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<journal-id journal-id-type="publisher-id">Front. Pharmacol.</journal-id>
<journal-title>Frontiers in Pharmacology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Pharmacol.</abbrev-journal-title>
<issn pub-type="epub">1663-9812</issn>
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<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1348297</article-id>
<article-id pub-id-type="doi">10.3389/fphar.2024.1348297</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Pharmacology</subject>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Probiotics as modulators of gut-brain axis for cognitive development</article-title>
<alt-title alt-title-type="left-running-head">Kumar et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fphar.2024.1348297">10.3389/fphar.2024.1348297</ext-link>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Kumar</surname>
<given-names>Akash</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<contrib contrib-type="author">
<name>
<surname>Sivamaruthi</surname>
<given-names>Bhagavathi Sundaram</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
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<contrib contrib-type="author">
<name>
<surname>Dey</surname>
<given-names>Swarnima</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
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<contrib contrib-type="author">
<name>
<surname>Kumar</surname>
<given-names>Yogesh</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<contrib contrib-type="author">
<name>
<surname>Malviya</surname>
<given-names>Rishabha</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Prajapati</surname>
<given-names>Bhupendra G.</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Chaiyasut</surname>
<given-names>Chaiyavat</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
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<aff id="aff1">
<sup>1</sup>
<institution>Department of Food Technology, SRM University</institution>, <addr-line>Sonipat</addr-line>, <addr-line>Delhi</addr-line>, <country>India</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Office of Research Administration</institution>, <institution>Chiang Mai University</institution>, <addr-line>Chiang Mai</addr-line>, <country>Thailand</country>
</aff>
<aff id="aff3">
<sup>3</sup>
<institution>Innovation Center for Holistic Health, Nutraceuticals, and Cosmeceuticals</institution>, <institution>Faculty of Pharmacy</institution>, <institution>Chiang Mai University</institution>, <addr-line>Chiang Mai</addr-line>, <country>Thailand</country>
</aff>
<aff id="aff4">
<sup>4</sup>
<institution>Amity Institute of Food Technology</institution>, <institution>Amity University</institution>, <addr-line>Noida</addr-line>, <addr-line>Uttar Pradesh</addr-line>, <country>India</country>
</aff>
<aff id="aff5">
<sup>5</sup>
<institution>Department of Paramedical and Allied Sciences</institution>, <institution>School of Medical and Allied Sciences</institution>, <institution>Galgotias University</institution>, <addr-line>Greater Noida</addr-line>, <addr-line>Uttar Pradesh</addr-line>, <country>India</country>
</aff>
<aff id="aff6">
<sup>6</sup>
<institution>Shree S. K. Patel College of Pharmaceutical Education and Research</institution>, <institution>Ganpat University</institution>, <addr-line>Mehsana</addr-line>, <country>India</country>
</aff>
<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/129670/overview">Budheswar Dehury</ext-link>, Regional Medical Research Center (ICMR), India</p>
</fn>
<fn fn-type="edited-by">
<p>
<bold>Reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/1267868/overview">Attayeb Mohsen</ext-link>, National Institutes of Biomedical Innovation, Health and Nutrition, Japan</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Bhupendra G. Prajapati, <email>bhupen27@gmail.com</email>; Chaiyavat Chaiyasut, <email>chaiyavat@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="epub">
<day>20</day>
<month>02</month>
<year>2024</year>
</pub-date>
<pub-date pub-type="collection">
<year>2024</year>
</pub-date>
<volume>15</volume>
<elocation-id>1348297</elocation-id>
<history>
<date date-type="received">
<day>02</day>
<month>12</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>05</day>
<month>02</month>
<year>2024</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2024 Kumar, Sivamaruthi, Dey, Kumar, Malviya, Prajapati and Chaiyasut.</copyright-statement>
<copyright-year>2024</copyright-year>
<copyright-holder>Kumar, Sivamaruthi, Dey, Kumar, Malviya, Prajapati and Chaiyasut</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Various microbial communities reside in the gastrointestinal tract of humans and play an important role in immunity, digestion, drug metabolism, intestinal integrity, and protection from pathogens. Recent studies have revealed that the gut microbiota (GM) is involved in communication with the brain, through a bidirectional communication network known as the gut-brain axis. This communication involves humoral, immunological, endocrine, and neural pathways. Gut dysbiosis negatively impacts these communication pathways, leading to neurological complications and cognitive deficits. Both pre-clinical and clinical studies have demonstrated that probiotics can restore healthy GM, reduce intestinal pH, and reduce inflammation and pathogenic microbes in the gut. Additionally, probiotics improve cell-to-cell signaling and increase blood-brain-derived neurotrophic factors. Probiotics emerge as a potential approach for preventing and managing neurological complications and cognitive deficits. Despite these promising findings, the safety concerns and possible risks of probiotic usage must be closely monitored and addressed. This review article provides a brief overview of the role and significance of probiotics in cognitive health.</p>
