Christopher T A, Lopez B L, Yue T L, Feuerstein G Z, Ruffolo R R, Ma X L
Division of Emergency Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
J Pharmacol Exp Ther. 1995 Apr;273(1):64-71.
Splanchnic artery occlusion (SAO) followed by reperfusion results in circulatory shock in which oxygen-derived free radicals play an important role. Carvedilol, a novel beta adrenoceptor antagonist and a vasodilator, has been recently shown to exert potent antioxidant effects in multiple cell model systems. In the present experiment, we investigated the effect of carvedilol on SAO shock. Pentobarbital-anesthetized rats were subjected to 60 min of SAO followed by 120 min of reperfusion. Administration of 1 mg/kg carvedilol 10 min before reperfusion prolonged survival time (P < .05) and attenuated the increases in tissue myeloperoxidase activities (P < .01) and hematocrits (P < .001). Moreover, carvedilol significantly preserved superior mesenteric artery endothelial function (P < .01). Similar protection was seen in SAO shock rats treated with the superoxide free-radical scavenger superoxide dismutase. Except for a moderate attenuation of an increase in hematocrits, protective effects were not seen in SAO shock rats treated with the prototypic beta blocker propranolol. These results indicate that in murine SAO shock, carvedilol affords significant protection, which may be achieved through maintenance of tissue blood perfusion, quenching of oxygen free radicals, preservation of vascular endothelial function, and inhibition of neutrophil-endothelial interaction and its resultant increased microvascular permeability.
内脏动脉闭塞(SAO)后再灌注会导致循环性休克,其中氧衍生的自由基起重要作用。卡维地洛是一种新型β肾上腺素能受体拮抗剂和血管扩张剂,最近已证明在多种细胞模型系统中具有强大的抗氧化作用。在本实验中,我们研究了卡维地洛对SAO休克的影响。用戊巴比妥麻醉的大鼠接受60分钟的SAO,然后再灌注120分钟。在再灌注前10分钟给予1mg/kg卡维地洛可延长存活时间(P <.05),并减弱组织髓过氧化物酶活性(P <.01)和血细胞比容的升高(P <.001)。此外,卡维地洛显著保留了肠系膜上动脉内皮功能(P <.01)。在用超氧化物自由基清除剂超氧化物歧化酶治疗的SAO休克大鼠中也观察到类似的保护作用。除了血细胞比容升高的适度减弱外,在用原型β受体阻滞剂普萘洛尔治疗的SAO休克大鼠中未观察到保护作用。这些结果表明,在小鼠SAO休克中,卡维地洛提供了显著的保护作用,这可能是通过维持组织血液灌注、淬灭氧自由基、保留血管内皮功能以及抑制中性粒细胞与内皮细胞的相互作用及其导致的微血管通透性增加来实现的。