Pain and Regional Anesthesia
Somatotopy in Human Primary Somatosensory Cortex in Pain System
Ogino, Yuichi M.D.*; Nemoto, Hidenori M.D., Ph.D.†; Goto, Fumio M.D., Ph.D.‡
Background: Compared with somatotopical organization (somatotopy) in the postcentral gyrus in the tactile system, somatotopy in the pain system is not well understood. The aim of this study is to elucidate whether there is somatotopy in the human pain system.
Methods: To elucidate the somatotopy of nociceptive neurons in the postcentral gyrus, the authors recorded pain-evoked cortical responses to noxious intraepidermal electrical stimulation applied to the left hand and left foot in 11 male subjects, using magnetoencephalography.
Results: Brief painful stimuli evoked sustained cortical activity in the primary somatosensory cortex (SI) in the hemisphere contralateral to the stimulated side and in the secondary somatosensory cortex in both hemispheres. In SI, representations of the hand and foot were distinctly separated, with a more medial and posterior location for the foot, whereas no significant difference was found in the locations for the secondary somatosensory cortex dipole. The SI arrangement along the central sulcus was compatible with the homunculus revealed by Penfield using direct cortical stimulation during surgery.
Conclusions: The human pain system contains a somatotopical representation in SI but with less somatotopical organization in the secondary somatosensory cortex. The current results provide supporting evidence of SI involvement in human pain perception and suggest that human SI subserves the localization of the stimulated site in nociceptive processing.
THE human postcentral gyrus is associated with somatic sensation, as is represented by the well-known “penfieldian homunculus” (a bizarre-shaped human body projected to the brain cortical section). Since the landmark study of Penfield and Boldrey,1
somatotopy (an orderly representation of the skin surface) has been demonstrated by various methods, such as the direct stimulation of the cortical surface,1
the recording of somatosensory-evoked responses on the cortical surface,2–4
and magnetoencephalographic approaches.5,6
However, all of these somatotopy-related studies were performed in the processing of innocuous tactile somatosensory information.
Pain processing in humans, particularly in terms of primary somatosensory cortex (SI) involvement in pain perception, remains largely unknown in contrast to the processing of innocuous tactile sensation. Recent functional imaging studies in humans have provided evidence that multiple regions of the brain are involved in pain perception. For example, the secondary somatosensory cortex (SII), insula, and anterior cingulate cortex have been shown to be activated by noxious stimuli.7
Bushnell et al.8
reported SI to be activated in approximately one half of all pain imaging studies (see table 1
in Bushnell et al.
), and its contribution to pain perception is still controversial7,8
since Tarkka and Treede9
first reported activity in the vicinity of SI using electroencephalography. Only a few recent magnetoencephalography studies have demonstrated pain-induced SI activity.10–12
The probable reason half of the studies did not identify the SI activity is that early SI components are very weak and easily overlooked.13
As for the location of noxious stimulation–evoked activation in SI, only a few studies, such as somatosensory-evoked potential9,14
and positron emission tomography15
studies, have indicated an arrangement along the central sulcus consistent with somatotopical organization. However, these indications regarding somatotopy in pain perception remains to be confirmed, because SI involvement in pain perception is still controversial and somatotopical investigation essentially requires high spatial and temporal resolutions. In addition, it has been technically difficult to record cortical activities in humans noninvasively, and selectively apply painful stimulation.
Magnetoencephalography noninvasively records weak magnetic fields produced by electric currents flowing in neurons in the human brain.16
Multichannel magnetoencephalography has an advantage of detecting cortical activities at higher spatial resolutions (on the millimeter order) than those of somatosensory-evoked potential (recorded by electroencephalography), and at much higher temporal resolutions (on the millisecond order) than those of functional magnetic resonance imaging and positron emission tomography.
