Feng Wen-Jing, Mou Jie, Liao Ping-Ping, Zhou Jing, Zhang Nan-Nan, Hu Ting, Wang Shan, Zhang Shi-Yuan, Mao Yong-Jun
Department of Geriatric Medicine, The Affiliated Hospital of Qingdao University, Qingdao, 266003 Shandong China.
Department of Epidemiology and Health Statistics, The School of Public Health of Qingdao University, Qingdao, 266021 Shandong China.
Food Sci Biotechnol. 2024 Feb 19;33(12):2835-2844. doi: 10.1007/s10068-024-01534-y. eCollection 2024 Sep.
Aging is a known independent risk factor for several cardiovascular diseases. Here, we evaluated potential effects and possible mechanisms through which alginate oligosaccharides (AOS) affect hydrogen peroxide (HO)-induced senescence in H9C2 cardiomyocytes. A series of AOS molecules, including oligoM, oligoG, M-5, and G-5, were investigated. AOS significantly decreased SA-β-gal and DAPI-stained positive cells, downregulated p53 and p21 (aging-related markers) expression, and eventually protected H9C2 cells from HO-induced senescence. AOS decreased reactive oxygen species and malondialdehyde production, recovered mitochondrial function, and alleviated the oxidative stress state by regulating PGC-1α and NADPH oxidase subunit expression. Furthermore, AOS treatment restored the expression of antioxidant enzymes in senescent H9C2 cells. Thus, our results show in vitro evidence that AOS alleviate senescence in H9C2 cells by regulating the redox state; thus, AOS may be an effective therapeutic agent that could protect against cardiomyocyte senescence.
衰老已知是多种心血管疾病的独立风险因素。在此,我们评估了海藻酸钠寡糖(AOS)影响过氧化氢(HO)诱导的H9C2心肌细胞衰老的潜在作用及可能机制。研究了一系列AOS分子,包括oligoM、oligoG、M - 5和G - 5。AOS显著减少了SA-β-半乳糖苷酶和DAPI染色阳性细胞,下调了p53和p21(衰老相关标志物)的表达,并最终保护H9C2细胞免受HO诱导的衰老。AOS减少了活性氧和丙二醛的产生,恢复了线粒体功能,并通过调节PGC - 1α和NADPH氧化酶亚基的表达减轻了氧化应激状态。此外,AOS处理恢复了衰老H9C2细胞中抗氧化酶的表达。因此,我们的结果在体外证明AOS通过调节氧化还原状态减轻H9C2细胞衰老;因此,AOS可能是一种有效的治疗剂,可预防心肌细胞衰老。