Curcumin interacts with macrophages, muscle cells, adipocytes, hepatic stellate, and pancreatic cells via targeting multiple molecular components including transcription factors, inflammatory mediators, enzymes, such as protein kinases (31, 32), histone acetyltransferase (33, 34), DNA methyltransferases, histone deacetylases, and modulation of micro RNAs (Figure 2) (35). Furthermore, many of the protein targets are components of multiple cell signaling pathways involved in the development of metabolic disorders, such as Peroxisome proliferator-activated receptor gamma (PPARγ), nuclear factor κB (NF-κB)/nuclear factor-erythroid 2 related factor 2 (NRF2), Wnt/β-catenin, NRF2/Kelch-like ECH-associated protein 1 (KEAP1), FOXO, and phosphatidylinositol-3-kinase(PI-3-K)/Akt/tumor necrosis factor-α (TNF-α) (Figure 3) (36).

By stimulating PPARγ and NRF2 signaling pathways, curcumin consequently up-regulates adiponectin and other gene products, leading to the downregulation of adipokines including resistin, leptin, TNF, interleukin (IL)-6, and monocyte chemotactic protein-1 (37). In a recent in silico study, Shakour et al. reported that curcumin and its derivatives such as bisdemethoxycurcumin, cyclocurcumin, and demethoxy curcumin have an important regulatory function in oxidative and inflammatory processes involved in many diseases (38).

Obesity is a chronic disease associated with inflammation; it has a main role in MS development as well as increasing the risk of atherosclerosis. Alteration of adipose tissue reduces lipid metabolism, causing an imbalance in the energy storage in fat tissue, thus affecting endocrine system and immune response. These alterations are primarily marked by the secretion of leptin, adipocyte-specific hormone resistin, and plasminogen activator inhibitor type-1 (PAI-1). In addition, inflammatory cytokines are also released such as TNF, IL-1, IL-6, and monocyte chemotactic protein (MCP)-1. These cytokines and chemokines significantly promote insulin resistance and mediate chronic inflammation.

Curcumin in turmeric is notable for its antioxidant and anti-inflammatory effects (Figure 3) (39, 40) and for ameliorating obesity risk factors (41) via the inhibition of NF-κB in adipose tissue, thereby reducing the expression of TNF-α, IL-6, MCP-1, PAI-1, and increasing adiponectin expression (40).

Some molecular pathways of inflammation and obesity are cross-talked with insulin resistance and diabetes (42, 43). Oxidative stress induced by elevated levels of circulating free fatty acids, endoplasmic reticulum (ER) stress, and proinflammatory signaling pathways also contribute to the induction of insulin resistance (43–45). Curcumin acts mainly as a signaling modulator that activates endogenous antioxidant responses such as the NRF2-KEAP1 (45) and has been demonstrated to reduce ER stress in a high-fat diet mice model, in vitro in primary adipocytes (46), and in palmitate-induced insulin resistance in human umbilical vein endothelial cells (HUVECs) (47). Lipolysis decreases and insulin resistance improves with decreased ER stress (47) but the relationship between ER stress, mitochondrial stress, and inflammation is complex (43). Thus, the curcumin effects require further investigation to elucidate the mechanism and links to other metabolic processes.

Cardiovascular diseases (CVDs) are the notable cause of death globally. Curcumin has been shown to prevent and treat CVDs via modulation of multiple signaling pathways related to cellular proliferation, growth, survival, oxidative stress, and inflammation. Curcumin prevents cardiovascular dysfunction and its primary risk factors (atherosclerosis, aortic aneurysm, myocardial infarction, and stroke) (48, 49) by activating endogenous antioxidant, anti-inflammatory, and anti-apoptotic responses, thereby improving cardiovascular complications, heart failure, and cardiotoxicity (50–52).

