Reversal of learned helplessness by morphine
in rats: involvement of a dopamine mediation

by
Besson A, Privat AM, Eschalier A, Fialip J
Laboratoire de Pharmacologie,
Faculte de Pharmacie,
Equipe NPPUA,
Clermont-Ferrand, France.
Pharmacol Biochem Behav 1998 Jun; 60(2):519-25


ABSTRACT

The aim of this study was to examine the role of dopamine neurotransmission in the effects of morphine in the learned helplessness paradigm in rats, a generally recognized model of depression. In this model, rats first exposed to inescapable shocks (stressed rats) exhibited an escape deficit in a subsequent shuttle-box test performed 48 h later for 3 consecutive days. The numbers of escape failures and intertrial crossings (motor activity during each intertrial interval) were recorded. Morphine was injected twice daily for 5 days (6 mg/kg/day, s.c.), and haloperidol, a preferential D2-dopamine receptor antagonist, was injected i.p. 15 min before each shuttle-box session. At the highest dose tested (150 microg/kg) haloperidol mimicked the behavioral deficit produced by inescapable shocks. A 37.5 microg/kg dose of haloperidol, which was ineffective by itself, reversed the morphine-induced improvement of escape behavior in previously stressed rats and the morphine-induced increase in intertrial activity in both stressed and nonstressed animals. These results support roles (a) for a dysregulation of dopaminergic neuronal activity in the expression of escape deficit subsequent to an inescapable aversive situation, and (b) for a dopaminergic mediation in the effects of morphine in the learned helplessness paradigm.
Opioids
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Dopamine
Anhedonia
Adenylyl cyclase
Drugs and reward
CRH-R antagonists
Animal depression
Social rank theory
Learned helpless rats
Glucocorticoids and mood
Depression and chronic pain
Depression, opioids and the HPA
Types of depression and mood-disorder
Imipramine and the delta opioid receptors


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