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体外孕酮对去卵巢雌激素处理的雌性大鼠纹状体中苯丙胺刺激的多巴胺释放的调节作用:反应特征

In vitro progesterone modulation of amphetamine-stimulated dopamine release from the corpus striatum of ovariectomized estrogen-treated female rats: response characteristics.

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. 1990 May 28;517(1-2):117-22. doi: 10.1016/0006-8993(90)91016-a.

DOI:10.1016/0006-8993(90)91016-a
PMID:2375984
Abstract

We have previously reported that a pulsatile infusion of progesterone directly into superfusion chambers containing corpus striatal tissue fragments of ovariectomized estrogen-treated female rats augmented amphetamine-stimulated dopamine release in vitro. In an attempt to understand some of the means by which progesterone modulates dopamine release under these in vitro conditions, we examined two characteristics of this effect of progesterone. First, to determine the threshold dose of progesterone and whether it was necessary for progesterone to be administered in a pulsatile mode, in Expt. I we examined the effect of a single, brief infusion of progesterone at doses of 2, 4 and 40 ng/ml. Second, to evaluate the temporal relationship between progesterone infusion and its capacity to augment amphetamine-stimulated dopamine release, in Expt. II we varied the interval between progesterone infusion and amphetamine challenge, with amphetamine infused at 10, 30, 50 or 90 min post-progesterone. The results of Expt. I indicate that a single 10-min infusion of progesterone at 2 ng/ml was adequate to produce an accentuated response to amphetamine infusion. Although further increases were obtained following the 4 and 40 ng/ml doses, these values failed to differ significantly from the levels obtained with the 2 ng/ml dose. From Expt. II, we observed that this effect of progesterone was relatively rapid with statistically significant increases in amphetamine-stimulated dopamine release occurring at 30 min post-progesterone and similar responses being maintained at 50 and 90 min post-progesterone.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前报道过,将黄体酮以脉冲式注入含有去卵巢并用雌激素处理的雌性大鼠纹状体组织碎片的灌注室中,可在体外增强苯丙胺刺激的多巴胺释放。为了了解在这些体外条件下黄体酮调节多巴胺释放的一些方式,我们研究了黄体酮这种作用的两个特征。首先,为了确定黄体酮的阈值剂量以及黄体酮是否必须以脉冲模式给药,在实验I中,我们研究了以2、4和40 ng/ml的剂量单次短暂注入黄体酮的效果。其次,为了评估黄体酮注入与其增强苯丙胺刺激的多巴胺释放能力之间的时间关系,在实验II中,我们改变了黄体酮注入与苯丙胺激发之间的间隔时间,在注入黄体酮后10、30、50或90分钟注入苯丙胺。实验I的结果表明,以2 ng/ml的剂量单次注入10分钟的黄体酮足以对苯丙胺注入产生增强反应。尽管在4和40 ng/ml的剂量后获得了进一步的增加,但这些值与2 ng/ml剂量获得的水平没有显著差异。从实验II中,我们观察到黄体酮的这种作用相对较快,在注入黄体酮后3分钟苯丙胺刺激的多巴胺释放有统计学上的显著增加,并且在注入黄体酮后50和90分钟保持类似的反应。(摘要截短至250字)

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