Regulation of AMPA and NMDA receptor-mediated EPSPs in dendritic trees of thalamocortical cells

被引:6
|
作者
Lajeunesse, Francis [1 ,2 ]
Kroeger, Helmut [2 ]
Timofeev, Igor [1 ,3 ]
机构
[1] Univ Laval, CRIUSMQ, Quebec City, PQ G1J 2G3, Canada
[2] Univ Laval, Dept Phys, Quebec City, PQ G1J 2G3, Canada
[3] Univ Laval, Dept Psychiat & Neurosci, Quebec City, PQ G1J 2G3, Canada
基金
加拿大健康研究院;
关键词
thalamus; synaptic integration; neuronal morphology; signal propagation; LATERAL GENICULATE-NUCLEUS; THALAMIC NEURONS; PYRAMIDAL NEURON; RELAY NEURONS; COINCIDENCE DETECTION; MEMBRANE-PROPERTIES; CABLE PROPERTIES; INTEGRATION; CAT; MORPHOLOGY;
D O I
10.1152/jn.01090.2011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Lajeunesse F, Kroger H, Timofeev I. Regulation of AMPA and NMDA receptor-mediated EPSPs in dendritic trees of thalamocortical cells. J Neurophysiol 109: 13-30, 2013. First published October 24, 2012; doi:10.1152/jn.01090.2011.-Two main excitatory synapses are formed at the dendritic arbor of first-order nuclei thalamocortical (TC) neurons. Ascending sensory axons primarily establish contacts at large proximal dendrites, whereas descending corticothalamic fibers form synapses on thin distal dendrites. With the use of a multicomparment computational model based on fully reconstructed TC neurons from the ventroposterolateral nucleus of the cat, we compared local responses at the site of stimulation as well as somatic responses induced by both alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor (AMPAR)- and N-methyl-D-aspartate receptor (NMDAR)-mediated currents. We found that AMPAR-mediated responses, when synapses were located at proximal dendrites, induced a larger depolarization at the level of soma, whereas NMDAR-mediated responses were more efficient for synapses located at distal dendrites. The voltage transfer and transfer impedance were higher for NMDAR than for AMPAR activation at any location. For both types of synaptic current and for both input locations at the dendritic arbor, somatic responses were characterized by a low variability despite the large variability found in local responses in dendrites. The large neurons had overall smaller somatic responses than small neurons, but this relation was not found in local dendritic responses. We conclude that in TC cells, the dendritic location of small synaptic inputs does not play a major role in the amplitude of a somatic response, but the size of the neuron does. The variability of response amplitude between cells was much larger than the variability within cells. This suggests possible functional segregation of TC neurons of different size.
引用
收藏
页码:13 / 30
页数:18
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