Anti-inflammatory effect of a sulphated polysaccharide fraction extracted from the red algae Hypnea musciformis via the suppression of neutrophil migration by the nitric oxide signalling pathway

Author:

de Brito Tarcisio Vieira1,Prudêncio Rafael da Silva1,Sales Adriano Bezerra1,Vieira Júnior Francisco das Chagas1,Candeira Starley Jone Nogueira1,Franco Álvaro Xavier2,Aragão Karoline Sabóia2,Ribeiro Ronaldo de Albuquerque2,Ponte de Souza Marcellus Henrique Loiola2,Chaves Luciano de Sousa3,Freitas Ana Lúcia Ponte3,Medeiros Jand-Venes Rolim1,dos Reis Barbosa André Luiz1

Affiliation:

1. LAFFEX – Laboratory of Experimental Physiopharmacology, Biotechnology and Biodiversity Center Research (BIOTEC), Federal University of Piauí-CMRV, Parnaíba, Brazil

2. LAFICA – Laboratory of Pharmacology of Inflammation and Cancer, Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Brazil

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

Abstract

Abstract Objectives The aim of this study was to evaluate the anti-inflammatory effect of a sulphated polysaccharide fraction (PLS) extracted from the alga Hypnea musciformis and investigate the possible involvement of the nitric oxide (NO) pathway in this effect. Methods The anti-inflammatory activity of PLS was evaluated using inflammatory agents (carrageenan and dextran) to induce paw oedema and peritonitis in Swiss mice. Samples of paw tissue and peritoneal fluid were removed to determine myeloperoxidase (MPO) activity, NO3/NO2 levels, and interleukin-1β (IL-1β) level. The involvement of NO in the modulation of neutrophil migration in carrageenan-induced paw oedema or peritonitis was also investigated. Key findings Compared with vehicle-treated mice, mice pretreated with PLS (10 mg/kg) inhibited carrageenan-induced and dextran-induced oedema; it also inhibited total and differential peritoneal leucocyte counts in a model of peritonitis. These PLS effects were reversed by l-arginine treatment and recovered with the administration of a NO synthase blocker (aminoguanidine). Furthermore, PLS reduced the MPO activity, decreased IL-1β levels, and increased NO3/NO2 levels in the peritoneal cavity. Conclusions PLS reduced the inflammatory response by modulating neutrophil migration, which appeared to be dependent on the NO pathway.

Funder

UFPI/CNPq

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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