Myocardial infarction-induced anxiety-like behavior is associated with epigenetic alterations in the hippocampus of rat

被引:5
|
作者
Zhou, Ying [1 ]
Tian, Qiuyun [2 ]
Zheng, Chenfei [1 ]
Yang, Jinge [3 ]
Fan, Junming [2 ]
Shentu, Yangping [4 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp 1, Dept Nephrol, Wenzhou 325000, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Sch Basic Med Sci, Inst Hypoxia Med, Wenzhou 325035, Zhejiang, Peoples R China
[3] Jiangxi Med Coll, Dept Med Technol, Shangrao 334709, Jiangxi, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 1, Dept Pathol, Wenzhou 325000, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Myocardial infarction; Anxiety-like behavior; Epigenetic; Inflammation; Apoptosis; Hippocampus; DEPRESSIVE-LIKE BEHAVIOR; MEDIAL PREFRONTAL CORTEX; NF-KAPPA-B; HEART-FAILURE; UP-REGULATION; STRESS; SIRT1; RESVERATROL; INHIBITION; MECHANISMS;
D O I
10.1016/j.brainresbull.2020.08.023
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Epidemiological and experimental animal studies indicate that there is a high risk for the incidence of neuropsychiatric disorders suffering from cardiovascular diseases such as myocardial infarction (MI). However, the potential mechanism of this association remains largely unknown. This study sought to evaluate whether epigenetic alterations in the hippocampus is associated with MI-induced anxiety-like behavior in rats. MI was induced by occlusion of the left anterior descending artery in adult female rats. Anxiety-like behavior was examined by elevated plus maze, light-dark box, and open field test. Relative gene and protein levels expression in the hippocampus were tested by qRT-PCR and western blotting, respectively. We found that MI rats exhibited anxiety-like behavior compared with those in controls, and there is a positive correlation between MI and anxiety-like behavior. We also found that MI decreased KDM6B while increased SIRT1 expression in the hippocampus of MI rats relative to those in controls. In addition, MI not only increased levels of IL-1 beta, box, and cleaved-caspase 3, but also increased Iba-1 and GFAP expression in the hippocampus, as compared to those in controls, suggesting a promotion of neuro-inflammation and apoptosis in hippocampus. Co-immunoprecipitation assay illustrated that H3K27me3 functioned by counteracting with YAP activation in the hippocampus of MI rats relative to those in controls. Together, these results suggest a potential role of hippocampal epigenetic signaling in MI-induced anxiety-like behavior in rats, and pharmacological targeting KDM6B or SIRT1 could be a strategy to ameliorate anxiety-like behavior induced by MI.
引用
收藏
页码:172 / 183
页数:12
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