Plans for the fifth year of funding involve four general research areas: 1 The development and improvement of standardized methods for the tracer kinetic study of brain function, 2. Standardization of anatomical approaches to functional image analysis. 3. The evaluation of normal subjects in resting states and during specific sensory, motor and cognitive tasks and 4. The continued evaluation and collaboration with other investigators in the study of patients with Huntington's Disease, Aphasia, Epilepsy, Affective Disorders and Dementia. In the area of methodological development, I will continue the human and animal experimentation needed to validate the bolus approach to oxygen utilization studies. In the realm of anatomical standardization, I will complete a series of NIMH sponsored workshops for the standardization and identification of regions from functional images obtained with PET and SPECT. In our own laboratory these approaches will be implemented and a laboratory wide data base will be established for the integrated exchange of data between experimental protocols in both animals and humans. Studies in normal subjects with PET will include the use of oxygen-15 labeled compounds and FDG for our new tomograph. These studies will provide new values for kinetic rate constants of the deoxyglucose model and initial high resolution values for the human brain for cerebral glucose metabolism, blood flow, blood volume, oxygen utilization and oxygen extraction fraction. Continued studies of the motor system will expand our original approach in normal subjects to evaluate tasks in patients with motor system diseases including Huntington's Disease, Wilson's Disease, Tardive Dyskinesia and Parkinson's Disease. Other patient studies will include the continuation of our work in Huntington's Disease with emphasis on correlating our studies in at risk patients with genetic linkage studies performed for the identification of the Huntington's Disease gene. Expansion of our work in patients with affective disorders will include provocative stimuli from both behavioral tasks and pharmacological manipulations with antidepressant drugs and stimulants.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Academic/Teacher Award (ATA) (K07)
Project #
5K07NS000588-05
Application #
3078057
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1981-07-01
Project End
1986-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
5
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
Schools of Medicine
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Metter, E J; Kempler, D; Jackson, C et al. (1989) Cerebral glucose metabolism in Wernicke's, Broca's, and conduction aphasia. Arch Neurol 46:27-34
Baxter Jr, L R; Schwartz, J M; Mazziotta, J C et al. (1988) Cerebral glucose metabolic rates in nondepressed patients with obsessive-compulsive disorder. Am J Psychiatry 145:1560-3
Baxter Jr, L R; Schwartz, J M; Phelps, M E et al. (1988) Localization of neurochemical effects of cocaine and other stimulants in the human brain. J Clin Psychiatry 49 Suppl:23-6
Baxter Jr, L R; Thompson, J M; Schwartz, J M et al. (1987) Trazodone treatment response in obsessive-compulsive disorder--correlated with shifts in glucose metabolism in the caudate nuclei. Psychopathology 20 Suppl 1:114-22
Baxter Jr, L R; Mazziotta, J C; Phelps, M E et al. (1987) Cerebral glucose metabolic rates in normal human females versus normal males. Psychiatry Res 21:237-45
Mazziotta, J C; Phelps, M E; Pahl, J J et al. (1987) Reduced cerebral glucose metabolism in asymptomatic subjects at risk for Huntington's disease. N Engl J Med 316:357-62
Schwartz, J M; Baxter Jr, L R; Mazziotta, J C et al. (1987) The differential diagnosis of depression. Relevance of positron emission tomography studies of cerebral glucose metabolism to the bipolar-unipolar dichotomy. JAMA 258:1368-74
Metter, E J; Kempler, D; Jackson, C A et al. (1987) Cerebellar glucose metabolism in chronic aphasia. Neurology 37:1599-606
Metter, E J; Jackson, C; Kempler, D et al. (1986) Left hemisphere intracerebral hemorrhages studied by ( (F-18)-fluorodeoxyglucose PET. Neurology 36:1155-62
Metter, E J; Mazziotta, J C; Itabashi, H H et al. (1985) Comparison of glucose metabolism, x-ray CT, and postmortem data in a patient with multiple cerebral infarcts. Neurology 35:1695-701

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