Progenies of gestational diabetes mellitus exhibit sex disparity in metabolism after respective therapies of insulin, glibenclamide, and metformin in dams during pregnancy.

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Yao Lu, Yajing Jia, Jing Lu, Juan Liu, Yuxin Xu, Yong Liu, Keyang Chen
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引用次数: 0

Abstract

Background: The aim of this study was to compare the sex-dependent intergenerational effects of insulin, glibenclamide, and metformin on glucose and lipid metabolism in the offspring born to GDM mice.

Methods: The murine GDM was induced by high fat diet. The offspring were grouped based on the treatments in maternal mice. ITT and GTT were performed at 4th and 8th weeks of age, respectively. Serum levels of TC, TG, HDL-C, and LDL-C plus hepatic levels of TG and TC, were respectively determined by enzymatic kits. Western blotting was conducted to detect related proteins in the livers from offspring.

Results: The dyslipidaemia, hepatic lipid abnormality, and insulin insensitivity caused by GDM were persistently normalised in male adult offspring by the respective therapies of insulin, glibenclamide, and metformin during maternal pregnancy. Specifically, the decreases in plasma TC, TG, and LDL-C levels (29%, 37.8%, and 57.7%, respectively, p ˂ .05) and in hepatic lipid contents (TC 31.3% and TG 39.2%, p ˂ .05), the increases in hepatic phosphorylation levels of AKT, CPT1A, PPAR-α, and PPAR-γ (57.1%, 91.7%, 68%, and 173.3%, respectively, p ˂ .05) and the inhibition of G6Pase, PEPCK, and HMGCS1 (35.7%, 68.8%, and 77.3% respectively, p ˂ .05) were still observed in the male offspring born to treated GDM mice from 4th to 8th week of age. Unexpectedly, the aforementioned parameters in female progenies in different groups were not significantly changed compared with controls.

Conclusions: Respective treatments in GDM mice during pregnancy with insulin, glibenclamide, and metformin have the long-term persistent effects in male offspring, while female progenies born to untreated dams showed an autonomous inhibition of intergenerational relay of glucose and lipid dysregulation. Our current findings may imply a sex-dependent strategy of medical care for GDM mothers and their offspring.NoveltiesRespective interventions of insulin, glibenclamide, and metformin on dams exerted the persisted effects on male progenies.Therapies of three drugs on dams had the similarly improved effects in offspring.Female offspring autonomously corrected their dysregulated glucose-lipid metabolism caused by gestational diabetes mellitus (GDM) in dams.

母体在怀孕期间分别使用胰岛素、格列本脲和二甲双胍治疗后,妊娠糖尿病的后代在新陈代谢方面表现出性别差异。
背景:本研究旨在比较胰岛素、格列本脲和二甲双胍对GDM小鼠所生后代葡萄糖和脂质代谢的性别依赖性代间效应:方法:通过高脂饮食诱导小鼠 GDM。方法:通过高脂饮食诱导小鼠 GDM,根据母鼠的治疗方法对子代进行分组。分别在小鼠 4 周龄和 8 周龄时进行 ITT 和 GTT 试验。血清中的 TC、TG、HDL-C 和 LDL-C 含量以及肝脏中的 TG 和 TC 含量分别由酶联试剂盒测定。用 Western 印迹法检测后代肝脏中的相关蛋白质:结果:在母体妊娠期间,通过胰岛素、格列本脲和二甲双胍的治疗,成年男性后代中由 GDM 引起的血脂异常、肝脏脂质异常和胰岛素不敏感持续恢复正常。具体而言,血浆 TC、TG 和 LDL-C 水平的降低(分别为 29%、37.8% 和 57.7%,p ˂ .05)和肝脏脂质含量的降低(TC 31.3% 和 TG 39.2%,p ˂ .05),肝脏 AKT、CPT1A、PPAR-α 和 PPAR-γ 磷酸化水平的升高(57.1%、91.7% 和 68.0%,p ˂ .05),以及胰岛素、格列本脲和二甲双胍对 GDM 引起的胰岛素不敏感性的降低(分别为 29%、37.8% 和 57.7%,p ˂ .05)。在第 4 至第 8 周龄的 GDM 小鼠所生的雄性后代中,仍能观察到 AKT、CPT1A、PPAR-α 和 PPAR-γ 的肝磷酸化水平(分别为 57.1%、91.7%、68% 和 173.3%,p ˂ .05)以及 G6Pase、PEPCK 和 HMGCS1 的抑制水平(分别为 35.7%、68.8% 和 77.3%,p ˂ .05)。意外的是,与对照组相比,不同组别雌性后代的上述参数没有显著变化:结论:胰岛素、格列本脲和二甲双胍对妊娠期GDM小鼠的不同治疗对雄性后代具有长期持续的影响,而未经治疗的母鼠所生的雌性后代则表现出自主抑制血糖和血脂失调代际传递的作用。雌性后代可自主纠正由母体妊娠糖尿病(GDM)引起的糖脂代谢紊乱。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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