Evidence of deprenyl-insensitive apoptosis of nigral dopamine neurons during development

被引:10
作者
Groc, L
Levine, RA
Foster, JA
Normile, HJ
Weissmann, D
Bezin, L
机构
[1] Henry Ford Hosp, William T Gossett Neurol Labs, Detroit, MI 48202 USA
[2] John D Dingell Vet Adm Med Ctr, Detroit, MI USA
[3] Wayne State Univ, Dept Pharmaceut Sci, Detroit, MI USA
[4] Wayne State Univ, Dept Psychiat & Behav Neurosci, Wayne, MI USA
[5] Wayne State Univ, Dept Phys Assistant Studies, Detroit, MI USA
[6] Univ Lyon 1, CNRS, UMR 5542, Lab Neuropharmacol Mol, F-69365 Lyon, France
来源
DEVELOPMENTAL BRAIN RESEARCH | 2000年 / 120卷 / 01期
关键词
deprenyl; apoptosis; substantia nigra;
D O I
10.1016/S0165-3806(99)00195-9
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Apoptosis of dopamine neurons occurs naturally in the substantia nigra during development, culminating in approximately 30% loss of these cells during the perinatal period. Deprenyl, independent of its monoamine oxidase (MAO)-B inhibitory properties, can prevent dopamine neuronal apoptosis in models of neurodegeneration. Our current study demonstrate that apoptotic death of dopamine neurons during development is insensitive to daily treatment of pregnant mothers and then newborns with deprenyl (0.1, 1, or 10 mg/kg). This result is not due to poor crossing of the placental and blood-brain barriers, since deprenyl caused a dose-dependent inhibition of brain MAO-B activity in pups at birth. Determining the pathway(s) leading to deprenyl-insensitive apoptosis of nigral dopamine neurons in development may shed light on mechanisms underlying the premature death of dopamine neurons in neurodegenerative disorders. (C) 2000 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:95 / 98
页数:4
相关论文
共 19 条
[1]  
ANSARI KS, 1993, J NEUROSCI, V13, P4042
[2]   EFFECTS OF SELECTIVE MONOAMINE-OXIDASE INHIBITORS ON THE INVIVO RELEASE AND METABOLISM OF DOPAMINE IN THE RAT STRIATUM [J].
BUTCHER, SP ;
FAIRBROTHER, IS ;
KELLY, JS ;
ARBUTHNOTT, GW .
JOURNAL OF NEUROCHEMISTRY, 1990, 55 (03) :981-988
[3]   Free radicals and the pathobiology of brain dopamine systems [J].
Cadet, JL ;
Brannock, C .
NEUROCHEMISTRY INTERNATIONAL, 1998, 32 (02) :117-131
[4]   Selective reduction of monoamine oxidase A and B in the frontal cortex of subordinate rats [J].
Dhingra, NK ;
Raju, TR ;
Meti, BL .
BRAIN RESEARCH, 1997, 758 (1-2) :237-240
[5]   PROTECTION AGAINST DSP-4-INDUCED NEUROTOXICITY BY DEPRENYL IS NOT RELATED TO ITS INHIBITION OF MAO-B [J].
FINNEGAN, KT ;
SKRATT, JJ ;
IRWIN, I ;
DELANNEY, LE ;
LANGSTON, JW .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 184 (01) :119-126
[6]   NATURALLY-OCCURRING CELL-DEATH DURING POSTNATAL-DEVELOPMENT OF THE SUBSTANTIA-NIGRA PARS COMPACTA OF RAT [J].
JANEC, E ;
BURKE, RE .
MOLECULAR AND CELLULAR NEUROSCIENCE, 1993, 4 (01) :30-35
[7]   L-DEPRENYL REDUCES BRAIN-DAMAGE IN RATS EXPOSED TO TRANSIENT HYPOXIA-ISCHEMIA [J].
KNOLLEMA, S ;
AUKEMA, W ;
HOM, H ;
KORF, J ;
TERHORST, GJ .
STROKE, 1995, 26 (10) :1883-1887
[8]   DNA fragmentation and prolonged expression of c-fos, c-jun, and hsp 70 in kainic acid-induced neuronal cell death in transgenic mice overexpressing human CuZn-superoxide dismutase [J].
Kondo, T ;
Sharp, FR ;
Honkaniemi, J ;
Mikawa, S ;
Epstein, CJ ;
Chan, PH .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1997, 17 (03) :241-256
[9]   RATE OF CELL-DEATH IN PARKINSONISM INDICATES ACTIVE NEUROPATHOLOGICAL PROCESS [J].
MCGEER, PL ;
ITAGAKI, S ;
AKIYAMA, H ;
MCGEER, EG .
ANNALS OF NEUROLOGY, 1988, 24 (04) :574-576
[10]   Behavioral and neurochemical effects induced by subchronic l-deprenyl administration [J].
Molinengo, L ;
Ghi, P .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 58 (03) :649-655