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α-肾上腺素能激动剂对人脂肪细胞中腺苷酸环化酶活性的抑制作用。

Inhibition of adenylate cyclase activity in human fat cells by alpha-adrenergic agonists.

作者信息

Wright E E, Simpson E R

出版信息

Horm Metab Res. 1982 Sep;14(9):475-9. doi: 10.1055/s-2007-1019051.

Abstract

The effects of the alpha 1-adrenergic agonist methoxamine and the alpha 2-adrenergic agonist clonidine on isoproterenol stimulated adenylate cyclase activity were examined in plasma membranes prepared from female human subcutaneous adipose tissue. It was found that in the presence of 10 microM GTP and 100 mM NaCl increasing concentrations of both agonists inhibited basal and isoproterenol-stimulated adenylate cyclase activity. The inhibitory action of 5 x 10(-7) M clonidine could not be overcome by increasing concentrations of isoproterenol. These results suggest both alpha 1- and alpha 2-adrenergic agonists inhibit beta-agonist-stimulated adenylate cyclase activity in human adipose tissue.

摘要

在从女性人体皮下脂肪组织制备的质膜中,研究了α1 - 肾上腺素能激动剂甲氧明和α2 - 肾上腺素能激动剂可乐定对异丙肾上腺素刺激的腺苷酸环化酶活性的影响。发现在存在10微摩尔GTP和100毫摩尔氯化钠的情况下,两种激动剂浓度增加均抑制基础和异丙肾上腺素刺激的腺苷酸环化酶活性。5×10(-7)M可乐定的抑制作用不能通过增加异丙肾上腺素的浓度来克服。这些结果表明,α1和α2肾上腺素能激动剂均抑制人脂肪组织中β - 激动剂刺激的腺苷酸环化酶活性。

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