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Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats

OBJECTIVE: Evaluation of traditionally used royal jelly (RJ) for the management of hepato-renal damage and gastrointestinal ulcerations caused by diclofenac. METHODS: Forty adult male Wistar rats were allocated into four groups. Rats of the 1(st) group received only saline and served as normal group...

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Autores principales: Mostafa, Rasha E., El-Marasy, Salma A., Abdel Jaleel, Gehad A., Bakeer, Rofanda M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997571/
https://www.ncbi.nlm.nih.gov/pubmed/32025584
http://dx.doi.org/10.1016/j.heliyon.2020.e03330
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author Mostafa, Rasha E.
El-Marasy, Salma A.
Abdel Jaleel, Gehad A.
Bakeer, Rofanda M.
author_facet Mostafa, Rasha E.
El-Marasy, Salma A.
Abdel Jaleel, Gehad A.
Bakeer, Rofanda M.
author_sort Mostafa, Rasha E.
collection PubMed
description OBJECTIVE: Evaluation of traditionally used royal jelly (RJ) for the management of hepato-renal damage and gastrointestinal ulcerations caused by diclofenac. METHODS: Forty adult male Wistar rats were allocated into four groups. Rats of the 1(st) group received only saline and served as normal group. The remaining 3 groups received diclofenac (50 mg/kg/day, I.P.) for 7 days. Group 2 served as diclofenac-control group. Groups 3 and 4 received RJ (150 and 300 mg/kg/day, P.O.) respectively for 30 days. Twenty-four hours after the last treatment, blood samples were collected, rats were sacrificed, and livers, kidneys, stomachs & intestines were harvested. Stomachs and intestines were tested for ulcer counts. Serum levels of AST, ALT, creatinine and urea were investigated. Hepatic, renal, gastric and intestinal tissue contents of myeloperoxidase (MPO) and prostaglandin-E2 (PGE2) were measured. Histopathological examinations were also performed followed by immunohistochemical determination of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression. RESULTS: Diclofenac administration caused significant deterioration of all the above mentioned parameters. RJ improved hepatic and renal functions. Gastric and intestinal ulcer counts were significantly ameliorated. Hepatic, renal, gastric and intestinal tissue PGE-2 contents and COX-2 expression were significantly elevated. RJ also significantly reduced MPO content and iNOS expression as compared to diclofenac-control group. Improvements of the histopathological pictures of hepatic, renal, gastric and intestinal tissues were also apparent. CONCLUSION: The study demonstrates promising protective effects of RJ against diclofenac-induced hepato-renal damage and gastrointestinal ulceration in rats.
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spelling pubmed-69975712020-02-05 Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats Mostafa, Rasha E. El-Marasy, Salma A. Abdel Jaleel, Gehad A. Bakeer, Rofanda M. Heliyon Article OBJECTIVE: Evaluation of traditionally used royal jelly (RJ) for the management of hepato-renal damage and gastrointestinal ulcerations caused by diclofenac. METHODS: Forty adult male Wistar rats were allocated into four groups. Rats of the 1(st) group received only saline and served as normal group. The remaining 3 groups received diclofenac (50 mg/kg/day, I.P.) for 7 days. Group 2 served as diclofenac-control group. Groups 3 and 4 received RJ (150 and 300 mg/kg/day, P.O.) respectively for 30 days. Twenty-four hours after the last treatment, blood samples were collected, rats were sacrificed, and livers, kidneys, stomachs & intestines were harvested. Stomachs and intestines were tested for ulcer counts. Serum levels of AST, ALT, creatinine and urea were investigated. Hepatic, renal, gastric and intestinal tissue contents of myeloperoxidase (MPO) and prostaglandin-E2 (PGE2) were measured. Histopathological examinations were also performed followed by immunohistochemical determination of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression. RESULTS: Diclofenac administration caused significant deterioration of all the above mentioned parameters. RJ improved hepatic and renal functions. Gastric and intestinal ulcer counts were significantly ameliorated. Hepatic, renal, gastric and intestinal tissue PGE-2 contents and COX-2 expression were significantly elevated. RJ also significantly reduced MPO content and iNOS expression as compared to diclofenac-control group. Improvements of the histopathological pictures of hepatic, renal, gastric and intestinal tissues were also apparent. CONCLUSION: The study demonstrates promising protective effects of RJ against diclofenac-induced hepato-renal damage and gastrointestinal ulceration in rats. Elsevier 2020-02-01 /pmc/articles/PMC6997571/ /pubmed/32025584 http://dx.doi.org/10.1016/j.heliyon.2020.e03330 Text en © 2020 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Mostafa, Rasha E.
El-Marasy, Salma A.
Abdel Jaleel, Gehad A.
Bakeer, Rofanda M.
Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title_full Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title_fullStr Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title_full_unstemmed Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title_short Protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
title_sort protective effect of royal jelly against diclofenac-induced hepato-renal damage and gastrointestinal ulcerations in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997571/
https://www.ncbi.nlm.nih.gov/pubmed/32025584
http://dx.doi.org/10.1016/j.heliyon.2020.e03330
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