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The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement
BACKGROUND AND PURPOSE: Gastritis is one of the most current gastrointestinal disorders worldwide. Alcohol consumption is one of the major factors, which provides gastritis. Rosmarinic acid (RA) is found in many plants and has powerful antioxidant and anti-inflammatory effects. In this study, the pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216161/ https://www.ncbi.nlm.nih.gov/pubmed/34221064 http://dx.doi.org/10.4103/1735-5362.314829 |
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author | Heidari, Fatemeh Komeili-Movahhed, Tahereh Hamidizad, Zeinab Moslehi, Azam |
author_facet | Heidari, Fatemeh Komeili-Movahhed, Tahereh Hamidizad, Zeinab Moslehi, Azam |
author_sort | Heidari, Fatemeh |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Gastritis is one of the most current gastrointestinal disorders worldwide. Alcohol consumption is one of the major factors, which provides gastritis. Rosmarinic acid (RA) is found in many plants and has powerful antioxidant and anti-inflammatory effects. In this study, the protective effect of RA was evaluated on the histopathological indices, antioxidant ability, and prostaglandin E2 (PGE2) secretion in male rats. EXPERIMENTAL APPROACH: Forty-two animals were divided into control, ethanol-induced gastritis, and RA groups, 6 each. The protective groups included RA administration before gastritis induction at 50 mg (R-G50), 100 mg (R-G100), 150 mg (R-G150), and 200 mg (R-G200) doses. Gastritis was induced by gavage of 1 mL pure ethanol in fasted animals. After 1 h of gastritis induction, the rats were sacrificed and stomach tissue was removed. FINDINGS/RESULTS: Histological evaluation revealed that RA significantly attenuated gastric ulcers, leucocyte infiltration, and hyperemia. It also increased mucosal layer thickness and restored gastric glands. Furthermore, RA decreased malondialdehyde level, increased superoxide dismutase, catalase, and glutathione in the stomach tissue, and raised gastric PGE2 level. CONCLUSION AND IMPLICATIONS: Our study demonstrated that rosmarinic acid has a notable effect on gastritis protection that could be due to increased antioxidant defense and PGE2 secretion, eventually maintenance of mucosal barrier integrity and gastric glands. |
format | Online Article Text |
id | pubmed-8216161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-82161612021-07-02 The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement Heidari, Fatemeh Komeili-Movahhed, Tahereh Hamidizad, Zeinab Moslehi, Azam Res Pharm Sci Original Article BACKGROUND AND PURPOSE: Gastritis is one of the most current gastrointestinal disorders worldwide. Alcohol consumption is one of the major factors, which provides gastritis. Rosmarinic acid (RA) is found in many plants and has powerful antioxidant and anti-inflammatory effects. In this study, the protective effect of RA was evaluated on the histopathological indices, antioxidant ability, and prostaglandin E2 (PGE2) secretion in male rats. EXPERIMENTAL APPROACH: Forty-two animals were divided into control, ethanol-induced gastritis, and RA groups, 6 each. The protective groups included RA administration before gastritis induction at 50 mg (R-G50), 100 mg (R-G100), 150 mg (R-G150), and 200 mg (R-G200) doses. Gastritis was induced by gavage of 1 mL pure ethanol in fasted animals. After 1 h of gastritis induction, the rats were sacrificed and stomach tissue was removed. FINDINGS/RESULTS: Histological evaluation revealed that RA significantly attenuated gastric ulcers, leucocyte infiltration, and hyperemia. It also increased mucosal layer thickness and restored gastric glands. Furthermore, RA decreased malondialdehyde level, increased superoxide dismutase, catalase, and glutathione in the stomach tissue, and raised gastric PGE2 level. CONCLUSION AND IMPLICATIONS: Our study demonstrated that rosmarinic acid has a notable effect on gastritis protection that could be due to increased antioxidant defense and PGE2 secretion, eventually maintenance of mucosal barrier integrity and gastric glands. Wolters Kluwer - Medknow 2021-05-12 /pmc/articles/PMC8216161/ /pubmed/34221064 http://dx.doi.org/10.4103/1735-5362.314829 Text en Copyright: © 2021 Research in Pharmaceutical Sciences https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Heidari, Fatemeh Komeili-Movahhed, Tahereh Hamidizad, Zeinab Moslehi, Azam The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title | The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title_full | The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title_fullStr | The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title_full_unstemmed | The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title_short | The protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
title_sort | protective effects of rosmarinic acid on ethanol-induced gastritis in male rats: antioxidant defense enhancement |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8216161/ https://www.ncbi.nlm.nih.gov/pubmed/34221064 http://dx.doi.org/10.4103/1735-5362.314829 |
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