JN Add DOIs to your references at manuscript stage!
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 100: 1879-1884, 2008. First published August 6, 2008; doi:10.1152/jn.90511.2008
0022-3077/08 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
100/4/1879    most recent
90511.2008v1
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 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 Google Scholar
Google Scholar
Right arrow Articles by Stüttgen, M. C.
Right arrow Articles by Schwarz, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stüttgen, M. C.
Right arrow Articles by Schwarz, C.

Responses of Rat Trigeminal Ganglion Neurons to Longitudinal Whisker Stimulation

Maik C. Stüttgen1, Stephanie Kullmann1,2 and Cornelius Schwarz1

1Abteilung für Kognitive Neurologie, Hertie-Institut für Klinische Hirnforschung and 2Graduate School for Neural and Behavioural Sciences, Universität Tübingen, Tübingen, Germany

Submitted 28 April 2008; accepted in final form 31 July 2008

Responses of rat trigeminal ganglion neurons to longitudinal whisker stimulation. Rats use their mobile set of whiskers to actively explore their environment. Parameters that play a role to generate movement dynamics of the whisker shaft within the follicle, thus activating primary afferents, are manifold: among them are mechanical properties of the whiskers (curvature, elasticity and taper), active movements (head, body, and whiskers), and finally, object characteristics (surface, geometry, position, and orientation). Hence the whisker system is confronted with forces along all three axes in space. Movements along the two latitudinal axes of the whisker (horizontal and vertical) have been well studied. Here we focus on movement along the whisker's longitudinal axis that has been neglected so far. We employed ramp-and-hold movements that pushed the whisker shaft toward the skin and quantified the resulting activity in trigeminal first-order afferents in anesthetized rats. Virtually all recorded neurons were highly sensitive to longitudinal movement. Neurons could be perfectly segregated into two groups according to their modulation by stimulus amplitude and velocity, respectively. This classification regimen correlated perfectly with the presence or absence of slowly adapting responses in longitudinal stimulation but agreed with classification derived from latitudinal stimulation only if the whisker was engaged in its optimal direction and set point. We conclude that longitudinal stimulation is an extremely effective means to activate the tactile pathway and thus is highly likely to play an important role in tactile coding on the ascending somatosensory pathway. In addition, compared with latitudinal stimulation, it provides a reliable and easy to use method to classify trigeminal first-order afferents.


Address for reprint requests and other correspondence: C. Schwarz, Hertie Institut für Klinische Hirnforschung, Universität Tübingen, Abteilung für Kognitive Neurologie, Otfried Müller Str. 27, 72076 Tübingen, Germany (E-mail: cornelius.schwarz{at}uni-tuebingen.de)




This article has been cited by other articles:


Home page
J. Neurosci.Home page
H. J. Chiel, L. H. Ting, O. Ekeberg, and M. J. Z. Hartmann
The Brain in Its Body: Motor Control and Sensing in a Biomechanical Context
J. Neurosci., October 14, 2009; 29(41): 12807 - 12814.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2008 by the The American Physiological Society.