Shuai Yi, Guo Jun, Peng Shuang-qing, Zhang Li-shi
Beijing Institute of Pharmacology and Toxicology, National Beijing Center for Drug Safety Evaluation and Research, Beijing 100850, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2007 Jul;38(4):620-3.
To investigate the inhibitive effect of metallothionein (MT) on DOX-induced cardiac apoptosis and the involved possible mechanisms.
Adult male C57BL mice (6-8 weeks old) were randomly assigned into four groups and given the following treatment: Zinc (ZnSO4, 300 micromol/kg, s.c., once a day for 2 days) or equal volume of physiological saline prior to a single dose of DOX (15 mg/kg, i.p.) or equal volume of saline. Animals were sacrificed on the 4th day after DOX administration and hearts were excised for further studies, including cadmium-hemoglobin affinity assay for MT concentration, ELISA detection of DNA fragmentation and Western blot analysis of Bax and Bcl-2.
DOX administration decreased heart weight by 10% and caused remarkable cardiac apoptosis as demonstrated by DNA fragments, while Zinc pretreatment significantly increased the MT levels and therefore inhibited the cardiac apoptotic effect of DOX. Elevated expression of Bax was obviously observed after DOX treatment, while this elevation was prevented by MT induction by Zinc. On the contrary, Bcl-2 protein level was not altered significantly among each group.
These findings suggest that metallothionein induced by Zinc exhibits protective effects on the cardiac apoptosis of DOX, which might be mediated through the prevention of Bax protein up-regulation by DOX and associated elevation of Bax/Bcl-2 ratio.
研究金属硫蛋白(MT)对阿霉素(DOX)诱导的心脏细胞凋亡的抑制作用及其可能的机制。
将成年雄性C57BL小鼠(6 - 8周龄)随机分为四组,给予以下处理:在单次注射DOX(15 mg/kg,腹腔注射)或等量生理盐水之前,给予锌(硫酸锌,300 μmol/kg,皮下注射,每天一次,共2天)或等量生理盐水。在DOX给药后第4天处死动物,取出心脏进行进一步研究,包括用镉 - 血红蛋白亲和力测定法检测MT浓度、用ELISA法检测DNA片段化以及用Western blot法分析Bax和Bcl - 2。
DOX给药使心脏重量减轻10%,并导致明显的心脏细胞凋亡,DNA片段可证明这一点,而锌预处理显著提高了MT水平,从而抑制了DOX的心脏凋亡作用。DOX处理后明显观察到Bax表达升高,而锌诱导MT可防止这种升高。相反,各组间Bcl - 2蛋白水平无明显变化。
这些发现表明,锌诱导的金属硫蛋白对DOX诱导的心脏细胞凋亡具有保护作用,这可能是通过防止DOX引起的Bax蛋白上调以及相关的Bax/Bcl - 2比值升高来介导的。