JN Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
QUICK SEARCH:   [advanced]


     

J Neurophysiol 92: 665-668, 2004. First published March 3, 2004; doi:10.1152/jn.00031.2004
0022-3077/04 $5.00
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
92/1/665    most recent
00031.2004v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (29)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jones, L. M.
Right arrow Articles by Keller, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jones, L. M.
Right arrow Articles by Keller, A.

REPORT

Precise Temporal Responses in Whisker Trigeminal Neurons

Lauren M. Jones1, SooHyun Lee2, Jason C. Trageser1, Daniel J. Simons2 and Asaf Keller1

1Department of Anatomy and Neurobiology and the Program in Neuroscience, University of Maryland School of Medicine, Baltimore, Maryland 21201; and 2Department of Neurobiology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261

Submitted 2 March 2004; accepted in final form 2 March 2004


   ABSTRACT
TOP
 ABSTRACT
INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
The ability of rats using their whiskers to perform fine tactile discrimination rivals that of humans using their fingertips. Rats must perform these discriminations rapidly and accurately while palpating the environment with their whiskers. This suggests that whisker-derived inputs produce a robust and reliable code, capable of capturing complex, high-frequency information. The first neural representation of whisker-derived stimulus information is in primary afferent neurons of the trigeminal ganglion. Here we demonstrate that there is a continuum of direction-dependent response profiles in trigeminal neurons and provide the first quantitative analysis of the encoding of complex stimuli by these neurons. We show that all classes of trigeminal ganglion neurons respond with highly reproducible temporal spike patterns to transient stimuli. Such a robust coding mechanism may allow rapid perception of complex tactile features.


   INTRODUCTION
TOP
 ABSTRACT
 INTRODUCTION
METHODS
 RESULTS
 DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
Coding of sensory stimuli has been traditionally studied by analyzing changes in mean neuronal firing rates. However, in many sensory systems, stimuli elicit sparse spike trains in individual neurons (Hahnloser et al. 2002Go; Theunissen 2003Go; Vinje and Gallant 2000Go), including the rodent whisker-trigeminal system (Simons and Carvell 1989Go). The limited numbers of spikes elicited in these systems, combined with the complex stimuli that the systems can distinguish, imply that individual neurons cannot encode stimuli with a rate-based coding scheme. There is mounting evidence that sensory perception involves temporal coding schemes in which the timing of individual spikes encodes information beyond that provided by a rate coding scheme (Dayan and Abbott 2001Go; Rieke et al. 1997Go). Temporal coding requires that a sensory stimulus elicit a highly reproducible pattern of spikes. Our goal was to test the hypothesis that in the whisker-trigeminal system, sensory inputs evoke such reproducible spike patterns. We started by analyzing responses in the whisker primary afferents of the trigeminal ganglion, because they necessarily constrain all subsequent processing.

Response properties of whisker-related trigeminal ganglion neurons were previously investigated with the use of ramp-and-hold whisker deflections (Gibson and Welker 1983a,bGo; Lichtenstein et al. 1990Go; Shoykhet et al. 2000Go). In this paradigm, an individual whisker is attached to a computer-controlled piezoelectric device that rapidly deflects the whisker in a specified direction, and maintains the whisker at this deflection angle for tens of milliseconds. This paradigm permits accurate control of stimulus parameters, and studies taking advantage of this approach have elucidated many important response characteristics of trigeminal neurons (Gibson and Welker 1983a,bGo; Lichtenstein et al. 1990Go; Shoykhet et al. 2000Go; see also Szwed et al. 2003Go). In all of these studies, response properties were characterized based on the neurons' mean firing rates. To test the hypothesis that temporal firing patterns reliably encode stimulus parameters, we focused here on the precise timing of individual spikes in stimulus-evoked spike trains.


