Suppr超能文献

可可摄入量通过改善葡萄糖稳态来减轻 Zucker 糖尿病肥胖大鼠的肾脏损伤。

Cocoa intake attenuates renal injury in Zucker Diabetic fatty rats by improving glucose homeostasis.

机构信息

Department of Metabolism and Nutrition, Institute of Food Science and Technology and Nutrition (ICTAN), Consejo Superior de Investigaciones Científicas (CSIC), José Antonio Novais 10, Ciudad Universitaria, 28040, Madrid, Spain.

Sección Departamental de Fisiología. Facultad de Farmacia, Universidad Complutense de Madrid (UCM), Spain.

出版信息

Food Chem Toxicol. 2019 May;127:101-109. doi: 10.1016/j.fct.2019.03.002. Epub 2019 Mar 7.

Abstract

Glucotoxicity (high levels of glucose) is a major factor in the pathogenesis of diabetic kidney disease. Cocoa has anti-diabetic effects by lowering glucose levels. However, whether cocoa exerts beneficial effects on the renal cortex glucose homeostasis and the molecular mechanisms responsible for this possible protective activity remain largely unknown. Thus, the potential anti-diabetic properties of cocoa on insulin signalling, glucose transporters and gluconeogenic enzymes were evaluated in the renal cortex of Zucker Diabetic fatty (ZDF) rats. Male ZDF rats were fed a control or cocoa-rich diet (10%), and Zucker Lean animals received the control diet. ZDF rats supplemented with cocoa (ZDF-Co) showed decreased body weight gain, glucose and insulin levels, improved glucose tolerance, insulin resistance and structural alterations in renal cortex. Moreover, cocoa-rich diet ameliorated insulin resistance by reverting decreased tyrosine-phosphorylated-insulin receptor levels and by preventing the inactivation of glycogen synthase kinase-3/glycogen synthase pathway (GSK-3/GS) in the renal cortex of ZDF-Co rats. Cocoa antihyperglycaemic effect also appeared to be mediated through the diminution of phosphoenolpyruvate-carboxykinase (PEPCK), glucose-6-phosphatase (G-6-Pase), sodium-glucose-co-transporter-2 (SGLT-2), and glucose-transporter-2 (GLUT-2) levels in ZDF-Co rat's renal cortex. These findings demonstrate that cocoa alleviates renal injury by contributing to maintain the glucose homeostasis in type 2 diabetic ZDF rats.

摘要

高血糖(葡萄糖水平升高)是糖尿病肾病发病机制中的一个主要因素。可可具有降血糖作用,因此对糖尿病有治疗作用。然而,可可是否对肾皮质葡萄糖稳态具有有益作用,以及负责这种可能的保护活性的分子机制在很大程度上仍然未知。因此,在 Zucker 糖尿病肥胖(ZDF)大鼠的肾皮质中评估了可可对胰岛素信号、葡萄糖转运蛋白和糖异生酶的潜在抗糖尿病特性。雄性 ZDF 大鼠喂食对照或富含可可的饮食(10%),Zucker 瘦型动物接受对照饮食。补充可可的 ZDF 大鼠(ZDF-Co)体重增加减少,葡萄糖和胰岛素水平降低,葡萄糖耐量、胰岛素抵抗和肾皮质结构改变得到改善。此外,富含可可的饮食通过恢复降低的酪氨酸磷酸化胰岛素受体水平和防止 ZDF-Co 大鼠肾皮质中糖原合酶激酶-3/糖原合酶途径(GSK-3/GS)失活来改善胰岛素抵抗。可可的降血糖作用似乎也通过降低磷酸烯醇丙酮酸羧激酶(PEPCK)、葡萄糖-6-磷酸酶(G-6-Pase)、钠-葡萄糖协同转运蛋白-2(SGLT-2)和葡萄糖转运蛋白-2(GLUT-2)在 ZDF-Co 大鼠肾皮质中的水平来介导。这些发现表明,可可通过有助于维持 2 型糖尿病 ZDF 大鼠的葡萄糖稳态来减轻肾脏损伤。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验