</abstract>
<kwd-group>
<kwd>cognition</kwd>
<kwd>gut-brain axis</kwd>
<kwd>
<italic>Lactobacillus</italic>
</kwd>
<kwd>
<italic>Bifidobacterium</italic>
</kwd>
<kwd>inflammation</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Neuropharmacology</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="s1">
<title>1 Introduction</title>
<p>Cognition was once assumed to be controlled only by the central nervous system (CNS) (<xref ref-type="bibr" rid="B76">Zhu et al., 2020</xref>), but recent studies have revealed that a diverse range of factors plays a role in its regulation and influence. The gastrointestinal tract of humans is a habitat of various microbial communities, referred to as gut microbiota (GM) (<xref ref-type="bibr" rid="B52">Patel et al., 2023</xref>). GM may impact host health and is regulated by various factors such as stress, age, food, and host genetics (<xref ref-type="bibr" rid="B43">Long-Smith et al., 2020</xref>). The gut and brain communicate through a bidirectional communication network, known as the gut-brain axis (GBA) (<xref ref-type="bibr" rid="B40">Kumar et al., 2023</xref>). GM dysbiosis may alter brain structure, brain vascular physiology, and blood-brain barrier (BBB) permeability which may cause neurological disorders and cognitive impairment (<xref ref-type="bibr" rid="B76">Zhu et al., 2020</xref>). Therefore, GM may be a potential target for preventing and treating cognitive impairment (<xref ref-type="bibr" rid="B63">Sun et al., 2020</xref>; <xref ref-type="bibr" rid="B21">Eastwood et al., 2021</xref>).</p>
<p>Probiotics are &#x201c;live microorganisms that, when administrated in sufficient amounts, confer a health benefit to the host&#x201d; (<xref ref-type="bibr" rid="B45">Mart&#xed;n and Langella_2019</xref>). Probiotic administration results in the restoration of GM, changes in microbiota-derived metabolites, reduction in inflammation, and maintains hypothalamic pituitary adrenal (HPA) axis function and gut barrier integrity (<xref ref-type="bibr" rid="B53">Plaza-Diaz et al., 2019</xref>). In recent years, pre-clinical and clinical studies have described the role of probiotics in cognitive health (<xref ref-type="bibr" rid="B60">Sivamaruthi et al., 2019</xref>; <xref ref-type="bibr" rid="B65">Thangaleela et al., 2022</xref>). This review aims to provide a concise summary of the probiotic potential for preventing and treating cognitive impairments.</p>
</sec>
<sec id="s2">
<title>2 Gut-brain communication</title>
<p>The gut and brain communicate through a complex network which includes various pathways. The neurological pathway includes the enteric nervous system (ENS), vagus nerves (VN), and gastrointestinal neurotransmitters. Modulation of afferent sensory nerves produces biologically active catecholamines and local neurotransmitters such as histamine. GM may impact the availability of nutrients, resulting in the alteration of peptide release from enteroendocrine cells and affecting the GBA. The dysbiosis of GM may cause inflammation and release of cytokines, which influence the GBA. Bacterial metabolites may affect the humoral system, cross from the BBB, and regulate microglia for cognitive development (<xref ref-type="bibr" rid="B4">Appleton, 2018</xref>; <xref ref-type="bibr" rid="B25">Gwak and Chang, 2021</xref>). The communication pathways of the microbiota-GBA have been represented in <xref ref-type="fig" rid="F1">Figure 1</xref> (<xref ref-type="bibr" rid="B41">Lin et al., 2020</xref>).</p>
<fig id="F1" position="float">
<label>FIGURE 1</label>
<caption>
<p>The communication pathways of the microbiota-gut-brain axis (Adapted with permission from <xref ref-type="bibr" rid="B41">Lin et al., 2020</xref>).</p>
</caption>
<graphic xlink:href="fphar-15-1348297-g001.tif"/>
</fig>
<sec id="s2-1">
<title>2.1 GM and GBA in cognition and neurological diseases</title>
<p>Studies have demonstrated that gut bacteria can produce neurotransmitters and other signaling chemicals that affect brain function and development (<xref ref-type="bibr" rid="B49">Morais et al., 2020</xref>; <xref ref-type="bibr" rid="B11">Chen et al., 2021</xref>). Recent studies detailed the associations between GM, mental health, and psychological diseases and disorders including anxiety and depression (<xref ref-type="bibr" rid="B40">Kumar et al., 2023</xref>). Genetics, nutrition, environment, and early life experiences play a role in mental health and development via GM. However, to completely understand the influence of GBA on human health and wellbeing, further studies are required (<xref ref-type="bibr" rid="B36">Kelsey et al., 2019</xref>). According to a meta-analysis, infants born via cesarean section had a slightly higher chance of developing attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) than those born vaginally (<xref ref-type="bibr" rid="B14">Curran et al., 2015</xref>). A study revealed that children with ASD specifically exhibit different patterns of bacterial classes, for example, ASD children have an abundance of toxin-producing bacteria, like <italic>Clostridia</italic> (<xref ref-type="bibr" rid="B36">Kelsey et al., 2019</xref>).</p>
