Ligand-gated ion channels in the enteric nervous system

被引:111
作者
Galligan, JJ
机构
[1] Michigan State Univ, Dept Pharmacol & Toxicol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Program Neurosci, E Lansing, MI 48824 USA
关键词
electrophysiology; enteric nervous system; ion channels; receptors;
D O I
10.1046/j.1365-2982.2002.00363.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There are many cell surface receptors expressed by neurones in the enteric nervous system ( ENS). These receptors respond to synaptically released neurotransmitters, circulating hormones and locally released substances. Cell surface receptors are also targets for many therapeutically used drugs. This review will focus on ligand-gated ion channels, i.e. receptors in which the ligand binding site and the ion channel are parts of a single multimeric receptor. Ligand-gated ion channels expressed by enteric nerves are: nicotinic acetylcholine receptors (nAChRs), P2X receptors, 5-hydroxytryptamine(3) (5-HT3) receptors, gamma-aminobutyric acid (GABA(A)) receptors, N-methyl-D-aspartate ( NMDA) receptors, alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid ( AMPA) receptors and glycine receptors. P2X, 5-HT3 and nAChRs participate in fast synaptic transmission in S-type neurones in the ENS. Fast synaptic transmission occurs in some AH-type neurones, and AH neurones express all the ligand-gated ion channels listed above. Ligand-gated ion channels may be localized at extra-synaptic sites in some AH neurones and these extra-synaptic receptors may be useful targets for drugs that can be used to treat disorders of gastrointestinal function.
引用
收藏
页码:611 / 623
页数:13
相关论文
共 119 条
[1]   Comparison of the effects of neurokinin-3 receptor blockade on two forms of slow synaptic transmission in myenteric AH neurons [J].
Alex, G ;
Kunze, WAA ;
Furness, JB ;
Clerc, N .
NEUROSCIENCE, 2001, 104 (01) :263-269
[2]   Functional interactions between nicotinic and P2X channels in short-term cultures of guinea-pig submucosal neurons [J].
Barajas-López, C ;
Espinosa-Luna, R ;
Zhu, YH .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 513 (03) :671-683
[3]   5-Hydroxytryptamine and atropine inhibit nicotinic receptors in submucosal neurons [J].
Barajas-López, C ;
Karanjia, R ;
Espinosa-Luna, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2001, 414 (2-3) :113-123
[4]   P-2x-purinoceptors of myenteric neurones from the guinea-pig ileum and their unusual pharmacological properties [J].
BarajasLopez, C ;
Huizinga, JD ;
Collins, SM ;
Gerzanich, V ;
EspinosaLuna, R ;
Peres, AL .
BRITISH JOURNAL OF PHARMACOLOGY, 1996, 119 (08) :1541-1548
[5]  
BARAJASLOPEZ C, 1994, J PHARMACOL EXP THER, V268, P1396
[6]  
Bardhan KD, 2000, ALIMENT PHARM THERAP, V14, P23
[7]   The terminals of myenteric intrinsic primary afferent neurons of the guinea-pig ileum are excited by 5-hydroxytryptamine acting at 5-hydroxytryptamine-3 receptors [J].
Bertrand, PP ;
Kunze, WAA ;
Furness, JB ;
Bornstein, JC .
NEUROSCIENCE, 2000, 101 (02) :459-469
[8]   A simple mathematical model of second-messenger mediated slow excitatory postsynaptic potentials [J].
Bertrand, PP ;
Thomas, EA ;
Kunze, WAA ;
Bornstein, JC .
JOURNAL OF COMPUTATIONAL NEUROSCIENCE, 2000, 8 (02) :127-142
[9]  
BERTRAND PP, 1992, J PHARMACOL EXP THER, V262, P677
[10]   ATP as a putative sensory mediator: Activation of intrinsic sensory neurons of the myenteric plexus via P2X receptors [J].
Bertrand, PP ;
Bornstein, JC .
JOURNAL OF NEUROSCIENCE, 2002, 22 (12) :4767-4775