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Vol. 297, Issue 3, 1074-1081, June 2001
School of Physiology and Pharmacology, University of New South
Wales, Australia
Radioiodinated neurotensin (125I-NT) was used to
characterize and localize NT binding sites in normal human sigmoid
colon. Specimens were obtained from patients (30-77 years old)
undergoing resection for colon carcinoma. Specific binding of
125I-NT to sigmoid circular muscle membranes was enhanced
by o-phenanthroline (1 mM) but other peptidase
inhibitors were ineffective. 125I-NT bound to a
high-affinity site of Kd = 0.88 ± 0.09 nM and Bmax = 4.03 ± 0.66 fmol/mg of wet weight tissue (n = 14), although in
the majority of patients another site, of low but variable affinity,
could also be detected. Specific binding of 50 pM 125I-NT
was inhibited by NT(8-13) > NT > SR142948A
neuromedin N
SR48692, consistent with binding to the NT1
receptor. In autoradiographic studies, dense specific binding of
125I-NT was seen over myenteric and submucosal ganglia,
moderate binding over circular muscle, and sparse binding over
longitudinal muscle and taenia coli. Levocabastine, which has affinity
for the NT2 receptor, did not inhibit specific binding of
125I-NT in membrane competition or autoradiographic
studies. NT contracted sigmoid colon circular muscle strips with a
pD2 value of 6.8 ± 0.2 nM (n = 25). The contractile responses to NT were significantly potentiated in
the presence of tetrodotoxin (1 µM), indicating a neural
component. Results from functional studies support actions for NT on
both muscle and enteric neurons, consistent with the presence of NT
receptors on circular muscle and ganglia of human sigmoid colon. The
lack of inhibition by levocabastine suggests that the second binding
site detected does not correspond to the NT2 receptor.