The fluctuating response to levodopa in Parkinson's disease (""""""""on- off"""""""" phenomenon) is a common, disabling problem that occurs during chronic levodopa therapy and is resistant to current modes of therapeutic manipulation. Our goal is to understand why this fluctuating response develops and what determines the minute-to- minute motor function. This understanding is to foundation on which to design improved therapeutic strategies to treat the fluctuating response or prevent its development. This proposal will 1) explore the importance of plasma large neutral amino acid (LNAA) concentrations on response to levodopa in parkinsonian patients by determining how much plasma amino acids vary during the day, whether the ratio of plasma levodopa to LNAA concentrations is a better predictor of response and whether fasting LNAA concentrations correlate with minimum therapeutically effective plasma levodopa concentrations; 2) to investigate the possibility of a biphasic response to levodopa (both inhibitory and excitatory actions) by comparing responses to placebo, subthreshold, threshold, and suprathreshold infusion rates and the possibility of tolerance by determining the effect of constant intraduodenal infusions for 5 days on sensitivity to apomorphine and; 3) examine central pharmacokinetics of levodopa in stable and fluctuating patients by establishing dose response curves for levodopa and apomorphine to judge whether sensitivity to drug kinetics in the effector compartment is different between stable and fluctuating patients and; 4) as another index of central pharmacokinetics; study the relationship between plasma and CSF levodopa in dogs and neurosurgical patients and subsequently CSF levodopa and response in parkinsonian patients. These experiments will help define factors which modify the response to levodopa as well as the phenomenon which underlie the development of the fluctuating response.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021062-05
Application #
3401834
Study Section
Neurological Sciences Subcommittee 1 (NLS)
Project Start
1984-07-01
Project End
1992-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
5
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Oregon Health and Science University
Department
Type
Schools of Medicine
DUNS #
009584210
City
Portland
State
OR
Country
United States
Zip Code
97239
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Kay, D M; Stevens, C F; Hamza, T H et al. (2010) A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology 75:1189-94
Chung, Kathryn A; Lobb, Brenna M; Nutt, John G et al. (2010) Objective measurement of dyskinesia in Parkinson's disease using a force plate. Mov Disord 25:602-8
Brodsky, Matthew A; Park, Byung S; Nutt, John G (2010) Effects of a dopamine agonist on the pharmacodynamics of levodopa in Parkinson disease. Arch Neurol 67:27-32
Nutt, John G; Chung, Kathy A; Holford, Nicholas H G (2010) Dyskinesia and the antiparkinsonian response always temporally coincide: a retrospective study. Neurology 74:1191-7
Chung, Kathryn A; Lobb, Brenna M; Nutt, John G et al. (2010) Effects of a central cholinesterase inhibitor on reducing falls in Parkinson disease. Neurology 75:1263-9
Gunzler, Steven A; Pavel, Misha; Koudelka, Caroline et al. (2009) Foot-tapping rate as an objective outcome measure for Parkinson disease clinical trials. Clin Neuropharmacol 32:97-102
Peterson, Amie L; Nutt, John G (2008) Treatment of Parkinson's disease with trophic factors. Neurotherapeutics 5:270-80
Holford, Nick; Nutt, John G (2008) Disease progression, drug action and Parkinson's disease: why time cannot be ignored. Eur J Clin Pharmacol 64:207-16

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