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毒蕈碱M1受体在大鼠5-羟色胺诱导的贝佐尔德-雅里什反射中枢通路中的作用

Involvement of muscarinic M1 receptor in the central pathway of the serotonin-induced Bezold-Jarisch reflex in rats.

作者信息

Saito K, Yoshioka M, Kohya T, Kitabatake A

机构信息

Department of Cardiovascular Medicine, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

J Auton Nerv Syst. 1994 Sep;49(1):61-8. doi: 10.1016/0165-1838(94)90021-3.

Abstract

The involvement of central muscarinic receptors in mediating the Bezold-Jarisch reflex elicited by injection of 5-hydroxytryptamine (5-HT) was studied in urethane/chloralose-anesthetized rats. Intravenous bolus injection of 5-HT (3.1 to 50 micrograms/kg) evoked a short-lasting dose-related bradycardia and hypotension, the Bezold-Jarisch reflex, accompanied with bursts of the efferent cervical vagus nerve. Systemic administration of atropine (0.1 and 1 mg/kg) blocked not only the cardiac responses but also the efferent cervical vagus nerve activity changes. Although the afferent cervical vagus nerve was also activated by an intravenous bolus injection of 5-HT, these responses were not altered by the systemic administration of even a high dose of atropine (1 mg/kg). Intracerebroventricular (i.c.v.) administration of pirenzepine (1 and 10 micrograms/10 microliters), a selective M1 receptor antagonist, caused a rightward shift of the 5-HT dose-response curve for efferent vagus nerve activity. In contrast, i.c.v. administration of muscarinic type 2 receptor antagonist, gallamine, and type 3 receptor antagonist, p-fluorohexahydrosiladifenidol, failed to alter the response in nerve activity to 5-HT. These results suggest that the activation of central nervous muscarinic receptors might be involved in mediating the Bezold-Jarisch reflex and that the subtype might belong to type 1.

摘要

在乌拉坦/氯醛糖麻醉的大鼠中,研究了中枢毒蕈碱受体在介导由注射5-羟色胺(5-HT)引发的贝佐尔德-雅里什反射中的作用。静脉推注5-HT(3.1至50微克/千克)可诱发短暂的剂量相关心动过缓和低血压,即贝佐尔德-雅里什反射,并伴有传出颈迷走神经的爆发活动。全身给予阿托品(0.1和1毫克/千克)不仅阻断了心脏反应,还阻断了传出颈迷走神经活动的变化。尽管静脉推注5-HT也会激活传入颈迷走神经,但即使全身给予高剂量的阿托品(1毫克/千克),这些反应也不会改变。脑室内(i.c.v.)给予选择性M1受体拮抗剂哌仑西平(1和10微克/10微升),导致传出迷走神经活动的5-HT剂量反应曲线向右移动。相比之下,脑室内给予毒蕈碱2型受体拮抗剂加拉明和3型受体拮抗剂对氟己基六氢硅二苯胺未能改变神经活动对5-HT的反应。这些结果表明,中枢神经毒蕈碱受体的激活可能参与介导贝佐尔德-雅里什反射,且该亚型可能属于1型。

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