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Vol. 283, Issue 3, 1495-1502, 1997
Basic Research Group, Tsukuba Research Laboratories, Fujisawa
Pharmaceutical Co. Ltd., Tsukuba, Ibaraki 300-26, Japan
Acute pancreatitis was induced in mice by feeding with a
choline-deficient ethionine-supplemented diet. All the mice developed acute pancreatitis, and approximately 80% of them died within 4 days.
Stereomicroscopic and light microscopic examinations revealed that
pancreatic necrosis and circulatory disturbance that were not apparent
on day 1 were increased markedly on days 2 and 3. Serum levels of
pancreatic enzymes were normal or reduced on day 1 but then increased
to peak on day 3. Plasma 5-hydroxyindoleacetic acid levels, which may
indicate serotonin release, were significantly increased on days 1 through 3. Pretreatment with D,L-p-chlorophenylalanine methylester hydrochloride (200-400 mg/kg) significantly attenuated the
mortality of the mice with pancreatitis. Dose-dependent attenuation was
also obtained with ketaserin (0.01-10 mg/kg), cyproheptadine (0.01-10
mg/kg), pindolol (0.1-100 mg/kg) and NAN-190 (0.1-100 mg/kg), but not
with 0.01 to 10 mg/kg of ICS205-930 or M-840, and the activities were
significantly correlated with the binding affinities for serotonin2
receptor on the rat cerebral cortex. In addition, ketanserin or
cyproheptadine attenuated the morphologic changes in the
choline-deficient ethionine-supplemented diet mice at a dose (3.2 mg/kg) that hardly affected the serum enzyme levels. We propose that
serotonin2 receptor activation plays an important role in the
aggravation of diet-induced acute pancreatitis.
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