The gastroprotective effect of Sicyos angulatus against hydrochloric acid/ethanol-induced acute gastritis and gastric ulcer in mice

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Title
The gastroprotective effect of Sicyos angulatus against hydrochloric acid/ethanol-induced acute gastritis and gastric ulcer in mice
Author(s)
Hye Rin Kim; Min Chan Kim; Eun-Jung KangJung-Hyeon ChoiYoung Keun ChoiIn-Bok LeeDong Hee ChoiYun Jeong SeoJung Ran NohYong-Hoon KimChul-Ho Lee
Bibliographic Citation
Journal of Medicinal Food, vol. 27, no. 12, pp. 1219-1230
Publication Year
2024
Abstract
Gastritis and gastric ulcers are common gastric diseases that are caused by infection, drugs, alcohol consumption, or stress. These conditions lead to increased inflammatory cytokines and recruitment of leukocytes, which damage the stomach mucosa and exacerbate disease severity. Sicyos angulatus (SA), an annual vine in the Cucurbitaceae family, is known to have an anti-inflammatory effect, but its efficacy for preventing gastritis and gastric ulcers has not yet been evaluated. In the present study, we investigated the gastroprotective effect of SA using a hydrochloric acid/ethanol-induced gastric mucosal injury mouse model and lipopolysaccharide (LPS)-stimulated KATO III cells. Macroscopic analysis revealed a reduction in gastric ulcer area. Similarly, histopathological analysis showed a dose-dependent decrease in gastric mucosal injury, with significant improvement at 750 mg/kg of SA treatment. Gene expressions of inflammatory cytokines, chemokines, and adhesion molecule were reduced in the SA-administered group. Immunohistochemical staining indicated that SA significantly decreased neutrophil infiltration in the lamina propria and epithelium of the stomach. Kaempferol, a major bioactive flavonoid of SA, also improved gastric injury by reducing macroscopic and microscopic lesions, inflammatory mediator gene expression, and neutrophil infiltration. Furthermore, both SA and kaempferol downregulated LPS-mediated increases in inflammatory cytokines and chemokines following inhibition of p38 and c-Jun N-terminal kinase (JNK) phosphorylation in KATO III cells. These results suggest that SA can ameliorate gastric mucosal injury by inhibiting the recruitment of inflammatory cells, particularly neutrophils, and by suppressing p38 and JNK phosphorylation.
Keyword
Anti-inflammatory effectGastric ulcerGastritisKaempferolNeutrophilSicyos angulatus
ISSN
1096-620X
Publisher
Mary Ann Liebert, Inc
Full Text Link
http://dx.doi.org/10.1089/jmf.2024.k.0091
Type
Article
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Laboratory Animal Resource & Research Center > 1. Journal Articles
Ochang Branch Institute > Division of National Bio-Infrastructure > 1. Journal Articles
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