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牛磺酸对异丙肾上腺素诱导的心肌损伤的保护作用机制。

Mechanism of the protective action of taurine against isoprenaline induced myocardial damage.

作者信息

Ohta H, Azuma J, Awata N, Hamaguchi T, Tanaka Y, Sawamura A, Kishimoto S, Sperelakis N

机构信息

Third Department of Internal Medicine, Osaka University Medical School, Japan.

出版信息

Cardiovasc Res. 1988 Jun;22(6):407-13. doi: 10.1093/cvr/22.6.407.

Abstract

The effect of the sulphur amino acid, taurine, on the biochemical changes induced by a toxic dose of isoprenaline was examined in chick hearts. Isoprenaline treatment (80 and 240 mg.kg-1 subcutaneously twice a day for four days) caused a dose dependent increase in heart to body weight ratio. Isoprenaline administration induced a substantial accumulation of calcium and caused a profound decrease of adenosine triphosphate content and creatine phosphokinase activity in the myocardium. A pronounced increase in lipoperoxide and decrease in phospholipid and reduced glutathione concentrations were also seen. Oral administration of taurine (200 mg.kg-1 for seven days) partially protected against these changes induced by isoprenaline. It is suggested that the beneficial effect of taurine may be due in part to inhibition of lipoperoxide formation and calcium accumulation and to protection against the deterioration of membrane phospholipids.

摘要

在鸡心脏中研究了含硫氨基酸牛磺酸对中毒剂量异丙肾上腺素诱导的生化变化的影响。异丙肾上腺素处理(每天皮下注射80和240mg·kg-1,共四天)导致心脏与体重比呈剂量依赖性增加。给予异丙肾上腺素会导致钙大量蓄积,并使心肌中三磷酸腺苷含量和肌酸磷酸激酶活性显著降低。还观察到脂质过氧化物明显增加,磷脂和还原型谷胱甘肽浓度降低。口服牛磺酸(200mg·kg-1,共七天)可部分预防异丙肾上腺素诱导的这些变化。提示牛磺酸的有益作用可能部分归因于抑制脂质过氧化物形成和钙蓄积,以及保护膜磷脂免于降解。

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