Curcumin is a popular traditional medicine for inflammatory conditions (39). Inflammation is involved in MS as elevated visceral adipose tissue modulates adipokine secretion leading to decreasing adiponectin levels, increasing leptin and proinflammatory cytokines (i.e. TNF-α and IL-6), thereby promoting endothelial cell dysfunction and atherosclerosis (85). Non-bio-enhanced curcuminoid can lower C-Reactive Protein (CRP), while other forms of curcumin, such as bio-enhanced curcuminoids, bio-enhanced curcumin, curcumin without bio-enhancement, and turmeric had no effect, showing the tendency of curcumin to lower IL-6 regardless of bio-enhancement (69). Qin et al. (70) also showed that malondialdehyde (MDA), a stress oxidative marker, is lowered by curcumin regardless of intervention dose, duration, and underlying disease, except for osteoarthritis. Moreover, the combination of curcuminoids and piperine is more effective than curcumin alone to reduce MDA levels (70) but does not affect TNF-α, leptin, or adiponectin (27, 69, 71–74, 84). Consumption of nanoparticles of curcumin for 6 weeks, along with regular exercise in 44 older women with MS, decreased IL-6, increased IL-10, and increased brain-derived neurotrophic (BDNF) level (86).

Curcumin has been reported to activate AMP-activated protein kinase (AMPK) to inhibit adipocyte differentiation. Stimulation of AMPK down-regulated PPAR-γ in 3T3-L1 adipocytes to prevent insulin resistance and obesity (87). Di Piero et al. reported that curcumin has a beneficial effect on weight management in 44 overweight subjects by improving weight loss, reducing body fat, increasing waistline reduction, improving hip circumference reduction, and enhancing reduction of BMI (p < 0.01 for all comparisons) without significant statistical effect on phosphatidylserine (88). Akbari et al. (84) reported that curcumin in a dose of 70–2,400 mg/day for 4–36 weeks can significantly reduce BMI and body weight compared to placebo. The effect of curcumin based on dose and duration of intervention, however, showed high heterogeneity among clinical studies. Waist circumference was also significantly reduced but there was no clinical data regarding a clinical significance in the hip ratio (84). Azhdari et al. and Altobelli et al. also reported the insignificant effect of curcumin in reducing BMI and waist circumference (28, 75), thus the effectiveness of curcumin in improving obesity is unclear.

Diabetes mellitus (DM) is a metabolic disorder with hyperglycemia as the main clinical feature. The association between insulin and its producing organ, the pancreas, forms the fundamental understanding of the diseases. Over the last 100 years, clear evidence has distinct two types of diabetes: “insulin-dependent” (Type 1–T1DM) in which the pancreas completely fails to produce insulin and “non-insulin-dependent” (Type 2–T2DM). In T2DM, insulin hypersecretion by β-cell (hyperinsulinemia) causes the inability of the pancreas to cope with required insulin and later can experience insulin resistance, resulting in elevated blood glucose levels (hyperglycaemic hyperinsulinemia). Insulin resistance, as an onset of hyperinsulinemia, can cause the inability of β-cell to secrete insulin, apparently due to the manifestation of hyperglycemia (hyperglycaemic hypoinsulinemia). In addition, the liver contributes to systemic insulin resistance in which gluconeogenesis is undertaken, and hepatic insulin resistance can occur during the hyperglycemia state. Muscle insulin resistance can also occur when fat accumulation disturbs glucose uptake and affects insulin signaling. Fat accumulation in pancreatic cells causes β-cell dysfunction, increases plasma glucose, and reduces insulin response. Understanding the complex pathologies of DM promotes the evidence that DM is associated with greater risk factors related to cardiovascular diseases, such as coronary heart diseases and stroke, and non-vascular diseases, including cancer, neuro disorder, and liver diseases (89).

