Department of Biochemistry, School of Bioengineering and Biosciences, Lovely Professional University, Phagwara, Punjab, 144411, India.
Department of Microbiology, School of Bioengineering and Biosciences, Lovely Professional University, Phagwara, Punjab, 144411, India.
Biogerontology. 2023 Oct;24(5):609-662. doi: 10.1007/s10522-023-10050-1. Epub 2023 Jul 30.
Aging accompanied by several age-related complications, is a multifaceted inevitable biological progression involving various genetic, environmental, and lifestyle factors. The major factor in this process is oxidative stress, caused by an abundance of reactive oxygen species (ROS) generated in the mitochondria and endoplasmic reticulum (ER). ROS and RNS pose a threat by disrupting signaling mechanisms and causing oxidative damage to cellular components. This oxidative stress affects both the ER and mitochondria, causing proteopathies (abnormal protein aggregation), initiation of unfolded protein response, mitochondrial dysfunction, abnormal cellular senescence, ultimately leading to inflammaging (chronic inflammation associated with aging) and, in rare cases, metastasis. RONS during oxidative stress dysregulate multiple metabolic pathways like NF-κB, MAPK, Nrf-2/Keap-1/ARE and PI3K/Akt which may lead to inappropriate cell death through apoptosis and necrosis. Inflammaging contributes to the development of inflammatory and degenerative diseases such as neurodegenerative diseases, diabetes, cardiovascular disease, chronic kidney disease, and retinopathy. The body's antioxidant systems, sirtuins, autophagy, apoptosis, and biogenesis play a role in maintaining homeostasis, but they have limitations and cannot achieve an ideal state of balance. Certain interventions, such as calorie restriction, intermittent fasting, dietary habits, and regular exercise, have shown beneficial effects in counteracting the aging process. In addition, interventions like senotherapy (targeting senescent cells) and sirtuin-activating compounds (STACs) enhance autophagy and apoptosis for efficient removal of damaged oxidative products and organelles. Further, STACs enhance biogenesis for the regeneration of required organelles to maintain homeostasis. This review article explores the various aspects of oxidative damage, the associated complications, and potential strategies to mitigate these effects.
衰老是多种与年龄相关的并发症的伴随物,是一个涉及多种遗传、环境和生活方式因素的多方面不可避免的生物学过程。这个过程的主要因素是氧化应激,由线粒体和内质网(ER)中产生的大量活性氧物种(ROS)引起。ROS 和 RNS 通过破坏信号机制并对细胞成分造成氧化损伤,对身体造成威胁。这种氧化应激会影响 ER 和线粒体,导致蛋白病(异常蛋白质聚集)、未折叠蛋白反应的启动、线粒体功能障碍、异常细胞衰老,最终导致炎症老化(与衰老相关的慢性炎症),在极少数情况下还会导致转移。氧化应激期间的 RONS 会使 NF-κB、MAPK、Nrf-2/Keap-1/ARE 和 PI3K/Akt 等多种代谢途径失调,这可能通过细胞凋亡和坏死导致细胞死亡。炎症老化会导致神经退行性疾病、糖尿病、心血管疾病、慢性肾病和视网膜病变等炎症和退行性疾病的发展。机体的抗氧化系统、沉默调节蛋白、自噬、细胞凋亡和生物发生在维持体内平衡方面发挥作用,但它们存在局限性,无法达到理想的平衡状态。某些干预措施,如热量限制、间歇性禁食、饮食习惯和定期运动,已显示出对对抗衰老过程的有益效果。此外,如 senotherapy(针对衰老细胞)和 sirtuin-activating compounds (STACs) 等干预措施,可增强自噬和细胞凋亡,以有效清除受损的氧化产物和细胞器。此外,STACs 还增强生物发生,以再生所需的细胞器,维持体内平衡。本文综述了氧化损伤的各个方面、相关并发症以及减轻这些影响的潜在策略。