Kurihara J, Tamaoki S, Kato H
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Eur J Pharmacol. 1993 Aug 10;240(1):73-6. doi: 10.1016/0014-2999(93)90547-u.
Ifenprodil, phentolamine, yohimbine or idazoxan, 1 mg/kg i.v., administered 5 min prior to 5-min global cerebral ischemia, completely prevented the post-ischemic dysfunction of the vagal baroreflex in anesthetized dogs. Idazoxan, 0.1 mg/kg i.v., was cerebroprotective against mild ischemia, but ineffective against severe ischemia. The post-ischemic administration of idazoxan, 1 mg/kg i.v., failed to restore the damaged vagal baroreflex. These results suggest that blockade of alpha 2-adrenoceptors during ischemia and the early reperfusion period may protect the vagal component of baroreflex from cerebral ischemia.
在给麻醉犬造成5分钟全脑缺血前5分钟静脉注射1毫克/千克的艾芬地尔、酚妥拉明、育亨宾或咪唑克生,可完全预防缺血后迷走神经压力反射功能障碍。静脉注射0.1毫克/千克的咪唑克生对轻度缺血具有脑保护作用,但对重度缺血无效。静脉注射1毫克/千克的咪唑克生在缺血后给药未能恢复受损的迷走神经压力反射。这些结果表明,在缺血和早期再灌注期间阻断α2 -肾上腺素能受体可能保护压力反射的迷走神经成分免受脑缺血的影响。