Quan Junjun, Jia Zhongli, Liu Lingjuan, Tian Jie
Department of Cardiology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing 400014, China.
Chongqing Key Laboratory of Structural Birth Defect and Reconstruction, Chongqing 400014, China.
Genes Dis. 2024 Apr 3;12(2):101284. doi: 10.1016/j.gendis.2024.101284. eCollection 2025 Mar.
Aging is an independent risk factor for cardiovascular diseases. Cardiac diastolic dysfunction (CDD), ultimately leading to heart failure with preserved ejection fraction (HFpEF), is prevalent among older individuals. Although therapeutics have made great progress, preventive strategies remain unmet medical needs. Green tea catechins have been shown to be effective in improving aging-related cardiovascular and cerebral disorders in animal models and patients. However, little attention has been paid to whether long-term administration of epigallocatechin gallate (EGCG), the major bioactive ingredient of green tea catechins, could prevent the onset and progression of CDD. In this study, 12-month-old female mice were orally administered 50, 100 and 200 mg EGCG mixed with drinking water for 6 months. Aged mice (18 months old) exhibited the major features of HFpEF, including CDD with pEF, cardiac fibrosis, increased cardiomyocyte apoptosis, and mitochondrial damages, as well as elevated A/B-type natriuretic peptide. Cardiac troponin I (cTnI) expression was also reduced. Long-term administration of 100 or 200 mg EGCG prevented aging-related CDD and exercise capacity decline, along with alleviating myocardial apoptosis and mitochondria damage. The transcription and protein expression of cTnI were increased, which might be achieved by inhibiting the expression and activity of histone deacetylase 1 (HDAC1), and reducing its binding level near cTnI's promoter, thereby elevating acetylated histone 3 (AcH3) and acetylated lysine 9 on histone H3 (AcH3K9) in the aged mice. We provide a novel insight that long-term administration of EGCG is a potentially effective strategy in preventing aging-related CDD and cTnI expression decline.
衰老为心血管疾病的独立危险因素。心脏舒张功能障碍(CDD)最终会导致射血分数保留的心力衰竭(HFpEF),在老年人中很常见。尽管治疗方面已取得巨大进展,但预防策略仍是未被满足的医疗需求。绿茶儿茶素已被证明在动物模型和患者中可有效改善与衰老相关的心血管和脑部疾病。然而,很少有人关注长期给予绿茶儿茶素的主要生物活性成分表没食子儿茶素没食子酸酯(EGCG)是否能预防CDD的发生和进展。在本研究中,给12月龄雌性小鼠口服50、100和200mg与饮用水混合的EGCG,持续6个月。老年小鼠(18月龄)表现出HFpEF的主要特征,包括伴有射血分数保留的CDD、心脏纤维化、心肌细胞凋亡增加、线粒体损伤,以及A/B型利钠肽升高。心肌肌钙蛋白I(cTnI)表达也降低。长期给予100或200mg EGCG可预防与衰老相关的CDD和运动能力下降,同时减轻心肌细胞凋亡和线粒体损伤。cTnI的转录和蛋白表达增加,这可能是通过抑制组蛋白去乙酰化酶1(HDAC1)的表达和活性,并降低其在cTnI启动子附近的结合水平,从而提高老年小鼠中组蛋白H3上的乙酰化组蛋白3(AcH3)和乙酰化赖氨酸9(AcH3K9)来实现的。我们提供了一个新的见解,即长期给予EGCG是预防与衰老相关的CDD和cTnI表达下降的潜在有效策略。