Front. Immunol. Frontiers in Immunology Front. Immunol. 1664-3224 Frontiers Media S.A. 10.3389/fimmu.2025.1642001 Immunology Review Natural antidepressants in neuroimmunomodulation: molecular mechanisms, action targets, and therapeutic potential Lv Shimeng 1 † Kong Linghui 1 † Zhong Xia 2 † Shang Ruirui 3 Lu Yitong 1 Zhang Guangheng 1 Gao Haonan 1 Hou Xin 4 Li Guoqiang 5 * Yu Xiaowen 6 * 1 First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, China 2 Institute of Child and Adolescent Health, School of Public Health, Peking University, Beijing, China 3 College of Rehabilitation Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China 4 The Second Clinical College of Guangzhou University of Chinese Medicine, Guangdong, China 5 Department of Pain Medicine, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, China 6 Division 4 of Neurology Department, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, China

Edited by: Carolina Otero, Universidad Andrés Bello, Chile

Reviewed by: Benjamín Cárdenas, Universidad Andrés Bello, Chile

Cristian Arredondo, Universidad Andres Bello, Chile

*Correspondence: Xiaowen Yu, yuxiaowen@sdutcm.edu.cn; Guoqiang Li, star_guoqiang@163.com

†These authors have contributed equally to this work

 27 08 2025 2025 16 1642001 05 06 2025 11 08 2025 Copyright © 2025 Lv, Kong, Zhong, Shang, Lu, Zhang, Gao, Hou, Li and Yu. 2025 Lv, Kong, Zhong, Shang, Lu, Zhang, Gao, Hou, Li and Yu

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Depression is a major global public health issue, yet key bottlenecks remain in understanding its pathophysiological mechanisms, which significantly hinder breakthroughs in precision treatment strategies. Recent studies have highlighted the neuroimmune system as a primary pathogenic contributor to the onset and progression of depression. Meanwhile, natural products, characterized by multi-component synergy, multi-target activity, and multi-pathway regulation, have shown significant potential in regulating neuroimmunity. However, a systematic review of the role of neuroimmunity in the pathological process of depression and the therapeutic effects of natural products is still lacking. This review aims to comprehensively elucidate the core role of neuroimmunity in the pathological mechanisms of depression through literature analysis, explore in depth the molecular mechanisms and targets involved in natural product interventions, and critically evaluate the limitations and current challenges in clinical translation. Ultimately, this review provides a solid theoretical foundation and guidance for future research and the development of precision antidepressant therapies based on natural products.

 neuroimmunity immunoregulation depression natural product molecular biology function section-in-acceptance Immunological Tolerance and Regulation Introduction

Major depressive disorder (MDD), commonly referred to as depression, is one of the leading causes of disability worldwide. Its main features include significant physiological symptoms such as fatigue, weight loss, and decreased appetite. Currently, approximately 300 million people are affected by MDD globally, and its prevalence continues to rise, posing a significant public health burden (1). However, the underlying pathological and physiological mechanisms of MDD remain incompletely understood, which severely limits progress in developing precision treatment strategies. At present, first-line clinical treatment mainly relies on selective serotonin reuptake inhibitors, but these medications are often accompanied by adverse effects such as nausea. In addition, they often have a delayed onset of action, and the non-response rate remains relatively high (2, 3). Therefore, an in-depth analysis of the pathological mechanisms of MDD and the development of new antidepressants with rapid onset, sustained efficacy, and improved safety profiles has become a pressing and central challenge in the field of psychopharmacology.

The immune system plays a central role in the pathophysiological processes of MDD. Immune cells and the cytokines they secrete interact with the brain through the neuro-endocrine-immune network, influencing mood, cognition, and behavioral functions. The neuroimmune system contributes to the progression of depression through multidimensional mechanisms; Therefore, targeting neuroimmune regulation has become one of the key strategic directions in the development of novel antidepressant therapies (4–6). Natural products refer to bioactive substances derived from a wide range of sources, including animals, plants, insects, microorganisms, marine organisms, and endogenous substances in humans and animals. For decades, natural products and their derivatives have been widely studied in the context of health promotion and disease intervention due to their structural diversity, favorable safety profiles, and cost-effectiveness. Among them, numerous natural bioactive molecules have been shown to exert significant immunomodulatory effects (7, 8).

Recent advances in molecular biology have significantly accelerated research into the neuro-immunomodulatory mechanisms of depression, leading to a growing body of compelling evidence. Within this context, natural products have demonstrated unique and promising therapeutic potential in antidepressant strategies due to their characteristic multi-target, synergistic modulation. However, current research still faces critical challenges, including fragmented mechanistic understanding, an unclear network of action targets, and limited clinical translation. These issues severely hinder the development of novel natural antidepressants targeting neuroimmune pathways. This review aims to integrate the existing literature, systematically clarify the central role of the neuroimmune axis in the pathophysiology of depression, and summarize the molecular mechanisms by which natural compounds modulate neuroimmunity. In addition, it critically evaluates the limitations of current research. Ultimately, this review provides a theoretical foundation and offers direction for future research and the clinical translation of neuroimmune-targeted natural antidepressants.

 Review method

To investigate the pathological mechanisms of depression mediated by neuroimmunity and the neuro-immunomodulatory effects of natural products in treating depression, we conducted a comprehensive search of the PubMed, Web of Science, and ScienceDirect databases based on the PRISMA. The keywords used were “natural product,” “depression,” “major depressive disorder,” “neuroimmunity,” “neuroimmune modulation,” “antidepressant,” “neuroinflammation,” “proinflammatory cytokine,” “NLRP3 inflammasome,” “glial cells,” “microglia,” “astrocyte,” “microbial-gut-brain axis,” “programmed cell death,” “pyroptosis,” “autophagy,” “mitochondrion,” “neuroplasticity,” “synaptic plasticity,” “neurogenesis,” “epigenetics,” and “circadian rhythm.” Retrieve articles published from January 2000 to Jun 2025. The retrieved articles were reviewed by two independent reviewers based on their title, abstract, and full text, adhering to inclusion and exclusion criteria. The inclusion criteria included: (1) original articles written in English; (2) the article investigates the mechanisms by which natural products regulate neuroimmune therapy for depression. Exclusion criteria include: (1) articles written in any language other than English; (2) gray literature; (3) editorials; and (4) duplicate publications. After completing the literature search and screening process, a total of 227 articles were included in the final evaluation.

 Neuroimmunity and depression Immune dysregulation in depression

There is ample evidence suggesting the presence of peripheral and neuroimmune dysregulation in patients with depression. In the brains of suicidal patients with depression, upregulation of NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome expression has been observed (9). In patients with MDD, genes related to endoplasmic reticulum stress (ERS) and inflammasomes (such as NLRC4 and NLRP3) are significantly upregulated, suggesting that the enhancement of immune-inflammatory mechanisms in MDD may be closely related to the synergistic effects of organelle dysfunction (involving the endoplasmic reticulum and mitochondria) and inflammasome activation (10). Elevated levels of interleukin-6 (IL-6) and interleukin-8 (IL-8) in MDD patients, as well as abnormal functional connectivity between the prefrontal cortex (PFC), anterior cingulate cortex (ACC), visual cortex, postcentral gyrus, and striatum, suggest that inflammation may contribute to the neuropathological mechanisms of MDD by altering the functional connectivity of key brain regions such as the PFC (11). Moreover, pro-inflammatory cytokines, including tumor necrosis factor-alpha (TNF-α) and IL-1β, serve as important indicators reflecting systemic inflammatory status, offering objective and indispensable measures for evaluating the degree of immune activation in patients with MDD (1). In clinical studies, Li et al. found that the volume of gray matter in the right frontal gyrus is a key mediating factor between IL-1β levels and antidepressant response. IL-1β may indirectly reduce treatment efficacy by decreasing the volume of this brain region (12).

In addition, patients with MDD exhibit increased choroid plexus volume and decreased lymphatic system function, which are closely related to systemic inflammation and oxidative stress, and may contribute to the pathological process of MDD through immune mechanisms (13). In a recent cross-sectional study based on the National Health and Nutrition Examination Survey in the United States, it was found that the aggregate index of systemic inflammation (AISI) level has a U-shaped correlation with depression, and maintaining AISI within a reasonable range may help reduce the incidence of depression (14). A study investigating sex differences in patients with depression revealed that the association between inflammation and depression differs by gender, with female patients more likely to exhibit elevated levels of C-reactive protein and IL-6 (15). Systemic inflammation, as indicated by elevated IL-6 levels, may affect the severity and progression of depressive symptoms, especially in adolescent women (16).

Overall, there is a significant correlation between depression and immune homeostasis imbalance. Patients with depression exhibit immune dysregulation in both peripheral blood and the central nervous system (CNS). Further analysis of the key molecular mechanisms involved in neuroimmune interactions, particularly the elucidation of the biological effects of specific inflammatory mediators within the CNS, will help overcome the limitations of traditional antidepressant treatments that primarily target monoamine neurotransmitters. This will provide an important theoretical foundation for the development of precision treatment strategies based on immune regulation.

 Neuroimmune mediated pathological mechanism of depression Cytokine

In depression, there is a pathological phenomenon characterized by the upregulation of pro-inflammatory cytokines, as evidenced by a meta-analysis showing a significant increase in pro-inflammatory cytokines in patients with MDD (17). However, the potential molecular mechanisms underlying this phenomenon have not yet been fully elucidated.Interleukin-33 (IL-33), a tissue-derived nuclear cytokine from the IL-1 family, has been implicated in this process (18). Studies suggest that IL-33 may disrupt the coordination between hippocampal metabolic rhythms and circadian clock genes by activating inflammatory signaling and interfering with mitochondrial metabolism, ultimately leading to depression-like behavior (19). In addition, interleukin-1β (IL-1β) plays a significant regulatory role in the connection between the mid-frontal gyrus and the middle cingulate cortex/insula junction and depressive symptoms, suggesting that inflammation may serve as a bridge linking brain dysfunction and depressive symptoms (20). An imbalance between IL-1 receptor antagonist (IL-1ra) and IL-1β reduces the expression of the cAMP response element-binding protein (CREB)-brain-derived neurotrophic factor (BDNF) in the hippocampus and disrupts neurotransmission mediated by α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs), resulting in depression-like behavior (21). Knockout of IL-1β in the hippocampus significantly reduces lipopolysaccharide (LPS)-induced anxiety and depression-like behavior. IL-1β knockdown also inhibits oxidative and neuroinflammatory responses and upregulates vascular endothelial growth factor and BDNF levels in the hippocampus (22). Another essential pro-inflammatory cytokine involved in immune modulation is interleukin-18 (IL-18) (23). It has been reported that IL-18-deficient mice are more susceptible to stress, exhibiting significantly increased expression of inflammatory factors (TNF-α, IL-1β, and IL-6) in the hippocampus, along with increased numbers of activated microglia and astrocytes (24). During antidepressant treatments, such as Integrative Body-Mind-Sleep and Qigong interventions, significant reductions in depressive symptoms, sleep disturbances, and levels of IL-6 and IL-1β have been observed (25). A comprehensive analysis of existing evidence indicates that pro-inflammatory cytokines play a key regulatory role in the pathological progression of depression. Building upon this foundation, further exploration of the upstream molecular mechanisms regulating their release (such as the activation of the NLRP3 inflammasome pathway) may provide crucial insights into the multifaceted molecular processes underlying neuroimmune dysregulation in depression.

