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Vol. 287, Issue 2, 625-632, November 1998
Departments of
Pharmacology (A.E.R., M.J.C., X.Y.L., F.M.)and
Biological Chemistry (F.M.), University of Michigan Medical School, Ann
Arbor, Michigan
Chronic treatment of C6 glioma cells stably expressing the rat
delta opioid receptor (C6
) with full agonists resulted in receptor down-regulation. Chronic
[D-Ser2,L-Leu5]enkephalyl-Thr
treatment caused a decrease in cell surface as well as a decrease in
agonist-stimulated
[35S]guanosine-5'-O-(3-thio)triphosphate binding.
Treatment with full agonists for 12 hr resulted in a 90% decrease in
receptor number that was paralleled by a decrease in the ability of
agonist to stimulate
[35S]guanosine-5'-O-(3-thio)triphosphate binding and
inhibit forskolin-stimulated adenylyl cyclase. Of the remaining
receptors, a smaller fraction of receptors (41 ± 4 vs.
56 ± 4% in control) exhibited high affinity for agonist as
compared to receptors in control membranes. Elimination of
functional guanosine triphosphate binding protein (G protein) by
Pertussis toxin pretreatment did not alter the ability of agonist to
down regulate receptor. We hypothesized that agonist affinity (not
efficacy) would be a predictor of an agonist's ability to down-regulate receptor. However, we found that only full agonists were
able to down-regulate receptor number, G protein activation and
adenylyl cyclase inhibition. Chronic exposure to partial agonist 7-spiroindinooxymorphone, which has a very high affinity for the receptor, as well as morphine, did not cause receptor down-regulation. Taken together, these results suggest that full agonists alter receptor
conformation such that the altered conformation is recognized by G
protein as well as proteins involved in receptor down-regulation. In
addition, down-regulation is independent of agonist-mediated G protein
activation and subsequent down-stream signaling.
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