Morphine alters the locomotor responses to a D2/D3 dopamine receptor agonist differentially in adolescent and adult mice

Rebecca S. Hofford, Paul J. Wellman, Shoshana Eitan

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


The D2-like dopamine receptors mediate the emotional/aversive state during morphine withdrawal. Given age-dependent differences in the affective responses to withdrawal, this study examined whether the response to dopamine receptor agonists is altered differentially across ages following morphine administration. Adolescent and adult mice were injected with morphine (twice daily, 10-40 mg/kg, s.c.) or saline for 6 days. Subsequently, they were examined for their locomotor response to quinpirole, a D2/D3 receptor agonist, and SKF 38393, a D1 receptor agonist. Quinpirole dose-dependently reduced locomotion in drug-naïve animals. Initial suppression was also observed in morphine-treated animals, but was followed by enhanced locomotion. Notably, this enhanced locomotion was markedly greater in adolescents than adults. Quinpirole-induced hypo-locomotion is thought to be mediated by the presynaptic D2Short receptors, whereas its activating effect is mediated by postsynaptic D2Long/D3 receptors. This suggests that following morphine administration, the postsynaptic, but not the presynaptic, dopaminergic signaling is differentially modulated across ages. This locomotor supersensitivity was not observed for SKF 38393, a D1 dopamine receptor agonist. The D2/D3 receptors are involved in the pathophysiology of many mental illnesses. Thus, this study offers a potential explanation for the increased psychiatric disorder co-morbidities when drug use begins during adolescence.

Original languageEnglish
Pages (from-to)1355-1365
Number of pages11
JournalJournal of Psychopharmacology
Issue number10
StatePublished - Oct 2012
Externally publishedYes


  • Quinpirole
  • SKF 38393
  • age-dependent
  • drugs of abuse
  • locomotion
  • opioid
  • withdrawal


Dive into the research topics of 'Morphine alters the locomotor responses to a D2/D3 dopamine receptor agonist differentially in adolescent and adult mice'. Together they form a unique fingerprint.

Cite this