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3,5-Dicaffeoyl-4-malonylquinic acid reduced oxidative stress and inflammation in a experimental model of inflammatory bowel disease.

AbstractAIM:
The aim of the present study was to examine the effects of 3,5-dicaffeoyl-4-malonylquinic acid (CA1), extract from Centella Asiatica, in rats subjected to experimental colitis.
RESULTS:
Colitis was induced in rats by intracolonic instillation of dinitrobenzene sulphonic acid (DNBS). CA1 was administered daily orally (0.2 or 2 mg/kg). Four days after DNBS administration, treatment with CA1 significantly reduced the appearance of diarrhoea and the loss of body weight. This was associated with a significant reduction in colonic MPO activity. CA1 also reduced NF-kappaB activation, the pro-inflammatory cytokines release, the appearance of I-NOS, nitrotyrosine, PARP and proMMP-9 and -2 activity in the colon and reduced the up-regulation of ICAM-1 and the expression of P-Selectin.
CONCLUSIONS:
The results of this study suggested that administration of CA1 may be beneficial for treatment of inflammatory bowel disease.
AuthorsRosanna di Paola, Emanuela Esposito, Emanuela Mazzon, Rocco Caminiti, Roberto Dal Toso, Giovanna Pressi, Salvatore Cozzocrea
JournalFree radical research (Free Radic Res) Vol. 44 Issue 1 Pg. 74-89 (Jan 2010) ISSN: 1029-2470 [Electronic] England
PMID19886745 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • 3,5-dicaffeoyl-4-malonylquinic acid
  • Anti-Inflammatory Agents
  • Caffeic Acids
  • Centella asiatica extract
  • Plant Extracts
  • Triterpenes
  • Quinic Acid
  • Chlorogenic Acid
Topics
  • Animals
  • Anti-Inflammatory Agents (pharmacology, therapeutic use)
  • Caffeic Acids (pharmacology, therapeutic use)
  • Cells, Cultured
  • Centella
  • Chlorogenic Acid (analogs & derivatives)
  • Colon (drug effects, metabolism, pathology)
  • Disease Models, Animal
  • Down-Regulation (drug effects)
  • Drug Evaluation, Preclinical
  • Inflammation (drug therapy, metabolism, pathology)
  • Inflammatory Bowel Diseases (drug therapy, immunology, metabolism, pathology)
  • Male
  • Models, Biological
  • Oxidative Stress (drug effects)
  • Plant Extracts
  • Quinic Acid (analogs & derivatives, pharmacology, therapeutic use)
  • Rats
  • Rats, Sprague-Dawley
  • Triterpenes (pharmacology)

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