首页> 美国卫生研究院文献>Endocrinology >Maternal Dietary Restriction During the Periconceptional Period in Normal-Weight or Obese Ewes Results in Adrenocortical Hypertrophy an Up-Regulation of the JAK/STAT and Down-Regulation of the IGF1R Signaling Pathways in the Adrenal of the Postnatal Lamb
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Maternal Dietary Restriction During the Periconceptional Period in Normal-Weight or Obese Ewes Results in Adrenocortical Hypertrophy an Up-Regulation of the JAK/STAT and Down-Regulation of the IGF1R Signaling Pathways in the Adrenal of the Postnatal Lamb

机译:正常体重或肥胖母羊在围孕期的母亲饮食限制导致肾上腺皮质肥大JAK / STAT的上调和产后羔羊肾上腺的IGF1R信号通路的下调

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摘要

Maternal dietary restriction during the periconceptional period results in an increase in adrenal growth and in the cortisol stress response in the offspring. The intraadrenal mechanisms that result in the programming of these changes are not clear. Activation of the IGF and the signal transducer and activator of transcription (STAT)/suppressors of cytokine signaling (SOCS) pathways regulate adrenal growth. We have used an embryo transfer model in sheep to investigate the impact of exposure to either dietary restriction in normal or obese mothers or to maternal obesity during the periconceptional period on adrenal growth and function in the offspring. We assessed the adrenal abundance of key signaling molecules in the IGF-I and Janus kinase/STAT/SOCS pathways including IGF-I receptor, IGF-II receptor, Akt, mammalian target of rapamycin, ribosomal protein S6, eukaryotic translation initiation factor 4E-binding protein 1, eukaryotic translation initiation factor 4E, STAT1, STAT3, STAT5, SOCS1, and SOCS3 in female and male postnatal lambs. Maternal dietary restriction in the periconceptional period resulted in the hypertrophy of the adrenocortical cells in the zona fasciculata-reticularis and an up-regulation in STAT1, phospho-STAT1, and phospho-STAT3 (Ser727) abundance and a down-regulation in IGF-I receptor, Akt, and phospho-Akt abundance in the adrenal cortex of the postnatal lamb. These studies highlight that weight loss around the time of conception, independent of the starting maternal body weight, results in the activation of the adrenal Janus kinase/STAT pathway and adrenocortical hypertrophy. Thus, signals of adversity around the time of conception have a long-term impact on the mechanisms that regulate adrenocortical growth.
机译:围孕期的母体饮食限制会导致后代肾上腺的生长和皮质醇应激反应的增加。导致这些改变的编程的肾上腺内机制尚不清楚。 IGF的激活以及信号转导和转录激活因子(STAT)/细胞因子信号传导(SOCS)通路的抑制因子调节肾上腺的生长。我们已经在绵羊中使用了胚胎移植模型来研究正常或肥胖母亲的饮食限制或在围孕期暴露于母体肥胖对后代肾上腺生长和功能的影响。我们评估了IGF-I和Janus激酶/ STAT / SOCS途径中关键信号分子的肾上腺丰度,包括IGF-I受体,IGF-II受体,Akt,雷帕霉素哺乳动物靶标,核糖体蛋白S6,真核翻译起始因子4E-雌性和雄性产后羔羊中的结合蛋白1,真核翻译起始因子4E,STAT1,STAT3,STAT5,SOCS1和SOCS3。围孕期的母体饮食限制导致筋膜带状肾上腺皮质细胞肥大,STAT1,磷酸STAT1和磷酸STAT3(Ser727)丰度上调,而IGF-I则下调产后羔羊肾上腺皮质中的受体,Akt和磷酸化Akt丰度。这些研究强调,受孕前后体重的减轻与母体的起始体重无关,导致肾上腺Janus激酶/ STAT通路的激活和肾上腺皮质肥大。因此,受孕前后的逆境信号对调节肾上腺皮质生长的机制具有长期影响。

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