Xiao L, Becker J B
Department of Psychology, University of Michigan, Ann Arbor 48109-1109, USA.
Synapse. 1998 Aug;29(4):379-91. doi: 10.1002/(SICI)1098-2396(199808)29:4<379::AID-SYN10>3.0.CO;2-M.
Based upon the observation that estrogen acts in the striatum to rapidly modulate dopamine (DA) neural transmission and DA-mediated behaviors, it has been postulated that these effects of estrogen are mediated by a specific, membrane-bound receptor mechanism. To further characterize the pharmacological specificity of the estrogen binding site, the present experiments examine effects of various estrogen agonists on amphetamine (AMPH)-induced DA release from striatal tissue of ovariectomized female rats, using a superfusion method. Catechol estrogens 4-, and 2-hydroxyestradiol, but not 2-methoxyestradiol, significantly enhance AMPH-induced striatal DA release. Estrogen metabolites, estrone and estriol, and the non-steroidal estrogen analog, diethylstilbestrol, are without effects. Estradiol conjugated to bovine serum albumin (BSA) mimics the effect of estradiol to enhance stimulated striatal DA release. These results indicate that the steroidal configuration and hydroxylation on the A-ring of estrogenic compounds may be important determinants of ligand binding to the putative estrogen binding site in the striatum. Furthermore, the effectiveness of the estradiol conjugated to BSA reinforces the idea of an external membrane-bound receptor binding site in the striatum.
基于雌激素在纹状体中作用于快速调节多巴胺(DA)神经传递及DA介导行为的观察结果,有人推测雌激素的这些作用是由一种特定的膜结合受体机制介导的。为了进一步明确雌激素结合位点的药理学特异性,本实验采用灌流法研究了各种雌激素激动剂对去卵巢雌性大鼠纹状体组织中苯丙胺(AMPH)诱导的DA释放的影响。儿茶酚雌激素4-羟基雌二醇和2-羟基雌二醇能显著增强AMPH诱导的纹状体DA释放,而2-甲氧基雌二醇则无此作用。雌激素代谢产物雌酮和雌三醇以及非甾体雌激素类似物己烯雌酚均无作用。与牛血清白蛋白(BSA)结合的雌二醇模拟了雌二醇增强刺激的纹状体DA释放的作用。这些结果表明,雌激素化合物A环上的甾体构型和羟基化可能是配体与纹状体中假定的雌激素结合位点结合的重要决定因素。此外,与BSA结合的雌二醇的有效性强化了纹状体中存在外部膜结合受体结合位点的观点。