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促甲状腺激素释放激素对食欲素/下丘脑泌素神经元的刺激作用。

Stimulation of orexin/hypocretin neurones by thyrotropin-releasing hormone.

作者信息

González J Antonio, Horjales-Araujo Emilia, Fugger Lars, Broberger Christian, Burdakov Denis

机构信息

Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.

出版信息

J Physiol. 2009 Mar 15;587(Pt 6):1179-86. doi: 10.1113/jphysiol.2008.167940. Epub 2009 Feb 9.

Abstract

Central orexin/hypocretin neurones are critical for sustaining consciousness: their firing stimulates wakefulness and their destruction causes narcolepsy. We explored whether the activity of orexin cells is modulated by thyrotropin-releasing hormone (TRH), an endogenous stimulant of wakefulness and locomotor activity whose mechanism of action is not fully understood. Living orexin neurones were identified by targeted expression of green fluorescent protein (GFP) in acute brain slices of transgenic mice. Using whole-cell patch-clamp recordings, we found that TRH robustly increased the action potential firing rate of these neurones. TRH-induced excitation persisted under conditions of synaptic isolation, and involved a Na(+)-dependent depolarization and activation of a mixed cation current in the orexin cell membrane. By double-label immunohistochemistry, we found close appositions between TRH-immunoreactive nerve terminals and orexin-A-immunoreactive cell bodies. These results identify a new physiological modulator of orexin cell firing, and suggest that orexin cell excitation may contribute to the arousal-enhancing actions of TRH.

摘要

中枢食欲素/下丘脑泌素神经元对于维持意识至关重要:它们的放电刺激清醒,而它们的破坏会导致发作性睡病。我们探究了食欲素细胞的活动是否受促甲状腺激素释放激素(TRH)调节,TRH是一种内源性清醒和运动活动刺激物,其作用机制尚未完全明确。通过在转基因小鼠的急性脑片中靶向表达绿色荧光蛋白(GFP)来识别活的食欲素神经元。使用全细胞膜片钳记录,我们发现TRH显著提高了这些神经元的动作电位发放率。在突触隔离条件下,TRH诱导的兴奋持续存在,并且涉及食欲素细胞膜中Na(+)依赖性去极化和混合阳离子电流的激活。通过双重标记免疫组织化学,我们发现TRH免疫反应性神经末梢与食欲素-A免疫反应性细胞体之间紧密相邻。这些结果确定了食欲素细胞放电的一种新的生理调节因子,并表明食欲素细胞兴奋可能有助于TRH的唤醒增强作用。

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