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Vol. 283, Issue 3, 1367-1374, 1997
Department of Pharmaceutical Biology and Pharmacology, Victorian
College of Pharmacy, Monash University, Parkville, Victoria, Australia
The aims of this study were to examine how the imidazoline
(I)1/alpha-2 receptor agonist moxonidine and
the putative endogenous imidazoline receptor agonist agmatine might
affect intestinal motility and fluid transport. The effects of
moxonidine were compared with those of UK 14,304, a highly selective
alpha-2 adrenoceptor agonist with very low affinity for
I1 receptors. Moxonidine and UK 14,304 inhibited the
peristaltic reflex in the isolated rat ileum. The inhibitory effects
were antagonized by the selective alpha-2 adrenoceptor
antagonist yohimbine and the I1/alpha-2
antagonist efaroxan and almost completely blocked by the irreversible
alpha-2 adrenoceptor antagonist EEDQ
(N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline), whichhas a
low affinity for imidazoline receptors. Yohimbine (3 µM) and efaroxan
(0.01 and 1 µM) caused parallel rightward shifts to the
concentration-response curves of moxonidine and UK 14,304, yielding
pKB values corresponding to those
at alpha-2 binding sites. Moxonidine induced
dose-dependent proabsorptive effects in the jejunum and ileum and also
reversed the secretory phase of the vasoactive intestinal
peptide-induced responses. The degree of antagonism by yohimbine and
efaroxan was similar against moxonidine and UK 14,304 on the
proabsorptive and antisecretory effects. We conclude that the effects
of moxonidine in mediating inhibition of intestinal motility and
enhancing fluid transport are attributed predominantly to interaction
with alpha-2 adrenoceptors. Agmatine had no effect on
peristalsis but significantly decreased the rate of fluid absorption
from the jejunum and ileum, an effect in contrast to moxonidine. A
physiological role for agmatine in the regulation of intestinal
transport remains to be clarified.