Nine-month curcumin consumption improves β-cell function by increasing Homeostatic Model Assessment (HOMA)-β, lowering Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) and C-peptide (90). In the meta-analysis by Huang et al. (76), curcumin significantly improved fasting plasma glucose, HOMA-IR, and glycated hemoglobin (HbA1c). Subgroup analysis confirmed the significant effects of curcumin (≥300 mg/day dose and ≥12-week intervention) in improving plasma fasting glucose and HbA1c in the diabetes subgroup, with no significant effects in the non-diabetic subgroup (76). Melo et al. also reported that curcumin treatment was more effective in the higher blood glucose baseline (77). Hodaei et al. confirmed the findings reporting daily administration of 1,500 mg curcumin has a beneficial influence in decreasing weight and fasting blood glucose in subjects with type 2 diabetes (91).

Hypertension is a common component of MS and there are two meta-analyses of curcumin in hypertension. Hadi et al. reported no significant effect of curcumin on systolic blood pressure (SBP) and diastolic blood pressure (DBP), although SBP was reduced (average reduction of 1.24 mmHg) but not significantly at ≥ 12-week (78). Azhdari et al. confirmed that curcumin has no significant effect on SBP but significantly improved DBP (heterogeneity <50%) (28).

Dyslipidemia is a clinical condition described as elevated total or LDL-cholesterol (LDL-C) or low HDL cholesterol (HDL-C) levels and is considered a serious risk factor for coronary heart disease and stroke (92). Yuan et al. (83) reported that curcumin might reduce total cholesterol when administrated to diabetic patients for a minimum of 12 weeks (>300 mg/day), reduce LDL-C after a minimum 12-week intervention, and triglycerides after a minimum 8-week intervention. More prolonged administration may be required to improve the efficacy of curcumin on dyslipidemia. However, Simental-Mendía et al. found that curcumin did not affect HDL-C regardless of intervention duration (<12-week and ≥12-week) (79). Another meta-analysis also confirmed the non-significant effect of curcumin in improving HDL-C with low heterogeneity (75, 80, 81).

NAFLD and MS are two different disorders with overlapping clinical and pathophysiological characteristics. NALFD indicates mere liver steatosis to overt liver cirrhosis (93). Oxidative stress and inflammation play major roles in the progression of NAFLD. As an anti-inflammatory modulator, curcumin might improve health parameters related to NAFLD (94). Some RCT reported the effectiveness of curcumin and curcuminoids in improving various health parameters in NAFLD patients, i.e., serum levels of pro-inflammatory cytokines (IL-1α, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, TNF-α, monocyte chemoattractant protein-1, interferon γ, vascular endothelial growth factor, and epidermal growth factor, fasting plasma insulin (FPI), HOMA-IR, liver transaminases, fatty liver index, serum cortisol, ultrasound morphological of the liver, and other parameters included in MS (p < 0.05) (94–112). The findings were consistent regarding the beneficial effects on improving NAFLD risk factors (113), with only one study having conflicting results, whereby curcumin was reported to have no impact on liver transaminases, metabolic and inflammatory parameters. This inconsistency is probably due to the low curcumin dose of only 35 mg curcumin per intake, thus reducing its bioavailability and effectiveness (114). The combination of curcumin with other substances, such as ursodeoxycholic and piperine, has shown a positive outcome in improving NAFLD (115–117). Dose and term administration should be critically appraised.

Sleep duration might be linked to MS and a short sleep duration has been associated with obesity. Sleep deprivation could increase oxidative stress mediators in the brain and since curcumin may relieve oxidative stress, it may be beneficial in suppressing stress and prolonging sleep duration. However, according to a trial by Saberi-Karimian et al. curcumin did not have any impact on sleep duration in patients with MS (118).

