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.
Rats
Animals
Stomach Ulcer
/ chemically induced
Ethanol
/ therapeutic use
Onions
NF-kappa B
/ metabolism
Ulcer
/ drug therapy
Anthocyanins
NF-E2-Related Factor 2
/ metabolism
Plant Extracts
/ pharmacology
Anti-Ulcer Agents
/ pharmacology
Flavonoids
/ therapeutic use
Phytochemicals
/ adverse effects
HMGB Proteins
/ metabolism
Gastric Mucosa
/ pathology
Ethanol-induced gastric ulcer rat model
Metabolomics
Nrf2/HO-1 and HMGB-1/NF-κB
Red onion peel (Allium cepa L.)
UPLC-qTOF-MS
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
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
117115Informations 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.