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Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model

dc.contributor.authorLeite, Alberto Andrade
dc.contributor.authorReiter, Russel Joseph
dc.contributor.authorMendes Brandao, Julio Cezar
dc.contributor.authorSakae, Thiago Mamoru
dc.contributor.authorMarinho, Marcia [UNESP]
dc.contributor.authorCamargo, Celia Regina
dc.contributor.authorOliveira-Junior, Itamar Souza
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUT Hlth Sci Ctr San Antonio
dc.contributor.institutionUniversidade Federal de Sergipe (UFS)
dc.contributor.institutionUniv Santa Catarina
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T15:05:24Z
dc.date.available2021-06-25T15:05:24Z
dc.date.issued2021-01-01
dc.description.abstractOBJECTIVES: The current study compared the impact of pretreatment with melatonin and N-acetylcysteine (NAC) on the prevention of rat lung damage following intestinal ischemia-reperfusion (iIR). METHODS: Twenty-eight Wistar rats were subjected to intestinal ischemia induced by a 60 min occlusion of the superior mesenteric artery, followed by reperfusion for 120 min. Animals were divided into the following groups (n=7 per group): sham, only abdominal incision; SS+iIR, pretreated with saline solution and iIR; NAC+iIR, pretreated with NAC (20 mg/kg) and iIR; MEL+iIR, pretreated with melatonin (20 mg/kg) and iIR. Oxidative stress and inflammatory mediators were measured and histological analyses were performed in the lung tissues. RESULTS: Data showed a reduction in malondialdehyde (MDA), myeloperoxidase (MPO), and TNF-alpha in the animals pretreated with NAC or MEL when compared to those treated with SS+iIR (p<0.05). An increase in superoxide dismutase (SOD) levels in the NAC- and MEL-pretreated animals as compared to the SS+iIR group (34 +/- 8 U/g of tissue; p<0.05) was also observed. TNF-alpha levels were lower in the MEL+iIR group (91 +/- 5 pg/mL) than in the NAC+iIR group (101 +/- 6 pg/mL). Histological analysis demonstrated a higher lung lesion score in the SS+iIR group than in the pretreated groups. CONCLUSION: Both agents individually provided tissue protective effect against intestinal IR-induced lung injury, but melatonin was more effective in ameliorating the parameters analyzed in this study.en
dc.description.affiliationUniv Fed Sao Paulo, Programa Posgrad Med Translac, Sao Paulo, SP, Brazil
dc.description.affiliationUT Hlth Sci Ctr San Antonio, Dept Cell Syst & Anat, San Antonio, TX USA
dc.description.affiliationUniv Fed Sergipe, Dept Cirurgia, Disciplina Anestesiol Dor & Med Paliat, Aracaju, SE, Brazil
dc.description.affiliationUniv Santa Catarina, Santa Catarina, SC, Brazil
dc.description.affiliationUniv Estadual Paulista, Fac Med Vet, Dept Prod & Saude Anim, Aracatuba, SP, Brazil
dc.description.affiliationUniv Fed Sao Paulo, Dept Cirurgia, Disciplina Anestesiol Dor & Med Intens, Sao Paulo, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Fac Med Vet, Dept Prod & Saude Anim, Aracatuba, SP, Brazil
dc.format.extent7
dc.identifierhttp://dx.doi.org/10.6061/clinics/2021/e2513
dc.identifier.citationClinics. Sao Paulo: Hospital Clinicas, Univ Sao Paulo, v. 76, 7 p., 2021.
dc.identifier.doi10.6061/clinics/2021/e2513
dc.identifier.issn1807-5932
dc.identifier.urihttp://hdl.handle.net/11449/210340
dc.identifier.wosWOS:000651623600001
dc.language.isoeng
dc.publisherHospital Clinicas, Univ Sao Paulo
dc.relation.ispartofClinics
dc.sourceWeb of Science
dc.subjectMelatonin
dc.subjectIntestinal Ischemia-Reperfusion
dc.subjectNAC
dc.subjectAcute Respiratory Distress Syndrome
dc.subjectExperimental Model
dc.titleMelatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat modelen
dc.typeArtigopt
dcterms.rightsHolderHospital Clinicas, Univ Sao Paulo
dspace.entity.typePublication
relation.isOrgUnitOfPublication1f8041b8-563c-4766-90b9-4dd9c0101666
relation.isOrgUnitOfPublication.latestForDiscovery1f8041b8-563c-4766-90b9-4dd9c0101666
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Medicina Veterinária, Araçatubapt
unesp.departmentApoio, Produção e Saúde Animal - FMVApt

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