 NLRP3 signaling pathway

A cytoplasmic multiprotein complex known as the NLRP3 inflammasome responds to external environmental stress and cellular injury. Upon activation, the assembled NLRP3 inflammasome promotes the maturation and release of inflammatory cytokines, including IL-18 and IL-1β, by activating caspase-1 (26). NLRP3 is closely associated with depression. Chronic mild stress (CMS) activates the NLRP3 inflammasome, enhances the maturation and release of IL-1β, and subsequently triggers neuroinflammation, ultimately leading to depression-like behavior (27). Furthermore, the NLRP3 inflammasome contributes to LPS-induced depression-like behavior through the induction of indoleamine 2,3-dioxygenase (28). It is also involved in chronic unpredictable mild stress (CUMS)-induced Alzheimer’s disease-like pathological changes and related cognitive impairment (29). In addition, NLRP3 mediates the activation of inflammasomes, leading to depression-like behaviors caused by estrogen deficiency and hippocampal inflammation in mice (30). The expression of proteins related to the NLRP3 inflammasome pathway is significantly upregulated in the ischemic hippocampus of post-stroke depression (PSD) mice. However, when the hyperpolarization-activated cyclic nucleotide-gated cation channel 1(HCN1) was knocked out by injecting a virus into the hippocampus, the expression of NLRP3 inflammasome-related proteins in PSD mice decreased, and both anxiety- and depression-like behaviors were alleviated (31).

On the other hand, NLRP3 also mediates associated signaling pathways involved in the pathology of depressive symptoms. One key purinergic receptor that plays a central role in inflammation and immunity is the P2X7 receptor (P2X7R), which is expressed in almost all cells of the innate and adaptive immune systems. P2X7R mediates various key biological processes (32). In depression, rats exposed to CUMS exhibit upregulation of the P2X7R/NLRP3/IL-1β signaling axis and display depression-like behaviors (33). Moreover, CUMS activates P2X7R in microglia, triggering neuroinflammatory responses through the activation of the NLRP3 inflammasome and the release of inflammatory molecules such as IL-1β (34). Activation of P2X7R and the downstream NLRP3 inflammasome in hippocampal microglia also mediates depression-like behavior (35). Although psychological stress is known to contribute to emotional disorders such as depression, the underlying molecular mechanisms require further elucidation. Recent studies by Li et al. demonstrated that psychological stress activates the P2X7R/NLRP3 inflammasome pathway, leading to amygdala demyelination and oligodendrocyte dysfunction, ultimately resulting in emotional disturbances, particularly depression (36). These findings highlight the critical role of the P2X7R/NLRP3 signaling pathway in emotional disorders, especially depression. Therapeutically targeting this pathway, for example, through transcutaneous auricular vagus nerve stimulation, can suppress microglia-mediated neuroinflammation and alleviate diabetes-related depression induced by a high-fat diet via modulation of the P2X7R/NLRP3/IL-1β signaling pathway in the prefrontal cortex (37). In addition, NLRP3 mediates other signaling pathways relevant to depression. For example, in CUMS-induced depression-like behavior in mice, activation of the ERS-NLRP3 signaling pathway contributes to both depressive behavior and cognitive dysfunction (38). Silent Information Regulator 2 Homolog 1 (SIRT1), a member of the nicotinamide adenine dinucleotide (NAD+)-dependent deacetylase family, is closely associated with the onset and progression of inflammation-related disorders through the SIRT1/NLRP3 signaling pathway (39). Recent studies indicate that nicotinic acid may exert a protective effect against LPS-induced depression-like behavior in mice by modulating the SIRT1/poly (ADP-ribose) polymerase-1 (PARP-1)/NLRP3 signaling cascade (40). Melatonin alleviates LPS-induced acute depression-like behavior and suppresses NLRP3 inflammasome activation in microglia via the SIRT1/nuclear factor erythroid 2-related factor 2 (Nrf2) pathway (41).

In summary, the NLRP3 inflammasome and its associated inflammatory signaling pathways play significant roles in both the pathogenesis and potential therapeutic intervention of depression. Further elucidation of the specific molecular mechanisms underlying glial cell-mediated neuroinflammation will enhance our understanding of the pathophysiological mechanisms of CNS in depression from a multidimensional perspective.

 Microglia

Microglia are resident macrophages of the brain that play a vital role in immune surveillance and the maintenance of CNS homeostasis. They are functionally implicated in various cerebrovascular diseases by regulating neuroinflammatory responses and facilitating tissue repair processes (42). An integrated spatial and mononuclear transcriptomic analysis revealed that gene changes related to depression-like behavior were predominantly localized in microglia. In particular, a pro-inflammatory microglial subpopulation was identified, characterized by the expression of genes involved in neuroinflammation and potentially contributing to the pathology of depression through the activation of inflammatory pathways such as nuclear factor kappa B (NF-κB) (43). In the ACC, the innate immune receptors known as triggering receptors expressed on myeloid cells-1 and -2 (TREM-1/2) in microglia have been shown to mediate visceral hypersensitivity and depression-like behavior after colitis (44). Furthermore, early-life inflammation can impair the phagocytic capacity of microglia, potentially leading to maladaptive responses of ACC glutamatergic neurons to stress, thereby promoting the emergence of depression-like symptoms during adolescence (45). When early-life stress is combined with heightened cortisol reactivity, it may further exacerbate neuroimmune disturbances in adulthood. This is evidenced by increased microglial activation in the hippocampus and elevated expression of TNF-α and microRNA-342 (miR-342) (46).

Exposure to chlorpyrifos induces a primed state in microglia, rendering them more susceptible to subsequent stress, which then promotes their inflammatory activation. This sequence leads to impaired neural plasticity and the development of depression-like behavior in the hippocampus (47). Additionally, there is growing evidence that the NLRP3 inflammasome plays a pathogenic role within microglia. Specifically, activation of the glucocorticoid receptor (GR)-NF-κB-NLRP3 signaling pathway in hippocampal microglia has been shown to mediate neuroinflammation and promote depression-like behaviors under chronic stress conditions (48). Furthermore, Pan et al. demonstrated that IL-1β-related inflammation in the prefrontal cortex of depressed rats is mediated by microglial NLRP3 inflammasome activation in response to chronic stress (49). Similarly, depression-like behavior induced by streptozotocin (STZ) in diabetic mice may be associated with activation of the NLRP3 inflammasome, primarily within hippocampal microglia (50). In addition, retinal injury may initiate hippocampal microglial activation via the NLRP3/IL-1β pathway, leading to neuroinflammation and subsequent depression-like behavior (51).

Targeting microglia regulation offers promising therapeutic strategies for alleviating depressive-like behaviors. For instance, poly (ADP-ribose) polymerase 14 (PARP14) has been shown to inhibit microglial activation by promoting reactive oxygen species (ROS) clearance through nicotinamide nucleoside transhydrogenase (NNT), thereby reducing depression-like behavior in mice (52). Minocycline, a tetracycline antibiotic with broad anti-neuroinflammatory properties, readily crosses the blood–brain barrier (BBB) and inhibits the activation of pro-inflammatory microglia, exerting neuroprotective effects (53). In depression models, minocycline alleviates depression-like symptoms by blocking microglial activation and phagocytosis, which helps restore neurogenesis in the dorsal hippocampus (54). Furthermore, Forkhead box O3a (FOXO3a) regulates microglial phenotype by suppressing peroxisome proliferator-activated receptor gamma (PPAR-γ). Inhibition of FOXO3a can polarize microglia from the pro-inflammatory M1 phenotype to the anti-inflammatory M2 phenotype, thereby reducing hippocampal neuroinflammation and ameliorating depressive-like behaviors in LPS-induced mouse models (55).

 Astrocyte

Astrocytes are the most abundant glial cells in the CNS and perform a variety of essential homeostatic functions in vivo. These include supporting other CNS-resident cells, such as neurons, by buffering excess neurotransmitters and regulating synaptic activity and BBB integrity (56). In patients with MDD, astrocyte derived extracellular vesicles exhibit significantly elevated levels of pro-inflammatory cytokines such as IL-6, TNF-α, and IL-1β, indirectly reflecting the involvement of astrocytes in depressive neuropathology (57). Moreover, during depression, bidirectional interactions occur between astrocytes and microglia. Chronic social defeat stress (CSDS) induces microglial activation of P2X7Rs and subsequent IL-6 release, which binds to IL-6 receptors on astrocytes, triggering apoptotic pathways, reducing astrocyte numbers, and impairing their function—contributing to anxiety- and depression-like behaviors (58). In astrocytes lacking the sigma-1 receptor, the NF-κB inflammatory pathway is activated. Interactions between reactive astrocytes and activated microglia further amplify neuroinflammation and exacerbate stress-induced neuronal damage (59). In a mouse model of sepsis-associated encephalopathy, astrocytic A1 adenosine receptors mediate the pro-inflammatory effects of adenosine, promoting microglial activation, BBB disruption, peripheral immune cell infiltration, neuronal dysfunction, and depression-like behaviors (60). In astrocyte-specific Orai1 knockout mice, Orai1 deficiency significantly suppresses LPS-induced hippocampal cytokine release and microglial activation, while also preventing calcium signaling enhancement and metabolic disturbances in astrocytes (61). Additionally, in astrocyte-specific NR2C knockout mice, NR2C deficiency preserves the activity of the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt)/mechanistic target of rapamycin (mTOR) pathway, inhibits downstream NF-κB signaling, and maintains synaptic protein expression and dendritic spine integrity, thereby reversing LPS-induced synaptic damage (62). Furthermore, LPS stimulation increases Kir4.1 expression in astrocytes, enhances N-methyl-D-aspartate receptor activity via GluN2B phosphorylation, activates calpain-1 through calcium influx, and triggers the NLRP3 inflammasome, leading to IL-1β release, impaired synaptic plasticity, and depression-like behaviors (63).

