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Towards an Understanding of Integrative Brain Functions


Integrated events in central dopamine transmission as analyzed at multiple levels.

Evidence for intramembrane adensine A2A/dopamine D2 and adenosine A1/dopamine D1 receptor intractions in the basal ganglia

Kjell Fuxea,* Sergi Ferré a, Michele Zolib, Luigi F. Agnatib

aDept. of Neuroscience, Karolinska Institutet, 171 77 Stockholm, bSection of Physiology, Dept. of Biomedical Sciences, University of Medina, 4100 Modena, Italy




Abstract
An analysis at the network and membrane level has provided evidence that antagonistic interactions between adenosine A2A/dopamine D2 and adenosine A1/dopamine D1 receptors in the ventral and dorsal striatum are at least in part responsible for the motor stimulant effects of adenosine receptor antagonists like caffeine and for the motor depressant actions of adenosine receptor agonists. The results obtained in stably cotransfected cells also underline the hypothesis that the intramembrane A2A/D2 and A1/D1 receptor interactions represent functionally important mechanisms that may be the major mechanism for the demonstrated antagonistic A2A/D2 and A1/D1 receptor interactions found in vivo in behavioural studies and in studies on in vivo microdialysis of the striopallidal and strioentopeduncular GABAergic pathways. A major mechanism for the direct intramembrane A2A/D2 and A1/D1 receptor interactions may involve formation of A2A/D2 and A1/D1 heterodimers leading to allosteric changes that will alter the affinity as wells as the G protein coupling and thus the efficacy to control the target proteins in the membranes. This is the first molecular network to cellular integration in the nerve cell membrane and may be well suited for a number of integrated tasks and can be performed in a short-time scale, in comparison with the very long-time scale observed when receptor heteroregulation involves phosphorylation or receptor resynthesis. Multiple receptor-receptor interactions within the membranes through formation of receptor clusters may lead to the storage of information within the membranes. Such molecular circuits can represent hidden layers within the membranes that substantially increase the computational potential of neuronal networks. These molecular circuits are biased and may therefore represent part of the molecular mechanism for the storage of memory traces (engrams) in the membranes.


*Corresponding author: Kjell.Fuxe@neuro.ki.si

Brain Research Reviews 26 (1998) 258-273
Copyright © 1998 Elsevier Science B. V. All rights reserved.

 

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