<p>The association of GM with the cognitive function of the infant has been reported. Three different microbial clusters have been identified, based on the variations in the prevalence of three important bacterial species, <italic>Faecalibacterium, Bacterioides</italic>, and <italic>Ruminococcaceae</italic>. The study showed the differences between the three groups in the Early Learning Composite Score (measures an infant&#x2019;s overall performance in activities involving cognitive and motor development). The newborns with a comparatively high abundance of <italic>Bacteroides</italic> had the greatest scores. In contrast, newborns with a reasonably high abundance of <italic>Faecalibacterium</italic> had the lowest cognitive and motor development scores. Also, the research findings revealed structural variations in the brain; the newborns with a substantial abundance of <italic>Bacteroides</italic> showing a bigger right superior occipital gyrus at age one compared to infants in the other two groups (<xref ref-type="bibr" rid="B9">Carlson et al., 2018</xref>). Kelsey et al. reported that gut microbial diversity at first year of life reflected cognitive development at second year of age. So, the result was predicted that the microbiome affects the functions of cognitive development differently during infancy than in later stages in the developing phases of life (<xref ref-type="bibr" rid="B36">Kelsey et al., 2019</xref>).</p>
<p>The microbiome&#x2019;s initial formation and the nervous system&#x2019;s growth and maturation co-occur from the very earliest stages of fetal development. Recent studies reveal the role of microbiomes in brain development and neurological diseases and disorders (<xref ref-type="bibr" rid="B16">Dash et al., 2022</xref>; <xref ref-type="bibr" rid="B50">Nandwana et al., 2022</xref>). Any issue impairing brain function might also potentially result in several neurodevelopmental disorders (NDDs) (<xref ref-type="bibr" rid="B16">Dash et al., 2022</xref>; <xref ref-type="bibr" rid="B70">Wang et al., 2022</xref>). Several NDDs have been reported, including intellectual development disorder, ADHD, ASD, specific learning disabilities like dyslexia or dyscalculia, conduct disorders, motor disorders (tic disorders, Tourette&#x2019;s syndrome), and a congenital disorder-cerebral palsy (<xref ref-type="bibr" rid="B3">Antolini and Colizzi, 2023</xref>). The people with NDD struggle to operate in social, intellectual, professional, and personal spheres of life. Impaired brain activities affect emotions, self-control, learning capacity, memory, intelligence quotient, and social skills. The first sign and behavioral difficulties may appear in early infancy, but the entire spectrum of NDDs becomes visible when the child grows. The spectrum of developmental impairments frequently persists throughout the person&#x2019;s lifetime (<xref ref-type="bibr" rid="B66">Thapar et al., 2017</xref>). The symptoms of NDDs might be alleviated by interventions that target GM (<xref ref-type="bibr" rid="B68">Vendrik et al., 2020</xref>).</p>
<p>A linkage was found between the brain&#x2019;s functions or dysfunction and the host&#x2019;s GM (<xref ref-type="bibr" rid="B34">Iliodromiti et al., 2023</xref>). A meta-analysis study compared GM of kids with and without ASD. The gut of children with ASD has significantly higher concentrations of <italic>Bacteroides, Parabacteroides</italic>, and <italic>Clostridium</italic> species, while <italic>Bifidobacterium</italic> species are lower. This dysbiosis could contribute to the development of ASD (<xref ref-type="bibr" rid="B32">Iglesias-V&#xe1;zquez et al., 2020</xref>). Also, another study showed that autistic kids had high concentrations of specific bacteria such as <italic>Clostridium, Desulfovibrio, Sutterella</italic>, and <italic>Lactobacillus</italic>. Still, the results are inconsistent (<xref ref-type="bibr" rid="B7">Bezawada et al., 2020</xref>), indicating that further studies are needed to know whether the altered microbiome is the cause or consequence of the condition.</p>
<p>Bundgaard-Nielsen et al. reported that the people with ADHD and ASD share GM sign (both alpha and beta diversity), which was different from the control. A high abundance of <italic>Eggerthella</italic>, <italic>Hungatelle</italic> and <italic>Ruminococcus gnavus</italic>, and a lower relative abundance of <italic>Coprobacter</italic> and <italic>Howardella</italic> were found among the ADHD and ASD subjects (<xref ref-type="bibr" rid="B8">Bundgaard-Nielsen et al., 2023</xref>). Meta-analysis reported no significant differences in ADHD patients, in terms of their alpha diversity indexes. Especially, genus <italic>Blautia</italic> abundance was higher in ADHD subjects than controls (<xref ref-type="bibr" rid="B70">Wang et al., 2022</xref>). The meta-analysis showed that only heterogenic data is available on the GM of ADHD patients. So, further studies are required using more study subjects, which may explain the relationship between microbial dysbiosis and ADHD.</p>
