Gastroprotective potential of red onion (Allium cepa L.) peel in ethanol-induced gastric injury in rats: Involvement of Nrf2/HO-1 and HMGB-1/NF-κB trajectories.


Journal

Journal of ethnopharmacology
ISSN: 1872-7573
Titre abrégé: J Ethnopharmacol
Pays: Ireland
ID NLM: 7903310

Informations de publication

Date de publication:
30 Jan 2024
Historique:
received: 29 06 2023
revised: 26 08 2023
accepted: 30 08 2023
medline: 22 11 2023
pubmed: 3 9 2023
entrez: 2 9 2023
Statut: ppublish

Résumé

The utilization of plants with therapeutic properties in traditional medicine has a longstanding practice. Among them, the well-known Allium cepa L. commonly known as onion has been valued for its anti-inflammatory and antioxidant potential in the treatment of various ailments, including gastric ulcers. This study investigated the gastroprotective potential of red onion peel extract and its fractions in a rat model of ethanol-induced gastric ulcer. Moreover, their phytochemical profiles were compared to identify the active metabolites. Mass spectrometry-based metabolomics and chemometrics were performed for phytochemical analysis. Ethanol-induced gastric ulcer model was used to assess the gastroprotective activity. Nine groups of rats were allocated as follows: Group 1 was the normal control; Group 2 rats were used as a positive control/model and received 1 mL of absolute ethanol; and Group 3 rats were treated with famotidine at a dose of 20 mg/kg orally. Group 4 and 5 rats were treated with total acidified ethanolic extract (T1, T2). Group 6 and 7 rats were treated with anthocyanins-rich fractions (P1, P2). Groups 8 and 9 were the flavonoids-rich fraction (S1, S2) treatment. Prior to scarification, the ulcer index in mm was obtained from gastric tissues photographed beside a ruler with further analysis using ImageJ software. Seventy key major and discriminatory metabolites were identified including flavonoids, anthocyanins, phenolic acids, and miscellaneous compounds. The examined extract and its fractions significantly reduced the ulcer index and inflammatory cytokines via downregulating HMGB-1/NF-κB. Also, they augmented the expression of Nrf2/HO-1 and reduced NOX1/4 mRNA expression. Moreover, there was a significant reduction in the oxidative stress and apoptotic biomarkers as well as a noticeable enhancement in histopathological changes of the stomach tissues. Red onion peels have a promising dose dependent gastroprotective potential in alcohol-induced ulcers via modulating Nrf2/HO-1 and HMGB-1/NF-κB trajectories. This highlights the potential of red onion peels in treating gastric ulcers.

Identifiants

pubmed: 37659760
pii: S0378-8741(23)00983-2
doi: 10.1016/j.jep.2023.117115
pii:
doi:

Substances chimiques

Ethanol 3K9958V90M
NF-kappa B 0
Anthocyanins 0
NF-E2-Related Factor 2 0
Plant Extracts 0
Anti-Ulcer Agents 0
Flavonoids 0
Phytochemicals 0
HMGB Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

117115

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest We wish to confirm that there are no known conflicts of interest associated with this publication of “Gastroprotective Potential of Red Onion (Allium cepa L.) Peel in Ethanol-Induced Gastric Injury in Rats: Involvement of Nrf2/HO-1 and HMGB-1/NF-κB Trajectories” to be published in Journal of Ethnopharmacology. With the submission of this manuscript I would like to undertake that the above mentioned manuscript has not been published elsewhere, accepted for publication elsewhere or under editorial review for publication elsewhere; and that my Institute's (Faculty of Pharmacy, Cairo University) representative is fully aware of this submission.

Auteurs

Nermeen B Ali (NB)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt.

Sherihan Salaheldin Abdelhamid Ibrahim (SS)

Department of Pharmacology and Therapeutics, Faculty of Pharmacy, Pharos University in Alexandria, Alexandria, Egypt.

Muhammad A Alsherbiny (MA)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt; Innovation Centre, Victor Chang Cardiac Research Institute, Darlinghurst, Sydney, Australia; NICM Health Research Institute, Western Sydney University, Penrith, NSW, 2747, Australia.

Eman Sheta (E)

Department of Pathology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.

Riham A El-Shiekh (RA)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt. Electronic address: riham.adel@pharma.cu.edu.eg.

Rehab M Ashour (RM)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt.

Amira A El-Gazar (AA)

Department of Pharmacology and Toxicology, Faculty of Pharmacy, October 6 University, 12585, Egypt.

Ghada M Ragab (GM)

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Misr University for Science and Technology, 12585, Egypt.

Sabah H El-Gayed (SH)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt; Department of Pharmacognosy, Faculty of Pharmacy, 6th October University, Cairo, Egypt.

Chun Guang Li (CG)

NICM Health Research Institute, Western Sydney University, Penrith, NSW, 2747, Australia.

Essam Abdel-Sattar (E)

Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo, 11562, Egypt. Electronic address: essam.abdelsattar@pharma.cu.edu.eg.

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Classifications MeSH