Serum copper and zinc and the ratio of Zn/Cu are often used to identify oxidative stress and inflammation (119, 120). Furthermore, protein chaperones, such as heat shock proteins (HSP) are highly expressed during oxidative stress (121). Some recent studies reported the effects of curcumin and its derivatives on some oxidative stress markers in MS patients (122), for instance, serum copper, zinc, and trace elements are elevated in patients with MS compared to healthy subjects (120). A double-blind clinical trial of 120 subjects with MS reported increased serum zinc and Zn/Cu ratio after administration of curcumin and phospholipid curcumin complex at a dose of 1 g/day for 6 weeks (123). However, Mohammadi et al. reported no significant difference in the alteration of HSP 27 serum concentrations among the study groups (group received curcumin, phospholipid -curcumin complex, or a placebo for 6 weeks) (124). Oxidative stress occurs as a result of an imbalance between pro-oxidant and antioxidant defense systems, resulting in cellular damage and associated diseases including MS. The redox stress index indicates the pro-oxidant/antioxidant balance in human serum due to oxidation and reduction reactions that coincide (125). Ghazimoradi et al. (126) conducted a double-blind, randomized, placebo-controlled trial over 6 weeks of 120 individuals with MS and three groups of subjects received curcumin, phospholipid curcumin, and placebo. Serum PAB was elevated significantly in the curcumin group. Still, the study did not assess different doses of curcumin and did not consider the impact of other adjuvants and its possible interaction that may affect the efficacy of curcumin (126). No significant effect was observed on the serum antioxidant vitamin E level after administration of 1 g curcumin supplement per day for 6 weeks, indicating that the reported antioxidant effect of curcumin is mainly via the modulatory action on the intracellular antioxidant system rather than serum vitamin E (127).

One of the limitations of using phytochemicals often is their poor bioavailability in the human body, thus nano formulations have been employed to improve the delivery of phytochemicals such as curcumin, berberine, naringenin, quercetin, emodin, myricitrin, stevioside, and resveratrol to the target organ and cells (128). Nano-based formulations for the MS that are biodegradable, biocompatible, nontoxic, and stable after oral administration should be developed focusing on the multifactorial effects rather than a single factor (128). A recent study by Bateni et al. reported that nano-micelle curcumin supplement at a dose of 80 mg/day significantly improved serum triglycerides in patients with MS, although no significant difference was observed in anthropometric measurements, blood pressure, and several biochemical factors (129). Nano curcumin supplementation (80 mg/day for 6 weeks) along with regular exercise significantly reduced inflammation in an elderly woman with MS, as well as decreased the percentage of fat and IL-6, and increased IL-10 and BDNF (86).

Curcumin had been approved as a safe agent under the Generally Recognized as Safe (GRAS) category by the FDA (130). Nevertheless, the European Medicine Agency (EMA) released a revised version of the guideline for using C. longa with special warnings and precautions for patients with obstruction of the bile duct, cholangitis, liver disease, gallstones, and any other forms other biliary diseases. Due to a lack of data on children, adolescents under 18 years, pregnancy, and lactation, the use of C. longa is not recommended to those groups of the population (131). Mild undesirable side effects such as dry mouth, flatulence, and gastric irritation should also be critically appraised (131). Panahi et al. reported curcumin is well tolerated with the possibility of minor side effects, including diarrhea, constipation, headache, skin rash (132). A clinical study also reported nausea and colds in the curcumin group (20).

Acceptable Daily Intake (ADI) for curcumin as food additive defined by the European Food Safety Agency (EFSA) is 3 mg/kg BW/day based on No Observed Adverse Effect Level (NOAEL) of 250–320 mg/kg BW/day from the toxicity study (133). Some studies reported curcumin is considered safe even at high doses of up to 4–8 g/day (40, 134). Rigorous studies to understand curcumin's safety as a single modality and/or combination with other substances are warranted, including human trials, to repulse possible hepatotoxicity and genotoxicity disputes (135–137).

There are currently six ongoing trials examining the efficacy of curcumin in improving MS parameters, including five trials assessing blood glucose, four trials evaluating serum lipid profile, three trials measuring blood pressure, two trials examining body weight, and three trials evaluating oxidative stress and inflammation markers. Due to the fast metabolism and low gut absorption of curcumin, three of these trials are also examining specific curcumin formulations for enhanced bioavailability, e.g., micellar curcumin, nano curcumin, and nano micelles. Another trial is also investigating the effects of curcumin in combination with other agents including inulin, resveratrol, and omega-3 fatty acids to enhance its effectiveness. One study in Thailand is recruiting many participants (n = 200) with a long intervention duration (12 months) of regular curcumin that anticipates that the long-term supplementation with this new curcumin formulation may result in a better outcome (138).

