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Journal of Clinical and
Basic Psychosomatics FND and gut microbiome

doi: 10.3389/fimmu.2014.00136 via free fatty acid receptor 2 in rodents. Int J Obes (Lond).
2015;39(3):424-429.
43. Apazoglou K, Mazzola V, Wegrzyk J, Frasca Polara G,
Aybek S. Biological and perceived stress in motor functional doi: 10.1038/ijo.2014.153
neurological disorders. Psychoneuroendocrinology.
2017;85:142-150. 54. Porter DW, Irwin N, Flatt PR, Gault VA. Prolonged
GIP receptor activation improves cognitive function,
doi: 10.1016/j.psyneuen.2017.08.023 hippocampal synaptic plasticity and glucose homeostasis in
44. Morais LH, Schreiber HL 4 , Mazmanian SK. The gut high-fat fed mice. Eur J Pharmacol. 2011;650(2-3):688-693.
th
microbiota-brain axis in behaviour and brain disorders. Nat doi: 10.1016/j.ejphar.2010.10.059
Rev Microbiol. 2021;19(4):241-255.
55. Borrego-Ruiz A, Borrego JJ. Influence of human gut
doi: 10.1038/s41579-020-00460-0 microbiome on the healthy and the neurodegenerative
45. Ullah H, Arbab S, Tian Y, et al. The gut microbiota-brain axis aging. Exp Gerontol. 2024;194:112497.
in neurological disorder. Front Neurosci. 2023;17:1225875. doi: 10.1016/j.exger.2024.112497
doi: 10.3389/fnins.2023.1225875 56. Muller PA, Schneeberger M, Matheis F, et al. Microbiota
46. Chen Y, Xu J, Chen Y. Regulation of neurotransmitters by modulate sympathetic neurons via a gut-brain circuit.
the gut microbiota and effects on cognition in neurological Nature. 2020;583(7816):441-446.
disorders. Nutrients. 2021;13(6):2099. doi: 10.1038/s41586-020-2474-7
doi: 10.3390/nu13062099 57. Kennedy PJ, Cryan JF, Dinan TG, Clarke G. Kynurenine
47. Strandwitz P, Kim KH, Terekhova D, et al. GABA- pathway metabolism and the microbiota-gut-brain axis.
modulating bacteria of the human gut microbiota. Nat Neuropharmacology. 2017;112(Pt B):399-412.
Microbiol. 2019;4(3):396-403. doi: 10.1016/j.neuropharm.2016.07.002
doi: 10.1038/s41564-018-0307-3 58. Dinan TG, Cryan J. Regulation of the stress response by the
48. Liu XF, Shao JH, Liao YT, et al. Regulation of short- gut microbiota: Implications for psychoneuroendocrinology.
chain fatty acids in the immune system. Front Immunol. Psychoneuroendocrinology. 2012;37(9):1369-1378.
2023;14:1186892. doi: 10.1016/j.psyneuen.2012.03.007
doi: 10.3389/fimmu.2023.1186892 59. Farooq RK, Alamoudi W, Alhibshi A, Rehman S,
49. Łoniewska B, Fraszczyk-Tousty M, Tousty P, Skonieczna- Sharma AR, Abdulla FA. Varied composition and underlying
Żydecka K, Maciejewska-Markiewicz D, Łoniewski I. mechanisms of gut microbiome in neuroinflammation.
Analysis of fecal short-chain fatty acids (SCFAs) in healthy Microorganisms. 2022;10(4):705.
children during the first two years of life: An observational doi: 10.3390/microorganisms10040705
prospective cohort study. Nutrients. 2023;15(2):367.
60. Stolzer I, Scherer E, Süß P, et al. Impact of microbiome-
doi: 10.3390/nu15020367 brain communication on neuroinflammation and
50. Dalile B, Van Oudenhove L, Vervliet B, Verbeke K. neurodegeneration. Int J Mol Sci. 2023;24(19):14925.
The role of short-chain fatty acids in microbiota gut- doi: 10.3390/ijms241914925
brain communication. Nat Rev Gastroenterol Hepatol.
2019;16(8):461-478. 61. Acioglu C, Heary RF, Elkabes S. Roles of neuronal toll-like
receptors in neuropathic pain and central nervous system
doi: 10.1038/s41575-019-0157-3 injuries and diseases. Brain Behav Immun. 2022;102:163-178.
51. Morris G, Berk M, Carvalho A, et al. The role of the doi: 10.1016/j.bbi.2022.02.016
microbial metabolites including tryptophan catabolites and
short chain fatty acids in the pathophysiology of immune- 62. Mitchell L, Smith SH, Braun JS, Herzog KH, Weber JR,
inflammatory and neuroimmune disease. Mol Neurobiol. Tuomanen EI. Dual phases of apoptosis in pneumococcal
2017;4(6):4432-4451. meningitis. J Infect Dis. 2004;190(11):2039-2046.
doi: 10.1007/s12035-016-0004-2 doi: 10.1086/425520
52. Larraufie P, Martin-Gallausiaux C, Lapaque N, et al. 63. Arentsen T, Qian Y, Gkotzis S, et al. The bacterial peptidoglycan-
SCFAs strongly stimulate PYY production in human sensing molecule Pglyrp2 modulates brain development and
enteroendocrine cells. Sci Rep. 2018;8(1):74. behavior. Mol Psychiatry. 2017;22(2):257-266.
doi: 10.1038/s41598-017-18259-0 doi: 10.1038/mp.2016.182
53. Psichas A, Sleeth ML, Murphy KG, et al. The short chain 64. Acarin L, González B, Castellano B. Neuronal, astroglial and
fatty acid propionate stimulates GLP-1 and PYY secretion microglial cytokine expression after an excitotoxic lesion in the

Volume 2 Issue 4 (2024) 8 doi: 10.36922/jcbp.4160