The ovarian reserve as target of insulin/IGF and ROS in metabolic disorder-dependent ovarian dysfunctions.

Reproduction & Fertility Pub Date : 2021-08-17 eCollection Date: 2021-07-01 DOI:10.1530/RAF-21-0038
Maria Dri, Francesca Gioia Klinger, Massimo De Felici
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引用次数: 4

Abstract

It is known for a long time that metabolic disorders can cause ovarian dysfunctions and affect a woman's fertility either by direct targeting follicular cells and/or the oocytes or by indirect interference with the pituitary-hypothalamic axis, resulting in dysfunctional oogenesis. Such disorders may also influence the efficiency of the embryo implantation and the quality of the embryo with permanent effects on the fertility and health of the offspring. Thanks to the expanding knowledge on the molecular mechanisms governing oogenesis and folliculogenesis in mammals, we are beginning to understand how such disorders can negatively affect this process and consequently fertility in women. In the present review, we point out and discuss how the disturbance of insulin/IGF-dependent signalling and increased reactive oxygen species (ROS) level in the ovary typically associated to metabolic disorders such as type II diabetes and obesity can dysregulate the dynamics of the ovarian reserve and/or impair the survival and competence of the oocytes.

Lay summary: In women, a progressive decline and depletion of the primary ovary reserve, which represents the reserve of immature eggs, are a challenging condition in the field of reproductive medicine. This decline, occurring physiological with age, is the main determinant of the age at the onset of menopause. Concomitant with the reduction in their number, the quality of the eggs also decreases with age. Metabolic disorders such as diabetes and obesity can cause ovarian dysfunctions and affect a woman's fertility mainly by direct targeting the egg stockpile or by indirect interference with the production of reproductive hormones. Here, we report up-to-date data and discuss results about how disturbance of insulin-dependent signalling and increased oxidative stress in the ovary, usually associated to metabolic disorders, can dysregulate the dynamics of the primary ovary reserve and/or impair the survival and quality of the eggs.

Abstract Image

Abstract Image

卵巢储备作为胰岛素/IGF和ROS在代谢紊乱依赖性卵巢功能障碍中的靶点。
长期以来,人们都知道代谢紊乱会导致卵巢功能障碍,影响女性的生育能力,要么直接针对卵泡细胞和/或卵母细胞,要么间接干扰垂体-下丘脑轴,导致排卵功能障碍。这些疾病还可能影响胚胎着床的效率和胚胎的质量,对后代的生育能力和健康产生永久性影响。由于对哺乳动物卵子发生和卵泡发生的分子机制的了解不断扩大,我们开始了解这些疾病如何对这一过程产生负面影响,从而影响女性的生育能力。在本综述中,我们指出并讨论了胰岛素/ igf依赖性信号的紊乱和卵巢中活性氧(ROS)水平的增加通常与代谢紊乱(如II型糖尿病和肥胖)相关,如何调节卵巢储备的动态和/或损害卵母细胞的生存和能力。摘要:在女性中,代表未成熟卵子储备的初级卵巢储备的逐渐下降和枯竭是生殖医学领域的一个具有挑战性的条件。随着年龄的增长,这种生理上的下降是更年期开始时年龄的主要决定因素。随着卵子数量的减少,卵子的质量也随着年龄的增长而下降。代谢紊乱,如糖尿病和肥胖,可导致卵巢功能障碍,影响妇女的生育能力,主要是通过直接针对卵子储备或间接干扰生殖激素的产生。在这里,我们报告了最新的数据,并讨论了卵巢中胰岛素依赖性信号的干扰和氧化应激的增加,通常与代谢紊乱有关,如何调节初级卵巢储备的动态和/或损害卵子的存活和质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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