</sec>
</sec>
<sec id="s3">
<title>3 Role of probiotics in gut health</title>
<p>Probiotics are living, non-pathogenic bacteria and yeast that are beneficial for the human body when administrated and improve and promote microbial balance, particularly in the digestive system (<xref ref-type="bibr" rid="B45">Mart&#xed;n and Langella, 2019</xref>). They primarily comprise <italic>Lactobacillus</italic> and <italic>Bifidobacterium</italic> species or <italic>Saccharomyces boulardii</italic> (<xref ref-type="bibr" rid="B48">Mishra and Acharya, 2021</xref>). The probiotic strains are involved in several physiological events, including reducing the pH of the intestine, cell-to-cell signaling, lower and preventing the colonization of pathogenic microbes and regulating the immune response of the host (<xref ref-type="bibr" rid="B31">Iacob et al., 2019</xref>). A separate probiotic group is called &#x201c;psychobiotics&#x201d;, which could improve psychological and mental health and influence mood, anxiety, focus, memory, and cognition (<xref ref-type="bibr" rid="B58">Sharma and Kaur, 2020</xref>; <xref ref-type="bibr" rid="B65">Thangaleela et al., 2022</xref>).</p>
<p>The collection of microbes, their genomes, and their products that inhabit the human intestine is referred to as the gut &#x201c;microbiome&#x201d; as opposed to the microbes themselves, which are referred to as &#x201c;microbiota&#x201d; (<xref ref-type="bibr" rid="B17">De Vos et al., 2022</xref>). The most common strain of GM belongs to the phyla like <italic>Bacteroides, Proteobacteria,</italic> and <italic>Actinobacteria</italic> while the most prevalent genera are <italic>Streptococcus, Pseudomonas, Bacteroides, Fusobacteria, Clostridium,</italic> and <italic>Lactobacillus</italic> (<xref ref-type="bibr" rid="B34">Iliodromiti et al., 2023</xref>). The gut bacteria associated with the host chronic inflammation and defense system (<xref ref-type="bibr" rid="B23">Ferreira et al., 2014</xref>), preserve the underlying framework of the mucosal barrier (<xref ref-type="bibr" rid="B51">Paone and Cani, 2020</xref>), and aid in the host&#x2019;s metabolism (<xref ref-type="bibr" rid="B42">Lindsay et al., 2020</xref>). GM is associated with the production of several gastrointestinal hormones, short-chain fatty acids and vitamins, and medication uptake (<xref ref-type="bibr" rid="B46">Mendoza-Le&#xf3;n et al., 2023</xref>). It is known that the disruption in healthy GM results in inflammation (<xref ref-type="bibr" rid="B30">Huang et al., 2019</xref>). Additionally, it has been claimed that inflammatory states are linked to diseases like depression and anxiety. The GBA is thought to be responsible for this phenomenon (<xref ref-type="bibr" rid="B40">Kumar et al., 2023</xref>).</p>
</sec>
<sec id="s4">
<title>4 Probiotics, cognitive development, and neurological diseases and disorders</title>
<p>GM may influence various brain growth and operations elements, such as microglia and astrocyte polarisation, maturation, and control of neurotransmission, neurogenesis, and myelination (<xref ref-type="bibr" rid="B24">Ghezzi et al., 2021</xref>). Probiotics could influence the composition of GM and restore the gut ecosystem and be used as a potential approach for preventing and treating cognitive deficits (<xref ref-type="bibr" rid="B60">Sivamaruthi et al., 2019</xref>; <xref ref-type="bibr" rid="B65">Thangaleela et al., 2022</xref>). For example, the supplementation of a probiotic mixture (<italic>Lactobacillus acidophilus</italic>, <italic>L. rhamnosus</italic> and <italic>Bifidobacteria longum</italic>) for 3&#xa0;months improved the abundance of <italic>Bifidobacteria</italic> and <italic>Lactobacilli</italic> levels and symptoms of autism assessed by the Autism Treatment Evaluation Checklist (<xref ref-type="bibr" rid="B57">Shaaban et al., 2018</xref>).</p>
<p>Probiotics maintain a healthy environment in the intestine and reduce the various risk factors (<xref ref-type="bibr" rid="B67">Varela-Trinidad et al., 2022</xref>). Ishii et al. reported the facilitation of hippocampus learning and memory in mice model of Parkinson&#x2019;s disease after administering <italic>Bifidobacterium breve (B. breve)</italic> strain A1. <italic>B. breve</italic> A1 supplementation recovered the transcriptional level expression of synaptophysin (SYP) and postsynaptic density protein-95 (PSD95) synaptic protein, which is involved in synaptic formation and stability (<xref ref-type="bibr" rid="B35">Ishii et al., 2021</xref>). Likely, the supplementation of a probiotic mixture containing <italic>B. bifidum, B. longum, L. rhamnosus, L. rhamnosus</italic> GG, <italic>L. plantarum</italic> LP28, and <italic>Lactococcus lactis</italic> subsp. <italic>lactis</italic> has improved the motor neuron function in mice models of Parkinson&#x2019;s disease. Probiotic interventions could provide neuroprotection and reduce the exerts, improving dopaminergic neuronal degeneration (<xref ref-type="bibr" rid="B27">Hsieh et al., 2020</xref>). <italic>B. animalis</italic> subsp. <italic>Lactis</italic> and arginine administration improved cognitive flexibility in C57BL/6 mice, and the study proposed that maintaining a controlled intestinal environment with functional foods like probiotics could improve cognitive flexibility (<xref ref-type="bibr" rid="B33">Ikuta et al., 2023</xref>).</p>
