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衰老会增加精子染色质损伤,并损害过氧化物酶体增殖物激活受体6基因敲除小鼠的生育能力。

Advancing age increases sperm chromatin damage and impairs fertility in peroxiredoxin 6 null mice.

作者信息

Ozkosem Burak, Feinstein Sheldon I, Fisher Aron B, O'Flaherty Cristian

机构信息

Urology Research Laboratory, Research Institute of the McGill University Health Centre, McGill University, Montréal, Québec, Canada; Department of Surgery (Urology Division), Research Institute of the McGill University Health Centre, McGill University, Montréal, Québec, Canada.

Institute for Environmental Medicine, University of Pennsylvania, Philadelphia, PA, USA; Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Redox Biol. 2015 Aug;5:15-23. doi: 10.1016/j.redox.2015.02.004. Epub 2015 Feb 25.

Abstract

Due to socioeconomic factors, more couples are choosing to delay conception than ever. Increasing average maternal and paternal age in developed countries over the past 40 years has raised the question of how aging affects reproductive success of males and females. Since oxidative stress in the male reproductive tract increases with age, we investigated the impact of advanced paternal age on the integrity of sperm nucleus and reproductive success of males by using a Prdx6(-/-) mouse model. We compared sperm motility, cytoplasmic droplet retention sperm chromatin quality and reproductive outcomes of young (2-month-old), adult (8-month-old), and old (20-month-old) Prdx6(-/-) males with their age-matched wild type (WT) controls. Absence of PRDX6 caused age-dependent impairment of sperm motility and sperm maturation and increased sperm DNA fragmentation and oxidation as well as decreased sperm DNA compaction and protamination. Litter size, total number of litters and total number of pups per male were significantly lower in Prdx6(-/-) males compared to WT controls. These abnormal reproductive outcomes were severely affected by age in Prdx6(-/-) males. In conclusion, the advanced paternal age affects sperm chromatin integrity and fertility more severely in the absence of PRDX6, suggesting a protective role of PRDX6 in age-associated decline in the sperm quality and fertility in mice.

摘要

由于社会经济因素,越来越多的夫妇选择推迟受孕。在过去40年里,发达国家男性和女性的平均生育年龄不断增加,这引发了衰老如何影响男性和女性生殖成功率的问题。由于男性生殖道中的氧化应激会随着年龄增长而增加,我们通过使用Prdx6(-/-)小鼠模型,研究了高龄父亲对精子核完整性和男性生殖成功率的影响。我们比较了年轻(2个月大)、成年(8个月大)和年老(20个月大)的Prdx6(-/-)雄性小鼠与年龄匹配的野生型(WT)对照小鼠的精子活力、胞质滴滞留、精子染色质质量和生殖结果。PRDX6的缺失导致精子活力和精子成熟出现年龄依赖性损伤,增加了精子DNA片段化和氧化,同时降低了精子DNA压缩和鱼精蛋白化。与WT对照相比,Prdx6(-/-)雄性小鼠的窝仔数、总窝数和每只雄性的幼崽总数显著降低。这些异常的生殖结果在Prdx6(-/-)雄性小鼠中受到年龄的严重影响。总之,在缺乏PRDX6的情况下,高龄父亲对精子染色质完整性和生育能力的影响更为严重,这表明PRDX6在小鼠精子质量和生育能力与年龄相关的下降中起保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1a5/4371547/6c3108438fb5/fx1.jpg

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