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Vol. 282, Issue 1, 378-384, 1997
Department of Medicine, Division of Gastroenterology and
Hepatology, Jefferson Medical College, Thomas Jefferson University,
Philadelphia, Pennsylvania
Studies were performed on the internal anal sphincter (IAS) smooth
muscle strips obtained from opossums (Didelphis
virginiana). Isometric tension and L-arginine
levels of the tissues were measured under basal conditions, in the
presence of electrical field stimulation (EFS) and after treatment with
different concentrations of arginase. For the nonadrenergic
noncholinergic nerve stimulation, short trains (4 sec) as well as
continuous EFS were used. During continuous EFS, after the initial IAS
relaxation, the response began to fade within several min to ~80%
recovery of the basal tone. We also examined the influence of
L-arginine and L-citrulline on these responses.
For some studies, the tissues were pretreated with L-glutamine (an inhibitor of L-citrulline
uptake), L-glutamate or
NG-hydroxy-L-arginine (an inhibitor of
arginase). Interestingly, the basal levels of L-arginine
were found to be significantly higher in the IAS (tonic smooth muscle)
than in the rectal (phasic smooth muscle) smooth muscle. Arginase
caused a concentration-dependent attenuation of the IAS relaxation
caused by EFS. L-Citrulline and L-arginine were
equipotent in reversing the attenuation. Both arginase (60 min
pretreatment) and continuous EFS (tissues collected at the time of
maximal recovery of the basal IAS tone after the initial relaxation)
caused significant decreases in L-arginine levels. The
decreases in the levels of L-arginine were restored by the
exogenous administration of either L-arginine or
L-citrulline. The restoration of L-arginine
levels by L-citrulline but not by L-arginine
was selectively blocked by L-glutamine. Furthermore, the
IAS relaxation, attenuated by arginase was unaffected by
L-glutamine but was restored by
NG-hydroxy-L-arginine pretreatment. The studies
suggest that L-citrulline-L-arginine recycling
may play a significant role in the maintenance of IAS relaxation in
response to nonadrenergic noncholinergic nerve stimulation.