HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Acute pancreatitis affects non-parenchymal liver cells by a mechanism dependent on platelet-activating factor.

AbstractBACKGROUND/AIM:
During acute experimental pancreatitis, inflammatory mediators/cytokines are released by the pancreas and enter the portal venous system, reaching the liver. We investigate some aspects of the liver cell function under conditions of acute pancreatitis and the effect of in vivo treatment with a selective platelet-activating factor (PAF) antagonist.
METHODS:
Cells were isolated from Wistar rats 24 h after induction of acute pancreatitis by retrograde injection of sodium taurocholate into the main pancreatic duct. The non-parenchymal cell population was separated by Percoll gradient and the adherent cell population (Kupffer cells) obtained. The cells were cultured for 24 h and supernatants assayed for nitrite by Griess reaction and for tumour necrosis factor (TNF) by bioassay in L929 cells. The microbicidal activity was evaluated by killing of Candida albicans. The PAF antagonist WEB2170 (10 mg/kg i.v.) was administered 30 min before induction of pancreatitis.
RESULTS:
We found that liver cells produce nitric oxide (NO) only under lipopolysaccharide stimulation and that WEB-2170 treatment reduces the NO production by liver cells in the pancreatitis group only. Cells from both groups produced TNF spontaneously, and the levels were further increased after lipopolysaccharide stimulation. WEB-2170 treatment did not affect the TNF levels. Moreover, killing of C. albicans by Kupffer cells wassignificantly increased by the PAF antagonist.
CONCLUSION:
These results suggest that PAF released during acute pancreatitis upregulates the NO production by non-parenchymal liver cells and inhibits Kupffer cell microbicidal activity which could explain the increased bacterial dissemination observed in acute pancreatitis.
AuthorsLourenilson J Souza, Marina T Shio, Nilza A T Molan, Marcel C C Machado, Sonia Jancar
JournalPancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.] (Pancreatology) Vol. 7 Issue 1 Pg. 67-73 ( 2007) ISSN: 1424-3903 [Print] Switzerland
PMID17449968 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Azepines
  • Lipopolysaccharides
  • Platelet Activating Factor
  • Platelet Aggregation Inhibitors
  • Platelet Membrane Glycoproteins
  • Receptors, G-Protein-Coupled
  • Triazoles
  • Tumor Necrosis Factors
  • platelet activating factor receptor
  • Nitric Oxide
  • Taurocholic Acid
  • bepafant
Topics
  • Acute Disease
  • Animals
  • Azepines (pharmacology)
  • Candida albicans (immunology)
  • Kupffer Cells (immunology)
  • Lipopolysaccharides (pharmacology)
  • Liver (immunology)
  • Male
  • Nitric Oxide (antagonists & inhibitors, metabolism)
  • Pancreatitis (chemically induced, immunology)
  • Platelet Activating Factor (antagonists & inhibitors, physiology)
  • Platelet Aggregation Inhibitors (pharmacology)
  • Platelet Membrane Glycoproteins (antagonists & inhibitors)
  • Rats
  • Rats, Wistar
  • Receptors, G-Protein-Coupled (antagonists & inhibitors)
  • Taurocholic Acid (toxicity)
  • Triazoles (pharmacology)
  • Tumor Necrosis Factors (analysis, metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: