Cerebral processing of acute skin and muscle pain in humans.

The human cerebral processing of noxious input from skin and muscle was compared with the use of positron emission tomography with intravenous H2(15)O to detect changes in regional cerebral blood flow (rCBF) as an indicator of neuronal activity. During each of eight scans, 11 normal subjects rated the intensity of stimuli delivered to the nondominant (left) forearm on a scale ranging from 0 to 100 with 70 as pain threshold. Cutaneous pain was produced with a high-energy CO2 laser stimulator. Muscle pain was elicited with high-intensity intramuscular electrical stimulation. The mean ratings of perceived intensity for innocuous and noxious stimulation were 32.6 +/- 4.5 (SE) and 78.4 +/- 1.7 for cutaneous stimulation and 15.4 +/- 4.2 and 73.5 +/- 1.4 for intramuscular stimulation. The pain intensity ratings and the differences between noxious and innocuous ratings were similar for cutaneous and intramuscular stimuli (P > 0.05). After stereotactic registration, statistical pixel-by-pixel summation (Z score) and volumes-of-interest (VOI) analyses of subtraction images were performed. Significant increases in rCBF to both noxious cutaneous and intramuscular stimulation were found in the contralateral secondary somatosensory cortex (SII) and inferior parietal lobule [Brodmann area (BA) 40]. Comparable levels of rCBF increase were found in the contralateral anterior insular cortex, thalamus, and ipsilateral cerebellum. Noxious cutaneous stimulation caused significant activation in the contralateral lateral prefrontal cortex (BA 10/46) and ipsilateral premotor cortex (BA 4/6). Noxious intramuscular stimulation evoked rCBF increases in the contralateral anterior cingulate cortex (BA 24) and subsignificant responses in the contralateral primary sensorimotor cortex (MI/SI) and lenticular nucleus. These activated cerebral structures may represent those recruited early in nociceptive processing because both forms of stimuli were near pain threshold. Correlation analyses showed a negative relationship between changes in rCBF for thalamus and MI/SI for cutaneous stimulation, and positive relationships between thalamus and anterior insula for both stimulus modalities. Direct statistical comparisons between innocuous cutaneous and intramuscular stimulation with the use of Z scores and VOI analyses showed no reliable differences between these two forms of noxious stimulation, indicating a substantial overlap in brain activation pattern. The comparison of noxious cutaneous and intramuscular stimulation indicated more activation in the premotor cortex, SII, and prefrontal cortex with cutaneous stimulation, but these differences did not reach statistical significance. The similar cerebral activation patterns suggest that the perceived differences between acute skin and muscle pain are mediated by differences in the intensity and temporospatial pattern of neuronal activity within similar sets of forebrain structures.

[1]  M. Wiesendanger Input from muscle and cutaneous nerves of the hand and forearm to neurones of the precentral gyrus of baboons and monkeys , 1973, The Journal of physiology.

[2]  J. B. Preston,et al.  Responses of cortical neurons (areas 3a and 4) to ramp stretch of hindlimb muscles in the baboon. , 1976, Journal of neurophysiology.

[3]  R. Schmidt,et al.  Convergence of muscle and cutaneous input onto primate spinothalamic tract neurons , 1977, Brain Research.

[4]  H. Burton,et al.  Somatic submodality distribution within the second somatosensory (SII), 7b, retroinsular, postauditory, and granular insular cortical areas of M. fascicularis , 1980, The Journal of comparative neurology.

[5]  Y. Iwamura,et al.  Responses of feline si neurones to noxious stimulation of muscle and tendon , 1981, PAIN.

[6]  K. Reinikainen,et al.  Neuromagnetic localization of cortical activity evoked by painful dental stimulation in man , 1983, Neuroscience Letters.

[7]  T. Morrow,et al.  Ventral posterior thalamic neurons differentially responsive to noxious stimulation of the awake monkey. , 1983, Science.

[8]  B. Sessle,et al.  Corticobulbar projections and orofacial and muscle afferent inputs of neurons in primate sensorimotor cerebral cortex , 1983, Experimental Neurology.

[9]  M. Raichle,et al.  Stimulus rate dependence of regional cerebral blood flow in human striate cortex, demonstrated by positron emission tomography. , 1984, Journal of neurophysiology.

[10]  D. Burke,et al.  The projection of muscle afferents from the hand to cerebral cortex in man. , 1984, Brain : a journal of neurology.

[11]  J. Hanson Hypoglossal high threshold afferents projecting to the secondary somatosensory area in the cat. , 1985, Archives italiennes de biologie.

