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M1和M2受体对大鼠颈上神经节的突触诱发电位介导不同的效应。

M1 and M2 receptors mediate different effects on synaptically evoked potentials of the rat superior cervical ganglion.

作者信息

Newberry N R

机构信息

Merck Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Harlow, Essex U.K.

出版信息

Neurosci Lett. 1988 May 16;88(1):100-6. doi: 10.1016/0304-3940(88)90322-9.

Abstract

The application of muscarine, carbachol or methylfurmethide to the rat superior cervical ganglion in vitro resulted in a complex mixture of effects as recorded from the internal carotid nerve using a greased-gap technique. In addition to the previously described depolarizing and hyperpolarizing responses, increases and decreases in the amplitudes of the synaptically evoked compound action potential and its related afterhyperpolarization were observed. The depolarization and the enhancing effects of the agonists were selectively antagonized by pirenzepine (0.3 microM) whereas the hyperpolarization and depressant effects were antagonized by gallamine (10 microM). Methylfurmethide only induced the pirenzepine-sensitive effects. It is concluded that M1 and M2 (cardiac-like) receptors exert different effects on the synaptically evoked potentials of this preparation.

摘要

使用油隙技术记录大鼠离体颈上神经节内颈动脉神经的反应时,向其中施加毒蕈碱、卡巴胆碱或甲基呋索氯铵会产生复杂的效应混合物。除了先前描述的去极化和超极化反应外,还观察到突触诱发复合动作电位及其相关后超极化的幅度增加和减少。激动剂的去极化和增强作用可被哌仑西平(0.3微摩尔)选择性拮抗,而超极化和抑制作用则被加拉明(10微摩尔)拮抗。甲基呋索氯铵仅诱导哌仑西平敏感的效应。结论是,M1和M2(类心脏)受体对该制剂的突触诱发电位发挥不同作用。

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