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Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats

BACKGROUND: Diabetic nephropathy (DN) is one of the complex complications of Diabetes Mellitus (DM). The present study has been designed to examine protective role of hydrogen Sulphide (H(2)S) donor against streptozotocin (STZ) -induced behavioral, oxidative abnormalities and its DN like symptoms in...

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Autores principales: Kaur, Manpreet, Sachdeva, Shilpi, Bedi, Onkar, Kaur, Tavleen, Kumar, Puneet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517497/
https://www.ncbi.nlm.nih.gov/pubmed/26221579
http://dx.doi.org/10.1186/s40200-015-0185-7
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author Kaur, Manpreet
Sachdeva, Shilpi
Bedi, Onkar
Kaur, Tavleen
Kumar, Puneet
author_facet Kaur, Manpreet
Sachdeva, Shilpi
Bedi, Onkar
Kaur, Tavleen
Kumar, Puneet
author_sort Kaur, Manpreet
collection PubMed
description BACKGROUND: Diabetic nephropathy (DN) is one of the complex complications of Diabetes Mellitus (DM). The present study has been designed to examine protective role of hydrogen Sulphide (H(2)S) donor against streptozotocin (STZ) -induced behavioral, oxidative abnormalities and its DN like symptoms in rats. METHODS: For the induction of DN single intraperitoneal administration of STZ (45 mg/kg) was given till third week. Behavioral parameters were measured on 1st, 7th, 21st and 42nd days and biochemical parameters were performed on 42nd day. All the drug treatments [NaHS (10 & 30 μmol/kg i.p), DL-propargylglycine (10 mg/kg i.p), standard drug- Losartan (5 mg/kg p.o)] were given for 3 weeks staring from 21st day after the STZ injection. RESULTS: Three weeks treatment with sodium hydrosulphide (NaHS) (10 and 30 μmol/kg i.p,) significantly attenuated the behavioral and biochemical abnormalities in STZ-treated animals. DL-propargylglycine (10 mg/kg i.p) pretreatment with sub-effective dose of NaHS (30 μmol/kg i.p) significantly reversed the protective effect of NaHS. However, combination of both NaHS (30 μmol/kg i.p) and standard drug losartan (5 mg/kg p.o) potentiated their effects as compared to their effect alone. CONCLUSION: The results of the present study suggest that H(2)S treatment showed significant improvement in behavioral and biochemical abnormalities induced by STZ administration. Thus H(2)S represents a target of treatment to prevent the progression of complications by DN.
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spelling pubmed-45174972015-07-29 Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats Kaur, Manpreet Sachdeva, Shilpi Bedi, Onkar Kaur, Tavleen Kumar, Puneet J Diabetes Metab Disord Research Article BACKGROUND: Diabetic nephropathy (DN) is one of the complex complications of Diabetes Mellitus (DM). The present study has been designed to examine protective role of hydrogen Sulphide (H(2)S) donor against streptozotocin (STZ) -induced behavioral, oxidative abnormalities and its DN like symptoms in rats. METHODS: For the induction of DN single intraperitoneal administration of STZ (45 mg/kg) was given till third week. Behavioral parameters were measured on 1st, 7th, 21st and 42nd days and biochemical parameters were performed on 42nd day. All the drug treatments [NaHS (10 & 30 μmol/kg i.p), DL-propargylglycine (10 mg/kg i.p), standard drug- Losartan (5 mg/kg p.o)] were given for 3 weeks staring from 21st day after the STZ injection. RESULTS: Three weeks treatment with sodium hydrosulphide (NaHS) (10 and 30 μmol/kg i.p,) significantly attenuated the behavioral and biochemical abnormalities in STZ-treated animals. DL-propargylglycine (10 mg/kg i.p) pretreatment with sub-effective dose of NaHS (30 μmol/kg i.p) significantly reversed the protective effect of NaHS. However, combination of both NaHS (30 μmol/kg i.p) and standard drug losartan (5 mg/kg p.o) potentiated their effects as compared to their effect alone. CONCLUSION: The results of the present study suggest that H(2)S treatment showed significant improvement in behavioral and biochemical abnormalities induced by STZ administration. Thus H(2)S represents a target of treatment to prevent the progression of complications by DN. BioMed Central 2015-07-28 /pmc/articles/PMC4517497/ /pubmed/26221579 http://dx.doi.org/10.1186/s40200-015-0185-7 Text en © Kaur et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kaur, Manpreet
Sachdeva, Shilpi
Bedi, Onkar
Kaur, Tavleen
Kumar, Puneet
Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title_full Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title_fullStr Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title_full_unstemmed Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title_short Combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
title_sort combined effect of hydrogen sulphide donor and losartan in experimental diabetic nephropathy in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517497/
https://www.ncbi.nlm.nih.gov/pubmed/26221579
http://dx.doi.org/10.1186/s40200-015-0185-7
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