P2 receptor-mediated modulation of neurotransmitter release -: an update

被引:49
作者
Sperlagh, Beata [1 ]
Heinrich, Attila [1 ]
Csolle, Cecilia [1 ]
机构
[1] Hungarian Acad Sci, Inst Expt Med, Mol Pharmacol Lab, H-1450 Budapest, Hungary
关键词
neuromodulation; presynaptic; P2X receptor; P2Y receptors; release; transmitter;
D O I
10.1007/s11302-007-9080-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Presynaptic nerve terminals are equipped with a number of presynaptic auto- and heteroreceptors, including ionotropic P2X and metabotropic P2Y receptors. P2 receptors serve as modulation sites of transmitter release by ATP and other nucleotides released by neuronal activity and pathological signals. A wide variety of P2X and P2Y receptors expressed at pre- and postsynaptic sites as well as in glial cells are involved directly or indirectly in the modulation of neurotransmitter release. Nucleotides are released from synaptic and nonsynaptic sites throughout the nervous system and might reach concentrations high enough to activate these receptors. By providing a fine-tuning mechanism these receptors also offer attractive sites for pharmacotherapy in nervous system diseases. Here we review the rapidly emerging data on the modulation of transmitter release by facilitatory and inhibitory P2 receptors and the receptor subtypes involved in these interactions.
引用
收藏
页码:269 / 284
页数:16
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