Hubei Key Laboratory of Bioinorganic Chemistry & Materia Medica, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 1037 Luoyu Road, Hongshan, Wuhan, Hubei 430074, People's Republic of China.
Exp Eye Res. 2011 May;92(5):401-7. doi: 10.1016/j.exer.2011.02.014. Epub 2011 Mar 21.
To determine the influences of early-stage diabetes mellitus on methionine sulfoxide reductases (Msrs) expression in lenses, streptozocin (STZ)-induced diabetic mice as animal models were used in this study. The results showed that the contents of methionine sulfoxide (MetO), protein carbonyl (PC) and Malondialdehyde (MDA) in the lenses of STZ-induced diabetic mice after 14 days were significantly higher than that in the normal control, level of total sulfhydryl groups (TSH) was 60% of normal control, and mRNA expressing levels of the MsrA and MsrBs were significantly decreased compared with normal group, as was the expression of MsrB1 protein. These results suggest that STZ not only causes increased oxidative stress, but also suppresses Msr mRNA and MsrB1 protein expression during early-stage diabetes in mice. However, the mechanism remains to research.
为了确定早期糖尿病对晶状体中天冬氨酸硫氧化物还原酶(Msr)表达的影响,本研究采用链脲佐菌素(STZ)诱导的糖尿病小鼠作为动物模型。结果表明,STZ 诱导的糖尿病小鼠晶状体中天冬氨酸硫氧化物(MetO)、蛋白质羰基(PC)和丙二醛(MDA)的含量在 14 天后明显高于正常对照组,总巯基(TSH)含量为正常对照组的 60%,MsrA 和 MsrBs 的 mRNA 表达水平与正常组相比明显降低,MsrB1 蛋白的表达也降低。这些结果表明,STZ 不仅引起氧化应激增加,而且在糖尿病早期还抑制了小鼠 Msr mRNA 和 MsrB1 蛋白的表达。然而,其机制仍有待研究。