Activation of post-synaptic dopamine D₁ receptors promotes the release of tissue plasminogen activator in the nucleus accumbens via PKA signaling

J Neurochem. 2007 Dec;103(6):2589-96. doi: 10.1111/j.1471-4159.2007.04946.x.

Abstract

We have previously demonstrated that tissue plasminogen activator (tPA) plays an important role through the conversion of plasminogen to plasmin in the release of dopamine in the nucleus accumbens (NAc) evoked by depolarization or the systemic administration of drugs of abuse such as morphine and nicotine. In the present study, we examined the mechanisms by which drugs of abuse increase extracellular tPA activity in the NAc in vivo using in situ zymography. The dopamine D(1) receptor (D(1) R) agonist SKF38393, but not D(2) receptor agonist quinpirole, significantly increased extracellular tPA activity in the NAc. The effect of SKF38393 was blocked by pre-treatment with the dopamine D(1) R antagonist SCH23390. Microinjection of Rp-cAMPs, a protein kinase A inhibitor, into the NAc completely blocked the effect of SKF38393. Systemic administration of morphine and methamphetamine increased extracellular tPA activity in the NAc, and these effects were completely blocked by pre-treatment with SCH23390 and raclopride. The results suggest that activation of post-synaptic dopamine D(1) Rs in the NAc leads to an increase in extracellular tPA activity via protein kinase A signaling. Furthermore, dopamine D(2) receptors are also involved in the release of tPA induced by morphine and methamphetamine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine / pharmacology
  • Analgesics, Opioid / pharmacology
  • Animals
  • Benzazepines / pharmacology
  • Brain Chemistry / drug effects
  • Cyclic AMP-Dependent Protein Kinases / antagonists & inhibitors
  • Cyclic AMP-Dependent Protein Kinases / physiology*
  • Dopamine Agonists / pharmacology
  • Dopamine Antagonists / pharmacology
  • Dopamine Uptake Inhibitors / pharmacology
  • Immunohistochemistry
  • Male
  • Methamphetamine / pharmacology
  • Mice
  • Mice, Inbred ICR
  • Morphine / pharmacology
  • Nucleus Accumbens / metabolism*
  • Oxidopamine / toxicity
  • Protein Kinase Inhibitors / pharmacology
  • Raclopride / pharmacology
  • Receptors, Dopamine D1 / agonists*
  • Signal Transduction / drug effects
  • Sympatholytics / toxicity
  • Synapses / physiology*
  • Tissue Plasminogen Activator / metabolism*
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Analgesics, Opioid
  • Benzazepines
  • Dopamine Agonists
  • Dopamine Antagonists
  • Dopamine Uptake Inhibitors
  • Protein Kinase Inhibitors
  • Receptors, Dopamine D1
  • SCH 23390
  • Sympatholytics
  • Raclopride
  • Methamphetamine
  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  • Morphine
  • Oxidopamine
  • Tyrosine 3-Monooxygenase
  • Cyclic AMP-Dependent Protein Kinases
  • Tissue Plasminogen Activator