dihydroxyphenylalanine has been researched along with Multiple System Atrophy in 11 studies
Dihydroxyphenylalanine: A beta-hydroxylated derivative of phenylalanine. The D-form of dihydroxyphenylalanine has less physiologic activity than the L-form and is commonly used experimentally to determine whether the pharmacological effects of LEVODOPA are stereospecific.
dopa : A hydroxyphenylalanine carrying hydroxy substituents at positions 3 and 4 of the benzene ring.
Multiple System Atrophy: A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92)
Excerpt | Relevance | Reference |
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"We used PET with the tracers [18F]fluorodeoxyglucose (FDG), [18F]fluorodopa (FDOPA) and [11C]raclopride (RACLO) to study striatal glucose and dopa metabolism, and dopamine D2 receptor binding, respectively, in nine patients with multiple system atrophy." | 3.69 | Complementary PET studies of striatal neuronal function in the differential diagnosis between multiple system atrophy and Parkinson's disease. ( Antonini, A; Günther, I; Leenders, KL; Maguire, RP; Missimer, J; Psylla, M; Vontobel, P, 1997) |
"The third part of the unified Parkinson's disease rating scale (UPDRS) was used to evaluate the development of PD symptom before and 1 hour after taking the medicine." | 1.35 | [Acute dopaminergic responsiveness test in diagnosis of Parkinson's disease and Parkinsonian disorders]. ( Feng, T; Li, W; Lin, JX; Wang, YJ; Xu, XT, 2008) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (18.18) | 18.2507 |
2000's | 4 (36.36) | 29.6817 |
2010's | 4 (36.36) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
da Silva Schmitt, G | 1 |
Martinez, ARM | 1 |
da Graça, FF | 1 |
de Lima, FD | 1 |
Bonadia, LC | 1 |
Amorim, BJ | 1 |
Nucci, A | 1 |
França, MC | 1 |
Goldstein, DS | 4 |
Sullivan, P | 2 |
Holmes, C | 4 |
Kopin, IJ | 2 |
Sharabi, Y | 4 |
Mash, DC | 1 |
Wu, T | 1 |
Jinsmaa, Y | 1 |
Li, W | 1 |
Feng, T | 1 |
Wang, YJ | 1 |
Lin, JX | 1 |
Xu, XT | 1 |
Lewis, SJ | 1 |
Pavese, N | 1 |
Rivero-Bosch, M | 1 |
Eggert, K | 1 |
Oertel, W | 1 |
Mathias, CJ | 1 |
Brooks, DJ | 1 |
Gerhard, A | 1 |
Eckert, T | 1 |
Feigin, A | 1 |
Lewis, DE | 1 |
Dhawan, V | 1 |
Frucht, S | 1 |
Eidelberg, D | 1 |
Bentho, O | 1 |
Sato, T | 1 |
Moak, J | 1 |
Imrich, R | 1 |
Conant, S | 1 |
Eldadah, BA | 1 |
Otsuka, M | 1 |
Kuwabara, Y | 1 |
Ichiya, Y | 1 |
Hosokawa, S | 1 |
Sasaki, M | 1 |
Yoshida, T | 1 |
Fukumura, T | 1 |
Kato, M | 1 |
Masuda, K | 1 |
Antonini, A | 1 |
Leenders, KL | 1 |
Vontobel, P | 1 |
Maguire, RP | 1 |
Missimer, J | 1 |
Psylla, M | 1 |
Günther, I | 1 |
Jankovic, J | 1 |
Kapadia, AS | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Does N-Acetylcysteine Decrease Spontaneous Oxidation of Central Neural Dopamine in Parkinson's Disease?[NCT03104725] | Phase 1 | 6 participants (Actual) | Interventional | 2017-09-25 | Terminated (stopped due to Difficulty with recruitment and participant accrual due to study eligibility criteria and required study procedures (e.g., multiple lumbar punctures).) | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Patients with Parkinson's Disease (PD) who took N-acetylcysteine (NAC), and healthy volunteers who did not take NAC, each had two separate lumbar punctures (LPs) to obtain spinal fluid. The spinal fluid samples were used to measure the ratio of the brain chemical called 5-S-cysteinyl-dopamine (Cys-DA) to the brain chemical called 3,4-Dihydroxyphenylacetic acid (Cys-DOPAC). Dopamine has 2 metabolic fates. One is the breakdown of dopamine by an enzyme to form DOPAC. The other is spontaneous oxidation to form Cys-DA. The ratio of Cys-DA/DOPAC may reflect these relative fates. If NAC reduced spontaneous oxidation to Cys-DA, then the ratio Cys-DA/DOPAC would decrease between LP 1 and LP 2, which would be reflected as a percent decrease. (NCT03104725)
Timeframe: All participants underwent a baseline LP. For PD participants, the second LP occurred approximately 2 hours after the participant had taken NAC the last NAC dose. For HV participants the second LP takes place approximately 48 hours after the first LP.
