4.6 Article

PI3K signaling supports amphetamine-induced dopamine efflux

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2008.05.091

Keywords

dopamine transporter (DAT); amphetamine (AMPH); dopamine (DA); phosphatidylinositol 3-kinase (PI3K); insulin; drug abuse; transient current

Funding

  1. NIDA NIH HHS [K05 DA022413-01A1, DA21069, R01 DA013975, R01 DA026947, F31 DA021069-02, R56 DA013975, DA12408, P01 DA012408-100004, P01 DA012408-109001, DA022413, F31 DA021069, K05 DA022413, P01 DA012408, F31 DA021069-01A1, R01 DA013975-08, DA13975] Funding Source: Medline
  2. NIDDK NIH HHS [R01 DK062722, R01 DK062722-05, DK62722] Funding Source: Medline
  3. NIMH NIH HHS [R01 MH058921, R01 MH058921-14, MH058921] Funding Source: Medline

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The dopamine (DA) transporter (DAT) is a major molecular target of the psychostimulant amphetamine (AMPH). AMPH, as a result of its ability to reverse DAT-mediated inward transport of DA, induces DA efflux thereby increasing extracellular DA levels. This increase is thought to underlie the behavioral effects of AMPH. We have demonstrated previously that insulin, through phosphatidylinositol 3-kinase (PI3K) signaling, regulates DA clearance by fine-tuning DAT plasma membrane expression. PI3K signaling may represent a novel mechanism for regulating DA efflux evoked by AMPH, since only active DAT at the plasma membrane can efflux DA. Here, we show in both a heterologous expression system and DA neurons that inhibition of PI3K decreases DAT cell surface expression and, as a consequence, AMPH-induced DA efflux. (c) 2008 Elsevier Inc. All rights reserved.

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