In addition, several astrocyte-specific molecular mechanisms have been implicated in the regulation of neuroinflammation and the development of depression. The multiple endocrine neoplasia type 1 (Menin) gene in astrocytes regulates neuroinflammation by inhibiting the NF-κB/IL-1β pathway; functional deficiencies or genetic mutations in Menin may contribute to the onset of depressive disorders (64). The β-arrestin2-biased signaling pathway downstream of dopamine receptor D2 is significantly disrupted during the progression of depression. Notably, genetic deletion of β-arrestin2 exacerbates neuroinflammatory responses and promotes depression-like behaviors (65). Furthermore, neural precursor cell expressed, developmentally downregulated 4 (NEDD4)-like E3 ubiquitin protein ligase (NEDD4L) regulates P2X7R expression by ubiquitinating paired box 6, thereby modulating astrocyte function and neuroinflammatory signaling (66).

In summary, the glial cell system demonstrates a complex molecular network involved in the neuroimmunomodulation of depression. In particular, molecular interactions between microglia and astrocytes play a pivotal role in the neuroimmune pathogenesis and therapeutic targeting of depression. However, beyond these classical glial cell types, the functional heterogeneity and regulatory mechanisms of oligodendrocytes and their precursor cells within the neuroinflammatory microenvironment remain largely unexplored. Furthermore, expanding beyond a CNS-centric perspective to investigate the potential remote modulatory effects of peripheral organs (e.g., the gut) on CNS neuroinflammation may contribute to a more integrative understanding of systemic immune dysregulation in depression and offer novel theoretical perspectives for research and treatment.

 Microbial-gut-brain axis

The term MGB axis refers to a complex network of interconnected biological systems that enables bidirectional communication between gut microbiota and the brain. Maintaining homeostasis among the microbiota, CNS, and gastrointestinal tract is essential for overall health (67). Recent studies have revealed that individuals with MDD exhibit altered diversity and composition of gut microbiota, which strongly correlate with levels of inflammatory factors (68). Research into the relationship between gut microbiota and neuroimmune mechanisms shows that gut dysbiosis induces depression-like behavior via complement C3-mediated abnormalities in microglial synaptic pruning (69). Additionally, gut microbiota can modulate NLRP3 inflammasome involvement in the pathogenesis of depression. For example, CUMS can cause the dysbiosis of gut microbiota, increase harmful bacteria, disrupt the intestinal barrier, and permit bacterial metabolites such as LPS to enter the bloodstream. This activates NLRP3 inflammasomes in immune cells, exacerbates CNS inflammation, and triggers depression-like behavior (70). In addition, chronic ethanol exposure (CEE) induces gut microbiota dysbiosis and impairs gut homeostasis, resulting in elevated circulating LPS and inflammatory cytokines that activate hippocampal NLRP3 inflammasomes, resulting in neuroinflammation and depression-like symptoms (71). In NLRP3-deficient mice, gut microbiota regulates astrocyte dysfunction through circular RNA HIPK2, thereby ameliorating depression-like behavior (72).

The primary byproducts of microbial fermentation of dietary fiber are short-chain fatty acids (SCFAs), which are essential for maintaining immune function, neurological health, and metabolic balance (73). Shen et al. found that CEE leads to gut microbiota dysbiosis and reduces SCFA levels. This reduction damages gut structure and function, promotes CNS inflammation, disrupts the blood-brain barrier, causes neurological nutritional deficiencies, and leads to neuronal injury, ultimately resulting in anxiety- and depression-like behaviors. Importantly, fecal microbiota transplantation combined with SCFA supplementation significantly alleviates these adverse effects (74). In addition, in inflammatory bowel disease (IBD), perforin produced by colon CD8+ T cells promotes the expression of C-X-C motif chemokine ligand 9 (CXCL9), inducing ERS in hippocampal neurons and exacerbating depression associated with IBD (75). The splenic nerves may play a key role in LPS-induced depression-like phenotypes and inflammatory responses, while gut microbiota may regulate the function of microglia through the MGB axis, contributing to depression-like behaviors (76). Furthermore, mutations in the Fzd6 gene regulate the composition of gut microbiota by reducing the relative abundance of inflammation-related bacterial families such as Ruminococcaceae and Lachnospiraceae, which significantly mediates neuroinflammatory processes associated with depression (77).

In conclusion, the MGB axis plays a critical regulatory role in the onset and progression of depression through multiple mechanisms that alter the neuroimmune microenvironment, especially by mediating the aberrant activation of the NLRP3 inflammasome and microglia. Importantly, molecularly targeted interventions aimed at modulating the gut microbiota offer a crucial theoretical foundation for developing novel antidepressant therapies. Future research should integrate gut microbiome analysis, neuroimaging techniques, and molecular pharmacology to establish a multimodal research framework. This approach will systematically clarify the specific regulatory mechanisms of the MGB axis in depression and advance its potential as a therapeutic target.

 Programmed cell death

The development and homeostasis of multicellular organisms depend on regulating cell proliferation and the timely removal of harmful cells, such as damaged cells that may become cancerous or cells exploited by pathogens. This process is primarily achieved through PCD (78). PCD includes apoptosis, autophagy, and pyroptosis, all involving tightly regulated gene expression events (79). Pyroptosis is a lytic and inflammatory form of PCD, typically triggered by inflammasomes and executed by gasdermin (GSDM) proteins (80). In endocrine diseases, hyperglycemia induces apoptosis and pyroptosis of hippocampal neurons via an NLRP3-dependent pathway, which is associated with depression-like symptoms in STZ-induced diabetes models (81). In depression, deficiency of Kir6.1 activates the NLRP3 inflammasome through excessive accumulation of mitochondrial ROS, triggering caspase-1-dependent cleavage of gasdermin D (GSDMD), leading to astrocyte pyroptosis and the release of the pro-inflammatory cytokine IL-1β (82). Similarly, Li et al. found that CMS induces hippocampal astrocyte pyroptosis via activation of the NLRP3/caspase-1/GSDMD signaling pathway, causing a reduction in astrocyte numbers and depression-like behavior (83). In addition, knockout of the NLRP3 gene in astrocytes ameliorates depression-like pathology in mice with mild traumatic brain injury by inhibiting astrocytic pyroptosis (84). Methamphetamine exposure activates the NLRP6 inflammasome in astrocytes through regulation of miR-152, leading to caspase-1 cleavage, maturation and release of IL-1β and IL-18, and GSDMD pore formation on the plasma membrane. This triggers pyroptosis and results in pathological behaviors including depression (85). Moreover, ghrelin reduces neuroinflammation and alleviates depression-like behavior by inhibiting activation of the NLRP2/NLRP3 inflammasomes and pyroptosis in astrocytes (86).

Autophagy is a cellular process that enables the degradation and recycling of proteins and organelles to maintain cellular homeostasis (87). Dysfunctional autophagy worsens neuroinflammatory responses and induces depression-like behavior through the NLRP1-PI3K/Akt/mTOR signaling axis (88). The autophagy process is related to the activation of NLRP3 inflammasomes. Impaired lysosomal function within the autophagy-lysosome pathway can delay the degradation of NLRP3 inflammasomes, promoting the production of pro-inflammatory cytokines and leading to depressive behavior in CUMS mouse models (89). The high mobility group box 1/signal transducer and activator of transcription 3/p65 axis plays a key role in chronic stress-induced depression by driving microglial activation and autophagy (90). In addition, melatonin reduces autophagic damage by regulating FOXO3a, thereby preventing neuroinflammation and alleviating depressive symptoms (91). In summary, pyroptosis and autophagy-related regulatory mechanisms within PCD play significant roles in neuroinflammatory responses. Emerging research suggests their involvement in the pathological progression of depression and therapeutic outcomes. However, a systematic understanding of the specific molecular mechanisms underlying autophagy and pyroptosis in neuroinflammation, as well as their potential crosstalk, is currently lacking. There is an urgent need to deeply explore their intrinsic connections and synergistic interaction networks.

 Mitochondrion

Mitochondria are essential organelles found in most eukaryotic cells, responsible for key physiological processes such as energy production, signal transmission and regulation, maintenance of intracellular calcium balance, and ROS generation. When mitochondrial biogenesis is impaired, ROS levels increase, mitochondrial autophagy is impaired, and mitochondrial dynamics are altered, leading to mitochondrial dysfunction (92). Recent studies have shown that CUMS alters inflammation and brain mitochondrial activity, causing rats to exhibit depression-like behaviors. The mitochondrial function marker ATP is negatively correlated with levels of pro-inflammatory cytokines (93). This suggests a potential link between mitochondria and neuroinflammation in depression. Mechanistically, TNF-α inhibits NIP3-like protein X-mediated mitochondrial autophagy, leading to mitochondrial dysfunction and synaptic defects that trigger passive stress responses (94). Chronic restraint stress (CRS) increases cell-free mitochondrial DNA levels, activating the Toll-like receptor 9 signaling pathway, which induces neuroinflammation and social behavior deficits (95). Furthermore, mitochondrial uncoupling protein 2 (UCP2) regulates the ROS-thioredoxin-interacting protein (TXNIP)-NLRP3 signaling pathway to mediate NLRP3 inflammasome activation in astrocytes. UCP2 deficiency worsens CMS-induced depression-like behaviors, impairs neurogenesis, and causes astrocyte loss (96). O-[3-piperidino-2-hydroxy-1-propyl]-nicotinic acid amidoxime dihydrochloride (BGP-15) alleviates depression-like behavior by promoting PTEN-induced putative kinase 1/Parkin-dependent mitophagy, which mitigates LPS-induced mitochondrial dysfunction, neuroinflammation, and neuronal apoptosis (97).

 Neuroplasticity

Neuroplasticity is fundamental to brain development, learning, and CNS homeostasis (98). Neuroinflammation affects neuronal plasticity in the basolateral amygdala (BLA), leading to behaviors resembling anxiety and depression. For instance, LPS induces anxiety- and depression-like behaviors by activating microglia in the BLA, which enhances excitatory synaptic transmission and increases intrinsic neuronal excitability (99). In addition, chronic stress triggers inflammation induced by microglia and macrophages, worsening defects in synaptic phagocytosis and neuronal plasticity, leading to neurological dysfunction and depression-related behaviors (100). The transcription factor nuclear receptor subfamily 4 group A member 2 (Nr4a2), predominantly expressed in CNS neurons, plays a vital role in synaptic plasticity (101). Recent studies show that Nr4a2 can modulate depression-like behavior induced by LPS by reducing the morphological and functional damage caused by chronic neuroinflammation to microglia and calcium/calmodulin-dependent protein kinase II (CaMKII)-expressing neurons (102).

