Planta Med 2010; 76(2): 113-119
DOI: 10.1055/s-0029-1186003
Pharmacology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Assessment of Zymosan-Induced Leukocyte Influx in a Rat Model using Sulfated Polysaccharides

Maria Leila Cardoso1 , Caroline A. C. Xavier2 , Maria B. Emilia Bezerra2 , Almino O. Afonso Paiva1 , Maria F. Goretti Carvalho3 , Norma M. B. Benevides3 , Francisco A. C. Rocha4 , Edda Lisboa Leite1 , 5
  • 1Departamento de Bioquímica, Universidade Federal do Rio Grande do Norte, Natal-RN, Brasil
  • 2Departamento de Farmacologia da UERN, Universidade Estadual do Rio Grande do Norte, Natal-RN, Brazil
  • 3Departamento de Patologia, UNP, Rio Grande do Norte, Natal-RN, Brasil
  • 4Departamento de Bioquímica, Universidade Federal do Ceará, UFC, Fortaleza-CE, Brazil
  • 5Departamento de Farmacologia, Universidade Federal do Ceará. Fortaleza-CE, Brazil
Further Information

Publication History

received January 4, 2009 revised June 29, 2009

accepted July 3, 2009

Publication Date:
03 August 2009 (online)

Preview

Abstract

Fucoidan, a sulfated polysaccharide from the brown algae Fucus vesiculosus, has diverse biological properties, including anti-inflammatory, anticoagulant and antithrombotic activity. This study analyzed the therapeutic activity of total fucoidan (TF) from F. vesiculosus and that of purified fractions (F1 and F2) on zymosan-induced arthritis. Arthritis was induced by injecting zymosan into the knee joint. Thus, three fucoidan fractions were obtained by acetone fractionation. Due to the yield obtained from F3, we used only fucoidans F1 and F2 in the induced inflammation tests. Chemical analyses and electrophoretic characterization of these fractions demonstrated that they contain polysaccharides, sulfate ester and very low protein levels. The fucoidans obtained from TF showed only an electrophoretic band in agarose gel with much lower polydispersion. The F2 fraction showed a migration between fucoidans F1 and F3. We administered TF (15, 30, 50 mg/kg i. p.), F1 or F2 (10, 25 and 50 mg/kg i. p.), diclofenac sodium (10 mg/kg i. p.), lumiracoxib (5 mg/kg o. a.) or L-NAME (30 mg/kg i. p.), 1 hour after induction of articular inflammation. We analyzed cell influx and nitrite levels in addition to performing histopathological analysis. TF (total fucoidan) at 15, 30, 50 mg/kg i. p. and its fractions (F1 and F2 at concentrations of 25 and 50 mg/kg i. p.) significantly reduced cellular influx and nitric oxide concentration. Moreover, the articular inflammation in zymosan-induced arthritis caused a progressive loss in glycosaminoglycan content. This loss decreased when TF (30 mg/kg) was administered. These data suggest that fucoidan exerts anti-inflammatory action in a zymosan-induced model of acute inflammation in rats. Taken together with the fact that these natural compounds have minimal toxicity, this may have important therapeutic implications.

References

Prof. Dr. Edda Lisboa Leite

Departamento de Bioquímica
Centro de Biociências
Universidade Federal do Rio Grande do Norte

Avenida Salgado Filho 3000

Campus Universitário

Lagoa Nova

Cep: 59072-940

Natal, RN

Brazil

Phone: + 55 84 32 15 34 16

Fax: + 55 84 32 11 92 08

Email: eddaleite@cb.ufrn.br