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纳米硒和/或蜂毒对链脲佐菌素诱导的糖尿病性心肌病和肾病的影响。

Effect of Selenium Nanoparticles and/or Bee Venom against STZ-Induced Diabetic Cardiomyopathy and Nephropathy.

作者信息

Lotfy Mona M, Dowidar Mohamed F, Ali Haytham A, Ghonimi Wael A M, Al-Farga Ammar, Ahmed Amany I

机构信息

Biochemistry Departments, Faculty of Vet. Med., Zagazig University, Zagazig 44519, Egypt.

Department of Biochemistry, College of science, University of Jeddah, Jeddah 23218, Saudi Arabia.

出版信息

Metabolites. 2023 Mar 8;13(3):400. doi: 10.3390/metabo13030400.

Abstract

The main purpose of our study was to examine the role of selenium nanoparticles (SeNPs) and/or bee venom (BV) in ameliorating diabetic cardiomyopathy (DCM) and nephropathy (DN) at the biochemical, histopathological and molecular levels. Fifty male albino rats were used in this experiment, divided into five groups: control, Streptozocin (STZ) diabetic, STZ-diabetic treated with SeNPs, STZ-diabetic treated with BV, and STZ-diabetic treated with SeNPs and BV. Biochemically, STZ injection resulted in a significant increase in serum glucose, BUN, creatinine, CRP, CK-MB, AST, LDH and cardiac troponins with a significant decrease in the serum insulin and albumin concentrations. Histopathologically, STZ injection resulted in diabetes, as revealed by glomerulonephritis, perivascular hemorrhage, inflammatory cell infiltrations and fibrosis, with widening of interstitial spaces of cardiomyocytes, loss of muscle cells continuity and some hyaline degeneration. At the molecular levels, the expression levels of miRNA 328, miRNA-21, TGFβ1, TGFβ1R, JAK1, STST-3, SMAD-1 and NFκβ genes were significantly up-regulated, whereas the expression levels of SMAD-7 were significantly down-regulated. It is concluded that SeNPs and/or BV administration ameliorates the deleterious effects resulting from STZ administration through improving the biochemical, histopathological and molecular effects, suggesting their protective role against the long-term diabetic complications of DCM and DN.

摘要

我们研究的主要目的是在生化、组织病理学和分子水平上,研究硒纳米颗粒(SeNPs)和/或蜂毒(BV)在改善糖尿病性心肌病(DCM)和肾病(DN)方面的作用。本实验使用了50只雄性白化大鼠,分为五组:对照组、链脲佐菌素(STZ)糖尿病组、用SeNPs治疗的STZ糖尿病组、用BV治疗的STZ糖尿病组以及用SeNPs和BV治疗的STZ糖尿病组。生化方面,注射STZ导致血清葡萄糖、尿素氮、肌酐、CRP、肌酸激酶同工酶(CK-MB)、天冬氨酸转氨酶(AST)、乳酸脱氢酶(LDH)和心肌肌钙蛋白显著升高,而血清胰岛素和白蛋白浓度显著降低。组织病理学上,注射STZ导致糖尿病,表现为肾小球肾炎、血管周围出血、炎性细胞浸润和纤维化,心肌细胞间质间隙增宽、肌肉细胞连续性丧失以及一些玻璃样变性。在分子水平上,miRNA 328、miRNA-21、转化生长因子β1(TGFβ1)、TGFβ1受体(TGFβ1R)、Janus激酶1(JAK1)、信号转导与转录激活因子3(STST-3)、SMAD-1和核因子κB(NFκβ)基因的表达水平显著上调,而SMAD-7的表达水平显著下调。结论是,给予SeNPs和/或BV可通过改善生化、组织病理学和分子效应来减轻STZ给药所产生的有害影响,表明它们对DCM和DN的长期糖尿病并发症具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907f/10057804/7c4e1733720d/metabolites-13-00400-g001.jpg

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