Izumi N, Yasuda H
Nihon Yakurigaku Zasshi. 1985 Oct;86(4):323-8. doi: 10.1254/fpj.86.323.
The anti-anoxic effect of sufoxazine was investigated in various cerebral anoxia models with mice, in comparison with those of various cerebroactive drugs. Sufoxazine reduced dose-dependently the duration of coma induced by a sublethal dose of KCN (1.8 mg/kg, i.v.), significantly stimulating recovery from the coma at 5 mg/kg, i.p. and 30 mg/kg, p.o. It also protected against a lethal dose of KCN (2.5 mg/kg, i.v.). Sufoxazine prolonged the survival time of mice subjected to hypobaric and normobaric hypoxia. Dihydroergotoxin and ifenprodil gave similar protection in the KCN-induced anoxia models, but produced adverse effects in the hypoxia models. Calcium hopantenate exerted similar but weak protection only at a dose as high as 300 mg/kg, i.p. These findings suggest that sufoxazine has an anti-anoxic action superior to those of the other cerebroactive drugs used.
与多种脑活性药物相比,在多种小鼠脑缺氧模型中研究了舒伏沙嗪的抗缺氧作用。舒伏沙嗪能剂量依赖性地缩短由亚致死剂量的氰化钾(1.8毫克/千克,静脉注射)诱导的昏迷持续时间,腹腔注射5毫克/千克和口服30毫克/千克时能显著促进昏迷苏醒。它还能保护小鼠免受致死剂量氰化钾(2.5毫克/千克,静脉注射)的影响。舒伏沙嗪可延长低压和常压缺氧小鼠的存活时间。双氢麦角毒碱和艾芬地尔在氰化钾诱导的缺氧模型中具有类似的保护作用,但在缺氧模型中产生了不良反应。泛酸钙仅在腹腔注射高达300毫克/千克的剂量时才具有类似但较弱的保护作用。这些发现表明,舒伏沙嗪具有优于其他所用脑活性药物的抗缺氧作用。