Curcumin is unstable with low bioavailability (20, 21). There is much evidence that the pharmacological effects of curcumin are mainly due to its metabolites (151). Holder et al. suggest that curcumin elimination will mainly undergoes through bile: The primary biliary metabolites of curcumin consist of the two glucuronide conjugates [tetrahydrocurcumin (THC) and hexahydrocurcumin (HHC)], whereas the minor metabolites consist of ferulic acid and dihydro ferulic acid (152). Glucuronide and sulfate derivatives are the main detectable metabolites in urine and after five days, about 40% are excreted in an unchanged form. Another in vivo study indicated that less than half of the curcumin remains in the lower part of the gut, attributed to the biotransformation of curcumin to other components in the gut (153). Kunnumakkara et al. reported that curcumin is undetectable in the heart, blood, and at a very low concentration in the liver, kidney, and portal blood (154).

The intravenous administration of curcumin in rats was associated with a low concentration of THC and dihydrocurcumin (DHC) in plasma. Curcumin was detected in the kidney, liver, and brain. In contrast, THC and DHC were detected in only the kidney and liver, indicating that curcumin crosses the blood-brain barrier, converting a prodrug molecule and possibly targeting neuron dysfunction and disorder (155).

Some investigations in human and rat intestinal tissues showed that curcumin is metabolized in the human intestinal tissue. The extent of curcumin conjugation in the human intestine is much higher than in the rat intestine, however, there is less curcumin conjugation in the human liver compared to rat liver, indicating that curcumin is biotransformed into THC and DHC, thereafter converted into glucuronide conjugates (156).

Enzymes involved in sulphation and glucuronidation are also found in the kidney, liver, and intestinal mucosa. In the intestine, curcuminoids, including curcumin, are conjugated to glucuronide, then form a glucuronide conjugates in the portal vein and subsequently conjugate into glucuronide/sulfate in the liver. Unlike oral administration, curcuminoids administrated intravenously in rats enter the blood circulation and dispose of in the liver as a free form (157).

To date, there are two known phases of curcumin metabolism, phase I and phase II. Phase I metabolism involves saturating double bonds to form several curcumin metabolites such as di, tetra, hexa, and octahydrocurcumin, whereas, in phase II metabolism, glucuronide or sulfate is conjugated to curcumin as well as its metabolites (154). Curcumin and its metabolites can form conjugation to any of their phenol-OH groups (21). Additionally, curcumin metabolism may occur in the intestine by microorganisms such as Escherichia coli whereby the NADPH-dependent enzyme converts curcumin into di- and tetrahydrocurcumin (158).

Curcumin degradation products including its metabolites may involve in the observed therapeutic effects. A few curcumin metabolites have been investigated in preclinical studies, for example, DHC exhibited lipid biosynthesis and increased lipid oxidation in HepG2 and LO₂ cells. A molecular docking study revealed that DHC showed more affinity for binding to the phospholipase A2 active site than curcumin, indicating that DHC possesses anti-inflammatory activity (159), decreasing oxidative stress by upregulating NRF2, decreasing insulin resistance by increasing glucose uptake, and modulating the PI3K/AKT pathway (160).

Based on the chemical structure, THC is more stable and soluble in an aqueous medium than curcumin, as the former lacks α, β dienes, so it is unable to form Michael adducts with intracellular proteins. Nevertheless, the therapeutic activities of THC have been reported such as anti-aging, anti-neurodegeneration, and anticancer effects with significant antioxidant activity, so it can prevent human diseases related to oxidative stress (36). Hexahydrocurcumin (HHC), a hydrogenated metabolite of curcumin, is not well studied but it has been documented to have anticancer, antioxidant, antiinflammatory, and cardioprotective activities. Some of which have been reported to be more potent than the parent compound, curcumin, such as free radical scavenging activities (161). Octahydrocurcumin (OHC) exhibits several activities similar to the parent compound, curcumin, while its antitumor and anti-inflammatory activities were more potent than curcumin (162–164).

