Lifespan and Population Health, School of Medicine, University of Nottingham, Nottingham, NG7 2UH, UK.
Core Metabolomics and Lipidomics Laboratory, Wellcome-MRC Institute of Metabolic Science, University of Cambridge, Addenbrooke's Treatment Centre, Keith Day Road, Cambridge, CB2 0QQ, UK.
Commun Biol. 2022 Sep 8;5(1):929. doi: 10.1038/s42003-022-03914-8.
The underlying mechanisms driving paternally-programmed metabolic disease in offspring remain poorly defined. We fed male C57BL/6 mice either a control normal protein diet (NPD; 18% protein) or an isocaloric low protein diet (LPD; 9% protein) for a minimum of 8 weeks. Using artificial insemination, in combination with vasectomised male mating, we generated offspring using either NPD or LPD sperm but in the presence of NPD or LPD seminal plasma. Offspring from either LPD sperm or seminal fluid display elevated body weight and tissue dyslipidaemia from just 3 weeks of age. These changes become more pronounced in adulthood, occurring in conjunction with altered hepatic metabolic and inflammatory pathway gene expression. Second generation offspring also display differential tissue lipid abundance, with profiles similar to those of first generation adults. These findings demonstrate that offspring metabolic homeostasis is perturbed in response to a suboptimal paternal diet with the effects still evident within a second generation.
导致后代父系编程代谢疾病的潜在机制仍未得到明确界定。我们用正常蛋白饮食(NPD;18%蛋白)或等热量低蛋白饮食(LPD;9%蛋白)喂养雄性 C57BL/6 小鼠至少 8 周。通过人工授精,并结合输精管切除术雄性交配,我们用 NPD 或 LPD 精子生成后代,但存在 NPD 或 LPD 精浆。来自 LPD 精子或精液的后代仅在 3 周龄时就表现出体重增加和组织血脂异常。这些变化在成年期更为明显,同时伴有肝代谢和炎症途径基因表达的改变。第二代后代也表现出组织脂质丰度的差异,其谱与第一代成年人相似。这些发现表明,后代的代谢稳态受到亚最佳父系饮食的干扰,即使在第二代中仍能观察到这些影响。