4.7 Article

D2 dopamine receptor subtype-mediated hyperactivity and amphetamine responses in a model of ADHD

Journal

NEUROBIOLOGY OF DISEASE
Volume 37, Issue 1, Pages 228-236

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2009.10.009

Keywords

Hyperactivity; coloboma; D2 dopamine receptor; D3 dopamine receptor; D4 dopamine receptor; Amphetamine; ADHD; Microdialysis; SNAP-25; Knockout; S33084, L-745.870, L-741.626

Categories

Funding

  1. U.S. Public Health Service [R01 NS34845]
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS034845] Funding Source: NIH RePORTER

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Low doses of psychostimulants produce beneficial behavioral effects in ADHD patients but the mechanisms underlying the response are not understood. Here we use the hyperactive mouse mutant coloboma to identify D2-like dopamine receptor subtypes that mediate the hyperactivity and response to amphetamine; we have previously demonstrated that D1-like dopamine receptors are not involved. Targeted deletion of the D2, but not the D3 or the D4, dopamine receptor in coloboma mice eliminated the hyperactivity; depleting D2 dopamine receptors also restored the excess dopamine overflow that may drive the hyperactivity to normal concentrations. Similar to its effects on ADHD patients. amphetamine reduced the hyperactivity of coloboma mice. The D2 dopamine receptor-selective antagonist L-741.626. but not D3 or D4 dopamine receptor-selective antagonists, blocked the amphetamine-induced reduction in locomotor activity. Thus, the D2 dopamine receptor subtype mediates both the hyperactivity and response to amphetamine. suggesting a specific target for novel therapeutics in ADHD. (C) 2009 Elsevier Inc All rights reserved.

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