Affiliation:
1. Department of Pharmaceutical Science, University of Vale do Itajaí , Itajaí , Santa Catarina, Brazil
2. Department of Pharmacology, Laboratory of Pharmacology Applied to the Gastrointestinal Tract and its Interactions, Federal University of Santa Catarina , Florianópols , Brazil
3. Center of Exact Sciences, Federal University of Espírito Santo , Vitória, Espírito Santo , Brazil
4. School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo , Ribeirão Preto , Brazil
Abstract
Abstract
Objective
To investigate the effects of Araucaria sp. brown propolis (ABP) against trinitrobenzenesulfonic acid (TNBS)-induced colitis in rats.
Methods
Animals received vehicle (1% DMSO, 1 ml/kg) or hydroalcoholic extract of ABP (hydroalcoholic extract of Araucaria sp. brown propolis (HEABP), 30, 100, and 300 mg/kg) orally, or dexamethasone (25 mg/kg, s.c.) for 5 days. On day 4, the animals received intracolonic TNBS (150 mg/kg), on day 6 they were euthanized. The weight of the animals, the macroscopic and microscopic colonic damage, reduced glutathione (GSH) and malondialdehyde (MDA) levels, and the activity of glutathione S-transferase (GST), catalase (CAT), superoxide dismutase (SOD), and myeloperoxidase (MPO) were measured in colon homogenate. The action of HEABP and two isolated compounds in neutrophil migration was recorded.
Key findings
HEABP (100 and 300 mg/kg), but not dexamethasone, decreased colonic lesion, and increased colonic mucin staining. In parallel, HEABP decreased MDA and restored GSH levels and the activity of SOD, CAT, and GST in the colon. A dose-dependent inhibition of MPO activity was observed (LogIC50 = 1.9). Moreover, HEBPA and the junicedric and abietic acids inhibited the neutrophil chemotaxis in vitro and HEBPA reduced neutrophil migration in vivo.
Conclusion
HEABP may be promising in the therapies for inflammatory bowel diseases, reducing oxidative and inflammatory damage, especially mediated by neutrophils.
Funder
São Paulo Scientific Foundations-FAPESP
Publisher
Oxford University Press (OUP)