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Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure

OBJECTIVES: The aim was to investigate the nephroprotective effect of combination of aliskiren (ASK), a direct renin inhibitor and pentoxifylline (PTX), inhibitor of tumor necrotic factor-alpha (TNF-alpha), in rat remnant kidney model of chronic kidney disease (CKD). MATERIALS AND METHODS: Nephrecto...

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Autores principales: Soni, Hitesh M., Patel, Praful P., Patel, Savan, Rath, Akshyaya C., Acharya, Aviseka, Trivedi, Harshkant D., Jain, Mukul R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375824/
https://www.ncbi.nlm.nih.gov/pubmed/25821316
http://dx.doi.org/10.4103/0253-7613.150351
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author Soni, Hitesh M.
Patel, Praful P.
Patel, Savan
Rath, Akshyaya C.
Acharya, Aviseka
Trivedi, Harshkant D.
Jain, Mukul R.
author_facet Soni, Hitesh M.
Patel, Praful P.
Patel, Savan
Rath, Akshyaya C.
Acharya, Aviseka
Trivedi, Harshkant D.
Jain, Mukul R.
author_sort Soni, Hitesh M.
collection PubMed
description OBJECTIVES: The aim was to investigate the nephroprotective effect of combination of aliskiren (ASK), a direct renin inhibitor and pentoxifylline (PTX), inhibitor of tumor necrotic factor-alpha (TNF-alpha), in rat remnant kidney model of chronic kidney disease (CKD). MATERIALS AND METHODS: Nephrectomized (NPX) rats were treated with ASK (10 mg/kg, p.o.), PTX (100 mg/kg, p.o.), and combination of PTX + ASK once daily for 28 days. We have performed analysis of various renal injury parameters after 4 weeks of treatment. RESULTS: Treatment with PTX, ASK and combination showed significant improvement in urea, creatinine and total protein in plasma when compared with vehicle treated group in NPX rats. ASK and combination of PTX + ASK elicited significant reduction in blood pressure but PTX alone did not produce blood pressure reduction. ASK treatment showed significant elevation in TNF-alpha, whereas PTX and ASK + PTX showed significant reduction in TNF-alpha in plasma. Histopathologically, the extent of the kidney injury was similar in NPX + vehicle and NPX + ASK-treated rats. PTX and ASK + PTX-treated group showed lesser extent of kidney injury. There was good correlation of mRNA expression levels of kidney injury molecule-1 and bradykinin B1 receptor data with histopathological findings in kidney samples and elevated TNF-alpha levels in plasma. CONCLUSIONS: We conclude that combination of PTX + ASK may be better therapeutic intervention for nephroprotection in CKD patients.
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spelling pubmed-43758242015-03-27 Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure Soni, Hitesh M. Patel, Praful P. Patel, Savan Rath, Akshyaya C. Acharya, Aviseka Trivedi, Harshkant D. Jain, Mukul R. Indian J Pharmacol Research Article OBJECTIVES: The aim was to investigate the nephroprotective effect of combination of aliskiren (ASK), a direct renin inhibitor and pentoxifylline (PTX), inhibitor of tumor necrotic factor-alpha (TNF-alpha), in rat remnant kidney model of chronic kidney disease (CKD). MATERIALS AND METHODS: Nephrectomized (NPX) rats were treated with ASK (10 mg/kg, p.o.), PTX (100 mg/kg, p.o.), and combination of PTX + ASK once daily for 28 days. We have performed analysis of various renal injury parameters after 4 weeks of treatment. RESULTS: Treatment with PTX, ASK and combination showed significant improvement in urea, creatinine and total protein in plasma when compared with vehicle treated group in NPX rats. ASK and combination of PTX + ASK elicited significant reduction in blood pressure but PTX alone did not produce blood pressure reduction. ASK treatment showed significant elevation in TNF-alpha, whereas PTX and ASK + PTX showed significant reduction in TNF-alpha in plasma. Histopathologically, the extent of the kidney injury was similar in NPX + vehicle and NPX + ASK-treated rats. PTX and ASK + PTX-treated group showed lesser extent of kidney injury. There was good correlation of mRNA expression levels of kidney injury molecule-1 and bradykinin B1 receptor data with histopathological findings in kidney samples and elevated TNF-alpha levels in plasma. CONCLUSIONS: We conclude that combination of PTX + ASK may be better therapeutic intervention for nephroprotection in CKD patients. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4375824/ /pubmed/25821316 http://dx.doi.org/10.4103/0253-7613.150351 Text en Copyright: © Indian Journal of Pharmacology 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 Research Article
Soni, Hitesh M.
Patel, Praful P.
Patel, Savan
Rath, Akshyaya C.
Acharya, Aviseka
Trivedi, Harshkant D.
Jain, Mukul R.
Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title_full Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title_fullStr Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title_full_unstemmed Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title_short Effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
title_sort effects of combination of aliskiren and pentoxyfylline on renal function in the rat remnant kidney model of chronic renal failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375824/
https://www.ncbi.nlm.nih.gov/pubmed/25821316
http://dx.doi.org/10.4103/0253-7613.150351
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