Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage

ABSTRACT: Objective: The aim of this study was to compare in vivo efect of fve pharmacological options on infammation and pulmonary fbrosis induced by paraquat. Methods: 54 Wistar SPF rats were used. After 2 h post-intoxication with paraquat ion, groups of 9 animals were ran domly assigned to (1) cy...

Full description

Autores:
Buendía Rodríguez, Jefferson Antonio
Justinico Castro, José Armando
Tapia Vela, Laura Joanna
Sinisterra Espejo, Denis María
Sánchez Villamil, Juana Patricia
Zuluaga Salazar, Andrés Felipe
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38529
Acceso en línea:
https://hdl.handle.net/10495/38529
Palabra clave:
Antioxidantes - Farmacología
Antioxidants - pharmacology
Ácido Ascórbico - Farmacología
Ascorbic Acid - pharmacology
Atorvastatina
Atorvastatin
Pulmón
Lung
Paraquat
Ciclofosfamida
Cyclophosphamide
Dexametasona
Dexamethasone
Quimioterapia Combinada
Drug Therapy, Combination
Heparina de Bajo-Peso-Molecular
Heparin, Low-Molecular-Weight
Neumonía
Pneumonia
Alveolos Pulmonares
Pulmonary Alveoli
Fibrosis Pulmonar
Pulmonary Fibrosis
Ratas Wistar
Rats, Wistar
Resultado del Tratamiento
Treatment Outcome
https://id.nlm.nih.gov/mesh/D000975
https://id.nlm.nih.gov/mesh/D001205
https://id.nlm.nih.gov/mesh/D000069059
https://id.nlm.nih.gov/mesh/D008168
https://id.nlm.nih.gov/mesh/D010269
https://id.nlm.nih.gov/mesh/D003520
https://id.nlm.nih.gov/mesh/D003907
https://id.nlm.nih.gov/mesh/D004359
https://id.nlm.nih.gov/mesh/D006495
https://id.nlm.nih.gov/mesh/D011014
https://id.nlm.nih.gov/mesh/D011650
https://id.nlm.nih.gov/mesh/D011658
https://id.nlm.nih.gov/mesh/D017208
https://id.nlm.nih.gov/mesh/D016896
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
id UDEA2_3ada6eb752d32d89630e5afdd33a1da3
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/38529
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
title Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
spellingShingle Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
Antioxidantes - Farmacología
Antioxidants - pharmacology
Ácido Ascórbico - Farmacología
Ascorbic Acid - pharmacology
Atorvastatina
Atorvastatin
Pulmón
Lung
Paraquat
Ciclofosfamida
Cyclophosphamide
Dexametasona
Dexamethasone
Quimioterapia Combinada
Drug Therapy, Combination
Heparina de Bajo-Peso-Molecular
Heparin, Low-Molecular-Weight
Neumonía
Pneumonia
Alveolos Pulmonares
Pulmonary Alveoli
Fibrosis Pulmonar
Pulmonary Fibrosis
Ratas Wistar
Rats, Wistar
Resultado del Tratamiento
Treatment Outcome
https://id.nlm.nih.gov/mesh/D000975
https://id.nlm.nih.gov/mesh/D001205
https://id.nlm.nih.gov/mesh/D000069059
https://id.nlm.nih.gov/mesh/D008168
https://id.nlm.nih.gov/mesh/D010269
https://id.nlm.nih.gov/mesh/D003520
https://id.nlm.nih.gov/mesh/D003907
https://id.nlm.nih.gov/mesh/D004359
https://id.nlm.nih.gov/mesh/D006495
https://id.nlm.nih.gov/mesh/D011014
https://id.nlm.nih.gov/mesh/D011650
https://id.nlm.nih.gov/mesh/D011658
https://id.nlm.nih.gov/mesh/D017208
https://id.nlm.nih.gov/mesh/D016896
title_short Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
title_full Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
title_fullStr Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
title_full_unstemmed Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
title_sort Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damage
dc.creator.fl_str_mv Buendía Rodríguez, Jefferson Antonio
Justinico Castro, José Armando
Tapia Vela, Laura Joanna
Sinisterra Espejo, Denis María
Sánchez Villamil, Juana Patricia
Zuluaga Salazar, Andrés Felipe
dc.contributor.author.none.fl_str_mv Buendía Rodríguez, Jefferson Antonio
Justinico Castro, José Armando
Tapia Vela, Laura Joanna
Sinisterra Espejo, Denis María
Sánchez Villamil, Juana Patricia
Zuluaga Salazar, Andrés Felipe
