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几种术前用药对脂肪细胞脂解及脂肪组织环磷酸腺苷磷酸二酯酶活性的影响。

Effects of several preoperative medications on fat cell lipolysis, and activity of adipose tissue cyclic AMP phosphodiesterase.

作者信息

Curtis-Prior P B, Jenner M, Chan Y H, McColl I

出版信息

Experientia. 1979 Nov 15;35(11):1430-1. doi: 10.1007/BF01962766.

Abstract

Effects were examined of atropine, diazepam, pethidene, promethazine, scopolamine, omnopon and papaverine on basal and noradrenaline-stimulated lipolysis in rat isolated fat cells and on rat adipose tissue cyclic AMP phosphodiesterase activity. Papaverine at high concentration (1 mM) inhibited both basal and hormone-stimulated lipolysis, whereas diazepam enhanced basal lipolysis. At a 'clinical dose', omnopon increased both basal and noradrenaline-stimulated lipolysis. Adipose tissue cAMP phosphodiesterase activity was strongly inhibited by 1 mM diazepam, papaverine, promethazine and omnopon (280 microgram ml-1). Lack of enhancement of lipolysis by the established cAMP phosphodiesterase antagonist papaverine, is compatible with simultaneous inhibition also of adipose adenyl cyclase. Diazepam-stimulated lipolysis is compatible with its phosphodiesterase inhibitory activity. It is proposed that papaverine-containing omnopon may offer some survival advantages during surgical stress by facilitating a caloric supply.

摘要

研究了阿托品、地西泮、哌替啶、异丙嗪、东莨菪碱、阿片全碱和罂粟碱对大鼠分离脂肪细胞基础脂解及去甲肾上腺素刺激的脂解的影响,以及对大鼠脂肪组织环磷酸腺苷磷酸二酯酶活性的影响。高浓度(1 mM)的罂粟碱抑制基础脂解和激素刺激的脂解,而地西泮增强基础脂解。在“临床剂量”下,阿片全碱增加基础脂解和去甲肾上腺素刺激的脂解。1 mM地西泮、罂粟碱、异丙嗪和阿片全碱(280微克/毫升)强烈抑制脂肪组织环磷酸腺苷磷酸二酯酶活性。已确定的环磷酸腺苷磷酸二酯酶拮抗剂罂粟碱未增强脂解,这与同时抑制脂肪腺苷酸环化酶相符。地西泮刺激的脂解与其磷酸二酯酶抑制活性相符。有人提出,含罂粟碱的阿片全碱可能通过促进热量供应在手术应激期间提供一些生存优势。

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