Propyl Gallate Mitigates Gastric Injury Caused by Indomethacin in Wistar Rats

Propyl gallate (PG) is an edible food-grade antioxidant, but its gastroprotective potential has not been extensively evaluated. This study evaluated the protective effects of PG on indomethacin-induced gastric mucosal injury in Wistar rats. Male rats were assigned to control (C), vehicle (Vehicle), PG-treated (20, 40, and 100 mg/kg; LPG, MPG, and HPG), and positive control (omeprazole, 30 mg/kg; OM). Following 7 days of pretreatment, indomethacin (100 mg/kg) was administered to all groups except group C, and the gastric tissues were collected for further analysis. PG pretreatment significantly reduced ulcer area in a dose-dependent manner (<i>p</i> < 0.05). PG also suppressed gastric inflammatory protein expression (NF-κB, COX-2, TNF-α, IL-6, and iNOS), restoring prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) levels, and enhanced antioxidant defenses, as evidenced by increased glutathione (GSH) levels and superoxide dismutase (SOD) activity. These findings demonstrate that PG exerts marked gastroprotective effects through combined anti-inflammatory and antioxidant mechanisms.

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Journal
Journal of Agricultural and Food Chemistry
Published
2025-12-22
DOI
https://doi.org/10.1021/acs.jafc.5c13909
Primary Topic
Tannin, Tannase and Anticancer Activities
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article
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article

Propyl Gallate Mitigates Gastric Injury Caused by Indomethacin in Wistar Rats

Kuo‐An Tseng, Y M WANG, Felix Widodo, Yu-Hsiang Chen et al.
Journal of Agricultural and Food Chemistry
Tannin, Tannase and Anticancer Activities
article

Propyl Gallate Mitigates Gastric Injury Caused by Indomethacin in Wistar Rats

Kuo‐An Tseng, Y M WANG, Felix Widodo, Yu-Hsiang Chen, Yu-Kuo Chen, Shih-Chao Lin, Pei-Shan Tsai, Tsair-Bor Yen
article en

Abstract

Propyl gallate (PG) is an edible food-grade antioxidant, but its gastroprotective potential has not been extensively evaluated. This study evaluated the protective effects of PG on indomethacin-induced gastric mucosal injury in Wistar rats. Male rats were assigned to control (C), vehicle (Vehicle), PG-treated (20, 40, and 100 mg/kg; LPG, MPG, and HPG), and positive control (omeprazole, 30 mg/kg; OM). Following 7 days of pretreatment, indomethacin (100 mg/kg) was administered to all groups except group C, and the gastric tissues were collected for further analysis. PG pretreatment significantly reduced ulcer area in a dose-dependent manner (<i>p</i> < 0.05). PG also suppressed gastric inflammatory protein expression (NF-κB, COX-2, TNF-α, IL-6, and iNOS), restoring prostaglandin E<sub>2</sub> (PGE<sub>2</sub>) levels, and enhanced antioxidant defenses, as evidenced by increased glutathione (GSH) levels and superoxide dismutase (SOD) activity. These findings demonstrate that PG exerts marked gastroprotective effects through combined anti-inflammatory and antioxidant mechanisms.

Journal of Agricultural and Food ChemistryVol. 74(1)
National Taiwan Ocean University (TW), National Pingtung University of Science and Technology (TW), Institute of Marine Biotechnology (DE), University School (US), Indiana University School of Medicine, Indiana University (US)
Zero hunger
Openalex Percentile: Top 31%
Tannin, Tannase and Anticancer Activities
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