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Investigación en Farmacología y Toxicología
dc.subject.decs.none.fl_str_mv Antioxidantes - Farmacología
Antioxidants - pharmacology
Ácido Ascórbico - Farmacología
Ascorbic Acid - pharmacology
Atorvastatina
Atorvastatin
Pulmón
Lung
Paraquat
Ciclofosfamida
Cyclophosphamide
Dexametasona
Dexamethasone
Quimioterapia Combinada
Drug Therapy, Combination
Heparina de Bajo-Peso-Molecular
Heparin, Low-Molecular-Weight
Neumonía
Pneumonia
Alveolos Pulmonares
Pulmonary Alveoli
Fibrosis Pulmonar
Pulmonary Fibrosis
Ratas Wistar
Rats, Wistar
Resultado del Tratamiento
Treatment Outcome
topic Antioxidantes - Farmacología
Antioxidants - pharmacology
Ácido Ascórbico - Farmacología
Ascorbic Acid - pharmacology
Atorvastatina
Atorvastatin
Pulmón
Lung
Paraquat
Ciclofosfamida
Cyclophosphamide
Dexametasona
Dexamethasone
Quimioterapia Combinada
Drug Therapy, Combination
Heparina de Bajo-Peso-Molecular
Heparin, Low-Molecular-Weight
Neumonía
Pneumonia
Alveolos Pulmonares
Pulmonary Alveoli
Fibrosis Pulmonar
Pulmonary Fibrosis
Ratas Wistar
Rats, Wistar
Resultado del Tratamiento
Treatment Outcome
https://id.nlm.nih.gov/mesh/D000975
https://id.nlm.nih.gov/mesh/D001205
https://id.nlm.nih.gov/mesh/D000069059
https://id.nlm.nih.gov/mesh/D008168
https://id.nlm.nih.gov/mesh/D010269
https://id.nlm.nih.gov/mesh/D003520
https://id.nlm.nih.gov/mesh/D003907
https://id.nlm.nih.gov/mesh/D004359
https://id.nlm.nih.gov/mesh/D006495
https://id.nlm.nih.gov/mesh/D011014
https://id.nlm.nih.gov/mesh/D011650
https://id.nlm.nih.gov/mesh/D011658
https://id.nlm.nih.gov/mesh/D017208
https://id.nlm.nih.gov/mesh/D016896
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D000975
https://id.nlm.nih.gov/mesh/D001205
https://id.nlm.nih.gov/mesh/D000069059
https://id.nlm.nih.gov/mesh/D008168
https://id.nlm.nih.gov/mesh/D010269
https://id.nlm.nih.gov/mesh/D003520
https://id.nlm.nih.gov/mesh/D003907
https://id.nlm.nih.gov/mesh/D004359
https://id.nlm.nih.gov/mesh/D006495
https://id.nlm.nih.gov/mesh/D011014
https://id.nlm.nih.gov/mesh/D011650
https://id.nlm.nih.gov/mesh/D011658
https://id.nlm.nih.gov/mesh/D017208
https://id.nlm.nih.gov/mesh/D016896
description ABSTRACT: Objective: The aim of this study was to compare in vivo efect of fve pharmacological options on infammation and pulmonary fbrosis induced by paraquat. Methods: 54 Wistar SPF rats were used. After 2 h post-intoxication with paraquat ion, groups of 9 animals were ran domly assigned to (1) cyclophosphamide plus dexamethasone (2) low molecular weight heparin (3) unfractionated heparin (4) vitamin C every 24 h, (5) atorvastatin or (6) placebo with intraperitoneal saline. Lung infammation, alveolar injury, hepatocyte damage, hepatic regeneration, acute tubular necrosis and kidney congestion were evaluated. Results: In the control group 100% of animals presented moderate and severe lung infammation, while in the groups with atorvastatin and intratracheal heparin this proportion was lower (55.5%; CI 26.6–81.3%) (p=0.025). A lower degree of moderate or severe hepatic regeneration was evident in the treatment groups with atorvastatin (p=0.009). In this study was demonstrated that statins and heparin might have a protective efect in the paraquat induced destructive phase. More evidence is needed to evaluated of dose–response efects of these drugs before to study in clinical trials
publishDate 2019
dc.date.issued.none.fl_str_mv 2019
dc.date.accessioned.none.fl_str_mv 2024-03-10T01:00:51Z
dc.date.available.none.fl_str_mv 2024-03-10T01:00:51Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Buendía JA, Justinico Castro JA, Vela LJT, Sinisterra D, Sánchez Villamil JP, Zuluaga Salazar AF. Comparison of four pharmacological strategies aimed to prevent the lung inflammation and paraquat-induced alveolar damage. BMC Res Notes. 2019 Sep 18;12(1):584. doi: 10.1186/s13104-019-4598-0.
