NF-kappa B/Rel activation in cerulein pancreatitis

Citation
Au. Steinle et al., NF-kappa B/Rel activation in cerulein pancreatitis, GASTROENTY, 116(2), 1999, pp. 420-430
Citations number
38
Categorie Soggetti
Gastroenerology and Hepatology","da verificare
Journal title
GASTROENTEROLOGY
ISSN journal
00165085 → ACNP
Volume
116
Issue
2
Year of publication
1999
Pages
420 - 430
Database
ISI
SICI code
0016-5085(199902)116:2<420:NBAICP>2.0.ZU;2-A
Abstract
Background & Aims: Recent evidence suggests that a number of rapid signalin g cascades are initiated during secretagogue-induced pancreatitis. However, little is known about the nuclear events. The aim of this study was to exp lore activation of the transcription factor NF-kappa B/Rel after supramaxim al stimulation with the cholecystokinin analogue cerulein in the pancreas. Methods & Results: Nuclear appearance of NF-kappa B/Rel-binding activity wa s detectable 15 minutes after cerulein injection. The DNA-binding activity consisted of NF-kappa B1 p50, NF-kappa B2 p52, and RelA p65 as judged by su pershift assays and Western blot analysis. The onset and termination of NF- kappa B/Rel activation correlated with the degradation and reappearance of I kappa B alpha. Cerulein in supramaximal but not in physiological doses ac tivated NF-kappa B/Rel in vitro. After blocking of NF-kappa B/Rel activatio n with pyrrolidine dithiocarbamate, the degree of morphological alterations was more pronounced than in controls, serum amylase and lactate dehydrogen ase levels were significantly increased, and messenger RNA levels of pancre atitis-associated protein were more strongly induced, reflecting a more sev ere degree of pancreatitis. Similar results were obtained when N-acetyl-L-c ysteine was used as an inhibitor of NF-kappa B activation. Conclusions: The se data show that NF-kappa B/Rel is rapidly activated during cerulein pancr eatitis. This activation may induce a self-defending genetic program before the onset of cellular injury, which might prevent higher degrees of damage of pancreatic acinar cells after secretagogue hyperstimulation.