<p>The administration of <italic>L. plantarum</italic> and <italic>B. bifidum</italic> in Wistar rats for 8 weeks increased the concentration of choline acetyltransferase and brain-derived neurotrophic factor in the hippocampus (<xref ref-type="bibr" rid="B1">A&#x11f;ag&#xfc;nd&#xfc;z et al., 2022</xref>). <italic>L. plantarum</italic> DP189 strain helps in the regulation of the P13K/AKE/GSK-3&#x3b2; pathway in Alzheimer&#x2019;s disease mice, resulting in the improvement of dysbiosis and prevented <italic>tau</italic> hyperphosphorylation (<xref ref-type="bibr" rid="B61">Song et al., 2022</xref>). It has been reported that <italic>L. plantarum</italic> PS128 aids in regulating glycogen synthase kinase 3&#x3b2; activity in streptozotocin-accelerated cognitive dysfunction mice (<xref ref-type="bibr" rid="B29">Huang et al., 2021</xref>).</p>
<p>There were several probiotic strains like <italic>B. fragilis, Prevotella histicola, Lactobacillus</italic> sp., <italic>B. animalis</italic>, <italic>L. plantarum</italic>, <italic>L. paracasei</italic> administered to the animal model, which showed the essential impact on the level of anti-inflammatory markers and delay the onset of multiple sclerosis. There would be enhancement in the level of Treg&#x2019;s (CD4<sup>&#x2b;</sup> CD25<sup>&#x2b;</sup> Fox P3<sup>&#x2b;</sup>) and regulate the balance of Th1/Th17 and Th2 cytokines by probiotics in multiple sclerosis (<xref ref-type="bibr" rid="B20">Dziedzic and Saluk, 2022</xref>).</p>
</sec>
<sec id="s5">
<title>5 Mechanisms underlying probiotic effects on the gut-brain axis</title>
<p>Gut microbial disruption can negatively impact mental health. Therefore, restoration of gut microbiota could be used as an intervention to improve mental health. Modifying the GM could affect the functioning of the hippocampus. Bacterial toxins (Lipopolysaccharides; typical consequences of dysbiosis) and amyloid beta (A&#x3b2;) may interact with certain pathways like the vagus nerve pathway, the immune pathway related to the cytokines, and the systemic pathway, which is related to hormones and neurotransmitters to enhance the permeability of blood-brain barrier, mucosal-intestine barrier and finally results in the malfunctioning of the hippocampus (<xref ref-type="bibr" rid="B64">Tang et al., 2021</xref>).</p>
<p>Probiotics play a crucial role in reducing oxidative stress by producing various antioxidant enzymes (catalase and superoxide dismutase), antioxidants (butyrate, folate, and glutathione), and chelating metal ions. Probiotics may prevent immune actions like inflammatory responses by inhibiting TLR activation (<xref ref-type="bibr" rid="B19">Dobielska et al., 2022</xref>). The reduced inflammatory state could enhance the blood-brain barrier integrity and improve neurological functions (<xref ref-type="bibr" rid="B72">Wang et al., 2023</xref>). In addition to probiotic&#x2019;s antioxidant and anti-inflammatory properties, they may improve cognitive function in depression by reducing hypothalamic-pituitary-adrenal (HPA)-axis dysfunction, and by increasing monoamine levels and neuroplasticity (<xref ref-type="bibr" rid="B19">Dobielska et al., 2022</xref>).</p>
<p>Studies have demonstrated that probiotics are associated with increased expression of BDNF and may be responsible for better cognitive performance (<xref ref-type="bibr" rid="B30">Huang et al., 2019</xref>). Prolonged supplementation of probiotics increases the concentration of tryptophan in the peripheral system and improves mental health. Probiotics exert their antidepressant effects by upregulating enzymes involved in serotonin synthesis (<xref ref-type="bibr" rid="B44">Luki&#x107; et al., 2022</xref>). Probiotics can change 5-hydroxytryptamine receptors, dopamine, and protein c-Fos levels; they may be responsible for modulation in the biochemistry of the CNS (<xref ref-type="bibr" rid="B69">Wang et al., 2016</xref>). Probiotics (<italic>Rouxiella badensis</italic> subsp. <italic>acadiensis</italic>) also increase the expression of certain mRNA, serotonin-1A (5-HT1A), and serotonin (5-HT)-2C receptors in the hippocampus (<xref ref-type="bibr" rid="B74">Yahfoufi et al., 2021</xref>), which could improve cognition.</p>
<p>Probiotics could modify the levels of neurotransmitters and neuromodulators, including serotonin, gamma-aminobutyric acid, acetylcholine, norepinephrine, N-acetyl aspartate, dopamine, and glutamate, which regulates the brain&#x2019;s activity via metabolic pathways (<xref ref-type="bibr" rid="B12">Chudzik et al., 2021</xref>; <xref ref-type="bibr" rid="B18">Dicks, 2022</xref>). Though the previous studies provide established knowledge of the possible mechanisms of probiotics-mediated cognitive improvement, further studies are needed to improve the probiotic-based treatment opportunities for cognitive declines.</p>
</sec>
<sec id="s6">
<title>6 Clinical trials and observational studies</title>