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/38529
dc.identifier.doi.none.fl_str_mv 10.1186/s13104-019-4598-0
dc.identifier.eissn.none.fl_str_mv 1756-0500
identifier_str_mv Buendía JA, Justinico Castro JA, Vela LJT, Sinisterra D, Sánchez Villamil JP, Zuluaga Salazar AF. Comparison of four pharmacological strategies aimed to prevent the lung inflammation and paraquat-induced alveolar damage. BMC Res Notes. 2019 Sep 18;12(1):584. doi: 10.1186/s13104-019-4598-0.
10.1186/s13104-019-4598-0
1756-0500
url https://hdl.handle.net/10495/38529
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv BMC Res. Notes.
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dc.relation.citationissue.spa.fl_str_mv 1
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dc.relation.citationvolume.spa.fl_str_mv 12
dc.relation.ispartofjournal.spa.fl_str_mv BMC Research Notes
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spelling Buendía Rodríguez, Jefferson AntonioJustinico Castro, José ArmandoTapia Vela, Laura JoannaSinisterra Espejo, Denis MaríaSánchez Villamil, Juana PatriciaZuluaga Salazar, Andrés FelipeGrupo de Investigación en Farmacología y Toxicología2024-03-10T01:00:51Z2024-03-10T01:00:51Z2019Buendía JA, Justinico Castro JA, Vela LJT, Sinisterra D, Sánchez Villamil JP, Zuluaga Salazar AF. Comparison of four pharmacological strategies aimed to prevent the lung inflammation and paraquat-induced alveolar damage. BMC Res Notes. 2019 Sep 18;12(1):584. doi: 10.1186/s13104-019-4598-0.https://hdl.handle.net/10495/3852910.1186/s13104-019-4598-01756-0500ABSTRACT: Objective: The aim of this study was to compare in vivo efect of fve pharmacological options on infammation and pulmonary fbrosis induced by paraquat. Methods: 54 Wistar SPF rats were used. After 2 h post-intoxication with paraquat ion, groups of 9 animals were ran domly assigned to (1) cyclophosphamide plus dexamethasone (2) low molecular weight heparin (3) unfractionated heparin (4) vitamin C every 24 h, (5) atorvastatin or (6) placebo with intraperitoneal saline. Lung infammation, alveolar injury, hepatocyte damage, hepatic regeneration, acute tubular necrosis and kidney congestion were evaluated. Results: In the control group 100% of animals presented moderate and severe lung infammation, while in the groups with atorvastatin and intratracheal heparin this proportion was lower (55.5%; CI 26.6–81.3%) (p=0.025). A lower degree of moderate or severe hepatic regeneration was evident in the treatment groups with atorvastatin (p=0.009). In this study was demonstrated that statins and heparin might have a protective efect in the paraquat induced destructive phase. More evidence is needed to evaluated of dose–response efects of these drugs before to study in clinical trialsColombia. Ministerio de Ciencia, Tecnología e InnovaciónCOL00399025 páginasapplication/pdfengBMC (BioMed Central)Londres, Inglaterrahttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Comparison of four pharmacological strategies aimed to prevent the lung infammation and paraquat-induced alveolar damageArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAntioxidantes - FarmacologíaAntioxidants - pharmacologyÁcido Ascórbico - FarmacologíaAscorbic Acid - pharmacologyAtorvastatinaAtorvastatinPulmónLungParaquatCiclofosfamidaCyclophosphamideDexametasonaDexamethasoneQuimioterapia CombinadaDrug Therapy, CombinationHeparina de Bajo-Peso-MolecularHeparin, Low-Molecular-WeightNeumoníaPneumoniaAlveolos PulmonaresPulmonary AlveoliFibrosis PulmonarPulmonary FibrosisRatas WistarRats, WistarResultado del TratamientoTreatment Outcomehttps://id.nlm.nih.gov/mesh/D000975https://id.nlm.nih.gov/mesh/D001205https://id.nlm.nih.gov/mesh/D000069059https://id.nlm.nih.gov/mesh/D008168https://id.nlm.nih.gov/mesh/D010269https://id.nlm.nih.gov/mesh/D003520https://id.nlm.nih.gov/mesh/D003907https://id.nlm.nih.gov/mesh/D004359https://id.nlm.nih.gov/mesh/D006495https://id.nlm.nih.gov/mesh/D011014https://id.nlm.nih.gov/mesh/D011650https://id.nlm.nih.gov/mesh/D011658https://id.nlm.nih.gov/mesh/D017208https://id.nlm.nih.gov/mesh/D016896BMC Res. 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