A common mechanism mediates long-term changes in synaptic transmission after chronic cocaine and morphine.

Abstract:

:The mesolimbic system is known to play a role in self-administration of opioids and psychostimulants. Although morphine and cocaine act by separate cellular mechanisms initially, the present study describes a common change in synaptic regulation of dopamine cells in the ventral tegmental area 1 week after termination of chronic treatment with either drug. Normally, D1 receptor activation augmented the amplitude of a gamma-aminobutyric acid type B (GABA(B)) inhibitory postsynaptic potential (IPSP), but in drug-experienced animals, D1 receptor activation caused an inhibition of the GABA(B) IPSP. The inhibition was blocked by adenosine A1 receptor antagonists and by agents that disrupted the metabolism of cAMP. This long-lasting dopamine-adenosine interaction may be one mechanism involved in dopamine-mediated craving and relapse to drug-seeking behaviors.

journal_name

Neuron

journal_title

Neuron

authors

Bonci A,Williams JT

doi

10.1016/s0896-6273(00)80082-3

subject

Has Abstract

pub_date

1996-03-01 00:00:00

pages

631-9

issue

3

eissn

0896-6273

issn

1097-4199

pii

S0896-6273(00)80082-3

journal_volume

16

pub_type

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