A Positron Emission Tomography (PET) Facility has been established at the University of Michigan for the development of a new, non-invasive approach to human brain research utilizing positron emitting metabolic and pharmacologic probes. A dedicated TCC CS-30 medical cyclotron, a TCC PCT-4600A tomographic scanner, the radiochemical/radiopharmaceutical facilities and a small image processing computer facility will be used in the performance of PET studies and complement the existing Nuclear Medicine facilities. Proposed studies involve the use of positron emitting probes 15-0-C0, 15-0-H20, 15-0-02, 18-F-2-deoxyglucose, 11-C-BCNU, 68-Ga-EDTA and 11-C-Scopolamine to study cerebral blood volume, blood flow and partition coefficients, oxygen utilization, glucose utilization, tumor uptake, blood-brain barrier integrity and muscarinic receptors respectively. Patients with Huntington's disease, epilepsy, brain tumors, the hypotonic and hypertonic phases of paralysis associated with stroke, dystonia, olivopontocerebellar atrophy and aging in the human brain will also be studied. Studies of the normal brain with several agents will continue. New positron-emitting radiopharmaceuticals will be synthesized and new labeling techniques will be investigated. 11-C-Scopolamine will be available for high specific activity in vivo receptor studies and 11-C-amine cyclopentane carbocylic acid (ACPC) will be developed for amino acid uptake studies. New physiological modeling techniques will be instituted for mapping receptor sites. Parameter estimation techniques will be developed to determine rate constants from dynamic PET studies of FDG metabolism.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS015655-07
Application #
3099562
Study Section
(SRC)
Project Start
1979-12-01
Project End
1989-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
7
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Bohnen, Nicolaas I; Kanel, Prabesh; Müller, Martijn L T M (2018) Molecular Imaging of the Cholinergic System in Parkinson's Disease. Int Rev Neurobiol 141:211-250
Rektor, Ivan; Bohnen, Nicolaas I; Korczyn, Amos D et al. (2018) An updated diagnostic approach to subtype definition of vascular parkinsonism - Recommendations from an expert working group. Parkinsonism Relat Disord 49:9-16
Kim, Kamin; Bohnen, Nicolaas I; Müller, Martijn L T M et al. (2018) Compensatory dopaminergic-cholinergic interactions in conflict processing: Evidence from patients with Parkinson's disease. Neuroimage :
Beaulieu, Mélanie L; Müller, Martijn L T M; Bohnen, Nicolaas I (2018) Peripheral neuropathy is associated with more frequent falls in Parkinson's disease. Parkinsonism Relat Disord 54:46-50
Bohnen, Nicolaas I; Grothe, Michel J; Ray, Nicola J et al. (2018) Recent advances in cholinergic imaging and cognitive decline-Revisiting the cholinergic hypothesis of dementia. Curr Geriatr Rep 7:1-11
Nejad-Davarani, Siamak; Koeppe, Robert A; Albin, Roger L et al. (2018) Quantification of brain cholinergic denervation in dementia with Lewy bodies using PET imaging with [18F]-FEOBV. Mol Psychiatry :
Kotagal, Vikas; Albin, Roger L; Müller, Martijn L T M et al. (2018) Cardiovascular Risk Factor Burden in Veterans and Non-Veterans with Parkinson Disease. J Parkinsons Dis 8:153-160
Bohnen, Nicolaas I; Müller, Martijn L T M; Frey, Kirk A (2017) Molecular Imaging and Updated Diagnostic Criteria in Lewy Body Dementias. Curr Neurol Neurosci Rep 17:73
Chou, Kelvin L; Gilman, Sid; Bohnen, Nicolaas I (2017) Association between autonomic dysfunction and fatigue in Parkinson disease. J Neurol Sci 377:190-192
Kim, Kamin; Müller, Martijn L T M; Bohnen, Nicolaas I et al. (2017) The cortical cholinergic system contributes to the top-down control of distraction: Evidence from patients with Parkinson's disease. Neuroimage :

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