Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations

Detalhes bibliográficos
Autor(a) principal: Attiq, Ali
Data de Publicação: 2018
Outros Autores: Ashraf, Muhammad, Jalil, Juriyati, Javeed, Aqeel, Anjum, Aftab Ahmad, Ullah, Asad, Umair, Muhammad, Ali, Sarwat
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/146838
Resumo: It is understood that drugs regardless of their order of administration can exhibit drug interactions. Established on the fact that treatment of hypertension may last for decades and prolong usage of multiple drug regimen may induce substantial pathophysiological changes. Hence, This study was designed to evaluate the possible synergistic toxic effects of anti-hypertensive (carvedilol), and anti-inflammatory drug (celecoxib) alone and in combinations. Well-established MTT assay, Single Cell Gel Electrophoresis (SCGE) and Ames assay were employed to evaluate the toxicity at cellular level. Results from MTT assay on Vero cell line revealed that drug combinations have more pronounced anti-proliferative activity with combine IC50 value of 13.7:47.8 µg/mL. Likewise, exposure of peripheral blood mononuclear cells with drug combinations revealed significant (P
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spelling Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinationsCarvedilolCelecoxibMutagenicityGenotoxicityCytotoxicity. It is understood that drugs regardless of their order of administration can exhibit drug interactions. Established on the fact that treatment of hypertension may last for decades and prolong usage of multiple drug regimen may induce substantial pathophysiological changes. Hence, This study was designed to evaluate the possible synergistic toxic effects of anti-hypertensive (carvedilol), and anti-inflammatory drug (celecoxib) alone and in combinations. Well-established MTT assay, Single Cell Gel Electrophoresis (SCGE) and Ames assay were employed to evaluate the toxicity at cellular level. Results from MTT assay on Vero cell line revealed that drug combinations have more pronounced anti-proliferative activity with combine IC50 value of 13.7:47.8 µg/mL. Likewise, exposure of peripheral blood mononuclear cells with drug combinations revealed significant (PUniversidade de São Paulo. Faculdade de Ciências Farmacêuticas2018-06-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/14683810.1590/s2175-97902018000117292Brazilian Journal of Pharmaceutical Sciences; Vol. 54 Núm. 1 (2018); e17292Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 1 (2018); e17292Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 1 (2018); e172922175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/146838/140367Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessAttiq, AliAshraf, MuhammadJalil, JuriyatiJaveed, AqeelAnjum, Aftab AhmadUllah, AsadUmair, MuhammadAli, Sarwat2018-06-07T16:31:56Zoai:revistas.usp.br:article/146838Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2018-06-07T16:31:56Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
title Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
spellingShingle Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
Attiq, Ali
Carvedilol
Celecoxib
Mutagenicity
Genotoxicity
Cytotoxicity.
title_short Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
title_full Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
title_fullStr Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
title_full_unstemmed Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
title_sort Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
author Attiq, Ali
author_facet Attiq, Ali
Ashraf, Muhammad
Jalil, Juriyati
Javeed, Aqeel
Anjum, Aftab Ahmad
Ullah, Asad
Umair, Muhammad
Ali, Sarwat
author_role author
author2 Ashraf, Muhammad
Jalil, Juriyati
Javeed, Aqeel
Anjum, Aftab Ahmad
Ullah, Asad
Umair, Muhammad
Ali, Sarwat
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Attiq, Ali
Ashraf, Muhammad
Jalil, Juriyati
Javeed, Aqeel
Anjum, Aftab Ahmad
Ullah, Asad
Umair, Muhammad
Ali, Sarwat
dc.subject.por.fl_str_mv Carvedilol
Celecoxib
Mutagenicity
Genotoxicity
Cytotoxicity.
topic Carvedilol
Celecoxib
Mutagenicity
Genotoxicity
Cytotoxicity.
description It is understood that drugs regardless of their order of administration can exhibit drug interactions. Established on the fact that treatment of hypertension may last for decades and prolong usage of multiple drug regimen may induce substantial pathophysiological changes. Hence, This study was designed to evaluate the possible synergistic toxic effects of anti-hypertensive (carvedilol), and anti-inflammatory drug (celecoxib) alone and in combinations. Well-established MTT assay, Single Cell Gel Electrophoresis (SCGE) and Ames assay were employed to evaluate the toxicity at cellular level. Results from MTT assay on Vero cell line revealed that drug combinations have more pronounced anti-proliferative activity with combine IC50 value of 13.7:47.8 µg/mL. Likewise, exposure of peripheral blood mononuclear cells with drug combinations revealed significant (P
publishDate 2018
dc.date.none.fl_str_mv 2018-06-07
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/146838
10.1590/s2175-97902018000117292
url https://www.revistas.usp.br/bjps/article/view/146838
identifier_str_mv 10.1590/s2175-97902018000117292
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/146838/140367
dc.rights.driver.fl_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
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. 54 Núm. 1 (2018); e17292
Brazilian Journal of Pharmaceutical Sciences; v. 54 n. 1 (2018); e17292
Brazilian Journal of Pharmaceutical Sciences; Vol. 54 No. 1 (2018); e17292
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
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