<p>Both clinical trials and observational studies are crucial for assessing the effectiveness of probiotics in cognitive health. During aging, the chances of dementia and changes in their behavior also increase. Several studies reported the impact of supplementation probiotics on cognition and GM (<xref ref-type="table" rid="T1">Table 1</xref>). The supplementation of <italic>Lactiplantibacillus plantarum</italic> OLL 2712 for 12 weeks reduces inflammation by lowering the abundance of certain genera such as <italic>Oscillibacter, Monoglobus</italic>, and <italic>Lachnoclostridium</italic> in elderly adults (aged &#x3e;65 years). The OLL2712 supplementation improved visual and composite memory (<xref ref-type="bibr" rid="B55">Sakurai et al., 2022</xref>). Tang et al. reported that probiotics (Lactobacilli and Bifidobacteria) act as neuroprotective agents in cognitively impaired elderly individuals and AD patients (<xref ref-type="bibr" rid="B64">Tang et al., 2021</xref>). Patients with Parkinson&#x2019;s disease was supplemented with probiotics containing <italic>L. casei</italic> Shirota (6.5 &#xd7; 10<sup>9</sup> colony forming units) daily for 5 weeks, which increases the bowel opening and reduces constipation, bloating, and abdominal pain. This study suggested that probiotics can effectively alleviate constipation symptoms in Parkinsons patients (<xref ref-type="bibr" rid="B10">Cassani et al., 2011</xref>).</p>
<table-wrap id="T1" position="float">
<label>TABLE 1</label>
<caption>
<p>The representative studies on the influences of probiotic intervention on cognitive impairment.</p>
</caption>
<table>
<thead valign="top">
<tr>
<th align="left">Study type</th>
<th align="left">Subjects</th>
<th align="left">Interventions, dose, and duration</th>
<th align="left">Findings</th>
<th align="left">References</th>
</tr>
</thead>
<tbody valign="top">
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Elderly patients following non-cardiac surgery (<italic>n</italic> &#x3d; 120)</td>
<td align="left">Capsule containing <italic>L. acidophilus, B. longum,</italic> and <italic>Enterococcus faecalis</italic> (&#x2265;10<sup>7</sup> CFU of each strain/capsule); Two capsules/day; During their hospital stay</td>
<td align="left">Reduced the plasma IL-6 and cortisol levels. Probiotic supplementation could relieve post-operative cognitive impairment after non-cardiac surgery in elderly patients</td>
<td align="left">
<xref ref-type="bibr" rid="B71">Wang et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Healthy adults with mild Cognitive Impairment (Age 50&#x2013;79&#xa0;years) (<italic>n</italic> &#x3d; 80)</td>
<td align="left">
<italic>B. breve</italic> MCC1274 (1 &#xd7; 10<sup>10</sup> CFU/capsule); Two capsules/day; For 16&#xa0;weeks</td>
<td align="left">Slow down the mild cognitive impairment symptoms. Improved the anti-inflammatory system</td>
<td align="left">
<xref ref-type="bibr" rid="B6">Bernier et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Elderly with memory impairment and 3rd repletion value of WLMIR. (<italic>n</italic> &#x3d; 93)</td>
<td align="left">
<italic>Limosilactobacillus fermentum</italic> A2.8 (10<sup>7</sup> or 10<sup>8</sup> CFU); For 12&#xa0;weeks</td>
<td align="left">10<sup>7</sup> CFU supplemented group showed improvement in memory and visuospatial function. 10<sup>7</sup>&#xa0;CFU supplemented group showed improvement in memory, learning, and verbal fluency</td>
<td align="left">
<xref ref-type="bibr" rid="B26">Handajani et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Patients undergoing hip or knee arthroplasty. (Age &#x2265;60&#xa0;years) (<italic>n</italic> &#x3d; 106)</td>
<td align="left" style="color:#282828">
<italic>L. acidophilus, B. longum</italic> and <italic>Enterococcus faecalis</italic> (&#x3e;10<sup>7</sup> CFU each strain); Four capsules, twice/day; During hospital stay</td>
<td align="left">Improved verbal memory domain. Aid in preventing perioperative development of POCD.</td>
<td align="left">
<xref ref-type="bibr" rid="B28">Hu et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Healthy elderly subjects (Age &#x2265;65&#xa0;years) (<italic>n</italic> &#x3d; 63)</td>
<td align="left">
<italic>B. bifidum</italic> BGN4 and <italic>B. longum</italic>&#xa0;BORI (1 &#xd7; 10<sup>9</sup> CFU each strain); Four capsules/day; For 12&#xa0;weeks</td>
<td align="left">Improved the mental flexibility test and stress score. Reduced stress and inflammation-causing gut bacteria</td>
<td align="left">
<xref ref-type="bibr" rid="B37">Kim et al. (2021)</xref>
</td>
</tr>
<tr>
<td align="left">RCT</td>
<td align="left">Middle aged (Age 52&#x2013;59&#xa0;years) and older adult (Age 60&#x2013;75&#xa0;years) with mild cognitive impairment (<italic>n</italic> &#x3d; 169)</td>
<td align="left">
<italic>L. rhamnosus</italic> GG (10<sup>9</sup> CFU) and Prebiotic inulin from chicory root extract (200&#xa0;mg)/capsule. Two capsules/day; For 12&#xa0;weeks</td>
<td align="left">Reduced the abundances of <italic>Prevotella</italic> and <italic>Dehalobacterium.</italic> Improved the cognitive score</td>
<td align="left">
<xref ref-type="bibr" rid="B2">Aljumaah et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Older adults with mild cognitive impairment (Age 65&#x2013;88&#xa0;years) (<italic>n</italic> &#x3d; 130)</td>
<td align="left">
<italic>B. breve</italic> MCC1274 (2 &#xd7; 10<sup>9</sup> CFU); For 24&#xa0;weeks</td>
<td align="left">ADAS&#x2019; subscales &#x201c;orientation in time&#x201d; and &#x201c;writing&#x201d; were significantly improved. Suppressed brain atrophy progression</td>
<td align="left">
<xref ref-type="bibr" rid="B5">Asaoka et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">RDB-PCT</td>
