T. Tsuchiya et al., DISTRIBUTION AND REGULATION OF ORNITHINE DECARBOXYLASE ACTIVITY ALONGTHE VILLUS-CRYPT AXIS IN THE SMALL-INTESTINE, Biochimica et biophysica acta (G). General subjects, 1336(2), 1997, pp. 202-210
Distribution of ornithine decarboxylase activity in rat intestinal vil
li and crypts was determined by serially sectioning frozen mucosa and
measuring enzyme activity in pools of sections composed of villi or cr
ypts. Contents of the pools was determined by histological examination
of representative sections, and simultaneous measurement of sucrase a
s a marker of villus samples demonstrated excellent separation of vill
i and crypts. In fasted and ad lib fed rats, enzyme activity was highe
st in the villus-crypt junctional area and in crypts (P < 0.05). Refee
ding after a fast increased enzyme activity 15-fold, with greatest act
ivity in villus tips and the villus-crypt junctional area. Luminal 0.4
M glycine stimulated enzyme activity only in villus and villus-crypt
junctional samples, while luminal 10 mM putrescine stimulated activity
only in crypts. Parenteral epidermal growth factor caused increased e
nzyme activity in all mucosal areas, but the 18-28-fold increase in th
e three villus samples (top, middle and bottom) was significantly grea
ter(P < 0.05) than the 7-9-fold increase in crypt and junctional sampl
es. In rats refed after a fast, parenteral putrescine (2 mmol/kg) depr
essed enzyme activity in all mucosal areas. Ornithine decarboxylase ac
tivity is usually greatest in junctional and crypt cells, and villus a
nd crypt cells respond differently to luminal and systemic stimuli.