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去甲肾上腺素、普瑞特罗和美托洛尔对新生大鼠棕色脂肪组织中腺苷酸环化酶活性组织化学定位的影响。

Effect of norepinephrine, prenalterol and metoprolol on the histochemical localization of adenylate cyclase activity in the brown adipose tissue of newborn rat.

作者信息

Rechardt L, Hervonen H

出版信息

Histochemistry. 1982;76(4):489-95. doi: 10.1007/BF00489904.

Abstract

Norepinephrine-stimulated adenylate cyclase enzyme (EC 4.6.1.1.) was histochemically demonstrated by electron microscope in the plasmalemmas of the newborn rat adipocytes. The precipitating agent in the histochemical reaction was cobalt salt. Metoprolol, a selective beta 1-blocker given in vivo abolished almost totally the reaction products from the outer surfaces of the plasmalemmas. In vitro treatment did not yield constantly reproducible results. Prenalterol (H 133/22-CGP 7760/B Hässle) a selective beta-agonist given in vivo stimulated enzyme activity in the plasmalemmas. The reaction, however, showed different localization patterns and enhanced amounts of reaction products in the membranes. It is proposed that the histochemical demonstration of amine-stimulated adenylate cyclase activity in the adipocyte plasmalemmas corresponds to the hormonal receptor sites. The question of the sensitivity of the receptors is discussed.

摘要

通过电子显微镜在新生大鼠脂肪细胞的质膜中组织化学地证实了去甲肾上腺素刺激的腺苷酸环化酶(EC 4.6.1.1.)。组织化学反应中的沉淀剂是钴盐。体内给予的选择性β1受体阻滞剂美托洛尔几乎完全消除了质膜外表面的反应产物。体外处理未产生恒定可重复的结果。体内给予的选择性β激动剂普瑞特罗(H 133/22-CGP 7760/B 哈塞尔)刺激了质膜中的酶活性。然而,反应在膜中显示出不同的定位模式和增加的反应产物量。有人提出,脂肪细胞质膜中胺刺激的腺苷酸环化酶活性的组织化学证实对应于激素受体位点。讨论了受体敏感性的问题。

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