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Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats
OBJECTIVE(S): Some pathologic situations such as diabetes and metabolic syndrome are associated with alternation in nitric oxide level. Incidence of these condition increases with aging. On the other hand, insulin secretion is modulated by nitric oxide, and nitric oxide synthase (NOS) activity is al...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366721/ https://www.ncbi.nlm.nih.gov/pubmed/25810884 |
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author | Farrokhfall, Khadije Hashtroudi, Mehri Seyed Ghasemi, Asghar Mehrani, Hossein |
author_facet | Farrokhfall, Khadije Hashtroudi, Mehri Seyed Ghasemi, Asghar Mehrani, Hossein |
author_sort | Farrokhfall, Khadije |
collection | PubMed |
description | OBJECTIVE(S): Some pathologic situations such as diabetes and metabolic syndrome are associated with alternation in nitric oxide level. Incidence of these condition increases with aging. On the other hand, insulin secretion is modulated by nitric oxide, and nitric oxide synthase (NOS) activity is also altered in diabetes. In this study, modification in the enzyme activity associated with aging and also optimized procedure for islet NOS assay was investigated. MATERIALS AND METHODS: Male Wistar rats were randomly divided in two experimental groups: A: adult rats; were 4 month old and B: old rats; were 12 month old. In all groups, plasma glucose, insulin and NO(X) (nitrite + nitrate = NO(X)) were measured, and also insulin secretion in isolated pancreatic islet with or without L-NAME was investigated. Furthermore, the inducible NOS activity with L-citrulline measurement in islets was measured. RESULTS: L-citrulline was quantified using one step HPLC column. Aging induced hyperglycemia (P<0.05) and excess plasma NO(X) (17.74 ± 1.664 and 26.25 ± 2.166 μmol/l in A and B groups respectively, P<0.05) with unaltered plasma insulin. Islet insulin secretion was significantly reduced in aging rats. L-NAME induced islet insulin secretion especially in aging rats (P=0.003). Inducible NOS activity in islets of aging rats was significantly higher than adult rats (1.082 ± 0.084 and 6.277 ± 0.475 pmol/min per mg protein in adult and aging rats, respectively, P<0.001). CONCLUSION: These findings show that decreased in islet insulin secretion may be related to increase in iNOS activity in islets, which follows impaired carbohydrate metabolism in aging. |
format | Online Article Text |
id | pubmed-4366721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-43667212015-03-25 Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats Farrokhfall, Khadije Hashtroudi, Mehri Seyed Ghasemi, Asghar Mehrani, Hossein Iran J Basic Med Sci Original Article OBJECTIVE(S): Some pathologic situations such as diabetes and metabolic syndrome are associated with alternation in nitric oxide level. Incidence of these condition increases with aging. On the other hand, insulin secretion is modulated by nitric oxide, and nitric oxide synthase (NOS) activity is also altered in diabetes. In this study, modification in the enzyme activity associated with aging and also optimized procedure for islet NOS assay was investigated. MATERIALS AND METHODS: Male Wistar rats were randomly divided in two experimental groups: A: adult rats; were 4 month old and B: old rats; were 12 month old. In all groups, plasma glucose, insulin and NO(X) (nitrite + nitrate = NO(X)) were measured, and also insulin secretion in isolated pancreatic islet with or without L-NAME was investigated. Furthermore, the inducible NOS activity with L-citrulline measurement in islets was measured. RESULTS: L-citrulline was quantified using one step HPLC column. Aging induced hyperglycemia (P<0.05) and excess plasma NO(X) (17.74 ± 1.664 and 26.25 ± 2.166 μmol/l in A and B groups respectively, P<0.05) with unaltered plasma insulin. Islet insulin secretion was significantly reduced in aging rats. L-NAME induced islet insulin secretion especially in aging rats (P=0.003). Inducible NOS activity in islets of aging rats was significantly higher than adult rats (1.082 ± 0.084 and 6.277 ± 0.475 pmol/min per mg protein in adult and aging rats, respectively, P<0.001). CONCLUSION: These findings show that decreased in islet insulin secretion may be related to increase in iNOS activity in islets, which follows impaired carbohydrate metabolism in aging. Mashhad University of Medical Sciences 2015-02 /pmc/articles/PMC4366721/ /pubmed/25810884 Text en Copyright: © Iranian Journal of Basic Medical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Farrokhfall, Khadije Hashtroudi, Mehri Seyed Ghasemi, Asghar Mehrani, Hossein Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title | Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title_full | Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title_fullStr | Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title_full_unstemmed | Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title_short | Comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
title_sort | comparison of inducible nitric oxide synthase activity in pancreatic islets of young and aged rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366721/ https://www.ncbi.nlm.nih.gov/pubmed/25810884 |
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