Arafa Manar Hamed, Mohammad Nanies Sameeh, Atteia Hebatallah Husseini, Abd-Elaziz Hesham Radwan
Department of Forensic Medicine and Clinical Toxicology, Faculty of Medicine, Zagazig University, Zagazig, Sharkia Gov, Egypt,
J Physiol Biochem. 2014 Sep;70(3):701-11. doi: 10.1007/s13105-014-0339-y. Epub 2014 Jun 18.
The possible effectiveness of resveratrol, a polyphenol present in different plants comprising berries, grapes and peanuts, on the prevention of doxorubicin-induced cardiac toxicity and fibrosis was investigated. Forty adult male Wistar albino rats were divided into four groups. Group I received normal saline, group II gavaged with resveratrol (20 mg/kg, daily for 4 weeks), group III received doxorubicin (2.5 mg/kg i.p. in six injections for 2 weeks; accumulative dose of 15 mg/kg), and group IV received doxorubicin + resveratrol (starting resveratrol intake 2 weeks before doxorubicin administration). Resveratrol significantly alleviated the increase in left ventricular lipid peroxidation, hydroxyproline, and tumor necrosis factor alpha levels as well as serum creatine kinase-myocardial band (CK-MB) activity and prevented the decrease in body and heart weights in doxorubicin-treated group. However, a marked protection against reduced glutathione content depletion and superoxide dismutase activity reduction was observed in the left ventricles of rats pretreated with resveratrol in combination with doxorubicin. Resveratrol also ameliorated the up-regulation of left ventricular caspase-3 and transforming growth factor-beta1 gene expression as well as left ventricular histopathological changes including necrosis and fibrosis induced by doxorubicin. Collectively, our results suggest that resveratrol provides a significant protection against doxorubicin-induced cardiotoxicity and fibrosis in rats. Therefore, it may be used as a promising cardioprotective agent in patients treated with doxorubicin due to malignant diseases. So, further clinical trials are required to confirm these findings.
白藜芦醇是一种存在于包括浆果、葡萄和花生在内的不同植物中的多酚,研究了其对预防阿霉素诱导的心脏毒性和纤维化的可能效果。40只成年雄性Wistar白化大鼠被分为四组。第一组接受生理盐水,第二组灌胃白藜芦醇(20毫克/千克,每日一次,共4周),第三组接受阿霉素(腹腔注射2.5毫克/千克,分6次注射,共2周;累积剂量为15毫克/千克),第四组接受阿霉素+白藜芦醇(在阿霉素给药前2周开始摄入白藜芦醇)。白藜芦醇显著减轻了阿霉素治疗组左心室脂质过氧化、羟脯氨酸和肿瘤坏死因子α水平的升高以及血清肌酸激酶同工酶(CK-MB)活性,并防止了体重和心脏重量的下降。然而,在联合阿霉素预处理的大鼠左心室中,观察到对白藜芦醇显著保护了谷胱甘肽含量的消耗和超氧化物歧化酶活性的降低。白藜芦醇还改善了左心室半胱天冬酶-3和转化生长因子-β1基因表达的上调以及阿霉素诱导的左心室组织病理学变化,包括坏死和纤维化。总体而言,我们的结果表明,白藜芦醇对阿霉素诱导的大鼠心脏毒性和纤维化具有显著的保护作用。因此,它可能作为一种有前景的心脏保护剂用于因恶性疾病接受阿霉素治疗的患者。所以,需要进一步的临床试验来证实这些发现。