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大鼠肠道黏膜屏障功能对模拟失重的反应

Responses of Intestinal Mucosal Barrier Functions of Rats to Simulated Weightlessness.

作者信息

Jin Mingliang, Zhang Hao, Zhao Ke, Xu Chunlan, Shao Dongyan, Huang Qingsheng, Shi Junling, Yang Hui

机构信息

Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi'an, China.

College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi'an, China.

出版信息

Front Physiol. 2018 Jun 14;9:729. doi: 10.3389/fphys.2018.00729. eCollection 2018.

Abstract

Exposure to microgravity or weightlessness leads to various adaptive and pathophysiological alterations in digestive structures and physiology. The current study was carried out to investigate responses of intestinal mucosal barrier functions to simulated weightlessness, by using the hindlimb unloading rats model. Compared with normal controls, simulated weightlessness damaged the intestinal villi and structural integrity of tight junctions, up-regulated the expression of pro-apoptotic protein Bax while down-regulated the expression of anti-apoptotic protein Bcl-2, thus improved the intestinal permeability. It could also influence intestinal microbiota composition with the expansion of Bacteroidetes and decrease of Firmicutes. The predicted metagenomic analysis emphasized significant dysbiosis associated differences in genes involved in membrane transport, cofactors and vitamins metabolism, energy metabolism, and genetic information processing. Moreover, simulated weightlessness could modify the intestinal immune status characterized by the increase of proinflammatory cytokines, decrease of secretory immunoglobulin A, and activation of TLR4/MyD88/NF-κB signaling pathway in ileum. These results indicate the simulated weightlessness disrupts intestinal mucosal barrier functions in animal model. The data also emphasize the necessity of monitoring and regulating astronauts' intestinal health during real space flights to prevent breakdowns in intestinal homeostasis of crewmembers.

摘要

暴露于微重力或失重环境会导致消化结构和生理功能发生各种适应性和病理生理学改变。本研究通过使用后肢卸载大鼠模型,旨在探究肠道黏膜屏障功能对模拟失重的反应。与正常对照组相比,模拟失重破坏了肠绒毛和紧密连接的结构完整性,上调了促凋亡蛋白Bax的表达,同时下调了抗凋亡蛋白Bcl-2的表达,从而增加了肠道通透性。它还会影响肠道微生物群组成,使拟杆菌门扩张,厚壁菌门减少。预测宏基因组分析强调了在膜转运、辅因子和维生素代谢、能量代谢以及遗传信息处理等相关基因中存在显著的失调相关差异。此外,模拟失重可改变肠道免疫状态,其特征为促炎细胞因子增加、分泌型免疫球蛋白A减少以及回肠中TLR4/MyD88/NF-κB信号通路激活。这些结果表明模拟失重会破坏动物模型中的肠道黏膜屏障功能。这些数据还强调了在实际太空飞行期间监测和调节宇航员肠道健康以防止机组人员肠道稳态失衡的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789d/6011188/8467e1855964/fphys-09-00729-g001.jpg

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