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全身腺苷酸环化酶 5()缺乏对全身胰岛素敏感性和脂肪组织的影响。

Effects of Whole-Body Adenylyl Cyclase 5 () Deficiency on Systemic Insulin Sensitivity and Adipose Tissue.

机构信息

Medical Center, Medical Department III-Endocrinology, Nephrology, Rheumatology, University of Leipzig, 04103 Leipzig, Germany.

Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG) of the Helmholtz Zentrum München at the University of Leipzig and University Hospital Leipzig, 04103 Leipzig, Germany.

出版信息

Int J Mol Sci. 2021 Apr 21;22(9):4353. doi: 10.3390/ijms22094353.

Abstract

Genome-wide association studies have identified adenylyl cyclase type 5 () as candidate gene for diabetes-related quantitative traits and an increased risk of type 2 diabetes. Mice with a whole-body deletion of do not develop obesity, glucose intolerance and insulin resistance, have improved cardiac function and increased longevity. Here, we investigated knockout mice () to test the hypothesis that changes in adipose tissue (AT) may contribute to the reported healthier phenotype. In contrast to previous reports, we found that deletion of did not confer any physiological or biochemical benefits. However, this unexpected finding allowed us to investigate the effects of depletion on AT independently of lower body weight and a metabolically healthier phenotype. mice exhibited an increased number of smaller adipocytes, lower mean adipocyte size and a distinct AT gene expression pattern with midline 1 () as the most significantly downregulated gene compared to control mice. Our model challenges previously described beneficial effects of deficiency and suggests that targeting Adcy5 does not improve insulin sensitivity and may therefore limit the relevance of ADCY5 as potential drug target.

摘要

全基因组关联研究已经确定腺苷酸环化酶 5()为与糖尿病相关的定量性状和 2 型糖尿病风险增加的候选基因。全身缺失的小鼠不会发生肥胖、葡萄糖不耐受和胰岛素抵抗,心脏功能得到改善,寿命延长。在这里,我们研究了 Adcy5 基因敲除小鼠(),以验证脂肪组织(AT)的变化可能有助于解释报道的更健康表型的假说。与之前的报道相反,我们发现缺失并没有带来任何生理或生化上的益处。然而,这一意外的发现使我们能够在不考虑体重降低和代谢更健康表型的情况下,研究 Adcy5 缺失对 AT 的影响。Adcy5 基因敲除小鼠表现出更多数量的较小脂肪细胞、更小的平均脂肪细胞大小和独特的 AT 基因表达模式,与对照组小鼠相比,中线 1()是下调最显著的基因。我们的 Adcy5 基因敲除小鼠模型挑战了之前描述的 Adcy5 缺乏的有益影响,并表明靶向 Adcy5 并不能提高胰岛素敏感性,因此可能限制了 ADCY5 作为潜在药物靶点的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1387/8122634/ddea142b186c/ijms-22-04353-g001.jpg

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