HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Phospholipase A2 isoforms in acute pancreatitis.

AbstractOBJECTIVE:
To assess phospholipase A2 isoforms during human and experimental acute necrotizing pancreatitis. Phospholipase A2 isoforms (group I, II, and IV) were examined in acute pancreatitis tissues in humans and rats to determine whether the exocrine pancreas itself is a source of these mediators.
SUMMARY BACKGROUND DATA:
Phospholipase A2 has important regulatory functions, especially in inflammation.
METHODS:
Using Northern blot analysis and immunohistochemistry, the expression and localization of phospholipase A2 isoforms were analyzed in pancreatic tissue obtained from 21 patients with acute necrotizing pancreatitis and in pancreatic tissues of rats with acute edematous and necrotizing pancreatitis. Rat samples were examined daily for 1 week.
RESULTS:
In human acute pancreatitis, phospholipase A2-I mRNA expression was 8.9-fold decreased. By contrast, phospholipase A2-II (7.8-fold) and phospholipase A2-IV (8.1-fold) mRNA levels were increased. By in situ hybridization, phospholipase A2-IV was found to be expressed in remaining acinar and ductal cells adjacent to the necrotic areas. Immunostaining revealed moderate to intense phospholipase A2-II immunoreactivity in remaining acinar and ductal cells next to the necrosis. In rat pancreatitis, phospholipase A2-II mRNA levels in the pancreas were unchanged in the early phase (8 hours) but markedly increased after 24 hours, with a fluctuating pattern until day 7.
CONCLUSIONS:
Enhanced expression of phospholipase A2-II and A2-IV isoenzymes in human and experimental acute pancreatitis suggests that these enzymes play a role in modulating the inflammatory reaction in the pancreas. Because phospholipase A2-II and A2-IV mRNA was strongly present in remaining viable pancreatic acinar and ductal cells, the pancreas itself seems to be at least partly a source and a regulator of phospholipase A2-II- and A2-IV-dependent inflammatory reactions in acute pancreatitis.
AuthorsH Friess, S Shrikhande, E Riesle, M Kashiwagi, K Baczako, A Zimmermann, W Uhl, M W Büchler
JournalAnnals of surgery (Ann Surg) Vol. 233 Issue 2 Pg. 204-12 (Feb 2001) ISSN: 0003-4932 [Print] United States
PMID11176126 (Publication Type: Journal Article)
Chemical References
  • Phospholipases A
  • Phospholipases A2
Topics
  • Adolescent
  • Adult
  • Animals
  • Blotting, Northern
  • Densitometry
  • Female
  • Humans
  • Male
  • Middle Aged
  • Pancreas (enzymology, pathology)
  • Pancreatitis, Acute Necrotizing (enzymology)
  • Phospholipases A (metabolism)
  • Phospholipases A2
  • Rats
  • Rats, Wistar

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: