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有证据表明,孤束核和其他脑干区域的5-羟色胺3(5-HT3)受体可调节麻醉大鼠中由贝佐尔德-贾里斯反射激活所诱发的迷走神经性心动过缓。

Evidence that 5-HT3 receptors in the nucleus tractus solitarius and other brainstem areas modulate the vagal bradycardia evoked by activation of the von Bezold-Jarisch reflex in the anesthetized rat.

作者信息

Pires J G, Silva S R, Ramage A G, Futuro-Neto H A

机构信息

Departamento de Ciências Fisiológicas, Centro Biomédico, Universidade Federal do Espírito Santo, Av. Marechal Campos 1468, Vitória, ES 29040-090, Brazil.

出版信息

Brain Res. 1998 Apr 27;791(1-2):229-34. doi: 10.1016/s0006-8993(98)00109-7.

Abstract

The effects of intracisternal (i.c.) application of the 5-HT3 receptor antagonist granisetron (0.016-0.16 microg kg-1) and the agonist phenylbiguanide (0.3-3 microg kg-1) on reflex bradycardia evoked by injection of phenylbiguanide (i.v.; 10 microg kg-1) were investigated in urethane anesthetized atenolol-pretreated rats. The effect of bilateral microinjection of granisetron (10 nmol per side, 100 nl) into the nucleus tractus solitarius (NTS) on the reflex was also investigated. Intracisternal administration of granisetron dose-dependently (0.016-0.16 microg kg-1) and significantly attenuated the reflex bradycardia whilst the highest dose given i.v. had no significant effect on the reflex bradycardia. Phenylbiguanide given i.c. only caused significant potentiation at the middle dose (1 microg kg-1), having no significant effects at the other doses. Neither granisetron nor phenylbiguanide given i.c. affected resting heart rate or blood pressure. Granisetron microinjected bilaterally into the NTS also significantly attenuated both reflex bradycardia and hypotension. It is concluded that excitation of cardiac vagal motoneurones evoked by cardiopulmonary afferents involves activation of 5-HT3 receptors located in the nucleus tractus solitarius and other brainstem areas.

摘要

在乌拉坦麻醉且预先用阿替洛尔处理的大鼠中,研究了脑池内(i.c.)注射5-羟色胺3(5-HT3)受体拮抗剂格拉司琼(0.016 - 0.16微克/千克)和激动剂苯乙双胍(0.3 - 3微克/千克)对静脉注射(i.v.;10微克/千克)苯乙双胍诱发的反射性心动过缓的影响。还研究了双侧微量注射格拉司琼(每侧10纳摩尔,100纳升)到孤束核(NTS)对该反射的影响。脑池内给予格拉司琼剂量依赖性地(0.016 - 0.16微克/千克)显著减弱反射性心动过缓,而静脉注射最高剂量对反射性心动过缓无显著影响。脑池内给予苯乙双胍仅在中等剂量(1微克/千克)时引起显著增强,在其他剂量时无显著影响。脑池内给予格拉司琼或苯乙双胍均不影响静息心率或血压。双侧微量注射到NTS的格拉司琼也显著减弱反射性心动过缓和低血压。结论是心肺传入神经诱发的心脏迷走运动神经元兴奋涉及位于孤束核和其他脑干区域的5-HT3受体的激活。

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