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促甲状腺激素释放激素在体外刺激围产期大鼠呼吸。

Thyrotropin-releasing hormone stimulates perinatal rat respiration in vitro.

作者信息

Greer J J, al-Zubaidy Z, Carter J E

机构信息

Department of Physiology, University of Alberta Perinatal Research Centre, Edmonton, Canada.

出版信息

Am J Physiol. 1996 Nov;271(5 Pt 2):R1160-4. doi: 10.1152/ajpregu.1996.271.5.R1160.

Abstract

In the present study, we test whether thyrotropin-releasing hormone (TRH) stimulates respiratory frequency in perinatal rats by acting at regions of the medulla responsible for respiratory rhythmogenesis, the pre-Bötzinger complex. We also test whether TRH stimulates respiration in the fetal rat at a time shortly after the inception of respiratory rhythmogenesis [embryonic days (E) 17-18]. Two in vitro experimental models were utilized: the isolated brain stem-spinal cord preparation from fetal (E17-E18) and neonatal [postnatal days (P) 0-2] rats and the medullary slice preparation isolated from neonatal rats (P1-P2). Bath application of TRH caused a dose-dependent, reversible increase (maximum increase approximately 60%) in the frequency of respiratory rhythmic neural discharge generated by brain stem-spinal cord [half-maximal effective concentration (EC50) approximately 9 nM] and medullary slice (EC50 approximately 2.5 nM) neonatal rat preparations. Pressure injection of TRH unilaterally into the region of the pre-Bötzinger complex of the neonatal medullary slice caused an approximately 28% increase in the frequency of respiratory discharge. Application of TRH to the medium bathing fetal rat brain stem-spinal cord preparations caused an approximately threefold increase in respiratory discharge frequency. We conclude that TRH stimulates respiratory discharge frequency from the time near inception of respiratory motor discharge and acts directly at the pre-Bötzinger complex.

摘要

在本研究中,我们测试促甲状腺激素释放激素(TRH)是否通过作用于延髓中负责呼吸节律产生的区域——前包钦格复合体,来刺激围产期大鼠的呼吸频率。我们还测试了TRH是否在呼吸节律产生开始后不久(胚胎期第17 - 18天)刺激胎鼠呼吸。使用了两种体外实验模型:来自胎鼠(胚胎期第17 - 18天)和新生鼠(出生后第0 - 2天)的离体脑干-脊髓标本,以及来自新生鼠(出生后第1 - 2天)的延髓切片标本。浴槽中加入TRH导致新生鼠脑干-脊髓标本(半数最大效应浓度[EC50]约为9 nM)和延髓切片标本(EC50约为2.5 nM)产生的呼吸节律性神经放电频率出现剂量依赖性、可逆性增加(最大增加约60%)。将TRH单侧压力注射到新生鼠延髓切片的前包钦格复合体区域,导致呼吸放电频率增加约28%。将TRH应用于浸泡胎鼠脑干-脊髓标本的培养基中,导致呼吸放电频率增加约三倍。我们得出结论,TRH从呼吸运动放电开始时就刺激呼吸放电频率,并且直接作用于前包钦格复合体。

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