首页> 外文期刊>Endocrine journal >Analysis of hepatic gene expression profile in a spontaneous mouse model of type 2 diabetes under a high sucrose diet
【24h】

Analysis of hepatic gene expression profile in a spontaneous mouse model of type 2 diabetes under a high sucrose diet

机译:高蔗糖饮食对自发性2型糖尿病小鼠模型肝基因表达谱的影响

获取原文
获取原文并翻译 | 示例
       

摘要

Both genetic factors and diabetogenic environmental factors, such as a high-sucrose diet (HSD), are involved in the development of type 2 diabetes. In this study, the Nagoya-Shibata-Yasuda (NSY) mouse, an animal model of type 2 diabetes and C3H mice used as controls, were fed a HSD, a high-fat diet (HFD) or a regular diet (RD) from weaning. In C3H mice, HFD significantly increased body weight gain, but maintained glucose tolerance. In contrast, in NSY mice, HSD resulted in increased body weight gain and liver steatosis and increased glucose intolerance to a greater extent than HFD. Furthermore, we performed DNA microarray analysis to detect differences in hepatic gene expression levels in both strains under HSD. We then performed RT-PCR analysis on selected genes to evaluate basal expression level under RD and changes under HSD conditions. HSD-fed NSY, but not C3H mice, exhibited increased hepatic expression levels of Pparg2, an isoform of Pparg as well as G0s2, a target of Pparg, which are known to be adipocyte-specific genes. Compared to RD-fed C3H mice, hepatic expression levels of Kat2b (transcriptional regulation), Hsd3b5 (steroid hormone metabolism) and Cyplbl (bile acid metabolism) were initially lower in RD-fed NSY mice, and were further decreased in HSD-fed NSY mice. Expression of Metallothionein (Mil) and Metallothionein 2 (Mt2) was significantly lower in NSY mice compared to C3H mice, irrespective of dietary condition. These data suggest that elucidation of this heterogeneity in response to HSD might contribute to further understanding of the gene-environment interactions leading to diabetes in humans.
机译:遗传因素和糖尿病形成环境因素(例如高蔗糖饮食(HSD))都参与了2型糖尿病的发展。在这项研究中,对名古屋-柴田-安田(NSY)小鼠(一种2型糖尿病动物模型和C3H小鼠作为对照)进行了HSD,高脂饮食(HFD)或常规饮食(RD)的喂养断奶。在C3H小鼠中,HFD显着增加了体重增加,但维持了葡萄糖耐量。相反,在NSY小鼠中,HSD与HFD相比,导致体重增加和肝脂肪变性增加,以及葡萄糖耐量增加。此外,我们进行了DNA芯片分析,以检测HSD下两个菌株中肝基因表达水平的差异。然后,我们对选定的基因进行了RT-PCR分析,以评估RD下的基础表达水平和HSD条件下的变化。由HSD喂养的NSY,但不是C3H小鼠,表现出肝表达水平升高,Pparg2是Pparg的同种型,而G0s2是Pparg的靶标,已知是脂肪细胞特异性基因。与RD喂养的C3H小鼠相比,Kat2b(转录调节),Hsd3b5(类固醇激素代谢)和Cyplbl(胆汁酸代谢)的肝表达水平最初在RD喂养的NSY小鼠中较低,而在HSD喂养的NSY中进一步降低。老鼠。与C3H小鼠相比,NSY小鼠的金属硫蛋白(Mil)和金属硫蛋白2(Mt2)的表达均显着降低,而与饮食条件无关。这些数据表明,阐明对HSD的异质性可能有助于进一步理解导致人类糖尿病的基因与环境之间的相互作用。

著录项

  • 来源
    《Endocrine journal》 |2013年第3期|261-274|共14页
  • 作者单位

    Department of Geriatric Medicine and Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-Oka, Suita, Osaka 565-0871, Japan,Department of Molecular Endocrinology, Osaka University Graduate School of Medicine, Osaka, Japan;

    Department of Geriatric Medicine and Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-Oka, Suita, Osaka 565-0871, Japan;

    Department of Molecular Endocrinology, Osaka University Graduate School of Medicine, Osaka, Japan;

    Department of Endocrinology, Metabolism and Diabetes, Kinki University School of Medicine, Osaka, Japan;

    Department of Endocrinology, Metabolism and Diabetes, Kinki University School of Medicine, Osaka, Japan;

    Department of Geriatric Medicine and Nephrology, Osaka University Graduate School of Medicine, 2-2 Yamada-Oka, Suita, Osaka 565-0871, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    type 2 diabetes; hepatosteatosis; NSY mouse; high-sucrose diet; hepatic gene expression;

    机译:2型糖尿病;肝脂肪变性NSY小鼠;高蔗糖饮食;肝基因表达;
  • 入库时间 2022-08-18 01:32:45

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号