Analysis of the Potential Topical Anti-Inflammatory Activity ofAverrhoa carambolaL. in Mice

Author:

Cabrini Daniela Almeida1,Moresco Henrique Hunger2,Imazu Priscila1,Silva Cíntia Delai da1,Pietrovski Evelise Fernandes1,Mendes Daniel Augusto Gasparin Bueno1,Prudente Arthur da Silveira1,Pizzolatti Moacir Geraldo2,Brighente Inês Maria Costa2,Otuki Michel Fleith3

Affiliation:

1. Laboratory of Inflammation, Department of Pharmacology, Universidade Federal do Paraná, Curitiba, PR, Brazil

2. Department of Chemistry, Universidade Federal de Santa Catarina, Campus Universitário, Trindade, Florianópolis, SC, Brazil

3. Department of Pharmaceutical Sciences, Universidade Estadual de Ponta Grossa, Ponta Grossa, Campus Uvaranas, Av. General Carlos Cavalcanti 4748, Bloco M, Sala 94, 84030-900, PR, Brazil

Abstract

Inflammatory skin disorders, such as psoriasis and atopic dermatitis, are very common in the population; however, the treatments currently available are not well tolerated and are often ineffective.Averrhoa carambolaL. (Oxalidaceae) is an Asian tree that has been used in traditional folk medicine in the treatment of several skin disorders. The present study evaluates the topical anti-inflammatory effects of the crude ethanolic extract ofA. carambolaleaves, its hexane, ethyl acetate, and butanol fractions and two isolated flavonoids on skin inflammation. Anti-inflammatory activity was measured using a croton oil-induced ear edema model of inflammation in mice. Topically applied ethanolic extract reduced edema in a dose-dependent manner, resulting in a maximum inhibition of 73 ± 3% and an ID50value of 0.05 (range: 0.02–0.13) mg/ear. Myeloperoxidase (MPO) activity was also inhibited by the extract, resulting in a maximum inhibition of 60 ± 6% (0.6 mg/ear). All of the fractions tested caused inhibition of edema formation and of MPO activity. Treatment with the ethyl acetate fraction was the most effective, resulting in inhibition levels of 75 ± 5 and 54 ± 8% for edema formation and MPO activity, respectively. However, treatment of mice with isolated compounds [apigenin-6-C-β-l-fucopyranoside and apigenin-6-C-(2-O-α-l-rhamnopyranosyl)-β-l-fucopyranoside] did not yield successful results. Apigenin-6-C-(2-O-α-l-rhamnopyranosyl)-β-l-fucopyranoside caused only a mild reduction in edema formation (28 ± 11%). Taken together, these preliminary results support the popular use ofA. carambolaas an anti-inflammatory agent and open up new possibilities for its use in skin disorders.

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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