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β3 -肾上腺素能受体激动剂BRL 37344对清醒禁食家兔脂肪动员和血浆葡萄糖水平的影响。

Effects of the beta 3-adrenoceptor agonist BRL 37344 on lipomobilization and plasma glucose levels in conscious fasted rabbits.

作者信息

Reverte M, Rivas-Cabañero L

机构信息

Departamento de Fisiología y Farmacología, Facultad de Medicina, Universidad de Salamanca, Spain.

出版信息

Can J Physiol Pharmacol. 1996 Mar;74(3):251-6.

PMID:8773403
Abstract

The existence of a functional beta 3-adrenoceptor in conscious 24 h fasted rabbits was investigated by studying the effect of BRL 37344 (a beta 3-adrenoceptor agonist) in comparison with CGP 12177 (a beta 1- and beta 2-adrenoceptor antagonist, which also acts as a partial beta 3 agonist) and isoproterenol (a nonselective beta 1-, beta 2-, and beta 3-adrenoceptor agonist) on plasma nonesterified fatty acids (NEFA) and its possible relation with glucose metabolism. All drugs were intravenously infused at the same dose, 0.3 microgram.kg-1.min-1 (30 min), BRL 37344, CGP 12177, and isoproterenol significantly elevated plasma NEFA levels without increasing plasma glucose levels. Isoproterenol elevated plasma insulin and lactate levels, but BRL 37344 and CGP 12177 did not. Bupranolol (0.1 mg/kg, subcutaneously) blocked the BRL 37344 mediated effect on plasma NEFA levels. In the presence of CGP 20712A (1 mg/kg, subcutaneously), ICI 118551 (30 micrograms/kg, subcutaneously), or the mixture of both selective beta-antagonists, BRL 37344 also evoked an increase in plasma NEFA levels, but the response was less pronounced when compared with BRL 37344 alone. These data suggest that in conscious rabbits deprived of food for 24 h (i) BRL 37344 induces lipomobilization through beta 3-adrenoceptor stimuli, but the effect is less than by beta 1- and beta 2-adrenoceptor stimuli, and (ii) an excess of plasma NEFA evoked by BRL 37344 may not necessarily contribute to plasma glucose increases.

摘要

通过研究BRL 37344(一种β3肾上腺素能受体激动剂)与CGP 12177(一种β1和β2肾上腺素能受体拮抗剂,也作为部分β3激动剂)以及异丙肾上腺素(一种非选择性β1、β2和β3肾上腺素能受体激动剂)对血浆非酯化脂肪酸(NEFA)的影响及其与葡萄糖代谢的可能关系,来研究清醒禁食24小时家兔体内功能性β3肾上腺素能受体的存在情况。所有药物均以相同剂量0.3微克·千克-1·分钟-1静脉输注(30分钟),BRL 37344、CGP 12177和异丙肾上腺素均显著提高血浆NEFA水平,而不增加血浆葡萄糖水平。异丙肾上腺素提高了血浆胰岛素和乳酸水平,但BRL 37344和CGP 12177没有。布普洛尔(0.1毫克/千克,皮下注射)阻断了BRL 37344对血浆NEFA水平的介导作用。在存在CGP 20712A(1毫克/千克,皮下注射)、ICI 118551(30微克/千克,皮下注射)或两种选择性β拮抗剂混合物的情况下,BRL 37344也引起血浆NEFA水平升高,但与单独使用BRL 37344相比,反应不那么明显。这些数据表明,在清醒禁食24小时的家兔中,(i)BRL 37344通过β3肾上腺素能受体刺激诱导脂肪动员,但其作用小于β1和β2肾上腺素能受体刺激,(ii)BRL 37344引起的血浆NEFA过量不一定会导致血浆葡萄糖升高。

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