Department of Morphology, Health Sciences Center, Federal University of Espirito Santo, Av. Marechal Campos, 1468, CEP: 290440-090 Vitória, ES, Brazil.
Department of Morphology, Health Sciences Center, Federal University of Espirito Santo, Av. Marechal Campos, 1468, CEP: 290440-090 Vitória, ES, Brazil; Bachelor of Physical Education and Sports, Faculty of Human Sciences and Education, Universidad de los Llanos, Villavicencio-Meta, Colombia.
Reprod Toxicol. 2021 Aug;103:108-123. doi: 10.1016/j.reprotox.2021.06.004. Epub 2021 Jun 5.
Exposure to the obesogen tributyltin (TBT) alone or high carbohydrate diet (HCD) alone leads to obesity and reproductive complications, such as premature ovary failure (POF) features. However, little is known about interactions between TBT and nutrition and their combined impact on reproduction. In this study, we assessed whether acute TBT and HCD exposure results in reproductive and metabolic irregularities. Female rats were treated with TBT (100 ng/kg/day) and fed with HCD for 15 days and metabolic and reproductive outcomes were assessed. TBT and HCD rats displayed metabolic impairments, such as increased adiposity, abnormal lipid profile and triglyceride and glucose (TYG) index, worsening adipocyte hypertrophy in HCD-TBT rats. These metabolic consequences were linked with reproductive disorders. Specifically, HCD-TBT rats displayed irregular estrous cyclicity, high follicle-stimulating hormone (FSH) levels, low anti-Müllerian hormone (AMH) levels, reduction in ovarian reserve, and corpora lutea (CL) number, with increases in atretic follicles, suggesting that HCD-TBT exposure exacerbated POF features. Further, strong negative correlations were observed between adipocyte hypertrophy and ovarian reserve, CL number and AMH levels. HCD-TBT exposure resulted in reproductive tract inflammation and fibrosis. Collectively, these data suggest that TBT plus HCD exposure leads to metabolic and reproductive abnormalities, exacerbating POF features in female rats.
单独暴露于肥胖物三丁基锡(TBT)或高碳水化合物饮食(HCD)单独可导致肥胖和生殖并发症,如卵巢早衰(POF)特征。然而,人们对 TBT 与营养之间的相互作用及其对生殖的综合影响知之甚少。在这项研究中,我们评估了急性 TBT 和 HCD 暴露是否会导致生殖和代谢异常。雌性大鼠接受 TBT(100ng/kg/天)处理并喂食 HCD15 天,评估代谢和生殖结果。TBT 和 HCD 大鼠表现出代谢损伤,如肥胖增加、脂质谱异常和甘油三酯和葡萄糖(TYG)指数升高,HCD-TBT 大鼠的脂肪细胞肥大恶化。这些代谢后果与生殖障碍有关。具体而言,HCD-TBT 大鼠表现出不规则的动情周期、高卵泡刺激素(FSH)水平、低抗苗勒管激素(AMH)水平、卵巢储备减少和黄体(CL)数量减少,同时有闭锁卵泡增加,表明 HCD-TBT 暴露加重了 POF 特征。此外,脂肪细胞肥大与卵巢储备、CL 数量和 AMH 水平之间存在强烈的负相关。HCD-TBT 暴露导致生殖道炎症和纤维化。总之,这些数据表明,TBT 加 HCD 暴露可导致代谢和生殖异常,加重雌性大鼠的 POF 特征。