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首页> 外文期刊>Neuropharmacology >Progesterone inhibition of dopamine-induced increase in frequency of spontaneous excitatory postsynaptic currents in rat prelimbic cortical neurons.
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Progesterone inhibition of dopamine-induced increase in frequency of spontaneous excitatory postsynaptic currents in rat prelimbic cortical neurons.

机译:孕酮抑制多巴胺诱导的大鼠前肢皮层神经元自发性兴奋性突触后突触电流频率增加。

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摘要

We examined the effects of progesterone on frequency of miniature excitatory postsynaptic currents (mEPSCs) and spontaneous excitatory postsynaptic currents (sEPSCs), and dopamine-induced increase in the frequency of sEPSCs in pyramidal cells of layers V-VI of the rat prelimbic cortex using whole-cell patch-clamp techniques in slices. The results showed that progesterone 100 microM had no effects on the frequency of mEPSCs and sEPSCs, but significantly inhibited dopamine-induced increase in frequency of sEPSCs. This was in contrast to the effect of progesterone on the effect of 5-HT, which showed no changes after progesterone. When studying the mechanism of the progesterone effect, we observed that GABA(A) receptor antagonist and progesterone receptor antagonist did not influence the effect of progesterone; progesterone had no effects on D1 receptor agonist, protein kinase A and protein kinase C activator-induced increase in the frequency of sEPSCs. Interestingly, sigma(1) receptor antagonist could inhibit the effect of dopamine and sigma(1) receptor agonist had a synergistic effect on the effect of D1 receptor agonist. These results suggest that progesterone may inhibit dopamine-induced increase in frequency of sEPSCs in rat prelimbic cortical neurons via inhibition of sigma(1)/D1 receptor synergism because progesterone has been known to be an antagonist of sigma(1) receptor.
机译:我们研究了黄体酮对微型兴奋性突触后突触电流(mEPSCs)和自发性兴奋性突触后突触电流(sEPSCs)频率的影响,以及多巴胺诱导的大鼠前肢皮层V-VI层锥体细胞中sEPSCs频率的增加切片中的细胞膜片钳技术。结果表明,孕酮100 microM对mEPSC和sEPSC的频率没有影响,但显着抑制了多巴胺引起的sEPSC的频率增加。这与孕酮对5-HT的作用相反,后者在孕酮后没有变化。在研究孕激素作用的机制时,我们观察到GABA(A)受体拮抗剂和孕激素受体拮抗剂不影响孕激素的作用。黄体酮对D1受体激动剂,蛋白激酶A和蛋白激酶C激活剂诱导的sEPSC频率增加没有影响。有趣的是,sigma(1)受体拮抗剂可以抑制多巴胺的作用,而sigma(1)受体激动剂对D1受体激动剂的作用具有协同作用。这些结果表明,孕酮可能通过抑制sigma(1)/ D1受体的协同作用而抑制多巴胺诱导的大鼠前肢皮层神经元sEPSCs频率的增加,因为已知孕酮是sigma(1)受体的拮抗剂。

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