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下丘脑γ-氨基丁酸能对压力感受器刺激的呼吸反应的调节

Hypothalamic GABAergic modulation of respiratory responses to baroreceptor stimulation.

作者信息

Dillon G H, Shonis C A, Waldrop T G

机构信息

Department of Physiology and Biophysics, University of Illinois, Urbana 61801.

出版信息

Respir Physiol. 1991 Sep;85(3):289-304. doi: 10.1016/0034-5687(91)90069-u.

Abstract

Little is known about possible hypothalamic modulation of the respiratory response to baroreceptor activation. The purpose of this study was to determine if the respiratory depression associated with the baroreceptor reflex is modulated by neurons in the posterior hypothalamus. Breathing frequency and tidal diaphragmatic activity were derived from diaphragmatic electromyographic recordings in anesthetized rats. Respiratory responses to baroreceptor activation were analyzed before and after unilateral microinjections of GABA antagonists (picrotoxin, bicuculline methiodide) or a GABA synthesis inhibitor (3-mercaptopropionic acid, 3-MP) into the posterior hypothalamus. Baroreceptor stimulation prior to microinjections elicited a decrease in both breathing frequency and tidal diaphragmatic activity. Microinjection of picrotoxin elicited an increase in respiratory activity. The decrease in tidal diaphragmatic activity evoked by baroreceptor stimulation was blocked after the microinjection. Furthermore, the baroreceptor-induced fall in breathing frequency was converted to an increase in breathing frequency. These effects of picrotoxin were reversed by microinjections of a GABA agonist (muscimol) into the same site. Microinjections of 3-MP also blocked the decrease in breathing frequency associated with baroreceptor stimulation. The GABA antagonist bicuculline methiodide elicited similar effects. These results indicate that a GABAergic mechanism in the posterior hypothalamus modulates the respiratory responses to baroreceptor stimulation.

摘要

关于下丘脑对压力感受器激活所致呼吸反应的可能调节作用,目前所知甚少。本研究的目的是确定与压力感受器反射相关的呼吸抑制是否受下丘脑后部神经元的调节。呼吸频率和膈肌潮气量活动通过麻醉大鼠的膈肌肌电图记录得出。在单侧向下丘脑后部微量注射GABA拮抗剂(印防己毒素、甲碘化荷包牡丹碱)或GABA合成抑制剂(3-巯基丙酸,3-MP)之前和之后,分析对压力感受器激活的呼吸反应。微量注射前的压力感受器刺激导致呼吸频率和膈肌潮气量活动均降低。微量注射印防己毒素引起呼吸活动增加。微量注射后,压力感受器刺激引起的膈肌潮气量活动降低被阻断。此外,压力感受器引起的呼吸频率下降转变为呼吸频率增加。向同一部位微量注射GABA激动剂(蝇蕈醇)可逆转印防己毒素的这些作用。微量注射3-MP也可阻断与压力感受器刺激相关的呼吸频率下降。GABA拮抗剂甲碘化荷包牡丹碱也产生类似作用。这些结果表明,下丘脑后部的GABA能机制调节对压力感受器刺激的呼吸反应。

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