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孕酮对去卵巢并用雌激素处理的大鼠纹状体中多巴胺释放的调节作用具有立体特异性。

Modulatory effects of progesterone upon dopamine release from the corpus striatum of ovariectomized estrogen-treated rats are stereo-specific.

作者信息

Dluzen D E, Ramirez V D

机构信息

Department of Physiology and Biophysics, University of Illinois, Urbana 61801.

出版信息

Brain Res. 1991 Jan 4;538(1):176-9. doi: 10.1016/0006-8993(91)90395-c.

Abstract

We have shown previously that progesterone linked with bovine serum albumin at position 3 of the progesterone molecule (P-3-BSA) was effective in modulating (both stimulating and inhibiting) amphetamine (AMPH)-evoked dopamine (DA) release in vitro from superfused corpus striatal (CS) tissue fragments of ovariectomized estrogen-primed rats. To examine the stereospecificity of this effect, progesterone linked with bovine serum albumin at position 11 (P-11-BSA) and deoxycorticosterone linked with bovine serum albumin at position 21 (DOC-BSA) were tested for their ability to modulate amphetamine-stimulated DA release in vitro when administered in either a pulsatile or a continuous infusion mode at different doses. The results demonstrate that a specific orientation of the P-BSA molecule is required for differential modulation of AMPH stimulated DA release from the CS of ovariectomized estrogen-treated rats, since DOC-BSA was ineffective and P-11-BSA showed only a stimulatory effect.

摘要

我们之前已经表明,孕酮分子第3位与牛血清白蛋白相连的孕酮(P-3-BSA)在体外能够有效调节(刺激和抑制)去卵巢并用雌激素预处理的大鼠的纹状体(CS)组织碎片在苯丙胺(AMPH)诱发下的多巴胺(DA)释放。为了检验这种效应的立体特异性,对孕酮分子第11位与牛血清白蛋白相连的孕酮(P-11-BSA)以及第21位与牛血清白蛋白相连的脱氧皮质酮(DOC-BSA)进行了测试,观察它们在以不同剂量进行脉冲式或连续输注时,调节体外苯丙胺刺激的DA释放的能力。结果表明,P-BSA分子的特定取向对于差异调节去卵巢并用雌激素处理的大鼠CS中AMPH刺激的DA释放是必需的,因为DOC-BSA无效,而P-11-BSA仅显示出刺激作用。

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