   METHODS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
RESULTS
 DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
Data were obtained from nine adult female rats, prepared for electrophysiological recordings as previously described (Lichtenstein et al. 1990Go). Extracellular recordings of well-isolated single units were obtained under halothane or urethan anesthesia. Spikes were discriminated off-line using amplitude threshold and/or principal component analysis. Autocorrelograms were computed for each unit, and units with interspike intervals <1 ms were discarded. We recorded responses to ramp-and-hold whisker deflections from 85 trigeminal ganglion neurons. As previously described (Gibson and Welker 1983a,bGo; Lichtenstein et al. 1990Go; Shoykhet et al. 2000Go), these neurons had either a phasic response, firing only to stimulus onset and offset, or a phasic-tonic response, firing at stimulus onset/offset and throughout the stimulus hold period (Fig. 1, A and C). These firing patterns are traditionally used to characterize neurons as either rapidly adapting (RA) or slowly adapting (SA), respectively. However, individual neurons can respond with both RA and SA profiles, depending on the direction of whisker deflection. For example, the neuron depicted in Fig. 1B responded tonically (SA response) in five of eight directions, but phasically (RA response) in two of eight directions. Although some cells do respond with an RA or SA profile in every direction of stimulation (Fig. 1, A and C), we found that 43% of the neurons can respond in either slowly and rapidly fashions, depending on the direction of whisker deflection (Fig. 1B).



View larger version (25K):
[in this window]
[in a new window]
  		FIG. 1. Direction-dependent response profiles in trigeminal ganglion neurons. A–C: peri-event rasters and peristimulus time histograms (PSTHs; 1-ms bins) recorded in response to ramp and hold whisker deflections (200-ms duration), delivered 50 times in each of 8 directions. Neurons that respond with a slowly adapting profile only (A) were classified as category 0. Those responding only with a rapidly adapting profile (C) were classified as category 8. Neurons with mixed response profiles (B) were classified as categories 1 to 7, depending on the number of rapidly adapting response profiles to different deflection angles. D: percentage of all cells (n = 85) in each response profile category.

 
To quantify this direction-dependent response property, we categorized trigeminal neurons into eight different groups. Category 8 cells respond in a rapidly adapting fashion in all eight directions (pure RA profiles). Category 0 cells respond in a slowly adapting fashion in all eight directions (pure SA profiles). Categories 1–7 respond in a rapidly adapting fashion in one to seven directions and in a slowly adapting fashion (or no spikes) in the remaining directions. For example, the cell depicted in Fig. 1B was classified as a category 2 neuron because it responded to two of eight directions in a rapidly adapting fashion. Of the 85 neurons we analyzed, 40% were classified as category 8 (pure RA), and the remaining 60% responded to one or more directions in a sustained, SA-like response (Fig. 1D). This finding indicates that trigeminal neurons express a directionally dependent continuum of firing patterns. Gibson and Welker (1983bGo) found a similar, amplitude-dependent continuum in sustained responses. Thus this and other classification schemes must take into account the stimulus-dependent response profile continuum—including responses in different directions—of trigeminal ganglion neurons.


   RESULTS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
In peristimulus time histograms (PSTHs) computed for cells in every category (pure RA, mixed RA/SA, pure SA), the precise timing of the initial spikes was highly reproducible from trial to trial. This reproducibility is evidenced in the early response to the ramp-and-hold stimulus, as seen in Fig. 1. We quantified reproducibility by calculating the time of occurrence of the PSTH bin having the highest probability. For all neurons, the mean peak probability was 89 ± 14% and occurred at 5.6 ± 2.4 ms after stimulus onset. These findings indicate that stimulus transients—such as occur at the beginning of the ramp and hold deflection—produce highly reliable temporal firing patterns in all types of trigeminal neurons.

We then tested the reliability of temporal firing patterns in response to more complex time-varying whisker deflections that may occur during discrimination behaviors (Bermejo et al. 2002Go; Carvell and Simons 1990Go; Guic-Robles et al. 1989Go; Hartmann et al. 2003Go; Neimark et al. 2003Go). We deflected an individual whisker in a complex pattern described by a "pink noise" waveform, low-pass filtered at 200 or 700 Hz (Fig. 2, A and D). We chose these frequency ranges because they encompass the range of frequencies rats are likely to encounter in their environment (Bermejo et al. 2002Go; Carvell and Simons 1990Go; Hartmann et al. 2003Go; Neimark et al. 2003Go). These waveforms were presented at each cell's preferred direction, as determined from responses to ramp-and-hold stimuli (see preceding text). As expected, individual neurons responded to 700-Hz stimulation with a significantly higher mean firing rate compared with their responses to 200-Hz stimulation (paired t-test, P ≤ 10–13). However, the mean firing rates of the three classes of neurons in response to 200 Hz stimuli (122 ± 57 Hz) were equivalent (ANOVA, P = 0.70). Similarly, the mean firing rates of these neuronal classes to 700 Hz stimuli were indistinguishable from each other (273 ± 115 Hz, ANOVA, P = 0.75).



