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Eldepryl - Selegiline

Eldepryl (Selegiline hydrochloride). Orion Pharma (UK) Ltd. UK Summary of product characteristics, July 2006. [Pg.688]

The mechanism of action of amantadine (Symmetrel) and selegiline (Eldepryl) in die treatment of parkinsonism is not fully understood. [Pg.265]

Selegiline (Eldepryl ) Blocks MAOB metabolism and presynaptic reuptake of DA in the brain Start with 5 mg in the morning if symptoms continue, add 5 mg at noon 5 mg daily may be as clinically effective as 10 mg daily with fewer side effects... [Pg.479]

Selegiline (deprenyl Eldepryl) is an irreversible MAO-B inhibitor that blocks dopamine breakdown and can modestly extend the duration of action of L-dopa (up to 1 hour). It often permits reduction of L-dopa dose by as much as one-half. [Pg.647]

A final pharmacological strategy for treatment of Parkinson s disease comes from enzyme inhibition. This was initally done with an MAO inhibitor, L-deprenyl (selegiline, Eldepryl), but more recent drugs have become available that are COMT inhibitors. L-Deprenyl is an inhibitor of MAOB, which is the form of MAO selective to dopamine. Thus, it may increase the amount of available dopamine for release. Second, it may protect dopamine neurons by reducing the oxidative stress concomitant with dopamine metabolism (Olanow 1997). Third, L-deprenyl is metabolized into amphetamine and methamphetamine, which may contribute to their antiparkinsonian effects. Unlike other treatments for Parkinson s disease, L-deprenyl seems to slow the progression of the disease. Tolcapone (Tasmar) is a COMT inhibitor, which prevents extracellular breakdown of dopamine. [Pg.155]

Yet another MAOI is selegiline (Eldepryl). Unlike the other MAOls, selegiline is seldom used to treat depression. At low doses, selegiline only inhibits the M AO-B enzyme. Therefore, it increases dopamine activity but does not have any pronounced effect on norepinephrine or serotonin. For this reason, it has been less useful as an antidepressant however, its primary use has been to treat Parkinson s disease. Of course, this selectivity for dopamine suggests that it may be helpful for ADHD as well. [Pg.245]

This drug is a selective inhibitor of monoaminooxidase B, which suppresses dopamine-inactivation processes and facilitates an increase of its level in the brain. In treating Parkinsonism, selegiline is usually used in combination with levodopa. The most common synonyms of selegiline are deprenyl, eldepryl, eldopal, and others. [Pg.138]

Another drug used in the treatment of Parkinson s disease is selegiline (also known as deprenyl, or Eldepryl). It is an irreversible inhibitor of MAO-B, an important enzyme in the metabolism of dopamine (Fig. 33.2). Blockade of dopamine metabolism makes more dopamine available for stimulation of its receptors. Selegiline, as monotherapy, may be effective in the newly diagnosed patient with parkinsonism because its pharmacological effect enhances the actions of endogenous dopamine. [Pg.369]

In the United States, the three MAOIS available for the treatment of psychiatric conditions are phenelzine (Nardil), tranylcypromine (Parnate), and isocarboxazid (Marplan). All three agents have indications for adult major depression (>16 years old) and, more specifically, atypical depression (anergia, hypersomnia, hy-perphagia, somatization, and anxiety symptoms). Although not indicated for anxiety, the MAOIs can also be particularly helpful in treatment of these disorders. Selegiline or L-deprenyl (Eldepryl) is also available in the United States and indicated for symptoms of Parkinson s disease and depression. [Pg.296]

Isocarboxazid (Marplan) Moclobemide (Aurorix, Manerix, Moclodura ) Phenelzine (Nardil) Tranylcypromine Selegiline (Selegiline, Eldepryl)... [Pg.690]


See other pages where Eldepryl - Selegiline is mentioned: [Pg.1696]    [Pg.59]    [Pg.151]    [Pg.650]    [Pg.87]    [Pg.1696]    [Pg.1696]    [Pg.1696]    [Pg.59]    [Pg.151]    [Pg.650]    [Pg.87]    [Pg.1696]    [Pg.1696]    [Pg.645]    [Pg.834]    [Pg.251]    [Pg.364]    [Pg.51]    [Pg.42]    [Pg.281]    [Pg.621]    [Pg.41]    [Pg.281]    [Pg.217]    [Pg.128]    [Pg.655]    [Pg.488]    [Pg.632]    [Pg.821]    [Pg.159]   


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