Melatonin can be, more effective than N-acetylcysteine, protecting acute lung injury induced by intestinal ischemia-reperfusion in rat model
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1834482841649414144 |