The aim of this study is to elucidate whether there is somatotopy along the central gyrus in the human pain system by recording pain-evoked somatosensory-evoked magnetic field (pain SEF). In this study, we used two methods to detect SI activities along the central gyrus in human pain perception: One is magnetoencephalography, and another is noxious intraepidermal electrical stimulation that preferentially provides Aδ-fiber nociceptive stimuli without tactile sensations. We recorded pain SEF by whole-head–type magnetoencephalography after acute pain evoked by noxious intraepidermal electrical stimulation inflicted to the dorsum of the left hand and left foot in healthy human subjects.
Materials and Methods
The experiment was performed on 11 healthy male volunteers, aged 24–35 yr (mean age ± SD, 29.0 ± 3.6). The study was approved by the Gunma University Hospital Clinical Investigation and Research Unit (ethics committee; Maebashi, Japan), and written consent was obtained from all of the subjects. All of the subjects were right-handed, none had a history of neurologic disease, and all had normal magnetic resonance (MR) brain images.
Painful Electrical Stimulation
For painful stimulation, an intraepidermal stimulation method developed by Inui et al.12,17
was used. However, the original method was modified slightly to provide a higher selectivity for the activation of nociceptors.18
We used a concentric bipolar needle electrode (patent pending: inventors, Koji Inui and Yasuyuki Takeshima; assignee, National Institute for Physiologic Sciences, Okazaki, Japan; date patent applied for, November 30, 2004) for intraepidermal stimulation in this study with its inventors’ permission. The anode was an outer ring 1.2 mm in diameter, and the cathode was an inner needle that protruded 0.2 mm from the outer ring. By gently pressing the electrode against the skin, the needle tip was inserted in the epidermis, while the outer ring was attached to the skin surface.
This method has some major advantages as follows: (1) Aδ fibers can be selectively stimulated. The method has been shown to be useful in pain SEF studies in humans12,18
to detect signals ascending through Aδ fibers without the contamination of tactile responses due to fast conducting fibers, such as Aβ fibers. (2) Its stimulation induces sharp and well-defined pricking pain sensations without any innocuous sensations in humans. (3) It is a noninvasive and simple method involving only electrical stimulation and therefore activates skin nociceptors directly without a time delay, unlike laser stimulation. The method provides a constant activation time, which is the condition required for stimulus-locked averaging in somatosensory-evoked magnetic field (SEF) studies.
Using such a method, we could evoke sharp-pain stimulus preferentially without any tactile sensation. The electric stimulus was a current-constant square wave pulse delivered at random intervals of 0.2–0.4 Hz. The stimulus duration was 1.0 ms. Current intensity was scaled sufficient to produce a definite pain sensation and a pain intensity from 3 to 5 on a visual analog scale, where 0 represents not painful and 10 represents extremely painful in each subject. Stimulus intensity was determined before the recordings.
We stimulated the left hand and left foot. The hand site was the dorsum of the left hand between the first and second metacarpal bones. The foot site was the instep of the left foot between the first and second metatarsal bones. The mean stimulus intensities were 0.58 ± 0.08 mA (mean ± SD) for the hand stimulation and 0.59 ± 0.16 mA for the foot stimulation. The mean visual analog scale scores were 3.6 ± 0.6 for the hand stimulation and 3.8 ± 0.6 for the foot stimulation. The insertion of the needle electrode caused no bleeding or visible damage to the skin.
Two different conditions were used for each subject: conditions under which the pain stimuli were applied to the left hand (hand condition) and left foot (foot condition). The first stimulus place (the hand or foot) was randomized across subjects. The subjects were required to relax and count the stimuli applied silently, i.e., to pay attention to the stimuli. Each condition contains 130 stimuli. To avoid habituation and maintain the subject’s vigilance, we took three intervals of 2–3 min randomly under each condition and divided one condition into four sessions. During the interval between sessions, the subjects were asked how many stimuli were applied in the preceding session to confirm their arousal and whether they recognized definite pain stimuli without tactile sensation.
