Blocking
of enhanced sensitivity to behavioral effects
of naloxone induced by narcotic agonists in rats
Raka Jain* and Rajat Ray
Department of Psychiatry,
National Drug Dependence Treatment Centre,
All India Institute of Medical Sciences,
New Delhi 110 029
( Received on March 27, 2003 )
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Abstract
The present experiment evaluated
whether prior treatment with naloxone could block the sensitization
to opiate antagonist induced by single dose administration
of pure agonist (morphine) or mixed agonist (buprenorphine).
Food deprived male Wistar rats were trained to respond for
food on a multiple-trial, fixed-interval 3 min schedule. Reinforcement
was contingent upon a response within a 10-s limited hold
period following a fixed-interval of 3 min. A trial consisted
of three fixed interval of 3 min separated by a 10 min timeout
period during which responses were not reinforced. The rate
decreasing effects of the opioid antagonist naloxone was determined
by cumulative dosing. Pretreatment with morphine (0.3 mg/kg,
SC) and buprenorphine (0.03 mg/kg, SC) resulted in an increase
sensitivity to the rate decreasing effect of naloxone compared
to saline pretreatment. Administration of naloxone (0.3 mg/kg)
10 min prior to pretreatment doses of buprenorphine (0.03
mg/kg; 1.0 mg/kg) and morphine (0.3 mg/kg) increased sensitization
to naloxone. However, greater sensitization was observed at
low dose of buprenorphine. The increased sensitivity was partially
blocked at high dose of buprenorphine (1.0 mg/kg) by naloxone
pretreatment. These results suggest that the doses of naloxone
used to block opioid induced sensitization might be different
from those required in animals with normal sensitivity to
opioid antagonists. Further agonist-induced sensitization
to behavioral effects of opioid antagonist appears to be opioid
receptor specific.