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Polysaccharide fraction isolated from Passiflora edulis inhibits the inflammatory response and the oxidative stress in mice.
Silva, Renan O; Damasceno, Samara R B; Brito, Tarcísio V; Dias, Jordana M; Fontenele, Amanda M; Braúna, Isabela S; Júnior, José S C; Maciel, Jeanny S; de Paula, Regina C M; Ribeiro, Ronaldo A; Souza, Marcellus H L P; Freitas, Ana L P; Medeiros, Jand-Venes R; Silva, Draulio C; Barbosa, André L R.
Afiliação
  • Silva RO; Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Damasceno SR; Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Brito TV; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Dias JM; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Fontenele AM; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Braúna IS; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Júnior JS; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Maciel JS; Laboratory of Polymer, Department of Organic and Inorganic Chemistry, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • de Paula RC; Laboratory of Polymer, Department of Organic and Inorganic Chemistry, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Ribeiro RA; Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Souza MH; Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Freitas AL; Laboratory of Proteins and Carbohydrates of Marine Algae, Department of Biochemistry and Molecular Biology, Federal University of Ceará, Fortaleza, Ceará, Brazil.
  • Medeiros JV; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
  • Silva DC; Laboratory of Biochemistry, Core of Molecular Ecology (NECMOL), Federal University of San Francisco Valley, Petrolina, Pernambuco, Brazil.
  • Barbosa AL; Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil.
J Pharm Pharmacol ; 67(7): 1017-27, 2015 Jul.
Article em En | MEDLINE | ID: mdl-25808583
ABSTRACT

OBJECTIVES:

The aim of the study was to investigate the anti-inflammatory, antioxidant and antinociceptive actions of PFPe, a polysaccharide fraction isolated from the dried fruit of the Passiflora edulis.

METHODS:

Animals were pretreated with PFPe (0.3, 1 or 3 mg/kg, i.p.) 1 h before induction of paw oedema by carrageenan, histamine, serotonin, compound 48/80 or prostaglandin E2 (PGE2). Neutrophil migration and vascular permeability were measured after carrageenan injection into the peritoneum, and the action of the PFPe on the tumour necrosis factor-alpha, interleukin-1 beta (IL-1ß), myeloperoxidase (MPO), glutathione (GSH) and malondialdehyde (MDA) levels was also evaluated. To assay nociception, we examined acetic acid-induced writhing, formalin-induced paw licking and response latency in the hot plate test. KEY

FINDINGS:

Pretreatment with PFPe significantly inhibited carrageenan-induced paw oedema. PFPe also reduced paw oedema induced by compound 48/80, histamine, serotonin, and PGE2 and compound 48/80-induced vascular permeability. In addition, PFPe significantly reduced the MPO activity, MDA and GSH concentrations, and IL-1ß level. In the nociception tests, PFPe reduced acetic acid-induced writhing and formalin-induced paw licking and did not increase the response latency time.

CONCLUSIONS:

Our results suggest that PFPe administration reduces the inflammatory response by modulation of the liberation or synthesis of histamine and serotonin, by reduction of neutrophil migration, IL-1ß levels, and oxidative stress and nociception.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Estresse Oxidativo / Passiflora / Inflamação / Anti-Inflamatórios Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polissacarídeos / Estresse Oxidativo / Passiflora / Inflamação / Anti-Inflamatórios Idioma: En Ano de publicação: 2015 Tipo de documento: Article