The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats

Detalhes bibliográficos
Autor(a) principal: Keshavarzi, Zakieh
Data de Publicação: 2022
Outros Autores: Ashekar, Aleme, Vatanchian, Mehran, Abbaspour, Alireza, Bibak, Bahram, Behnamfar, Morteza, Barzegar, Saeid, Shakeri, Farzaneh
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/205001
Resumo: Various pharmacological effects including anti-inflammatory and anti-oxidant properties were shown for woody endocarpium of walnut alcoholic extract (WEW). In the study, the effect of the WEW extract in acetic acid induced ulcerative colitis in rats was evaluated. Thiol, glutathione peroxidase (GPX), malondialdehyde (MDA), superoxide dismutase (SOD) and gastric acid levels and pathological changes in the colon were investigated in the control group (C), ulcerative colitis group (UC), UC groups treated with WEW extract (10, 20, and 50 mg/kg) and sulfasalazine. Levels of gastric acid, MDA and pathological scores in colon were increased but SOD, GPX and thiol levels were decreased in UC animals compared to those of the control group (p<0.001). Treatment with the highest concentration of extract significantly improved level of thiol and pathological scores compared to the UC group (p<0.05 to p<0.001). Treatment with the two higher concentrations of extract also significantly decreased acid level compared to the UC group (p<0.01 to p<0.001). There was significant improvement in MDA due to treatment with the all concentrations of the extract (p<0.001). Sulfasalazine treatment also significantly improved most parameters compared to the UC group but did not changed pathological scores (p<0.05 to p<0.001). These results indicated a possible preventive therapeutic effect for the WEW extract on UC.
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spelling The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in ratsWEWOxidative stressGastric acid InflammationUlcerative colitisVarious pharmacological effects including anti-inflammatory and anti-oxidant properties were shown for woody endocarpium of walnut alcoholic extract (WEW). In the study, the effect of the WEW extract in acetic acid induced ulcerative colitis in rats was evaluated. Thiol, glutathione peroxidase (GPX), malondialdehyde (MDA), superoxide dismutase (SOD) and gastric acid levels and pathological changes in the colon were investigated in the control group (C), ulcerative colitis group (UC), UC groups treated with WEW extract (10, 20, and 50 mg/kg) and sulfasalazine. Levels of gastric acid, MDA and pathological scores in colon were increased but SOD, GPX and thiol levels were decreased in UC animals compared to those of the control group (p<0.001). Treatment with the highest concentration of extract significantly improved level of thiol and pathological scores compared to the UC group (p<0.05 to p<0.001). Treatment with the two higher concentrations of extract also significantly decreased acid level compared to the UC group (p<0.01 to p<0.001). There was significant improvement in MDA due to treatment with the all concentrations of the extract (p<0.001). Sulfasalazine treatment also significantly improved most parameters compared to the UC group but did not changed pathological scores (p<0.05 to p<0.001). These results indicated a possible preventive therapeutic effect for the WEW extract on UC.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2022-12-19info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/20500110.1590/s2175-97902022e19520Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/205001/196180Copyright (c) 2022 Brazilian Journal of Pharmaceutical Scienceshttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessKeshavarzi, ZakiehAshekar, AlemeVatanchian, MehranAbbaspour, AlirezaBibak, BahramBehnamfar, MortezaBarzegar, SaeidShakeri, Farzaneh2023-08-21T18:24:06Zoai:revistas.usp.br:article/205001Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2023-08-21T18:24:06Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
title The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
spellingShingle The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
Keshavarzi, Zakieh
WEW
Oxidative stress
Gastric acid
Inflammation
Ulcerative colitis
title_short The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
title_full The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
title_fullStr The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
title_full_unstemmed The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
title_sort The effect of woody endocarpium of walnut alcoholic extract on acetic acid-induced ulcerative colitis in rats
author Keshavarzi, Zakieh
author_facet Keshavarzi, Zakieh
Ashekar, Aleme
Vatanchian, Mehran
Abbaspour, Alireza
Bibak, Bahram
Behnamfar, Morteza
Barzegar, Saeid
Shakeri, Farzaneh
author_role author
author2 Ashekar, Aleme
Vatanchian, Mehran
Abbaspour, Alireza
Bibak, Bahram
Behnamfar, Morteza
Barzegar, Saeid
Shakeri, Farzaneh
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Keshavarzi, Zakieh
Ashekar, Aleme
Vatanchian, Mehran
Abbaspour, Alireza
Bibak, Bahram
Behnamfar, Morteza
Barzegar, Saeid
Shakeri, Farzaneh
dc.subject.por.fl_str_mv WEW
Oxidative stress
Gastric acid
Inflammation
Ulcerative colitis
topic WEW
Oxidative stress
Gastric acid
Inflammation
Ulcerative colitis
description Various pharmacological effects including anti-inflammatory and anti-oxidant properties were shown for woody endocarpium of walnut alcoholic extract (WEW). In the study, the effect of the WEW extract in acetic acid induced ulcerative colitis in rats was evaluated. Thiol, glutathione peroxidase (GPX), malondialdehyde (MDA), superoxide dismutase (SOD) and gastric acid levels and pathological changes in the colon were investigated in the control group (C), ulcerative colitis group (UC), UC groups treated with WEW extract (10, 20, and 50 mg/kg) and sulfasalazine. Levels of gastric acid, MDA and pathological scores in colon were increased but SOD, GPX and thiol levels were decreased in UC animals compared to those of the control group (p<0.001). Treatment with the highest concentration of extract significantly improved level of thiol and pathological scores compared to the UC group (p<0.05 to p<0.001). Treatment with the two higher concentrations of extract also significantly decreased acid level compared to the UC group (p<0.01 to p<0.001). There was significant improvement in MDA due to treatment with the all concentrations of the extract (p<0.001). Sulfasalazine treatment also significantly improved most parameters compared to the UC group but did not changed pathological scores (p<0.05 to p<0.001). These results indicated a possible preventive therapeutic effect for the WEW extract on UC.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-19
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/205001
10.1590/s2175-97902022e19520
url https://www.revistas.usp.br/bjps/article/view/205001
identifier_str_mv 10.1590/s2175-97902022e19520
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/205001/196180
dc.rights.driver.fl_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Brazilian Journal of Pharmaceutical Sciences
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 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. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; v. 58 (2022)
Brazilian Journal of Pharmaceutical Sciences; Vol. 58 (2022)
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
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