3 results match your criteria: "10 Center Dr. MSC 1264[Affiliation]"

Anxiety and otovestibular disorders: linking behavioral phenotypes in men and mice.

Behav Brain Res

January 2008

Laboratory of Clinical Science, Building 10, Room 3D41, National Institute of Mental Health, 10 Center Dr. MSC 1264, NIH, Bethesda, MD 20892-1264, USA.

Human anxiety and vestibular disorders have long been known to co-occur. Paralleling human clinical and non-clinical data, mounting genetic, pharmacological and behavioral evidence confirms that animal anxiety interplays and co-exists with vestibular/balance deficits. However, relatively few animal models have addressed the nature of this relationship.

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Locomotory patterns, spatiotemporal organization of exploration and spatial memory in serotonin transporter knockout mice.

Brain Res

September 2007

Laboratory of Clinical Science, Building 10, Room 3D41, National Institute of Mental Health, 10 Center Dr. MSC 1264, Bethesda, MD 20892-1264, USA.

Serotonin transporter knockout (SERT-/-) mice are extensively used as a genetic model of several neuropsychiatric disorders, and consistently display anxiety-like behaviors and inactivity in different tests. To better understand how these mice organize their behavior, we assessed the open field and elevated plus maze spatiotemporal patterning of activity in adult male SERT wild type (+/+), heterozygous (+/-) and -/- mice on C57BL/6J genetic background using new videotracking and analytic procedures. In addition, we analyzed their spatial memory, assessing within- and between-trial habituation, and examined specific motor characteristics of their movement in these two tests.

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Mapping convulsants' binding to the GABA-A receptor chloride ionophore: a proposed model for channel binding sites.

Neurochem Int

January 2007

Laboratory of Clinical Science, Building 10, Room 3D41, National Institute of Mental Health (NIMH), NIH, 10 Center Dr. MSC 1264, Bethesda, MD 20892-1264, USA.

Gamma-aminobutyric acid (GABA) type A receptors play a key role in brain inhibitory neurotransmission, and are ligand-activated chloride channels blocked by numerous convulsant ligands. Here we summarize data on binding of picrotoxin, tetrazoles, beta-lactams, bicyclophosphates, butyrolactones and neurotoxic pesticides to GABA-A ionophore, and discuss functional and structural overlapping of their binding sites. The paper reviews data on convulsants' binding sensitivity to different point mutations in ionophore-lining second trans-membrane domains of GABA-A subunits, and maps possible location of convulsants' sites within the chloride ionophore.

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