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单剂量及重复剂量的血管舒张剂/β-肾上腺素能拮抗剂卡维地洛可阻断在清醒大鼠中可乐唑啉和异丙肾上腺素介导的血流动力学反应。

Single and repeated doses of the vasodilator/beta-adrenergic antagonist, carvedilol, block cirazoline- and isoproterenol-mediated hemodynamic responses in the conscious rat.

作者信息

Smith E F, Slivjak M J, Gagnon R

机构信息

SmithKline Beecham Pharmaceuticals, Department of Pharmacology, King of Prussia, PA 19406.

出版信息

Cardiovasc Drugs Ther. 1992 Oct;6(5):499-504. doi: 10.1007/BF00055608.

Abstract

The purpose of this study was to evaluate the effects of carvedilol, a beta 1&2-adrenergic blocker and vasodilator, on cirazoline-mediated changes in arterial blood pressure and isoproterenol-mediated changes in heart rate after acute and chronic administration. Conscious, chronically instrumented male Sprague-Dawley rats were injected with carvedilol (1 mg/kg, IV), prazosin (0.3 mg/kg, IV), or propranolol (1 mg/kg, twice daily for 8 days. After administration of the first dose of carvedilol on day 1, the vasopressor response to cirazoline (60 +/- 3 mmHg predrug) and the isoproterenol-induced tachycardia (152 +/- 13 beats/min predrug) were blocked (e.g., 7 +/- 4 mmHg postdrug and 11 +/- 3 beats/min postdrug, respectively). After the administration of carvedilol on day 8, the cirazoline vasopressor response was 2 +/- 1 mmHg and the isoproterenol-induced tachycardia was 4 +/- 3 beats/min, indicating effective alpha 1- and beta-adrenergic blockade after chronic dosing with carvedilol. Prazosin blocked the cirazoline-induced vasopressor response on both days 1 and 8 but had no effect on the isoproterenol-induced tachycardia. Propranolol blocked the isoproterenol-induced tachycardia on both days 1 and 8 but had no effect on the cirazoline vasopressor response. These data indicate that only carvedilol effectively blocked both alpha- and beta-adrenergic hemodynamic responses and that the antagonism of these responses with carvedilol was not diminished after chronic dosing of twice-a-day treatment for 8 days.

摘要

本研究的目的是评估卡维地洛(一种β1&2肾上腺素能阻滞剂和血管扩张剂)在急性和慢性给药后对西拉唑啉介导的动脉血压变化以及异丙肾上腺素介导的心率变化的影响。对有意识的、长期植入仪器的雄性Sprague-Dawley大鼠注射卡维地洛(1mg/kg,静脉注射)、哌唑嗪(0.3mg/kg,静脉注射)或普萘洛尔(1mg/kg,每日两次,共8天)。在第1天给予第一剂卡维地洛后,对西拉唑啉的升压反应(给药前60±3mmHg)和异丙肾上腺素诱导的心动过速(给药前152±13次/分钟)被阻断(例如,给药后分别为7±4mmHg和11±3次/分钟)。在第8天给予卡维地洛后,西拉唑啉升压反应为2±1mmHg,异丙肾上腺素诱导的心动过速为4±3次/分钟,表明卡维地洛长期给药后α1和β肾上腺素能阻滞有效。哌唑嗪在第1天和第8天都阻断了西拉唑啉诱导的升压反应,但对异丙肾上腺素诱导的心动过速没有影响。普萘洛尔在第1天和第8天都阻断了异丙肾上腺素诱导的心动过速,但对西拉唑啉升压反应没有影响。这些数据表明,只有卡维地洛能有效阻断α和β肾上腺素能血流动力学反应,并且在每天两次治疗8天的长期给药后,卡维地洛对这些反应的拮抗作用并未减弱。

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