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犬在跑步机运动期间的α1肾上腺素能受体阻断和/或5-羟色胺1A激动作用。

Alpha 1-adrenoceptor blockade and/or 5-HT1A agonism during treadmill exercise in dogs.

作者信息

Grohs J G, Fischer G, Huber S, Raberger G

机构信息

Pharmakologisches Institut, Universität Wien, Austria.

出版信息

J Auton Pharmacol. 1991 Apr;11(2):101-7. doi: 10.1111/j.1474-8673.1991.tb00249.x.

Abstract
  1. The hypotensive effects of alpha 1-adrenergic blockade and/or stimulation of central nervous 5-HT1A receptors were studied using drugs with different affinity for central nervous 5-HT1A and peripheral alpha 1-adrenoceptors. Urapidil, 5-methylurapidil, flesinoxan and 8-OH-DPAT were compared under states of different activation of the autonomic nervous system, i.e. at rest and during graded treadmill exercise. 2. The rank order of hypotensive potency as derived from the most extensive decrease in resting diastolic arterial blood pressure was urapidil greater than 5-methylurapidil greater than flesinoxan much greater than 8-OH-DPAT. 3. The reflex increase in heart rate due to the decrease in arterial blood pressure at rest was suppressed after 0.1 mumol kg-1 flesinoxan. 4. The reflex increase in heart rate due to the decrease in arterial blood pressure at rest was less accentuated after high doses of urapidil and 5-methylurapidil. 5. During exercise both 5HT1A receptor agonists, flesinoxan and 8-OH-DPAT, decreased sympathetic tone. 6. The combined effects of alpha 1-adrenoceptor blockade and 5-HT1A receptor stimulation (urapidil and 5-methylurapidil) result in distinct decreases in blood pressure and slight suppression of reflex tachycardia at rest after high doses. Stimulation of 5-HT1A receptors alone (flesinoxan) suppresses reflex tachycardia by modulation of baroreceptor reflex and at high dose also diminishes exercise-induced increase in sympathetic tone.
摘要
  1. 使用对中枢神经系统5-HT1A和外周α1-肾上腺素能受体具有不同亲和力的药物,研究了α1-肾上腺素能阻断和/或中枢神经系统5-HT1A受体刺激的降压作用。在自主神经系统不同激活状态下,即静息时和分级跑步机运动期间,比较了乌拉地尔、5-甲基乌拉地尔、氟司必林和8-羟基二丙胺苯丙酮。2. 根据静息舒张压最大降幅得出的降压效力排序为:乌拉地尔>5-甲基乌拉地尔>氟司必林>>8-羟基二丙胺苯丙酮。3. 静息时,0.1μmol/kg氟司必林后,因动脉血压下降引起的心率反射性增加受到抑制。4. 高剂量乌拉地尔和5-甲基乌拉地尔给药后,静息时因动脉血压下降引起的心率反射性增加减弱。5. 在运动期间,5-HT1A受体激动剂氟司必林和8-羟基二丙胺苯丙酮均降低交感神经张力。6. α1-肾上腺素能受体阻断和5-HT1A受体刺激(乌拉地尔和5-甲基乌拉地尔)的联合作用导致高剂量给药后静息时血压明显下降,反射性心动过速轻度受抑制。单独刺激5-HT1A受体(氟司必林)通过调节压力感受器反射抑制反射性心动过速,高剂量时也可减少运动诱导的交感神经张力增加。

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