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有证据表明,新型抗高血压药物氟西诺生可引起不同程度的交感神经抑制,并通过中枢作用增加迷走神经张力。

Evidence that the novel antihypertensive agent, flesinoxan, causes differential sympathoinhibition and also increases vagal tone by a central action.

作者信息

Ramage A G, Wouters W, Bevan P

机构信息

Academic Department of Pharmacology, Royal Free Hospital School of Medicine, Hampstead, London, U.K.

出版信息

Eur J Pharmacol. 1988 Jul 14;151(3):373-9. doi: 10.1016/0014-2999(88)90533-x.

Abstract

The effects of flesinoxan were studied on thoracic preganglionic, splanchnic and renal sympathetic nerve activity, carotid sinus nerve activity, blood pressure and heart rate in anaesthetised cats. In some experiments femoral or renal arterial conductance was also recorded. Flesinoxan (3-300 micrograms kg-1) caused a dose-related fall in blood pressure and heart rate and also caused sympathoinhibition. This fall in blood pressure was not associated with changes in femoral arterial conductance but was with a large increase in renal arterial conductance. In this respect flesinoxan had a greater sympathoinhibitory action on the renal nerve compared with the other sympathetic outflows. The bradycardia was unaffected by the 5-HT3 antagonist, MDL 72222, but was reversed by atropine and was abolished in bi-vagotomised cats. Flesinoxan also caused sympathoinhibition in bi-vagotomised cats and decreased carotid sinus nerve activity and blood pressure. It is concluded that flesinoxan acts centrally to cause sympathoinhibition and an increase in vagal tone.

摘要

研究了氟西诺生对麻醉猫的胸段节前神经、内脏神经和肾交感神经活动、颈动脉窦神经活动、血压和心率的影响。在一些实验中,还记录了股动脉或肾动脉传导率。氟西诺生(3 - 300微克/千克)引起血压和心率呈剂量依赖性下降,并导致交感神经抑制。血压下降与股动脉传导率变化无关,但与肾动脉传导率大幅增加有关。在这方面,与其他交感神经传出纤维相比,氟西诺生对肾神经的交感神经抑制作用更强。5 - HT3拮抗剂MDL 72222对心动过缓无影响,但阿托品可使其逆转,在双侧迷走神经切断的猫中则消失。氟西诺生在双侧迷走神经切断的猫中也引起交感神经抑制,并降低颈动脉窦神经活动和血压。结论是,氟西诺生通过中枢作用引起交感神经抑制和迷走神经张力增加。

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