Probiotics from Thai Fermented Foods Reduced Anxiety and Enhanced Neuroplasticity in a Wistar Rat Model doi.org/10.26538/tjnpr/v6i6.15

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Vijitra L.-In
Worachot Saengha
Thipphiya Karirat
Ampa Konsue
Eakapol Wangkahart
Teeraporn Katisart

Abstract

Probiotics have a significant impact on mental health through the gut-brain axis mechanism. From Thai fermented foods, various probiotic bacterial strains have been isolated. The present study was aimed at investigating the effects of probiotics from Thai fermented foods on anxiety and neuroplasticity in a Wistar rat model. Six bacterial strains were isolated from Thai fermented foods and used to prepare a probiotic cocktail. Male rats were divided into three groups. Group 1 (CON) rats were given sterile, distilled water for 21 days. Group 2 (ANT) rats received four antibiotics over 21 days. Each rat in Group 3 (PRO) was administered antibiotics every day for seven days, followed by 14 days of probiotics. Compulsiveness, anxiety-like behavior, depression, and neuroplasticity were evaluated. The rat brain tissue specimens were collected at the end of the experiment and analyzed histologically. The expressions of the genes linked with brain inflammation, neuroplasticity, and HPA axis regulation were also examined. The results showed that 14 days of probiotic mixture treatment in the PRO group significantly improved anxiety levels (p<0.05), compared to the rats in the ANT group, but did not affect depression. Probiotics showed positive effects on neuroplasticity by lowering Bax but increasing Igf-1 and Gr mRNA gene expressions in PRO compared to ANT. They also demonstrated neuroprotectivity in the dentate gyrus. The findings of this study suggest that probiotics from Thai fermented foods decrease anxiety and improve neuroplasticity, thereby having the potential to become a functional food, enriched with psychobiotics to promote human mental behavior.

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L.-In, V., Saengha, W., Karirat, T., Konsue, A., Wangkahart, E., & Katisart, T. (2022). Probiotics from Thai Fermented Foods Reduced Anxiety and Enhanced Neuroplasticity in a Wistar Rat Model: doi.org/10.26538/tjnpr/v6i6.15. Tropical Journal of Natural Product Research (TJNPR), 6(6), 910-914. https://tjnpr.org/index.php/home/article/view/24
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How to Cite

L.-In, V., Saengha, W., Karirat, T., Konsue, A., Wangkahart, E., & Katisart, T. (2022). Probiotics from Thai Fermented Foods Reduced Anxiety and Enhanced Neuroplasticity in a Wistar Rat Model: doi.org/10.26538/tjnpr/v6i6.15. Tropical Journal of Natural Product Research (TJNPR), 6(6), 910-914. https://tjnpr.org/index.php/home/article/view/24

References

Rezac S, Kok CR, Heermann M, Hutkins R. Fermented foods as a dietary source of live organisms. Front Microbiol. 2018; 9(1785):1-29.

Dinan TG, Stanton C, Cryan JF. Psychobiotics: A novel class of psychotropic. Biol Psych. 2013; 74(10):720-726.

Guida F. Turco F, Iannotta M, De Gregorio D, Palumbo I, Sarnelli G. Antibiotics-induced microbiota perturbation causes gut endocannabinoidome changes, hippocampal neuroglial reorganization and depression in mice. Brain Behav Immunol. 2018; 67(1):230-245.

Zommiti M, Cambronel M, Maillot O, Barreau M, Sebei K, Feuilloley M, Connil N. Evaluation of probiotic properties and safety of Enterococcus faecium isolated from Artisanal Tunisian meat “Dried Ossban”. Front Microbiol. 2018; 9(1685):1-12.

Luang-In V, Katisart T, Konsue A, Nudmamud-Thanoi S, Narbad A, Saengha W, Wangkahart E, Pumriw S, Samappito W, Ma NL. Psychobiotic effects of multi-strain probiotics originated from Thai fermented foods in a rat model. Food Sci Anim Resourc. 2020; 40(6):1014-1032.

Angoa-Pérez M, Kane MJ, Briggs DI, Francescutti DM, Kuhn DM. Marble burying and nestlet shredding as tests of repetitive, compulsive-like behaviors in mice. J Visual Exp. 2013; 82(50978):1-7.

Pramoolsilpa G, Nudmamud-Thanoi S, Khongsombat O. The neuroprotective effects of germinated black glutinous rice diet on Aβ25-35 peptide induced learning and memory deficits in male rats. Thai J Pharmacol. 2017; 39(1):48-61.

