Dluzen D E, Ramirez V D
Department of Physiology and Biophysics, University of Illinois, Urbana 61801.
Brain Res. 1991 Jan 4;538(1):176-9. doi: 10.1016/0006-8993(91)90395-c.
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.
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。