Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Research, Society and Development |
Texto Completo: | https://rsdjournal.org/index.php/rsd/article/view/33047 |
Resumo: | This study aimed to histologically evaluate the pharmacological activity of meloxicam, COX-2 inhibitor, on liver function in arthritic rats. Meloxicam is a non-steroidal anti-inflammatory drug (NSAID), COX-2 inhibitor, generally prescribed in the area of rheumatology. Thus, 18 Wistar rats were divided into 3 groups with 6 animals each: G1 (Negative Control), G2 (Arthritis induced with Zymosan [Zy]), G3 (Arthritis induced with Zymosan [Zy] and treated with meloxicam). The G3 treatment started on the 21st day after induction. The animals were sacrificed, by overdose of Ketamine/Xylazine, seven, 14 and 21 days after the beginning of the meloxicam treatment. Liver samples were collected from the animals, fixed in Millonig buffer containing 10% formaldehyde and processed for conventional histological analysis. G1 animals showed absence of inflammation and degeneration of hepatocytes. In the G2 group, a slight cytoplasmic alteration was observed at seven and 14 days. At 21 days, intense cytoplasmic and nuclear disorganization was detected, accompanied by cell necrosis. In G3, large spacing between sinusoid capillaries was detected. In some 14-day-old animals, amyloidosis was observed, with the presence of a large number of vacuolated hepatocytes involved in an amorphous mass of necrotic cells. Most of the hepatocyte nuclei had compacted chromatin, evidencing cellular degeneration. Meloxican, used as an anti-inflammatory in the synovial region, showed that, in addition to its beneficial effects for the treatment of rheumatological diseases, it is capable of, when administered orally, promoting a high level of liver damage. |
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Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental studyArtritis inducida, citotoxicidad de hepatocitos y fármacos antiinflamatorios no esteroideos (AINE) – estudio experimentalArtrite induzida, citotoxicidade dos hepatócitos e anti-inflamatórios não esteroidais (AINES) – estudo experimentalMeloxicamZymosanArtritis inducida.MeloxicamZymosanInduced arthritis.MeloxicamZymosanArtrite induzida.This study aimed to histologically evaluate the pharmacological activity of meloxicam, COX-2 inhibitor, on liver function in arthritic rats. Meloxicam is a non-steroidal anti-inflammatory drug (NSAID), COX-2 inhibitor, generally prescribed in the area of rheumatology. Thus, 18 Wistar rats were divided into 3 groups with 6 animals each: G1 (Negative Control), G2 (Arthritis induced with Zymosan [Zy]), G3 (Arthritis induced with Zymosan [Zy] and treated with meloxicam). The G3 treatment started on the 21st day after induction. The animals were sacrificed, by overdose of Ketamine/Xylazine, seven, 14 and 21 days after the beginning of the meloxicam treatment. Liver samples were collected from the animals, fixed in Millonig buffer containing 10% formaldehyde and processed for conventional histological analysis. G1 animals showed absence of inflammation and degeneration of hepatocytes. In the G2 group, a slight cytoplasmic alteration was observed at seven and 14 days. At 21 days, intense cytoplasmic and nuclear disorganization was detected, accompanied by cell necrosis. In G3, large spacing between sinusoid capillaries was detected. In some 14-day-old animals, amyloidosis was observed, with the presence of a large number of vacuolated hepatocytes involved in an amorphous mass of necrotic cells. Most of the hepatocyte nuclei had compacted chromatin, evidencing cellular degeneration. Meloxican, used as an anti-inflammatory in the synovial region, showed that, in addition to its beneficial effects for the treatment of rheumatological diseases, it is capable of, when administered orally, promoting a high level of liver damage.Este estudio tuvo como objetivo evaluar histológicamente la actividad farmacológica del meloxicam, inhibidor de la COX-2, sobre la función hepática en ratas artríticas. El meloxicam es un fármaco antiinflamatorio no esteroideo (AINE), inhibidor de la COX-2, generalmente prescrito en el área de la reumatología. Así, 18 ratas Wistar se dividieron en 3 grupos de 6 animales cada uno: G1 (Control Negativo), G2 (Artritis inducida con Zymosan [Zy]), G3 (Artritis inducida con Zymosan [Zy] y tratada con meloxicam). El tratamiento G3 comenzó el día 