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α2 - 肾上腺素能效应对胎鼠棕色脂肪组织中腺苷酸环化酶活性及(3H)-可乐定特异性结合的影响

Occurrence of alpha 2-adrenergic effects on adenylate cyclase activity and (3H)-clonidine specific binding in brown adipose tissue from foetal rats.

作者信息

Domínguez M J, Fernández M, Elliott K, Benito M

出版信息

Biochem Biophys Res Commun. 1986 Aug 14;138(3):1390-4. doi: 10.1016/s0006-291x(86)80437-5.

Abstract

Noradrenaline maximally stimulates adenylate cyclase activity in brown adipocytes from foetal rats by 400%. Isoproterenol maximally stimulates the adenylate cyclase activity by 600%. The differences observed in the dose-response curves of adenylate cyclase activity to isoproterenol or noradrenaline were prevented in the presence of clonidine (a alpha 2-agonist) or yohimbine (alpha 2-antagonist) respectively. (3H)-clonidine binds specifically to brown fat membranes saturable (from 1.75 to 20 nM). Scatchard analysis revealed a Bmax of 22 fmol/mg and a KD of 10 nM.

摘要

去甲肾上腺素能使胎鼠棕色脂肪细胞中的腺苷酸环化酶活性最大程度地提高400%。异丙肾上腺素能使腺苷酸环化酶活性最大程度地提高600%。在可乐定(一种α2-激动剂)或育亨宾(α2-拮抗剂)存在的情况下,分别阻止了观察到的腺苷酸环化酶活性对异丙肾上腺素或去甲肾上腺素的剂量反应曲线的差异。(3H)-可乐定特异性结合至棕色脂肪膜,具有饱和性(1.75至20 nM)。Scatchard分析显示Bmax为22 fmol/mg,KD为10 nM。

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