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塞利洛尔和阿替洛尔对清醒犬静息及运动时大的心外膜冠状动脉的不同作用。

Differential effects of celiprolol and atenolol on large epicardial coronary arteries in conscious dogs at rest and during exercise.

作者信息

Drieu la Rochelle C, Giudicelli J F, Berdeaux A

机构信息

Département de Pharmacologie, Faculté de Médecine Paris-Sud, Le Kremlin-Bicêtre, France.

出版信息

J Cardiovasc Pharmacol. 1993 Jul;22(1):15-21. doi: 10.1097/00005344-199307000-00003.

Abstract

The effects of celiprolol (1 mg/kg), a selective beta 1-adrenoceptor antagonist with partial agonist activity (PAA), on large and small coronary arteries and on systemic hemodynamics were investigated and compared with those of atenolol (1 mg/kg) and saline at rest and during three levels of treadmill exercise in the same 7 conscious dogs. Control exercise after saline administration induced increases in heart rate (HR 131 +/- 4%), left ventricular (LVdP/dt 117 +/- 5%), coronary blood flow (CBF 133 +/- 13%), and circumflex artery diameter (CxAD, 6.6 +/- 1.3%) and a decrease in coronary vascular resistance (CVR, -47 +/- 3%). Atenolol decreased LVdP/dt (-19 +/- 2%) and CxAD (-3.2 +/- 0.3%, p < 0.05) at rest, but large epicardial coronary arteries remained constricted during exercise (-4.7 +/- 1.4% at 12 km/h, p < 0.05) despite simultaneous dilation of coronary resistance vessels. In contrast to atenolol, celiprolol did not constrict large coronary arteries at rest (CxAD -0.2 +/- 0.9%, NS), and this beneficial effect of celiprolol was maintained throughout the exercise period. LVdP/dt was not modified and HR was slightly increased (14.3 +/- 2.6%) at rest by celiprolol. Atenolol and celiprolol reduced the exercise-induced positive inotropic and chronotropic effects, atenolol being the most potent. Thus, in dogs at rest when basal sympathetic tone was low, celiprolol, most likely because of its PAA, induced slight cardiac stimulation and prevented vasoconstriction of the large coronary arteries usually observed after beta-adrenoceptor blockade.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了具有部分激动活性(PAA)的选择性β1肾上腺素能受体拮抗剂塞利洛尔(1毫克/千克)对大、小冠状动脉及全身血流动力学的影响,并在7只清醒犬休息时及三个跑步机运动水平下,将其与阿替洛尔(1毫克/千克)和生理盐水的作用进行比较。生理盐水给药后的对照运动使心率(HR升高131±4%)、左心室(LVdP/dt升高117±5%)、冠状动脉血流量(CBF升高133±13%)、回旋动脉直径(CxAD,增大6.6±1.3%)增加,冠状动脉血管阻力(CVR,降低47±3%)降低。阿替洛尔在休息时降低LVdP/dt(-19±2%)和CxAD(-3.2±0.3%,p<0.05),但尽管冠状动脉阻力血管同时扩张,大的心外膜冠状动脉在运动时仍收缩(12千米/小时时为-4.7±1.4%,p<0.05)。与阿替洛尔不同,塞利洛尔在休息时不收缩大冠状动脉(CxAD -0.2±0.9%,无显著性差异),且在整个运动期间这种有益作用得以维持。塞利洛尔在休息时不改变LVdP/dt,使HR略有升高(14.3±2.6%)。阿替洛尔和塞利洛尔均降低运动诱导的正性肌力和变时作用,阿替洛尔作用最强。因此,在休息时基础交感神经张力较低的犬中,塞利洛尔很可能因其部分激动活性,引起轻微的心脏刺激,并防止通常在β肾上腺素能受体阻断后出现的大冠状动脉血管收缩。(摘要截取自250字)

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