衰老过程中线粒体damps依赖性炎性体激活诱导低有氧能力大鼠血管平滑肌细胞功能障碍和主动脉僵硬

Chandrika Canugovi, M. Stevenson, Aleksandr E. Vendrov, A. Lozhkin, S. Britton, L. Koch, M. Runge, N. Madamanchi
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摘要

前言:低有氧运动能力是心血管疾病(CVD)的独立危险因素和过早死亡的预测因子。随着年龄的增长,低有氧能力降低了心血管疾病的阈值。目的:由于低有氧能力和衰老与线粒体氧化应激和功能障碍有关,我们研究了老年低容量跑者(LCR)大鼠(27个月)与高容量跑者(HCR)大鼠相比是否存在血管功能障碍。方法和结果:与年龄和性别匹配的HCR大鼠相比,老龄LCR大鼠主动脉eNOS水平和血管舒张度显著降低,主动脉胶原蛋白和硬度显著增加。年龄相关性血管功能障碍与LCR大鼠主动脉ROS水平升高及DNA损伤存在相关性。老龄LCR大鼠VSMCs的线粒体耗氧量、膜电位、ATP水平和线粒体自噬均较低。老年LCR大鼠VSMCs显示AIM2炎性体活化。用纯化的线粒体损伤相关分子模式(DAMP)处理的年轻(4个月大)LCR大鼠的VSMCs再现了与老年大鼠VSMCs相似的炎性体激活表型。雷帕霉素是一种有效的免疫抑制剂,在老年LCR大鼠VSMCs中诱导线粒体自噬,刺激电子传递链活性,降低炎症小体活性,线粒体ROS和DAMP水平。MitoTEMPO是一种线粒体ROS清除剂,对老年大鼠的VSMCs同样有效。结论:衰老过程中有氧运动能力低的情况下,血管中线粒体自噬和炎性体激活受损导致动脉功能障碍和主动脉僵硬。对于有氧能力降低的老年人,线粒体抗氧化剂、线粒体自噬诱导和炎症小体抑制可能是增强血管健康的有效治疗策略。
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Mitochondrial DAMPs-dependent inflammasome activation during aging induces vascular smooth muscle cell dysfunction and aortic stiffness in low aerobic capacity rats
Introduction: Low aerobic exercise capacity is an independent risk factor for cardiovascular disease (CVD) and a predictor of premature death. In combination with aging, low aerobic capacity lowers the threshold for CVD. Aim: Since low aerobic capacity and aging have been linked to mitochondrial oxidative stress and dysfunction, we investigated whether aged Low-Capacity Runner (LCR) rats (27 months) had vascular dysfunction compared to High-Capacity Runner (HCR) rats. Methods and Results: A significant decrease in aortic eNOS levels and vasodilation as well as an increase in aortic collagen and stiffness were observed in aged LCR rats compared to age and sex-matched HCR rats. There was a correlation between age-related vascular dysfunction and increased levels of ROS and DNA damage in aortas of LCR rats. Moreover, mitochondrial oxygen consumption, membrane potential, ATP levels, and mitophagy were lower in VSMCs of aged LCR rats. VSMCs from older LCR rats showed AIM2 inflammasome activation. VSMCs of young (4 months old) LCR rats treated with purified mitochondrial damage-associated molecular patterns (DAMP) recapitulated an inflammasome activation phenotype similar to that seen in aged rat VSMCs. Rapamycin, a potent immunosuppressant, induced mitophagy, stimulated electron transport chain activity, reduced inflammasome activity, mitochondrial ROS and DAMP levels in VSMCs from aged LCR rats. MitoTEMPO, a mitochondrial ROS scavenger, was similarly effective on VSMCs from aged rats. Conclusion: The findings suggest that impaired mitophagy and inflammasome activation in the vasculature under conditions of low aerobic exercise capacity during aging results in arterial dysfunction and aortic stiffness. In older adults with reduced aerobic capacity, mitochondrial antioxidants, mitophagy induction, and inflammasome inhibition may be effective therapeutic strategies for enhancing vascular health.
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