Intervention | percent change (Mean) |
---|---|
Healthy Volunteers (HVs) | 50.1 |
Parkinson's Disease (PD) Patients | 27.2 |
Patients with Parkinson's Disease (PD) who took N-acetylcysteine (NAC), and healthy volunteers who did not take NAC, each had two separate lumbar punctures (LP 1 and LP 2) to obtain spinal fluid. The spinal fluid samples were used to measure the amount of a brain chemical called 5-S-cysteinyl-dopamine (Cys-DA). The primary outcome measure is the mean change in CSF Cys-DA levels between pre and post-NAC treatment, which is calculated as the difference of CSF Cys-DA levels at pre-treatment (LP 1) and post-treatment (LP 2) divided by CSF Cys-DA at pre-treatment (LP 1). A greater percent decrease in Cys-DA levels in the brain would suggest that NAC may contribute to a reduction in the oxidation of brain dopamine, while a smaller percent decrease would suggest that NAC had no effect on the oxidation of brain dopamine. (NCT03104725)
Timeframe: All participants underwent a baseline LP. For PD participants, the second LP occurred approximately 2 hours after the participant had taken NAC the last NAC dose. For HV participants the second LP takes place approximately 48 hours after the first LP.
Intervention | percent change (Mean) |
---|---|
Healthy Volunteers (HVs) | 45.7 |
Parkinson's Disease (PD) Patients | 20.1 |
Patients with Parkinson's Disease (PD) who took N-acetylcysteine (NAC), and healthy volunteers who did not take NAC, each had two separate lumbar punctures (LPs) to obtain spinal fluid. The spinal fluid samples were used to measure the ratio of the brain chemical called 5-S-cysteinyl-dopamine (Cys-DA) to the brain chemical called 3,4-Dihydroxyphenylacetic acid (Cys-DOPAC). Dopamine has 2 possible metabolic fates or processes of degradation. One fate is the breakdown of Dopamine by an enzyme to form DOPAC. The other fate is spontaneous oxidation to form Cys-DA. The ratio of Cys-DA to DOPAC may reflect these relative fates. If NAC reduced spontaneous oxidation to Cys-DA, then the ratio Cys-DA/DOPAC ratio would decrease between LP 1 and LP 2. (NCT03104725)
Timeframe: All participants underwent a baseline LP. For PD participants, the second LP occurred approximately 2 hours after the participant had taken NAC the last NAC dose. For HV participants the second LP takes place approximately 48 hours after the first LP.
Intervention | ratio (Mean) | |
---|---|---|
Cys-DA/DOPAC LP1 | Cys-DA/DOPAC LP2 | |
Healthy Volunteers (HVs) | 0.12 | 0.05 |
Parkinson's Disease (PD) Patients | 0.16 | 0.13 |
11 other studies available for dihydroxyphenylalanine and Multiple System Atrophy
Article | Year |
---|---|
Dopa-Responsive Parkinsonism in a Patient With Homozygous RFC1 Expansions.
Topics: Atrophy; Dihydroxyphenylalanine; Homozygote; Humans; Multiple System Atrophy; Parkinsonian Disorders | 2020 |
Decreased vesicular storage and aldehyde dehydrogenase activity in multiple system atrophy.
Topics: 3,4-Dihydroxyphenylacetic Acid; Aged; Aged, 80 and over; Aldehyde Dehydrogenase; Corpus Striatum; Di | 2015 |
Survival in synucleinopathies: A prospective cohort study.
Topics: Aged; alpha-Synuclein; Brain; Cerebellar Diseases; Cohort Studies; Dihydroxyphenylalanine; Female; F | 2015 |
Elevated cerebrospinal fluid ratios of cysteinyl-dopamine/3,4-dihydroxyphenylacetic acid in parkinsonian synucleinopathies.
Topics: 3,4-Dihydroxyphenylacetic Acid; Aged; Animals; Catechols; Dihydroxyphenylalanine; Dopamine; Female; | 2016 |
[Acute dopaminergic responsiveness test in diagnosis of Parkinson's disease and Parkinsonian disorders].
Topics: Adult; Aged; Diagnosis, Differential; Dihydroxyphenylalanine; Dopamine; Female; Humans; Male; Middle | 2008 |
Brain monoamine systems in multiple system atrophy: a positron emission tomography study.
Topics: Aged; Biogenic Monoamines; Brain; Dihydroxyphenylalanine; Dopamine; Female; Fluorine Radioisotopes; | 2012 |
Regional metabolic changes in parkinsonian patients with normal dopaminergic imaging.
Topics: Brain; Corpus Striatum; Dihydroxyphenylalanine; Dopamine; Female; Ganglia; Humans; Male; Middle Aged | 2007 |
Biomarkers to detect central dopamine deficiency and distinguish Parkinson disease from multiple system atrophy.
Topics: 3,4-Dihydroxyphenylacetic Acid; Analysis of Variance; Biomarkers; Brain; Dihydroxyphenylalanine; Dop | 2008 |
Differentiating between multiple system atrophy and Parkinson's disease by positron emission tomography with 18F-dopa and 18F-FDG.
Topics: Adult; Aged; Diagnosis, Differential; Dihydroxyphenylalanine; Female; Fluorodeoxyglucose F18; Glucos | 1997 |
Complementary PET studies of striatal neuronal function in the differential diagnosis between multiple system atrophy and Parkinson's disease.
Topics: Aged; Carbon Radioisotopes; Caudate Nucleus; Corpus Striatum; Diagnosis, Differential; Dihydroxyphen | 1997 |
Functional decline in Parkinson disease.
Topics: Adolescent; Adult; Age of Onset; Aged; Aged, 80 and over; Autonomic Nervous System Diseases; Demogra | 2001 |