PT  - JOURNAL ARTICLE
AU  - Magdalena  Mas Nieto
AU  - Jodie Wilson
AU  - Annie Cupo
AU  - Bernard P. Roques
AU  - Florence Noble
TI  - Chronic Morphine Treatment Modulates the Extracellular Levels of Endogenous Enkephalins in Rat Brain Structures Involved in Opiate Dependence: A Microdialysis Study
AID  - 10.1523/JNEUROSCI.22-03-01034.2002
DP  - 2002 Feb 01
TA  - The Journal of Neuroscience
PG  - 1034--1041
VI  - 22
IP  - 3
4099  - http://www.jneurosci.org/content/22/3/1034.short
4100  - http://www.jneurosci.org/content/22/3/1034.full
SO  - J. Neurosci.2002 Feb 01; 22
AB  - The endogenous opioid system is often assumed to play a role in vulnerability to drug abuse. However, controversial results have been reported regarding the levels of enkephalins or preproenkephalin in neurons of rodent brains after opiate administration. The present study was performed to determine the extracellular levels of enkephalins and its physiological antagonist cholecystokinin (CCK), usingin vivo microdialysis in freely moving rats after morphine-induced physical dependence or positive place conditioning. A large increase (340%) of Met-enkephalin was observed in the periaqueductal gray matter, a structure involved in morphine withdrawal syndrome, in morphine-dependent rats. No change in CCK immunoreactivity occurred in these conditions. Moreover, using the conditioning place preference paradigm, we observed for the first time opposite changes of enkephalin outflow in the nucleus accumbens (NAc). Thus, an increase in enkephalin levels was observed in rats placed in the drug-associated compartment and a decrease in the saline-paired side. These changes in opioid peptides in the NAc may reflect an “emotional state” of the animals in relation to the expectation of drug reward (reinforcing effects of morphine). Moreover, the lack of regulation in CCK outflow suggests that CCK–opioid interactions in morphine dependence involve probably post-receptor events.