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Vol. 286, Issue 1, 481-488, July 1998
Department of Biological Sciences, Rutgers University, Piscataway,
New Jersey
Regulation of serotonin (5-HT) release may be altered during the
development of opioid tolerance and dependency. To test this hypothesis, changes in extracellular 5-HT during prolonged
administration of morphine were determined by microdialysis in the
dorsal raphe nucleus (DRN) of freely behaving rats. Morphine or placebo
pellets were implanted s.c. As compared to placebo, morphine pellets
induced a sustained, ~50% increase in DRN 5-HT and a significant
elevation in hot plate latency during the 12-hr period after
implantation. One week later DRN 5-HT had returned to control levels,
and implanting additional morphine pellets had no effect on 5-HT or hot
plate latency. One day after removing the pellets from rats exposed to
morphine for 2 wk, acute challenge with morphine (20 mg/kg, s.c.) had a
significantly smaller effect on 5-HT in the DRN as compared to the
placebo treatment group. Administration of naltrexone to rats implanted
with morphine pellets for 2 wk induced signs of withdrawal and a
significant decrease in DRN 5-HT. These results suggest that the
regulation of 5-HT release is altered during the development of
tolerance to morphine. Thus, DRN 5-HT may be one of the factors
involved in the changes in physiology and behavioral state during
opioid withdrawal.