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长效α1-肾上腺素能拟交感神经药可抑制人体肌肉的交感神经输出。

Long-acting alpha 1-adrenoceptive sympathomimetic agent suppresses sympathetic outflow to muscles in humans.

作者信息

Iwase S, Mano T, Saito M, Ishida G

机构信息

Department of Higher Nervous Control, Nagoya University, Japan.

出版信息

J Auton Nerv Syst. 1991 Dec;36(3):193-9. doi: 10.1016/0165-1838(91)90043-3.

Abstract

To clarify the effect of a long-acting selective alpha 1-adrenoceptive sympathomimetic agent on sympathetic outflow to muscles (muscle sympathetic activity, MSA) in humans, 5 mg of midodrine hydrochloride was injected intravenously in ten healthy male subjects aged 19-25. Spontaneous MSA was significantly suppressed as well as plasma norepinephrine level without changing heart rate, or systemic blood pressure. The suppression continued for more than 90 min, and this is supposed to be due to negative feedback action on the baroreflex loop. The absence of significant changes in heart rate or systemic blood pressure in healthy subjects suggests that hemodynamic homeostasis is maintained by reducing the MSA in response to a long-acting sympathomimetic agent, like midodrine hydrochloride, which constricts peripheral vessels directly.

摘要

为阐明长效选择性α1 -肾上腺素能拟交感神经药对人体肌肉交感神经输出(肌肉交感神经活动,MSA)的影响,对10名年龄在19 - 25岁的健康男性受试者静脉注射5毫克盐酸米多君。自发性MSA以及血浆去甲肾上腺素水平显著受到抑制,而心率和全身血压未发生变化。这种抑制持续超过90分钟,推测这是由于对压力感受性反射环的负反馈作用。健康受试者心率和全身血压无显著变化,这表明通过减少对长效拟交感神经药(如直接收缩外周血管的盐酸米多君)的反应性MSA来维持血流动力学稳态。

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