[12]  K. Berkley,et al.  Diencephalic mechanisms of pain sensation , 1985, Brain Research Reviews.

[13]  G Kobal,et al.  Cortical responses to painful CO2 stimulation of nasal mucosa; a magnetoencephalographic study in man. , 1986, Electroencephalography and clinical neurophysiology.

[14]  David P. Friedman,et al.  Thalamic connectivity of the second somatosensory area and neighboring somatosensory fields of the lateral sulcus of the macaque , 1986, The Journal of comparative neurology.

[15]  David P. Friedman,et al.  Cortical connections of the somatosensory fields of the lateral sulcus of macaques: Evidence for a corticolimbic pathway for touch , 1986, The Journal of comparative neurology.

[16]  N. Mizuno,et al.  Cingulate gyrus of the cat receives projection fibers from the thalamic region ventral to the ventral border of the ventrobasal complex , 1988, The Journal of comparative neurology.

[17]  T. Morrow,et al.  Cutaneous pain and detection thresholds to short CO2 laser pulses in humans: Evidence on afferent mechanisms and the influence of varying stimulus conditions , 1988, Pain.

[18]  Eric H. Chudler,et al.  SI nociceptive neurons participate in the encoding process by which monkeys perceive the intensity of noxious thermal stimulation , 1988, Brain Research.

[19]  Fred L. Bookstein,et al.  Principal Warps: Thin-Plate Splines and the Decomposition of Deformations , 1989, IEEE Trans. Pattern Anal. Mach. Intell..

[20]  M. Torrens Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268 , 1990 .

[21]  D. Pandya,et al.  Anatomical investigation of projections from thalamus to posterior parietal cortex in the rhesus monkey: A WGA‐HRP and fluorescent tracer study , 1990, The Journal of comparative neurology.

[22]  R Dubner,et al.  Responses of nociceptive SI neurons in monkeys and pain sensation in humans elicited by noxious thermal stimulation: effect of interstimulus interval. , 1990, Journal of neurophysiology.

[23]  Chen Pei-xi,et al.  Cerebellar evoked potential elicited by stimulation of C-fiber in saphenous nerve of cat , 1990, Brain Research.

[24]  Karl J. Friston,et al.  Comparing Functional (PET) Images: The Assessment of Significant Change , 1991, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[25]  Dan R. KenshaloJr.,et al.  The Role of the Cerebral Cortex in Pain Sensation , 1991 .

[26]  Alan C. Evans,et al.  Multiple representations of pain in human cerebral cortex. , 1991, Science.

[27]  Alan C. Evans,et al.  Attention modulates somatosensory cerebral blood flow response to vibrotactile stimulation as measured by positron emission tomography , 1991, Annals of neurology.

[28]  Karl J. Friston,et al.  Cortical and subcortical localization of response to pain in man using positron emission tomography , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[29]  R. Treede,et al.  Laser-evoked cerebral potentials in the assessment of cutaneous pain sensitivity in normal subjects and patients. , 1991, Revue neurologique.

[30]  J. Schouenborg,et al.  Topography and nociceptive receptive fields of climbing fibres projecting to the cerebellar anterior lobe in the cat. , 1991, The Journal of physiology.

[31]  J Schouenborg,et al.  The postsynaptic dorsal column pathway mediates cutaneous nociceptive information to cerebellar climbing fibres in the cat. , 1991, The Journal of physiology.

[32]  D. Perani,et al.  Chronic pain: a PET study of the central effects of percutaneous high cervical cordotomy , 1991, Pain.

[33]  J. Greenspan,et al.  Reversible pain and tactile deficits associated with a cerebral tumor compressing the posterior insula and parietal operculum , 1992, Pain.

[34]  J. Schmahmann,et al.  Parietal pseudothalamic pain syndrome. Clinical features and anatomic correlates. , 1992, Archives of neurology.

[35]  B. Vogt,et al.  Nociceptive neurons in area 24 of rabbit cingulate cortex. , 1992, Journal of neurophysiology.

[36]  Alan C. Evans,et al.  A Three-Dimensional Statistical Analysis for CBF Activation Studies in Human Brain , 1992, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

[37]  S Minoshima,et al.  An automated method for rotational correction and centering of three-dimensional functional brain images. , 1992, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[38]  J. Arndt,et al.  The role of nociceptors of cutaneous veins in the mediation of cold pain in man. , 1992, The Journal of physiology.

[39]  M. Giamberardino,et al.  Experimental referred pain and hyperalgesia from muscles in humans , 1993 .

[40]  Alan C. Evans,et al.  Role of the human anterior cingulate cortex in the control of oculomotor, manual, and speech responses: a positron emission tomography study. , 1993, Journal of neurophysiology.

