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仓鼠脂肪细胞中的前列腺素、α-肾上腺素能受体与脂肪分解

Prostaglandins, alpha-adrenergic receptors and lipolysis in hamster fat cells.

作者信息

Tan S, Curtis-Prior P B

出版信息

Prostaglandins Leukot Med. 1985 Jan;17(1):117-23. doi: 10.1016/0262-1746(85)90040-x.

Abstract

In hamster fat cells, PGE2, PGI1 and clonidine (alpha 2-adrenoceptor agonist) were shown to inhibit markedly lipolysis stimulated by methylisobutylxanthine (MIX) (2 X 10(-4) M) and slightly that provoked by isoprenaline (5 X 10(-7) M). The similar inhibitory actions of the alpha 2-adrenoceptor agonist clonidine and PGE2 on lipolysis stimulated by MIX led us to examine possible reversal of the antilipolytic effect of PGE2 by yohimbine (alpha 2-adrenoceptor antagonist). However, the absence of an effect of yohimbine on PGE2, antilipolytic action indicated that the PGE2 receptor was different from the alpha 2-adrenoceptor of hamster fat cells. In these studies, PGE2 was shown to be a more potent antilipolytic agent that PGI2 (IC50 values 2 X 10(-9) and greater than 10(-4) M respectively).

摘要

在仓鼠脂肪细胞中,前列腺素E2(PGE2)、前列环素I1(PGI1)和可乐定(α2-肾上腺素能受体激动剂)可显著抑制由甲基异丁基黄嘌呤(MIX,2×10⁻⁴ M)刺激引起的脂解作用,并轻微抑制由异丙肾上腺素(5×10⁻⁷ M)引发的脂解作用。α2-肾上腺素能受体激动剂可乐定和PGE2对MIX刺激的脂解作用具有相似的抑制作用,这促使我们研究育亨宾(α2-肾上腺素能受体拮抗剂)是否能逆转PGE2的抗脂解作用。然而,育亨宾对PGE2的抗脂解作用没有影响,这表明PGE2受体与仓鼠脂肪细胞的α2-肾上腺素能受体不同。在这些研究中,PGE2被证明是比前列环素I2(PGI2)更有效的抗脂解剂(IC50值分别为2×10⁻⁹ M和大于10⁻⁴ M)。

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