Downregulating mammalian STE20-like kinase 1 in the hippocampus significantly alleviates depression-like behavior and restores synaptic plasticity impaired by chronic stress by inhibiting the p38 signaling pathway and neuroinflammation (103). Targeting phosphatase and actin regulator 4 (Phactr4) also reverses chronic stress-induced depression-like behavior in rats by regulating neuroinflammation and neuroplasticity (104). Sleep deprivation reduces depression-like behavior in CRS mice by reducing neuroinflammatory responses in the ACC and improving neuroplasticity in both the PFC and ACC (105). Pharmacologically, activation of BDNF/tropomyosin receptor kinase B (TrkB) signaling improves synaptic plasticity and suppresses pro-inflammatory cytokine expression, resulting in rapid antidepressant-like effects (106). Leflunacetam ameliorates LPS-induced synaptic plasticity deficits and neuroinflammation by activating the BDNF/TrkB-mediated PI3K/Akt/mTOR signaling pathway (107). Additionally, pramipexole improves the depressive behavior in diabetic rats by inhibiting NLRP3 inflammasome-mediated neuroinflammation and protecting neural plasticity (108).

 Other types

Epigenetics is the study of heritable changes in gene expression caused by modifications that do not alter the DNA sequence itself (109). One key mechanism is DNA methylation, which regulates numerous cellular processes (110). In patients with MDD, five significant differential methylation positions were identified in the NLRP3 gene. The methylation levels at these sites correlated with abnormal changes in cortical thickness across the occipital, parietal, temporal, and frontal lobes, suggesting that NLRP3 inflammasome-associated neuroinflammation may mediate brain structural remodeling through epigenetic mechanisms (111). Moreover, immunomethylation patterns serve as a potential tool to stratify immune-related subtypes of MDD (112). Abnormal hydroxymethylation of the BDNF gene in the hippocampus, driven by neuroinflammation, is another important epigenetic factor associated with depression-like behavior (113). Furthermore, epigenetics-related circular RNAs may contribute to depression pathogenesis. For instance, Cai et al. found that circular RNA ubiquitin conjugating enzyme E2 K (circ-UBE2K) promotes aberrant microglial activation and neuroinflammation by binding to heterogeneous nuclear ribonucleoprotein U and regulating UBE2K expression, thus contributing to MDD development (114). Polycomb group 1 alleviates neuroinflammation and improves depressive behaviors by epigenetic inhibition of matrix metalloproteinase 10 (MMP10) expression in microglia (115).

In living organisms, the metabolism of carbohydrates, lipids, proteins, and other substances follows a circadian rhythm to maintain the energy supply and material circulation necessary for normal biological functions. Circadian rhythms are crucial for organismal health but can be disrupted by pathological conditions, which may accelerate disease progression and create a vicious cycle (116). Brain and muscle ARNT-like protein 1 (BMAL1) is an important transcription factor that regulates these circadian rhythms (117). LPS triggers an “inflammatory storm” by activating microglia, disrupting the balance of circadian rhythm genes, particularly BMAL1, and promoting depression-like behavior by impairing synaptic plasticity and hypothalamic-pituitary-adrenal axis function (118). In addition, acute sleep deprivation in mice causes dysregulation of circadian rhythm-related gene expression and imbalances in gut microbiota, leading to excessive neuroinflammation and depression-like behaviors (119).Period genes 2 mediate the association between neuroinflammation and depressive behavior by affecting the expression of BMAL1 and its regulation of chemokine (C-C motif) ligand 5 (RANTES) (120). Exposure to polystyrene microplastics induces depression-like behavior in zebrafish by disrupting core circadian clock genes and triggering overactive neuroinflammation, marked by increased pro-inflammatory cytokines and microglial activation (121). In models with disrupted circadian rhythms, agomelatine has been shown to alleviate depression-like behavior, inhibit neuroinflammation, and promote hippocampal neurogenesis (122) ( Figure 1 ).

Neuroimmune mediated depression. In a healthy brain, the BBB remains structurally intact, neuronal functions are normal, neurotransmitter homeostasis is maintained, and glial cells show no signs of aberrant activation or damage. Conversely, in the context of depression under stress, BBB integrity is compromised. This breach allows peripheral harmful agents to enter the CNS, triggering aberrant microglial activation. Consequently, associated inflammatory signaling pathways become hyperactive, ultimately leading to neuronal injury. CNS, central nervous system. ATP, Adenosine Triphosphate. LPS, lipopolysaccharide. NF-κB, nuclear factor-kappaB. GSDM, gasdermin.

Diagram comparing healthy and depressed brains. The healthy brain shows neurogenesis, stable neural plasticity, and neuroprotective signaling with a stable blood-brain barrier. The depressed brain highlights stress-induced neuroinflammation, damage to the blood-brain barrier, and overactive inflammation pathways. Key elements include neurons, astrocytes, microglia, synapses, and capillaries, showcasing cellular interactions and differences in immune responses, such as the activation of microglia and inflammasomes.

In summary, research on the molecular mechanisms underlying neuroinflammation in depression reveals a complex pathological network involving coordinated interactions across multiple systems. Pro-inflammatory cytokines, inflammasome activation, and dysfunctional glial cells form the core pathological basis of neuroinflammation in depression. Key biological processes, such as mitochondrial dysfunction, disruption of the MGB axis, abnormal PCD, impaired neuroplasticity, epigenetic modifications, and circadian rhythm disturbances, contribute to the progression of depression by causing imbalances within neuroinflammatory networks, either directly or through cascading effects. Importantly, targeted modulation of these interconnected molecular pathways represents a promising direction for the development of developing novel antidepressant therapies.

Under this research framework, the multi-target regulatory strategy based on natural products demonstrates unique advantages. By systematically investigating how natural bioactive compounds modulate neuroinflammatory pathways, this approach not only deepens our understanding of the molecular pathology underlying depression but also identifies lead compounds with clearly defined therapeutic targets for clinical translation. This integrated research paradigm, combining molecular mechanism exploration with natural product-based drug development, holds promise for advancing antidepressant discovery from single-target interventions to innovative multi-system regulation. Such progress may provide a strong scientific foundation for overcoming current limitations in antidepressant therapy.

 Molecular mechanism of natural product Flavonoids

Flavonoids, as specialized plant secondary metabolites, are low-molecular-weight natural compounds known for their broad-spectrum bioactivities, including anticancer, antioxidant, and anti-inflammatory effects (123). Bavachin, a natural flavonoid extracted from Fructus Psoraleae, inhibits the NF-κB pathway by targeting protein kinase C delta. This action reduces neuroinflammation and oxidative stress, thereby improving the survival and function of diabetic neurons and ultimately alleviating diabetes-induced depressive behavior in mice (124). Schaftoside, found in traditional Chinese herbs such as Dendrobium nobile, exerts antidepressant effects by decreasing pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α) in the serum and hippocampus of mice (125). Phloretin, a natural dihydrochalcone primarily isolated from apples, inhibits the NF-κB-C3 axis and microglia-mediated synaptic phagocytosis, providing neuroprotection in depression models (126). Quercetin, a flavonoid abundant in fruits and vegetables, suppresses neuroinflammation and alleviates LPS-induced depressive symptoms by modulating the NLRP3/NF-κB/inducible nitric oxide synthase (iNOS) signaling pathway in microglia (127). Astragolin is a flavonoid glycoside derived from Astragalus sinicus L. It effectively improves LPS-induced depressive-like behavior through maintenance of BBB integrity, inhibition of microglial activation, reduction of pro-inflammatory cytokines, and regulation of the receptor-interacting serine/threonine-protein kinase 1 (RIPK1)/RIPK3/mixed lineage kinase domain-like protein (MLKL) and mTOR/NF-κB inflammatory signaling pathways (128). Baicalin, extracted from dried roots of Scutellaria, has been shown through network pharmacology to regulate neuroinflammation, apoptosis, and oxidative stress, contributing to its antidepressant effects (129). In addition, baicalin can inhibit the activation of the glycogen synthase kinase-3 beta (GSK3β)/NF-κB/NLRP3 pathway, promoting neuronal maturation and protecting against neuronal damage, thereby alleviating CUMS-induced depression-like behavior (130).

Hyperoside is a flavonol glycoside found in various herbs, including Artemisia capillaris (131). It downregulates pro-inflammatory cytokine levels in the serum, intestinal tissue, and hippocampus, while also improving gut microbiota dysbiosis and SCFA concentrations caused by CRS (132). In addition, hyperoside alleviates microglial polarization and neuroinflammation through the thioredoxin-1/NLRP1/caspase-1 signaling pathway, thereby reducing depression-like behavior in CSDS mice (133). Seabuckthorn (Hippophae rhamnoides L.) is an excellent dietary source of flavonoids. Flavonoids derived from seabuckthorn can alleviate CUMS-induced gut microbiota disruption and downregulate inflammation-related factors (134). Kaempferol, a naturally occurring flavonoid present in many fruits and vegetables (such as onions, broccoli, strawberries, and grapes),and traditional Chinese medicines like Ginkgo biloba (135). It inhibits NLRP3 inflammasome activation and improves depression-like behavior by modulating microglial polarization and shifting the balance between PPARγ and signal transducer and activator of transcription 1 (STAT1) signaling pathways (136). Furthermore, Kaempferol-3-O-sophoroside not only improves depression-like behavior in mice but also promotes BDNF production in the hippocampus and induces autophagy to reduce NLRP3-mediated neuroinflammation (137).

Puerarin is the main bioactive compound extracted from Pueraria lobata (138). It can alleviate gut microbiota dysbiosis, inhibit the expression of pro-inflammatory cytokines and NF-κB in rats, and effectively treat depression (139). Puerarin generally exhibits low toxicity in both animals and humans. Among its adverse reactions, febrile responses are most common, followed by drug-induced dermatitis and hemolytic reactions. Although the incidence of hemolytic reactions combined with anaphylactic shock is extremely low, this potentially life-threatening complication poses a significant clinical risk for the use of puerarin (140). Therefore, further systematic evaluation of puerarin’s toxicity and potential side effects is recommended. Neohesperidin, a citrus-derived flavonoid, acts as a health-promoting phytochemical due to its diverse bioactivities and favorable safety profile. Its antidepressant effects are mediated through modulation of the NLRP3 inflammasome pathway (141). Luteolin, a flavonoid widely distributed in plants such as honeysuckle, is primarily found in fruits, vegetables, and medicinal herbs (142). It alleviates CRS-induced depressive behaviors by promoting PPARγ-dependent Arg-1+ microglial polarization, which suppresses neuroinflammation and reverses phagocytosis-driven synaptic pruning (143). Luteolin has demonstrated a favorable safety profile in clinical settings, with no significant adverse reactions reported in preclinical studies or human trials (144). However, its long-term safety and potential risks still need to be systematically validated through multi-center, large-sample clinical studies, especially regarding its use in populations with special physiological conditions. Establishing a comprehensive evidence-based medicine framework is necessary to address these concerns.