[41]  M. Mintun,et al.  Automated detection of the intercommissural line for stereotactic localization of functional brain images. , 1993, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[42]  C Bassetti,et al.  Sensory syndromes in parietal stroke , 1993, Neurology.

[43]  S. Mense,et al.  Nociception from skeletal muscle in relation to clinical muscle pain , 1993, Pain.

[44]  K L Casey,et al.  Afferent modulation of warmth sensation and heat pain in the human hand. , 1993, Somatosensory & motor research.

[45]  J. R. Sper Parietal “Pseudothalamic” Pain Syndrome , 1993 .

[46]  K L Casey,et al.  Variability of laser-evoked potentials: attention, arousal and lateralized differences. , 1993, Electroencephalography and clinical neurophysiology.

[47]  M. Raichle,et al.  Tactile-vibration-activated foci in insular and parietal-opercular cortex studied with positron emission tomography: mapping the second somatosensory area in humans. , 1993, Somatosensory & motor research.

[48]  Karl J. Friston,et al.  Cerebral responses to pain in patients with atypical facial pain measured by positron emission tomography. , 1994, Journal of neurology, neurosurgery, and psychiatry.

[49]  R A Koeppe,et al.  Positron emission tomographic analysis of cerebral structures activated specifically by repetitive noxious heat stimuli. , 1994, Journal of neurophysiology.

[50]  M. Bushnell,et al.  A thalamic nucleus specific for pain and temperature sensation , 1994, Nature.

[51]  J. Ochoa,et al.  Identification of muscle afferents subserving sensation of deep pain in humans. , 1994, Journal of neurophysiology.

[52]  E. Chudler,et al.  Somatosensory, multisensory, and task-related neurons in cortical area 7b (PF) of unanesthetized monkeys. , 1994, Journal of neurophysiology.

[53]  P. Strick,et al.  Anatomical evidence for cerebellar and basal ganglia involvement in higher cognitive function. , 1994, Science.

[54]  P. Strick,et al.  Activation of a cerebellar output nucleus during cognitive processing. , 1994, Science.

[55]  M Ingvar,et al.  Urge to scratch represented in the human cerebral cortex during itch. , 1994, Journal of neurophysiology.

[56]  R. Koeppe,et al.  Anatomic standardization: linear scaling and nonlinear warping of functional brain images. , 1994, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[57]  Alan C. Evans,et al.  Distributed processing of pain and vibration by the human brain , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[58]  R. Kakigi,et al.  Pain-related magnetic fields following painful CO2 laser stimulation in man , 1995, Neuroscience Letters.

[59]  R. Meyer,et al.  Evidence for two different heat transduction mechanisms in nociceptive primary afferents innervating monkey skin. , 1995, The Journal of physiology.

[60]  K. Berkley,et al.  Are there separate central nervous system pathways for touch and pain? , 1995, Nature Medicine.

[61]  Jen-Chuen Hsieh,et al.  Central representation of chronic ongoing neuropathic pain studied by positron emission tomography , 1995, PAIN®.

[62]  R. Passingham,et al.  Functional anatomy of the mental representation of upper extremity movements in healthy subjects. , 1995, Journal of neurophysiology.

[63]  Karen Faith Berman,et al.  Unilateral decrease in thalamic activity observed with positron emission tomography in patients with chronic neuropathic pain , 1995, Pain.

[64]  E. Chudler,et al.  The role of the basal ganglia in nociception and pain , 1995, Pain.

[65]  L. Arendt-Nielsen,et al.  Induction and assessment of experimental muscle pain. , 1995, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

[66]  F. Lenz,et al.  Stimulation in the human somatosensory thalamus can reproduce both the affective and sensory dimensions of previously experienced pain , 1995, Nature Network Boston.

[67]  R. Koeppe,et al.  Comparison of human cerebral activation pattern during cutaneous warmth, heat pain, and deep cold pain. , 1996, Journal of neurophysiology.

[68]  A Weindl,et al.  Deactivation of human visual cortex during involuntary ocular oscillations. A PET activation study. , 1996, Brain : a journal of neurology.

[69]  S. Stone-Elander,et al.  Traumatic nociceptive pain activates the hypothalamus and the periaqueductal gray: a positron emission tomography study , 1996, Pain.

[70]  E. Chudler,et al.  Behavioral outcome of posterior parietal cortex injury in the monkey , 1996, Pain.

[71]  J. M. Ollinger,et al.  Positron Emission Tomography , 2018, Handbook of Small Animal Imaging.