Suppr超能文献

人绒毛膜促性腺激素与大鼠脂肪组织的相互作用:人绒毛膜促性腺激素——促黄体生成素受体明显缺乏。

The interaction of hCG with rat adipose tissue: apparent lack of hCG--LH receptors.

作者信息

Tell G P, Haour F, Saez J M

出版信息

Mol Cell Endocrinol. 1977 Jan;6(3):171-9. doi: 10.1016/0303-7207(77)90083-1.

Abstract

The interaction of human chorionic gonadotropin (hCG) with rat adipose tissue was investigated by both metabolic and binding studies. Highly purified preparations of hCG did not affect the adenylate cyclase activity nor the lipolysis of rat adipocytes in the presence or in the absence of GTP. However, it was demonstrated that (a) the hCGs used were biologically active since they stimulated cAMP and testosterone production by rat Leydig cells, and (b) there are receptor sites on the rat ovary that bind [125I]hCG and recognize rat luteinizing hormone (LH). The lack of response cannot then be attributed to a loss of activity of the hormone preparation tested nor to a failure of the rat tissues to recognize an hormone of human origin, but rather to an absence of hCG--LH receptors on the fat cell membrane surface. It is suggested that results previously reported in other laboratories could be explained by the presence of contaminating amounts of lipolytic hormones in their preparations.

摘要

通过代谢研究和结合研究对人绒毛膜促性腺激素(hCG)与大鼠脂肪组织的相互作用进行了研究。在存在或不存在鸟苷三磷酸(GTP)的情况下,高度纯化的hCG制剂既不影响腺苷酸环化酶活性,也不影响大鼠脂肪细胞的脂解作用。然而,已证明:(a)所使用的hCG具有生物活性,因为它们能刺激大鼠睾丸间质细胞产生环磷酸腺苷(cAMP)和睾酮;(b)大鼠卵巢上存在能结合[125I]hCG并识别大鼠促黄体生成素(LH)的受体位点。因此,缺乏反应不能归因于所测试的激素制剂活性丧失,也不能归因于大鼠组织无法识别源自人类的激素,而是由于脂肪细胞膜表面不存在hCG-LH受体。有人提出,其他实验室先前报道的结果可能是由于其制剂中存在污染量的脂解激素所致。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验