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α-肾上腺素能受体对人体静息及交感-肾上腺激活状态下神经肽Y样免疫反应性和儿茶酚胺血浆水平的影响。

Alpha-adrenoceptor influence on plasma levels of neuropeptide Y-like immunoreactivity and catecholamines during rest and sympathoadrenal activation in humans.

作者信息

Pernow J, Lundberg J M, Kaijser L

机构信息

Department of Pharmacology, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Cardiovasc Pharmacol. 1988;12(5):593-9. doi: 10.1097/00005344-198811000-00014.

Abstract

Antecubital venous plasma neuropeptide Y-like immunoreactivity (NPY-LI) and catecholamines were analyzed in six healthy volunteers performing a graded bicycle exercise without medication and after acute administration of clonidine, phentolamine, and nifedipine. During the control exercise, plasma noradrenaline (NA), adrenaline (A), and NPY-LI increased to 17-, 7-, and 3-fold the resting values, respectively, at a maximal workload. Clonidine (300 micrograms p.o.) reduced resting and exercising heart rate (HR) and systolic blood pressure (SBP). Plasma NA at rest decreased and NA, A, and NPY-LI were 40-60% lower during the exercise after clonidine compared to the control. Phentolamine (0.07 mg X kg-1 every 10 min i.v.) and nifedipine (20 mg p.o.) increased HR and reduced SBP during the exercise. Plasma NA at rest was elevated threefold and the exercise-induced increases in NA and A were also enhanced after phentolamine. Plasma NPY-LI at rest was unchanged by phentolamine, while it was increased five-fold, as compared to the control, at the highest workload. Nifedipine slightly enhanced plasma NA and NPY-LI but not A during exercise. It is suggested that NPY is released mainly at high levels of sympathetic activity and that blood-pressure-lowering drugs acting on alpha adrenoceptors acutely influence the release of both NA and NPY-LI from sympathetic nerves in humans.

摘要

对6名健康志愿者进行了研究,分析他们在未用药情况下以及急性给予可乐定、酚妥拉明和硝苯地平后进行分级自行车运动时肘前静脉血浆神经肽Y样免疫反应性(NPY-LI)和儿茶酚胺的情况。在对照运动期间,在最大工作量时,血浆去甲肾上腺素(NA)、肾上腺素(A)和NPY-LI分别增加至静息值的17倍、7倍和3倍。可乐定(口服300微克)降低了静息和运动时的心率(HR)及收缩压(SBP)。静息时血浆NA下降,与对照相比,可乐定给药后运动期间NA、A和NPY-LI降低40%-60%。酚妥拉明(静脉注射0.07毫克/千克,每10分钟一次)和硝苯地平(口服20毫克)在运动期间使HR增加而SBP降低。静息时血浆NA升高3倍,酚妥拉明给药后运动诱导的NA和A增加也增强。酚妥拉明对静息时血浆NPY-LI无影响,而在最高工作量时,与对照相比,其增加了5倍。硝苯地平在运动期间轻微增强了血浆NA和NPY-LI,但对A无影响。提示NPY主要在高交感神经活动水平时释放,作用于α肾上腺素能受体的降压药物可急性影响人体交感神经中NA和NPY-LI的释放。

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