Data Acquisition and Analysis
Somatosensory-evoked magnetic fields were recorded with a helmet-shaped 306-channel detector array (Vectorview; ELEKTA Neuromag, Helsinki, Finland) comprising 102 identical triple sensor elements in a magnetically shielded room. Each sensor element consisted of two orthogonal planar gradiometers and one magnetometer coupled to a multisuperconducting quantum interference device, thus providing three independent measurements of magnetic field. The signals were recorded at a band-pass of 0.1–100 Hz and digitized at 600 Hz. The analysis period of 550 ms included a prestimulus baseline of 50 ms. Pain SEF data, i.e., the averaged magnetoencephalographic values after painful somatosensory stimulation, were collected and averaged after 130 stimuli for each condition. The signals recorded from the 204 gradiometers were used for source localization.
To identify the sources of the evoked activities, the equivalent current dipole (ECD), which best explained the measured data, was computed using a least-squares search method.16
A subset of 10–18 channels including the local signal maxima were used for the estimation of ECDs. These calculations gave the three-dimensional location, orientation, and strength of the ECD in a spherical conductor model, which was based on each subject’s MR images to determine the source location. The x-axis passed through preauricular points pointing to the right, the positive y-axis traversed the nasion, and the positive z-axis pointed up. The goodness of fit of an ECD was calculated to indicate in percentage terms how much the dipole accounts for the measured field variance. We used the goodness of fit to determine whether the model was an appropriate one. Only ECDs explaining more than 90% of the field variance (goodness of fit > 90%) at selected periods of time were used for further analysis.
The analysis period was extended to the entire time period, and all of the channels were taken into account in computing a time-varying multidipole model because several cortical activities after painful stimulation overlapped temporally. The strengths of the previously found ECDs were allowed to change while their locations and orientations were maintained. The resulting source strength waveforms were used in the determination of peak and onset latencies and dipole strength (peak amplitude). The data acquisition and analysis followed Hamalainen et al. 16
On the basis of point markers, MR image and magnetoencephalography coordinate systems were aligned, and source locations were superposed on the individual MR images. MR image scans were obtained from all the subjects with a 3.0-T Siemens Allegra scanner (Siemens Medical Systems, Erlangen, Germany). T1-weighted coronal, axial, and sagittal image slices obtained every 2.0 mm were used for rendering the three-dimensional reconstruction of the brain’s surface.
After confirming the dipole moments between two different conditions, to determine the statistical significance of the source location on a three-dimensional coordinate system, we adopted a discriminant analysis, using the x-, y-, and z-coordinates as variables. Furthermore, the Wilcoxon paired signed rank test was used to assess the difference in the coordinates (x, y, and z) of the dipole source, onset latency, peak latency, and dipole moment strength between the hand and foot conditions. P < 0.05 was considered to be significant. Data were expressed as mean ± SD.
The epidermal stimulation elicited well-defined pricking sensations without tactile sensations in all of the subjects. There was no significant difference in visual analog scale score or stimulus intensity between the hand and foot conditions.
shows representative data obtained from subject 1 and its analysis procedure. Under both the hand and foot conditions, clear and consistent evoked magnetic fields were detected in three spatially segregated areas, namely the right centroparietal area and the right and left frontotemporal areas, which are shown in figure 1a
as circles A
, and C
under the hand condition, and as circles A′:
, and C′:
under the foot condition, respectively. By the ECD analysis, circles A
in figure 1a
were estimated to be located in the right posterior wall of the central sulcus, corresponding to SI in the hemisphere contralateral to the stimulated side (fig. 1b
). Similarly, circles B
were estimated in the upper bank of the sylvian fissure, corresponding to SII in the right and left hemispheres, respectively (fig. 1b
). We termed the three ECDs cSI (contralateral SI), cSII (contralateral SII), and iSII (ipsilateral SII) under each condition. The SI sources were located in or around the crown of the postcentral gyrus under both the hand and foot conditions, corresponding to Brodmann’s area 1 or 2 (figs. 1b and 2
). Their x-, y-, and z-coordinates are shown in table 1
. The traces in figure 1c
indicate the time course of these activities in both the hand and foot.