<td align="left">Healthy older adults without cognitive impairment (Age 60&#x2013;75&#xa0;years) (<italic>n</italic> &#x3d; 60)</td>
<td align="left">
<italic>B. longum</italic> BB68S (5 &#xd7; 10<sup>10</sup> CFU/sachet); One sachet/day; For 8 weeks</td>
<td align="left">Increased the relative abundances of <italic>Cellulosilyticum, Dorea, Lachnospira</italic>, and <italic>Bifidobacterium</italic>. Decreased the relative abundances of <italic>Porphyromonas, Bilophila, Parabacteroides, Tyzzerella, Collinsella, Epulopiscium, Granulicatella,</italic> and <italic>unclassified_c_Negativicutes</italic>. RBANS score was significantly improved</td>
<td align="left">
<xref ref-type="bibr" rid="B59">Shi et al. (2022)</xref>
</td>
</tr>
<tr>
<td align="left">RCT</td>
<td align="left">Older adults with mild cognitive impairment (Age &#x3e;60&#xa0;years) (<italic>n</italic> &#x3d; 42)</td>
<td align="left">
<italic>Lactococcus lactis</italic> BioF-224, <italic>Lactococcus lactis</italic> LY-66, <italic>B. lactis</italic> CP-9, <italic>B. animalis</italic> BB-115, <italic>B. infantis</italic> BLI-02, <italic>B. lactis</italic> HNO19, <italic>L. plantarum</italic> CN 2018, <italic>L. plantarum</italic> BioF-228, <italic>L. rhamnosus</italic> Bv-77, <italic>L. rhamnosus</italic> HNO01, <italic>L. johnsonii</italic> MH-68, <italic>L. paracasei</italic> MP137, <italic>L. paracasei</italic> GL-156, <italic>L. salivarius</italic> AP-32, <italic>L. acidophilus</italic> TYCA06, <italic>L. casei</italic> CS-773, <italic>L. reuteri</italic> TSR332, <italic>L. fermentum</italic> TSF331 (&#x3e;2 &#xd7; 10<sup>10</sup> CFU/g); 2g/day; For 12&#xa0;weeks</td>
<td align="left">The relative abundances of <italic>Haemophilus, Pantoea, Erysipelotrichaceae, Anaerostipes, Ruminococcus, Prevotellaceae, Lachnospiraceae, Muribaculaceae, Coprococcus</italic>, and <italic>Blautia</italic> were increased. Cognitive function (based on the MMSE and MCA scores) and sleep quality were improved</td>
<td align="left">
<xref ref-type="bibr" rid="B22">Fei et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left">RCT</td>
<td align="left">Healthy adult females (Age 19&#x2013;31&#xa0;years) (<italic>n</italic> &#x3d; 53)</td>
<td align="left">
<italic>L. acidophilus</italic> LA02 and <italic>B. lactis</italic> BS01 (2 &#xd7; 10<sup>9</sup> CFU/capsule); For 6&#xa0;weeks</td>
<td align="left">No significant impact on cognition in the healthy population</td>
<td align="left">
<xref ref-type="bibr" rid="B15">Czajeczny et al. (2023)</xref>
</td>
</tr>
<tr>
<td align="left">RCT</td>
<td align="left">Adults with active physical activity (Average age &#x223c;64.3&#xa0;years) (<italic>n</italic> &#x3d; 127)</td>
<td align="left">
<italic>L. rhamnosus</italic> GG</td>
<td align="left">No significant improvement in cognitive function</td>
<td align="left">
<xref ref-type="bibr" rid="B56">Sanborn et al. (2022)</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>RDB-PCT, Randomized double-blind and placebo-controlled trial; RCT, Randomized clinical trial; CFU, Colony forming unit; WLMIR, Word List Memory Immediate Recall; POCD, Postoperative cognitive dysfunction; ADAS, Alzheimer disease assessment scale; RBANS, Repeatable Battery for the Assessment of Neuropsychological Status; MMSE, Mini-mental state examination; MCA, Montreal cognitive assessment.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>Hu et al. reported that the supplementation of <italic>Lactobacillus acidophilus</italic>, <italic>Bifidobacterium longum</italic> and <italic>Enterococcus faecalis</italic> (&#x3e;10<sup>7</sup>&#xa0;CFU of each strain &#xd7; 4; twice/day) improved the verbal memory domain of performance in elderly subjects. The intervention group had a lower incidence of decline in specific verbal memory tests like the Hopkins Verbal Learning Test-Revised. Hospital stay duration, mortality rates, inflammatory markers, and white blood cell levels did not change significantly in both groups (<xref ref-type="bibr" rid="B28">Hu et al., 2023</xref>). <italic>Bifidobacterium bifidum</italic> BGN4 and <italic>Bifidobacterium longum</italic> BORI intervention for 12 weeks reduced the inflammation-causing gut bacteria, increased blood brain-derived neurotrophic factor (BDNF), and reduced stress levels in healthy elders. The study revealed that probiotic intake had no significant impact on cognitive domains such as language, memory, visuo-spatial processing, or other executive functions. However, after 12&#xa0;weeks of intervention, mental flexibility significantly improved in the probiotic group. Additionally, probiotics intake decreased stress levels and the abundance of specific bacterial genera, including <italic>Eubacterium, Allisonella, Clostridiales,</italic> and <italic>Prevotellaceae</italic> (<xref ref-type="bibr" rid="B37">Kim et al., 2021</xref>).</p>
<p>A meta-analysis by <xref ref-type="bibr" rid="B75">Zhu et al. (2021)</xref> reported that probiotics significantly improved cognitive functions, particularly in mild cognitive impairment. At the same time, some factors can influence these benefits, such as probiotic strains, dosage, duration of intervention, and disease severity. In another meta-analysis, the impact of probiotics on cognitive function in patients with AD, mild cognitive impairment, and PD was analyzed. The study suggested probiotics could improve insulin resistance, lipid metabolisms, and cognitive and gastrointestinal health (<xref ref-type="bibr" rid="B73">Xiang et al., 2022</xref>). Not all the randomized clinical trials showed the positive impacts of probiotics on the subject&#x2019;s cognitive health (<xref ref-type="table" rid="T1">Table 1</xref>).</p>