Drug metabolism is categorized into phase I and phase II metabolism. Cytochrome P450 (CYP) enzymes, a large superfamily of heme proteins, play a major role in modulating phase I metabolism by catalyzing oxidative biotransformation of drugs and xenobiotics (165, 166). At least 57 CYP genes have been identified in humans. Of 18 families and 44 subfamilies human CYPs, only families 1–3 are most active in hepatic metabolism with five of them (CYP 1A2, 2C9, 2C19, 2D6, and 3A4) contributing to metabolism of 75% of drugs (165, 167). Drug therapy can induce or inhibit CYP enzymes resulting in drug-drug interaction. Induction or inhibition of CYP may decrease or increase plasma drug levels causing adverse drug reactions or toxicity (168). After CYP enzyme metabolism, most drugs are metabolized by conjugation reaction in phase II metabolism. Phase II enzymes contribute significantly to metabolic inactivation of drug compounds and biotransformation of xenobiotics to make them easier to excrete from the body. Phase II enzymes are mainly transferases, including glutathione S-transferases (GSTs), thiopurine-S-methyltransferase (TPMT), sulfotransferases (SULTs), uridine-diphosphate glucuronosyltransferases (UGTs), N-acetyltransferases (NATs), and NADH quinone oxidases (169).

Curcumin can modulate the activity of drug-metabolizing enzymes, both phase I and phase II metabolic enzymes (170). Curcumin is reported to significantly inhibit CYP2D6 activity in in vitro as well as in vivo. In vitro studies using human liver microsomes showed that 100 μg/mL of tumeric extract inhibited about 70% dextrorphan (metabolites of dextromethorphan mediated by CYP2D6) formation. Meanwhile, in vivo model exhibited a significant increase in human urinary metabolic ratio of dextromethorphan/dextrorphan after administration of tumeric extract (171). Similarly, CYP inhibitory activity assay using human recombinant CYP enzymes demonstrated that curcumin inhibited CYP2D6 by 60% at concentration of 120 μM and effectively inhibited CYP3A4 by almost eliminating the enzyme function at concentration ≥ 60 μM (172). In contrast, other in vivo and ex-vivo studies found that curcumin significantly activated CYP3A4. The study showed that 50 and 100 mg/Kg of curcumin markedly reduced the AUC₀₋₅₄₀ of everolimus (a probe drug of P-glycoprotein/CYP3A4) by 70.6 and 71.5%, respectively (173). Meanwhile, Mach et al. reported that curcumin in liposomal formulation did not inhibit CYP2D6 and CYP3A4 activity, but liposomal curcumin at concentration of 58.3 μM inhibited CYP2C9 (10.5%) and CYP2C8 (22.5%) by in vitro assay (174).

Chen et al. investigated that 14 days of treatment with curcumin after caffeine administration significantly repressed CYP1A2 activity by 28.6% and significantly induced CYP2A6 activity by 48.9% in human subjects, but had no significant effect on N-acetyltransferase (NAT2) and xanthine oxidase (XO) (175). Volak et al. (176) reported that by in vitro assay using human liver microsomes, curcuminoid extract exhibits moderate to potent inhibitory activity (IC50<50 μM) toward various CYPs in the following ascending order CYP2C19 > CYP2B6 > CYP2C9 > CYP3A. In contrast, curcuminoid extract exhibits low inhibitory activity of CYP2D6, CYP1A2, and CYP2E1 (IC50 > 60 μM). Meanwhile, pure synthetic curcuminoids (curcumin, demethoxycurcumin, and bisdemethoxycurcumin) show similar inhibition to the CYP3A and CYP2C9 activities (176).

