Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/211875 |
Resumo: | Diclofenac sodium (DF) is a non-steroidal anti-inflammatory drug (NSAID) that possesses antipyretic, analgesic, antinociceptive and anti-inflammatory activities. Like other NSAIDs, DF is known to be associated with renal, cardiovascular, and gastrointestinal complications. The present study was carried out to evaluate the adverse effects of DF in vivo in wistar albino rats and to assess if oral administration of the organic osmolyte betaine mitigates the adverse effect of DF. Eighteen male Wistar rats were divided into three groups, one group of animals was fed orally with 20 mg/kg of DF once/day, and the other group received a combination of 20 mg/kg of DF and 30 mg/kg of betaine, once/day. Apart from the hematological and biochemical parameters, histopathological changes in the liver, lungs, brain, heart and kidney were also investigated. Histopathological alterations that were found in the liver, kidney, and lungs of DF-treated animals were found to be minimal or absent in DF + betaine-treated animals, as compared to untreated control. The results showed that betaine mitigates the adverse effects associated with DF treatment. |
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Brazilian Journal of Pharmaceutical Sciences |
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Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino ratsDiclofenac; Osmolytes; Betaine; Wister RatsDiclofenac sodium (DF) is a non-steroidal anti-inflammatory drug (NSAID) that possesses antipyretic, analgesic, antinociceptive and anti-inflammatory activities. Like other NSAIDs, DF is known to be associated with renal, cardiovascular, and gastrointestinal complications. The present study was carried out to evaluate the adverse effects of DF in vivo in wistar albino rats and to assess if oral administration of the organic osmolyte betaine mitigates the adverse effect of DF. Eighteen male Wistar rats were divided into three groups, one group of animals was fed orally with 20 mg/kg of DF once/day, and the other group received a combination of 20 mg/kg of DF and 30 mg/kg of betaine, once/day. Apart from the hematological and biochemical parameters, histopathological changes in the liver, lungs, brain, heart and kidney were also investigated. Histopathological alterations that were found in the liver, kidney, and lungs of DF-treated animals were found to be minimal or absent in DF + betaine-treated animals, as compared to untreated control. The results showed that betaine mitigates the adverse effects associated with DF treatment.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-05-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/21187510.1590/s2175-97902023e201178Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e201178Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e201178Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e2011782175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/211875/194625https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessBasheeruddin, Mohd.V., LavanyaAhmed, NeesarJamal, Shazia2023-05-31T19:22:49Zoai:revistas.usp.br:article/211875Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-05-31T19:22:49Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
title |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
spellingShingle |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats Basheeruddin, Mohd. Diclofenac; Osmolytes; Betaine; Wister Rats |
title_short |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
title_full |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
title_fullStr |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
title_full_unstemmed |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
title_sort |
Organic osmolyte betaine mitigates the deleterious effects of Diclofenac in vivo in wistar albino rats |
author |
Basheeruddin, Mohd. |
author_facet |
Basheeruddin, Mohd. V., Lavanya Ahmed, Neesar Jamal, Shazia |
author_role |
author |
author2 |
V., Lavanya Ahmed, Neesar Jamal, Shazia |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Basheeruddin, Mohd. V., Lavanya Ahmed, Neesar Jamal, Shazia |
dc.subject.por.fl_str_mv |
Diclofenac; Osmolytes; Betaine; Wister Rats |
topic |
Diclofenac; Osmolytes; Betaine; Wister Rats |
description |
Diclofenac sodium (DF) is a non-steroidal anti-inflammatory drug (NSAID) that possesses antipyretic, analgesic, antinociceptive and anti-inflammatory activities. Like other NSAIDs, DF is known to be associated with renal, cardiovascular, and gastrointestinal complications. The present study was carried out to evaluate the adverse effects of DF in vivo in wistar albino rats and to assess if oral administration of the organic osmolyte betaine mitigates the adverse effect of DF. Eighteen male Wistar rats were divided into three groups, one group of animals was fed orally with 20 mg/kg of DF once/day, and the other group received a combination of 20 mg/kg of DF and 30 mg/kg of betaine, once/day. Apart from the hematological and biochemical parameters, histopathological changes in the liver, lungs, brain, heart and kidney were also investigated. Histopathological alterations that were found in the liver, kidney, and lungs of DF-treated animals were found to be minimal or absent in DF + betaine-treated animals, as compared to untreated control. The results showed that betaine mitigates the adverse effects associated with DF treatment. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-05-08 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/211875 10.1590/s2175-97902023e201178 |
url |
https://www.revistas.usp.br/bjps/article/view/211875 |
identifier_str_mv |
10.1590/s2175-97902023e201178 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/211875/194625 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e201178 Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); e201178 Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); e201178 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1800222918044549120 |