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溴隐亭可增强鸟苷酸环化酶的活性。

Bromocriptine enhances guanylate cyclase activity.

作者信息

Vesely D L

出版信息

Endocrinology. 1981 Oct;109(4):1284-6. doi: 10.1210/endo-109-4-1284.

Abstract

Bromocriptine and its parent compound alpha-ergocryptine were investigated with respect to their ability to interact with the guanylate cyclase (E.C.4.6.1.2)-cyclic GMP system in vitro in the rat pituitary and ovary. Both bromocriptine and alpha-ergocryptine enhanced guanylate cyclase two- to threefold in both of these tissues over a concentration range of 1 nM to 1 microM. Since bromocriptine is thought to be a dopamine agonist in the pituitary, dopamine's effects on guanylate cyclase were also tested. Dopamine caused a twofold enhancement of guanylate cyclase activity in the pituitary and ovary. When bromocriptine and dopamine were used in combination, bromocriptine had to be in equal or a greater concentration with respect to dopamine in vitro to enhance guanylate cyclase activity. These findings suggest that bromocriptine's effect at the level of the pituitary and ovary may be mediated through enhancement of guanylate cyclase activity.

摘要

研究了溴隐亭及其母体化合物α-麦角隐亭在体外与大鼠垂体和卵巢中的鸟苷酸环化酶(E.C.4.6.1.2)-环鸟苷酸系统相互作用的能力。在1 nM至1 microM的浓度范围内,溴隐亭和α-麦角隐亭均可使这两种组织中的鸟苷酸环化酶活性增强两至三倍。由于溴隐亭在垂体中被认为是一种多巴胺激动剂,因此也测试了多巴胺对鸟苷酸环化酶的作用。多巴胺使垂体和卵巢中的鸟苷酸环化酶活性增强两倍。当联合使用溴隐亭和多巴胺时,在体外溴隐亭的浓度必须等于或高于多巴胺才能增强鸟苷酸环化酶活性。这些发现表明,溴隐亭在垂体和卵巢水平的作用可能是通过增强鸟苷酸环化酶活性来介导的。

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