Several studies reported that curcumin modulates phase II metabolism enzymes. Curcuminoids can inhibit acetaminophen glucuronidation (by UGT enzyme) and acetaminophen sulfonation (by SULT enzyme) in LS180 cells. Curcumin is a more significant potent inhibitor of acetaminophen glucuronidation than demethoxycurcumin and bisdemethoxycurcumin, but compared to other curcuminoids, curcumin is the least potent inhibitor of acetaminophen sulfonation (176). In addition, curcumin is a potent inhibitor of phenol sulfotransferase (SULT1A1) in human liver, kidney, colon, duodenum, and lung (177). However, in a clinical study, short-term use (2 days) of curcuminoid/piperine combination is unlikely to affect significantly the pharmacokinetic disposition of drugs involving UGT and SULT (178).

In addition, curcumin was reported to modulate GST activity. Liu et al. (179) investigated the therapeutic potential of curcumin and resveratrol in mice bearing lung carcinoma induced by benzo(a)pyrene. The result showed that curcumin and a combination of curcumin-resveratrol treatment for 22 weeks significantly increased GST level by 14 and 18%, respectively, compared to benzo(a)pyrene treatment (179). Similarly, a study reported that 2 weeks of curcumin oral administration (400 mg/kg) in mice increased GST activity by 20% (180).

Gut microbiota has recently gained great attention due to their role in understanding the pathobiology of diseases, efficacy of treatment, as well as diet and nutrition that affect human health (181). There is increasing evidence supporting the concept that the gut microbiota is responsible for the regulation of metabolic disorder including obesity, weight gain, and insulin sensitivity (162–164). Phyla Firmicutes and Bacteroidetes are associated with genetic obesity in rodents (182, 183), but efficacy may differ among specific genera and species. Bacteroides, for instance, are linked to a high fat/low-fiber intake, while Prevotella are associated with complex carbohydrate intake (184). In-depth knowledge of diet-microbiota interactions is also important to identify the risk factors of metabolic disorders closely related to diet and nutrition. The gut microbiome can be modified and regulated by probiotics and/or prebiotics, such as non-digestible carbohydrates (163, 185), that are considered as part of therapeutic strategies (186).

A preclinical study of obese mice showed that dietary supplementation of prebiotic oligofructose decreased Streptococcus intermedius, a cytolysin-producing microorganism that normally disturbs intestinal wall permeability. The human intestinal mucin-degrading bacterium, Akkermansia muciniphila, was also increased after the administration of prebiotics and correlated with elevated levels of Glucagon-like peptide-1 (GLP-1) and Glucagon-like peptide-2 (GLP-2) in L-cells (187). This organism is associated with metabolic-regulating proteins (188). In addition, the elevated concentration of these GLPs can improve gut barrier function and metabolism via the metabolism of fatty acids to short-chain fatty acids (189). Oral intake of curcumin enhanced the intestinal barrier function, improved glucose tolerance, and lowered circulating LPS levels in Western diet-fed LDL receptor knockout (LDLR) mice (190). Curcumin can act as a prebiotic to influence the microbiome, consequently, influence metabolic imbalance such as obesity (191). A double-blind, randomized, placebo-controlled pilot study revealed turmeric and curcumin alter gut microbiota, including the increases in most Clostridium spp., Bacteroides spp., Citrobacter spp., Cronobacter spp., Enterobacter spp., Enterococcus spp., Klebsiella spp., Parabacteroides spp., and Pseudomonas spp. and the reduction of several Blautia spp. and most Ruminococcus spp. (192). Although clinical trials are challenging, especially introducing prebiotics and probiotics to modulate the gut microbiome, constant and in-depth studies must be performed as there are several differences in metabolic profiles determined by gut microbiota (193). The microbiota response to treatment is highly personalized. The breakdown of curcumin and the biotransformed products must also be elucidated, as curcumin degradation products and/or metabolites possibly access the systemic circulation and metabolic system, albeit at great variability. Thus, the results from clinical trials must be facilitated by concomitant biofluids marker assessments to investigate curcumin administration and the correlated clinical outcomes.