Morus alba leaf extracts prevent indomethacin-induced intestinal ulcers via suppression of endoplasmic reticulum stress

dc.contributor.authorBoonyong C.
dc.contributor.authorAngkhasirisap W.
dc.contributor.authorLertnitikul N.
dc.contributor.authorKengkoom K.
dc.contributor.authorSuttisri R.
dc.contributor.authorJianmongkol S.
dc.contributor.correspondenceBoonyong C.
dc.contributor.otherMahidol University
dc.date.accessioned2025-04-01T18:12:37Z
dc.date.available2025-04-01T18:12:37Z
dc.date.issued2025-01-01
dc.description.abstractThis study investigated the gastrointestinal (GI) protective effect of water and ethanol extracts of Morus alba leaves in rats who received indomethacin. Rats were randomly distributed into nine groups: a control group, an indomethacin group, and seven groups pre-treated orally with either water and ethanol extracts of M. alba leaves (500, 1,000, and 2,000 mg/kg) or omeprazole (100 mg/kg) for 5 days before receiving oral indomethacin (40 mg/kg). After 24-hour treatment, GI lesions, apoptotic proteins, and prostaglandin E2 (PGE2) in gastric and jejunal tissues were evaluated by macro- and microscopic assessments, western blot analysis, and ELISA, respectively. Both extracts prevented ulcerative lesions in rat jejunum, but not in the stomach. Their intestinal protection involved suppressing protein kinase R-like ER kinase/C/EBP homologous protein signaling and the Bcl-2-associated X protein/B-cell leukemia/lymphoma 2 protein (Bax/Bcl-2) ratio. Both extracts did not affect PGE2 levels in rat GI tissues, which might explain their inability to prevent gastric ulcers.
dc.identifier.citationJournal of Applied Pharmaceutical Science Vol.15 No.3 (2025) , 101-111
dc.identifier.doi10.7324/JAPS.2025.210080
dc.identifier.eissn22313354
dc.identifier.scopus2-s2.0-105000132064
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/108543
dc.rights.holderSCOPUS
dc.subjectPharmacology, Toxicology and Pharmaceutics
dc.subjectMedicine
dc.titleMorus alba leaf extracts prevent indomethacin-induced intestinal ulcers via suppression of endoplasmic reticulum stress
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105000132064&origin=inward
oaire.citation.endPage111
oaire.citation.issue3
oaire.citation.startPage101
oaire.citation.titleJournal of Applied Pharmaceutical Science
oaire.citation.volume15
oairecerif.author.affiliationChulalongkorn University
oairecerif.author.affiliationRangsit University
oairecerif.author.affiliationMahidol University

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