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Inhibition of immediate-type allergic reactions by Prunella vulgaris in a murine model.

Abstract
We studied the effect of aqueous extract of Prunella vulgaris (Labiatae) (PVAE) on immediate-type allergic reactions. PVAE (0.005 to 1 g/kg) dose-dependently inhibited systemic anaphylactic shock induced by compound 48/ 80 in rats. When PVAE was given as pretreatment, at concentrations ranging from 0.005 to 1 g/kg, the serum histamine levels induced by compound 48/ 80 were reduced in a dose-dependent manner. PVAE (0.001 to 1 g/kg) inhibited the passive cutaneous anaphylaxis activated by anti-dinitrophenyl (DNP) IgE antibody dose dependently. PVAE also inhibited the histamine release induced by compound 48/80 or anti-DNP IgE from the rat peritoneal mast cells (RPMC). The level of cyclic AMP in RPMC, when PVAE was added, significantly increased, compared with that of normal control. Moreover, PVAE (0.01 and 0.1 mg/ml) had a significant inhibitory effect on anti-DNP IgE-mediated tumor necrosis factor-alpha production from RPMC. These results indicate that PVAE inhibits immediate-type allergic reactions in rats.
AuthorsT Y Shin, Y K Kim, H M Kim
JournalImmunopharmacology and immunotoxicology (Immunopharmacol Immunotoxicol) Vol. 23 Issue 3 Pg. 423-35 (Aug 2001) ISSN: 0892-3973 [Print] England
PMID11694032 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Dinitrobenzenes
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • Immunoglobulin E
  • p-Methoxy-N-methylphenethylamine
  • Cyclic AMP
Topics
  • Anaphylaxis (chemically induced, prevention & control)
  • Animals
  • Cyclic AMP (metabolism)
  • Dinitrobenzenes (immunology)
  • Histamine Release (drug effects)
  • Hypersensitivity, Immediate (prevention & control)
  • Immunoglobulin E (administration & dosage)
  • Lamiaceae
  • Male
  • Mast Cells (drug effects, immunology)
  • Passive Cutaneous Anaphylaxis (drug effects)
  • Plant Extracts (pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Tumor Necrosis Factor-alpha (biosynthesis)
  • p-Methoxy-N-methylphenethylamine (toxicity)

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