首页> 外文期刊>Journal of diabetes research. >Expression of CTRP3, a Novel Adipokine, in Rats at Different Pathogenic Stages of Type 2 Diabetes Mellitus and the Impacts of GLP-1 Receptor Agonist on It
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Expression of CTRP3, a Novel Adipokine, in Rats at Different Pathogenic Stages of Type 2 Diabetes Mellitus and the Impacts of GLP-1 Receptor Agonist on It

机译:CTRP3,一种新型己酮,在2型糖尿病的不同致病阶段的大鼠中的表达及GLP-1受体激动剂对其的影响

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摘要

This study aimed to investigate the expression of C1q/TNF-related protein-3 (CTRP3) in rats at different pathogenic stages of type 2 diabetes mellitus (T2DM) and the impacts of glucagon-like peptide-1 (GLP-1) receptor agonist on it. Male wistar rats were fed with high-fat diet for 10 weeks to induce insulin resistance (IR) and then were given low-dose streptozotocin (STZ) intraperitoneal injection to induce T2DM. Exendin-4 (Ex-4), a GLP-1 receptor agonist, was subcutaneous injected to the IR rats and T2DM rats for 4 weeks. The expression of CTRP3 mRNA and protein in epididymis adipose tissue of rats at the stage of IR was lower significantly than that of normal control (NC) rats and decreased more when they were at the stage of overt T2DM (all P < 0.05 or P < 0.01). After the treatment with Ex-4, the mRNA and protein expressions of CTRP3 were increased by 15.5% (P < 0.01) and 14.8% (P < 0.05), respectively, in IR rats and increased by 20.6% (P < 0.01) and 16.5% (P < 0.05), respectively, in T2DM rats. Overall, this study found that the expression of CTRP3 in visceral adipose tissue was progressively decreased in a T2DM rat model from the pathogenic stage of IR to overt diabetes, while Ex-4 treatment increased its expression in such animals.
机译:本研究旨在探讨2型糖尿病(T2DM)不同致病阶段的大鼠C1Q / TNF相关蛋白-3(CTRP3)的表达及胰高血糖素肽-1(GLP-1)受体激动剂的影响在上面。雄性Wistar大鼠用高脂饮食喂食10周,以诱导胰岛素抵抗(IR),然后给予低剂量链脲佐菌素(STZ)腹膜内注射以诱导T2DM。 exendin-4(前4),一种GLP-1受体激动剂,被皮下注射到IR大鼠和T2DM大鼠4周。在IR阶段的大鼠脂肪组织中的CtrP3 mRNA和蛋白质的表达明显低于正常对照(NC)大鼠的大鼠,并且当它们处于公开T2DM的阶段时减少(所有P <0.05或P <0. 0.01)。用EX-4治疗后,CTRP3的mRNA和蛋白表达分别增加15.5%(P <0.01)和14.8%(P <0.05),在IR大鼠中,增加20.6%(P <0.01)和分别在T2DM大鼠中分别为16.5%(P <0.05)。总体而言,该研究发现,从IR的致病性阶段的T2DM大鼠模型中,从IR到公开糖尿病的致病阶段,Ctrp3在内脏脂肪组织中的表达逐渐减少,而前4种治疗增加了其在这些动物中的表达。

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  • 来源
    《Journal of diabetes research.》 |2014年第2期|共6页
  • 作者单位

    Wuhan Univ Zhongnan Hosp Dept Endocrinol Wuhan 430071 Peoples R China;

    Wuhan Univ Zhongnan Hosp Dept Internal Med Wuhan 430071 Peoples R China;

    Wuhan Univ Zhongnan Hosp Dept Endocrinol Wuhan 430071 Peoples R China;

    Wuhan Univ Zhongnan Hosp Dept Endocrinol Wuhan 430071 Peoples R China;

    Wuhan Univ Zhongnan Hosp Dept Endocrinol Wuhan 430071 Peoples R China;

    Wuhan Univ Zhongnan Hosp Dept Endocrinol Wuhan 430071 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 内分泌腺疾病及代谢病;
  • 关键词

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