{"title":"Antagonism of doxorubicin cardiotoxicity by carnitine is specific of the L-diasteroisomer.","authors":"F Maccari, M T Ramacci","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The therapeutic use of Doxorubicin in the treatment of human solid tumors is restricted because of its cardiotoxicity. It has been demonstrated that D,L-Carnitine reduces or suppresses some of the cardiotoxic effects produced by the antibiotic. The results of this study, carried out on rat heart Langendorff preparation show that the decrease in heart rate, coronary flow, and contractile force, occurring after Doxorubicin infusion, was antagonized by the laevo-diasteroisomer; the dextroform was totally inactive. On the contrary, both forms increased phospholipid concentration in the myocardium. This would suggest that the reparatory effect of L-Carnitine against Doxorubicin cardiotoxicity is linked to the natural role played by this substance in metabolic processes.</p>","PeriodicalId":9217,"journal":{"name":"Biomedicine / [publiee pour l'A.A.I.C.I.G.]","volume":"35 2","pages":"65-7"},"PeriodicalIF":0.0000,"publicationDate":"1981-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine / [publiee pour l'A.A.I.C.I.G.]","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The therapeutic use of Doxorubicin in the treatment of human solid tumors is restricted because of its cardiotoxicity. It has been demonstrated that D,L-Carnitine reduces or suppresses some of the cardiotoxic effects produced by the antibiotic. The results of this study, carried out on rat heart Langendorff preparation show that the decrease in heart rate, coronary flow, and contractile force, occurring after Doxorubicin infusion, was antagonized by the laevo-diasteroisomer; the dextroform was totally inactive. On the contrary, both forms increased phospholipid concentration in the myocardium. This would suggest that the reparatory effect of L-Carnitine against Doxorubicin cardiotoxicity is linked to the natural role played by this substance in metabolic processes.
阿霉素在治疗人类实体肿瘤中的应用受到限制,因为它具有心脏毒性。已经证明D, l -肉碱减少或抑制抗生素产生的一些心脏毒性作用。本研究在大鼠心脏Langendorff制剂上进行的结果表明,阿霉素输注后发生的心率、冠状动脉血流和收缩力的降低被左旋异构体拮抗;右旋葡萄糖完全没有活性。相反,两种形式均增加心肌磷脂浓度。这表明左旋肉碱对阿霉素心脏毒性的修复作用与该物质在代谢过程中所起的天然作用有关。