 Terpenoids

Terpenes represent the largest class of plant-derived natural products, characterized by diverse chemical structures and a wide range of biological activities (145). 5-O-methylvisammioside, extracted from Saposhnikoviae Radix, inhibits NF-κB pathway activation and alleviates depression-like behavior by targeting SRC kinase (146). Carvacrol, a monoterpene found in the essential oils of aromatic plants such as Origanum vulgaris and Thymus vulgaris, reduces oxidative stress and decreases hippocampal IL-1β and TNF-α levels, thereby improving depression-like behavior induced by CUMS (147). Escin, a natural triterpenoid saponin from Aesculus chinensis (Suoluozi), alleviates CUMS-induced depression-like behaviors by modulating both the BDNF/TrkB/CREB and Toll-like receptor 4 (TLR4)/Myeloid differentiation factor 88 (MyD88)/NF-κB signaling pathways (148). Hyperibone J, a bioactive compound from Hypericum bellum, exerts antidepressant effects by adenosine kinase (ADK)-mediated suppression of P2X7R/TLR4-driven neuroinflammation in microglia (149). Total triterpenoids from Rosa roxburghii, primarily Kaji-ichigoside F1, demonstrate neuroprotective effects by activating the PPARγ/C-X3-C motif chemokine receptor 1 (CX3CR1)/Nrf2 pathway and inhibiting the NF-κB/NLRP3 signaling cascade to ameliorate LPS-induced depression-like behaviors (150). Yomogin, a sesquiterpenoid from Artemisia iwayomogi, mitigates LPS-induced depression by suppressing glial activation, pro-inflammatory cytokine expression, and mitogen-activated protein kinase (MAPK)-mediated neuroinflammation (151). Oridonin, a diterpenoid isolated from Rabdosia rubescens, exerts antidepressant effects by disrupting the interaction between NLRP3 and NEK7, thereby inhibiting neuroinflammation and autophagy impairment (152). Lycopene, a potent lipophilic antioxidant abundant in tomatoes, alleviates hippocampal microglial pyroptosis in chronic stress models by inhibiting the cathepsin B/NLRP3 pathway (153, 154).

Patchouli alcohol, the active constituent of Pogostemon cablin, exhibits anti-inflammatory and neuroprotective properties. It improves microglia-mediated neurogenesis impairment by inhibiting NLRP3 inflammasome activation, contributing to its antidepressant effects (155). Aucubin, an iridoid glycoside found in Eucommia ulmoides, has been shown by Liu et al. to alleviate depression-like behaviors in CUMS mice by targeting the GR/NF-κB/NLRP3 signaling pathway (156). Geniposide, an iridoid compound abundant in Gardenia jasminoides, mitigates inflammatory responses and abnormal glucose metabolism in depressed mice (157). However, due to its toxicity profile, geniposide dosage should be strictly controlled in clinical settings to balance efficacy and safety. Its pharmacokinetics vary with administration routes and disease models (158). Therefore, personalized dosing strategies based on metabolic and distribution parameters are recommended to optimize treatment and achieve precision medicine goals. Paeoniflorin, a water-soluble monoterpene glycoside and the main active ingredient of Paeonia lactiflora Pall (159), exerts antidepressant effects through multiple mechanisms. It reduces neuroinflammation by inhibiting microglia-induced caspase-11-dependent pyroptosis, suppresses NLRP3 inflammasome activation by promoting mitophagy, and modulates the SIRT1-NF-κB-NLRP3/pyroptosis axis to attenuate microglial activation (160–162). Acute toxicity of paeoniflorin is relatively low, with subacute and chronic toxicity studies showing minimal adverse effects. Experimental data indicate no significant genetic toxicity or mutagenicity (163). However, given the complexity of plant-derived natural products, long-term safety monitoring and in-depth drug interaction studies are essential to fully assess their safety profiles and potential clinical risks.

 Phenolic

Phenolic natural products are a diverse class of organic compounds widely found in nature. These secondary metabolites occur in plants, microorganisms, and some animals, exhibiting a broad range of biological activities and therapeutic potential. For example, Rhodomyrtone, a natural phenolic compound extracted from Rhodomyrtus tomentosa, improves depression-like behavior by reducing TNF-α and TNF receptor 1 expression, inhibiting astrocyte activation, and decreasing neuronal apoptosis (164). Resveratrol, a naturally occurring polyphenol abundant in grapes (165), plays a significant role in treating inflammatory depression. Its antidepressant effect is closely linked to an anti-inflammatory pathway mediated by hippocampal type 2 bitter taste receptors (166). In addition, resveratrol can alleviate inflammation and anxiety-like depression caused by maternal-infant separation by activating the Sirt1/NF-κB pathway (167). However, resveratrol has low oral bioavailability, and high doses may pose risks of nephrotoxicity and liver damage (168). Therefore, future research should focus on optimizing pharmacokinetics, exploring the molecular mechanisms of toxicity, and developing advanced drug delivery systems. Polydatin, a resveratrol derivative from Polygonum cuspidatum, alleviates depression-like behavior induced by CUMS primarily by inhibiting neuroinflammation and oxidative stress via the NF-κB and Nrf2 pathways (169). Paeonol, a small-molecule polyphenol mainly extracted from the traditional Chinese medicine Cortex Moutan, reduces neuroinflammation by suppressing the hypoxia-inducible factor 1 alpha signaling pathway in microglia, thereby alleviating depression (170).

Punicalin, a polyphenol found in pomegranate fruits, inhibits the TLR4/NF-κB signaling pathway and alleviates LPS-induced pathological behaviors, including depression (171). Raspberries, globally known for their pleasant flavor, contain raspberry ketone, a phenolic compound that reduces LPS-induced depression-like behaviors in mice by inhibiting the TLR4/NF-κB pathway and modulating the MGB axis (172). Magnolol, a natural phenolic compound derived from Magnolia officinalis, alleviates CUMS-induced depression by suppressing pro-inflammatory M1 microglial polarization and promoting anti-inflammatory M2 polarization through the Nrf2/heme oxygenase-1 (HO-1)/NLRP3 signaling pathway (173). Gastrodin, the primary phenolic glycoside from Gastrodia elata, mitigates LPS-induced neuroinflammation by modulating the Arg-1+ microglial phenotype via regulation of Nrf2 (174). Licochalcone A, a phenolic compound found in licorice, reduces gliosis, regulates microglial polarization, improves synaptic plasticity, and prevents cognitive decline and depression-like behavior caused by LPS (175).

 Saponin

Saponins are a class of amphiphilic compounds with diverse structures, widely distributed in many popular herbal plants (176). Akebia saponin D, a triterpenoid extracted from Dipsacus asper, preserves hippocampal neurogenesis by suppressing microglial inflammation through the PI3K/Akt signaling pathway, thereby improving depression-like behaviors and cognitive deficits in mice (177). Quinoa saponin shows potential as a natural dietary supplement for the treatment and prevention of anxiety and depression by regulating the MGB axis and inhibiting the activation of the TLR4/MyD88/NF-κB pathway (178). Saikosaponins, a group of triterpenoid saponins mainly derived from Radix Bupleuri (179), exert antidepressant effects primarily by reducing P2X7 expression in the brains of depressed mice, lowering central inflammation, and significantly inhibiting neuronal pyroptosis (180). Specifically, Saikosaponin A alleviates depressive symptoms by inhibiting hippocampal inflammation, increasing monoamine neurotransmitter levels, and modulating gut microbiota composition (181). Saikosaponin B2 also improves depression-like behavior by reducing microglial activation via the TLR4/NF-κB pathway, preventing ferroptosis, maintaining calcium homeostasis, and alleviating ERS (182). Saikosaponin C ameliorates CSDS-induced depression-like behaviors by inhibiting DNA methyltransferase 1, thereby decreasing IL-6 methylation and expression, while enhancing synaptic plasticity (183). Despite these neuroimmune regulatory effects, Saikosaponins carry potential risks of liver injury, and their pharmacological and toxicological effects are dose-dependent. High doses also pose a risk of nephrotoxicity (184). Therefore, future research should focus on defining the therapeutic window through systematic toxicology studies, establishing dosage guidelines balancing efficacy and safety, and elucidating the molecular mechanisms underlying liver and kidney toxicity, providing a theoretical basis for their rational clinical use.

Gypenosides from Gynostemma pentaphyllum ameliorate LPS-induced depressive behaviors through multitarget mechanisms, including normalizing systemic inflammation, modulating glial polarization, restoring hippocampal synaptic plasticity, and inhibiting PFC NLRP3 signaling to reinstate neurohomeostasis (185). Gypenosides-14 suppress pro-inflammatory cytokine expression, inhibit astrocyte activation, and attenuate hyperactivation of the NF-κB pathway (186). Ginsenosides are natural triterpenoid saponins obtained from different parts of ginseng, with diverse pharmacological activities such as anti-aging, immune regulation, and cognitive improvement (187). In antidepressant treatment, Ginsenoside Rb1 regulates mitochondrial autophagy and the NF-κB pathway, inhibits astrocyte pyroptosis, and maintains neural homeostasis by suppressing inflammation and enhancing synaptic plasticity (188). Ginsenoside Rc exerts antidepressant effects by modulating neuroinflammation, astrocyte-microglia crosstalk, and apoptosis pathways in the prefrontal cortex (189). Ginsenoside Re significantly reduces pro-inflammatory cytokine expression, inhibits microglial overactivation, and regulates BDNF signaling, thereby protecting neurons (190). Although certain ginsenosides have accumulated substantial scientific evidence supporting their safety and efficacy, their pharmacokinetic properties still require optimization. Current challenges include imbalanced or suboptimal solubility profiles (water versus lipid solubility) and metabolic instability, which limit their bioavailability in translational medical applications (191). To address these limitations, it is urgent to enhance their bioavailability and pharmacokinetic stability through formulation technology innovations, structural modifications, and the development of novel drug delivery systems.

