|
|
||||||||
From the Departments of Neurology (Dr. R. Baron) and Radiology (Drs. Y. Baron, Disbrow, and Roberts), University of California at San Francisco, CA; the Klinik für Neurologie (Dr. R. Baron), Christian-Albrechts-Universität Kiel, Germany; and the Radiologische Abteilung (Dr. Y. Baron), Städtisches Krankenhaus Kiel, Germany.
Address correspondence and reprint requests to Dr. Ralf Baron, Klinik für Neurologie, Christian-Albrechts-Universität Kiel, Niemannsweg 147, 24105 Kiel, Germany; e-mail: r.baron{at}neurologie.uni-kiel.de
OBJECTIVE: To investigate, using functional MRI (fMRI), the neural network that is activated by the pain component of capsaicin-induced secondary mechanical hyperalgesia.
BACKGROUND: Mechanical hyperalgesia (i.e., pain to innocuous tactile stimuli) is a distressing symptom of neuropathic pain syndromes. Animal experiments suggest that alterations in central pain processing occur that render tactile stimuli capable of activating central pain-signaling neurons. A similar central sensitization can be produced experimentally with capsaicin.
METHODS: In nine healthy individuals the cerebral activation pattern resulting from cutaneous nonpainful mechanical stimulation at the dominant forearm was imaged using fMRI. Capsaicin was injected adjacent to the stimulation site to induce secondary mechanical hyperalgesia. The identical mechanical stimulation was then perceived as painful without changing the stimulus intensity and location. Both activation patterns were compared to isolate the specific pain-related component of mechanical hyperalgesia from the tactile component.
RESULTS: The pattern during nonpainful mechanical stimulation included contralateral primary sensory cortex (SI) and bilateral secondary sensory cortex (SII) activity. During hyperalgesia, significantly higher activation was found in the contralateral prefrontal cortex: the middle (Brodmann areas [BAs] 6, 8, and 9) and inferior frontal gyrus (BAs 44 and 45). No change was present within SI, SII, and the anterior cingulate cortex.
CONCLUSIONS: Prefrontal activation is interpreted as a consequence of attention, cognitive evaluation, and planning of motor behavior in response to pain. The lack of activation of the anterior cingulate contrasts with physiologic pain after C-nociceptor stimulation. It might indicate differences in the processing of hyperalgesia and C-nociceptor pain or it might be due to habituation of affective sensations during hyperalgesia compared with acute capsaicin pain.
This article has been cited by other articles:
![]() |
M. Burgmer, M. Gaubitz, C. Konrad, M. Wrenger, S. Hilgart, G. Heuft, and B. Pfleiderer Decreased Gray Matter Volumes in the Cingulo-Frontal Cortex and the Amygdala in Patients With Fibromyalgia Psychosom Med, June 1, 2009; 71(5): 566 - 573. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. L. Whitsel, O. V. Favorov, Y. Li, M. Quibrera, and M. Tommerdahl Area 3a Neuron Response to Skin Nociceptor Afferent Drive Cereb Cortex, February 1, 2009; 19(2): 349 - 366. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Luo, M. Yu, S. D. Smith, M. Kritzer, C. Du, Y. Ma, N. D. Volkow, P. S. Glass, and H. Benveniste The Effect of Intravenous Lidocaine on Brain Activation During Non-Noxious and Acute Noxious Stimulation of the Forepaw: A Functional Magnetic Resonance Imaging Study in the Rat Anesth. Analg., January 1, 2009; 108(1): 334 - 344. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. Lee, L. Zambreanu, D. K. Menon, and I. Tracey Identifying Brain Activity Specifically Related to the Maintenance and Perceptual Consequence of Central Sensitization in Humans J. Neurosci., November 5, 2008; 28(45): 11642 - 11649. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. A. Boyle, M. Heinke, J. Gerber, J. Frasnelli, and T. Hummel Cerebral Activation to Intranasal Chemosensory Trigeminal Stimulation Chem Senses, May 1, 2007; 32(4): 343 - 353. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Mazzola, J. Isnard, and F. Mauguiere Somatosensory and Pain Responses to Stimulation of the Second Somatosensory Area (SII) in Humans. A Comparison with SI and Insular Responses Cereb Cortex, July 1, 2006; 16(7): 960 - 968. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Ducreux, N. Attal, F. Parker, and D. Bouhassira Mechanisms of central neuropathic pain: a combined psychophysical and fMRI study in syringomyelia Brain, April 1, 2006; 129(4): 963 - 976. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Maihofner, H. O. Handwerker, and F. Birklein Functional imaging of allodynia in complex regional pain syndrome Neurology, March 14, 2006; 66(5): 711 - 717. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. D. Iannetti, L. Zambreanu, R. G. Wise, T. J. Buchanan, J. P. Huggins, T. S. Smart, W. Vennart, and I. Tracey From The Cover: Pharmacological modulation of pain-related brain activity during normal and central sensitization states in humans PNAS, December 13, 2005; 102(50): 18195 - 18200. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Peyron, F. Schneider, I. Faillenot, P. Convers, F.-G. Barral, L. Garcia-Larrea, and B. Laurent An fMRI study of cortical representation of mechanical allodynia in patients with neuropathic pain Neurology, November 23, 2004; 63(10): 1838 - 1846. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Stiasny-Kolster, W. Magerl, W. H. Oertel, J. C. Moller, and R.-D. Treede Static mechanical hyperalgesia without dynamic tactile allodynia in patients with restless legs syndrome Brain, April 1, 2004; 127(4): 773 - 782. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Porro Functional Imaging and Pain: Behavior, Perception, and Modulation Neuroscientist, October 1, 2003; 9(5): 354 - 369. [Abstract] [PDF] |
||||
![]() |
J. Lorenz, S. Minoshima, and K. L. Casey Keeping pain out of mind: the role of the dorsolateral prefrontal cortex in pain modulation Brain, May 1, 2003; 126(5): 1079 - 1091. [Abstract] [Full Text] [PDF] |
||||
![]() |
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] |
||||
![]() |
C. A. Porro, P. Baraldi, G. Pagnoni, M. Serafini, P. Facchin, M. Maieron, and P. Nichelli Does Anticipation of Pain Affect Cortical Nociceptive Systems? J. Neurosci., April 15, 2002; 22(8): 3206 - 3214. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Witting, R. C. Kupers, P. Svensson, L. Arendt-Nielsen; A. Gjedde, and T. S. Jensen Experimental brush-evoked allodynia activates posterior parietal cortex Neurology, November 27, 2001; 57(10): 1817 - 1824. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. P.L. Roberts, E. A. Disbrow, H. C. Roberts, and H. A. Rowley Quantification and Reproducibility of Tracking Cortical Extent of Activation by Use of Functional MR Imaging and Magnetoencephalography AJNR Am. J. Neuroradiol., August 1, 2000; 21(8): 1377 - 1387. [Abstract] [Full Text] |
||||
![]() |
U. Ladabaum, S. Minoshima, and C. Owyang Pathobiology of Visceral Pain: Molecular Mechanisms and Therapeutic Implications V. Central nervous system processing of somatic and visceral sensory signals Am J Physiol Gastrointest Liver Physiol, July 1, 2000; 279(1): G1 - G6. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |