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Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney
OBJECTIVE: To investigate the association of hypertension coexisting with diabetes mellitus with oxidative stress and inflammation in the kidneys of streptozotocin (STZ)-induced diabetic rats. MATERIALS AND METHODS: Male Wistar rats were used for the experiments. Blood glucose (BG), urea, blood pres...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242028/ https://www.ncbi.nlm.nih.gov/pubmed/28163536 http://dx.doi.org/10.4103/0976-500X.195898 |
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author | Muthaian, Rupadevi Pakirisamy, Rajaa Muthu Parasuraman, Subramani Raveendran, Ramasamy |
author_facet | Muthaian, Rupadevi Pakirisamy, Rajaa Muthu Parasuraman, Subramani Raveendran, Ramasamy |
author_sort | Muthaian, Rupadevi |
collection | PubMed |
description | OBJECTIVE: To investigate the association of hypertension coexisting with diabetes mellitus with oxidative stress and inflammation in the kidneys of streptozotocin (STZ)-induced diabetic rats. MATERIALS AND METHODS: Male Wistar rats were used for the experiments. Blood glucose (BG), urea, blood pressure (BP), and heart rate (HR) were analyzed before and 48 h after STZ injection. Further, these parameters were monitored up to 3 months of diabetes induction. Subsequently, the inflammatory markers (C-reactive protein, tumor necrosis factor-alpha, and nitrate) and oxidative stress markers were estimated after 3 months of diabetes induction in the kidney homogenate. Histological analysis of renal tissue was also carried out. RESULTS: Linear elevation of BG, urea, mean arterial pressure (MAP), and HR was observed up to 3 months of diabetes induction. In the same manner, inflammatory and oxidative stress markers were also found to be significantly increased. Notably, the histological analysis revealed the signs of nephropathy such as increased mesangial cell number, thickness of basement membrane, and renal artery. Inflammatory and oxidative stress markers positively correlated with elevated BP and BG, but the correlation was better with BP rather than BG. CONCLUSION: Hypertension has a strong implication in the increased oxidative stress and inflammation of diabetic kidney at the very early stage of diabetes mellitus. |
format | Online Article Text |
id | pubmed-5242028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52420282017-02-03 Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney Muthaian, Rupadevi Pakirisamy, Rajaa Muthu Parasuraman, Subramani Raveendran, Ramasamy J Pharmacol Pharmacother Research Paper OBJECTIVE: To investigate the association of hypertension coexisting with diabetes mellitus with oxidative stress and inflammation in the kidneys of streptozotocin (STZ)-induced diabetic rats. MATERIALS AND METHODS: Male Wistar rats were used for the experiments. Blood glucose (BG), urea, blood pressure (BP), and heart rate (HR) were analyzed before and 48 h after STZ injection. Further, these parameters were monitored up to 3 months of diabetes induction. Subsequently, the inflammatory markers (C-reactive protein, tumor necrosis factor-alpha, and nitrate) and oxidative stress markers were estimated after 3 months of diabetes induction in the kidney homogenate. Histological analysis of renal tissue was also carried out. RESULTS: Linear elevation of BG, urea, mean arterial pressure (MAP), and HR was observed up to 3 months of diabetes induction. In the same manner, inflammatory and oxidative stress markers were also found to be significantly increased. Notably, the histological analysis revealed the signs of nephropathy such as increased mesangial cell number, thickness of basement membrane, and renal artery. Inflammatory and oxidative stress markers positively correlated with elevated BP and BG, but the correlation was better with BP rather than BG. CONCLUSION: Hypertension has a strong implication in the increased oxidative stress and inflammation of diabetic kidney at the very early stage of diabetes mellitus. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5242028/ /pubmed/28163536 http://dx.doi.org/10.4103/0976-500X.195898 Text en Copyright: © 2016 Journal of Pharmacology and Pharmacotherapeutics 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-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Research Paper Muthaian, Rupadevi Pakirisamy, Rajaa Muthu Parasuraman, Subramani Raveendran, Ramasamy Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title | Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title_full | Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title_fullStr | Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title_full_unstemmed | Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title_short | Hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
title_sort | hypertension influences the exponential progression of inflammation and oxidative stress in streptozotocin-induced diabetic kidney |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5242028/ https://www.ncbi.nlm.nih.gov/pubmed/28163536 http://dx.doi.org/10.4103/0976-500X.195898 |
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