Attenuation effect of Abnormal Savda Munziq on liver and heart toxicity caused by chemotherapy in mice

被引:17
作者
Aikemu, Ainiwaer [1 ]
Amat, Nurmuhamat [2 ]
Yusup, Abdiryim [2 ]
Shan, Lianlian [1 ]
Qi, Xinwei [3 ]
Upur, Halmurat [2 ]
机构
[1] Xinjiang Med Univ, Fac Pharm, Dept Drug Anal, 393 Xinyi Rd, Urumqi 830011, Xinjiang, Peoples R China
[2] Xinjiang Med Univ, Fac Tradit Uighur Med, 393 Xinyi Rd, Urumqi 830011, Xinjiang, Peoples R China
[3] Xinjiang Med Univ, Affiliated Hosp 1, Med Res Ctr, 393 Xinyi Rd, Urumqi 830011, Xinjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
abnormal Savda Munziq; chemotherapy; anthraquinone; toxicity; antioxidant effect; DOXORUBICIN-INDUCED CARDIOMYOPATHY; METASTATIC BREAST-CANCER; CELL LUNG-CANCER; LIPID-PEROXIDATION; ENZYME-ACTIVITIES; OXIDATIVE STRESS; RATS; 5-FLUOROURACIL; ADRIAMYCIN; CARDIOTOXICITY;
D O I
10.3892/etm.2016.3328
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Abnormal Savda Munziq (ASMq), an Uighur medicine formula commonly used in the treatment of cancer, has been speculated to possess antioxidative and antiproliferative effects, and to regulate immune activity. The present study was designed to systematically elucidate the toxicity-reducing activity of ASMq in mice undergoing combination chemotherapy with doxorubicin and 5-fluorouracil (5-FU). The mice were divided into normal (saline, 10 ml/kg) and doxorubicin + 5-FU groups (doxorubicin, 2.5 mg/kg; 5-FU, 10 mg/kg on alternate days). In addition, three groups received different doses of ASMq (2, 4 and 8 g/kg), in addition to doxorubicin (2.5 zmg/kg) and 5-FU (10 mg/kg) treatment on alternate days. The histology of the heart and liver, superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) activity, malondialdehyde (MDA) concentrations in heart homogenate, and various biochemical parameters of the liver were evaluated. Compared with the normal control group, ASMq dose-dependently improved a number of variables, including body weight, liver index, transaminase and total protein, and partially normalized liver and cardiac pathology. ASMq restored activities of defense antioxidant enzymes SOD and GSH-Px towards normal levels, and decreased MDA concentration in dose-dependent manner. These results demonstrated that ASMq provides significant protection against doxorubicin + 5-FU combination induced hepatotoxicity and cardiotoxicity. Further studies are required to determine the effects of ASMq against doxorubicin + 5-FU-induced toxicity during chemotherapy in vivo.
引用
收藏
页码:384 / 390
页数:7
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