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Vol. 284, Issue 3, 878-885, March 1998
Research Service, Clement J. Zablocki Veterans Affairs
Medical Center, Milwaukee, Wisconsin
Pentobarbital administered intracerebroventricularly to mice has been
shown previously to inhibit the analgesic action of morphine given
intrathecally. The purpose of the present study was to examine the
proposal that this antianalgesic action was mediated spinally by
cholecystokinin. First, intrathecal coadministration of
cholecystokinin-8 sulfate (CCK8s) with morphine inhibited the analgesic
action of morphine in the mouse tail-flick test. This rightward shift
of the morphine dose-response curve was reversed by the intrathecal
administration of either the CCKA receptor antagonist,
lorglumide, or the CCKB receptor antagonist, PD135,158. Second, lorglumide and PD135,158 given intrathecally also eliminated the antianalgesic effect of intracerebroventricularly administered pentobarbital against intrathecal morphine. Third, intrathecal pretreatment with CCK8 antiserum eliminated the effect of
pentobarbital. Thus, the results indicated that pentobarbital
antianalgesia was obtained through activation of a descending system to
the spinal cord where cholecystokinin inhibited the spinal analgesic
action of morphine.
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