View larger version (71K):
[in this window]
[in a new window]
  		FIG. 2. Trigeminal ganglion neurons respond to complex noise stimuli with highly reproducible spike trains. A: 1-s segment of the 200-Hz pink noise stimulus. B and C: peri-event rasters and PSTHs recorded in response to 50 presentations of the noise stimulus depicted in A. D: 1-s segment of the 700-Hz pink noise stimulus. E and F: peri-event rasters and PSTHs recorded in response to 50 presentations of the noise stimulus depicted in D. G: notched box and whisker plots (McGill et al. 1978Go) depicting the mean correlation coefficients among spike trains recorded from each cell class. Lines in each box depict the lower quartile, median, and upper quartile values. The whiskers extending from each end of a box depict the remaining data range. Notches on each box provide an estimate of 95% confidence intervals about the median; that the notches overlap supports the null hypothesis that the true medians in the population are equal.

 
Figure 2, B and C, depicts peri-event rasters and PSTHs in response to 50 presentations of the 200-Hz noise stimulus (Fig. 2A), recorded from representative RA and SA units. Figure 2, E and F, depicts the same for the 700-Hz stimulus (Fig. 2D). Note that responses to successive presentations of the same stimulus are highly reproducible, with most spikes—and even multiple spikes within a burst—occurring at precisely the same time in every trial. Highly reproducible response patterns were recorded from all categories of neurons, in response to either 200- or 700-Hz stimuli. Similarly, mechanoreceptors in the cat can precisely phase-lock to high-frequency vibratory stimuli (Gottschaldt and Vahle-Hinz 1981Go).

To quantify the temporal precision of stimulus evoked spikes, we calculated, for individual cells, the mean correlation coefficient between every pair of the 50 recorded spike trains. Single cell means ranged from 0.50 ± 0.07 to 0.93 ± 0.02, and the group mean across all cells was 0.65 ± 0.11. Figure 2G shows means for each cell class (RA, mixed, SA) at each stimulus frequency (200 and 700 Hz). Correlation values computed from responses recorded from all three classes of neuron, in response to either 200- or 700-Hz stimuli, were not significantly different (ANOVA, P = 0.82). Thus all classes of neurons respond to complex time-varying stimuli with precise, reproducible temporal patterns of spikes.


   DISCUSSION
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
These findings demonstrate two important characteristics of trigeminal ganglion neurons. First, responses to stimuli mimicking whisker contacts that occur during tactile discrimination are indistinguishable among all classes of neurons. This is evidenced by the similarity in the number and precise timing of spikes evoked in the different classes of neurons, and in the temporal patterns of their evoked responses. Thus the responses of these neurons to static whisker displacements (e.g., RA, SA, or mixed response profile) do not predict their responses to more natural, time-varying stimuli. This is due to the fact that these neurons display a stimulus-dependent continuum of response profiles (Fig. 1D) and to the fact that they respond most vigorously (Shoykhet et al. 2000Go) and reproducibly (Fig. 2) to stimulus transients.

A second important finding is the high temporal precision of responses to repeated presentations of time varying stimuli, including pink noise waveforms and transients in ramp-and-hold stimuli. Because of this precision, a single presentation of a complex stimulus evokes in trigeminal neurons specific and invariant spike patterns. This suggests that a single presentation of a stimulus provides sufficient information to encode complex stimulus features and that these features are encoded equally well in all cell classes. Such a robust coding mechanism may allow faithful detection of rapidly changing, complex tactile features.


   GRANTS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
ACKNOWLEDGMENTS
 REFERENCES
 
This work was supported by National Institute of Neurological Disorders and Stroke Grants: NS-31078 and NS-35360 to A. Keller, NS-19950 to D. J. Simons, and F31NS-46100 to L. M. Jones.


   ACKNOWLEDGMENTS
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
REFERENCES
 
We are indebted to Dr. D. Depireux for insightful comments and discussions.


