Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/8489
Title: Organ-related cigarette smoke-induced oxidative stress is strain-dependent.
Authors: Barroso, Carlos Romualdo Rueff
Trajano, Eduardo Tavares Lima
Alves, Jackson Nogueira
Paiva, Rojane Oliveira
Lanzetti, Manuella
Pires, Karla Maria Pereira
Bezerra, Frank Silva
Pinho, Ricardo Aurino
Valenca, Samuel Santos
Porto, Luís Cristovão de Moraes Sobrino
Keywords: Animal model
Issue Date: 2010
Citation: BARROSO, C. R. R. et al. Organ-related cigarette smoke-induced oxidative stress is strain-dependent. Medical Science Monitor, v. 16, p. 218-226, 2010. Disponível em: <https://www.medscimonit.com/download/index/idArt/880923>. Acesso em: 05 ago. 2017.
Abstract: Background: Cigarette smoke (CS) is associated with oxidative stress in several organs because it contains high concentrations of free radicals and reactive oxygen species. Experimental models, using different strains, provide important insights into the genetic basis of diseases. This study sought to identify, in different mouse strains, the organ that is most-susceptible to CS-induced oxidative stress to obtain an optimized experimental animal model of oxidative injury induced by CS. Material/Methods: Male Swiss, DBA/2, C3H, BALB/c, and C57BL/6 mice were exposed to CS 3 times a day (4 cigarettes per session) for 60 consecutive days. Control groups from the same strains were sham-treated. Protein content, malondialdehyde level, myeloperoxidase activity, and nitrite level were assayed in lung, liver, kidney, and brain from all strains. Catalase and glutathione peroxidase activities were measured. Analyses of data were done by using a 1-way ANOVA with Bonferroni’s post-test (P<.05). Results: Cigarette smoke exposure resulted in distinct, organ-specific responses among strains. The survival rate of DBA/2 mice was lowest. BALB/c and C57BL/6 strains were more-susceptible to oxidative damage in the lung and liver. C3H and C57BL/6 mice were more-susceptible to oxidative damage in the brain. No renal oxidative damage was seen. Conclusions: Mouse strains and individual organs display a range of susceptibilities to CS-induced oxidative stress. BALB/c and C57BL/6 strains appear to be the best choices as experimental models for studying CS effects on liver and lung, and C3H and C57BL/6 strains for CS-effects on the brain.
URI: http://www.repositorio.ufop.br/handle/123456789/8489
ISSN: 16433750
metadata.dc.rights.license: All articles are published under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) only allowing others to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially. Fonte: Medical Science Monitor <https://www.medscimonit.com/instructions>. Acesso em: 28 jul 2017.
Appears in Collections:DECBI - Artigos publicados em periódicos

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