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Diet-induced paternal obesity in the absence of diabetes diminishes the reproductive health of two subsequent generations of mice

机译:在没有糖尿病的情况下,饮食引起的父亲肥胖会降低随后两代小鼠的生殖健康

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Background Obesity and related conditions, notably subfertility, are increasingly prevalent. Paternal influences are known to influence offspring health outcome, but the impact of paternal obesity and subfertility on the reproductive health of subsequent generations has been overlooked. Methods A high-fat diet (HFD) was used to induce obesity but not diabetes in male C57Bl6 mice, which were subsequently mated to normal-weight females. First-generation offspring were raised on a control diet and their gametes were investigated for signs of subfertility. Second-generation offspring were generated from both first generation sexes and their gametes were similarly assessed.RESULTSWe demonstrate a HFD-induced paternal initiation of subfertility in both male and female offspring of two generations of mice. Furthermore, we have shown that diminished reproductive and gamete functions are transmitted through the first generation paternal line to both sexes of the second generation and via the first generation maternal line to second-generation males. Our previous findings that founder male obesity alters the epigenome of sperm, could provide a basis for the developmental programming of subfertility in subsequent generations. Conclusions This is the first observation of paternal transmission of diminished reproductive health to future generations and could have significant implications for the transgenerational amplification of subfertility observed worldwide in humans.
机译:背景肥胖症和相关疾病,特别是不育症,越来越普遍。众所周知,父亲的影响会影响后代的健康状况,但是,父亲的肥胖和生育力不足对后代生殖健康的影响却被忽略了。方法采用高脂饮食(HFD)诱导肥胖,但不诱导糖尿病的雄性C57B16小鼠,随后与正常体重的雌性交配。在控制饮食下饲养第一代后代,并研究其配子是否具有不育迹象。第二代后代均由第一代性别产生,并且对它们的配子也进行了类似的评估。结果我们证明了HFD诱导的两代小鼠的雄性和雌性后代的父本不育性开始。此外,我们已经表明,生殖功能和配子功能的减弱是通过第一代父系传给第二代男女,并通过第一代母系传给第二代男性。我们先前发现的发现,男性肥胖的建立者改变了精子的表观基因组,这可以为子孙后代的不育发展规划提供基础。结论这是生殖健康下降的父本传播给子孙后代的第一个观察结果,并且可能对人类在世界范围内观察到的亚生育力的世代放大具有重要意义。

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