Salacia campestris root bark extract: peroxidase inhibition, antioxidant and antiradical profile


Autoria(s): Rebuglio Vellosa, Jose Carlos; Khalil, Najeh Maissar; Gutierres, Vainia Ortega; Santos, Vainia Aparecida de Freitas Formenton Macedo dos; Furlan, Maysa; Brunetti, Iguatemy Lourenço; Oliveira, Olga Maria Mascarenhas de Faria
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/01/2009

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Reactive oxygen species (ROS) and free radical species have been implicated in initiating or accompanying many diseases in living organisms; there is thus, a continual need for antioxidants molecules to inactivate ROS/free radicals. Many studies of plants crude extracts have demonstrated free-radical scavenging and antioxidant action. Salacia species have long been used, in several countries, as traditional medicines against certain diseases and for their anti-inflammatory properties. In this Study, Salacia campestris Walp (Hippocrateaceae) root bark ethanol extract (ScEtOH) was assessed for its ability to scavenge free radicals and reactive oxygen species; the results were expressed as percentage inhibition of the active species. ScEtOH was efficient against studied species: DPPH radical (obtained inhibition = 30%), ABTS(center dot+) (IC(50) = 1.8 +/- 0.8 mu g/mL), HOCI (IC(50) = 1.7 +/- 0.1 mu g/mL), O2(center dot-) (obtained inhibition = 32%), and NO(center dot) (obtained inhibition = 18%). Peroxidase activity inhibition was evaluated through the guaiacol oxidation reaction catalyzed by hemin, HRP and. myeloperoxidase (MPO); data showed that ScEtOH at 10 mu g/mL led to 54 and 51% of inhibition, respectively, for the hemin and HRP systems. In the MPO system, ScEtOH promoted a 50% inhibition at 8.9 mu g/mL, whereas quercetin, a powerful MPO inhibitor, inhibited this system at 1.35 mu g/mL.

Formato

99-107

Identificador

http://dx.doi.org/10.1590/S1984-82502009000100012

Brazilian Journal of Pharmaceutical Sciences. São Paulo: Univ São Paulo, Conjunto Quimicas, v. 45, n. 1, p. 99-107, 2009.

1984-8250

http://hdl.handle.net/11449/25305

10.1590/S1984-82502009000100012

S1984-82502009000100012

WOS:000267750700012

WOS000267750700012.pdf

Idioma(s)

eng

Publicador

Universidade de São Paulo (USP), Conjunto Quimicas

Relação

Brazilian Journal of Pharmaceutical Sciences

Direitos

openAccess

Tipo

info:eu-repo/semantics/article