Skaznik-Wikiel Malgorzata E, Swindle Delaney C, Allshouse Amanda A, Polotsky Alex J, McManaman James L
Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Colorado School of Medicine, Aurora, Colorado
Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, University of Colorado School of Medicine, Aurora, Colorado.
Biol Reprod. 2016 May;94(5):108. doi: 10.1095/biolreprod.115.137414. Epub 2016 Mar 30.
Excess calorie consumption, particularly of a diet high in fat, is a risk factor for both obesity and reproductive disorders. Animal model studies indicate that elevated dietary fat can influence some reproductive functions independent of obesity. In the current study we sought to determine whether a high-fat diet (HFD) impacts ovarian function, long-term fertility, and local and systemic markers of inflammation independent of obesity. Five-week-old mice were fed either low-fat diet (control group-LF-Ln) or HFD for 10 wk and were divided based on body weight into high-fat obese (HF-Ob: >25 g) and high-fat lean (HF-Ln: <22 g). Ovaries were collected to assess ovarian follicles and to determine the degree of local inflammation. Serum proinflammatory cytokines were also measured. A group of animals was followed for breeding trials for 5 mo while being exposed to LFD or HFD. We found that both 10-wk and 32-wk exposure to HFD resulted in depleted primordial follicles regardless of obesity phenotype. Macrophage counts revealed increased tissue inflammation in the ovary independent of obesity. In addition, serum proinflammatory cytokines were increased in HF-Ln and HF-Ob in comparison to LF-Ln mice. Moreover, HFD had a sustained effect on litter production rate and number of pups per litter regardless of obese phenotype. This study describes for the first time that exposure to HFD causes significant reduction in primordial follicles, compromised fertility, produced higher proinflammatory cytokine levels, and increased ovarian macrophage infiltration, independent of obesity. The negative effects of HFD on primordial follicles may be mediated by increased tissue inflammation.
热量摄入过多,尤其是高脂肪饮食,是肥胖和生殖障碍的一个风险因素。动物模型研究表明,饮食中脂肪含量升高可独立于肥胖影响某些生殖功能。在本研究中,我们试图确定高脂饮食(HFD)是否会独立于肥胖影响卵巢功能、长期生育能力以及局部和全身炎症标志物。将5周龄的小鼠喂食低脂饮食(对照组-LF-Ln)或HFD 10周,并根据体重分为高脂肥胖组(HF-Ob:>25克)和高脂瘦小鼠组(HF-Ln:<22克)。收集卵巢以评估卵巢卵泡并确定局部炎症程度。还测量了血清促炎细胞因子。一组动物在暴露于LFD或HFD的同时进行5个月的繁殖试验。我们发现,无论肥胖表型如何,10周和32周暴露于HFD都会导致原始卵泡减少。巨噬细胞计数显示,卵巢组织炎症增加,与肥胖无关。此外,与LF-Ln小鼠相比,HF-Ln和HF-Ob组的血清促炎细胞因子增加。此外,无论肥胖表型如何,HFD对产仔率和每窝幼崽数量都有持续影响。本研究首次描述了暴露于HFD会导致原始卵泡显著减少、生育能力受损、促炎细胞因子水平升高以及卵巢巨噬细胞浸润增加,且与肥胖无关。HFD对原始卵泡的负面影响可能是由组织炎症增加介导的。