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β-肾上腺素能受体阻断药物对脂肪细胞非酯化脂肪酸释放的影响。

The effects of beta-adrenoceptor blocking drugs on non-esterified fatty acid release from adipocytes.

作者信息

Harms H H

出版信息

J Pharmacol. 1983;14 Suppl 2:209-15.

PMID:6138469
Abstract

A review is presented of the effects of beta-adrenoceptor blocking agents on lipolysis in adipose tissue. Considerable species differences appear to exist between the pharmacological characteristics of beta-adrenoceptors in adipocytes of rat, guinea pig, dog, cat, swine and man. Human adipocyte beta-adrenoceptors probably consist of two subtypes; insufficient data are available to ascertain whether they represent "classical" beta 1- and beta 2-adrenoceptors or atypical receptors similar but not identical to those in the rat. In vivo studies in man suggest that non-cardioselective beta-adrenoceptor blocking agents are more effective antilipolytic agents than cardioselective beta-adrenoceptor antagonists. No clinical evidence could be found to suggest that the quantitative differences in antilipolytic potency between cardioselective and non-cardioselective agents have more than speculative significance.

摘要

本文综述了β-肾上腺素能受体阻滞剂对脂肪组织脂肪分解的影响。大鼠、豚鼠、狗、猫、猪和人的脂肪细胞中β-肾上腺素能受体的药理学特性似乎存在显著的种属差异。人脂肪细胞β-肾上腺素能受体可能由两种亚型组成;目前尚无足够数据确定它们是否代表“经典”的β1和β2肾上腺素能受体,或与大鼠受体相似但不完全相同的非典型受体。人体的体内研究表明,非心脏选择性β-肾上腺素能受体阻滞剂比心脏选择性β-肾上腺素能拮抗剂更有效地发挥抗脂肪分解作用。未发现临床证据表明心脏选择性和非心脏选择性药物在抗脂肪分解效力上的定量差异具有超过推测的意义。

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