Ciplea A G, Kretzschmar R, Heimann W, Kirchengast M, Safer A
Gerhard-Domagk-Institute of Pathology, University of Münster, Münster/Westf., Fed. Rep. of Germany.
Arzneimittelforschung. 1988 Feb;38(2):215-21.
The new calcium antagonist anipamil (1,7-bis-(3-methoxyphenyl)-3-methylaza-7-cyano-nonadecane) exhibited a pronounced protective effect against isoprenaline-induced myocardial necrosis in rats. Anipamil was administered in single doses of 10 or 20 mg/kg daily for 4 days. 30 mg/kg isoprenaline was given by subcutaneous injection on the 3rd and 4th days of the study. The protective effect of anipamil was assessed by histological investigations, and its effect on the activity of the enzymes succinate dehydrogenase, NADH-NBT reductase, acid phosphatase and glucose-6-phosphate dehydrogenase in experimentally-induced myocardial damage was assessed quantitatively by microphotometry. The protective effect of anipamil against isoprenaline-induced myocardial necrosis was definitely dose-dependent: 10 mg/kg anipamil exhibited a partial protective effect, whilst 20 mg/kg anipamil protected the heart completely.
新型钙拮抗剂阿尼帕米(1,7-双-(3-甲氧基苯基)-3-甲基氮杂-7-氰基十九烷)对异丙肾上腺素诱导的大鼠心肌坏死具有显著的保护作用。阿尼帕米每日以10或20mg/kg的单剂量给药,持续4天。在研究的第3天和第4天,通过皮下注射给予30mg/kg异丙肾上腺素。通过组织学研究评估阿尼帕米的保护作用,并通过显微光度法对其在实验性诱导的心肌损伤中对琥珀酸脱氢酶、NADH-NBT还原酶、酸性磷酸酶和葡萄糖-6-磷酸脱氢酶活性的影响进行定量评估。阿尼帕米对异丙肾上腺素诱导的心肌坏死的保护作用具有明确的剂量依赖性:10mg/kg阿尼帕米表现出部分保护作用,而20mg/kg阿尼帕米则完全保护心脏。