TitleL-type Ca2+ channels mediate adaptation of extracellular signal-regulated kinase 1/2 phosphorylation in the ventral tegmental area after chronic amphetamine treatment.
Publication TypeJournal Article
Year of Publication2004
AuthorsRajadhyaksha A, Husson I, Satpute SS, Küppenbender KD, Ren JQ, Guerriero RM, Standaert DG, Kosofsky BE
JournalJ Neurosci
Volume24
Issue34
Pagination7464-76
Date Published2004 Aug 25
ISSN1529-2401
KeywordsAmphetamine, Animals, Calcium Channel Blockers, Calcium Channels, L-Type, Central Nervous System Stimulants, Dose-Response Relationship, Drug, Immunoblotting, Immunohistochemistry, In Situ Hybridization, Male, Mitogen-Activated Protein Kinase 1, Mitogen-Activated Protein Kinase 3, Nucleus Accumbens, Phosphoprotein Phosphatases, Phosphorylation, Protein Phosphatase 1, Rats, Rats, Sprague-Dawley, RNA, Messenger, Time Factors, Ventral Tegmental Area
Abstract

L-type Ca2+ channels (LTCCs) play an important role in chronic psychostimulant-induced behaviors. However, the Ca2+ second messenger pathways activated by LTCCs after acute and recurrent psychostimulant administration that contribute to drug-induced molecular adaptations are poorly understood. Using a chronic amphetamine treatment paradigm in rats, we have examined the role of LTCCs in activating the mitogen-activated protein (MAP) kinase pathway in the ventral tegmental area (VTA), a primary target for the reinforcing properties of psychostimulants. Using immunoblot and immunohistochemical analyses, we find that in chronic saline-treated rats a challenge injection of amphetamine increases phosphorylation of MAP [extracellular signal-regulated kinase 1/2 (ERK1/2)] kinase in the VTA that is independent of LTCCs. However, in chronic amphetamine-treated rats there is no increase in amphetamine-mediated ERK1/2 phosphorylation unless LTCCs are blocked, in which case there is robust phosphorylation in VTA dopamine neurons. Examination of the expression of phosphatases reveals an increase in calcineurin [protein phosphatase 2B (PP2B)] and MAP kinase phosphatase-1 (MKP-1) in the VTA. Using in situ hybridization histochemistry and immunoblot analyses, we further examined the mRNA and protein expression of the LTCC subtypes Ca(v)1.2 and Ca(v)1.3 in VTA dopamine neurons in drug-naive animals and in rats after chronic amphetamine treatment. We found an increase in Ca(v)1.2 mRNA and protein levels, with no change in Ca(v)1.3. Together, our results suggest that one aspect of LTCC-induced changes in second messenger pathways after chronic amphetamine exposure involves activation of the MAP kinase phosphatase pathway by upregulation of Ca(v)1.2 in VTA dopaminergic neurons.

DOI10.1523/JNEUROSCI.0612-04.2004
Alternate JournalJ. Neurosci.
PubMed ID15329393
PubMed Central IDPMC1201527
Grant ListK01 DA014057 / DA / NIDA NIH HHS / United States
K02 DA000354 / DA / NIDA NIH HHS / United States
K02DA00354 / DA / NIDA NIH HHS / United States
KO1DA14057 / DA / NIDA NIH HHS / United States