Literature DB >> 11264302

D1/D5 dopamine receptor activation differentially modulates rapidly inactivating and persistent sodium currents in prefrontal cortex pyramidal neurons.

N Maurice1, T Tkatch, M Meisler, L K Sprunger, D J Surmeier.   

Abstract

Dopamine (DA) is a well established modulator of prefrontal cortex (PFC) function, yet the cellular mechanisms by which DA exerts its effects in this region are controversial. A major point of contention is the consequence of D(1) DA receptor activation. Several studies have argued that D(1) receptors enhance the excitability of PFC pyramidal neurons by augmenting voltage-dependent Na(+) currents, particularly persistent Na(+) currents. However, this conjecture is based on indirect evidence. To provide a direct test of this hypothesis, we combined voltage-clamp studies of acutely isolated layer V-VI prefrontal pyramidal neurons with single-cell RT-PCR profiling. Contrary to prediction, the activation of D(1) or D(5) DA receptors consistently suppressed rapidly inactivating Na(+) currents in identified corticostriatal pyramidal neurons. This modulation was attenuated by a D(1)/D(5) receptor antagonist, mimicked by a cAMP analog, and blocked by a protein kinase A (PKA) inhibitor. In the same cells the persistent component of the Na(+) current was unaffected by D(1)/D(5) receptor activation-suggesting that rapidly inactivating and persistent Na(+) currents arise in part from different channels. Single-cell RT-PCR profiling showed that pyramidal neurons coexpressed three alpha-subunit mRNAs (Nav1.1, 1.2, and 1.6) that code for the Na(+) channel pore. In neurons from Nav1.6 null mice the persistent Na(+) currents were significantly smaller than in wild-type neurons. Moreover, the residual persistent currents in these mutant neurons-which are attributable to Nav1.1/1.2 channels-were reduced significantly by PKA activation. These results argue that D(1)/D(5) DA receptor activation reduces the rapidly inactivating component of Na(+) current in PFC pyramidal neurons arising from Nav1.1/1.2 Na(+) channels but does not modulate effectively the persistent component of the Na(+) current that is attributable to Nav1.6 Na(+) channels.

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Year:  2001        PMID: 11264302      PMCID: PMC6762404     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  67 in total

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Authors:  J Magistretti; D S Ragsdale; A Alonso
Journal:  J Neurosci       Date:  1999-09-01       Impact factor: 6.167

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Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

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Authors:  E Gershon; L Weigl; I Lotan; W Schreibmayer; N Dascal
Journal:  J Neurosci       Date:  1992-10       Impact factor: 6.167

5.  Differential subcellular localization of the RI and RII Na+ channel subtypes in central neurons.

Authors:  R E Westenbroek; D K Merrick; W A Catterall
Journal:  Neuron       Date:  1989-12       Impact factor: 17.173

6.  Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons.

Authors:  G Stuart; B Sakmann
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Journal:  J Neurosci       Date:  1995-12       Impact factor: 6.167

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Authors:  M R Costa; J E Casnellie; W A Catterall
Journal:  J Biol Chem       Date:  1982-07-25       Impact factor: 5.157

9.  Dopamine D1/D5 receptor activation modulates a persistent sodium current in rat prefrontal cortical neurons in vitro.

Authors:  N A Gorelova; C R Yang
Journal:  J Neurophysiol       Date:  2000-07       Impact factor: 2.714

10.  Inhibitory effects of ventral tegmental area stimulation on the activity of prefrontal cortical neurons: evidence for the involvement of both dopaminergic and GABAergic components.

Authors:  S Pirot; R Godbout; J Mantz; J P Tassin; J Glowinski; A M Thierry
Journal:  Neuroscience       Date:  1992-08       Impact factor: 3.590

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  77 in total

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2.  Phosphorylation-dependent differences in the activation properties of distal and proximal dendritic Na+ channels in rat CA1 hippocampal neurons.

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Journal:  J Physiol       Date:  2002-06-15       Impact factor: 5.182

3.  Action potential initiation and propagation in layer 5 pyramidal neurons of the rat prefrontal cortex: absence of dopamine modulation.

Authors:  Allan T Gulledge; Greg J Stuart
Journal:  J Neurosci       Date:  2003-12-10       Impact factor: 6.167

4.  The role of spiking and bursting pacemakers in the neuronal control of breathing.

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5.  Rapid dopaminergic and GABAergic modulation of calcium and voltage transients in dendrites of prefrontal cortex pyramidal neurons.

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Journal:  J Physiol       Date:  2012-05-28       Impact factor: 5.182

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Journal:  J Physiol       Date:  2005-10-06       Impact factor: 5.182

7.  Dopamine receptor activation can reduce voltage-gated Na+ current by modulating both entry into and recovery from inactivation.

Authors:  Yuki Hayashida; Andrew T Ishida
Journal:  J Neurophysiol       Date:  2004-11       Impact factor: 2.714

8.  Molecular determinants for modulation of persistent sodium current by G-protein betagamma subunits.

Authors:  Massimo Mantegazza; Frank H Yu; Andrew J Powell; Jeffrey J Clare; William A Catterall; Todd Scheuer
Journal:  J Neurosci       Date:  2005-03-30       Impact factor: 6.167

9.  Serotonin receptor activation inhibits sodium current and dendritic excitability in prefrontal cortex via a protein kinase C-dependent mechanism.

Authors:  David B Carr; Donald C Cooper; Sasha L Ulrich; Nelson Spruston; D James Surmeier
Journal:  J Neurosci       Date:  2002-08-15       Impact factor: 6.167

10.  Specificity of prenatal cocaine exposure effects on cortical interneurons is independent from dopamine D1 receptor co-localization.

Authors:  Barbara L Thompson; Gregg D Stanwood; Pat Levitt
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