Iliskovic N, Singal P K
Institute of Cardiovascular Sciences, St. Boniface General Hospital Research Centre, Winnipeg, Canada.
Am J Pathol. 1997 Feb;150(2):727-34.
The contribution of lipid lowering in protection against adriamycin cardiomyopathy achieved by probucol, an antioxidant and a lipid-lowering drug, was assessed by comparing its beneficial effects with that of lovastatin, another lipid-lowering drug with no known antioxidant properties. Adriamycin (cumulative dose, 15 mg/kg body weight) was given to rats in 6 equal injections (intraperitoneally) over a period of 2 weeks. Probucol (cumulative dose, 120 mg/kg body weight) or lovastatin (cumulative dose, 48 mg/kg body weight) was given in 12 equal injections (intraperitoneally) before and concurrent with adriamycin. After 3 weeks of post-treatment with adriamycin, congestive heart failure, ascites, congested liver, and depressed cardiac function were seen. Adriamycin treatment decreased glutathione peroxidase activity and increased lipid peroxidation. Adriamycin increased plasma triglycerides, total cholesterol, and high- and low-density lipoproteins. Myocardial triglycerides and total cholesterol were also increased. Probucol completely prevented the development of congestive heart failure and normalized myocardial and plasma triglycerides and total cholesterol, and significantly decreased plasma high- and low-density lipoproteins. Lovastatin significantly attenuated but did not completely prevent cardiomyopathic changes due to adriamycin. Lovastatin decreased plasma total cholesterol and low-density lipoproteins as well as myocardial triglycerides and total cholesterol. Plasma triglycerides and high-density lipoproteins were still high in the adriamycin plus lovastatin group. Probucol improved glutathione peroxidase activity and reduced lipid peroxidation whereas lovastatin had no effect on these adriamycin-induced changes. These data suggest that adriamycin cardiomyopathy is associated with an antioxidant deficit as well as increased myocardial and plasma lipids. Complete protection by probucol against adriamycin-induced congestive heart failure may be due to the unique combination of its antioxidant and lipid-lowering properties.
通过比较抗氧化降脂药物普罗布考与另一种无已知抗氧化特性的降脂药物洛伐他汀的有益作用,评估了普罗布考降低脂质在预防阿霉素诱导的心肌病中的作用。在2周内给大鼠腹腔注射6次等量阿霉素(累积剂量为15mg/kg体重)。在阿霉素给药前及给药期间,给大鼠腹腔注射12次等量的普罗布考(累积剂量为120mg/kg体重)或洛伐他汀(累积剂量为48mg/kg体重)。阿霉素治疗3周后,出现充血性心力衰竭、腹水、肝脏充血和心功能降低。阿霉素治疗降低了谷胱甘肽过氧化物酶活性,增加了脂质过氧化。阿霉素使血浆甘油三酯、总胆固醇以及高密度和低密度脂蛋白升高。心肌甘油三酯和总胆固醇也升高。普罗布考完全预防了充血性心力衰竭的发生,使心肌和血浆甘油三酯及总胆固醇恢复正常,并显著降低了血浆高密度和低密度脂蛋白。洛伐他汀显著减轻但未完全预防阿霉素引起的心肌病改变。洛伐他汀降低了血浆总胆固醇和低密度脂蛋白以及心肌甘油三酯和总胆固醇。在阿霉素加洛伐他汀组中,血浆甘油三酯和高密度脂蛋白仍然升高。普罗布考提高了谷胱甘肽过氧化物酶活性并减少了脂质过氧化,而洛伐他汀对这些阿霉素诱导的变化没有影响。这些数据表明,阿霉素心肌病与抗氧化剂缺乏以及心肌和血浆脂质增加有关。普罗布考对阿霉素诱导的充血性心力衰竭的完全保护作用可能归因于其抗氧化和降脂特性的独特组合。