TBARS公司
链脲佐菌素
基因沉默
细胞凋亡
下调和上调
糖尿病
标记法
链脲佐菌素
糖尿病性心肌病
医学
内分泌学
内科学
小RNA
污渍
甲基化
化学
男科
氧化应激
生物化学
脂质过氧化
免疫组织化学
心肌病
心力衰竭
基因
作者
Wei Huo,Hongyan Li,Yun Zhang,Hai Li
标识
DOI:10.1096/fj.201902086r
摘要
level and TBAR concentration. Nupr1 was targeted and inhibited by miR-874-3p (by luciferase activity and RNA immunoprecipitation assays), which was downregulated in DMED. miR-874-3p downregulation was due to increased methylation at the promoter region (methylation-specific PCR). miR-874-3p overexpression improved erection time and reduced apoptosis. In summary, miR-874-3p was downregulated which led to increased apoptosis and erectile dysfunction in DMED rats, through inhibition of Nupr1-mediated pathway. This study may also provide a new therapeutic direction for the treatment of DMED.
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