慢性约束应激与精子整体DNA超甲基化的关联:对大鼠雄性生殖功能的影响。

IF 2.5 3区 医学 Q2 BEHAVIORAL SCIENCES
Physiology & Behavior Pub Date : 2025-11-01 Epub Date: 2025-08-06 DOI:10.1016/j.physbeh.2025.115058
Daniellen Cristhine Castro Alves, Leandro Vaz Toffoli, Wyllian Rafael Silva, Viviane Batista Estrada, Luiz Fernando Veríssimo, Ana Paula Franco Punhagui, Rafaela Pires Erthal, Maria Vitória Oliveira Miguel, Marcus Vinicius de Matos Gomes, Glaura Scantamburlo Alves Fernandes, Gislaine Garcia Pelosi
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引用次数: 0

摘要

最近的证据表明,表观遗传机制参与了慢性约束应激的适应性生物反应。然而,应激对生殖细胞表观遗传编程的影响及其对生殖能力的后续影响仍未得到充分研究。因此,本研究旨在评估慢性约束应激对Wistar大鼠精子整体DNA甲基化和雄性生殖功能的影响。动物被分为两组:慢性约束应激组(14个疗程)和对照组。最后应激期结束后,收集所有动物的组织进行分析。应激组表现为精子DNA整体高甲基化(p=0.0095),精子活力降低(p=0.0079),精子异常增加(p=0.0159),精子小管异常增加(p=0.0159),附睾组织病理异常。此外,慢性抑制应激诱导附睾头区组织重组,改变了生精期。相对空泡重量(p=0.0317)和前列腺(p=0.0079)减少。精子数量在睾丸(p=0.0317)、附睾头/体(p=0.0285)和尾(p=0.0159)均下降。这些发现表明,慢性压力会对男性生殖参数产生不利影响,表明精子表观遗传程序对压力的脆弱性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic restraint stress associations with sperm global DNA hypermethylation: Impacts on male reproductive function in rats.

Recent evidence indicates the involvement of epigenetic mechanisms in the adaptive biological responses to chronic restraint stress. However, the impact of stress on the epigenetic programming of germ cells and subsequent effects on reproductive capacity remain understudied. Therefore, this study aimed to evaluate the effects of chronic restraint stress in sperm global DNA methylation and male reproductive function in Wistar rats. The animals were separated into two groups: the chronic restraint stress group (14 sessions) and the control group. After the final stress session, tissues of all the animals were collected for analysis. The stress group exhibited global sperm DNA hypermethylation (p = 0.0095), reduced sperm motility (p = 0.0079), increased sperm abnormalities (p = 0.0159), increased abnormal seminiferous tubules (p = 0.0159), and histopathological abnormalities in the epididymis. In addition, chronic restraint stress induced epididymal tissue reorganization in the caput region, and altered spermatogenic stages. There was a reduction of relative empty vesicle weight (p = 0.0317) and prostate (p = 0.0079). Sperm counts were decreased in the testis (p = 0.0317), in the caput /corpus of the epididymis (p = 0.0285) and cauda (p = 0.0159). These findings suggest that chronic stress can adversely affect male reproductive parameters, suggesting a vulnerability in the epigenetic programming of sperm to stress.

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来源期刊
Physiology & Behavior
Physiology & Behavior 医学-行为科学
CiteScore
5.70
自引率
3.40%
发文量
274
审稿时长
47 days
期刊介绍: Physiology & Behavior is aimed at the causal physiological mechanisms of behavior and its modulation by environmental factors. The journal invites original reports in the broad area of behavioral and cognitive neuroscience, in which at least one variable is physiological and the primary emphasis and theoretical context are behavioral. The range of subjects includes behavioral neuroendocrinology, psychoneuroimmunology, learning and memory, ingestion, social behavior, and studies related to the mechanisms of psychopathology. Contemporary reviews and theoretical articles are welcomed and the Editors invite such proposals from interested authors.
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