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乳糖诱导的慢性腹泻源于结肠腔内微生物发酵异常和离子转运紊乱。

Lactose-Induced Chronic Diarrhea Results From Abnormal Luminal Microbial Fermentation and Disorder of Ion Transport in the Colon.

作者信息

Xue Hong, Zhang Min, Ma Jinxin, Chen Ting, Wang Fengyun, Tang Xudong

机构信息

Digestive Laboratory of Traditional Chinese Medicine Research Institute of Spleen and Stomach Diseases, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

Front Physiol. 2020 Jul 29;11:877. doi: 10.3389/fphys.2020.00877. eCollection 2020.

Abstract

Diarrhea is one of the major abdominal symptoms in lactose-intolerant subjects. The changes in the large intestinal luminal environment and disorder of the epithelial ion transport in lactose-induced diarrhea remain unclear. The present study aimed to investigate the effect of an incremental high-lactose diet (IHLD, 30%/40%/50%) on luminal microbiota, microbiota-derived metabolite concentrations and colonic ion transport. Gut microbiota were analyzed by 16S rRNA amplicon sequencing and the concentration of SCFAs by gas chromatography, galactose, lactose and lactic acid through assay kit; Ussing chamber was performed to detect basal and stimulated ion transport; The expression and location of SCFA transporters, the Na-H exchanger 3(NHE3), cystic fibrosis transporter regulater (CFTR) and NKCC1 in the colon mucosa were analyzed by western and immunostaining. The concentrations of lactose, galactose and lactic acid of the cecal content were markedly increased ( < 0.01) and SCFA concentration was significantly decreased ( < 0.01). This was associated with depletion of the Lachnospiraceae NK4A136 group and Ruminococcaceae UCG-005 and increased relative abundance of Lactobacillus, escherichia-shigella and megamonas in the cecal microbiota. The expression of monocarboxylate transporter 1 was decreased in the colonic mucosa of the IHLD group. Low NHE3 expression and phosphorylation levels, and decreases in delta basal short circuit current after apical Na removal in the colonic mucosa of the IHLD group contributed to Na accumulation in the lumen and decrease stimulated Cl secretion with low CFTR and NKCC1 expression would compensate for water and electrolyte loss during the diarrhea process. These results indicated that the persistence of the diarrhea state was maintained by abnormal colonic microbiota fermentation leading to high concentrations of lactose, galactose and lactic acid and low SCFAs in the lumen, and decreased Na absorption with the low NHE3 expression and phosphorylation levels.

摘要

腹泻是乳糖不耐受患者的主要腹部症状之一。乳糖诱导的腹泻中大肠腔内环境的变化以及上皮离子转运紊乱仍不清楚。本研究旨在探讨递增高乳糖饮食(IHLD,30%/40%/50%)对肠道微生物群、微生物群衍生代谢物浓度和结肠离子转运的影响。通过16S rRNA扩增子测序分析肠道微生物群,用气相色谱法分析短链脂肪酸(SCFA)浓度,用试剂盒分析半乳糖、乳糖和乳酸浓度;采用Ussing chamber检测基础和刺激后的离子转运;通过蛋白质免疫印迹法和免疫染色分析结肠黏膜中SCFA转运体、钠氢交换体3(NHE3)、囊性纤维化跨膜传导调节因子(CFTR)和钠钾氯协同转运蛋白1(NKCC1)的表达和定位。盲肠内容物中乳糖、半乳糖和乳酸的浓度显著升高(<0.01),SCFA浓度显著降低(<0.01)。这与盲肠微生物群中毛螺菌科NK4A136组和瘤胃球菌科UCG - 005的减少以及乳酸杆菌、埃希氏菌 - 志贺氏菌属和巨单胞菌相对丰度的增加有关。IHLD组结肠黏膜中单羧酸转运体1的表达降低。IHLD组结肠黏膜中NHE3表达和磷酸化水平降低,顶端去除钠后基底短路电流降低,导致管腔内钠积累,刺激的氯分泌减少,CFTR和NKCC1低表达可补偿腹泻过程中的水和电解质损失。这些结果表明,腹泻状态的持续是由结肠微生物群异常发酵导致管腔内乳糖、半乳糖和乳酸浓度升高、SCFA浓度降低,以及NHE3低表达和磷酸化水平导致钠吸收减少所维持的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a3c/7403511/7d69dbfd721d/fphys-11-00877-g001.jpg

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