 Carbohydrates

Morinda officinalis is one of the four famous herbs in southern China (192). Morinda officinalis oligosaccharides (MOOs) have been used to treat mild and moderate depressive episodes. In preclinical studies, MOOs alleviate depression-like behaviors in PSD rats, mainly by regulating the NLRP3 inflammasome in microglia (193). In addition, MOOs inactivate the MyD88/PI3K pathway through E2F transcription factor 2 (E2F2), thereby reducing inflammation and depression-like behavior induced by CMS (194). In hypertension complicated with depression, astrocytes trigger neuroinflammatory responses due to mitochondrial damage, and MOOs upregulate Mitofusin 2 (Mfn2) expression, activating mitochondrial autophagy via the PI3K/Akt/mTOR pathway to clear damaged mitochondria in astrocytes (195). The antidepressant effects of Eucommiae cortex polysaccharides involve modulation of the MGB axis, including improvement of CUMS-induced gut dysbiosis by increasing Lactobacillaceae abundance and reducing LPS release, while simultaneously inhibiting microglia-mediated TLR4/NF-κB/MAPK signaling to attenuate neuroinflammation (196). Inulin, a soluble dietary fiber widely present in plants such as Jerusalem artichoke (197), protects the integrity of the intestinal barrier and blood-brain barrier, regulates TLR4/MyD88/NF-κB signaling to alleviate neuroinflammatory responses, and enhances CREB/BDNF signaling to promote neurogenesis and synaptic plasticity (198). Similarly, Rattan Pepper Polysaccharide (RPP) modulates the MGB axis by improving dextran sulfate sodium salt (DSS)-induced gut microbiota dysbiosis and SCFA disturbances, while restoring intestinal Th17/Treg homeostasis. In the brain, RPP mitigates neuroinflammation by suppressing the TLR4/NF-κB signaling pathway and enhances synaptic function through activation of CREB/BDNF signaling, thereby alleviating brain inflammation triggered by gut-derived inflammatory factors crossing the BBB and improving depression-like behaviors (199). In summary, current research indicates that natural saccharide compounds exert antidepressant effects by modulating the TLR4/NF-κB signaling pathway and MGB axis function to correct neuroinflammation-mediated immune imbalances. However, much remains to be explored in this field. Future studies should systematically clarify the biological functions and mechanisms of additional saccharide molecules in neuroimmune regulation.

 Alkaloid

Alkaloids are chemical molecules characterized by cyclic structures containing one or more basic nitrogen atoms (200). Higenamine, one of the earliest discovered benzylisoquinoline alkaloids, is known for its cardiotonic effects and was originally isolated from the traditional Chinese medicine Aconiti Lateralis Radix Praeparata (201). Higenamine can alleviate the inflammatory response following chronic unpredictable stress in rats by downregulating pro-inflammatory cytokine levels and improving astrocyte gap junctions (202). Arecoline, a bioactive alkaloid extracted from Areca nuts, reduces pro-inflammatory markers such as IL-1β and LPS in serum and colon, while enhancing hippocampal neural plasticity through increased expression of BDNF and postsynaptic density protein-95 (203). Matrine, a quinolizidine alkaloid derived from the traditional Chinese herb Sophora alopecuroides, acts on the MGB axis by modulating gut microbiota and metabolites, restoring intestinal barrier integrity, and reducing intestinal inflammation. This leads to decreased levels of pro-inflammatory cytokines in peripheral circulation and brain regions, along with upregulation of BDNF expression in the brain (204). Tabersonine is a natural alkaloid isolated from the medicinal plant Catharanthus roseus (205). In preclinical mouse models, tabersonine effectively inhibits NLRP3 inflammasome-mediated signaling, downregulates pro-inflammatory cytokine expression, inhibits the activation of microglia, and significantly improves LPS-induced depression-like behaviors (206).

Berberine is the main bioactive component of Rhizoma coptidis (207). Yang et al. found that berberine restricts NLRP3 inflammasome activity by promoting the binding of tripartite motif (TRIM)-containing protein 65 to NLRP3, enhancing NLRP3 ubiquitination, and reducing functional damage to hippocampal neurons in CUMS mice (208). In addition, in corticosterone-induced depression-like behavior, berberine inhibits NLRP3 inflammasome activation to alleviate neuroinflammation and rescues neuronal degeneration by improving synaptic plasticity and neurogenesis (209). In summary, berberine exerts its antidepressant effects mainly through targeted modulation of the NLRP3 inflammasome. However, whether it produces synergistic effects through other neuroimmune regulatory pathways requires further validation by multifaceted studies. From a safety perspective, berberine demonstrates a favorable profile at conventional therapeutic doses, although some patients experience transient gastrointestinal reactions such as diarrhea or constipation (210). Nevertheless, future research should focus on establishing a comprehensive systematic toxicological assessment and further investigating the compound’s in vivo metabolism to provide a stronger scientific basis for its rational clinical use.

 Other types

Betaine is abundant in various sources, such as sugar beet (211). Betaine protects nerves against Methamphetamine-induced nerve injury by suppressing the activation of the NLRP3 inflammasome pathway in the hippocampus, lowering IL-1β and TNF-α production, relieving pathogenic activation of microglia, and enhancing synaptic plasticity (212). In addition, betaine can significantly improve pain-related depression-like behavior induced by complete Freund’s adjuvant, specifically by regulating the phenotypic polarization of microglia and astrocytes, as well as modulating the expression of pro-inflammatory cytokines in the hippocampus (213). Schisandra has been a herbaceous plant resource with dual medicinal and edible functions since ancient times. It has multiple health and therapeutic effects (214). One of its potential natural compounds, Schisandrin B, downregulates the NF-κ B/TLR4/MyD88 signaling pathway and MAPK signaling pathway through miR-124, restoring M1/M2 balance and alleviating depressive symptoms (215).Schisandra chinensis Lignans can promote polarization of microglia towards the M2 phenotype, thereby exerting neuroprotective effects by activating the cannabinoid receptor type-2/STAT6 signaling pathway, and further exerting antidepressant effects (216). Arctiin is the main bioactive component of Fructus arctii. In depression, arctiin can bind to P2X7R to exert neuroprotective effects, thereby inhibiting the P2X7R/NLRP3 inflammasome signaling pathway (217). Yamogen is a natural compound with bioactive properties obtained from the Dioscorea species. It inhibits ERS and microglial activation, providing antidepressant benefits in an LPS-induced depression paradigm (218). Cajaninstilbene acid is a stilbene compound isolated from pigeon pea. It can alleviate depression like behavior in mice by inhibiting TLR4/NF-κ B mediated neuroinflammation and enhancing autophagy (219). Fucosterol is a plant sterol typically extracted from alginate. It has been confirmed that fuchosterol has anti-inflammatory activity. For example, in depression, fucosterol can regulate the activity of the MAPK/extracellular signal regulated kinase (ERK) 1/2 signaling pathway to inhibit microglial activation and neuroinflammation, thereby improving depression-like behaviors (220).

 Herbal extracts

Herbal extracts are natural and widely available active small-molecule ingredients commonly used to treat various diseases (221). Withania somnifera (L.) Dunal, known as Ashwagandha, is a small woody subshrub native to India, North Africa, and the Middle East. Its root extract suppresses the expression of inflammation-related proteins such as cyclooxygenase-2, iNOS, IL-6, IL-1β, and TNF-α, while modulating neuroendocrine and neurotransmitter systems to exert neuroprotective effects in mouse models of depression (222). Cannabis sativa L., an annual dioecious plant historically cultivated mainly in Central Asia, displays various pharmacological properties. Its inflorescence extract demonstrates antidepressant-like and anti-inflammatory effects in LPS-induced neuroinflammation models, potentially by regulating cytokine expression and mast cell activity (223). In addition, apple polyphenol extract inhibits MGB axis-mediated inflammatory responses, downregulates activation of the NF-κB inflammatory pathway, and significantly improves depression-like behavior (224). The methanolic extract of Aerva javanica leaves exerts antidepressant effects by downregulating brain tissue levels of TNF-α, IL-1β, and IL-6, inhibiting oxidative stress, and upregulating BDNF levels (225) ( Figure 2 ; Table 1 ).

Natural products regulate neuroimmune molecular mechanisms. In the depressive state, administration of natural products can exert their multi-target and multi-pathway neuroimmunomodulatory properties, thereby mitigating neuronal injury. NPs, natural product. BBB, blood-brain barrier. ATP, Adenosine Triphosphate. LPS, lipopolysaccharide. NF-κB, nuclear factor-kappaB. GSDM, gasdermin. TLR4, toll-like receptor 4. NLRP3, NOD-like receptor family pyrin domain containing 3. Nrf2, nuclear factor E2-related factor 2. HO-1, heme oxygenase-1. Mfn2, Mitofusion 2. PI3K, phosphatidylinositol-3-kinase. AKT, protein kinase (B) mTOR, mammalian target of rapamycin.

Diagram illustrating the effects of stress and natural products on neuroimmune injury in a mouse model. Natural products are shown to potentially mitigate stress-induced injuries. Arrows indicate pathways involving BBB injury, ATP, TLR4, NF-kB, and other molecular interactions like NLRP3, leading to neuroimmune injuries. The illustration includes detailed biological components such as astrocytes, microglia, and cellular processes like pyroptosis and mitophagy.

Natural product research information.

