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糖皮质激素对儿茶酚胺诱导的脂肪分解的允许作用:对脂肪细胞β-肾上腺素能受体偶联腺苷酸环化酶系统的直接“体外”效应

Permissive action of glucocorticoids on catecholamine-induced lipolysis: direct "in vitro" effects on the fat cell beta-adrenoreceptor-coupled-adenylate cyclase system.

作者信息

Lacasa D, Agli B, Giudicelli Y

机构信息

Department of Biochemistry, Faculty of Medecine Paris-Quest, C.H.I., Poissy, France.

出版信息

Biochem Biophys Res Commun. 1988 Jun 16;153(2):489-97. doi: 10.1016/s0006-291x(88)81121-5.

Abstract

Exposure of adipose tissue fragments to dexamethasone leads to enhanced lipolytic and cyclic AMP responses of isolated fat cells to isoproterenol. This permissive effect of the steroid is dose-dependent, prevented by the glucocorticoid receptor antagonist RU 38486, maximum after 48 h exposure to 10 nM dexamethasone and affects only the amplitude of the maximal response (+50%). Exposure to dexamethasone also induces an increase in both the number of beta-adrenergic receptors (+30%), and the adenylate cyclase-catalytic activity (+64%) and - responses to GTP (+114%) and isoproterenol (+55%). These data strongly suggest that the permissive effect of glucocorticoids towards lipolysis "in vivo" results at least in part from a glucocorticoid-receptor mediated action of these hormones on the fat cell membranous components involved in the beta-adrenergic control of lipolysis.

摘要

将脂肪组织碎片暴露于地塞米松会导致分离的脂肪细胞对异丙肾上腺素的脂解和环磷酸腺苷反应增强。这种类固醇的允许作用是剂量依赖性的,可被糖皮质激素受体拮抗剂RU 38486阻断,在暴露于10 nM地塞米松48小时后达到最大值,并且仅影响最大反应的幅度(增加50%)。暴露于地塞米松还会导致β-肾上腺素能受体数量增加(增加30%)、腺苷酸环化酶催化活性增加(增加64%)以及对GTP的反应(增加114%)和对异丙肾上腺素的反应(增加55%)。这些数据强烈表明,糖皮质激素对“体内”脂解的允许作用至少部分源于这些激素通过糖皮质激素受体介导对参与脂解β-肾上腺素能控制的脂肪细胞膜成分的作用。

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