Augmented cytotoxic, mutagenic and genotoxic response triggered by carvedilol and celecoxib combinations
Autor(a) principal: | |
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Data de Publicação: | 2018 |
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/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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oai:revistas.usp.br:article/146838 |
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Brazilian Journal of Pharmaceutical Sciences |
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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 |
_version_ |
1800222913681424384 |