One aim of this project is to use transcranial magnetic stimulation (TMS) of the brain to study physiological changes in different behavioral states and disorders. Since finding evidence of increased cortical excitability in obsessive-compulsive disorder (OCD), we have looked for an association between neurophysiological data and behavioral measures in the general population, using a dimensional approach. We found a highly significant positive association between the tendency to experience negative emotion (""""""""Neuroticism"""""""" in the 5-factor personality model) and cortical excitability measured with paired-pulse TMS which reflects cortical GABA-glutamate balance. We hypothesize that a condition of heightened excitability, as exists in high """"""""Neuroticism"""""""" individuals, should predispose to the development of long-term potentiation (LTP) of cortical synapses. We are looking for evidence of this with behavioral and electrophysiological tests before and after motor learning, again using a dimensional approach where possible. We further hypothesize that aberrant formation of associative LTP may underlie the development of OCD, focal dystonia, and other disorders and are initiating parallel studies to test these hypotheses. We have also initiated a study of the the possible contribution of genetic polymorphisms to the behavioral and neurophysiological dimensions mentioned above. For instance, we hypothesize that polymorphisms, such as that in the 5-HT transporter promoter region or the 5-HT1A receptor may contribute both to personality and to cortical excitability through their influence on GABAergic activity in the cortex. Other genes under study affect the 5-HT, dopamine, and GABA neurotransmitter systems. TMS measures of cortical excitability may provide intermediate phenotypes for genes affecting neural function and behavior

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Intramural Research (Z01)
Project #
1Z01NS002977-02
Application #
6432942
Study Section
(BSU)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2000
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Gilbert, Donald L; Zhang, Jie; Lipps, Tara D et al. (2007) Atomoxetine treatment of ADHD in Tourette syndrome: reduction in motor cortex inhibition correlates with clinical improvement. Clin Neurophysiol 118:1835-41
Huey, Edward D; Probasco, John C; Moll, Jorge et al. (2007) No effect of DC brain polarization on verbal fluency in patients with advanced frontotemporal dementia. Clin Neurophysiol 118:1417-8
Gilbert, Donald L; Wang, Zhewu; Sallee, Floyd R et al. (2006) Dopamine transporter genotype influences the physiological response to medication in ADHD. Brain 129:2038-46
Gilbert, Donald L; Ridel, Keith R; Sallee, Floyd R et al. (2006) Comparison of the inhibitory and excitatory effects of ADHD medications methylphenidate and atomoxetine on motor cortex. Neuropsychopharmacology 31:442-9
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Morales, Oscar G; Henry, Michael E; Nobler, Mitchell S et al. (2005) Electroconvulsive therapy and repetitive transcranial magnetic stimulation in children and adolescents: a review and report of two cases of epilepsia partialis continua. Child Adolesc Psychiatr Clin N Am 14:193-210, viii-ix
Wassermann, Eric M; Grafman, Jordan (2005) Recharging cognition with DC brain polarization. Trends Cogn Sci 9:503-5
Gilbert, Donald L; Sallee, Floyd R; Zhang, Jie et al. (2005) Transcranial magnetic stimulation-evoked cortical inhibition: a consistent marker of attention-deficit/hyperactivity disorder scores in tourette syndrome. Biol Psychiatry 57:1597-600
Leon-Sarmiento, Fidias E; Bara-Jimenez, William; Wassermann, Eric M (2005) Visual deprivation effects on human motor cortex excitability. Neurosci Lett 389:17-20
Garvey, Marjorie A; Barker, Christopher A; Bartko, John J et al. (2005) The ipsilateral silent period in boys with attention-deficit/hyperactivity disorder. Clin Neurophysiol 116:1889-96

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