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


     


J Neurophysiol 80: 2077-2088, 1998;
0022-3077/98 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 Lenz, F. A.
Right arrow Articles by Lesser, R. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lenz, F. A.
Right arrow Articles by Lesser, R. P.

The Journal of Neurophysiology Vol. 80 No. 4 October 1998, pp. 2077-2088
Copyright ©1998 The American Physiological Society

Painful Stimuli Evoke Potentials Recorded From the Parasylvian Cortex in Humans

F. A. Lenz, M. Rios, D. Chau, G. L. Krauss, T. A. Zirh, and R. P. Lesser

Departments of Neurosurgery and Neurology, Johns Hopkins Hospital, Baltimore, Maryland 21287-7713

Lenz, F. A., M. Rios, D. Chau, G. L. Krauss, T. A. Zirh, and R. P. Lesser. Painful stimuli evoke potentials recorded from the parasylvian cortex in humans. J. Neurophysiol. 80: 2077-2088, 1998. Cutaneous stimulation of the face and hand with a CO2 laser in three awake patients evoked potentials (LEPs) recorded from the dominant left parasylvian cortex. These were recorded by means of a subdural grid of electrodes implanted for evaluation of epilepsy. Stimulation of the contralateral face resulted in waveforms consisting of a negative potential (N2, 162 ± 5 ms; mean ± SE) followed by a positive potential (P2, 340 ± 18 ms). Both waves occurred at longer latency after hand than after facial stimulation. N2 and P2 potentials recorded from the grid correspond well in morphology to those recorded from the scalp in four additional patients tested with the same stimulation paradigm. The N2 waves recorded from the subdural grid occurred at significantly shorter latencies than did those recorded from the scalp (184 ± 6 ms), but the P2 waves at the grid occurred at significantly longer latencies than did those recorded at the scalp (281 ± 13 ms). The amplitudes of the potentials recorded from the grid were maximal over the parietal operculum both for contralateral stimulation of the face or hand and for ipsilateral stimulation of the face. Potentials also were recorded in this area after stimulation of the ipsilateral hand. The cortical distributions of these potentials suggest that their generators are located in the parietal operculum or in the insula, or in both, consistent with previous PET, magnetoencephalographic, and scalp LEP source analyses. These previous analyses provide indirect evidence of nociceptive input to parasylvian cortex because the interpretation of each analysis incorporates multiple assumptions. The present results are the first direct evidence of nociceptive input to the human parasylvian cortex.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
A. Mouraux and G. D. Iannetti
Nociceptive Laser-Evoked Brain Potentials Do Not Reflect Nociceptive-Specific Neural Activity
J Neurophysiol, June 1, 2009; 101(6): 3258 - 3269.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
K. Kobayashi, J. Winberry, C. C. Liu, R. D. Treede, and F. A. Lenz
A Painful Cutaneous Laser Stimulus Evokes Responses From Single Neurons in the Human Thalamic Principal Somatic Sensory Nucleus Ventral Caudal (Vc)
J Neurophysiol, May 1, 2009; 101(5): 2210 - 2217.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. D. Greenspan, S. Ohara, P. Franaszczuk, D. S. Veldhuijzen, and F. A. Lenz
Cold Stimuli Evoke Potentials That Can Be Recorded Directly From Parasylvian Cortex in Humans
J Neurophysiol, October 1, 2008; 100(4): 2282 - 2286.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
T. Weiss, W. Hesse, M. Ungureanu, H. Hecht, L. Leistritz, H. Witte, and W. H. R. Miltner
How Do Brain Areas Communicate During the Processing of Noxious Stimuli? An Analysis of Laser-Evoked Event-Related Potentials Using the Granger Causality Index
J Neurophysiol, May 1, 2008; 99(5): 2220 - 2231.
[Abstract] [Full Text] [PDF]


Home page
NeuroscientistHome page
C. A. Bagley, S. Ohara, H. C. Lawson, and F. A. Lenz
Psychophysics of CNS Pain-Related Activity: Binary and Analog Channels and Memory Encoding
Neuroscientist, February 1, 2006; 12(1): 29 - 42.
[Abstract] [PDF]


Home page
J. Neurophysiol.Home page
S. Ohara, N. E. Crone, N. Weiss, R.-D. Treede, and F. A. Lenz
Cutaneous Painful Laser Stimuli Evoke Responses Recorded Directly From Primary Somatosensory Cortex in Awake Humans
J Neurophysiol, June 1, 2004; 91(6): 2734 - 2746.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
H. Vogel, J. D. Port, F. A. Lenz, M. Solaiyappan, G. Krauss, and R.-D. Treede
Dipole Source Analysis of Laser-Evoked Subdural Potentials Recorded From Parasylvian Cortex in Humans
J Neurophysiol, June 1, 2003; 89(6): 3051 - 3060.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
I. A. Strigo, G. H. Duncan, M. Boivin, and M. C. Bushnell
Differentiation of Visceral and Cutaneous Pain in the Human Brain
J Neurophysiol, June 1, 2003; 89(6): 3294 - 3303.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
M. Frot and F. Mauguiere
Dual representation of pain in the operculo-insular cortex in humans
Brain, February 1, 2003; 126(2): 438 - 450.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
M. Fabri, G. Polonara, A. Quattrini, and U. Salvolini
Mechanical Noxious Stimuli Cause Bilateral Activation of Parietal Operculum in Callosotomized Subjects
Cereb Cortex, April 1, 2002; 12(4): 446 - 451.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. Sawamoto, M. Honda, T. Okada, T. Hanakawa, M. Kanda, H. Fukuyama, J. Konishi, and H. Shibasaki
Expectation of Pain Enhances Responses to Nonpainful Somatosensory Stimulation in the Anterior Cingulate Cortex and Parietal Operculum/Posterior Insula: an Event-Related Functional Magnetic Resonance Imaging Study
J. Neurosci., October 1, 2000; 20(19): 7438 - 7445.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Ploner, F. Schmitz, H.-J. Freund, and A. Schnitzler
Parallel Activation of Primary and Secondary Somatosensory Cortices in Human Pain Processing
J Neurophysiol, June 1, 1999; 81(6): 3100 - 3104.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online