   FOOTNOTES
 
The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Address for reprint requests and other correspondence: A. Keller, Dept. of Anatomy and Neurobiology, University of Maryland School of Medicine, 685 W. Baltimore St., Baltimore, MD 21201 (E-mail: akeller{at}umaryland.edu).


   REFERENCES
TOP
 ABSTRACT
 INTRODUCTION
 METHODS
 RESULTS
 DISCUSSION
 GRANTS
 ACKNOWLEDGMENTS
 REFERENCES
 
Bermejo R, Vyas A, and Zeigler HP. Topography of rodent whisking—I. Two dimensional monitoring of whisker movements. Somatosens Mot Res 19: 341–346, 2002.[CrossRef][Web of Science][Medline]

Carvell G and Simons DJ. Biometric analyses of vibrissal tactile discrimination in the rat. J Neurosci 10: 2638–2648, 1990.[Abstract]

Dayan P and Abbott LF. Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems. Cambridge, MA: MIT Press, 2001.

Gibson JM and Welker WI. Quantitative studies of stimulus coding in first-order vibrissa afferents of rats. I. Receptive field properties and threshold distributions. Somatosens Res 1: 51–67, 1983a.[Web of Science][Medline]

Gibson JM and Welker WI. Quantitative studies of stimulus coding in first-order vibrissa afferents of rats. II. Adaptation and coding of stimulus parameter. Somatosens Res 1: 95–117, 1983b.[Web of Science][Medline]

Gottschaldt KM and Vahle-Hinz C. Merkel cell receptors: structure and transducer function. Science 214: 183–186, 1981.[Abstract/Free Full Text]

Guic-Robles E, Valdivieso C, and Guajardo G. Rats can learn a roughness discrimination using only their vibrissal system. Behav Brain Res 31: 285–289, 1989.[CrossRef][Web of Science][Medline]

Hahnloser RH, Kozhevnikov AA, and Fee MS. An ultra-sparse code underlies the generation of neural sequences in a songbird. Nature 419: 65–70, 2002.[CrossRef][Medline]

Hartmann MJ, Johnson NJ, Towal RB, and Assad C. Mechanical characteristics of rat vibrissae: resonant frequencies and damping in isolated whiskers and in the awake behaving animal. J Neurosci 23: 6510–6519, 2003.[Abstract/Free Full Text]

Lichtenstein SH, Carvell GE and Simons DJ. Responses of rat trigeminal ganglion neurons to movements of vibrissae in different directions. Somat Motor Res 7: 47–65, 1990.

McGill R, Tukey JW, and Larsen WA. Variations of box plots. Am Stat 32: 12–16, 1978.[CrossRef]

Neimark MA, Andermann ML, Hopfield JJ, and Moore CI. Vibrissa resonance as a transduction mechanism for tactile encoding. J Neurosci 23: 6499–6509, 2003.[Abstract/Free Full Text]

Rieke F, Warland D, de Ruyter van Steveninck R, and Bialek W. Spike: Exploring the Neural Code. Cambridge, MA: MIT Press, 1997.

Shoykhet M, Doherty D, and Simons DJ. Coding of deflection velocity and amplitude by whisker primary afferent neurons: implications for higher level processing. Somatosens Mot Res 17: 171–180, 2000.[CrossRef][Web of Science][Medline]

Simons DJ and Carvell GE. Thalamocortical response transformation in rat vibrissa/barrel system. J Neurophysiol 61: 311–330, 1989.[Abstract/Free Full Text]

Szwed M, Bagdasarian K, and Ahissar E. Encoding of vibrissal active touch. Neuron 40: 621–630, 2003.[CrossRef][Web of Science][Medline]

Theunissen FE. From synchrony to sparseness. Trends Neurosci 26: 61–64, 2003.[CrossRef][Web of Science][Medline]

Vinje WE and Gallant JL. Sparse coding and decorrelation in primary visual cortex during natural vision. Science 287: 1273–1276, 2000.[Abstract/Free Full Text]




This article has been cited by other articles:


