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β-肾上腺素能激动剂对二硫键的还原作用:支持肾上腺素能药物作用机制的“还原激活”假说的证据。

Reduction of a disulfide bond by beta-adrenergic agonists: evidence in support of a general "reductive activation" hypothesis for the mechanism of action of adrenergic agents.

作者信息

Peterson D A, Gerrard J M

出版信息

Med Hypotheses. 1987 Jan;22(1):45-9. doi: 10.1016/0306-9877(87)90007-7.

Abstract

Beta-adrenergic agonists, but not antagonists, were found to reduce the disulfide bond of 5,5'-dithiobis-2-nitrobenzoic acid (DTNB). The extent of DTNB reduction was proportional to the intrinsic activity for these agonists. The results suggest a novel mechanism for transmission of the signal when a beta-adrenergic agonist occupies its receptor. We proposed that beta-adrenergic agonists exert their effects to activate the adenylate cyclase by reducing a disulfide bond in the receptor (R) or guanyl nucleotide binding protein (G) component of the adenylate cyclase complex leading to tight binding of GTP to G and activation of G.

摘要

已发现β-肾上腺素能激动剂而非拮抗剂可降低5,5'-二硫代双-2-硝基苯甲酸(DTNB)的二硫键。DTNB的还原程度与这些激动剂的内在活性成正比。结果提示了β-肾上腺素能激动剂占据其受体时信号传递的一种新机制。我们提出,β-肾上腺素能激动剂通过还原腺苷酸环化酶复合物的受体(R)或鸟苷酸结合蛋白(G)组分中的二硫键,从而使GTP与G紧密结合并激活G,进而发挥其激活腺苷酸环化酶的作用。

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