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普罗布考可促进内源性抗氧化剂生成,并对阿霉素诱导的大鼠心肌病具有保护作用。

Probucol promotes endogenous antioxidants and provides protection against adriamycin-induced cardiomyopathy in rats.

作者信息

Siveski-Iliskovic N, Kaul N, Singal P K

机构信息

Division of Cardiovascular Sciences, St Boniface General Hospital Research Centre, Winnipeg, Manitoba, Canada.

出版信息

Circulation. 1994 Jun;89(6):2829-35. doi: 10.1161/01.cir.89.6.2829.

Abstract

BACKGROUND

The potential usefulness of adriamycin (ADR) is restricted because of its cardiotoxic side effects. Since free radicals and lipid peroxidation are suggested to be involved in ADR cardiomyopathy, we examined the beneficial effects of probucol, a lipid-lowering drug with strong antioxidant properties.

METHODS AND RESULTS

ADR was administered to rats in six equal intraperitoneal injections over a period of 2 weeks (cumulative dose of 15 mg/kg). After a 3-week posttreatment period, cardiomyopathy and congestive heart failure were characterized by ascites, congested liver, depressed cardiac function, elevated left ventricular end-diastolic pressure, and myocardial cell damage. Myocardial glutathione peroxidase (GSHPx) activity was decreased, and lipid peroxidation was increased. Probucol (cumulative dose, 60 mg/kg IP) was administered in six equal injections over a 2-week period on days alternating with ADR treatment. Probucol significantly attenuated the myocardial effects of ADR, improved left ventricular function, and lowered mortality as well as the amount of ascites. Treatment with probucol was also accompanied by an increase in myocardial GSHPx and superoxide dismutase activities, with a concomitant decrease in lipid peroxidation.

CONCLUSIONS

These data provide evidence that ADR cardiomyopathy is associated with an antioxidant deficit. Improved cardiac function resulting from treatment with probucol may be related to the maintenance of the antioxidant status of the heart. The study suggests potential usefulness of antioxidant (probucol) therapy in ADR cardiomyopathy.

摘要

背景

阿霉素(ADR)的潜在效用因其心脏毒性副作用而受到限制。由于自由基和脂质过氧化被认为与阿霉素诱导的心肌病有关,我们研究了普罗布考(一种具有强大抗氧化特性的降脂药物)的有益作用。

方法与结果

在2周内给大鼠腹腔注射6次等量的阿霉素(累积剂量为15mg/kg)。在3周的治疗后期,心肌病和充血性心力衰竭表现为腹水、肝脏充血、心功能降低、左心室舒张末期压力升高以及心肌细胞损伤。心肌谷胱甘肽过氧化物酶(GSHPx)活性降低,脂质过氧化增加。在与阿霉素治疗交替的日子里,在2周内分6次等量注射普罗布考(累积剂量,60mg/kg腹腔注射)。普罗布考显著减轻了阿霉素对心肌的影响,改善了左心室功能,降低了死亡率以及腹水量。普罗布考治疗还伴随着心肌GSHPx和超氧化物歧化酶活性的增加,同时脂质过氧化减少。

结论

这些数据证明阿霉素诱导的心肌病与抗氧化剂缺乏有关。普罗布考治疗导致的心功能改善可能与维持心脏的抗氧化状态有关。该研究表明抗氧化剂(普罗布考)疗法在阿霉素诱导的心肌病中具有潜在效用。

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