Objective To explore the mechanism of gut microbiota in intestinal damage in high-altitude hypoxic environment. Methods Twenty C57BL/6 mice were randomly divided into a control group and an exposure group according to the ratio of 1:1. After the successful modeling of the 6000-meter high-altitude hypoxia model, the feces, blood and proximal colon tissue of these two groups were collected. The structure of gut microbiota in feces was determined by 16S rDNA analysis. The blood biochemical indexes were detected. The pathological changes of intestinal mucosal structure were observed by HE and PAS staining. The mRNA expression levels of ZO-1, Occludin, IL-6 and TNFα of colon tissue were measured by RT-qPCR. Results Compared with the control group, the red blood cell, hemoglobin and hematocrit values of the exposure group significantly increased. The high-altitude hypoxia model was successfully established. The 16S rDNA showed that the gut microbiota was disordered and the diversity declined, the content of the mucin-degrading bacteria Akkermansia and pathogenic bacterias Clostridium XVIII, Prevotella increased, the relative content of the short-chain fatty acids producing bacteria Roseburia, Odoribacter, Lachnospiracea, Butyricicoccus and Olsenella decreased. HE and PAS staining results showed that the interruption of colon epithelial continuity, atrophy of glands, shortening of crypts and reduction of goblet cells, which indicated the damage of intestinal structure and mucosal barrier. The expression levels of tight junction protein Occludin and ZO-1 mRNA decreased, which confirmed the disruption of intestinal mucosal of the exposure group. The expression level of inflammatory factors IL-6 and TNFα increased, which may be related to intestinal inflammatory reaction. Conclusions The intestinal damage caused by high-altitude hypoxic environment may be related to the change of gut microbiota. Gut microbiota disorder and diversity decreased, the relative abundance of pathogenic bacteria increased and probiotics decreased. These alterations cause the intestinal mucosal damage, intestinal inflammation, intestinal damage, and finally lead to high-altitude intestinal related diseases.
Key words
High-altitude hypoxia /
Gut microbiota /
Intestinal damage /
Intestinal mucosal barrier
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References
[1] Zhou Y, Lu H, Liu Y, et al. Cirbp-PSD95 axis protects against hypobaric hypoxia-induced aberrant morphology of hippocampal dendritic spines and cognitive deficits[J]. Mol Brain, 2021,14(1):129. DOI: 10.1186/s13041-021-00827-1.
[2] Pickard JM, Zeng MY, Caruso R, et al. Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease[J]. Immunol Rew, 2017,279(1):70-89.DOI: 10.1111/imr.12567.
[3] 周静, 许琴, 刘江伟, 等. 不同海拔高原低压缺氧环境下大鼠肠道病理损伤特点[J]. 现代生物医学进展, 2017,17(27):5238-5241. DOI: 10.13241/j.cnki.pmb.2017.27.009.
[4] Fruehauf H, Vavricka SR, Lutz TA, et al. Evaluation of acute mountain sickness by unsedated transnasal esophagogastroduodenoscopy at high altitude[J]. Clin Gastroenterol Hepatol, 2020,18(10):2218-2225.DOI: 10.1016/j.cgh.2019.11.036.
[5] Khanna K, Mishra KP, Ganju L, et al. High-altitude-induced alterations in gut-immune axis: a review[J]. Int Rev Immunol, 2018,37(2):119-126.DOI: 10.1080/08830185.2017.1407763.
[6] Li A, Wang Y, Li Zet al. Probiotics isolated from yaks improves the growth performance, antioxidant activity, and cytokines related to immunity and inflammation in mice[J]. Microb Cell Fact, 2019,18(1):112.DOI: 10.1186/s12934-019-1161-6.
[7] Pujo J, Petitfils C, Le Faouder P, et al. Bacteria-derived long chain fatty acid exhibits anti-inflammatory properties in colitis[J]. Gut, 2021,70(6):1088-1097.DOI: 10.1136/gutjnl-2020-321173.
[8] Gao R, Gao Z, Huang L, et al. Gut microbiota and colorectal cancer[J]. Eur J Clin Microbiol Infect Dis, 2017,36(5):757-769.DOI: 10.1007/s10096-016-2881-8.
[9] Suzuki TA, Martins FM, Nachman MW. Altitudinal variation of the gut microbiota in wild house mice[J]. Mol Ecol, 2019,28(9):2378-2390.DOI: 10.1111/mec.14905.
[10]Seregin SS, Golovchenko N, Schaf B, et al. NLRP6 Protects Il10(-/-) Mice from Colitis by Limiting Colonization of Akkermansia muciniphila[J]. Cell Rep, 2017,19(4):733-745.DOI: 10.1016/j.celrep.2017.05.074.
[11]Derrien M, Vaughan EE, Plugge CM, et al. Akkermansia muciniphila gen. nov., sp. nov., a human intestinal mucin-degrading bacterium[J]. Int Jl Syst Microbiol, 2004,54(Pt 5):1469-1476. DOI:10.1099/ijs. 0.02873-0.
[12]Ananthakrishnan AN, Bernstein CN, Iliopoulos D, et al. Environmental triggers in IBD: a review of progress and evidence[J]. Nat Rev Gastroenterol Hepatol, 2017, 15(1):39-49.DOI: 10.1038/nrgastro. 2017. 136.
[13]Li XW, Chen HP, He YY, et al. Effects of rich-polyphenols extract of dendrobium loddigesii on anti-diabetic, anti-inflammatory, anti-oxidant, and gut microbiota modulation in db/db mice[J]. Molecules, 2018,23(12):3245. DOI: 10.3390/molecules23123245.