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福司可林对人甲状腺膜中腺苷酸环化酶的刺激作用。

Forskolin stimulation of adenylate cyclase in human thyroid membranes.

作者信息

Kasai K, Suzuki Y, Hiraiwa M, Kuroda H, Emoto T, Nakamura T, Shimoda S

出版信息

Acta Endocrinol (Copenh). 1985 Feb;108(2):200-5. doi: 10.1530/acta.0.1080200.

Abstract

Forskolin stimulates adenylate cyclase in human thyroid membranes approximately 7-fold with half-maximal stimulation occurring at 5-10 microM. Guanine nucleotides are not required for stimulation of the enzyme by forskolin. Forskolin-stimulation is additive or greater than additive with that of TSH or Gpp(NH)p- (above 1 microM). Different from TSH- or Gpp(NH)p-stimulation of adenylate cyclase, uncoupling of the guanine nucleotide-binding regulatory component by increasing concentrations of MnCl2 did not result in uncoupling of forskolin stimulation. The finding indicates that forskolin may mainly act on the catalytic component of adenylate cyclase. From the present study, it is suggested that the diterpene forskolin stimulates adenylate cyclase in human thyroid membranes by a novel mechanism that differs from TSH- or Gpp(NH)p-stimulation, and that the diterpene may be a useful tool to investigate the metabolism of thyroid and its regulation in normal and pathological situations.

摘要

福斯可林可使人类甲状腺膜中的腺苷酸环化酶活性增强约7倍,在5 - 10微摩尔浓度时达到最大刺激效应的一半。福斯可林刺激该酶并不需要鸟嘌呤核苷酸。福斯可林的刺激作用与促甲状腺激素(TSH)或Gpp(NH)p(浓度高于1微摩尔)的刺激作用相加或大于相加效应。与TSH或Gpp(NH)p对腺苷酸环化酶的刺激不同,增加氯化锰浓度使鸟嘌呤核苷酸结合调节成分解偶联,并不会导致福斯可林刺激作用的解偶联。这一发现表明,福斯可林可能主要作用于腺苷酸环化酶的催化成分。从本研究来看,二萜类化合物福斯可林通过一种不同于TSH或Gpp(NH)p刺激的新机制刺激人类甲状腺膜中的腺苷酸环化酶,并且该二萜类化合物可能是研究甲状腺代谢及其在正常和病理情况下调节作用的有用工具。

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