Center of Safety Evaluation, Zhejiang Academy of Medical Sciences, Hangzhou, Zhejiang, China.
Food Chem Toxicol. 2011 Jan;49(1):259-64. doi: 10.1016/j.fct.2010.10.028. Epub 2010 Nov 5.
The present study aims to investigate whether Lycium barbarum polysaccharides (LBP) could protect against acute doxorubicin (DOX)-induced cardiotoxicity. Rats received daily treatment of either distilled water (4 ml/kg) or LBP (200mg/kg) for 10 days and then followed by an intravenous injection at day 7 of either saline (10 ml/kg) or DOX (10 mg/kg). DOX induced significantly myocardial damage in rats, which were characterized as conduction abnormalities, decreased heart-to-body weight ratio, increased serum CK, and myofibrillar disarrangement. DOX treatment also increased MDA and decreased SOD and GSH-Px activity in cardiac tissues. Pretreatment with LBP significantly reduced DOX-induced oxidative injury in cardiac tissue, suggesting by the fact that LBP significantly attenuated DOX-induced cardiac myofibrillar disarrangement and LBP was effective in decreasing the levels of serum CK and thus improving conduction abnormalities caused by DOX. LBP treatment significantly increased SOD and GSH-Px activity and decreased the MDA level of heart tissues damaged by DOX exposure in rats. Furthermore, the cytotoxic study showed that LBP protect against cytotoxicity of DOX in cardiac myoblasts H9c2 but dose not attenuate the anti-tumor activity of DOX. In summary, our evidence indicates that LBP elicited a typical protective effect on DOX-induced acute cardiotoxicity via suppressing oxidative stress.
本研究旨在探讨枸杞多糖(LBP)是否能预防急性阿霉素(DOX)诱导的心脏毒性。大鼠每天接受蒸馏水(4 ml/kg)或 LBP(200mg/kg)治疗 10 天,然后在第 7 天分别静脉注射生理盐水(10 ml/kg)或 DOX(10 mg/kg)。DOX 诱导大鼠心肌损伤明显,表现为传导异常、心脏重量比降低、血清 CK 升高、肌原纤维排列紊乱。DOX 处理还增加了心肌组织中的 MDA 并降低了 SOD 和 GSH-Px 活性。LBP 预处理显著减轻了 DOX 诱导的心肌组织氧化损伤,这一事实表明,LBP 显著减轻了 DOX 诱导的心肌纤维排列紊乱,有效降低了血清 CK 水平,从而改善了 DOX 引起的传导异常。LBP 处理还显著增加了 SOD 和 GSH-Px 活性,降低了 DOX 暴露大鼠心脏组织中 MDA 的水平。此外,细胞毒性研究表明,LBP 可保护心肌细胞 H9c2 免受 DOX 的细胞毒性,但不能减弱 DOX 的抗肿瘤活性。综上所述,我们的证据表明,LBP 通过抑制氧化应激对 DOX 诱导的急性心脏毒性产生了典型的保护作用。