Lange S, Lönnroth I
Infect Immun. 1982 Feb;35(2):391-5. doi: 10.1128/iai.35.2.391-395.1982.
The influence of bile acids on adenosine 3',5'-phosphate-induced intestinal secretion was studied in mice. Bile flow was stopped by ligation of the common bile duct, and secretion was induced in ligated loops of the small intestine. The decrease of bile led to inhibition of hypersecretion after challenge with heat-labile enterotoxins from Vibrio cholerae and Escherichia coli, as well as with prostaglandin E1. In contrast, the fluid response induced by dibutyryl-adenosine 3',5'-phosphate was unaffected by intestinal bile. Injection of bile or bile acids into intestinal loops before cholera toxin challenge restored the toxin-induced secretion in the bile-depleted intestine. At the subcellular level the decrease of intestinal bile led to inhibition of cholera toxin-activated adenylate cyclase, whereas the bile concentration did not influence the binding of 125I-labeled toxin to the intestinal epithelial cells. The results suggest that intestinal bile interacts with adenylate cyclase in the induction of fluid secretion by enterotoxins and prostaglandin E1.
在小鼠中研究了胆汁酸对3',5'-磷酸腺苷诱导的肠道分泌的影响。通过结扎胆总管来阻断胆汁流动,并在小肠的结扎肠袢中诱导分泌。胆汁减少导致在用霍乱弧菌和大肠杆菌的不耐热肠毒素以及前列腺素E1刺激后,高分泌受到抑制。相比之下,二丁酰-3',5'-磷酸腺苷诱导的液体反应不受肠道胆汁的影响。在霍乱毒素攻击前向肠袢注射胆汁或胆汁酸可恢复胆汁缺乏的肠道中毒素诱导的分泌。在亚细胞水平上,肠道胆汁的减少导致霍乱毒素激活的腺苷酸环化酶受到抑制,而胆汁浓度不影响125I标记的毒素与肠上皮细胞的结合。结果表明,肠道胆汁在肠毒素和前列腺素E1诱导液体分泌过程中与腺苷酸环化酶相互作用。