21 después de la inducción. Los animales fueron sacrificados, por sobredosis de Ketamina/Xilazina, siete, 14 y 21 días después del inicio del tratamiento con meloxicam. Se recogieron muestras de hígado de los animales, se fijaron en tampón Millonig que contenía formaldehído al 10 % y se procesaron para análisis histológico convencional. Los animales G1 mostraron ausencia de inflamación y degeneración de hepatocitos. En el grupo G2 se observó una ligera alteración citoplasmática a los siete y 14 días. A los 21 días se detectó una intensa desorganización citoplasmática y nuclear, acompañada de necrosis celular. En G3, se detectó un gran espacio entre los capilares sinusoidales. En algunos animales de 14 días se observó amiloidosis, con presencia de un gran número de hepatocitos vacuolados envueltos en una masa amorfa de células necróticas. La mayoría de los núcleos de hepatocitos presentaban cromatina compactada, evidenciando degeneración celular. Meloxican, utilizado como antiinflamatorio en la región sinovial, demostró que, además de sus efectos beneficiosos para el tratamiento de enfermedades reumatológicas, es capaz, cuando se administra por vía oral, de promover un alto nivel de daño hepático.Este estudo teve como objetivo avaliar histologicamente a atividade farmacológica do meloxicam, inibidor da COX-2, sobre a função hepática em ratos artríticos. O meloxicam é um anti-inflamatório não esteroidal (AINE), inibidor da COX-2, geralmente prescrito na área de reumatologia. Assim, 18 ratos Wistar foram divididos em 3 grupos com 6 animais cada: G1 (Controle Negativo), G2 (Artrite induzida com Zymosan [Zy]), G3 (Artrite induzida com Zymosan [Zy] e tratados com meloxicam). O tratamento com G3 iniciou-se no 21º dia após a indução. Os animais foram sacrificados, por overdose de Cetamina/Xilazina, sete, 14 e 21 dias após o início do tratamento com meloxicam. Amostras de fígado foram coletadas dos animais, fixadas em tampão Millonig contendo 10% de formaldeído e processadas para análise histológica convencional. Os animais do G1 apresentaram ausência de inflamação e degeneração dos hepatócitos. No grupo G2, foi observada discreta alteração citoplasmática aos sete e 14 dias. Aos 21 dias, foi detectada intensa desorganização citoplasmática e nuclear, acompanhada de necrose celular. Em G3, foi detectado grande espaçamento entre os capilares sinusóides. Em alguns animais com 14 dias de idade foi observada amiloidose, com a presença de grande número de hepatócitos vacuolados envolvidos em uma massa amorfa de células necróticas. A maioria dos núcleos dos hepatócitos apresentava cromatina compactada, evidenciando degeneração celular. O meloxicano, utilizado como anti-inflamatório na região sinovial, mostrou que, além de seus efeitos benéficos para o tratamento de doenças reumatológicas, é capaz de, quando administrado por via oral, promover alto nível de dano hepático.Research, Society and Development2022-08-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/3304710.33448/rsd-v11i10.33047Research, Society and Development; Vol. 11 No. 10; e526111033047Research, Society and Development; Vol. 11 Núm. 10; e526111033047Research, Society and Development; v. 11 n. 10; e5261110330472525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIenghttps://rsdjournal.org/index.php/rsd/article/view/33047/28049Copyright (c) 2022 Felipe Misael da Silva Morsoleto; Pedro Rondon Werneck; Juliana Aparecida Ramiro Moreira; Fernando Russo Costa do Bomfim; Marcelo Augusto Marretto Esquisatto; Maria Jose Misael da Silva Morsoletohttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessMorsoleto, Felipe Misael da Silva Werneck, Pedro Rondon Moreira, Juliana Aparecida Ramiro Bomfim, Fernando Russo Costa do Esquisatto, Marcelo Augusto Marretto Morsoleto, Maria Jose Misael da Silva 2022-08-12T22:23:03Zoai:ojs.pkp.sfu.ca:article/33047Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:48:49.569587Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false |
dc.title.none.fl_str_mv |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study Artritis inducida, citotoxicidad de hepatocitos y fármacos antiinflamatorios no esteroideos (AINE) – estudio experimental Artrite induzida, citotoxicidade dos hepatócitos e anti-inflamatórios não esteroidais (AINES) – estudo experimental |
title |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
