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Carroll D. Arnett

Researcher at Brookhaven National Laboratory

Publications -  29
Citations -  1888

Carroll D. Arnett is an academic researcher from Brookhaven National Laboratory. The author has contributed to research in topics: Receptor & Clorgyline. The author has an hindex of 17, co-authored 29 publications receiving 1852 citations.

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Glucose metabolic rate kinetic model parameter determination in humans: the lumped constants and rate constants for [18F]fluorodeoxyglucose and [11C]deoxyglucose.

TL;DR: Using the rate constants and lumped constants determined in humans for the glucose metabolic rate kinetic model used to measure local cerebral glucose consumption, the average whole-brain metabolic rates for glucose in normal subjects measured with [18F]FDG and [11C]DG are 5.66 ± 0.37 (n = 6) and 4.99 mg/100 g/min, respectively.
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Mapping human brain monoamine oxidase A and B with 11C-labeled suicide inactivators and PET.

TL;DR: Suicide enzyme inactivators labeled with positron emitters can be used to quantitate the distribution and kinetic characteristics of MAO in human brain structures and show rapid clearance of the inactive enantiomer and retention of the active enantiomers within MAO B-rich brain structures.
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Serial [18F]N-methylspiroperidol PET studies to measure changes in antipsychotic drug D-2 receptor occupancy in schizophrenic patients☆

TL;DR: Uptake and clearance of 18F-NMS in cerebellar tissue was not appreciably affected by antipsychotic medication or drug withdrawal, and an inverse relation between labeled competitor uptake and drug plasma level has been demonstrated.
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Turnover of brain monoamine oxidase measured in vivo by positron emission tomography using L-[11C]deprenyl.

TL;DR: The distribution of carbon‐11‐labeled L‐deprenyl, an irreversible inhibitor of monoamine oxidase type B (MAO‐B), was determined in the baboon brain by positron emission tomography and the half‐life for turnover was determined to be 30 days.
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Comparison of three 18F-labeled butyrophenone neuroleptic drugs in the baboon using positron emission tomography.

TL;DR: Analysis of the metabolic stability of the radioactively labeled compound in rat striatum indicated that greater than 95% of [18F]spiroperidol remains unchanged after 4 h, suggesting that spiro peridol either has a very slow dissociation rate or that it binds irreversibly to these receptors in vivo.