Garman RH, Li AA, Kaufmann W, Auer RN, Bolon B. Recommended methods for brain processing and quantitative analysis in rodent developmental neurotoxicity studies. Toxicol Pathol. 2015; 44(1):14-42.

Abildgaard A, Elfving B, Hokland M, Wegener G, Lund S. Probiotic treatment reduces depressive-like behaviour in rats independently of diet. Psychoneuroendocrinol. 2017; 79(5):40-48.

Liang S, Wang T, Hu X, Luo J, Li W, Wu X, Duan Y, Jin F. Administration of Lactobacillus helveticus NS8 improves behavioral, cognitive, and biochemical aberrations caused by chronic restraint stress. Neurosci. 2015; 310(27):561-577.

Witkin JM. Animal models of obsessive-compulsive disorder. Curr Protoc Neurosci. 2008; 45(1):1-9.

Estanislau C. Cues to the usefulness of grooming behavior in the evaluation of anxiety in the elevated plus-maze. Psychol Neurosci. 2012; 5(1):105112.

Llaneza DC and Frye CA. Progestogens and estrogen influence impulsive burying and avoidant freezing behavior of naturally cycling and ovariectomized rats. Pharmacol Biochem Behav. 2009; 93(3):337-342.

Kalueff AV, Stewart AM, Song C, Berridge KC, Graybiel AM, Fentress JC. Neurobiology of rodent self-grooming and its value for translational neuroscience. Nature Rev Neurosci. 2016; 17(1):45-59.

Marin I, Goertz J, Ren T. Microbiota alteration is associated with the development of stress-induced despair behavior. Sci Rep. 2017; 7(43859):1-10.

Bravo JA, Forsythe P, Chew MV, Escaravage E, Savignac HM, Dinan TG, Bienenstock J, Cryan JF. Ingestion of Lactobacillus strain regulates emotional behavior and central GABA receptor expression in a mouse via the vagus nerve. Proc Natl Acad Sci USA. 2011; 108(38):16050-

Li N, Wang Q, Wang Y, Sun A, Lin Y, Jin Y, Li X. Oral probiotics ameliorate the behavioral deficits induced by chronic mild stress in mice via the gut microbiotainflammation axis. Front Behav Neurosci. 2018; 12(266):1-11.

Kosten TA, Galloway MP, Duman RS, Russell DS, D’Sa C. Repeated unpredictable stress and antidepressants differentially regulate expression of the Bcl-2 family of apoptotic genes in rat cortical, hippocampal, and limbic brain structures. Neuropsychopharmacol. 2008; 33(7):1545-1558.

Arnett MG, Pan MS, Doak W, Cyr PEP, Muglia LM, Muglia LJ. The role of glucocorticoid receptor-dependent activity in the amygdala central nucleus and reversibility of early-life stress programmed behavior. Transl. Psych. 2015; 5(4):1-8.

Wyrwoll CS, Holmes MC, Seckl JR. 11β-hydroxysteroid dehydrogenases and the brain: from zero to hero, a decade of progress. Front Neuroendocrinol. 2011; 32(3):265-286.

Gallezot JD, Nabulsi N, Henry S, Pracitto R, Planeta B, Ropchan J, Lin SF, Labaree D, Kapinos M, Shirali A, LaraJaime T, Gao H, Matuskey D, Walzer M, Marek GJ, Bellaire S, Yuan N, Carson RE, Huang Y. Imaging the enzyme 11β-hydroxysteroid dehydrogenase type 1 with PET: evaluation of the novel radiotracer 11C-AS2471907 in human brain. J Nucl Med. 2019; 60(8):1140-1146.

Amaral DG, Scharfman HE, Lavenex P. The dentate gyrus: fundamental neuroanatomical organization (dentate gyrus for dummies). Prog Brain Res. 2007; 163:3–22.

Kheirbek MA, Drew LJ, Burghardt NS, Costantini DO, Tannenholz L, Ahmari SE, Zeng H, Fenton AA, Hen R. Differential control of learning and anxiety along the dorsoventral axis of the dentate gyrus. Neuron. 2013; 77(5):955–968.

Hazzaa SM, Abdelaziz S, Abd Eldaim MA, Abdel-Daim MM, Elgarawany GE. Neuroprotective potential of Allium sativum against monosodium glutamate-induced excitotoxicity: impact on short-term memory, gliosis, and oxidative stress. Nutr. 2020; 12(1028):1-17.