Temporal frequency of whisker movement. I. Representations in brain stem and thalamus

被引:124
作者
Sosnik, R [1 ]
Haidarliu, S [1 ]
Ahissar, E [1 ]
机构
[1] Weizmann Inst Sci, Dept Neurobiol, IL-76100 Rehovot, Israel
关键词
D O I
10.1152/jn.2001.86.1.339
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
How does processing of information change the internal representations used in subsequent stages of sensory pathways? To approach this question, we studied the representations of whisker movements in the lemniscal and paralemniscal pathways of the rat vibrissal system. We recently suggested that these two pathways encode movement frequency in different ways. We proposed that paralemniscal thalamocortical circuits, functioning as phase-locked loops (PLLs), translate temporally coded information into a rate code. Here we focus on the two major trigeminal nuclei of the brain stem, nucleus principalis and subnucleus interpolaris, and on their thalamic targets, the ventral posteromedial nucleus (VPM) and the medial division of the posterior nucleus (POm). This is the first study in which these brain stem and thalamic nuclei were explored together in the same animals and using the same stimuli. We studied both single- and multi-unit activity. We moved the whiskers both mechanically and by air puffs; here we present air-puff-induced movements because they are more similar to natural movements than movements induced by mechanical stimulations. We describe the basic properties of the responses in these brain stem and thalamic nuclei. The responses in both brain stem nuclei were similar; responses to air puffs were mostly tonic and followed the trajectory of whisker movement. The responses in the two thalamic nuclei were similar during low-frequency stimulations or during the first pulses of high-frequency stimulations, exhibiting more phasic responses than those of brain stem neurons. However, with frequencies >2 Hz, VPM and POm responses differed, generating different representations of the stimulus frequency. In the VPM, response amplitudes (instantaneous firing rates) and spike counts (total number of spikes per stimulus cycle) decreased as a function of the frequency. In the POm, latencies increased and spike count decreased as a function of the frequency. Having described the basic response properties in the four nuclei, we then focus on a specific test of our PLL hypothesis for coding in the paralemniscal pathway. We used short-duration air puffs, much shorter than whisker movements during natural whisking. The activity in this situation was consistent with the prediction we made on the basis of the PLL hypothesis.
引用
收藏
页码:339 / 353
页数:15
相关论文
共 65 条
[1]  
ABELES M, 1975, SIGNAL ANAL PATTERN, P41
[2]  
Abeles M., 1982, LOCAL CORTICAL CIRCU, DOI DOI 10.1007/978-3-642-81708-3
[3]   Transformation from temporal to rate coding in a somatosensory thalamocortical pathway [J].
Ahissar, E ;
Sosnik, R ;
Haidarliu, S .
NATURE, 2000, 406 (6793) :302-306
[5]  
Ahissar E, 2001, Prog Brain Res, V130, P75
[6]   Temporal frequency of whisker movement. II. Laminar organization of cortical representations [J].
Ahissar, E ;
Sosnik, R ;
Bagdasarian, K ;
Haidarliu, S .
JOURNAL OF NEUROPHYSIOLOGY, 2001, 86 (01) :354-367
[7]   Temporal-code to rate-code conversion by neuronal phase-locked loops [J].
Ahissar, E .
NEURAL COMPUTATION, 1998, 10 (03) :597-650
[8]   Decoding temporally encoded sensory input by cortical oscillations and thalamic phase comparators [J].
Ahissar, E ;
Haidarliu, S ;
Zacksenhouse, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11633-11638
[9]   THALAMOCORTICAL PROCESSING OF VIBRISSAL INFORMATION IN THE RAT .2. SPATIOTEMPORAL CONVERGENCE IN THE THALAMIC VENTROPOSTERIOR MEDIAL NUCLEUS (VPM) AND ITS RELEVANCE TO GENERATION OF RECEPTIVE-FIELDS OF S1 CORTICAL BARREL NEURONS [J].
ARMSTRONGJAMES, M ;
CALLAHAN, CA .
JOURNAL OF COMPARATIVE NEUROLOGY, 1991, 303 (02) :211-224
[10]   SPATIOTEMPORAL CONVERGENCE AND DIVERGENCE IN THE RAT S1 BARREL CORTEX [J].
ARMSTRONGJAMES, M ;
FOX, K .
JOURNAL OF COMPARATIVE NEUROLOGY, 1987, 263 (02) :265-281