Natural product Main sources PubChem CID Molecular formula Modeling method Study dosage Molecular mechanism References
Bavachin Fructus Psoraleae 14236566 C20H20O4 In vivo: Streptozotocin In vitro: LPS or high glucose In vivo: 50 and 100 mg/kg In vitro: 5 and 10 μM Acting on PKCδ to inhibit the NF- κB pathway (124)
Schaftoside Dendrobium nobile 442658 C26H28O14 CUMS and LPS 40, 80 and 160 mg/kg Inhibit neuroinflammation (125)
Phloretin Apple 4788 C15H14O5 CMS 10, 20 and 50 mg/kg Reduce synaptic phagocytosis mediated by microglia (126)
Quercetin Fruits and vegetables 5280343 C15H10O7 LPS 50 mg/kg Inhibition of neuroinflammatory signaling pathway (127)
Astragalin Astrolus sinicus L 5282102 C21H20O11 LPS In vitro: 0.2, 2 and 20 μM In vivo: 10 mg/kg Maintaining blood-brain barrier integrity and inhibiting neuroinflammation (128)
Baicalin Scutellaria 64982 C21H18O11 CUMS 60 mg/kg Inhibit neuroinflammation and cell apoptosis (129)
CUMS 20 and 40 mg/kg Inhibition of GSK3 β/NF-κB/NLRP3 signaling pathway (130)
Hyperoside Artemisia capillaris 5281643 C21H20O12 CRS 9 and 36 mg/kg Adjust MGB axis (132)
In vivo: CSDS In vitro: LPS In vivo: 1.875 and 3.75 mg/kg In vitro: 5, 10 and 20 μM Regulating the TRX1/NLRP1/Aspase-1 signaling pathway (133)
Flavonoids from Seabuckthorn (Hippophae rhamnoides L.) Hippophae rhamnoides L – – CUMS 20 and 100 mg/kg Adjust MGB axis (134)
Kaempferol Ginkgo biloba C15H10O6 5280863 LPS In vivo: 25 and 50 mg/kg In vitro: 5, 10, 20 and 40 μM Balance of PPARγ and STAT1 signals (136)
Kaempferol-3-O-sophoroside Crocus sativus (Saffron) C27H30O16 5282155 In vivo: CUMS In vitro: CORT In vivo: 10 and 20 mg/kg In vitro: 12.5-50 μM Binding with AMPK promotes the production of BDNF and enhances autophagy (137)
Puerarin Pueraria lobata C21H20O9 5281807 CUMS 30 and 100 mg/kg Adjust MGB axis (139)
Neohesperidin Citrus fruits C28H34O15 442439 CUMS 25, 50 and 100 mg/kg Regulating the NLRP3 signaling pathway (141)
Luteolin Honeysuckle C15H10O6 5280445 CRS 10, 30 and 40 mg/kg promoting the Arginase-1+ microglial phenotype (143)
5-O-methylvisammioside Saposhnikoviae Radix C22H28O10 21670038 LPS 4 mg/kg Inhibition of NF- κB pathway (146)
Carvacrol Origanum vulgare and Thymus vulgaris C10H14O 10364 CUMS 50 mg/kg Reduce oxidative stress and neuroinflammation (147)
Escin Aesculus chinensis (Suoluozi) C55H86O24 16211024 CUMS 1, 3 and 10 mg/kg Regulating BDNF/TrkB/CREB and TLR4/MyD88/NF-κB signaling pathways (148)
Hyperibone J Hypericum bellum C31H46O5 44575718 In vivo: CUMS and LPS In vitro: LPS In vivo: 10, 20 and 40 mg/kg In vitro: 10, 20 and 40 μM Inhibition of neuroinflammation mediated by P2X7R/TLR4 in microglia (149)
Kaji-ichigoside F1 R. roxburghii C36H58O10 14019178 LPS In vivo: 1, 2 and 4 mg/kg In vitro: 5, 10 and 20 μM Inhibition of NF-κB/NLRP3 signaling pathway expression and activation of PPARγ/CX3CR1/Nrf2 signaling pathway (150)
Yomogin Artemisia iwayomogi C15H16O3 174865 LPS In vivo: 5 mg/kg In vitro: 0.1, 1 and 10 μM Regulating the MAPK signaling pathway (151)
Oridonin Rabdosia rubescens C20H28O6 5321010 In vivo: CUMS In vitro: LPS In vivo: 5, 10 and 20 mg/kg In vitro: 5, 10, 20 and 40 μmol/L Blocking the interaction between NLRP3 and NEK7 to inhibit neuroinflammation and autophagic damage (152)
Lycopene Tomato C40H56 446925 CRS 50 mg/kg Inhibition of cathepsin B/NLRP3 pathway (154)
Patchouli alcohol Pogostemon cablin C15H26O 10955174 In vivo: CMS In vitro: LPS In vivo: 10, 20 and 40 mg/kg In vitro: 5, 10, 20, 40 and 80 μM Inhibition of NLRP3 inflammasome (155)
Aucubin E.ulmoides C15H22O9 91458 In vivo: CUMS In vitro: CORT In vivo: 10 and 20 mg/kg In vitro: 5, 10 and 20 μM Regulating the GR/NF-κB/NLRP3 signaling pathway (156)
Paeoniflorin Paeonia lactiflora pall C23H28O11 442534 In vivo: Reserpine In vitro: LPS and ATP In vivo: 10, 20 and 40 mg/kg In vitro: 0, 1, 10 and 100 μM Inhibition of CASP-11/GSDMD pathway (160)
In vivo: CUMS In vitro: CORT In vivo: 20, 40 and 80 mg/kg In vitro: 50, 100 and 200 μmol/L Promote mitochondrial autophagy and inhibit the activation of NLRP3 inflammasome (161)
In vivo: CUMS In vitro: LPS and ATP In vivo: 40 and 80 mg/kg In vitro: 10 and 100 μM Regulating SIRT1-NF-kB-NLRP3/pyroptosis pathway (162)
Resveratrol Grapes C14H12O3 445154 CUMS 80 mg/kg Inhibit neuroinflammation (166)
Maternal separation 40 mg/kg Downregulation of Sirt1/NF-kB signaling pathway (167)
Polydatin Polygonum cuspidatum C20H22O8 5281718 CUMS 100 and 200 mg/kg Inhibited the activation of NF-κB and Nrf2 pathways (169)
Paeonol Cortex Moutan C9H10O3 11092 LPS In vivo: 10 and 20 mg/kg In vitro: 0, 5, 10, 20, 40, 60 and 80 μM Regulating the HIF1A pathway (170)
Punicalin pomegranate fruits C34H22O22 92131301 LPS 1, 5 and 10 μg/mL Inhibition of TLR4/NF-κB pathway activity (171)
Raspberry ketone Raspberries C10H12O2 21648 LPS 100, 200 and 400 mg/kg Inhibition of TLR-4/NF-κB signaling pathway through MGB axis (172)
Magnolol Magnolia officinalis C18H18O2 72300 In vivo: CUMS In vitro: LPS/ATP In vivo: 50 and 100 mg/kg In vitro: 5, 10 and 20 μM Regulating Nrf2/HO-1/NLRP3 signal transduction (173)
Gastrodin Gastrodia elata C13H18O7 115067 LPS 25, 50 and 100 mg/kg Promote Arg-1+microglial phenotype through Nrf2 (174)
Licochalcone A Licorice C21H22O4 5318998 LPS 15 mg/kg Inhibit inflammation, enhance antioxidant response, prevent metabolic disorders, and improve synaptic related mechanisms (175)
Akebia saponin D Dipsacus asper Wall C47H76O18 14284436 LPS In vivo: 10, 50 and 100 mg/kg In vitro: 10, 50 and 100 μM Activate PI3K-AKT pathway (177)
Quinoa saponin Quinoa – – LPS 100 mg/kg Inhibition of TLR4/MyD88/NF- κB pathway activation (178)
Saikosaponins Radix Bupleuri – – LPS 120, 250 and 400 mg/kg Inhibition of P2X7 receptor to alleviate neuronal pyroptosis (180)
Saikosaponin A Radix Bupleuri C42H68O13 167928 Reserpine 50 mg/kg Adjust MGB axis (181)
Saikosaponins B2 Radix Bupleuri C42H68O13 21637642 In vivo: CUMS In vitro: LPS In vivo: 5 and 10 mg/kg In vitro: 0.2, 2 and 20 μM Regulating the TLR4/NF-κB signaling pathway (182)
Saikosaponin C Radix Bupleuri C48H78O17 167927 In vivo: CSDS In vitro: LPS In vivo: 0.5 and 1 mg/kg In vitro: 0.5, 1 and 2 μM Inhibition of DNMT1 protein reduces IL6 methylation (183)
Gypenosides G. pentaphyllum – – LPS 50, 100 and 200 mg/kg Inhibition of NLRP3/Caspase-1/ASC signaling pathway in PFC (185)
Gypenosides-14 G. pentaphyllum – – LPS In vivo: 100 mg/kg In vitro: 30, 60 and 90 μM Inhibition of NF- κB signaling pathway (186)
Ginsenosides Rb1 Ginseng C54H92O23 9898279 In vivo: CUMS In vitro: LPS In vivo: 10 mg/kg In vitro: 0, 4, 8, 16, 32, and 64 µg/mL Regulating mitochondrial autophagy and NF -κB pathway, inhibiting astrocyte pyroptosis (188)
Ginsenosides Rc Ginseng C53H90O22 12855889 L-alpha-aminoadipic acid 20 mg/kg Regulating neuroinflammation, astrocyte -microglial crosstalk, and apoptosis pathways (189)
Ginsenosides Re Ginseng C48H82O18 441921 In vivo: Reserpine In vitro: H2O2 In vivo: 10, 30 and 90 mg/kg In vitro: 0.1, 2 and 10 μM By inhibiting oxidative stress and inflammation, as well as activating the BDNF/TrkB/ERK/CREB pathway (190)
Morinda officinalis oligosaccharides Morinda officinalis – – tMCAO and CUMS 0.1 mg/g Regulating NLRP3 inflammasome in microglia (193)
In vivo: CMS In vitro: LPS In vivo: 25 and 50 mg/kg In vitro: 2.5, 5, 10 mg/mL Targeting the E2F2 mediated MyD88/PI3K signaling pathway (194)
In vivo: High-salt and CUMS In vitro: LPS In vivo: 0.1 mg/g In vitro: 5 mg/mL Upregulation of Mfn2 expression activates mitochondrial autophagy mediated by the PI3K/Akt/mTOR pathway (195)
Eucommiae cortex polysaccharides Eucommiae cortex – – CUMS 100 mg/kg Inhibiting gut microbiota mediated neuroinflammation (196)
Inulin Jerusalem artichoke – – CUMS 0.037 g inulin/kcal Regulating TLR4/MyD88/NF - κ B signaling transduction (198)
Rattan Pepper Polysaccharide Rattan Pepper – – Dextran sulfate sodium salt 200 mg/kg Adjust MGB axis (199)
Higenamine Aconiti Lateralis Radix Praeparata C16H17NO3 114840 CUS 5, 10 and 20 mg/kg Improve gap junctions and neuroinflammation in astrocytes (202)
Arecoline Areca nuts C8H13NO2 2230 CUMS 10 mg/kg Adjust MGB axis (203)
Matrine S. alopecuroides C15H24N2O 91466 CUMS 15, 30 and 60 mg/kg Adjust MGB axis (204)
Tabersonine Catharanthus roseus C21H24N2O2 20485 In vivo: LPS In vitro: LPS and ATP In vivo: 20 mg/kg In vitro: 1, 3, 6, 8, 10 and 20 μM Inhibition of NLRP3 inflammasome activation (206)
Berberine Rhizoma coptidis C20H18NO4 + 2353 In vivo: CUMS In vitro: LPS and ATP In vivo: 5 and 10 mg/kg In vitro: 0.5, 1, and 2 μM Inhibit NLRP3 inflammasome (208)
CORT 100 and 200 mg/kg Inhibition of NLRP3 inflammasome mediated neuroinflammation (209)
Betaine Sugar beet C5H11NO2 247 Methamphetamine 10, 30 and 100 mg/kg Inhibit NLRP3 inflammasome (212)
Complete Freund’s adjuvant 600 mg/kg Changing the polarization of microglia and astrocytes to reduce neuroinflammation (213)
Schisandrin B Schisandra C23H28O6 108130 LPS 31.25, 62.5, 125, 250, 500, and 1000 μg/mL Downregulation of NF-κ B/TLR4/MyD88 signaling pathway (215)
Schisandra chinensis Lignans Schisandra – – In vivo: CUMS In vitro: LPS In vivo: 600 and 1200 mg/kg In vitro: 0−2200 μg/mL Activate the CB2R/STAT6 signaling pathway (216)
Arctiin Fructus arctii C27H34O11 100528 In vivo: CUMS In vitro: CORT In vivo: 50 mg/kg In vitro: 0, 12.5, 25, 50, 100 and 200 μM Inhibition of P2X7R/NLRP3 inflammasome signaling pathway (217)
Yamogenin Dioscorea species C27H42O3 441900 LPS 5, 10 and 20 mg/kg Inhibit endoplasmic reticulum stress and microglial activation (218)
Cajaninstilbene acid Pigeon pea C21H22O4 9819225 CUMS and LPS 7.5, 15 and 30 mg/kg Inhibition of TLR4/NF -κB mediated neuroinflammation and enhancement of autophagy (219)
Fucosterol Algae C29H48O 5281328 CUMS and LPS 10 mg/kg Inhibition of excessive activation of microglia by MAPK/ERK1/2 signaling inhibition (220)
Ashwagandha root extract Ashwagandha (Withania somnifera (L.) Dunal) – – In vivo: CUMS In vitro: CORT In vivo: 60 and 100 mg/kg In vitro: 100 and 200 μg/mL Neuroprotection (222)
Cannabis sativa L. inflorescence extract Cannabis sativa L. inflorescence – – LPS 10, 20 and 30 mg/kg Regulating cytokine expression and mast cell activity (223)
Apple polyphenol extract Apple – – High sucrose diet 500 mg/kg Adjust MGB axis (224)
Methanolic Extract of Aerva javanica Leaves Aerva javanica – – LPS 100, 300, and 500 mg/kg Downregulate pro-inflammatory cytokines and inhibit oxidative stress (225)