shows the locations of cSI and cSII under the hand and foot conditions of four representative subjects, respectively, superimposed on three-dimensional brains constructed from each subject’s brain MR images. There was a significant difference between the hand and foot cSI locations based on three-dimensional cluster analysis (discriminant analysis, P
= 0.0014). On the other hand, the source locations of cSII (discriminant analysis, P
= 0.548) and iSII (P
= 0.547) did not differ significantly between the hand and foot conditions. Using the Wilcoxon paired signed rank test on the coordinates (x, y, and z) of ECD (cSI, cSII, iSII) locations between the hand and foot conditions, significant differences in the x- and y-coordinates in cSI were found. The cSI location under the foot condition was significantly medial (P
< 0.005) and posterior (P
< 0.05) to that under the hand condition (table 1
), whereas the bilateral SII (cSII and iSII) coordinates did not differ significantly between the two conditions (table 1
and figs. 1b and 2
Then, we compared the onset latencies, peak latencies, and dipole strengths of cSI, cSII, and iSII between the hand and foot conditions. Time course waveforms recorded in a representative subject under both the hand and foot conditions are shown in figure 1c
. The onset and peak latencies were significantly longer under the foot condition than under the hand condition in all the cSI, cSII, and iSII sources (table 2
). They were significantly longer in iSII than in cSII (P
< 0.01) under both conditions. In the iSII, the dipole strength under the foot condition was significantly smaller than that under the hand condition (P
< 0.05); there were no significant differences in the dipole strengths of cSI and cSII between the two conditions (table 2
This is the first magnetoencephalographic study that showed somatotopy in the human pain system. Using magnetoencephalography, which has high temporal and spatial resolutions, we verified somatotopy in SI activities along the central sulcus in early responses to noxious intraepidermal electrical stimulation. In contrast, bilateral SII shows less somatotopy. The current results provide supporting evidence of SI involvement in human pain perception and suggest that human SI subserves the localization of the stimulated site in nociceptive processing.
Pain Evoked by Intraepidermal Electrical Stimulation
We confirmed in all the subjects under both hand and foot conditions that brief, pricking, and well-localized pain sensations are evoked by intraepidermal electrical stimulation, which reflects preferential Aδ-fiber stimulation by this method. We consider this to be the greatest advantage of intraepidermal electrical stimulation, i.e., it enables selective technical stimulation of the nociceptive system with ordinary parts. There has been a problem with conventional transcutaneous electric stimulation methods such as that using a bipolar felt-tip electrode, which although is an easy method of producing painful sensations, activates large myelinated fibers (Aα fibers or Aβ fibers) related to tactile, vibration, and proprioception sensations, which are not “pure” pain-related components.
First pain is a brief, pricking, and well-localized pain, which mediate mainly Aδ fibers. The pain SEFs observed were generally compatible with results of previous studies using intraepidermal electrical stimulation12,19,20
and laser stimulation;11,21
they showed no activities during a 0- to 60-ms latency period in all subjects. For example, the activities of well-known 20- and 30-ms responses mediating Aβ-fiber inputs, which are known as the earliest cortical responses evoked by tactile stimulation, were completely lacking (fig. 1c
This observation could be well explained by the difference between the conduction velocities mediating Aβ fiber (innocuous) and Aδ fiber (noxious) inputs in both peripheral and spinal processing.19,23
Somatotopy in SI
The SI sources between the hand and foot in the current study are clearly separated along the central sulcus, and their spatial relationship is compatible with the penfieldian homunculus (fig. 2
). We consider our results to qualify as appropriate candidates for analyzing somatosensory areas in the human pain system. However, further studies are required to establish the entire body map in SI for the human nociceptive system. There were more individual variations in the foot source locations than in the hand source locations. This observation is compatible with those of previous studies investigating lower limb representations with tactile stimulation, suggesting complicated anatomical problems of the lower limb area in SI.14,24
In terms of SI activity, ECDs were found located in the anterior crown of the postcentral gyrus under both the hand and foot conditions in the MR images, suggesting that they correspond to Brodmann’s area 1 or 2 (figs. 1b and 2
). The current ECD locations are generally in accord with pain-induced SI source locations that recent magnetoencephalographic data have shown, different from those of tactile stimulation that originates from area 3b.11,20,21,25
To our knowledge, there are three magnetoencephalographic studies11,19,21
in which the locations of SI activation after noxious and innocuous stimuli were directly compared. All of these studies found the location of noxious stimulus-evoked SI activation probably in area 1 slightly more medial and superior than that of early SI activation in area 3b evoked by tactile stimuli. These studies clearly showed that the processing of noxious signals differed from tactile processing in SI. Within subdivisions in SI, area 3a is also suggested to be involved in the nociceptive system.26,27
Kenshalo et al.28
suggest that nociceptive neurons are located in area 1 of SI in monkeys, which is somatotopically organized. Therefore, it is presumed that subdivisions except 3b are involved in the nociceptive system.
