代谢组学分析显示,血清半胱氨酸水平在妊娠糖尿病进展过程中有所下降。

IF 5.3 2区 生物学 Q2 CELL BIOLOGY
Mengyu Lai, Jiaomeng Li, Jiaying Yang, Qingli Zhang, Yujia Gong, Yuhang Ma, Fang Fang, Na Li, Yingxiang Zhai, Tingting Shen, Yongde Peng, Jia Liu, Yufan Wang
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引用次数: 0

摘要

妊娠期糖尿病(GDM)是一种与妊娠有关的代谢紊乱疾病,与短期和长期不良健康后果相关,但其发病机制尚未明确阐明。对不同孕期代谢组标记物动态变化的研究可能会揭示 GDM 进展的潜在病理生理学。因此,在本研究中,我们分析了 75 名 GDM 妇女和 75 名糖耐量正常(NGT)妇女在三个妊娠期的代谢概况。我们发现,在 GDM 的发展过程中,38 种代谢物的变化趋势明显不同。具体来说,纵向分析表明,半胱氨酸(Cys)水平在 GDM 发展过程中明显下降。进一步的研究表明,Cys 可能通过抑制磷酸烯醇丙酮酸羧激酶来抑制肝脏葡萄糖生成,从而缓解雌性小鼠在妊娠 14.5 天时的 GDM。综上所述,这些研究结果表明,Cys 代谢途径可能在 GDM 中发挥着关键作用,补充 Cys 是治疗 GDM 患者的一种潜在新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolomic profiling reveals decreased serum cysteine levels during gestational diabetes mellitus progression.

Gestational diabetes mellitus (GDM) is a pregnancy-related metabolic disorder associated with short-term and long-term adverse health outcomes, but its pathogenesis has not been clearly elucidated. Investigations of the dynamic changes in metabolomic markers in different trimesters may reveal the underlying pathophysiology of GDM progression. Therefore, in the present study, we analysed the metabolic profiles of 75 women with GDM and 75 women with normal glucose tolerance throughout the three trimesters. We found that the variation trends of 38 metabolites were significantly changed during GDM development. Specifically, longitudinal analyses revealed that cysteine (Cys) levels significantly decreased over the course of GDM progression. Further study showed that Cys alleviated GDM in female mice at gestational day 14.5, possibly by inhibiting phosphoenolpyruvate carboxykinase to suppress hepatic gluconeogenesis. Taken together, these findings suggest that the Cys metabolism pathway might play a crucial role in GDM and Cys supplementation represents a potential new treatment strategy for GDM patients.

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来源期刊
CiteScore
9.60
自引率
1.80%
发文量
1383
期刊介绍: The Journal of Molecular Cell Biology ( JMCB ) is a full open access, peer-reviewed online journal interested in inter-disciplinary studies at the cross-sections between molecular and cell biology as well as other disciplines of life sciences. The broad scope of JMCB reflects the merging of these life science disciplines such as stem cell research, signaling, genetics, epigenetics, genomics, development, immunology, cancer biology, molecular pathogenesis, neuroscience, and systems biology. The journal will publish primary research papers with findings of unusual significance and broad scientific interest. Review articles, letters and commentary on timely issues are also welcome. JMCB features an outstanding Editorial Board, which will serve as scientific advisors to the journal and provide strategic guidance for the development of the journal. By selecting only the best papers for publication, JMCB will provide a first rate publishing forum for scientists all over the world.
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