In summary, plant-derived natural products show great therapeutic potential for depression associated with neuroinflammation. Current evidence suggests that certain bioactive phytochemicals can improve depression-like behaviors by modulating neuroinflammatory responses. However, the complex multi-component composition of plant extracts makes it challenging to clarify the synergistic interactions among their active constituents. Furthermore, the physicochemical properties of solvents used during extraction can greatly affect the bioavailability and pharmacodynamic stability of the final products. Therefore, future research should systematically characterize the neuroimmunomodulatory effects of plant extracts. Establishing standardized research protocols will lay a theoretical foundation for developing novel antidepressant strategies to overcome the limitations of existing treatments.

 Limitations and challenges

MDD is a highly prevalent chronic psychiatric condition worldwide, yet its underlying pathophysiological mechanisms remain incompletely understood. This knowledge gap severely impedes advances in developing targeted therapeutic strategies. Although conventional first-line antidepressants, such as fluoxetine, show moderate efficacy, their use is limited by single-target mechanisms and significant adverse effects. Recent research highlights the crucial role of neuroimmune regulatory networks in the pathogenesis, progression, and treatment outcomes of depression, presenting a promising direction for novel therapeutic approaches.

Natural products offer unique advantages in antidepressant therapy due to their multi-component synergistic mechanisms, which enable regulation of multiple targets within the neuroimmune system. This aligns well with the holistic regulatory principles of complex biological systems. Additionally, natural products possess bidirectional regulatory properties, capable of modulating both physiological functions and psychological states. This therapeutic approach of “harmonizing physiological and psychological states” closely matches the individualized treatment philosophy emphasized by precision medicine. Building on this foundation, scientifically integrating the multi-target benefits and precise actions of natural products to create a multidimensional synergistic framework, similar to “cocktail therapy”, will be pivotal for overcoming the limitations of single-target treatments and improving overall antidepressant effectiveness. This strategy represents a critical frontier in current translational medicine research.

Nevertheless, although natural products have demonstrated significant antidepressant potential in preclinical studies and suggest modulatory effects on the neuroimmune system, there remains a lack of high-quality evidence from large-scale, randomized, double-blind, placebo-controlled clinical trials. Therefore, their ability to produce clinically meaningful relief of depressive symptoms, deliver therapeutic benefits through neuroimmune modulation, and demonstrate strong safety profiles with long-term treatment sustainability requires rigorous validation through well-designed and methodologically robust clinical studies.

Special attention must be given to the risks of drug-drug interactions when combining natural products with conventional antidepressants. Clinically, co-administration can lead to pharmacokinetic interactions; for instance, concurrent use of miltirone and fluoxetine may cause toxic effects due to metabolic disturbances in individuals who are poor metabolizers of CYP2D6 or carry functional variants (226). Therefore, urgent research is needed to elucidate metabolic alterations during combination therapy and establish personalized medication guidelines for clinical practice.

Furthermore, the inherent physicochemical properties of certain natural products—such as inadequate chemical stability, low bioavailability, and limited BBB permeability—pose significant challenges to the targeted delivery of active compounds to the CNS. Meanwhile, natural resources from traditional medicinal systems (e.g., Chinese herbal medicine), face widespread issues including significant heterogeneity in cultivation conditions, lack of standardized processing methods, and substantial batch-to-batch variations in active components. The absence of standardized quality control systems not only limits their clinical application but also impedes rigorous investigation of their pharmacodynamic mechanisms.

On the other hand, although classical behavioral paradigms in rodents—such as the open field test, sucrose preference test, and forced swim test—allow relative quantification of depression-like behaviors, they fall short in capturing the complex psychological dimensions unique to human depression. Importantly, glial cells, including microglia and astrocytes, which are key mediators of neuroimmune regulation, play critical roles in the bioactivity of natural products. However, species differences in neurobiology between rodents and humans limit the ability of current models to accurately mimic the temporal progression of psychiatric symptoms. Moreover, existing models often fail to systematically simulate essential clinical features, such as the chronic nature of depression. These limitations in biological validity and clinical relevance inherently restrict the effective translation of preclinical findings into clinical practice.

Moreover, any biologically active substance on Earth can produce pharmacological effects and may cause non-specific off-target effects on normal tissues (227). Natural products are no exception in exerting antidepressant effects and carry potential toxicological risks and side effects. However, current research still lacks systematic evaluation of the possible adverse reactions and long-term risks associated with natural products, especially when multi-component synergistic interactions occur and their potential impacts on normal tissues. The absence of a comprehensive safety evaluation system has become a major barrier limiting the clinical translation of natural products.

 Conclusion

In conclusion, future research must urgently prioritize establishing a comprehensive clinical translation framework for natural products. This includes systematically conducting high-quality, multi-center, large-sample randomized double-blind controlled trials and developing standardized efficacy evaluation systems to objectively assess their antidepressant effects in clinical settings. Meanwhile, research should focus on exploring combination therapy models that integrate natural products with conventional antidepressants. Using adaptive clinical trial designs, the clinical benefits of these combined regimens should be rigorously validated under strict safety and efficacy monitoring. Furthermore, close surveillance of patients’ pharmacokinetic profiles and safety parameters is essential to ensure robust protection during clinical application.

Additionally, overcoming the bottleneck of low CNS delivery efficiency for natural products is crucial. This urgently requires the development of novel, intelligent targeted delivery systems. For example, priority should be given to exploring advanced delivery strategies based on multifunctional nanocarriers (such as liposomes and polymeric nanoparticles) combined with BBB-penetrating technologies, including active targeting ligands or cell-penetrating peptides. Meanwhile, establishing a standardized, whole-process quality control system for herbal medicines is essential to provide a solid scientific foundation for the clinical translation of natural products. In addition, future research can focus on the neuroimmune pathways mediated by neural circuits, and further explore the molecular mechanisms of natural products such as quercetin, ginsenosides, and resveratrol that have a certain research foundation, laying a solid foundation for their clinical translation.

More importantly, future research must integrate cutting-edge technological platforms such as single-cell transcriptomics and spatial multi-omics to systematically elucidate the dynamic molecular mechanisms underlying neuroimmune pathology in depression. Based on these insights, a dynamic staging model of the chronic evolution of depression’s neuroimmune pathology should be developed to identify optimal time windows for intervention with natural products. Furthermore, humanized organoid models combined with targeted gene editing technologies can be employed to deeply explore core, evolutionarily conserved pathological mechanisms across species, thereby optimizing and validating personalized treatment strategies.

In summary, there is an urgent need for systematic exploration in both preclinical and clinical translational research focused on the neuroimmune mechanisms of depression and targeted intervention strategies. Such efforts will provide essential theoretical support and clear translational pathways for developing novel antidepressants (especially natural products), while significantly accelerating their clinical application.

 Author contributions

SL: Writing – original draft. LK: Writing – review & editing. XZ: Writing – review & editing. RS: Writing – review & editing. YL: Writing – review & editing. GZ: Writing – review & editing. HG: Writing – review & editing. XH: Writing – review & editing. GL: Writing – review & editing. XY: Writing – review & editing.

 Funding

The author(s) declare financial support was received for the research and/or publication of this article. This work was supported by the 2025 Shandong University of Traditional Chinese Medicine Graduate Quality Improvement and Innovation Program (YJSTZCX2025020), Qilu Biancang TCM Talent Cultivation Project (Lu Wei Han (2024) No. 78), Postdoctoral Fellowship Program (Grade) of China Postdoctoral Science Foundation under Grant Number GZB20240036, Peking University Medical Youth Science and Technology Innovation Yangfan Program (BMU2025YFJHPY006), The Fundamental Research Funds for the Central Universities.

 Acknowledgments

Figure 1 (Created in BioRender. Lv, S. (2025) https://BioRender.com/m3gwuc4) and Figure 2 (Created in BioRender. Lv, S. (2025) https://BioRender.com/80ttvd2) were created by BioRender (https://www.biorender.com/).

 Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

 Generative AI statement

The author(s) declare that no Generative AI was used in the creation of this manuscript.

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 Publisher’s note

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