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脑啡肽及类似物FK - 33824对清醒绵羊平均动脉压和心率的影响。

Effects of enkephalins and the analogue FK-33824 on mean arterial pressure and heart rate in conscious sheep.

作者信息

Wang X M, Tresham J J, Scoggins B A, Coghlan J P

机构信息

Howard Florey Institute of Experimental Physiology and Medicine, University of Melbourne, Parkville, Australia.

出版信息

Clin Exp Hypertens A. 1989;11(3):427-45. doi: 10.3109/10641968909035352.

Abstract

Experiments were designed to evaluate the central and systemic effects by enkephalins and the enkephalin analogue FK-33824 on mean arterial pressure (MAP) and heart rate (HR) in conscious sheep. Intracerebroventricular infusion of FK-33824 increased both MAP and HR in a dose-dependent manner in normal sheep. The increases in MAP and HR were attenuated by naloxone administered centrally, but not systemically. Intracerebroventricular infusion of met-enkephalin, leu-enkephalin and naloxone failed to change both MAP and HR significantly. However, intravenous infusion of met-enkephalin, leu-enkephalin and FK-33824 resulted in bradycardia. Haemorrhage alone decreased both MAP and HR. Intracerebroventricular infusion of FK-33824 blunted the reduction in MAP in response to haemorrhage. The increases in MAP and HR following FK-33824 were also accompanied by elevated levels of plasma renin concentration. It is suggested that the tachycardia and pressor effect produced by the intracerebroventricular administration of FK-33824 in normal conscious sheep may result from a combined action of both neural and chemical pathways which are involved in cardiovascular control, and are mediated via the mu-opioid receptors. Opioids may have opposite effects on cardiovascular control depending on the route of administration.

摘要

实验旨在评估脑啡肽和脑啡肽类似物FK - 33824对清醒绵羊平均动脉压(MAP)和心率(HR)的中枢及全身效应。正常绵羊脑室内注入FK - 33824可使MAP和HR呈剂量依赖性升高。中枢给予纳洛酮可减弱MAP和HR的升高,但全身给药则无此作用。脑室内注入甲硫脑啡肽、亮脑啡肽和纳洛酮未能显著改变MAP和HR。然而,静脉注入甲硫脑啡肽、亮脑啡肽和FK - 33824会导致心动过缓。单纯失血会降低MAP和HR。脑室内注入FK - 33824可减轻因失血引起的MAP降低。FK - 33824引起的MAP和HR升高还伴有血浆肾素浓度升高。提示正常清醒绵羊脑室内给予FK - 33824产生的心动过速和升压效应可能是神经和化学途径共同作用的结果,这些途径参与心血管控制,并通过μ-阿片受体介导。阿片类药物对心血管控制的影响可能因给药途径而异。

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