Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes

Objective(s): Chronic hyperglycemia leads to activation of the advanced glycation end products (AGE)-receptor (RAGE) for AGE axis and oxidative stress, which promote diabetic renal damage. This study examines the effect of insulin-loaded trimethyl chitosan nanoparticles on the kidney tissue of diabe...

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Main Authors: Shirin Heidarisasan, Nasrin Ziamajidi, Jamshid Karimi, Roghayeh Abbasalipourkabir
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2018-10-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
AGE
Online Access:http://ijbms.mums.ac.ir/article_11328_5c92dea126b54cbbea11c64f99985ee8.pdf
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spelling doaj-d543d1e707a64277a60b18352d7b4fc32020-11-24T23:56:42ZengMashhad University of Medical SciencesIranian Journal of Basic Medical Sciences 2008-38662008-38742018-10-0121101035104210.22038/ijbms.2018.28463.689911328Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetesShirin Heidarisasan0Nasrin Ziamajidi1Jamshid Karimi2Roghayeh Abbasalipourkabir3Department of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IranDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IranDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IranDepartment of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, IranObjective(s): Chronic hyperglycemia leads to activation of the advanced glycation end products (AGE)-receptor (RAGE) for AGE axis and oxidative stress, which promote diabetic renal damage. This study examines the effect of insulin-loaded trimethyl chitosan nanoparticles on the kidney tissue of diabetic rats. Materials and Methods: Twenty-five male Wistar rats were randomly divided into 5 groups: normal control (C), diabetic group without treatment (DM), diabetic group treated with chitosan-based nanoparticle (DM+NP, 1 ml by gavage), diabetic group treated with 8 IU/kg insulin-loaded trimethyl chitosan nanoparticles (DM+N.in, 1 ml by gavage), and diabetic group treated with 8 IU/kg trade insulin (DM+SC.in, 0.2 ml by subcutaneous injection). The animals were treated from weeks 8 to 10. At the end of the study, serum urea, creatinine, and uric acid were measured. Also, the level of AGE and RAGE mRNA expression, and oxidative stress markers were studied in the kidney tissue.Results: Insulin-loaded nanoparticles similar to trade insulin could significantly reduce urea, creatinine, and uric acid parameters, while the elevated total antioxidant capacity (TAC), thiol groups, and catalase activity also reduced total oxidant status (TOS) and malondialdehyde (MDA) levels (Phttp://ijbms.mums.ac.ir/article_11328_5c92dea126b54cbbea11c64f99985ee8.pdfAGEAntioxidantDiabetes mellitusInsulinNanoparticlesOxidant
collection DOAJ
language English
format Article
sources DOAJ
author Shirin Heidarisasan
Nasrin Ziamajidi
Jamshid Karimi
Roghayeh Abbasalipourkabir
spellingShingle Shirin Heidarisasan
Nasrin Ziamajidi
Jamshid Karimi
Roghayeh Abbasalipourkabir
Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
Iranian Journal of Basic Medical Sciences
AGE
Antioxidant
Diabetes mellitus
Insulin
Nanoparticles
Oxidant
author_facet Shirin Heidarisasan
Nasrin Ziamajidi
Jamshid Karimi
Roghayeh Abbasalipourkabir
author_sort Shirin Heidarisasan
title Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
title_short Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
title_full Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
title_fullStr Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
title_full_unstemmed Effects of insulin-loaded chitosan-alginate nanoparticle on RAGE expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
title_sort effects of insulin-loaded chitosan-alginate nanoparticle on rage expression and oxidative stress status in the kidney tissue of rats with type 1 diabetes
publisher Mashhad University of Medical Sciences
series Iranian Journal of Basic Medical Sciences
issn 2008-3866
2008-3874
publishDate 2018-10-01
description Objective(s): Chronic hyperglycemia leads to activation of the advanced glycation end products (AGE)-receptor (RAGE) for AGE axis and oxidative stress, which promote diabetic renal damage. This study examines the effect of insulin-loaded trimethyl chitosan nanoparticles on the kidney tissue of diabetic rats. Materials and Methods: Twenty-five male Wistar rats were randomly divided into 5 groups: normal control (C), diabetic group without treatment (DM), diabetic group treated with chitosan-based nanoparticle (DM+NP, 1 ml by gavage), diabetic group treated with 8 IU/kg insulin-loaded trimethyl chitosan nanoparticles (DM+N.in, 1 ml by gavage), and diabetic group treated with 8 IU/kg trade insulin (DM+SC.in, 0.2 ml by subcutaneous injection). The animals were treated from weeks 8 to 10. At the end of the study, serum urea, creatinine, and uric acid were measured. Also, the level of AGE and RAGE mRNA expression, and oxidative stress markers were studied in the kidney tissue.Results: Insulin-loaded nanoparticles similar to trade insulin could significantly reduce urea, creatinine, and uric acid parameters, while the elevated total antioxidant capacity (TAC), thiol groups, and catalase activity also reduced total oxidant status (TOS) and malondialdehyde (MDA) levels (P
topic AGE
Antioxidant
Diabetes mellitus
Insulin
Nanoparticles
Oxidant
url http://ijbms.mums.ac.ir/article_11328_5c92dea126b54cbbea11c64f99985ee8.pdf
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