Striatal α6* nicotinic acetylcholine receptors:: Potential targets for Parkinson's disease therapy

被引:97
作者
Quik, M
McIntosh, JM
机构
[1] Parkinsons Inst, Sunnyvale, CA 94089 USA
[2] Univ Utah, Dept Biol, Salt Lake City, UT USA
[3] Univ Utah, Dept Psychiat, Salt Lake City, UT USA
关键词
D O I
10.1124/jpet.105.094375
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The presence of distinct nicotinic acetylcholine receptor ( nAChR) subtypes in specific central nervous system ( CNS) areas offers the possibility of developing targeted therapies for diseases involving the affected brain region. Parkinson's disease is a neurodegenerative movement disorder characterized by a progressive degeneration of the nigrostriatal system. alpha 6-containing nAChRs (designated alpha 6(star 1) nAChRs) have a relatively selective localization to the nigrostriatal pathway and a limited number of other CNS regions. In addition to a unique distribution, this subtype has a distinct pharmacology and specifically interacts with alpha-conotoxinMII, a toxin key in its identification and characterization. alpha 6(star) nAChRs are also regulated in a novel manner, with a decrease in their number after nicotine treatment rather than the increase observed for alpha 4(star) nAChRs. Striatal alpha 6(star) receptors were functional and mediate dopamine release, suggesting that they have a presynaptic localization. This is further supported by lesion studies showing that both alpha 6(star) nAChR sites and their functions are dramatically decreased with dopaminergic nerve terminal loss, in contrast to only small declines in alpha 4(star) and no change in alpha 7(star) receptors. Although the role of nigrostriatal alpha 6(star) nAChRs is only beginning to be understood, an involvement in motor behavior is emerging. This latter observation coupled with the finding that nicotine protects against nigrostriatal damage suggest that alpha 6(star) nAChRs may represent unique targets for neurodegenerative disorders linked to the nigrostriatal system such as Parkinson's disease.
引用
收藏
页码:481 / 489
页数:9
相关论文
共 85 条
[71]   Dose-related neuroprotective effects of chronic nicotine in 6-hydroxydopamine treated rats, and loss of neuroprotection in α4 nicotinic receptor subunit knockout mice [J].
Ryan, RE ;
Ross, SA ;
Drago, J ;
Loiacono, RE .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 132 (08) :1650-1656
[72]   An extracellular protein microdomain controls up-regulation of neuronal nicotinic acetylcholine receptors by nicotine [J].
Sallette, J ;
Bohler, S ;
Benoit, P ;
Soudant, M ;
Pons, S ;
Le Novère, N ;
Changeux, JP ;
Corringer, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (18) :18767-18775
[73]   Nicotine upregulates its own receptors through enhanced intracellular maturation [J].
Sallette, J ;
Pons, S ;
Devillers-Thiery, A ;
Soudant, M ;
de Carvalho, LP ;
Changeux, JP ;
Corringer, PJ .
NEURON, 2005, 46 (04) :595-607
[74]   Subunit composition and pharmacology of two classes of striatal presynaptic nicotinic acetylcholine receptors mediating dopamine release in mice [J].
Salminen, O ;
Murphy, KL ;
McIntosh, JM ;
Drago, J ;
Marks, MJ ;
Collins, AC ;
Grady, SR .
MOLECULAR PHARMACOLOGY, 2004, 65 (06) :1526-1535
[75]   Parkinson's disease [J].
Samii, A ;
Nutt, JG ;
Ransom, BR .
LANCET, 2004, 363 (9423) :1783-1793
[76]   Effects of SIB-1508Y, a novel neuronal nicotinic acetylcholine receptor agonist, on motor behavior in Parkinsonian monkeys [J].
Schneider, JS ;
Pope-Coleman, A ;
Van Velson, M ;
Menzaghi, F ;
Lloyd, GK .
MOVEMENT DISORDERS, 1998, 13 (04) :637-642
[77]  
SLAMINEN O, 2004, SOC NEUR 34 ANN M 20
[78]   Transdermal nicotine in PD - A randomized, double-blind, placebo-controlled study [J].
Vieregge, A ;
Sieberer, M ;
Jacobs, H ;
Hagenah, JM ;
Vieregge, P .
NEUROLOGY, 2001, 57 (06) :1032-1035
[79]   Desensitized nicotinic receptors in brain [J].
Wang, H ;
Sun, XL .
BRAIN RESEARCH REVIEWS, 2005, 48 (03) :420-437
[80]  
Whiteaker P, 2000, MOL PHARMACOL, V57, P913