Department of Experimental Biology, Faculty of Biology and Animal Science, Wrocław University of Environmental and Life Sciences, Norwida 27B, 50-375 Wrocław, Poland.
International Institute of Translational Medicine, Jesionowa 11, Malin, 55-114 Wisznia Mała, Poland.
Biomolecules. 2022 Jul 27;12(8):1039. doi: 10.3390/biom12081039.
Astaxanthin is gaining recognition as a natural bioactive component. This study aimed to test whether astaxanthin could protect adipose-derived stromal stem cells (ASCs) from apoptosis, mitochondrial dysfunction and oxidative stress. was used to extract astaxanthin, whose biocompatibility was tested after 24, 48 and 72 h of incubation with the cells; no harmful impact was found. ASCs were treated with optimal concentrations of astaxanthin. Several parameters were examined: cell viability, apoptosis, reactive oxygen levels, mitochondrial dynamics and metabolism, superoxide dismutase activity, and astaxanthin's antioxidant capacity. A RT PCR analysis was performed after each test. The astaxanthin treatment significantly reduced apoptosis by modifying the normalized caspase activity of pro-apoptotic pathways (p21, p53, and Bax). Furthermore, by regulating the expression of related master factors SOD1, SOD2, PARKIN, PINK 1, and MFN 1, astaxanthin alleviated the oxidative stress and mitochondrial dynamics failure caused by EMS. Astaxanthin restored mitochondrial oxidative phosphorylation by stimulating markers associated with the OXPHOS machinery: COX4I1, COX4I2, UQCRC2, NDUFA9, and TFAM. Our results suggest that astaxanthin has the potential to open new possibilities for potential bio-drugs to control and suppress oxidative stress, thereby improving the overall metabolic status of equine ASCs suffering from metabolic syndrome.
虾青素作为一种天然生物活性成分正受到越来越多的关注。本研究旨在测试虾青素是否能保护脂肪间充质干细胞(ASCs)免受细胞凋亡、线粒体功能障碍和氧化应激的影响。采用 法提取虾青素,将其与细胞共孵育 24、48 和 72 h 后检测其生物相容性,未发现有害影响。用最佳浓度的虾青素处理 ASCs。检测了几个参数:细胞活力、凋亡、活性氧水平、线粒体动力学和代谢、超氧化物歧化酶活性和虾青素的抗氧化能力。每次试验后进行 RT-PCR 分析。虾青素处理通过改变促凋亡途径(p21、p53 和 Bax)的标准化半胱氨酸天冬氨酸蛋白酶(caspase)活性显著降低了细胞凋亡。此外,通过调节相关主因子 SOD1、SOD2、PARKIN、PINK1 和 MFN1 的表达,虾青素缓解了 EMS 引起的氧化应激和线粒体动力学障碍。虾青素通过刺激与 OXPHOS 机制相关的标志物:COX4I1、COX4I2、UQCRC2、NDUFA9 和 TFAM,恢复了线粒体氧化磷酸化。我们的结果表明,虾青素有可能为控制和抑制氧化应激的潜在生物药物开辟新的可能性,从而改善患有代谢综合征的马 ASC 的整体代谢状态。