Planta Med 2000; 66(3): 284-286
DOI: 10.1055/s-2000-8572
Letter
Georg Thieme Verlag Stuttgart · New York

Anti-Inflammatory and Analgesic Activities of the Latex Containing Triterpenes from Himatanthus sucuuba

Ana Luísa P. de Miranda1 , Jefferson R. A. Silva2 , Claudia M. Rezende2 , Josiane S. Neves1 , Sérgio C. Parrini1 , Maria L. B. Pinheiro3 , Milade C. Cordeiro3 , Everaldo Tamborini3 , Angelo C. Pinto2,*
  • 1 Laboratório de Avaliação e Síntese de Substâncias Bioativas (LASSBio), Departamento de Fármacos, Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil
  • 2 Departamento de Química Orgânica, Instituto de Química, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ, Brazil
  • 3 Departamento de Química, Universidade Federal do Amazonas, Manaus, AM, Brazil
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Abstract

Some triterpenes and iridoids were previously isolated from the stem bark of Himatanthus sucuuba. The latex from Himatanthus sucuuba is used in popular amazonian medicine as an anti-inflammatory remedy. Fractions of the latex were pharmacologically evaluated with a view to verify this popular use in the carrageenan-induced rat paw edema and in the acetic acid-induced mouse constriction tests. The hexane fraction inhibited the edema formation by 35.9 % at a dose of 200 mg/kg (p.o.) but no activity was observed at 100 mg/kg (p.o.). The triterpenes present in the hexane fraction were identified as lupeol acetate, α-amyrin and lupeol cinnamates. The fraction containing only cinnamates inhibited the edema and the abdominal constrictions by 50 - 40 % and 57.9 %, respectively, at 100 mg/kg (p.o.). Among all the fractions studied, the fraction containing only cinnamates showed the greatest anti-inflammatory activity which suggests that these compounds were responsible for the previously described activity of the crude extract.

References

  • 1 Van den Berg  M E.. Plantas Medicinais na Amazônia: Contribuição ao seu Conhecimento Sistema¿tico,. CNPq/PRU/MPEG, Belém, Brasil; 1982: 212
  • 2 Perdue  G P,, Blomster  R N.. South American Plants III: Isolation of fulvoplumierin from Himatanthus sucuuba (M. Arg.) Woodson (Apocynaceae).  J. Pharm. Sci.. 1978;;  67 1322-3
  • 3 Endo  Y,, Hayashi  H,, Sato  T,, Maruno  M,, Ohta  T,, Nozoe  S.. Confluetic acid and 2′-O-methylperlatolic acid, monoamine oxidase B inhibitors in a Brazilian plant, Himatanthus sucuuba. .  Chem. Pharm. Bull.. 1994;;  42 1198-201
  • 4 Silva  J RA,, Rezende  C M,, Pinto  A C,, Pinheiro  M LB,, Cordeiro  M C,, Tamborini  E,, Young  C M,, Bolzani  V S.. Ésteres triterpênicos de Himatanthus sucuuba (Spruce) Woodson.  Quim. Nova. 1998;;  21 702-4
  • 5 Vinegar  R,, Truaux  J F,, Selph  J L.. Quantitative studies of pathway to acute carrageenan inflammation.  Fed. Proc.. 1976;;  35 2447-56
  • 6 Recio  M C,, Giner  R M,, Manez  S,, Rios  J L.. Structural requirements for the anti-inflammatory activity of natural triterpenoids.  Planta Medica. 1995;;  61 182-5
  • 7 Singh  S,, Bani  S,, Singh  G B,, Gupta  B D,, Banerjee  S K,, Singh  B.. Anti-inflammatory activity of lupeol.  Fitoterapia. 1997;;  LXVIII(1) 9-16
  • 8 Recio  M C,, Giner  R M,, Manez  S,, Gueho  J,, Julien  H R,, Hostettmann  K,, Rios  J L.. Investigations on the steroidal anti-inflammatory activity of triterpenoids from Diospyros leucomelas. .  Planta Medica. 1995;;  61 9-12
  • 9 Singh  G B,, Singh  S,, Bani  S,, Gupta  B D,, Banerjee  S K.. Anti-inflammatory activity of oleanolic acid in rats and mice.  J. Pharm. Pharmacol.. 1992;;  44 456-8
  • 10 Gupta  M B,, Bhalla  T N,, Tangri  K K,, Bhargava  K P.. Biochemical study of the anti-inflammatory activity of α- and β-amyrin acetate.  Biochem. Pharmacol.. 1971;;  20 401-5
  • 11 Gupta  M B,, Bhalla  T N,, Gupta  G P,, Mitra  C R,, Bhargava  K P.. Anti-inflammatory activity of natural products (1) triterpenoids.  Eur. J. Pharmacol.. 1969;;  6 67-70
  • 12 Ribeiro  I G,, Silva  K CM,, Parrini  S C,, Miranda  A LP,, Fraga  C AM,, Barreiro  E J.. Synthesis and antinociceptive properties of new structurally planned imidazo[1,2-a]pyridine 3-acylhydrazone derivatives.  Eur. J. Med. Chem.. 1998;;  33 225-35

Dr. Angelo da
Cunha
Pinto

Departamento de Química Orgânica Instituto de Química

UFRJ, 21945-970

Rio de Janeiro, RJ

Brazil

Email: angelo@iq.ufrj.br

Phone: +55.21.2904746

    >