SI in Nociceptive Processing
Kenshalo et al.29,30
clearly showed that a pathway from the ventral spinothalamic tract to SI via
the ventroposterior lateral nucleus of the thalamus plays a role in nociception in unitary recording studies in monkeys. Nociceptive neurons in both the ventroposterior lateral nucleus and SI have restricted contralateral receptive fields and are somatotopically organized.28–30
They also demonstrated that the activity of SI nociceptive neurons correlates with the monkey’s detection speed of noxious stimuli.31
These results suggest that nociceptive neurons in SI possess the ability to provide information on the sensory-discriminative component of nociceptive processing.
Accumulating evidence from human imaging studies9,10,15,32–35
also indicates the essential role of SI in the sensory-discriminative aspects of pain, such as localization, intensity, and temporal attributes of a noxious stimulus. The localization of painful laser-induced stimuli applied to the hand and foot areas was almost the same as that of tactile stimuli, with a mean error of 14 ± 3 mm.36
A recent study clearly showed that the spatial discrimination capacity does not differ between nociceptive and tactile systems in humans.37
These findings suggest that the human nociceptive system has a neural mechanism that provides precise spatial information. Among possible brain areas responsible for such mechanism, SI is the most frequently suggested area involved in stimulus localization for the nociceptive system.7
Despite these data, the role of SI in the discriminative aspect of pain remains controversial.27,38–40
In this study, we showed the somatotopical representations of the hand and foot in SI after painful stimulations, which are consistent with the evidence of small restricted receptive fields of SI nociceptive neurons that receive projections from somatotopically organized neurons in the ventroposterior lateral nucleus in monkeys.29,30
Our results suggest that human SI subserves the localization of the stimulated site in nociceptive processing. A case report of a patient with a lesion in SI also supports this notion; this patient had a selective loss of first pain sensation and pain localization, but a preserved pain affect.41
Somatotopy in SII
Our current data did not indicate a clear somatotopy in SII, for which we found strong responses from the hand and foot stimulations. Somatotopy in SII has been reported in monkeys2,42,43
Although no study has shown a clear topographic order of SII in humans, unlike the homunculus in SI, Maeda et al.47
have shown a tendency of the SII topographic order in humans as follows: medial–lateral direction: tibial nerve–middle finger–thumb–upper lip–lower lip. Our results of SII in pain perception showed a tendency of the topographic order hand–foot in the medial–lateral direction, opposite that reported by Maeda et al.
in tactile sensation.
Three magnetoencephalographic studies11,19,21
demonstrated no significant difference between the locations of tactile and nociceptive sources in human SII. In contrast, Vogel et al.48
suggested that the nociceptive SII area in humans activated by noxious stimulations may be separate from the tactile SII area. It is unclarified whether the tactile and nociceptive processings are both in the same SII areas or whether they exhibit different neuronal activities despite their being adjacent each other. In the current study, because bilateral SII locations showed no significant differences between the hand and foot conditions, we conclude that SII in the pain system does not have a strong somatotopy, unlike SI.
