Brain sites of movement disorder: Genetic and environmental agents in neurodevelopmental perturbations

被引:28
作者
Palomo, T
Beninger, RJ
Kostrzewa, RM
Archer, T
机构
[1] Univ Gothenburg, Dept Psychol, SE-40530 Gothenburg, Sweden
[2] Hosp 12 Octubre, Serv Psiquiatria, E-28041 Madrid, Spain
[3] Queens Univ, Dept Psychol & Psychiat, Kingston, ON K7L 3N6, Canada
[4] E Tennessee State Univ, Dept Pharmacol, Quillen Coll Med, Johnson City, TN 37614 USA
关键词
cerebellum; basal ganglia; limbic; striatum; glutamate; heavy metals; iron overload; tetrahydroisoquinolines; apoptosis; necrosis; neurotoxins; neurotrophins; dopamine; motor activity;
D O I
10.1007/BF03033369
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In assessing and assimilating the neurodevelopmental basis of the so-called movement disorders it is probably useful to establish certain concepts that will modulate both the variation and selection of affliction, mechanisms-processes and diversity of disease states. Both genetic, developmental and degenerative aberrations are to be encompassed within such an approach, as well as all deviations from the necessary components of behaviour that are generally understood to incorporate "normal" functioning. In the present treatise, both conditions of hyperactivity/hypoactivity, akinesia and bradykinesia together with a constellation of other symptoms and syndromes are considered in conjunction with the neuropharmacological and brain morphological alterations that may or may not accompany them, e.g. following neonatal denervation. As a case in point, the neuroanatomical and neurochemical points of interaction in Attention Deficit and Hyperactivity disorder (ADHD) are examined with reference to both the perinatal metallic and organic environment and genetic backgrounds. The role of apoptosis, as opposed to necrosis, in cell death during brain development necessitates careful considerations of the current explosion of evidence for brain nerve growth factors, neurotrophins and cytokines, and the processes regulating their appearance, release and fate. Some of these processes may possess putative inherited characteristics, like a-synudein, others may to greater or lesser extents be endogenous or semi-endogenous (in food), like the tetrahydroisoquinolines, others exogenous until inhaled or injested through environmental accident, like heavy metals, e.g. mercury. Another central concept of neurodevelopment is cellular plasticity, thereby underlining the essential involvement of glutamate systems and N-methyl-D-aspartate receptor configurations. Finally, an essential assimilation of brain development in disease must delineate the relative merits of inherited as opposed to environmental risks not only for the commonly regarded movement disorders, like Parkinson's disease, Huntington's disease and epilepsy, but also for afflictions bearing strong elements of psychosocial tragedy, like ADHD, autism and Savantism.
引用
收藏
页码:1 / 26
页数:26
相关论文
共 414 条
[1]   Stereoselective effect of (R)- and (S)-1-methyl-1,2,3,4-tetrahydroisoquinolines on a mouse model of Parkinson's disease [J].
Abe, K ;
Taguchi, K ;
Wasai, T ;
Ren, J ;
Utsunomiya, I ;
Shinohara, T ;
Miyatake, T ;
Sano, T .
BRAIN RESEARCH BULLETIN, 2001, 56 (01) :55-60
[2]   Biochemical and pathological study of endogenous 1-benzyl-1,2,3,4-tetrahydroisoquinoline-induced parkinsonism in the mouse [J].
Abe, K ;
Taguchi, K ;
Wasai, T ;
Ren, J ;
Utsunomiya, I ;
Shinohara, T ;
Miyatake, T ;
Sano, T .
BRAIN RESEARCH, 2001, 907 (1-2) :134-138
[3]   Mice lacking α-synuclein display functional deficits in the nigrostriatal dopamine system [J].
Abeliovich, A ;
Schmitz, Y ;
Fariñas, I ;
Choi-Lundberg, D ;
Ho, WH ;
Castillo, PE ;
Shinsky, N ;
Verdugo, JMG ;
Armanini, M ;
Ryan, A ;
Hynes, M ;
Phillips, H ;
Sulzer, D ;
Rosenthal, A .
NEURON, 2000, 25 (01) :239-252
[4]   Frequency of levodopa-related dyskinesias and motor fluctuations as estimated from the cumulative literature [J].
Ahlskog, JE ;
Muenter, MD .
MOVEMENT DISORDERS, 2001, 16 (03) :448-458
[5]   ANTERIOR CEREBELLAR VERMAL STIMULATION - EFFECT ON BEHAVIOR AND BASAL FOREBRAIN NEUROCHEMISTRY IN RAT [J].
ALBERT, TJ ;
DEMPESY, CW ;
SORENSON, CA .
BIOLOGICAL PSYCHIATRY, 1985, 20 (12) :1267-1276
[6]   Protective effects of neurotrophin-4/5 and transforming growth factor-alpha. On striatal neuronal phenotypic degeneration after excitotoxic lesioning with quinolinic acid [J].
Alexi, T ;
Venero, JL ;
Hefti, F .
NEUROSCIENCE, 1997, 78 (01) :73-86
[7]   Relationship of dopamine to serotonin in the neonatal 6-OHDA rat model of Lesch-Nyhan syndrome [J].
Allen, SM ;
Davis, WM .
BEHAVIOURAL PHARMACOLOGY, 1999, 10 (05) :467-474
[8]  
Altman J., 1997, DEV CEREBELLAR SYSTE
[9]   Different action on dopamine catabolic pathways of two endogenous 1,2,3,4-tetrahydroisoquinolines with similar antidopaminergic properties [J].
Antkiewicz-Michaluk, L ;
Michaluk, J ;
Mokrosz, M ;
Romanska, I ;
Lorenc-Koci, E ;
Ohta, S ;
Vetulani, J .
JOURNAL OF NEUROCHEMISTRY, 2001, 78 (01) :100-108
[10]   Neurochemical changes induced by acute and chronic administration of 1,2,3,4-tetrahydroisoquinoline and salsolinol in dopaminergic structures of rat brain [J].
Antkiewicz-Michaluk, L ;
Romañska, I ;
Papla, I ;
Michaluk, J ;
Bakalarz, M ;
Vetulani, J ;
Krygowska-Wajs, A ;
Szczudlik, A .
NEUROSCIENCE, 2000, 96 (01) :59-64