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Updated: Jan 6, 2026

Extraction and Analysis of Taiwanese Green Propolis
Published on: January 7, 2019
Uncovering the gastroprotective properties of araucaria brown propolis and its active compound, abietic acid
Benhur Judah Cury1, Heloizy de Fátima Teixeira de Silva2, Luiza Pereira Makowieski2
1Department of Pharmacology, Postgraduate Program in Pharmacology, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil.
Abstract:
Although Araucaria brown propolis is a singular propolis with potential therapeutic applications, its anti-ulcer activity remains unexplored. This study investigated the gastroprotective effects of Araucaria brown propolis hydroalcoholic extract (HeBPA, 30- 300 mg/kg and its isolated compound, abietic acid (AA) in corresponding doses to its content in HEBPA. The extract's anti-ulcer activity was evaluated using acidified ethanol-induced gastric ulcers and pylorus ligation to assess gastric antisecretory activity. Additionally, the study examined histological, oxidative, and inflammatory parameters, and the extract's anti-Helicobacter pylori and cytotoxic effects. The 100 mg/kg oral dose of HeBPA promoted gastroprotection by 69.63% by increasing antioxidant defenses (GSH, CAT, and SOD) and reducing MPO activity and MDA levels in ulcerated mucosa. This gastroprotective effect was not due to antisecretory activity, but rather involved non-protein sulfhydryl compounds, alpha-2 adrenergic receptors, prostaglandins, and nitric oxide, as evidenced by the abolition of the effect with L-NAME, NEM, indomethacin, or yohimbine pre-treatment. HeBPA increased mucin stained by PAS in the gastric mucosa and prevented histological damage, reducing edema and inflammatory infiltrate. Additionally, HeBPA promoted fibroblast proliferation at 1 µg/mL, but showed no antibacterial activity against H. pylori (MIC > 1000 µg/mL). In addition, AA at 17 mg/kg reduced by 44.82% the ethanol induced- ulcers. These findings contribute to validate the anti-ulcer effect of Brazilian Araucaria brown propolis, highlighting its potential as a natural resource for developing new gastric ulcer treatments. Notably, AA does appear to be a key bioactive compound responsible for this effect.
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