SII in Nociceptive Processing
The secondary somatosensory cortex has been suggested to be part of the cognitive-evaluative components of pain perception.10,32–35
Our result of no significant somatotopy in SII activities supports the suggestion that SII is associated more with the cognitive-evaluative aspects of the painful nature of a stimulus, such as pain-related emotion, learning, and memory, rather than with the sensory-discriminative aspects of pain.
The authors thank Koji Inui, M.D., Ph.D. (Assistant Professor), and Ryusuke Kakigi, M.D., Ph.D. (Professor, Department of Integrative Physiology, National Institute for Physiologic Sciences, Okazaki, Japan). The needle electrodes for pain stimulus in this study were used with the permission of Dr. Inui, who developed the method. The authors also thank Koji Koyama (Technician, Elekta K. K., Tokyo, Japan) for his technical support.
1. Penfield W, Boldray E: Somatic motor and sensory representation in the cerebral cortex of man as studied by electrical stimulation. Brain 1937;60:389–443
2. Woolsey CN, Fairman D: Contralateral, ipsilateral and bilateral representation of cutaneous receptors in somatic areas I and II of the cerebral cortex of pig, sheep and other mammals. Surgery 1946;19:684–702
3. Wood CC, Cohen D, Cun BN, Yarita M, Allison T: Electrical sources in human somatosensory cortex: Identification by combined magnetic and potential recordings. Science 1985;227:1051–3
4. Allison T, McCarthy G, Wood CC, Williamson PD, Spencer DD: Human cortical potentials evoked by stimulation of the median nerve: I. Cytoarchitectonic areas generating short-latency activity. J Neurophysiol 1989;62:694–710
5. Narich L, Madonna I, Opsomer RJ, Pizzella V, Romani GL, Torrioli G, Traversa R, Rossini PM: Neuromagnetic somatosensory homunculus: A non-invasive approach in humans. Neurosci Lett 1991;121:51–4
6. Nakamura A, Yamada T, Goto A, Kato T, Ito K, Abe Y, Kachi T, Kakigi R: Somatosensory homunculus as drawn by MEG. Neuroimage 1998;7:377–86
7. Treede RD, Kenshalo DR, Gracely RH, Jones AK: The cortical representation of pain. Pain 1999;79:105–11
8. Bushnell MC, Duncan GH, Hofbauer RK, Ha B, Chen JI, Carrier B: Pain perception: Is there a role for primary somatosensory cortex? Proc Natl Acad Sci U S A 1999;96:7705–9
9. Tarkka IM, Treede RD: Equivalent electrical source analysis of pain-related somatosensory evoked potentials elicited by a CO2 laser. J Clin Neurophysiol 1993;10:513–9
10. Ploner M, Schmitz F, Freund HJ, Schnitzler A: Parallel activation of primary and secondary somatosensory cortices in human pain processing. J Neurophysiol 1999;81:3100–4
11. Kanda M, Nagamine T, Ikeda A, Ohara S, Kunieda T, Fujiwara N, Yazawa S, Sawamoto N, Matsumoto R, Taki W, Shibasaki H: Primary somatosensory cortex is actively involved in pain processing in human. Brain Res 2000;853:282–9
12. Inui K, Tran TD, Qiu Y, Wang X, Hoshiyama M, Kakigi R: Pain-related magnetic fields evoked by intra-epidermal electrical stimulation in humans. Clin Neurophysiol 2002;113:298–304
13. Kakigi R, Inui K, Tamura Y: Electrophysiological studies on human pain perception. Clin Neurophysiol 2005;116:743–63
14. Xu X, Kanda M, Shindo K, Fujiwara N, Nagamine T, Ikeda A, Honda M, Tachibana N, Barrett G, Kaji R, et al: Pain-related somatosensory evoked potentials following CO2 laser stimulation of foot in man. Electroencephalogr Clin Neurophysiol 1995;96:12–23
