Electrophysiological and morphological properties of neurons in the substantia gelatinosa of the mouse trigeminal subnucleus caudalis

被引:33
作者
Davies, Alexander J. [1 ]
North, R. Alan [1 ,2 ]
机构
[1] Univ Manchester, Fac Life Sci, Manchester M13 9PT, Lancs, England
[2] Univ Manchester, Fac Med & Human Sci, Manchester M13 9PT, Lancs, England
基金
英国生物技术与生命科学研究理事会;
关键词
Voltage-gated channels; P2X receptors; Spontaneous synaptic current; TRPV1; Dorsal horn; DORSAL-HORN NEURONS; RAT SPINAL-CORD; MEMBRANE-PROPERTIES; CALCIUM-CHANNELS; P2X(3) RECEPTOR; NERVE INJURY; SYNAPTIC-TRANSMISSION; GLUTAMATE RELEASE; NUCLEUS-CAUDALIS; SENSORY NEURONS;
D O I
10.1016/j.pain.2009.07.038
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The excitability of the second order neurons within the trigeminal subnucleus caudalis underlies pain perception and processing in migraine and trigeminal neuralgia. These neurons were studied with whole-cell patch-clamp technique in slices from mouse brain stem. Electrical and morphological characteristics of 56 neurons were determined. Four categories were distinguished from electrophysiological properties: tonic (39%), phasic (34%). delayed (16%) and single spiking (11%). These categories did not show distinct morphological properties. Neurons had tetrodotoxin-sensitive sodium currents that activated and inactivated within milliseconds. They also showed a high voltage-activated, slowly inactivating calcium current: up to half of this current was blocked by omega-conotoxin GVIA (1 mu M) and omega-agatoxin IVA (100-300 nM), but it was not affected by nifedipine (10 mu M). Exogenously applied capsaicin (1 mu M) and alpha beta methylene-5'-adenosine triphosphate (100 mu M) elicited large amplitude, spontaneous excitatory postsynaptic currents that were blocked by capsazepine (10 mu M) and 5-[(3-phenoxybenzyl)-(1,2,3,4-tetrahydro-naphthalen-1-yl)-carbamoyl] -benzene-1,2,4-tricarboxylic acid (A-317491: 10 mu M), respectively. Thus, neurons of the mouse trigeminal subnucleus caudalis substantia gelatinosa exhibit N-type and P/Q-type voltage-gated calcium channels, and receive presynaptic afferents that express TRPV1 and P2X(2/3) receptors. These results suggest possible therapeutic interventions, and serve as a basis for the characterization of cellular changes that may underlie trigeminal neuropathic pain. (C) 2009 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:214 / 221
页数:8
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