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Transcriptome profiling of visceral adipose tissue in a novel obese rat model, WNIN/Ob & its comparison with other animal models

机译:新型肥胖大鼠模型WNIN / Ob内脏脂肪组织的转录组分析及其与其他动物模型的比较

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Background & objectives: Adipose tissue dysfunction in obesity is linked to the development of type 2 diabetes and cardiovascular diseases. We studied the differential gene expression in retroperitoneal adipose tissue of a novel obese rat model, WNIN/Ob, to understand the possible underlying transcriptional changes involved in the development of obesity and associatedcomorbidities in this model. Methods: Four month old, male WNIN/Ob lean and obese rats were taken, blood was collected and tissues were dissected. Body composition analysis and adipose tissue histology were performed. Global gene expression in retroperitoneal adipose tissue of lean and obese rats was studied by microarray using Affymetrix GeneChips. Results: One thousand and seventeen probe sets were downregulated and 963 probe sets were upregulated (more than two-fold) in adipose tissue of WNIN/Ob obese rats when compared to that of lean rats. Small nucleolar RNA (SnoRNA) made most of the underexpressed probe sets, whereas immune system-related genes werethe most overexpressed in the adipose tissues of obese rats. Genes coding for cytoskeletal proteinswere downregulated, whereas genes related to lipid biosynthesis were elevated in the adipose tissue of obese rats. Interpretation & conclusions: Majority of the altered genes and pathways in adipose tissue of WNIN/Ob obese rats were similar to the observations in other obese animal models and human obesity. Based on these observations, it is proposed that WNIN/Ob obese rat model may be a good model to study the mechanisms involved in the development of obesity and its comorbidities. Downregulation of SnoRNA appears to be a novel feature in this obese rat model.
机译:背景与目的:肥胖中的脂肪组织功能障碍与2型糖尿病和心血管疾病的发展有关。我们研究了新型肥胖大鼠模型WNIN / Ob在腹膜后脂肪组织中的差异基因表达,以了解在该模型中肥胖症和相关合并症的发展中可能涉及的潜在转录变化。方法:取4个月大的WNIN / Ob雄性肥胖和肥胖的大鼠,收集血液并解剖组织。进行身体成分分析和脂肪组织的组织学。使用Affymetrix GeneChips基因芯片研究了瘦和肥胖大鼠腹膜后脂肪组织中的整体基因表达。结果:与瘦大鼠相比,WNIN / Ob肥胖大鼠脂肪组织中的117个探针组被下调,而963个探针组被上调(两倍以上)。小核仁RNA(SnoRNA)构成了大多数表达不足的探针集,而与免疫系统相关的基因在肥胖大鼠的脂肪组织中表达最多。肥胖大鼠脂肪组织中编码细胞骨架蛋白的基因被下调,而与脂质生物合成相关的基因被升高。解释与结论:WNIN / Ob肥胖大鼠脂肪组织中基因和途径的大多数改变与其他肥胖动物模型和人类肥胖中的观察结果相似。基于这些观察结果,提出WNIN / Ob肥胖大鼠模型可能是研究肥胖症及其合并症发展机制的良好模型。 SnoRNA的下调似乎是这种肥胖大鼠模型中的新功能。

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