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通过微透析证明雌激素对大鼠内侧视前区γ-氨基丁酸能神经元的兴奋性A1去甲肾上腺素能输入的调节作用。

Oestrogen modulation of excitatory A1 noradrenergic input to rat medial preoptic gamma aminobutyric acid neurones demonstrated by microdialysis.

作者信息

Herbison A E, Heavens R P, Dyer R G

机构信息

Department of Neuroendocrinology, AFRC Institute of Animal Physiology and Genetics Research, Babraham, Cambridge, UK.

出版信息

Neuroendocrinology. 1990 Aug;52(2):161-8. doi: 10.1159/000125568.

Abstract

The effect of A1 cell group electrical stimulation on the simultaneous release of endogenous noradrenaline (NA) and gamma-aminobutyric acid (GABA) from the medial preoptic area (MPOA) was monitored with microdialysis. In ovariectomised (OVX) rats a 15-min period of A1 stimulation induced an immediate increase in both NA and GABA release in the MPOA. Electrical stimulation lateral to the A1 region did not alter NA or GABA release. The addition of the alpha-adrenergic antagonist phenoxybenzamine to the perfusion medium resulted in a significant increase in basal NA levels, and electrical stimulation during this period further increased NA release while GABA levels were not significantly altered throughout. The effect of oestrogen on this pathway was examined in animals at a time of oestrogen-negative feedback on luteinising hormone (LH) secretion (OVX-EBn) and prior to the expected oestrogen-induced LH surge (OVX-EBp). Activation of A1 neurones in OVX-EBn rats resulted in NA and GABA increases in the MPOA similar to that observed with OVX rats. In OVX-EBp animals, basal GABA levels were found to be significantly higher compared with OVX rats but NA release induced by A1 stimulation had no effect on GABA levels. Depolarisation of the MPOA by increasing the potassium ion concentration of the perfusion medium evoked significantly greater GABA release from OVX-EBp rats compared with the OVX and OVX-EBn animals. Potassium-stimulated NA release was not significantly altered by oestrogen administration. These results demonstrate an excitatory alpha-adrenergic mediated noradrenergic input to GABA neurones in the MPOA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用微透析技术监测A1细胞群电刺激对内侧视前区(MPOA)内源性去甲肾上腺素(NA)和γ-氨基丁酸(GABA)同时释放的影响。在去卵巢(OVX)大鼠中,15分钟的A1刺激可立即引起MPOA中NA和GABA释放增加。A1区域外侧的电刺激未改变NA或GABA的释放。向灌注介质中加入α-肾上腺素能拮抗剂酚苄明可使基础NA水平显著升高,在此期间的电刺激进一步增加了NA的释放,而GABA水平在整个过程中未发生显著改变。在雌激素对促黄体生成素(LH)分泌产生负反馈时(OVX-EBn)以及预期雌激素诱导LH峰出现之前(OVX-EBp),研究了雌激素对该通路的影响。激活OVX-EBn大鼠的A1神经元导致MPOA中NA和GABA增加,与OVX大鼠中观察到的情况相似。在OVX-EBp动物中,发现基础GABA水平与OVX大鼠相比显著更高,但A1刺激诱导的NA释放对GABA水平没有影响。与OVX和OVX-EBn动物相比,通过增加灌注介质中钾离子浓度使MPOA去极化,可引起OVX-EBp大鼠释放显著更多的GABA。雌激素给药对钾刺激的NA释放没有显著影响。这些结果表明,存在一种兴奋性的α-肾上腺素能介导的去甲肾上腺素能输入至MPOA中的GABA神经元。(摘要截短至250字)

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