(Q44374758)

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Previous exposure to VTA amphetamine enhances cocaine self-administration under a progressive ratio schedule in an NMDA, AMPA/kainate, and metabotropic glutamate receptor-dependent manner.

scientific article published on 5 March 2003

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Europe PubMed Central

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1 November 2019

Previous exposure to VTA amphetamine enhances cocaine self-administration under a progressive ratio schedule in an NMDA, AMPA/kainate, and metabotropic glutamate receptor-dependent manner (English)

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1 November 2019

Lauren M Tanabe

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1 November 2019

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Paul Vezina

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1 November 2019

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Nobuyoshi Suto

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1 November 2019

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Jennifer D Austin

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1 November 2019

Elizabeth Creekmore

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1 November 2019

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5 March 2003

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1 November 2019

Neuropsychopharmacology

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1 November 2019

28

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1 November 2019

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1 November 2019

629-639

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1 November 2019

Effect of 2,3-dihydroxy-6-nitro-7-sulfamoyl-benzo(f)quinoxaline on methamphetamine- and cocaine-induced behavioral sensitization

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Evidence of a complete independence of the neurobiological substrates for the induction and expression of behavioral sensitization to amphetamine

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Ca2+/calmodulin-kinase II enhances channel conductance of alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionate type glutamate receptors

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Sensitization and individual differences to IP amphetamine, cocaine, or caffeine following repeated intracranial amphetamine infusions

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Preexposure to amphetamine and nicotine predisposes rats to self-administer a low dose of cocaine

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Blockade of "reverse tolerance" to cocaine and amphetamine by MK-801.

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DNQX blockade of amphetamine behavioral sensitization

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Metabotropic glutamate receptors are necessary for sensitization by amphetamine

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21 January 2018

Effects of the AMPA receptor antagonist NBQX on the development and expression of behavioral sensitization to cocaine and amphetamine

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Repeated stimulation of L-type calcium channels in the rat ventral tegmental area mimics the initiation of behavioral sensitization to cocaine

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Stimulation of the pedunculopontine tegmental nucleus in the rat produces burst firing in A9 dopaminergic neurons.

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21 January 2018

Previous exposure to amphetamine increases incentive to obtain the drug: long-lasting effects revealed by the progressive ratio schedule.

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21 January 2018

Long-term potentiation--a decade of progress?

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Non-NMDA excitatory amino acid receptors in the ventral tegmental area mediate systemic dizocilpine (MK-801) induced hyperlocomotion and dopamine release in the nucleus accumbens

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21 January 2018

Pre-exposure of rats to amphetamine sensitizes self-administration of this drug under a progressive ratio schedule

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Factors that predict individual vulnerability to amphetamine self-administration.

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Predisposition to self-administer amphetamine: the contribution of response to novelty and prior exposure to the drug

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The metabotropic glutamate receptors: structure and functions

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Progressive ratio schedules in drug self-administration studies in rats: a method to evaluate reinforcing efficacy

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The neural basis of drug craving: an incentive-sensitization theory of addiction

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Characterization of multiple phosphorylation sites on the AMPA receptor GluR1 subunit

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21 January 2018

Effects of acute and repeated administration of N-methyl-d-aspartate (NMDA) into the ventral tegmental area: locomotor activating effects of NMDA and cocaine

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21 January 2018

Pre-exposure to amphetamine but not nicotine sensitizes rats to the motor activating effect of cocaine

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Previous exposure to VTA amphetamine enhances cocaine self-administration under a progressive ratio schedule in a D1 dopamine receptor dependent manner.

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Target-specific glutamatergic regulation of dopamine neurons in the ventral tegmental area

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21 January 2018

Single cocaine exposure in vivo induces long-term potentiation in dopamine neurons

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21 January 2018

Persistence of the ability of amphetamine preexposure to facilitate acquisition of cocaine self-administration

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21 January 2018

Alterations in dopaminergic and glutamatergic transmission in the induction and expression of behavioral sensitization: a critical review of preclinical studies

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Amphetamine injected into the ventral tegmental area sensitizes the nucleus accumbens dopaminergic response to systemic amphetamine: an in vivo microdialysis study in the rat.

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21 January 2018

The effect of dopamine receptor blockade on the development of sensitization to the locomotor activating effects of amphetamine and morphine

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21 January 2018

Electrophysiological evidence for the existence of NMDA and non‐NMDA receptors on rat ventral tegmental dopamine neurons

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Synaptic regulation of mesocorticolimbic dopamine neurons

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Amphetamine-induced glutamate efflux in the rat ventral tegmental area is prevented by MK-801, SCH 23390, and ibotenic acid lesions of the prefrontal cortex

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Laterodorsal tegmental stimulation elicits dopamine efflux in the rat nucleus accumbens by activation of acetylcholine and glutamate receptors in the ventral tegmental area

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Metabotropic glutamate receptors: electrophysiological properties and role in plasticity

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Control of GluR1 AMPA receptor function by cAMP-dependent protein kinase

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Double transduction with GTP cyclohydrolase I and tyrosine hydroxylase is necessary for spontaneous synthesis of L-DOPA by primary fibroblasts

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Properties and plasticity of excitatory synapses on dopaminergic and GABAergic cells in the ventral tegmental area.

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D-amphetamine-induced behavioral sensitization: implication of a glutamatergic medial prefrontal cortex-ventral tegmental area innervation

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Amphetamine-induced plasticity of AMPA receptors in the ventral tegmental area: effects on extracellular levels of dopamine and glutamate in freely moving rats.

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Metabotropic glutamate receptor antagonist, (R,S)-alpha-methyl-4-carboxyphenyglycine, blocks two distinct forms of long-term potentiation in area CA1 of rat hippocampus

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Amphetamine and D1 dopamine receptor agonists produce biphasic effects on glutamate efflux in rat ventral tegmental area: modification by repeated amphetamine administration.

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Identifiers

10.1038/SJ.NPP.1300075

1 reference

Europe PubMed Central

PubMed publication ID

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1 November 2019

PubMed publication ID

1 reference

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PubMed publication ID

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1 November 2019

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