Evaluation of oxidative stress in an experimental model of Crohn's disease treated with hyperbaric oxygen therapy
dc.contributor | Sistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP | |
dc.contributor.author | NAKUTIS, Fernanda Serafim | |
dc.contributor.author | NISHITOKUKADO, Ieda | |
dc.contributor.author | SANTOS, Fabiana Maria dos | |
dc.contributor.author | ORTIZ-AGOSTINHO, Carmen Lucia | |
dc.contributor.author | ALENCAR, Daniel Teixeira de | |
dc.contributor.author | ACHTSCHIN, Cassiana Ganem | |
dc.contributor.author | NUNES, Valeria Sutti | |
dc.contributor.author | LEITE, Andre Zonetti Arruda | |
dc.contributor.author | SIPAHI, Aytan Miranda | |
dc.date.accessioned | 2023-12-15T19:00:31Z | |
dc.date.available | 2023-12-15T19:00:31Z | |
dc.date.issued | 2023 | |
dc.description.abstract | Introduction: Treatments of Inflammatory Bowel Disease (IBD) are able to control symptoms in most cases, how-ever, a fraction of patients do not improve or have a loss of response to treatments, making it important to explore new therapeutic strategies. Hyperbaric oxygen therapy (HBO) may represent one of them. The aim of this study was to evaluate the effects of HBO therapy in an experimental model of IBD. Methods: Sixty male BALBc mice were divided into six groups. Group 1 was colitis-induced with trinitrobenzene sulfonic acid (TNBS) + ethanol, group 2 received TNBS + ethanol plus HBO, group 3 received only ethanol, group 4 received ethanol plus HBO, group 5 received saline solution, and group 6 received saline solution plus HBO. HBO was performed for four days, subsequently, the mice were evaluated daily. At the end of the study, samples from the intestine were collected for histological analysis as well as for measurement of antioxidant enzymes and cytokine levels. Results: HBO significantly improved the clinical and histological status of the animals. Treatment with HBO increased the activity of the antioxidant enzymes superoxide dismutase (SOD) and glutathione peroxidase (GPx) in all of the groups; moreover, the difference was only significant between the TNBS and TNBS + HBO groups and treatments promoted a reduction in the proinflammatory cytokines IFN-gamma, IL-12, IL-17 and TNF-alpha and increased the anti-inflammatory cytokines IL-4 and IL-10, with no changes in IL-13. Conclusion: HBO effectively treats TNBS-induced colitis by increasing the activity of antioxidant enzymes and modulating cytokine profiles. | eng |
dc.description.index | MEDLINE | |
dc.description.index | PubMed | |
dc.description.index | WoS | |
dc.description.index | Scopus | |
dc.identifier.citation | CLINICS, v.78, article ID 100305, 9p, 2023 | |
dc.identifier.doi | 10.1016/j.clinsp.2023.100305 | |
dc.identifier.eissn | 1980-5322 | |
dc.identifier.issn | 1807-5932 | |
dc.identifier.uri | https://observatorio.fm.usp.br/handle/OPI/57650 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER ESPANA | eng |
dc.relation.ispartof | Clinics | |
dc.rights | openAccess | eng |
dc.rights.holder | Copyright ELSEVIER ESPANA | eng |
dc.subject | Inflammatory bowel disease | eng |
dc.subject | Experimental model | eng |
dc.subject | Hyperbaric oxygen therapy | eng |
dc.subject.other | inflammatory-bowel-disease | eng |
dc.subject.other | ulcerative-colitis | eng |
dc.subject.other | double-blind | eng |
dc.subject.other | anti-tnf | eng |
dc.subject.other | alpha | eng |
dc.subject.other | pathogenesis | eng |
dc.subject.other | mechanisms | eng |
dc.subject.other | expression | eng |
dc.subject.other | challenges | eng |
dc.subject.other | rats | eng |
dc.subject.wos | Medicine, General & Internal | eng |
dc.title | Evaluation of oxidative stress in an experimental model of Crohn's disease treated with hyperbaric oxygen therapy | eng |
dc.type | article | eng |
dc.type.category | original article | eng |
dc.type.version | publishedVersion | eng |
dspace.entity.type | Publication | |
hcfmusp.author.external | NAKUTIS, Fernanda Serafim:Hosp Clin Fac Med Univ Sao Paulo HCFMUSP, Div Clin Gastroenterol & Hepatol, Lab Expt Clin Gastroenterol LIM 07, Sao Paulo, SP, Brazil | |
hcfmusp.author.external | ACHTSCHIN, Cassiana Ganem:Hosp Clin Fac Med Univ Sao Paulo HCFMUSP, Div Clin Gastroenterol & Hepatol, Lab Expt Clin Gastroenterol LIM 07, Sao Paulo, SP, Brazil | |
hcfmusp.author.external | LEITE, Andre Zonetti Arruda:Hosp Clin Fac Med Univ Sao Paulo HCFMUSP, Div Clin Gastroenterol & Hepatol, Lab Expt Clin Gastroenterol LIM 07, Sao Paulo, SP, Brazil; Hosp Clin Fac Med Univ Sao Paulo HCFMUSP, Div Clin Gastroenterol & Hepatol, Sao Paulo, SP, Brazil | |
hcfmusp.citation.scopus | 0 | |
hcfmusp.contributor.author-fmusphc | IEDA NISHITOKUKADO | |
hcfmusp.contributor.author-fmusphc | FABIANA MARIA DOS SANTOS | |
hcfmusp.contributor.author-fmusphc | CARMEN LUCIA ORTIZ AGOSTINHO | |
hcfmusp.contributor.author-fmusphc | DANIEL TEIXEIRA DE ALENCAR | |
hcfmusp.contributor.author-fmusphc | VALERIA SUTTI NUNES | |
hcfmusp.contributor.author-fmusphc | AYTAN MIRANDA SIPAHI | |
hcfmusp.description.articlenumber | 100305 | |
hcfmusp.description.volume | 78 | |
hcfmusp.origem | WOS | |
hcfmusp.origem.pubmed | 37976650 | |
hcfmusp.origem.scopus | 2-s2.0-85178536507 | |
hcfmusp.origem.wos | WOS:001113627400001 | |
hcfmusp.publisher.city | MADRID | eng |
hcfmusp.publisher.country | SPAIN | eng |
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hcfmusp.scopus.lastupdate | 2024-05-17 | |
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