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痢疾志贺氏菌I型肠毒素对肠粘膜腺苷酸环化酶的激活作用。

Activation of intestinal mucosal adenylate cyclase by Shigella dysenteriae I enterotoxin.

作者信息

Charney A N, Gots R E, Formal S B, Giannella R A

出版信息

Gastroenterology. 1976 Jun;70(6):1085-90.

PMID:178569
Abstract

Because the mechanism whereby Shigella dysenteriae I enterotoxin induces intestinal secretion is unclear, the effect of this toxin on adenylate cyclase activity in rabbit ileal mucosa was studied under various in vitro and in vivo conditions. Activation of adenylate cyclase by Shigella enterotoxin was observed only when substrate (ATP) concentrations above the Km of adenylate cyclase were employed. These concentrations of ATP are greater than those required to demonstrate activation of adenylate cyclase by cholera toxin. Under optimal assay conditions, doses of Shigella toxin between 5.4 and 900 mug of toxin protein and in vivo incubation times between 6 and 18 hr all increased adenylate cyclase activity by about 100%. Shigella toxin produced significant but highly variable increases in mucosal cyclic AMP concentrations, which were less that the rises seen with a comparable dose of cholera toxin. This variability in cyclic AMP response to Shigella toxin and the disparity between Shigella and cholera toxins' effects on mucosal cyclic AMP are probably the result of the different kinetics of adenylate cyclase activated by these enterotoxins. Mucosal Na-K-ATPase activity was unaffected by Shigella toxin. These observations suggest that alterations in fluid and electrolyte transport induced by Shigella enterotoxin may, in part, be mediated by the adenylate cyclase-cyclic AMP system.

摘要

由于痢疾志贺氏菌I型肠毒素诱导肠道分泌的机制尚不清楚,因此在各种体外和体内条件下研究了该毒素对兔回肠粘膜中腺苷酸环化酶活性的影响。仅当使用高于腺苷酸环化酶Km值的底物(ATP)浓度时,才观察到志贺氏菌肠毒素对腺苷酸环化酶的激活作用。这些ATP浓度高于证明霍乱毒素激活腺苷酸环化酶所需的浓度。在最佳测定条件下,5.4至900微克毒素蛋白剂量的志贺氏菌毒素以及6至18小时的体内孵育时间均使腺苷酸环化酶活性增加了约100%。志贺氏菌毒素使粘膜环磷酸腺苷(cAMP)浓度显著升高,但变化很大,低于同等剂量霍乱毒素引起的升高幅度。cAMP对志贺氏菌毒素反应的这种变异性以及志贺氏菌毒素和霍乱毒素对粘膜cAMP作用的差异,可能是这些肠毒素激活腺苷酸环化酶的不同动力学的结果。粘膜钠钾ATP酶活性不受志贺氏菌毒素影响。这些观察结果表明,志贺氏菌肠毒素诱导的液体和电解质转运改变可能部分由腺苷酸环化酶-环磷酸腺苷系统介导。

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