BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/219701 |
Resumo: | Our aim was to evaluate the effects of cisplatin and dexamethasone alone and combined on gastric contractility and histomorphometry of BALB/c and C57BL/6 mice. BALB/c and C57BL/6 male mice (8-week-old) were randomly separated into: Control; Cisplatin (7.5 mg/Kg); Dexamethasone (2.0 mg/Kg); and Dexamethasone plus Cisplatin (2.0 mg/Kg of dexamethasone 1-hour prior to 7.5 mg/Kg of cisplatin). Drugs were administered intraperitoneally for three days. Body weight and food intake were evaluated on 2nd day. Alternating Current Biosusceptometry technique was employed to measure gastric contractions on 3rd day. Afterward, mice were killed for gastric histomorphometric analysis. Cisplatin decreased food intake and caused bradygastria in BALB/c mice; however, the amplitude of gastric contractions decreased in both BALB/c and C57BL/6. Dexamethasone and cisplatin combined restored the gastric frequency and food intake only in BALB/c, but drug combination reduced the gastric amplitude of contractions in both strains. Dexamethasone alone increased gastric mucosa thickness in C57BL/6 and decreased muscular thickness in BALB/c. In conclusion, the mouse strains presented differences in acute effects of cisplatin and dexamethasone alone and combined on gastric function. This reinforces the importance of choosing the appropriate mouse strain for studying the acute effects of drugs on the gastrointestinal tract. |
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network_name_str |
Brazilian Journal of Pharmaceutical Sciences |
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BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasoneBALB/c;Bradygastria;C57BL/6;Gastric motility;StomachOur aim was to evaluate the effects of cisplatin and dexamethasone alone and combined on gastric contractility and histomorphometry of BALB/c and C57BL/6 mice. BALB/c and C57BL/6 male mice (8-week-old) were randomly separated into: Control; Cisplatin (7.5 mg/Kg); Dexamethasone (2.0 mg/Kg); and Dexamethasone plus Cisplatin (2.0 mg/Kg of dexamethasone 1-hour prior to 7.5 mg/Kg of cisplatin). Drugs were administered intraperitoneally for three days. Body weight and food intake were evaluated on 2nd day. Alternating Current Biosusceptometry technique was employed to measure gastric contractions on 3rd day. Afterward, mice were killed for gastric histomorphometric analysis. Cisplatin decreased food intake and caused bradygastria in BALB/c mice; however, the amplitude of gastric contractions decreased in both BALB/c and C57BL/6. Dexamethasone and cisplatin combined restored the gastric frequency and food intake only in BALB/c, but drug combination reduced the gastric amplitude of contractions in both strains. Dexamethasone alone increased gastric mucosa thickness in C57BL/6 and decreased muscular thickness in BALB/c. In conclusion, the mouse strains presented differences in acute effects of cisplatin and dexamethasone alone and combined on gastric function. This reinforces the importance of choosing the appropriate mouse strain for studying the acute effects of drugs on the gastrointestinal tract.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2023-08-28info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://www.revistas.usp.br/bjps/article/view/219701Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); 10Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); 10Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); 102175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/219701/200587https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessAlmeida Gama, Loyane Pirani Rocha Machado, Mariana Aparecida Corá, Luciana Simões Beckmann, Ana Paula Luz Alves, Wellington David Miranda, José Ricardo de ArrudaFrancely Américo , Madileine 2023-12-05T17:14:23Zoai:revistas.usp.br:article/219701Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-12-05T17:14:23Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
title |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
spellingShingle |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone Almeida Gama, Loyane BALB/c; Bradygastria; C57BL/6; Gastric motility; Stomach |
title_short |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
title_full |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
title_fullStr |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
title_full_unstemmed |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
title_sort |
BALB/c and C57BL/6 mouse strains influence gastric function outcomes with administration of cisplatin and dexamethasone |
author |
Almeida Gama, Loyane |
author_facet |
Almeida Gama, Loyane Pirani Rocha Machado, Mariana Aparecida Corá, Luciana Simões Beckmann, Ana Paula Luz Alves, Wellington David Miranda, José Ricardo de Arruda Francely Américo , Madileine |
author_role |
author |
author2 |
Pirani Rocha Machado, Mariana Aparecida Corá, Luciana Simões Beckmann, Ana Paula Luz Alves, Wellington David Miranda, José Ricardo de Arruda Francely Américo , Madileine |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Almeida Gama, Loyane Pirani Rocha Machado, Mariana Aparecida Corá, Luciana Simões Beckmann, Ana Paula Luz Alves, Wellington David Miranda, José Ricardo de Arruda Francely Américo , Madileine |
dc.subject.por.fl_str_mv |
BALB/c; Bradygastria; C57BL/6; Gastric motility; Stomach |
topic |
BALB/c; Bradygastria; C57BL/6; Gastric motility; Stomach |
description |
Our aim was to evaluate the effects of cisplatin and dexamethasone alone and combined on gastric contractility and histomorphometry of BALB/c and C57BL/6 mice. BALB/c and C57BL/6 male mice (8-week-old) were randomly separated into: Control; Cisplatin (7.5 mg/Kg); Dexamethasone (2.0 mg/Kg); and Dexamethasone plus Cisplatin (2.0 mg/Kg of dexamethasone 1-hour prior to 7.5 mg/Kg of cisplatin). Drugs were administered intraperitoneally for three days. Body weight and food intake were evaluated on 2nd day. Alternating Current Biosusceptometry technique was employed to measure gastric contractions on 3rd day. Afterward, mice were killed for gastric histomorphometric analysis. Cisplatin decreased food intake and caused bradygastria in BALB/c mice; however, the amplitude of gastric contractions decreased in both BALB/c and C57BL/6. Dexamethasone and cisplatin combined restored the gastric frequency and food intake only in BALB/c, but drug combination reduced the gastric amplitude of contractions in both strains. Dexamethasone alone increased gastric mucosa thickness in C57BL/6 and decreased muscular thickness in BALB/c. In conclusion, the mouse strains presented differences in acute effects of cisplatin and dexamethasone alone and combined on gastric function. This reinforces the importance of choosing the appropriate mouse strain for studying the acute effects of drugs on the gastrointestinal tract. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-08-28 |
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://www.revistas.usp.br/bjps/article/view/219701 |
url |
https://www.revistas.usp.br/bjps/article/view/219701 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/219701/200587 |
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.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); 10 Brazilian Journal of Pharmaceutical Sciences; v. 59 (2023); 10 Brazilian Journal of Pharmaceutical Sciences; Vol. 59 (2023); 10 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1800222918306693120 |