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糖尿病肾病使 Wistar 大鼠组织中孤儿受体 GPR149、GPR153、GPR176、TAAR3、TAAR5 和 TAAR9 的组织表达谱发生改变。

Diabetic nephropathy produces alterations in the tissue expression profile of the orphan receptors GPR149, GPR153, GPR176, TAAR3, TAAR5 and TAAR9 in Wistar rats.

机构信息

Departamento de Farmacología, Facultad de Medicina, Universidad Autónoma de Baja California, Mexicali, Baja California, México.

Laboratorio de Señalización Intracelular, Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Ciudad de México, México.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2020;39(8):1150-1161. doi: 10.1080/15257770.2020.1780437. Epub 2020 Jul 9.

Abstract

Diabetes mellitus is a debilitating health care problem affecting 382 million people around the world and one of the most common complications is diabetic nephropathy. For this reason, it is important to try to identify new mechanisms that could be involved in diabetes. A new class of receptors has been reported, called orphan receptors because the associated ligand and signaling cascades are unknown. These receptors could be an important source of targets for the treatment of many diseases such as diabetes and its associated complications like diabetic nephropathy. Therefore, the aim of this work was to study expression of the orphan receptors GPR149, GPR153, GPR176, TAAR3, TAAR5 and TAAR9 in the kidney of diabetic rats. We used male Wistar rats at 10-12 weeks of age. Diabetes was induced by a single dose of streptozotocin (60 mg/kg i.p.). After 4 weeks, tissues were obtained, and the expression of the mRNAs was measured by RT-PCR. Our results showed that the orphan receptors are expressed in a different way in the kidney. In conclusion, we suggest that orphan receptors could be involved in the development of diabetic nephropathy.

摘要

糖尿病是一种影响全球 3.82 亿人的使人衰弱的医疗保健问题,也是最常见的并发症之一。因此,重要的是要尝试确定可能涉及糖尿病的新机制。已经报道了一类新的受体,称为孤儿受体,因为相关的配体和信号级联是未知的。这些受体可能是治疗许多疾病(如糖尿病及其相关并发症,如糖尿病肾病)的重要靶点来源。因此,这项工作的目的是研究孤儿受体 GPR149、GPR153、GPR176、TAAR3、TAAR5 和 TAAR9 在糖尿病大鼠肾脏中的表达。我们使用了 10-12 周龄的雄性 Wistar 大鼠。糖尿病通过单次腹腔注射链脲佐菌素(60mg/kg)诱导。4 周后,获取组织,并通过 RT-PCR 测量 mRNA 的表达。我们的结果表明,孤儿受体在肾脏中的表达方式不同。总之,我们认为孤儿受体可能参与糖尿病肾病的发生。

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