Batalha Caio M P F, Vercesi Anibal Eugênio, Souza-Pinto Nadja C
Lab. Genética Mitocondrial, Departamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo, Brazil.
Departamento de Patologia Clínica, Faculdade de Medicina, Universidade de Campinas, Campinas, Brazil.
Antioxid Redox Signal. 2022 May;36(13-15):824-843. doi: 10.1089/ars.2021.0074. Epub 2022 Jan 4.
Aging is a natural process that affects most living organisms, resulting in increased mortality. As the world population ages, the prevalence of age-associated diseases, and their associated health care costs, has increased sharply. A better understanding of the molecular mechanisms that lead to cellular dysfunction may provide important targets for interventions to prevent or treat these diseases. Although the mitochondrial theory of aging had been proposed more than 40 years ago, recent new data have given stronger support for a central role for mitochondrial dysfunction in several pathways that are deregulated during normal aging and age-associated disease. Several of the experimental evidence linking mitochondrial alterations to age-associated loss of function are correlative and mechanistic insights are still elusive. Here, we review how mitochondrial dysfunction may be involved in many of the known hallmarks of aging, and how these pathways interact in an intricate net of molecular relationships. As it has become clear that mitochondrial dysfunction plays causative roles in normal aging and age-associated diseases, it is necessary to better define the molecular interactions and the temporal and causal relationship between these changes and the relevant phenotypes seen during the aging process. 36, 824-843.
衰老 是一个影响大多数生物的自然过程,会导致死亡率上升。随着世界人口老龄化,与年龄相关疾病的患病率及其相关医疗保健成本急剧增加。更好地理解导致细胞功能障碍的分子机制可能为预防或治疗这些疾病的干预措施提供重要靶点。尽管衰老的线粒体理论在40多年前就已提出,但最近的新数据为线粒体功能障碍在正常衰老和与年龄相关疾病中失调的几种途径中所起的核心作用提供了更有力的支持。将线粒体改变与与年龄相关的功能丧失联系起来的一些实验证据是相关性的,其机制性见解仍然难以捉摸。在这里,我们回顾线粒体功能障碍可能如何涉及许多已知的衰老标志,以及这些途径如何在复杂的分子关系网络中相互作用。由于线粒体功能障碍在正常衰老和与年龄相关疾病中起因果作用已变得清晰,因此有必要更好地定义分子相互作用以及这些变化与衰老过程中所见相关表型之间的时间和因果关系。36, 824 - 843。