Javascript must be enabled to continue!
L-Dopa Treatment in Parkinson’s Disease
View through CrossRef
Double-blind and non-blind therapeutic trials of orally administered L-Dopa in the long-term treatment of Parkinsonism were carried out with 126 patients. For correlative studies the amount of hornovanillic acid (HVA) in the cerebrospinal fluid (CSF) was analysed. A double-blind cross-over trial with 1.5 g of L-Dopa for 2 months was performed in 10 patients. During L-Dopa treatment 8 patients showed improvement but only 2 patients benefited with placebo. In a double-blind study 40 patients were treated with a daily dosage of 5 g of L-Dopa for 2 months. All patients showed benefit on L-Dopa during this trial period and L-Dopa induced highly significantly more improvement than placebo. During non-blind treatment with optimal dosage of L-Dopa followed up for 1 to 9 months, all but one of 76 parkinsonian patients showed overall improvement. The average dose needed for optimal improvement was usually between 4 and 5 g daily. 41 % of the patients were markedly or very markedly improved and 48 °/o moderately improved; only 11 % showed minimal benefit or none. All the cardinal symptoms of Parkinson’s disease were significantly alleviated. Patients with severe disease and with duration of disease of 15 years or more showed less marked improvement. In some patients changing of anticholinergic drug therapy during L-Dopa treatment indicated a synergistic effect. Nausea, vomiting, anorexia, postural hypotension and involuntary movements were the most frequent clinical side effects. L-Dopa treatment had to be discontinued in 2 patients after 2 months treatment because of mental disturbances. An increase in libido was reported by 25 % of the patients and 5 postmenopausal female patients had renewed menstrual bleeding. During L-Dopa treatment the amount of HVA in the CSF rose significantly in all patients and was correlated with the dose of L-Dopa but not clearly with the clinical improvement. The results indicated the significant value of high oral doses of L-Dopa in the long-term treatment of parkinsonian patients. It is concluded that the therapeutic response to L-Dopa is associated with an increase in brain dopamine metabolism but that there is not always a direct correlation.
Title: L-Dopa Treatment in Parkinson’s Disease
Description:
Double-blind and non-blind therapeutic trials of orally administered L-Dopa in the long-term treatment of Parkinsonism were carried out with 126 patients.
For correlative studies the amount of hornovanillic acid (HVA) in the cerebrospinal fluid (CSF) was analysed.
A double-blind cross-over trial with 1.
5 g of L-Dopa for 2 months was performed in 10 patients.
During L-Dopa treatment 8 patients showed improvement but only 2 patients benefited with placebo.
In a double-blind study 40 patients were treated with a daily dosage of 5 g of L-Dopa for 2 months.
All patients showed benefit on L-Dopa during this trial period and L-Dopa induced highly significantly more improvement than placebo.
During non-blind treatment with optimal dosage of L-Dopa followed up for 1 to 9 months, all but one of 76 parkinsonian patients showed overall improvement.
The average dose needed for optimal improvement was usually between 4 and 5 g daily.
41 % of the patients were markedly or very markedly improved and 48 °/o moderately improved; only 11 % showed minimal benefit or none.
All the cardinal symptoms of Parkinson’s disease were significantly alleviated.
Patients with severe disease and with duration of disease of 15 years or more showed less marked improvement.
In some patients changing of anticholinergic drug therapy during L-Dopa treatment indicated a synergistic effect.
Nausea, vomiting, anorexia, postural hypotension and involuntary movements were the most frequent clinical side effects.
L-Dopa treatment had to be discontinued in 2 patients after 2 months treatment because of mental disturbances.
An increase in libido was reported by 25 % of the patients and 5 postmenopausal female patients had renewed menstrual bleeding.
During L-Dopa treatment the amount of HVA in the CSF rose significantly in all patients and was correlated with the dose of L-Dopa but not clearly with the clinical improvement.
The results indicated the significant value of high oral doses of L-Dopa in the long-term treatment of parkinsonian patients.
It is concluded that the therapeutic response to L-Dopa is associated with an increase in brain dopamine metabolism but that there is not always a direct correlation.
Related Results
d‐DOPA IS UNIDIRECTIONALLY CONVERTED TOl‐DOPA BYd‐AMINO ACID OXIDASE, FOLLOWED BY DOPA TRANSAMINASE
d‐DOPA IS UNIDIRECTIONALLY CONVERTED TOl‐DOPA BYd‐AMINO ACID OXIDASE, FOLLOWED BY DOPA TRANSAMINASE
SUMMARYMany studies have shown that administration ofd‐3, 4‐dihydroxyphenylalanine (d‐dopa) produces contralateral rotation in hemi‐parkinsonian animals comparable tol‐dopa, with l...
Effect of the Dopa Decarboxylase Inhibitor MK-486 on L-dopa-Induced Inhibition of Prolactin Secretion: Evidence for CNS Participation in the L-dopa Effects
Effect of the Dopa Decarboxylase Inhibitor MK-486 on L-dopa-Induced Inhibition of Prolactin Secretion: Evidence for CNS Participation in the L-dopa Effects
The present studies were performed in order to determine whether the inhibition of prolactin (Prl) secretion which follows the systemic administration of L-dopa and its conversion ...
The Design and Evaluation of an l-Dopa–Lazabemide Prodrug for the Treatment of Parkinson’s Disease
The Design and Evaluation of an l-Dopa–Lazabemide Prodrug for the Treatment of Parkinson’s Disease
l-Dopa, the metabolic precursor of dopamine, is the treatment of choice for the symptomatic relief of the advanced stages of Parkinson’s disease. The oral bioavailability of l-dopa...
Doxycycline, an anti-inflammatory agent, alleviates dyskinesia induced by L-DOPA in Parkinsonian rats
Doxycycline, an anti-inflammatory agent, alleviates dyskinesia induced by L-DOPA in Parkinsonian rats
Background and Purpose L-DOPA induced dyskinesia is a debilitating side
effect of treating Parkinson’s disease with L-DOPA. There is a need to
discover a treatment that has the sam...
Striatal D1 medium spiny neuron activation induces dyskinesias in parkinsonian mice
Striatal D1 medium spiny neuron activation induces dyskinesias in parkinsonian mice
ABSTRACTBackgroundDyskinesias are a disabling motor complication that arises with prolonged l‐dopa treatment. Studies using D1 receptor drugs and genetically modified mice suggest ...
Development of Jelly Loaded with Nanogel Containing Natural L-Dopa from Mucuna pruriens Seed Extract for Neuroprotection in Parkinson’s Disease
Development of Jelly Loaded with Nanogel Containing Natural L-Dopa from Mucuna pruriens Seed Extract for Neuroprotection in Parkinson’s Disease
The first line therapy of patients with Parkinson’s disease, a neurodegenerative disorder caused by the degeneration of dopaminergic neurons, is levodopa (L-dopa) given orally. Rec...
Measuring L-dopa in plasma and urine to monitor therapy of elderly patients with Parkinson disease treated with L-dopa and a dopa decarboxylase inhibitor
Measuring L-dopa in plasma and urine to monitor therapy of elderly patients with Parkinson disease treated with L-dopa and a dopa decarboxylase inhibitor
Abstract
We have established a method for measuring L-dopa in plasma and urine, including the metabolites dopamine and L-dopac, using separation by ion-pair reversed...
Levodopa Inhibits the Development of Form‐Deprivation Myopia in Guinea Pigs
Levodopa Inhibits the Development of Form‐Deprivation Myopia in Guinea Pigs
ABSTRACT
Purpose.
It has been shown that visual deprivation leads to a myopic refractive error and...

