Neuronal nitric oxide synthase expression in cerebellar mutant mice

被引:24
作者
Abbott, LC
Nahm, SS
机构
[1] Texas A&M Univ, Dept Vet Anat & Publ Hlth, College Stn, TX 77843 USA
[2] Texas A&M Univ, Hlth Sci Ctr, Dept Human Anat & Med Neurobiol, College Stn, TX 77843 USA
关键词
cerebellum; nitric oxide; granule cell; Purkinje cell; cerebellar mutant mice;
D O I
10.1080/14734220410031927
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nitric oxide (NO) is a diffusible, multifunctional signaling molecule found in many areas of the brain. NO signaling is involved in a wide array of neurophysiological functions including synaptogenesis, modulation of neurotransmitter release, synaptic plasticity, central nervous system blood flow and cell death. NO synthase (NOS) activity regulates the production of NO and the cerebellum expresses high levels of nitric oxide synthase (NOS) in granule, stellate and basket cells. Cerebellar mutant mice provide excellent opportunities to study changes of NO/NOS concentrations and activities to gain a greater understanding of the roles of NO and NOS in cerebellar function. Here, we have reviewed the current understanding of the functional roles of NO and NOS in the cerebellum and present NO/NOS activities that have been described in various cerebellar mutant mice and NOS knockout mice. NO appears to exert neuroprotective effects at low to moderate concentrations, whereas NO becomes neurotoxic as the concentration increases. Excessive NO production can cause oxidative stress to neurons, ultimately impairing neuronal function and result in neuronal cell death. Based on their genetics and cerebellar histopathology, some of cerebellar mutant mice display similarities with human neurological conditions and may prove to be valuable models to study several human neurological disorders, such as autism and schizophrenia.
引用
收藏
页码:141 / 151
页数:11
相关论文
共 130 条
[51]   Interactions of nitric oxide with hemoproteins: roles of nitric oxide in mitochondria [J].
Henry, Y ;
Guissani, A .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (8-9) :1003-1014
[52]   Chronic hyperammonemia impairs the glutamate-nitric oxide-cyclic GMP pathway in cerebellar neurons in culture and in the rat in vivo [J].
Hermenegildo, C ;
Montoliu, C ;
Llansola, M ;
Muñoz, MD ;
Gaztelu, JM ;
Miñana, MD ;
Felipo, V .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 (10) :3201-3209
[53]   Chronic exposure to 2,5-hexanedione impairs the glutamate-nitric oxide-cyclic GMP pathway in cerebellar neurons in culture and in rat brain in vivo [J].
Hernandez-Viadel, M ;
Montoliu, C ;
Monfort, P ;
Canales, JJ ;
Erceg, S ;
Rowan, M ;
Ceccatelli, S ;
Felipo, V .
NEUROCHEMISTRY INTERNATIONAL, 2003, 42 (07) :525-533
[54]   ROLE OF STAGGERER GENE IN DETERMINING CELL NUMBER IN CEREBELLAR CORTEX .1. GRANULE CELL-DEATH IS AN INDIRECT CONSEQUENCE OF STAGGERER GENE-ACTION [J].
HERRUP, K .
DEVELOPMENTAL BRAIN RESEARCH, 1983, 11 (02) :267-274
[55]   CEREBELLAR CELL DEGENERATION IN THE LEANER MUTANT MOUSE [J].
HERRUP, K ;
WILCZYNSKI, SL .
NEUROSCIENCE, 1982, 7 (09) :2185-2196
[56]   Purkinje cells express neuronal nitric oxide synthase after methylmercury administration [J].
Himi, T ;
Ikeda, M ;
Sato, I ;
Yuasa, T ;
Murota, S .
BRAIN RESEARCH, 1996, 718 (1-2) :189-192
[57]   Nitric oxide, the enigmatic neuronal messenger: Its role in synaptic plasticity [J].
Holscher, C .
TRENDS IN NEUROSCIENCES, 1997, 20 (07) :298-303
[58]   TARGETED DISRUPTION OF THE NEURONAL NITRIC-OXIDE SYNTHASE GENE [J].
HUANG, PL ;
DAWSON, TM ;
BREDT, DS ;
SNYDER, SH ;
FISHMAN, MC .
CELL, 1993, 75 (07) :1273-1286
[59]   EFFECTS OF CEREBRAL-ISCHEMIA IN MICE DEFICIENT IN NEURONAL NITRIC-OXIDE SYNTHASE [J].
HUANG, ZH ;
HUANG, PL ;
PANAHIAN, N ;
DALKARA, T ;
FISHMAN, MC ;
MOSKOWITZ, MA .
SCIENCE, 1994, 265 (5180) :1883-1885
[60]  
Iadecola C, 1997, J NEUROSCI, V17, P9157