spellingShingle |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study Morsoleto, Felipe Misael da Silva Meloxicam Zymosan Artritis inducida. Meloxicam Zymosan Induced arthritis. Meloxicam Zymosan Artrite induzida. |
title_short |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
title_full |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
title_fullStr |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
title_full_unstemmed |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
title_sort |
Induced arthritis, hepatocytes cytotoxicity and non-steroidal anti-inflammatory drugs (NSAIDs) – experimental study |
author |
Morsoleto, Felipe Misael da Silva |
author_facet |
Morsoleto, Felipe Misael da Silva Werneck, Pedro Rondon Moreira, Juliana Aparecida Ramiro Bomfim, Fernando Russo Costa do Esquisatto, Marcelo Augusto Marretto Morsoleto, Maria Jose Misael da Silva |
author_role |
author |
author2 |
Werneck, Pedro Rondon Moreira, Juliana Aparecida Ramiro Bomfim, Fernando Russo Costa do Esquisatto, Marcelo Augusto Marretto Morsoleto, Maria Jose Misael da Silva |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Morsoleto, Felipe Misael da Silva Werneck, Pedro Rondon Moreira, Juliana Aparecida Ramiro Bomfim, Fernando Russo Costa do Esquisatto, Marcelo Augusto Marretto Morsoleto, Maria Jose Misael da Silva |
dc.subject.por.fl_str_mv |
Meloxicam Zymosan Artritis inducida. Meloxicam Zymosan Induced arthritis. Meloxicam Zymosan Artrite induzida. |
topic |
Meloxicam Zymosan Artritis inducida. Meloxicam Zymosan Induced arthritis. Meloxicam Zymosan Artrite induzida. |
description |
This study aimed to histologically evaluate the pharmacological activity of meloxicam, COX-2 inhibitor, on liver function in arthritic rats. Meloxicam is a non-steroidal anti-inflammatory drug (NSAID), COX-2 inhibitor, generally prescribed in the area of rheumatology. Thus, 18 Wistar rats were divided into 3 groups with 6 animals each: G1 (Negative Control), G2 (Arthritis induced with Zymosan [Zy]), G3 (Arthritis induced with Zymosan [Zy] and treated with meloxicam). The G3 treatment started on the 21st day after induction. The animals were sacrificed, by overdose of Ketamine/Xylazine, seven, 14 and 21 days after the beginning of the meloxicam treatment. Liver samples were collected from the animals, fixed in Millonig buffer containing 10% formaldehyde and processed for conventional histological analysis. G1 animals showed absence of inflammation and degeneration of hepatocytes. In the G2 group, a slight cytoplasmic alteration was observed at seven and 14 days. At 21 days, intense cytoplasmic and nuclear disorganization was detected, accompanied by cell necrosis. In G3, large spacing between sinusoid capillaries was detected. In some 14-day-old animals, amyloidosis was observed, with the presence of a large number of vacuolated hepatocytes involved in an amorphous mass of necrotic cells. Most of the hepatocyte nuclei had compacted chromatin, evidencing cellular degeneration. Meloxican, used as an anti-inflammatory in the synovial region, showed that, in addition to its beneficial effects for the treatment of rheumatological diseases, it is capable of, when administered orally, promoting a high level of liver damage. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-08-09 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/33047 10.33448/rsd-v11i10.33047 |
url |
https://rsdjournal.org/index.php/rsd/article/view/33047 |
identifier_str_mv |
10.33448/rsd-v11i10.33047 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://rsdjournal.org/index.php/rsd/article/view/33047/28049 |
dc.rights.driver.fl_str_mv |
https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Research, Society and Development |
publisher.none.fl_str_mv |
Research, Society and Development |
dc.source.none.fl_str_mv |
Research, Society and Development; Vol. 11 No. 10; e526111033047 Research, Society and Development; Vol. 11 Núm. 10; e526111033047 Research, Society and Development; v. 11 n. 10; e526111033047 2525-3409 reponame:Research, Society and Development instname:Universidade Federal de Itajubá (UNIFEI) instacron:UNIFEI |
instname_str |
Universidade Federal de Itajubá (UNIFEI) |
instacron_str |
UNIFEI |
institution |
UNIFEI |
reponame_str |
Research, Society and Development |
collection |
Research, Society and Development |
repository.name.fl_str_mv |
Research, Society and Development - Universidade Federal de Itajubá (UNIFEI) |
repository.mail.fl_str_mv |
rsd.articles@gmail.com |
_version_ |
1797052827398307840 |