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卵巢衰老:机制与干预策略

Ovarian aging: mechanisms and intervention strategies.

作者信息

Zhu Zhengmao, Xu Wanxue, Liu Lin

机构信息

Haihe Laboratory of Cell Ecosystem, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.

Department of Genetics and Cell Biology, College of Life Science, Nankai University, Tianjin, China.

出版信息

Med Rev (2021). 2022 Nov 22;2(6):590-610. doi: 10.1515/mr-2022-0031. eCollection 2022 Dec.

Abstract

Ovarian reserve is essential for fertility and influences healthy aging in women. Advanced maternal age correlates with the progressive loss of both the quantity and quality of oocytes. The molecular mechanisms and various contributing factors underlying ovarian aging have been uncovered. In this review, we highlight some of critical factors that impact oocyte quantity and quality during aging. Germ cell and follicle reserve at birth determines reproductive lifespan and timing the menopause in female mammals. Accelerated diminishing ovarian reserve leads to premature ovarian aging or insufficiency. Poor oocyte quality with increasing age could result from chromosomal cohesion deterioration and misaligned chromosomes, telomere shortening, DNA damage and associated genetic mutations, oxidative stress, mitochondrial dysfunction and epigenetic alteration. We also discuss the intervention strategies to delay ovarian aging. Both the efficacy of senotherapies by antioxidants against reproductive aging and mitochondrial therapy are discussed. Functional oocytes and ovarioids could be rejuvenated from pluripotent stem cells or somatic cells. We propose directions for future interventions. As couples increasingly begin delaying parenthood in life worldwide, understanding the molecular mechanisms during female reproductive aging and potential intervention strategies could benefit women in making earlier choices about their reproductive health.

摘要

卵巢储备对于生育能力至关重要,并影响女性的健康衰老。高龄产妇与卵母细胞数量和质量的逐渐丧失相关。卵巢衰老背后的分子机制和各种促成因素已被揭示。在这篇综述中,我们重点介绍了一些在衰老过程中影响卵母细胞数量和质量的关键因素。出生时的生殖细胞和卵泡储备决定了雌性哺乳动物的生殖寿命和绝经时间。卵巢储备加速减少会导致卵巢早衰或功能不全。随着年龄增长,卵母细胞质量差可能是由于染色体凝聚恶化和染色体排列不齐、端粒缩短、DNA损伤及相关基因突变、氧化应激、线粒体功能障碍和表观遗传改变所致。我们还讨论了延缓卵巢衰老的干预策略。讨论了抗氧化剂的衰老疗法对生殖衰老的疗效以及线粒体疗法。功能性卵母细胞和类卵巢组织可以从多能干细胞或体细胞中恢复活力。我们提出了未来干预的方向。随着全球范围内越来越多的夫妇开始推迟生育,了解女性生殖衰老过程中的分子机制和潜在的干预策略可能有助于女性更早地做出关于生殖健康的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85cf/10471094/4f95ec9a93f1/j_mr-2022-0031_fig_001.jpg

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