子痫前期胎盘脂质代谢的性别特异性失调

Obstetrics and gynecology research Pub Date : 2024-01-01 Epub Date: 2024-07-23 DOI:10.26502/ogr0159
Jay S Mishra, Hanjie Zhao, Jing Zheng, Sathish Kumar
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摘要

背景:子痫前期(PE)是一种妊娠期高血压疾病,与孕产妇和胎儿的不良结局有关。虽然胎盘功能障碍与子痫前期的发病机制有关,但人们对子痫前期对胎盘脂质代谢的影响及其潜在的性别二形性仍知之甚少:方法:我们对PE妊娠和血压正常妊娠的足月胎盘进行了全面分析。结果:PE 妊娠的胎盘表现出较高的性激素水平,而正常妊娠的胎盘则表现出较低的性激素水平:结果:PE妊娠胎盘中的脂质水平升高,与女性胎盘相比,男性胎盘中的三酰甘油、胆固醇酯和游离胆固醇的增加更为明显。基因表达分析显示了性别上的二态性改变,雄性 PE 胎盘中参与脂肪酸摄取、氧化和酯化的基因上调,而雌性 PE 胎盘则表现出更复杂的反应,某些基因既上调又下调。值得注意的是,男性PE胎盘中过氧体脂肪酸氧化基因上调,而女性PE胎盘中则受到抑制:我们的研究结果揭示了PE胎盘脂质代谢的性别双态性改变,表明男性胎盘可能更容易受到脂毒性的影响。这些发现可能有助于了解 PE 的发病机制,并制定针对不同性别的干预措施,以改善孕产妇和胎儿的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-Specific Dysregulation of Placental Lipid Metabolism in Preeclampsia.

Background: Preeclampsia (PE) is a hypertensive disorder of pregnancy associated with adverse maternal and fetal outcomes. While placental dysfunction is implicated in PE pathogenesis, the impact of PE on placental lipid metabolism and its potential sexual dimorphism remains poorly understood.

Methods: We conducted a comprehensive analysis of term placentas from PE and normotensive pregnancies with male and female fetuses. Lipid profiles were quantified using mass spectrometry, and mRNA expression of genes involved in fatty acid oxidation, esterification, and transport was assessed using qPCR.

Results: Placentas from PE pregnancies exhibited elevated lipid levels, with male placentas showing a more pronounced increase in triacylglycerols, cholesteryl esters, and free cholesterol compared to female placentas. Gene expression analysis revealed sexually dimorphic alterations, with male PE placentas exhibiting upregulation of genes involved in fatty acid uptake, oxidation, and esterification, while female PE placentas showed a more complex response with both upregulation and downregulation of certain genes. Notably, peroxisomal fatty acid oxidation was upregulated in male PE placentas but suppressed in female PE placentas.

Conclusions: Our findings reveal sexually dimorphic alterations in placental lipid metabolism in PE, suggesting that male placentas may be more vulnerable to lipotoxicity. These insights may have implications for understanding the pathogenesis of PE and developing sex-specific interventions to improve maternal and fetal outcomes.

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