Miller Sarah J, Hill Kaitlyn, Darby Isabella, Nusrat Fariha, Friedman Jacob E, Rudolph Michael C, Zimmerman Kurt A
Department of Internal Medicine, Division of Nephrology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States.
Department of Biochemistry and Physiology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States.
Am J Physiol Renal Physiol. 2025 Mar 1;328(3):F316-F327. doi: 10.1152/ajprenal.00227.2024. Epub 2025 Feb 5.
Due to the growing obesity epidemic in the United States, it is now estimated that approximately one third of all children are born to obese moms. These data, coupled with data indicating that obesity is associated with accelerated cyst growth in patients with autosomal dominant polycystic kidney disease (ADPKD), led us to hypothesize that maternal obesity may influence the rate of disease progression in offspring. To test this hypothesis, we induced maternal obesity by high-fat diet (HFD) feeding in the orthologous mouse model of ADPKD and followed polycystic kidney disease (PKD) progression in offspring for up to 1 year. Surprisingly, and in contrast to our initial hypothesis, exposure to maternal obesity during pregnancy and lactation did not significantly impact PKD severity in offspring at 3 mo or 1 yr of age. In contrast, reexposure to HFD for ∼3 m beginning at 12 wk of age worsened PKD severity in female, but not male, offspring born to obese dams as measured by cystic index, cyst number, and cyst area. Despite worsened cystic parameters, fibrosis and blood urea nitrogen were not altered in these animals. Collectively, these findings indicate that maternal obesity may accelerate PKD severity in female offspring exposed to an obesogenic diet. Due to the growing obesity pandemic, almost one third of all children are born to mothers with obesity; however, the impact of maternal obesity on polycystic kidney disease (PKD) is unknown. In this manuscript, we found that maternal obesity did not worsen PKD severity in mice at 3 mo or 1 yr of age when weaned onto normal chow diet. However, rechallenging pups born to obese mothers worsened PKD severity in female but not male mice.
由于美国肥胖症流行情况日益严重,目前估计约三分之一的儿童母亲为肥胖者。这些数据,再加上表明肥胖与常染色体显性多囊肾病(ADPKD)患者囊肿生长加速相关的数据,促使我们提出假设,即母亲肥胖可能会影响后代的疾病进展速度。为了验证这一假设,我们通过在ADPKD的直系同源小鼠模型中喂食高脂饮食(HFD)来诱发母鼠肥胖,并追踪后代多囊肾病(PKD)长达1年的进展情况。令人惊讶的是,与我们最初的假设相反,在怀孕和哺乳期接触母鼠肥胖并未对3个月或1岁后代的PKD严重程度产生显著影响。相比之下,从12周龄开始再次接触HFD约3个月,会使肥胖母鼠所生雌性后代(而非雄性后代)的PKD严重程度恶化,这通过囊肿指数、囊肿数量和囊肿面积来衡量。尽管囊肿参数恶化,但这些动物的纤维化和血尿素氮并未改变。总体而言,这些发现表明,母亲肥胖可能会加速接触致肥胖饮食的雌性后代的PKD严重程度。由于肥胖症大流行日益严重,几乎三分之一的儿童母亲患有肥胖症;然而,母亲肥胖对多囊肾病(PKD)的影响尚不清楚。在本论文中,我们发现当断奶后喂食正常食物时,母亲肥胖在3个月或1岁的小鼠中并未使PKD严重程度恶化。然而,再次挑战肥胖母亲所生的幼崽会使雌性而非雄性小鼠的PKD严重程度恶化。