Biomedical Sciences Research Institute, School of Biomedical Sciences, Ulster University, Coleraine, Northern Ireland, United Kingdom.
Biomedical Sciences Research Institute, School of Biomedical Sciences, Ulster University, Coleraine, Northern Ireland, United Kingdom.
Reprod Biol. 2023 Sep;23(3):100784. doi: 10.1016/j.repbio.2023.100784. Epub 2023 Jun 19.
Obesity is a major cause of infertility in females with a direct correlation between energy intake and reproductive dysfunction. To explore underlying mechanisms, disturbances in reproductive health and incretin/reproductive hormone receptor expression were studied in female Wistar rats fed a high-fat-diet for 20-weeks. Metabolic parameters and ovarian/adrenal gene expression were monitored along with estrous cycling and fertility upon mating. High-fat-feeding significantly increased body weight, plasma insulin and HOMA-IR, indicative of obesity and insulin resistance. Estrous cycles were prolonged compared to normal chow-fed rats, with 50 % having an average cycle length ≥ 7days. Reproductive outcomes revealed high-fat-diet reduced litter size by 48 %, with 16 % rats unable to achieve pregnancy. Furthermore, 80 % of the high-fat group took > 35 days to become pregnant compared to 33 % fed a normal-diet. Also, 35 % of pups born to high-fat-fed rats were eaten by mothers or born dead which was not observed with control rats. These changes were associated with downregulation of Amh, Npy2R and GcgR gene expression in ovaries with upregulation of InsR and Glp-1R genes. In adrenals, Glp-1R, GipR, Npy2R, InsR, GcgR, GshR and Esr-1 genes were upregulated. Histological analysis of high-fat-diet ovaries and adrenals revealed changes in morphology with significantly increased number of cysts and reduced adrenal capsule thickness. Circulating levels of insulin, testosterone and progesterone was significantly higher in high-fat group with reduced FSH levels in plasma. These data demonstrate that high-fat feeding disrupts female reproductive function and suggest important interactions between gut and reproductive hormones in ovaries and adrenals which merit further investigation.
肥胖是女性不孕的主要原因,能量摄入与生殖功能障碍之间存在直接相关性。为了探究其潜在机制,本研究观察了高脂肪饮食喂养 20 周的雌性 Wistar 大鼠的生殖健康和肠促胰岛素/生殖激素受体表达紊乱情况。同时监测了代谢参数和卵巢/肾上腺基因表达,并在交配后监测发情周期和生育能力。高脂肪喂养显著增加了体重、血浆胰岛素和 HOMA-IR,表明存在肥胖和胰岛素抵抗。发情周期与正常喂养大鼠相比延长,50%的大鼠平均周期长度≥7 天。生殖结果显示,高脂肪饮食使胎仔数减少了 48%,16%的大鼠无法怀孕。此外,与正常饮食组相比,80%的高脂肪组大鼠需要>35 天才能怀孕,而正常饮食组仅为 33%。此外,高脂肪喂养组的 35%的幼崽被母亲吃掉或出生后死亡,而对照组未观察到这种情况。这些变化与卵巢中 Amh、Npy2R 和 GcgR 基因表达下调以及 InsR 和 Glp-1R 基因表达上调有关。在肾上腺中,Glp-1R、GipR、Npy2R、InsR、GcgR、GshR 和 Esr-1 基因表达上调。高脂肪饮食卵巢和肾上腺的组织学分析显示形态发生变化,卵泡数量显著增加,肾上腺包膜厚度减少。高脂肪组的循环胰岛素、睾酮和孕酮水平显著升高,血浆中 FSH 水平降低。这些数据表明高脂肪喂养会破坏女性生殖功能,并提示肠道和生殖激素在卵巢和肾上腺之间存在重要相互作用,值得进一步研究。