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调节大鼠压力感受性反射性心动过缓的脑回路:楔束核与中脑导水管周围灰质之间的解剖学和功能联系。

Brain circuits mediating baroreflex bradycardia inhibition in rats: an anatomical and functional link between the cuneiform nucleus and the periaqueductal grey.

机构信息

UPMC/INSERM, UMR-S 975 and CNRS UMR 7225, Faculté de médecine UPMC, Site Pitie-Salpêtrière, Paris F-75013, France.

出版信息

J Physiol. 2011 Apr 15;589(Pt 8):2079-91. doi: 10.1113/jphysiol.2010.203737. Epub 2011 Feb 21.

Abstract

Defence responses triggered experimentally in rats by stimulation of the dorsomedial nucleus of the hypothalamus (DMH) and the dorsolateral periaqueductal grey matter (PAG) inhibit the cardiac baroreflex response (i.e. bradycardia). It has also been proposed that the midbrain cuneiform nucleus (CnF) is involved in active responses. Our aim was to identify the neurocircuitry involved in defence-induced baroreflex inhibition, with a particular focus on the link between DMH, CnF and dorsolateral PAG. Microinjection of the anterograde tracer Phaseolus vulgaris leucoaggutinin into the CnF revealed a dense projection to the dorsolateral PAG. Moreover, activation of neurons in the CnF induced increased expression of Fos protein in the dorsolateral PAG. Inhibition of neurons of the CnF or dorsolateral PAG prevented the inhibition of baroreflex bradycardia induced by DMH or CnF stimulation, respectively. These results provide a detailed description of the brain circuitry underlying acute baroreflex modulation by neurons of the DMH. Our data have shown for the first time that the CnF plays a key role in defence reaction-associated cardiovascular changes; its stimulation, from the DMH, activates the dorsolateral PAG, which, in turn, inhibits baroreflex bradycardia.

摘要

刺激下丘脑背内侧核(DMH)和外侧导水管周围灰质(PAG)可在大鼠中引发防御反应,抑制心脏压力反射反应(即心动过缓)。有人提出,中脑楔形核(CnF)参与了主动反应。我们的目的是确定防御诱导的压力反射抑制所涉及的神经回路,特别关注 DMH、CnF 和外侧 PAG 之间的联系。将顺行示踪剂菜豆白细胞凝集素注入 CnF 中,发现其与外侧 PAG 之间存在密集的投射。此外,CnF 中的神经元激活可诱导外侧 PAG 中 Fos 蛋白表达增加。抑制 CnF 或外侧 PAG 的神经元分别可防止 DMH 或 CnF 刺激引起的压力反射性心动过缓抑制。这些结果提供了 DMH 神经元对急性压力反射调节的详细描述。我们的数据首次表明,CnF 在防御反应相关的心血管变化中起关键作用;它从 DMH 刺激,激活外侧 PAG,反过来抑制压力反射性心动过缓。

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