...
首页> 外文期刊>Psychopharmacology >Effect of antidepressant drugs on dopamine D1 and D2 receptor expression and dopamine release in the nucleus accumbens of the rat.
【24h】

Effect of antidepressant drugs on dopamine D1 and D2 receptor expression and dopamine release in the nucleus accumbens of the rat.

机译:抗抑郁药对大鼠伏隔核中多巴胺D1和D2受体表达及多巴胺释放的影响。

获取原文
获取原文并翻译 | 示例

摘要

This study examined the effect of repeated treatment with the antidepressant drugs, fluoxetine, desipramine and tranylcypromine, on dopamine receptor expression (mRNA and binding site density) in sub-regions of the nucleus accumbens and striatum of the rat. The effect of these treatments on extracellular levels of dopamine in the nucleus accumbens was also measured. Experiments using in situ hybridisation showed that the antidepressants caused a region-specific increase in D2 mRNA, this effect being most prominent in the nucleus accumbens shell. In contrast, none of the treatments increased D1 mRNA in any of the regions examined. Measurement of D2-like binding by receptor autoradiography, using the ligand [3H]YM-09151-2, revealed that both fluoxetine and desipramine increased D2-like binding in the nucleus accumbens shell; fluoxetine had a similar effect in the nucleus accumbens core. Tranylcypromine, however, had no effect on D2-like binding in the nucleus accumbens but decreased binding in the striatum. In micro-dialysis experiments, our data showed that levels of extracellular dopamine in the nucleus accumbens were not altered in rats treated with either fluoxetine or desipramine, but increased by tranylcypromine. From our findings, we propose that the antidepressant drugs tested enhance dopamine function in the nucleus accumbens through either increased expression of post-synaptic D2 receptors (fluoxetine and desipramine) or increased dopamine release (tranylcypromine).
机译:这项研究检查了用抗抑郁药氟西汀,地昔帕明和反式环丙胺重复治疗对大鼠伏隔核和纹状体亚区域多巴胺受体表达(mRNA和结合位点密度)的影响。还测量了这些治疗对伏隔核中细胞外多巴胺水平的影响。使用原位杂交的实验表明,抗抑郁药引起D2 mRNA的区域特异性增加,这种作用在伏伏核壳中最为明显。相反,在所检查的任何区域中,没有一种处理增加D1 mRNA。使用配体[3H] YM-09151-2通过放射自显影法测量D2样结合,结果表明氟西汀和地昔帕明都增加了伏伏核壳中D2样结合。氟西汀在伏伏核核心中具有类似作用。但是,Tranylcypromine对伏隔核中的D2样结合没有影响,但在纹状体中的结合却减少了。在微透析实验中,我们的数据表明,用氟西汀或地昔帕明治疗的大鼠伏隔核中细胞外多巴胺的水平没有改变,但是反式环丙胺可增加这种浓度。根据我们的发现,我们建议所测试的抗抑郁药通过增加突触后D2受体的表达(氟西汀和地昔帕明)或增加多巴胺的释放(反式环丙胺)来增强伏隔核中的多巴胺功能。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号