Brooks Robert C, Garratt Michael G
Evolution & Ecology Research Centre, and School of Biological, Earth and Environmental Sciences, UNSW Australia, Kensington, Sydney, New South Wales, Australia.
Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
Ann N Y Acad Sci. 2017 Feb;1389(1):92-107. doi: 10.1111/nyas.13302. Epub 2016 Dec 23.
Males and females in many species differ in how they age and how long they live. These differences have motivated much research, concerning both their evolution and the underlying mechanisms that cause them. We review how differences in male and female life histories have evolved to shape patterns of aging and some of the mechanisms and pathways involved. We pay particular attention to three areas where considerable potential for synergy between mechanistic and evolutionary research exists: (1) the role of estrogens, androgens, the growth hormone/insulin-like growth factor 1 pathway, and the mechanistic target of rapamycin signaling pathway in sex-dependent growth and reproduction; (2) sexual conflict over mating rate and fertility, and how mate presence or mating can become an avenue for males and females to directly affect each other's life span; and (3) the link between dietary restriction and aging, and the emerging understanding that only the restriction of certain nutrients is involved and that this is linked to reproduction. We suggest that ideas about life histories, sex-dependent selection, and sexual conflict can inform and be informed by the ever more refined and complex understanding of the mechanisms that cause aging.
许多物种的雄性和雌性在衰老方式和寿命长短上存在差异。这些差异引发了大量关于其进化以及导致这些差异的潜在机制的研究。我们回顾了雄性和雌性生命历程的差异是如何进化以塑造衰老模式的,以及其中涉及的一些机制和途径。我们特别关注三个领域,在这些领域中,机制研究和进化研究之间存在相当大的协同潜力:(1)雌激素、雄激素、生长激素/胰岛素样生长因子1途径以及雷帕霉素信号通路的机制靶点在性别依赖性生长和繁殖中的作用;(2)交配率和生育力方面的性冲突,以及配偶的存在或交配如何成为雄性和雌性直接影响对方寿命的途径;(3)饮食限制与衰老之间的联系,以及新出现的认识,即只有某些营养素的限制才涉及其中,并且这与繁殖有关。我们认为,关于生命历程、性别依赖性选择和性冲突的观点可以为对导致衰老的机制的日益精细和复杂的理解提供信息,并从中获得信息。