15. Andersson JL, Lilja A, Hartvig P, Langstrom B, Gordh T, Handwerker H, Torebjork E: Somatotopic organization along the central sulcus, for pain localization in humans, as revealed by positron emission tomography. Exp Brain Res 1997;117:192–9
16. Hamalainen M, Hari R, Ilmoniemi RJ, Knuutila J, Lounasmaa OV: Magnetoencephalography—theory, instrumentation, and applications to noninvasive studies of the working human brain. Rev Mod Phys 1993;65:413–97
17. Inui K, Tran TD, Hoshiyama M, Kakigi R: Preferential stimulation of Aδ fibers by intra-epidermal needle electrode in humans. Pain 2002;96:247–52
18. Inui K, Tsuji T, Kakigi R: Temporal analysis of cortical mechanisms for pain relief by tactile stimuli in humans. Cereb Cortex 2005; (in press)
19. Inui K, Tran TD, Qiu Y, Wang X, Hoshiyama M, Kakigi R: A comparative magnetoencephalographic study of cortical activations evoked by noxious and innocuous somatosensory stimulations. Neuroscience 2003;120:235–48
20. Inui K, Wang X, Qiu Y, Nguyen BT, Ojima S, Tamura Y, Nakata H, Wasaka T, Tran TD, Kakigi R: Pain processing within the primary somatosensory cortex in humans. Eur J Neurosci 2003;18:2859–66
21. Ploner M, Schmitz F, Freund HJ, Schnitzler A: Differential organization of touch and pain in human primary somatosensory cortex. J Neurophysiol 2000;83:1770–6
22. Kakigi R, Hoshiyama M, Shimojo M, Naka D, Yamasaki H, Watanabe S, Xiang J, Maeda K, Lam K, Itomi K, Nakamura A: The somatosensory evoked magnetic fields. Prog Neurobiol 2000;61:495–523
23. Tran TD, Lam K, Hoshiyama M, Kakigi R: A new method for measuring the conduction velocities of Aβ-, Aδ- and C-fibers following electric and CO2 laser stimulation in humans. Neurosci Lett 2001;301:187–90
24. Shimojo M, Kakigi R, Hoshiyama M, Koyama S, Kitamura Y, Watanabe S: Differentiation of receptive fields in the sensory cortex following stimulation of various nerves of the lower limb in humans: A magnetoencephalographic study. J Neurosurg 1996;85:255–62
25. Ohara S, Crone NE, Weiss N, Treede RD, Lenz FA: Cutaneous painful laser stimuli evoke responses recorded directly from primary somatosensory cortex in awake humans. J Neurophysiol 2004;91:2734–46
26. Tommerdahl M, Delemos KA, Vierck Jr, CJ Favorov OV, Whitsel BL: Anterior parietal cortical response to tactile and skin-heating stimuli applied to the same skin site. J Neurophysiol 1996;75:2662–70
27. Craig AD: Pain mechanisms: Labeled lines versus convergence in central processing. Annu Rev Neurosci 2003;26:1–30
28. Kenshalo DR, Iwata K, Sholas M, Thomas DA: Response properties and organization of nociceptive neurons in area 1 of monkey primary somatosensory cortex. J Neurophysiol 2000;84:719–29
29. Kenshalo Jr, DR Giesler Jr, GJ Leonard RB, Willis WD: Responses of neurons in primate ventral posterior lateral nucleus to noxious stimuli. J Neurophysiol 1980;43:1594–614
30. Kenshalo Jr, DR Isensee O: Responses of primate SI cortical neurons to noxious stimuli. J Neurophysiol 1983;50:1479–96
31. Kenshalo Jr, DR Chudler EH, Anton F, Dubner R: SI nociceptive neurons participate in the encoding process by which monkeys perceive the intensity of noxious thermal stimulation. Brain Res 1988;454:378–82
32. Schnitzler A, Ploner M: Neurophysiology and functional neuroanatomy of pain perception. J Clin Neurophysiol 2000;17:592–603
33. Timmermann L, Ploner M, Haucke K, Schmitz F, Baltissen R, Schnitzler A: Differential coding of pain intensity in the human primary and secondary somatosensory cortex. J Neurophysiol 2001;86:1499–503
34. Ohara S, Crone NE, Weiss N, Treede RD, Lenz FA: Amplitudes of laser evoked potential recorded from primary somatosensory, parasylvian and medial frontal cortex are graded with stimulus intensity. Pain 2004;110:318–28
