Effects of thymoquinone against cisplatin-induced cardiac injury in rats

Detalhes bibliográficos
Autor(a) principal: Adalı,Fahri
Data de Publicação: 2016
Outros Autores: Gonul,Yucel, Kocak,Ahmet, Yuksel,Yasemin, Ozkececi,Gulay, Ozdemir,Cigdem, Tunay,Kamil, Bozkurt,Mehmet Fatih, Sen,Ozlem Gulec
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Acta Cirúrgica Brasileira (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502016000400271
Resumo: PURPOSE: T o investigate the possible protective effect of thymoquinone (TQ) in cisplatin (CP) induced myocardial injury. METHODS: A total of 28 adult male Wistar-Albino rats were randomly and equally divided into four groups as follows: Group 1 (control), Group 2 (CP at 15 mg/kg dose), Group 3 (TQ 40 mg/kg/day for two days prior to CP injection and on third day, CP at 15 mg/kg dose was intraperitoneally administered and TQ treatment continued until fifth day) and Group 4 (TQ at 40mg/kg/day dose for five days). RESULTS: There was a significant increment in CP group in terms of congestion, edema and pycnotic nuclei in myocardial fibers, comparing with other groups. TQ group exhibited significant increase in expression of antiapoptotic protein Bcl-2, comparing with CP group (p<0.05). In only CP administered group, expression of antiapoptotic protein Bcl-2 was lowest comparing with other groups. CONCLUSION: Established data indicate that cisplatin is cardiotoxic and thymoquinone may be useful in treating CP-induced cardiac injury.
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spelling Effects of thymoquinone against cisplatin-induced cardiac injury in ratsCisplatinCardiotoxicityGenes, bcl-2Rats PURPOSE: T o investigate the possible protective effect of thymoquinone (TQ) in cisplatin (CP) induced myocardial injury. METHODS: A total of 28 adult male Wistar-Albino rats were randomly and equally divided into four groups as follows: Group 1 (control), Group 2 (CP at 15 mg/kg dose), Group 3 (TQ 40 mg/kg/day for two days prior to CP injection and on third day, CP at 15 mg/kg dose was intraperitoneally administered and TQ treatment continued until fifth day) and Group 4 (TQ at 40mg/kg/day dose for five days). RESULTS: There was a significant increment in CP group in terms of congestion, edema and pycnotic nuclei in myocardial fibers, comparing with other groups. TQ group exhibited significant increase in expression of antiapoptotic protein Bcl-2, comparing with CP group (p<0.05). In only CP administered group, expression of antiapoptotic protein Bcl-2 was lowest comparing with other groups. CONCLUSION: Established data indicate that cisplatin is cardiotoxic and thymoquinone may be useful in treating CP-induced cardiac injury.Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia2016-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502016000400271Acta Cirúrgica Brasileira v.31 n.4 2016reponame:Acta Cirúrgica Brasileira (Online)instname:Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)instacron:SBDPC10.1590/S0102-865020160040000008info:eu-repo/semantics/openAccessAdalı,FahriGonul,YucelKocak,AhmetYuksel,YaseminOzkececi,GulayOzdemir,CigdemTunay,KamilBozkurt,Mehmet FatihSen,Ozlem Guleceng2016-05-06T00:00:00Zoai:scielo:S0102-86502016000400271Revistahttps://www.bvs-vet.org.br/vetindex/periodicos/acta-cirurgica-brasileira/https://old.scielo.br/oai/scielo-oai.php||sgolden@terra.com.br0102-86501678-2674opendoar:2016-05-06T00:00Acta Cirúrgica Brasileira (Online) - Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)false
dc.title.none.fl_str_mv Effects of thymoquinone against cisplatin-induced cardiac injury in rats
title Effects of thymoquinone against cisplatin-induced cardiac injury in rats
spellingShingle Effects of thymoquinone against cisplatin-induced cardiac injury in rats
Adalı,Fahri
Cisplatin
Cardiotoxicity
Genes, bcl-2
Rats
title_short Effects of thymoquinone against cisplatin-induced cardiac injury in rats
title_full Effects of thymoquinone against cisplatin-induced cardiac injury in rats
title_fullStr Effects of thymoquinone against cisplatin-induced cardiac injury in rats
title_full_unstemmed Effects of thymoquinone against cisplatin-induced cardiac injury in rats
title_sort Effects of thymoquinone against cisplatin-induced cardiac injury in rats
author Adalı,Fahri
author_facet Adalı,Fahri
Gonul,Yucel
Kocak,Ahmet
Yuksel,Yasemin
Ozkececi,Gulay
Ozdemir,Cigdem
Tunay,Kamil
Bozkurt,Mehmet Fatih
Sen,Ozlem Gulec
author_role author
author2 Gonul,Yucel
Kocak,Ahmet
Yuksel,Yasemin
Ozkececi,Gulay
Ozdemir,Cigdem
Tunay,Kamil
Bozkurt,Mehmet Fatih
Sen,Ozlem Gulec
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Adalı,Fahri
Gonul,Yucel
Kocak,Ahmet
Yuksel,Yasemin
Ozkececi,Gulay
Ozdemir,Cigdem
Tunay,Kamil
Bozkurt,Mehmet Fatih
Sen,Ozlem Gulec
dc.subject.por.fl_str_mv Cisplatin
Cardiotoxicity
Genes, bcl-2
Rats
topic Cisplatin
Cardiotoxicity
Genes, bcl-2
Rats
description PURPOSE: T o investigate the possible protective effect of thymoquinone (TQ) in cisplatin (CP) induced myocardial injury. METHODS: A total of 28 adult male Wistar-Albino rats were randomly and equally divided into four groups as follows: Group 1 (control), Group 2 (CP at 15 mg/kg dose), Group 3 (TQ 40 mg/kg/day for two days prior to CP injection and on third day, CP at 15 mg/kg dose was intraperitoneally administered and TQ treatment continued until fifth day) and Group 4 (TQ at 40mg/kg/day dose for five days). RESULTS: There was a significant increment in CP group in terms of congestion, edema and pycnotic nuclei in myocardial fibers, comparing with other groups. TQ group exhibited significant increase in expression of antiapoptotic protein Bcl-2, comparing with CP group (p<0.05). In only CP administered group, expression of antiapoptotic protein Bcl-2 was lowest comparing with other groups. CONCLUSION: Established data indicate that cisplatin is cardiotoxic and thymoquinone may be useful in treating CP-induced cardiac injury.
publishDate 2016
dc.date.none.fl_str_mv 2016-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502016000400271
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-86502016000400271
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0102-865020160040000008
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
publisher.none.fl_str_mv Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia
dc.source.none.fl_str_mv Acta Cirúrgica Brasileira v.31 n.4 2016
reponame:Acta Cirúrgica Brasileira (Online)
instname:Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
instacron:SBDPC
instname_str Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
instacron_str SBDPC
institution SBDPC
reponame_str Acta Cirúrgica Brasileira (Online)
collection Acta Cirúrgica Brasileira (Online)
repository.name.fl_str_mv Acta Cirúrgica Brasileira (Online) - Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia (SBDPC)
repository.mail.fl_str_mv ||sgolden@terra.com.br
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