Feuerstein G Z, Hamburger S A, Smith E F, Bril A, Ruffolo R R
Department of Pharmacology, SmithKline Beecham Pharmaceuticals p.l.c., King of Prussia, Pennsylvania 19406.
J Cardiovasc Pharmacol. 1992;19 Suppl 1:S138-41. doi: 10.1097/00005344-199219001-00027.
Carvedilol is a multiple-action cardiovascular agent that is both a beta-adrenoceptor antagonist and a vasodilator and has recently been made available for the treatment of mild-to-moderate hypertension. Clinical trials are ongoing to establish the efficacy of carvedilol in angina and congestive heart failure. beta-Adrenoceptor antagonists are known to reduce myocardial work secondary to reductions in heart rate and contractility; accordingly, they have been shown to be cardioprotective in animals and in humans. Because carvedilol has beta-adrenoceptor antagonist activity, it also should provide significant cardioprotection. The additional vasodilating activity of carvedilol, which will further reduce myocardial work by decreasing afterload and myocardial wall tension, should provide more salvage of ischemic myocardium than that afforded by a pure beta-adrenoceptor antagonist, such as propranolol. We investigated the ability of carvedilol and propranolol to reduce infarct size in experimental models of acute myocardial infarction in the rat, pig, and dog. The left anterior descending coronary artery was occluded for 30 (rat) or 45 min (pig) and then reperfused for 24 h (rat) or 4 h (pig). In the dog, the left circumflex coronary artery was occluded for 60 min and reperfused for 24 h. Vehicle, carvedilol, or propranolol was administered intravenously 15 min before ischemia (and, in the rat only, repeated 4 h after ischemia). An additional group of dogs was subjected to permanent left anterior descending coronary artery occlusion for 6 h, and carvedilol or propranolol was given 15 min after occlusion. Infarct size was examined on stained tissue sections using quantitative image analysis.(ABSTRACT TRUNCATED AT 250 WORDS)
卡维地洛是一种具有多种作用的心血管药物,它既是β肾上腺素能受体拮抗剂,又是血管扩张剂,最近已被用于治疗轻至中度高血压。目前正在进行临床试验以确定卡维地洛在心绞痛和充血性心力衰竭中的疗效。已知β肾上腺素能受体拮抗剂可通过降低心率和心肌收缩力来减少心肌做功;因此,它们已被证明在动物和人类中具有心脏保护作用。由于卡维地洛具有β肾上腺素能受体拮抗剂活性,它也应能提供显著的心脏保护作用。卡维地洛的额外血管扩张活性,通过降低后负荷和心肌壁张力进一步减少心肌做功,应该比单纯的β肾上腺素能受体拮抗剂如普萘洛尔提供更多的缺血心肌挽救。我们在大鼠、猪和狗的急性心肌梗死实验模型中研究了卡维地洛和普萘洛尔减少梗死面积的能力。左前降支冠状动脉闭塞30分钟(大鼠)或45分钟(猪),然后再灌注24小时(大鼠)或4小时(猪)。在狗中,左旋冠状动脉闭塞60分钟并再灌注24小时。在缺血前15分钟静脉注射溶媒、卡维地洛或普萘洛尔(仅在大鼠中,缺血后4小时重复给药)。另一组狗接受左前降支冠状动脉永久性闭塞6小时,并在闭塞后15分钟给予卡维地洛或普萘洛尔。使用定量图像分析在染色组织切片上检查梗死面积。(摘要截短至250字)