高脂饮食引起的肥胖和妊娠期 DMBA 暴露会改变卵泡生成和母体卵巢的蛋白质组。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-15 DOI:10.1093/biolre/ioae070
Gulnara Novbatova, Isabelle Fox, Kelsey Timme, Aileen F Keating
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引用次数: 0

摘要

肥胖和接触卵巢毒素会损害女性的生殖健康,据报道,肥胖女性的卵巢毒性比瘦弱女性更大。在妊娠期间,母亲和发育中的胎儿很容易受到这两种物质的影响。7,12-二甲基苯并[a]蒽(DMBA)在碳燃烧过程中释放,包括从香烟、煤炭、化石燃料和森林火灾中释放。本研究探讨了饮食引起的肥胖会增加卵巢对 DMBA 引起的卵巢毒性的敏感性这一假设,并确定了肥胖和 DMBA 暴露在妊娠期对母体卵巢的影响。给雌性 C57BL/6 J 小鼠喂食对照组(CT)或高糖高脂组(HSHF;45% 千卡热量来自脂肪;20% 千卡热量来自蔗糖)饮食,直到体重增加约 30%后再与未暴露的雄性小鼠交配。从妊娠第 7 天开始,小鼠腹腔暴露于载体对照组(玉米油)或 DMBA(1 毫克/千克稀释在玉米油中),持续 7 天,因此分为四组:瘦对照组(LC);瘦 DMBA 暴露组(LD);肥胖对照组(OC);肥胖 DMBA 暴露组(OD)。妊娠肥胖和暴露于 DMBA 会降低脾脏重量或孕酮(P 0.05)。此外,肥胖加剧了 DMBA 的减少(P
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High fat diet-induced obesity and gestational DMBA exposure alter folliculogenesis and the proteome of the maternal ovary†.

Obesity and ovotoxicant exposures impair female reproductive health with greater ovotoxicity reported in obese relative to lean females. The mother and developing fetus are vulnerable to both during gestation. 7,12-dimethylbenz[a]anthracene (DMBA) is released during carbon combustion including from cigarettes, coal, fossil fuels, and forest fires. This study investigated the hypothesis that diet-induced obesity would increase sensitivity of the ovaries to DMBA-induced ovotoxicity and determined impacts of both obesity and DMBA exposure during gestation on the maternal ovary. Female C57BL/6 J mice were fed a control or a High Sugar High Fat (45% kcal from fat; 20% kcal from sucrose) diet until ~30% weight gain was attained before mating with unexposed males. From gestation Day 7, mice were exposed intraperitoneally to either vehicle control (corn oil) or DMBA (1 mg/kg diluted in corn oil) for 7 d. Thus, there were four groups: lean control (LC); lean DMBA exposed; obese control; obese DMBA exposed. Gestational obesity and DMBA exposure decreased (P < 0.05) ovarian and increased liver weights relative to LC dams, but there was no treatment impact (P > 0.05) on spleen weight or progesterone. Also, obesity exacerbated the DMBA reduction (P < 0.05) in the number of primordial, secondary follicles, and corpora lutea. In lean mice, DMBA exposure altered abundance of 21 proteins; in obese dams, DMBA exposure affected 134 proteins while obesity alone altered 81 proteins in the maternal ovary. Thus, the maternal ovary is impacted by DMBA exposure and metabolic status influences the outcome.

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