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阿拉伯胶对阿霉素诱导的小鼠心脏毒性的保护作用:一种可能的保护机制。

Protective effect of arabic gum against cardiotoxicity induced by doxorubicin in mice: a possible mechanism of protection.

作者信息

Abd-Allah Adel R A, Al-Majed Abdulhakeem A, Mostafa Adel M, Al-Shabanah Othman A, Din Ayman Gamal E l, Nagi Mahmoud N

机构信息

Department of Pharmacology, College of Pharmacy, King Saud University, P O Box 2457, Riyadh 11451, Saudi Arabia.

出版信息

J Biochem Mol Toxicol. 2002;16(5):254-9. doi: 10.1002/jbt.10046.

Abstract

Arabic gum (AG) is a naturally occurring compound that has been proposed to possess potent antioxidant activity. In this study, the possible effects whereby AG could protect against cardiotoxicity induced by doxorubicin (DOX) in mice were carried out. Administration of single dose of DOX (15 mg/kg, i.p.) induced cardiotoxicity 72 h, manifested biochemically by a significant elevation of serum creatine kinase (CK) (EC 2.7.3.2). In addition, cardiotoxicity was further confirmed by the significant increase in lipid peroxides measured as malondialdehyde (MDA). Administration of AG (25 g/kg) orally for 5 days before and 72 h after DOX injection produced a significant protection against cardiotoxicity induced by DOX. This was evidenced by significant reductions in serum CK and cardiac lipid peroxides. The effect of AG was examined on the superoxide anion radical generated by enzymatic and nonenzymatic methods. The results indicate that AG is a potent superoxide scavenger. The superoxide scavenging effect of AG may explain, at least in part, the protective effect of AG against cardiotoxicity induced by DOX.

摘要

阿拉伯胶(AG)是一种天然存在的化合物,有人提出它具有强大的抗氧化活性。在本研究中,开展了关于AG对小鼠阿霉素(DOX)诱导的心脏毒性可能具有的保护作用的研究。单次注射DOX(15毫克/千克,腹腔注射)72小时后诱导产生心脏毒性,生化表现为血清肌酸激酶(CK)(EC 2.7.3.2)显著升高。此外,以丙二醛(MDA)衡量的脂质过氧化物显著增加进一步证实了心脏毒性。在DOX注射前5天及注射后72小时口服AG(25克/千克)对DOX诱导的心脏毒性产生了显著的保护作用。血清CK和心脏脂质过氧化物显著降低证明了这一点。通过酶法和非酶法检测了AG对超氧阴离子自由基的影响。结果表明AG是一种有效的超氧阴离子清除剂。AG的超氧阴离子清除作用至少可以部分解释其对DOX诱导的心脏毒性的保护作用。

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