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

Detalhes bibliográficos
Autor(a) principal: Leite, Alberto Andrade
Data de Publicação: 2021
Outros Autores: Reiter, Russel Joseph, Mendes Brandao, Julio Cezar, Sakae, Thiago Mamoru, Marinho, Marcia [UNESP], Camargo, Celia Regina, Oliveira-Junior, Itamar Souza
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.6061/clinics/2021/e2513
http://hdl.handle.net/11449/210340
Resumo: OBJECTIVES: 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.
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spelling Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat modelMelatoninIntestinal Ischemia-ReperfusionNACAcute Respiratory Distress SyndromeExperimental ModelOBJECTIVES: 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.Univ Fed Sao Paulo, Programa Posgrad Med Translac, Sao Paulo, SP, BrazilUT Hlth Sci Ctr San Antonio, Dept Cell Syst & Anat, San Antonio, TX USAUniv Fed Sergipe, Dept Cirurgia, Disciplina Anestesiol Dor & Med Paliat, Aracaju, SE, BrazilUniv Santa Catarina, Santa Catarina, SC, BrazilUniv Estadual Paulista, Fac Med Vet, Dept Prod & Saude Anim, Aracatuba, SP, BrazilUniv Fed Sao Paulo, Dept Cirurgia, Disciplina Anestesiol Dor & Med Intens, Sao Paulo, SP, BrazilUniv Estadual Paulista, Fac Med Vet, Dept Prod & Saude Anim, Aracatuba, SP, BrazilHospital Clinicas, Univ Sao PauloUniversidade Federal de São Paulo (UNIFESP)UT Hlth Sci Ctr San AntonioUniversidade Federal de Sergipe (UFS)Univ Santa CatarinaUniversidade Estadual Paulista (Unesp)Leite, Alberto AndradeReiter, Russel JosephMendes Brandao, Julio CezarSakae, Thiago MamoruMarinho, Marcia [UNESP]Camargo, Celia ReginaOliveira-Junior, Itamar Souza2021-06-25T15:05:24Z2021-06-25T15:05:24Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7http://dx.doi.org/10.6061/clinics/2021/e2513Clinics. Sao Paulo: Hospital Clinicas, Univ Sao Paulo, v. 76, 7 p., 2021.1807-5932http://hdl.handle.net/11449/21034010.6061/clinics/2021/e2513WOS:000651623600001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinicsinfo:eu-repo/semantics/openAccess2025-06-07T05:14:29Zoai:repositorio.unesp.br:11449/210340Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-06-07T05:14:29Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
title Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
spellingShingle Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
Leite, Alberto Andrade
Melatonin
Intestinal Ischemia-Reperfusion
NAC
Acute Respiratory Distress Syndrome
Experimental Model
title_short Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
title_full Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
title_fullStr Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
title_full_unstemmed Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
title_sort Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
author Leite, Alberto Andrade
author_facet Leite, Alberto Andrade
Reiter, Russel Joseph
Mendes Brandao, Julio Cezar
Sakae, Thiago Mamoru
Marinho, Marcia [UNESP]
Camargo, Celia Regina
Oliveira-Junior, Itamar Souza
author_role author
author2 Reiter, Russel Joseph
Mendes Brandao, Julio Cezar
Sakae, Thiago Mamoru
Marinho, Marcia [UNESP]
Camargo, Celia Regina
Oliveira-Junior, Itamar Souza
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
UT Hlth Sci Ctr San Antonio
Universidade Federal de Sergipe (UFS)
Univ Santa Catarina
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Leite, Alberto Andrade
Reiter, Russel Joseph
Mendes Brandao, Julio Cezar
Sakae, Thiago Mamoru
Marinho, Marcia [UNESP]
Camargo, Celia Regina
Oliveira-Junior, Itamar Souza
dc.subject.por.fl_str_mv Melatonin
Intestinal Ischemia-Reperfusion
NAC
Acute Respiratory Distress Syndrome
Experimental Model
topic Melatonin
Intestinal Ischemia-Reperfusion
NAC
Acute Respiratory Distress Syndrome
Experimental Model
description OBJECTIVES: 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.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T15:05:24Z
2021-06-25T15:05:24Z
2021-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.6061/clinics/2021/e2513
Clinics. Sao Paulo: Hospital Clinicas, Univ Sao Paulo, v. 76, 7 p., 2021.
1807-5932
http://hdl.handle.net/11449/210340
10.6061/clinics/2021/e2513
WOS:000651623600001
url http://dx.doi.org/10.6061/clinics/2021/e2513
http://hdl.handle.net/11449/210340
identifier_str_mv Clinics. Sao Paulo: Hospital Clinicas, Univ Sao Paulo, v. 76, 7 p., 2021.
1807-5932
10.6061/clinics/2021/e2513
WOS:000651623600001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 7
dc.publisher.none.fl_str_mv Hospital Clinicas, Univ Sao Paulo
publisher.none.fl_str_mv Hospital Clinicas, Univ Sao Paulo
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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