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吡啶甲酸铬对链脲佐菌素诱导糖尿病大鼠肾损伤和肾纤维化的保护作用。

Protective Effects of Chromium Picolinate Against Diabetic-Induced Renal Dysfunction and Renal Fibrosis in Streptozotocin-Induced Diabetic Rats.

机构信息

Vitamin D Research Institute, College of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, Shaanxi 723000, China.

College of Biological Science and Engineering, Shaanxi University of Technology, Hanzhong, Shaanxi 723000, China.

出版信息

Biomolecules. 2020 Mar 4;10(3):398. doi: 10.3390/biom10030398.

Abstract

Diabetic nephropathy (DN) is one of the most important complications of diabetes, and the leading cause of end-stage renal disease (ESRD). While Chromium picolinate (CrPic) supplementation has been found to be effective in treating diabetes, its effects on diabetic-induced nephropathy have not been studied. Therefore, in this study, CrPic (1 mg kg d ) was administered to a DN rat model by oral gavage for eight weeks to investigate its effects. The results show that CrPic supplementation caused a decrease in levels of blood glucose, serum insulin, blood urea nitrogen (BUN), serum creatinine, and urinary albumin in DN rats. It also reversed renal pathological changes, including renal glomerular sclerosis and interstitial fibrosis. In addition, the oxidative defense system in the kidneys of DN rats was found to be improved; the biological activities of superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) increased; and the content of malondialdehyde (MDA) lowered. Immunohistochemical results reveal that the expression levels of renal transforming growth factor-β1 (TGF-β1), Smad 2, and Smad 3 decreased significantly in the kidneys of rats in the CrPic-treated group. CrPic administration was thus found to ameliorate diabetic nephropathy in SD rats via an antioxidative stress mechanism, as well the ability to inhibit TGF-β1/Smad2/3 expression. This study suggests that CrPic could be a potential renal-protective nutrient against diabetic nephropathy.

摘要

糖尿病肾病(DN)是糖尿病最重要的并发症之一,也是终末期肾病(ESRD)的主要原因。虽然已经发现吡啶甲酸铬(CrPic)补充剂在治疗糖尿病方面有效,但它对糖尿病引起的肾病的影响尚未得到研究。因此,在这项研究中,通过口服灌胃向 DN 大鼠模型给予 CrPic(1mgkg-d),持续八周,以研究其作用。结果表明,CrPic 补充可降低 DN 大鼠的血糖、血清胰岛素、血尿素氮(BUN)、血清肌酐和尿白蛋白水平。它还逆转了肾脏的病理变化,包括肾小球硬化和间质纤维化。此外,DN 大鼠肾脏的氧化防御系统得到改善;超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽过氧化物酶(GPX)的生物活性增加;丙二醛(MDA)的含量降低。免疫组织化学结果显示,CrPic 治疗组大鼠肾脏中转化生长因子-β1(TGF-β1)、Smad2 和 Smad3 的表达水平显著降低。因此,CrPic 通过抗氧化应激机制以及抑制 TGF-β1/Smad2/3 表达来改善 SD 大鼠的糖尿病肾病。这项研究表明,CrPic 可能是一种潜在的肾脏保护营养素,可预防糖尿病肾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c2a/7175215/3dedef2f0015/biomolecules-10-00398-g001.jpg

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