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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography B: Biomedical Sciences and Applications 615 (1993), S. 169-173 
    ISSN: 0378-4347
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 45 (1993), S. 373-376 
    ISSN: 1432-1041
    Keywords: Eptastigmine ; Cholinesterase inhibition ; Elderly subjects ; adverse effects ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Eptastigmine is a new cholinesterase inhibitor, which may be potentially useful for the symptomatic treatment of Alzheimer's disease. A preliminary evaluation of its pharmacodynamic and pharmacokinetic profiles in the elderly has now been made in 6 healthy subjects (63–84 years of age) given 30 mg eptastigmine as a single oral dose. Blood was collected prior to and 1, 2, 3, 4, 6, 8, and 12 h after eptastigmine administration for measurement of cholinesterase inhibition in plasma and red blood cells and the plasma drug concentrations. The maximum plasma cholinesterase inhibition was 17%, which was reached 2.7 h after treatment. In red cells the maximum inhibition of the enzyme was 29% after 3.8 h. The estimated half-time of cholinesterase recovery was 12.4 h in plasma and 13.6 h in red blood cells. The peak plasma concentration of eptastigmine of 0.86 ng·ml−1 was reached after 1.4 h. Following absorption the drug was rapidly distributed into tissues (t1/2α = 0.44 h) and then eliminated with a half-life of 12.1 h. The drug was well tolerated in all but one subject, who showed bradycardia with hypertension and nausea for about 2 h after the dose. The results indicate that oral administration of eptastigmine to elderly subjects produces long lasting inhibition of cholinesterase activity in plasma and in red blood cells.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1590-3478
    Keywords: Bilirubin ; L-dopa ; Parkinson's disease ; Free radicals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Sommario Il danno ossidativo prodotto dai radicali liberi può contribuire a provocare il morbo di Parkinson (PD), inoltre il trattamento con L-dopa può determinare un aumento dello stress ossidativo nelle cellule nigrali dei pazienti con PD e questo suggerirebbe di ritardare il più a lungo possibile la terapia con L-dopa. La bilirubina è un potente antiossidantein vitro anche quando è legata all'albumina e questo propone un suo ruolo fisiologico come agente antiossidante. È stato calcolato che la bilirubina è in grado di attraversare la barriera emato-encefalica in quantità sufficienti da esercitare un effetto antiossidante nel cervello. Abbiamo trovato un aumento significativo (circa del 20%) della bilirubina plasmatica in 162 pazienti con PD in trattamento cronico con L-dopa in confronto a 93 pazienti parkinsoniani non trattati e 224 soggetti di controllo non parkinsoniani. Proponiamo che lo stress ossidativo nelle cellule nigrali prodotto dalla L-dopa nei pazienti parkinsoniani possa essere efficacemente controbilanciato da livelli aumentati di bilirubina. Il meccanismo con il quale la bilirubina plasmatica viene aumentata non è attualmente conosciuto.
    Notes: Abstract Oxidative damage by free radicals may contribute to the etiology of Parkinson's disease (PD), and increased oxidative stress in the nigral cells of PD patients may occur following L-dopa treatment, prompting suggestions that L-dopa therapy should be delayed as long as possible. Bilirubin is a potent antioxidantin vitro, even when bound to albumin, suggesting a physiological role as an antioxidant. Calculations indicate that bilirubin can pass the blood-brain barrier in sufficient quantity to exert a significant antioxidant effect in the brain. We have found a highly significant (about 20%) increase in plasma bilirubin in 162 PD patients on chronic L-dopa treatment compared to 93 untreated parkinsonians and 224 non-parkinsonian controls. We propose that L-dopa-induced increase in nigral oxidative stress in PD may be effectively counteracted by increased bilirubin levels. The mechanism by which plasma bilirubin is increased in patients receiving L-dopa is at present unknown.
    Type of Medium: Electronic Resource
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