35. Alkire MT, White NS, Hsieh R, Haier RJ: Dissociable brain activation responses to 5-Hz electrical pain stimulation: A high-field functional magnetic resonance imaging study. Anesthesiology 2004;100:939–46
36. Moore CE, Schady W: Cutaneous localisation of laser induced pain in humans. Neurosci Lett 1995;193:208–10
37. Schlereth T, Magerl W, Treede R: Spatial discrimination thresholds for pain and touch in human hairy skin. Pain 2001;92:187–94
38. Willis Jr, WD Zhang X, Honda CN, Giesler Jr, GJ: A critical review of the role of the proposed VMpo nucleus in pain. J Pain 2002;3:79–94
39. Craig AD, Blomqvist A: Is there a specific lamina I spinothalamocortical pathway for pain and temperature sensations in primates? J Pain 2002;3:95–101
40. Treede RD: Spinothalamic and thalamocortical nociceptive pathways. J Pain 2002;3:109–12
41. Ploner M, Freund HJ, Schnitzler A: Pain affect without pain sensation in a patient with a postcentral lesion. Pain 1999;81:211–4
42. Whitsel BL, Petrucelli LM, Werner G: Symmetry and connectivity in the map of the body surface in somatosensory area II of primates. J Neurophysiol 1969;32:170–83
43. Krubitzer L, Clarey J, Tweedale R, Elston G, Calford M: A redefinition of somatosensory areas in the lateral sulcus of macaque monkeys. J Neurosci 1995;15:3821–39
44. Hari R, Karhu J, Hamalainen M, Knuutila J, Salonen O, Sams M, Vilkman V: Functional organization of the human first and second somatosensory cortices: A neuromagnetic study. Eur J Neurosci 1993;5:724–34
45. Disbrow E, Roberts T, Krubitzer L: Somatotopic organization of cortical fields in the lateral sulcus of Homo sapiens: Evidence for SII and PV. J Comp Neurol 2000;418:1–21
46. Ruben J, Schwiemann J, Deuchert M, Meyer R, Krause T, Curio G, Villringer K, Kurth R, Villringer A: Somatotopic organization of human secondary somatosensory cortex. Cereb Cortex 2001;11:463–73
47. Maeda K, Kakigi R, Hoshiyama M, Koyama S: Topography of the secondary somatosensory cortex in humans: A magnetoencephalographic study. Neuroreport 1999;10:301–6
48. Vogel H, Port JD, Lenz FA, Solaiyappan M, Krauss G, Treede RD: Dipole source analysis of laser-evoked subdural potentials recorded from parasylvian cortex in humans. J Neurophysiol 2003;89:3051–60
This article has been cited 7 time(s).
SchmerzStudies on cerebral processing of pain using functional imaging - Somatosensory, emotional, cognitive, autonomic and motor aspectsSchmerz
Clinical NeurophysiologySomatotopic representation of pain in the primary somatosensory cortex (S1) in humansClinical Neurophysiology
Brain ResearchThe cortical representation of sensory inputs arising from boneBrain Research
Versatile effects of sildenafil: recent pharmacological applications
Pharmacological Reports, 59(2):
Neuroscience LettersSomatotopical relationships between cortical activity and reflex areas in reflexology: A functional magnetic resonance imaging studyNeuroscience Letters
European Journal of PainNociception-related somatosensory evoked potentials in awake dogs recorded after intra epidermal electrical stimulationEuropean Journal of Pain
PainMultiple pathways for noxious information in the human spinal cordPain
© 2005 American Society of Anesthesiologists, Inc.
Publication of an advertisement in Anesthesiology Online does not constitute endorsement by the American Society of Anesthesiologists, Inc. or Lippincott Williams & Wilkins, Inc. of the product or service being advertised.