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女性出生时体型小对其日后生活代谢性疾病风险的影响。

Effect of pregnancy for females born small on later life metabolic disease risk.

机构信息

Department of Physiology, The University of Melbourne, Melbourne, Victoria, Australia.

出版信息

PLoS One. 2012;7(9):e45188. doi: 10.1371/journal.pone.0045188. Epub 2012 Sep 13.

Abstract

There is a strong inverse relationship between a females own birth weight and her subsequent risk for gestational diabetes with increased risk of developing diabetes later in life. We have shown that growth restricted females develop loss of glucose tolerance during late pregnancy with normal pancreatic function. The aim of this study was to determine whether growth restricted females develop long-term impairment of metabolic control after an adverse pregnancy adaptation. Uteroplacental insufficiency was induced by bilateral uterine vessel ligation (Restricted) or sham surgery (Control) in late pregnancy (E18) in F0 female rats. F1 Control and Restricted female offspring were mated with normal males and allowed to deliver (termed Ex-Pregnant). Age-matched Control and Restricted Virgins were also studied and glucose tolerance and insulin secretion were determined. Pancreatic morphology and hepatic glycogen and triacylglycerol content were quantified respectively. Restricted females were born lighter than Control and remained lighter at all time points studied (p<0.05). Glucose tolerance, first phase insulin secretion and liver glycogen and triacylglycerol content were not different across groups, with no changes in β-cell mass. Second phase insulin secretion was reduced in Restricted Virgins (-34%, p<0.05) compared to Control Virgins, suggestive of enhanced peripheral insulin sensitivity but this was lost after pregnancy. Growth restriction was associated with enhanced basal hepatic insulin sensitivity, which may provide compensatory benefits to prevent adverse metabolic outcomes often associated with being born small. A prior pregnancy was associated with reduced hepatic insulin sensitivity with effects more pronounced in Controls than Restricted. Our data suggests that pregnancy ameliorates the enhanced peripheral insulin sensitivity in growth restricted females and has deleterious effects for hepatic insulin sensitivity, regardless of maternal birth weight.

摘要

女性自身的出生体重与妊娠糖尿病风险呈强烈负相关,出生体重越低,日后患糖尿病的风险越高。我们已经表明,生长受限的女性在妊娠晚期会出现葡萄糖耐量丧失,而胰腺功能正常。本研究旨在确定生长受限的女性在经历不良妊娠适应后是否会长期出现代谢控制受损。在妊娠晚期(E18),通过双侧子宫血管结扎(受限)或假手术(对照)诱导子宫胎盘不足,在 F0 雌性大鼠中。F1 对照组和受限组雌性后代与正常雄性交配并允许分娩(称为 Ex-Pregnant)。还研究了年龄匹配的对照组和受限组处女,并测定了葡萄糖耐量和胰岛素分泌。分别定量胰腺形态和肝糖原和三酰基甘油含量。受限组的出生体重比对照组轻,在所有研究的时间点都保持较轻(p<0.05)。葡萄糖耐量、第一相胰岛素分泌以及肝糖原和三酰基甘油含量在各组之间没有差异,β细胞质量没有变化。与对照组处女相比,受限组处女的第二相胰岛素分泌减少(-34%,p<0.05),提示外周胰岛素敏感性增强,但在妊娠后丧失。生长受限与增强的基础肝胰岛素敏感性相关,这可能提供代偿性益处,以防止与出生体重低相关的不良代谢结局。先前的妊娠与肝胰岛素敏感性降低有关,对照组的影响比受限组更明显。我们的数据表明,妊娠改善了生长受限女性的外周胰岛素敏感性,并且对肝胰岛素敏感性具有有害影响,而与母体出生体重无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3be/3441641/3f26ebba22a3/pone.0045188.g001.jpg

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