</sec>
<sec id="s7">
<title>7 Safety considerations and side effects of probiotics</title>
<p>Though probiotics have health benefits, they have some limitations (<xref ref-type="bibr" rid="B38">Kothari et al., 2019</xref>; <xref ref-type="bibr" rid="B62">Sotoudegan et al., 2019</xref>; <xref ref-type="bibr" rid="B13">Congur and Dalgic, 2023</xref>). Probiotics may cause systemic infection by bacterial translocation, gastrointestinal side effects, transfer of antibiotic resistance genes, toxic metabolic effects, and immune stimulation, The bacterial translocation is responsible for sepsis, fungemia, bacteremia, endocarditis (<xref ref-type="bibr" rid="B13">Congur and Dalgic, 2023</xref>). Premature infants, people with weak immunity, are more susceptible to infections. Immune stimulation may occur through bacterial toxins, including lipoteichoic acid, peptidoglycan, and lipopolysaccharides. Also, the risk of immune activation depends upon the strain of microorganisms and the dose administered (<xref ref-type="bibr" rid="B38">Kothari et al., 2019</xref>). Patients with short bowel syndrome risk developing probiotic-induced d-lactic acidosis due to unwarranted bacterial growth in the small intestine (<xref ref-type="bibr" rid="B54">Rao et al., 2018</xref>). <sc>d</sc>-lactic acidosis encephalopathy has neurologic symptoms such as memory loss, delirium, ataxia, and dysarthria (<xref ref-type="bibr" rid="B39">Kowlgi and Chhabra, 2015</xref>). Generally, infants, critically ill patients, patients with compromised immune systems, and cancers are considered risky subjects (<xref ref-type="bibr" rid="B62">Sotoudegan et al., 2019</xref>).</p>
</sec>
<sec id="s8">
<title>8 Recommendations for safe probiotic use</title>
<p>Certain key safety points must be adopted to recommend probiotics for safer use. Microbiome profiling is recommended because it can help identify factors affecting how individuals respond to probiotics differently and test various theories and processes. Manufacturers of older strains who might not have used modern techniques of assessing the risk of antibiotic resistance should re-evaluate their strains to ensure compliance. Manufacturers ought to disclose each probiotic strain&#x2019;s antibiogram and, if necessary, offer an empirical course of therapy. Research into animal models is encouraged to improve our knowledge of detecting possible long-term impacts of probiotics, particularly regarding next-generation strains. Companies must monitor and report adverse occurrences in compliance with regulatory regulations for foods, dietary supplements, and medications (<xref ref-type="bibr" rid="B47">Merenstein et al., 2023</xref>).</p>
</sec>
<sec sec-type="conclusion" id="s9">
<title>9 Conclusion</title>
<p>Preclinical studies have highlighted the effects of probiotics on neurotransmitters, brain structure, and cognitive function in animal models. At the same time, clinical trials have demonstrated potential human benefits, including improved cognitive outcomes and reduced anxiety and depression. However, the safety concerns and possible risks of probiotic usage must be closely monitored and addressed. The next-generation of probiotics, for example, <italic>Akkermansia muciniphilia</italic>, has protein Amuc-1100 and extracellular vesicles that help regulate the metabolic system and gut barrier integrity and reduce lipopolysaccharides leakage and inflammation. However, further investigations and microbiome characterization are required to understand individual reactions and optimize the therapeutic potential of probiotics in preventing and managing cognitive deficits.</p>
</sec>
</body>
<back>
<sec id="s10">
<title>Author contributions</title>
<p>AK: Formal Analysis, Methodology, Writing&#x2013;original draft. BS: Conceptualization, Formal Analysis, Project administration, Supervision, Writing&#x2013;original draft, Writing&#x2013;review and editing. SD: Data curation, Formal Analysis, Writing&#x2013;original draft. YK: Data curation, Formal Analysis, Writing&#x2013;original draft. RM: Data curation, Formal Analysis, Writing&#x2013;original draft. BP: Conceptualization, Project administration, Supervision, Validation, Writing&#x2013;original draft. CC: Funding acquisition, Project administration, Resources, Supervision, Writing&#x2013;original draft, Writing&#x2013;review and editing.</p>
</sec>
<sec sec-type="funding-information" id="s11">
<title>Funding</title>
<p>The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by Fundamental Fund 2024, Chiang Mai University, Chiang Mai, Thailand.</p>
</sec>
<ack>
<p>The authors (BS and CC) gratefully acknowledge Chiang Mai University, Chiang Mai, for its support.</p>
</ack>
<sec sec-type="COI-statement" id="s12">
<title>Conflict of interest</title>
<p>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.</p>
<p>The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
</sec>
<sec sec-type="disclaimer" id="s13">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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