Department of Animal Science and Reproductive and Developmental Sciences Program, Michigan State University , East Lansing, Michigan.
Arkansas Children's Nutrition Center , Little Rock, Arkansas.
Am J Physiol Endocrinol Metab. 2019 Mar 1;316(3):E383-E396. doi: 10.1152/ajpendo.00401.2018. Epub 2019 Jan 2.
Although obesity negatively influences the metabolic homeostasis of cells within a broad range of tissues, its impact on oocyte metabolism is not fully understood. Prior evidence suggests that obesity increases expression of oocyte genes associated with inflammation, oxidative stress, and lipid metabolism; however, the metabolic impact of these genetic differences is not known. To address this gap, we conducted an exploratory assessment of the follicular fluid (FF) metabolome in eight overweight/obese (OW) and nine normal-weight (NW) women undergoing in vitro fertilization. FF and serum were collected and analyzed by untargeted metabolomics using gas chromatography-quadrupole time-of-flight mass spectrometry and charged-surface hybrid column-electrospray ionization quadrupole time-of-flight tandem mass spectrometry. Untargeted metabolomics identified obesity-associated changes in FF metabolites related to oxidative stress/antioxidant capacity, xenometabolism/amino acid biosynthesis, and lipid metabolism. Discriminant FF metabolites included elevated uric acid, isothreonic acid, one unknown primary metabolite, and six unknown complex lipids in OW compared with NW women. Conversely, 2-ketoglucose dimethylacetal, aminomalonate, two unknown primary metabolites, and two unknown complex lipids were decreased in FF of OW relative to NW women. Indole-3-propionic acid (IPA), a bacteria-derived metabolite, was also decreased in both FF and serum of OW women ( P < 0.05). The significant correlation between antioxidant IPA in serum and FF ( R = 0.95, P < 0.0001) suggests a potential serum biomarker of FF antioxidant status or reflection of the gut metabolism interaction with the follicle. These results suggest that obesity has important consequences for the follicular environment during the preconception period, a window of time that may be important for lifestyle interventions to ameliorate obesity-associated risk factors.
虽然肥胖会对广泛组织内的细胞代谢稳态产生负面影响,但它对卵母细胞代谢的影响尚未完全了解。先前的证据表明,肥胖会增加与炎症、氧化应激和脂质代谢相关的卵母细胞基因的表达;然而,这些基因差异的代谢影响尚不清楚。为了解决这一差距,我们对 8 名超重/肥胖(OW)和 9 名正常体重(NW)接受体外受精的女性的卵泡液(FF)代谢组进行了探索性评估。采集 FF 和血清,使用气相色谱-四极杆飞行时间质谱和带电表面混合柱-电喷雾电离四极杆飞行时间串联质谱进行非靶向代谢组学分析。非靶向代谢组学鉴定出与氧化应激/抗氧化能力、异生物质代谢/氨基酸生物合成和脂质代谢相关的 FF 代谢物与肥胖相关的变化。判别性 FF 代谢物包括与 NW 女性相比,OW 女性的 FF 中尿酸、异苏氨酸、一种未知初级代谢物和六种未知复杂脂质升高。相反,2-酮葡萄糖二甲缩醛、氨基丙二酸、两种未知初级代谢物和两种未知复杂脂质在 OW 女性的 FF 中减少。OW 女性的 FF 和血清中吲哚-3-丙酸(IPA),一种细菌衍生的代谢物,也减少(P<0.05)。血清和 FF 中抗氧化 IPA 之间的显著相关性(R=0.95,P<0.0001)表明,IPA 可能是 FF 抗氧化状态的血清生物标志物,或反映肠道代谢与卵泡的相互作用。这些结果表明,肥胖对妊娠前期间卵泡环境有重要影响,这一时间窗口可能对改善肥胖相关危险因素的生活方式干预很重要。