Danilovich Natalia, Ram Sairam M
Molecular Reproduction Research Laboratory, Clinical Research Institute of Montreal, Montreal, Que., Canada H2W 1R7.
Exp Gerontol. 2006 Feb;41(2):117-22. doi: 10.1016/j.exger.2005.10.010. Epub 2005 Dec 13.
Reproductive senescence occurs in all female mammals with resultant changes in numerous body functional systems and several important features may be species-specific. Those features that appear to parallel human menopause and aging include general similarity of hormone profiles across the menopausal transition, progression to cycle termination through irregular cycles, declining fertility with age, disturbances in thermogenesis, age-related gains in body weight, fat distribution and disposition towards metabolic syndrome. Structural and hormonal changes in the brain and ovary play a critical role in determining the onset of reproductive senescence. The short life span of rodents such as mice (compared to humans) and the ability to generate specific and timed gene deletions, provide powerful experimental paradigms to understand the molecular and functional changes that precede and follow the loss of reproductive capacity. In theory, any manipulation that compromises ovarian function either partly or totally would impact reproductive events at various levels followed by other dysfunctions. In this article, we provide an overview of three mouse models for the study of female reproductive aging. They are derived from different strategies and their age related phenotypes have been characterized to varying degrees. The follitropin receptor knockout (FORKO) mouse, in its null and haploinsufficient state as well as the dioxin/aryl hydrocarbon receptor (AhR) knockout mouse, serve as two examples of single gene deletions. A third model, using administration of a chemical toxicant such as 4-vinylcyclohexene diepoxide (VCD) in the adult state, produces ovarian deficiencies accompanied by aging changes. These will serve as useful alternatives to previously used radical ovariectomy in young adults. It is anticipated that these new models and more that will be forthcoming will extend opportunities to understand reproductive aging and resolve controversies that abound on issues related to benefits and risks of hormone replacement therapy or other modalities for improving quality of life.
生殖衰老发生在所有雌性哺乳动物中,会导致众多身体功能系统发生变化,且一些重要特征可能具有物种特异性。那些似乎与人类更年期和衰老相似的特征包括:整个更年期过渡期间激素水平的总体相似性、通过月经周期不规律逐渐发展至月经周期终止、随着年龄增长生育能力下降、产热紊乱、与年龄相关的体重增加、脂肪分布以及对代谢综合征的易感性。大脑和卵巢的结构及激素变化在决定生殖衰老的起始方面起着关键作用。与人类相比,小鼠等啮齿动物寿命较短,且具备产生特定和定时基因缺失的能力,这为理解生殖能力丧失前后的分子和功能变化提供了强大的实验范例。理论上,任何部分或完全损害卵巢功能的操作都会在各个层面影响生殖事件,进而引发其他功能障碍。在本文中,我们概述了三种用于研究雌性生殖衰老的小鼠模型。它们源自不同的策略,其与年龄相关的表型也得到了不同程度的表征。促卵泡激素受体敲除(FORKO)小鼠,处于纯合缺失和单倍剂量不足状态,以及二噁英/芳烃受体(AhR)敲除小鼠,是单基因缺失的两个例子。第三种模型是在成年状态下给予化学毒物,如4 - 乙烯基环己烯二环氧化物(VCD),会导致卵巢功能缺陷并伴有衰老变化。这些将成为先前在年轻成年动物中使用的根治性卵巢切除术的有用替代方法。预计这些新模型以及即将出现的更多模型将为理解生殖衰老提供更多机会,并解决在激素替代疗法或其他改善生活质量方式的益处和风险相关问题上存在的诸多争议。