4.7 Article

Impaired spatial working memory and decreased frontal cortex BDNF protein level in dopamine transporter knockout mice

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 628, Issue 1-3, Pages 104-107

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2009.11.036

Keywords

Brain-derived neurotrophic factor (BDNF); Y-maze; Frontal cortex; (Dopamine transporter knockout (DAT KO) mouse)

Funding

  1. Ministry of Health, Labor and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan [17390315, 17022007, 18023007]
  3. Mitsubishi Pharma Research Foundation
  4. National Institute of Health Intramural Research Program (NIDA), DHHS (USA)
  5. Grants-in-Aid for Scientific Research [18023007, 17390315, 17022007] Funding Source: KAKEN

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Brain-derived neurotrophic factor (BDNF), one of the key brain neurotrophins, has been implicated in neuronal plasticity and memory. Recent studies document the importance of BDNF for normal long-term memory functions. However, there are few studies of the roles of BDNF in short-term memory. Dopamine is likely to play important roles in BDNF gene expression in specific brain regions, including frontal cortical regions that are implicated in short-term working memory processes that include spontaneous alternation. We have thus tested spatial working memory in dopamine transporter knockout (DAT KO) and wild-type mice. Spontaneous alternation in the Y-maze, an index of short-term spatial working memory in mice, was significantly decreased in DAT KO mice compared to wild-type mice. BDNF protein was significantly decreased in frontal cortex, though not in striatum or hippocampus, of the DAT KO mice. The data support the hypothesis that impaired spatial working memory in DAT KO mice may be related to decreased frontal cortical BDNF in these animals, and document apparent roles for BDNF in a short-term memory process. (C) 2009 Elsevier B.V. All rights reserved.

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