Home page
 J. Neurosci.Home page
G. Foffani, M. L. Morales-Botello, and J. Aguilar
Spike Timing, Spike Count, and Temporal Information for the Discrimination of Tactile Stimuli in the Rat Ventrobasal Complex
J. Neurosci., May 6, 2009; 29(18): 5964 - 5973.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
V. Khatri, R. Bermejo, J. C. Brumberg, A. Keller, and H. P. Zeigler
Whisking in Air: Encoding of Kinematics by Trigeminal Ganglion Neurons in Awake Rats
J Neurophysiol, April 1, 2009; 101(4): 1836 - 1846.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
S. Temereanca, E. N. Brown, and D. J. Simons
Rapid Changes in Thalamic Firing Synchrony during Repetitive Whisker Stimulation
J. Neurosci., October 29, 2008; 28(44): 11153 - 11164.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
R. B. Towal and M. J. Z. Hartmann
Variability in Velocity Profiles During Free-Air Whisking Behavior of Unrestrained Rats
J Neurophysiol, August 1, 2008; 100(2): 740 - 752.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
K. A. Moxon
Natural Whisking. Focus on "Variability in Velocity Profiles During Free-Air Whisking Behavior of Unrestrained Rats"
J Neurophysiol, August 1, 2008; 100(2): 551 - 553.
[Full Text] [PDF]

Home page
 J. Neurosci.Home page
T. A. S. Ewert, C. Vahle-Hinz, and A. K. Engel
High-Frequency Whisker Vibration Is Encoded by Phase-Locked Responses of Neurons in the Rat's Barrel Cortex
J. Neurosci., May 14, 2008; 28(20): 5359 - 5368.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
J. A. Birdwell, J. H. Solomon, M. Thajchayapong, M. A. Taylor, M. Cheely, R. B. Towal, J. Conradt, and M. J. Z. Hartmann
Biomechanical Models for Radial Distance Determination by the Rat Vibrissal System
J Neurophysiol, October 1, 2007; 98(4): 2439 - 2455.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
M. A. Montemurro, S. Panzeri, M. Maravall, A. Alenda, M. R. Bale, M. Brambilla, and R. S. Petersen
Role of Precise Spike Timing in Coding of Dynamic Vibrissa Stimuli in Somatosensory Thalamus
J Neurophysiol, October 1, 2007; 98(4): 1871 - 1882.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
A. Hasenstaub, R. N. S. Sachdev, and D. A. McCormick
State Changes Rapidly Modulate Cortical Neuronal Responsiveness
J. Neurosci., September 5, 2007; 27(36): 9607 - 9622.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
R. B. Towal and M. J. Hartmann
Right-left asymmetries in the whisking behavior of rats anticipate head movements.
J. Neurosci., August 23, 2006; 26(34): 8838 - 8846.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurosci.Home page
M. C. Stuttgen, J. Ruter, and C. Schwarz
Two psychophysical channels of whisker deflection in rats align with two neuronal classes of primary afferents.
J. Neurosci., July 26, 2006; 26(30): 7933 - 7941.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
S. C. Leiser and K. A. Moxon
Relationship Between Physiological Response Type (RA and SA) and Vibrissal Receptive Field of Neurons Within the Rat Trigeminal Ganglion
J Neurophysiol, May 1, 2006; 95(5): 3129 - 3145.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
D. Golomb, E. Ahissar, and D. Kleinfeld
Coding of Stimulus Frequency by Latency in Thalamic Networks Through the Interplay of GABAB-Mediated Feedback and Stimulus Shape
J Neurophysiol, March 1, 2006; 95(3): 1735 - 1750.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
M. Szwed, K. Bagdasarian, B. Blumenfeld, O. Barak, D. Derdikman, and E. Ahissar
Responses of Trigeminal Ganglion Neurons to the Radial Distance of Contact During Active Vibrissal Touch
J Neurophysiol, February 1, 2006; 95(2): 791 - 802.
[Abstract] [Full Text] [PDF]

Home page
 J. Neurophysiol.Home page
C. Boucsein, M. Nawrot, S. Rotter, A. Aertsen, and D. Heck
Controlling Synaptic Input Patterns In Vitro by Dynamic Photo Stimulation
J Neurophysiol, October 1, 2005; 94(4): 2948 - 2958.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
92/1/665    most recent
00031.2004v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (29)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Jones, L. M.
Right arrow Articles by Keller, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Jones, L. M.
Right arrow Articles by Keller, A.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the The American Physiological Society.