Literature DB >> 14697898

(-)-Deprenyl, a selective MAO-B inhibitor, with apoptotic and anti-apoptotic properties.

Kálmán Magyar1, Béla Szende.   

Abstract

(-)-Deprenyl (selegiline) is an irreversible inhibitor of monoamine oxidase (MAO) B, which was discovered in 1962 and become the "golden standard" of MAO research. Like the other MAO-B inhibitors, it was synthesized as an antidepressant, but in a selective MAO-B inhibitory dose it does not act in depression. It is used in the treatment of Parkinson's disease. (-)-Deprenyl potentiates the effect of dopamine, it has antioxidant activity and prevents the toxicity of the dopaminergic (6-OH-dopamine; 1-methyl-4-phenyl-1,2,3,6-tetrahydro-pyridine (MPTP)), the noradrenergic (DSP-4) and cholinergic (AF64A) neurotoxins after pre-treatment. When (-)-deprenyl was administered with levodopa in a long-term treatment of Parkinsonian patients, it induces adverse events (nausea, dizziness, confusion, hallucination, insomnia and cardiovascular changes), which could be due to dopamine potentiation in dopaminergic systems (limbic system), other than the nigrostriatal pathway. (-)-Deprenyl in much lower concentrations needed to induce MAO-B inhibition (10(-9) to 10(-13) M) potently inhibits MPTP or serum withdrawal induced apoptosis in tissue cultures of neuro-ectodermal origin (PC12, M1, M2058). The (+)-enantiomer of deprenyl lacks of this property. The anti-apoptotic activity of (-)-deprenyl can be prevented by inhibiting the metabolism of the drug with SKF-525A pre-treatment, which suggests that some of the presently unknown metabolites could be responsible for the anti-apoptotic activity. In high concentration (10(-3) M), (-)-deprenyl and its metabolites induce apoptosis in tissue cultures without serum withdrawal (biphasic action). Our findings support the view that 100, or even 1000 times lower dose of (-)-deprenyl can be offered in human therapy to protect, or slow down neuronal degeneration, than it is presently used. With low dose of the drug the dopaminergic adverse events could be avoided, while anti-apoptotic activity might be preserved.

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Year:  2004        PMID: 14697898     DOI: 10.1016/S0161-813X(03)00102-5

Source DB:  PubMed          Journal:  Neurotoxicology        ISSN: 0161-813X            Impact factor:   4.294


  34 in total

1.  Cytoprotective effect of (-)-deprenyl, (-)desmethyl-deprenyl and (-)deprenyl-N-oxide on glutathione depleted A-2058 melanoma cells.

Authors:  B Szende; G Barna; Kálmán Magyar
Journal:  J Neural Transm (Vienna)       Date:  2010-05-09       Impact factor: 3.575

2.  R-deprenyl: pharmacological spectrum of its activity.

Authors:  K Magyar; B Szende; V Jenei; T Tábi; M Pálfi; E Szöko
Journal:  Neurochem Res       Date:  2010-08-20       Impact factor: 3.996

3.  Amine oxidases and their inhibitors: what can they tell us about neuroprotection and the development of drugs for neuropsychiatric disorders?

Authors:  Glen B Baker; Bernard Sowa; Kathryn G Todd
Journal:  J Psychiatry Neurosci       Date:  2007-09       Impact factor: 6.186

Review 4.  The role of calcium and mitochondrial oxidant stress in the loss of substantia nigra pars compacta dopaminergic neurons in Parkinson's disease.

Authors:  D J Surmeier; J N Guzman; J Sanchez-Padilla; P T Schumacker
Journal:  Neuroscience       Date:  2011-08-25       Impact factor: 3.590

5.  Inhibition of human monoamine oxidase A and B by flavonoids isolated from two Algerian medicinal plants.

Authors:  Farida Larit; Khaled M Elokely; Narayan D Chaurasiya; Samira Benyahia; Manal A Nael; Francisco León; Mohammad Sanad Abu-Darwish; Thomas Efferth; Yan-Hong Wang; Djamila Belouahem-Abed; Samir Benayache; Babu L Tekwani; Stephen J Cutler
Journal:  Phytomedicine       Date:  2017-12-27       Impact factor: 5.340

6.  Trans-differentiation of the adipose tissue-derived stem cells into neuron-like cells expressing neurotrophins by selegiline.

Authors:  Alireza Abdanipour; Taki Tiraihi; Alireza Delshad
Journal:  Iran Biomed J       Date:  2011

7.  Neuroprotective effects of selegiline on rat neural stem cells treated with hydrogen peroxide.

Authors:  Alireza Abdanipour; Iraj Jafari Anarkooli; Saeed Shokri; Mehrdad Ghorbanlou; Vahid Bayati; Reza Nejatbakhsh
Journal:  Biomed Rep       Date:  2017-11-22

Review 8.  Calcium, cellular aging, and selective neuronal vulnerability in Parkinson's disease.

Authors:  D James Surmeier; Jaime N Guzman; Javier Sanchez-Padilla
Journal:  Cell Calcium       Date:  2010-01-06       Impact factor: 6.817

Review 9.  DSP4, a selective neurotoxin for the locus coeruleus noradrenergic system. A review of its mode of action.

Authors:  Svante B Ross; Carina Stenfors
Journal:  Neurotox Res       Date:  2014-06-26       Impact factor: 3.911

10.  The Neuroprotective Effect of Antidepressant Drug via Inhibition of TIEG2-MAO B Mediated Cell Death.

Authors:  Deyin Lu; Chandra Johnson; Shakevia Johnson; Shawna Tazik; Xiao-Ming Ou
Journal:  Drug Discov Ther       Date:  2008-10
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