| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4312526 | Behavioural Brain Research | 2014 | 9 Pages |
•Acute morphine did not alter mRNA expression and activity of CaMKII in hippocampus.•Morphine sensitization increased mRNA expression of CaMKII in the hippocampus.•Morphine sensitization increased CaMKII activity in the rat hippocampus.•Naloxone decreased mRNA expression of CaMKII in morphine-sensitized rats.•Naloxone decreased CaMKII activity in morphine-sensitized rats.
Repeated exposure to drugs of abuse, such as morphine, elicits a progressive enhancement of drug-induced behavioral responses, a phenomenon termed behavioral sensitization. These changes in behavior may reflect long-lasting changes in some of the important molecules involved in memory processing such as calcium/calmodulin-dependent protein kinase II (CaMKII). In the present study, we investigated the effect of morphine sensitization on mRNA expression of α and β isoforms and activity of CaMKII in the hippocampus of male rats. Animals were treated for 3 days with saline or morphine (20 mg/kg) and following a washout period of 5 days, a challenge dose of morphine (5 mg/kg) were administered. The results indicate that morphine administration in pre-treated animals produces behavioral sensitization, as determined by significant increase in locomotion and oral stereotypy behavior. In addition, repeated morphine treatment increased mRNA expression of both α and β isoforms of CaMKII in the hippocampus. The present study also showed that induction of morphine sensitization significantly increased both Ca2+/calmodulin-independent and Ca2+/calmodulin-dependent activities of CaMK II in the rat hippocampus. However, acute administration of morphine (5 mg/kg) did not alter either α and β CaMKII mRNA expression or CaMKII activity in the hippocampus. The stimulation effects of morphine sensitization on mRNA expression and activity of CaMKII were completely abolished by administration of naloxone, 30 min prior to s.c. injections of morphine (20 mg/kg/day × 3 days). Our data demonstrated that induction of morphine sensitization could effectively modulate the activity and the mRNA expression of CaMKII in the hippocampus and this effect of morphine was exerted by the activation of opioid receptors.
