Polysaccharide fraction isolated from P assiflora edulis inhibits the inflammatory response and the oxidative stress in mice

Author:

Silva Renan O1,Damasceno Samara R B1,Brito Tarcísio V2,Dias Jordana M2,Fontenele Amanda M2,Braúna Isabela S2,Júnior José S C2,Maciel Jeanny S3,de Paula Regina C M3,Ribeiro Ronaldo A1,Souza Marcellus H L P1,Freitas Ana L P4,Medeiros Jand-Venes R2,Silva Draulio C5,Barbosa André L R2

Affiliation:

1. Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil

2. Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí, Parnaíba, Piauí, Brazil

3. Laboratory of Polymer, Department of Organic and Inorganic Chemistry, Federal University of Ceará, Fortaleza, Ceará, Brazil

4. Laboratory of Proteins and Carbohydrates of Marine Algae, Department of Biochemistry and Molecular Biology, Federal University of Ceará, Fortaleza, Ceará, Brazil

5. Laboratory of Biochemistry, Core of Molecular Ecology (NECMOL), Federal University of San Francisco Valley, Petrolina, Pernambuco, Brazil

Abstract

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-1β), 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-1β 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-1β levels, and oxidative stress and nociception.

Funder

National Counsel of Technological and Scientific Development – CNPq

Research Foundation for the State of Piauí – FAPEPI

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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