Buck Institute for Research on Aging, Novato, California 94945, USA.
Physiol Genomics. 2013 Feb 4;45(3):106-9. doi: 10.1152/physiolgenomics.00155.2012. Epub 2012 Dec 18.
Estrogen provides many beneficial effects early in life by regulating normal tissue development and several physiological functions. While estrogen replacement therapy (ERT) in women was expected to reduce the health risks associated with the age-related decline in estrogen levels during menopause, ERT also resulted in increased progression to other types of diseases. Hence, distinguishing the signaling pathways that regulate the beneficial and detrimental effects of estrogen is important for developing interventions that selectively harness the hormone's beneficial effects, while minimizing its side effects. Estrogen can minimize mitochondrial dysfunction, which is thought to contribute to aging phenotypes. Decline in estrogen levels during menopause may lead to progressive mitochondrial dysfunction and may permanently alter cellular response, including that of estrogen (i.e., ERT). This review discusses the interplay between estrogen and mitochondrial function during the aging process and suggests a potential role of mitochondria in influencing the pleiotropic action of estrogen.
雌激素通过调节正常组织发育和多种生理功能,在生命早期提供许多有益的影响。虽然雌激素替代疗法(ERT)有望降低与绝经后雌激素水平下降相关的健康风险,但 ERT 也导致其他类型疾病的进展增加。因此,区分调节雌激素有益和有害作用的信号通路对于开发干预措施以选择性地利用激素的有益作用,同时最小化其副作用非常重要。雌激素可以最小化线粒体功能障碍,这被认为有助于衰老表型。绝经后雌激素水平下降可能导致进行性线粒体功能障碍,并可能永久改变细胞反应,包括雌激素(即 ERT)。本综述讨论了衰老过程中雌激素和线粒体功能之间的相互作用,并提出了线粒体在影响雌激素的多效性作用中的潜在作用。