Page 45 - JCBP-3-3
P. 45

Journal of Clinical and
            Basic Psychosomatics                                                  Microbiota in psychosomatic disorders



               gut organism from the discoveries in genus and species.   2021;11(8):1091.
               Front Cell Infect Microbiol. 2021;11:757718.
                                                                  doi: 10.3390/biom11081091
               doi: 10.3389/fcimb.2021.757718
                                                               31.  Qu S, Yu Z, Zhou Y,  et  al. Gut microbiota modulates
            21.  Krishnamurthy HK, Pereira M, Bosco J,  et al. Gut   neurotransmitter and gut-brain signaling.  Microbiol Res.
               commensals and their metabolites in health and disease.   2024;2024:127858.
               Front Microbiol. 2023;14:1244293.
                                                                  doi: 10.1016/j.micres.2024.127858
               doi: 10.3389/fmicb.2023.1244293
                                                               32.  Koutsokostas  C,  Merkouris  E,  Goulas  A,  et al.  Gut
            22.  Gradisteanu Pircalabioru G, Ilie I, Oprea L, et al. Microbiome,   microbes  associated  with  neurodegenerative  disorders:
               mycobiome and related metabolites alterations in patients   A comprehensive review of the literature. Microorganisms.
               with  metabolic  syndrome-A  pilot  study.  Metabolites.   2024;12(8):1735.
               2022;12(3):218.
                                                                  doi: 10.3390/microorganisms12081735
               doi: 10.3390/metabo12030218
                                                               33.  Nikolova VL, Pelton L, Moulton CD, et al. The Prevalence
            23.  Qin Q, Yan S, Yang Y, et al. A metagenome-wide association   and incidence of irritable bowel syndrome and inflammatory
               study of the gut microbiome and metabolic syndrome. Front   bowel  disease  in  depression  and  bipolar  disorder:
               Microbiol. 2021;12:682721.                         A  systematic  review  and  meta-analysis.  Psychosom Med.
                                                                  2022;84(3):313‑324.
               doi: 10.3389/fmicb.2021.682721
            24.  Sawant S, Meganathan P, Vedagiri H. Gut microbial      doi: 10.1097/psy.0000000000001046
               dysbiosis induced exacerbations influence the progression   34.  Lakshmanan AP, Mingione A, Pivari F,  et  al. Modulation
               of colorectal cancer. Biol Bull Rev. 2024;14(6):724‑739.  of  gut  microbiota:  The  effects  of  a  fruits  and  vegetables
               doi: 10.1134/S2079086424600528                     supplement. Front Nutr. 2022;9:930883.
                                                                  doi: 10.3389/fnut.2022.930883
            25.  Aho VT, Houser MC, Pereira PA,  et al. Relationships of
               gut microbiota, short-chain fatty acids, inflammation, and   35.  Archana N, Gupta AK, Noumani A, et al. Gut microbiota
               the  gut  barrier  in  Parkinson’s  disease.  Mol Neurodegener.   derived short‐chain fatty acids in physiology and pathology:
               2021;16:6.                                         An update. Cell Biochem Funct. 2024;42(7):e4108.
               doi: 10.1186/s13024‑021‑00427‑6                    doi: 10.1002/cbf.4108
            26.  Bagavant H, Araszkiewicz AM, Ingram JK, et al. Immune   36.  Cameron G, Nguyen T, Ciula M, Williams SJ, Godfrey DI.
               response  to  Enterococcus gallinarum in  lupus patients is   Glycolipids from the gut symbiont  Bacteroides fragilis are
               associated with a subset of lupus-associated autoantibodies.   agonists for natural killer T cells and induce their regulatory
               Front Immunol. 2021;12:635072.                     differentiation. Chem Sci. 2023;14(29):7887‑7896.
               doi: 10.3389/fimmu.2021.635072                     doi: 10.1039/d3sc02124f
            27.  Rasouli-Saravani A, Jahankhani K, Moradi S,  et al. Role   37.  Saturio S, Nogacka AM, Alvarado-Jasso GM,  et al. Role
               of microbiota short-chain fatty acids in the pathogenesis   of  bifidobacteria  on  infant  health.  Microorganisms.
               of  autoimmune  diseases.  Biomed  Pharmacother.   2021;9(12):2415.
               2023;162:114620.
                                                                  doi: 10.3390/microorganisms9122415
               doi: 10.1016/j.biopha.2023.114620
                                                               38.  Camilleri M, Vella A. What to do about the leaky gut. Gut.
            28.  Malik JA, Zafar MA, Lamba T, Nanda S, Khan MA,   2021;71(2):424‑435.
               Agrewala JN. The impact of aging-induced gut microbiome      doi: 10.1136/gutjnl‑2021‑325428
               dysbiosis on dendritic cells and lung diseases. Gut Microbes.
               2023;15(2):2290643.                             39.  Usuda H, Okamoto T, Wada K. Leaky gut: Effect of dietary
                                                                  fiber and fats on microbiome and intestinal barrier. Int J Mol
               doi: 10.1080/19490976.2023.2290643
                                                                  Sci. 2021;22(14):7613.
            29.  Noguera‐Fernández  N, Candela‐González J,  Orenes‐
               Piñero  E. Probiotics, prebiotics, fecal microbiota      doi: 10.3390/ijms22147613
               transplantation, and dietary patterns in inflammatory bowel   40.  Senarath RM, Burton M, Fernando WM, et al. Role of short
               disease. Mol Nutr Food Res. 2024;68(18):2400429.   chain fatty acids on astrocytes and microglia in Alzheimer’s
                                                                  disease brain. Int J Food Sci Technol. 2021;59(9):5902‑5911.
               doi: 10.1002/mnfr.202400429
                                                                  doi: 10.1111/ijfs.17380
            30.  Luck B, Horvath TD, Engevik KA, et al. Neurotransmitter
               profiles are altered in the gut and brain of mice mono-  41.  Xu J, He G, Chen L, et al. Farnesoid X receptor (FXR) and
               associated  with  Bifidobacterium dentium.  Biomolecules.   G protein-coupled bile acid receptor 1 (TGR5) signaling


            Volume 3 Issue 3 (2025)                         39                         doi: 10.36922/JCBP025040008
   40   41   42   43   44   45   46   47   48   49   50