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间歇性注射孕酮可增强,而持续注射则会减少去卵巢并用雌激素预处理的大鼠纹状体片段在体外灌流时由苯丙胺刺激引起的多巴胺释放。

Intermittent infusion of progesterone potentiates whereas continuous infusion reduces amphetamine-stimulated dopamine release from ovariectomized estrogen-primed rat striatal fragments superfused in vitro.

作者信息

Dluzen D E, Ramirez V D

出版信息

Brain Res. 1987 Mar 17;406(1-2):1-9. doi: 10.1016/0006-8993(87)90762-1.

Abstract

In the present experiment we examined the effect of a direct in vitro infusion of progesterone upon spontaneous and amphetamine-stimulated in vitro dopamine (DA) release and post-superfusion DA tissue concentration of corpus striatum tissue fragments from ovariectomized and estrogen-treated female rats. An intermittent infusion of progesterone at a dose of 2 ng/ml produced a significant increase in amphetamine-stimulated DA release and post-superfusion DA tissue concentration compared to similar superfusions infused with medium alone or cholesterol (2 ng/ml). Higher (50 ng/ml) or lower (0.2 ng/ml) doses of progesterone were ineffective and a continuous infusion of progesterone at an identical total concentration to that of the intermittent 2 ng/ml dose inhibited both amphetamine-stimulated DA release and post-superfusion DA tissue concentration. With the exception of 5 alpha DHP (dihydroxyprogesterone) intermittent infusions of various metabolites, a synthetic progestin (R5020) at 2 ng/ml and estradiol at both 0.2 ng/ml and 2 ng/ml failed to modify significantly the amphetamine-stimulated DA response. However, pregnanolone, 5 alpha DHP, R5020 at 2 ng/ml and estradiol at 0.2 ng/ml increased post-superfusion DA tissue concentration to levels comparable to that of progesterone. These results demonstrate that in vitro progesterone can directly alter the amphetamine-stimulated DA release from dopaminergic terminals of corpus striatal tissue fragments. This effect appears quite specific for progesterone as well as for a specific dose and mode of infusion of this gonadal steroid. Moreover, progesterone can exert opposite effects upon the amphetamine-evoked DA release from the corpus striatum as a function of its mode of infusion suggesting a means by which one hormone can differentially alter central nervous system function.

摘要

在本实验中,我们研究了直接体外输注孕酮对去卵巢并经雌激素处理的雌性大鼠纹状体组织碎片的自发和苯丙胺刺激的体外多巴胺(DA)释放以及灌注后DA组织浓度的影响。与单独灌注培养基或胆固醇(2 ng/ml)的类似灌注相比,以2 ng/ml的剂量间歇性输注孕酮可使苯丙胺刺激的DA释放和灌注后DA组织浓度显著增加。更高(50 ng/ml)或更低(0.2 ng/ml)剂量的孕酮无效,且以与间歇性2 ng/ml剂量相同的总浓度持续输注孕酮会抑制苯丙胺刺激的DA释放和灌注后DA组织浓度。除了5α二氢孕酮(dihydroxyprogesterone)外,各种代谢物的间歇性输注、2 ng/ml的合成孕激素(R5020)以及0.2 ng/ml和2 ng/ml的雌二醇均未显著改变苯丙胺刺激的DA反应。然而,孕烷醇酮、5α二氢孕酮、2 ng/ml的R5020以及0.2 ng/ml的雌二醇可使灌注后DA组织浓度升高至与孕酮相当的水平。这些结果表明,体外孕酮可直接改变纹状体组织碎片多巴胺能终末的苯丙胺刺激的DA释放。这种作用似乎对孕酮以及这种性腺甾体的特定剂量和输注方式具有相当的特异性。此外,孕酮根据其输注方式可对纹状体中苯丙胺诱发的DA释放产生相反的作用,提示一种激素可差异性改变中枢神经系统功能的方式。

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