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Using glutamate homeostasis as a target for treating addictive disorders

Journal

BEHAVIOURAL PHARMACOLOGY
Volume 21, Issue 5-6, Pages 514-522

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/FBP.0b013e32833d41b2

Keywords

cystine/glutamate exchanger; drug seeking; glial glutamate transporter; glutamate homeostasis

Funding

  1. NIH [DA015369, DA012513, DA003906]
  2. NATIONAL INSTITUTE ON DRUG ABUSE [P50DA015369, R01DA012513, F32DA026254, R37DA003906, R01DA003906] Funding Source: NIH RePORTER

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Well-developed cellular mechanisms exist to preserve glutamate homeostasis and regulate extrasynaptic glutamate levels. Accumulating evidence indicates that disruptions in glutamate homeostasis are associated with addictive disorders. The disruptions in glutamate concentrations observed after prolonged exposure to drugs of abuse are associated with changes in the function and activity of several key components within the homeostatic control mechanism, including the cystine/glutamate exchanger xc(-) and the glial glutamate transporter, EAAT2/GLT-1. Changes in the balance between synaptic and extrasynaptic glutamate levels in turn influence signaling through presynaptic and postsynaptic glutamate receptors, and thus affect synaptic plasticity and circuit-level activity. In this review, we describe the evidence for impaired glutamate homeostasis as a critical mediator of long-term drug-seeking behaviors, how chronic neuroadaptations in xc(-) and the glutamate transporter, GLT-1, mediate a disruption in glutamate homeostasis, and how targeting these components restores glutamate levels and inhibits drug-seeking behaviors. Behavioural Pharmacology 21:514-522 (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.

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