Department of Biochemistry & Biotechnology, Faculty of Science, Annamalai University, Tamil Nadu, India.
Basic Clin Pharmacol Toxicol. 2010 Oct;107(4):818-24. doi: 10.1111/j.1742-7843.2010.00579.x.
Our aim was to evaluate the protective effect of berberine on 7,12-dimethylbenz[a]anthracene (DMBA)-induced chromosomal aberrations and micro-nucleated polychromatic erythrocytes (MnPCEs) frequency in bone marrow cells of golden Syrian hamsters. The anti-clastogenic effect of berberine (50 mg/kg b.w. p.o.) was also assessed by measuring the status of phase II detoxification enzymes and oxidative stress, as biochemical endpoints, during DMBA (30 mg/kg b.w. i.p.) induced clastogenesis. Marked chromosomal aberrations, increased MnPCEs frequency and enhanced status of lipid peroxidation, antioxidants and phase I and II detoxification enzymes were noticed in hamsters treated with DMBA alone. Oral pre-treatment with berberine for 5 days to DMBA-treated hamsters significantly reduced the frequency of MnPCEs and chromosomal abnormalities as well as reversed the status of lipid peroxidation, antioxidants and phase I and II detoxification enzymes. The present study thus suggests that berberine has potent anti-clastogenic potential against DMBA-induced clastogenesis, which is probably due to its anti-lipid peroxidative potential and effect on modulation of phase I and II detoxification cascade.
我们的目的是评估小檗碱对 7,12-二甲基苯并[a]蒽(DMBA)诱导的金黄地鼠骨髓细胞染色体畸变和微核多染红细胞(MnPCE)频率的保护作用。还通过测量 DMBA(30mg/kg bw,ip)诱导的断裂剂的 II 期解毒酶和氧化应激状态,评估小檗碱(50mg/kg bw,po)的抗断裂剂作用。单独用 DMBA 处理的金黄地鼠出现明显的染色体畸变、MnPCE 频率增加和脂质过氧化、抗氧化剂以及 I 期和 II 期解毒酶的状态增强。用小檗碱对 DMBA 处理的金黄地鼠进行 5 天的口服预处理,可显著降低 MnPCE 和染色体异常的频率,并逆转脂质过氧化、抗氧化剂和 I 期和 II 期解毒酶的状态。因此,本研究表明,小檗碱对 DMBA 诱导的断裂剂具有很强的抗断裂作用,这可能是由于其抗脂质过氧化作用和对 I 期和 II 期解毒酶级联的调节作用。