Lucas A Chibli1, Kamilla C M Rodrigues2, Carolina M Gasparetto3, Nícolas C C Pinto4, Rodrigo L Fabri5, Elita Scio6, Maria S Alves7, Glauciemar Del-Vechio-Vieira8, Orlando V Sousa9. 1. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: lucano.farm@gmail.com. 2. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: kamillacoelho@yahoo.com.br. 3. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: carolina.gasparetto@ufjf.edu.br. 4. Department of Biochemistry, Institute of Biological Sciences, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: nickbioquimica@hotmail.com. 5. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: rodrigolfabri@yahoo.com.br. 6. Department of Biochemistry, Institute of Biological Sciences, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: elita.scio@ufjf.edu.br. 7. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: alves_ms2005@yahoo.com.br. 8. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: glauciemar@gmail.com. 9. Department of Pharmaceutical Sciences, Faculty of Pharmacy, Federal University of Juiz de Fora, Rua José Lourenço Kelmer, Campus Universitário, São Pedro, CEP 36036-330, Juiz de Fora, MG, Brazil. Electronic address: orlando.sousa@ufjf.edu.br.
Abstract
ETHNOPHARMACOLOGICAL RELEVANCE: Bryophyllum pinnatum (Lam.) Oken (Crassulaceae), popularly known in Brazil as "folha-da-fortuna", is a plant species used in folk medicine for the external and internal treatment of inflammation, infection, wound, burn, boil, ulcers and gastritis, and several other diseases. The present study aimed to perform the chemical characterization and the evaluation of the topical anti-inflammatory effect of the ethanol extract of Bryophyllum pinnatum leaves (EEBP) in acute and chronic mice ear edema models induced by different irritant agents. MATERIALS AND METHODS: The EEBP chemical characterization was performed by HPLC-UV DAD. Ear edema on Swiss mice was induced by the topical application of Croton oil (single and multiple applications), arachidonic acid, phenol, capsaicin and ethyl phenylpropiolate (EPP). The topical anti-inflammatory effect of EEBP was evaluated by measuring the ear weight (acute inflammation models) and thickness (chronic inflammation model). Histopathological analyses of ear tissue samples sensitized with Croton oil (single and multiple applications) were also performed. RESULTS: The flavonoids rutin, quercetin, luteolin and luteolin7-O-β-d-glucoside were detected in EEBP. Topical application of EEBP significantly (P<0.001) inhibited the ear edema induced by Croton oil single application (inhibition of 57%), arachidonic acid (inhibition of 67%), phenol (inhibition of 80%), capsaicin (inhibition of 72%), EPP (inhibition of 75%) and Croton oil multiple application (55% after 9 days). Histopathological analyses confirmed the topical anti-inflammatory effect of EEBP since it was observed reduction of edema, epidermal hyperplasia, inflammatory cells infiltration and vasodilation. CONCLUSIONS: The results suggest that EEBP is effective as a topical anti-inflammatory agent in acute and chronic inflammatory processes possibly due to inhibition of arachidonic acid pathway, which justify the traditional use of Bryophyllum pinnatum as a remedy for skin disorders.
ETHNOPHARMACOLOGICAL RELEVANCE: Bryophyllum pinnatum (Lam.) Oken (Crassulaceae), popularly known in Brazil as "folha-da-fortuna", is a plant species used in folk medicine for the external and internal treatment of inflammation, infection, wound, burn, boil, ulcers and gastritis, and several other diseases. The present study aimed to perform the chemical characterization and the evaluation of the topical anti-inflammatory effect of the ethanol extract of Bryophyllum pinnatum leaves (EEBP) in acute and chronic mice ear edema models induced by different irritant agents. MATERIALS AND METHODS: The EEBP chemical characterization was performed by HPLC-UV DAD. Ear edema on Swiss mice was induced by the topical application of Croton oil (single and multiple applications), arachidonic acid, phenol, capsaicin and ethyl phenylpropiolate (EPP). The topical anti-inflammatory effect of EEBP was evaluated by measuring the ear weight (acute inflammation models) and thickness (chronic inflammation model). Histopathological analyses of ear tissue samples sensitized with Croton oil (single and multiple applications) were also performed. RESULTS: The flavonoidsrutin, quercetin, luteolin and luteolin7-O-β-d-glucoside were detected in EEBP. Topical application of EEBP significantly (P<0.001) inhibited the ear edema induced by Croton oil single application (inhibition of 57%), arachidonic acid (inhibition of 67%), phenol (inhibition of 80%), capsaicin (inhibition of 72%), EPP (inhibition of 75%) and Croton oil multiple application (55% after 9 days). Histopathological analyses confirmed the topical anti-inflammatory effect of EEBP since it was observed reduction of edema, epidermal hyperplasia, inflammatory cells infiltration and vasodilation. CONCLUSIONS: The results suggest that EEBP is effective as a topical anti-inflammatory agent in acute and chronic inflammatory processes possibly due to inhibition of arachidonic acid pathway, which justify the traditional use of Bryophyllum pinnatum as a remedy for skin disorders.
Authors: Rafael P Pinheiro; Muiara A Moraes; Bruna C S Santos; Rodrigo L Fabri; Glauciemar Del-Vechio-Vieira; Célia H Yamamoto; Ana Lúcia S M Araújo; Aílson L A Araújo; Orlando V Sousa Journal: Inflammopharmacology Date: 2017-11-14 Impact factor: 4.473
Authors: Kamilla C M Rodrigues; Lucas A Chibli; Bruna C S Santos; Vanessa S Temponi; Nícolas C C Pinto; Elita Scio; Glauciemar Del-Vechio-Vieira; Maria S Alves; Orlando V Sousa Journal: Int J Mol Sci Date: 2016-12-01 Impact factor: 5.923