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2010 | 70 | 1 |

Tytuł artykułu

Cortical stimulation and tooth pulp evoked potentials in rats: A model of direct anti-nociception

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
While the effect of cortex stimulation on pain control is widely accepted, its physiological basis remains poorly understood. We chose an animal model of pain to study the influence of sensorimotor cortex stimulation on tooth pulp stimulation evoked potentials (TPEPs). Fifteen awake rats implanted with tooth pulp, cerebral cortex, and digastric muscle electrodes were divided into three groups, receiving 60 Hz, 40 Hz and no cortical stimulation, respectively. TPEPs were recorded before, one, three and five hours after continuous stimulation. We observed an inverse relationship between TPEP amplitude and latency with increasing tooth pulp stimulation. The amplitudes of the early components of TPEPs increased and their latency decreased with increasing tooth pulp stimulation intensity. Cortical stimulation decreased the amplitude of TPEPs; however, neither the latencies of TPEPs nor the jaw-opening reflex were changed after cortical stimulation. The decrease in amplitude of TPEPs after cortical stimulation may reflect its anti-nociceptive effect.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

70

Numer

1

Opis fizyczny

p.47-55,fig.,ref.

Twórcy

autor
  • Department of Normal, Pathological and Clinical Physiology, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic
autor
  • Laboratory of Physiology of Mastication, University Paris VII Denis Diderot, Paris, France
autor
  • Department of Normal, Pathological and Clinical Physiology, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic
autor
  • Laboratory of Physiology of Mastication, University Paris VII Denis Diderot, Paris, France
autor
  • Department of Normal, Pathological and Clinical Physiology, 3rd Faculty of Medicine, Charles University, Prague, Czech Republic

Bibliografia

  • Alantar A, Azerad J, Limoge A, Robert C, Rokyta R, Pollin B (1997) Potentiation of fentanyl suppression of the jaw-opening reflex by transcranial electrical stimulation. Brain Res 763: 14-20.
  • Azerad J, Woda A (1976) Tooth pulp projection to the trigeminal complex and jaw opening reflex in cat. J Biol Buccale 4: 109-115.
  • Barek S, Rusina R, Pollin B, Azerad J (2007) Somatosensory evoked response and jaw opening reflex elicited by tooth pulp stimulation in awake freely moving rats. Neuroendocrinol Lett 28: 101-105.
  • Bertrand O, Bohorquez J, Pernier J (1994) Time-frequency digital filtering based on an invertible wavelet transform: an application to evoked potentials. IEEE Trans Biomed Eng 41: 77-88.
  • Boucher Y, Pollin B, J. Azerad J (1993) Microinfusions of excitatory aminoacid antagonists into the trigeminal sen­sory complex antagonize the jaw opening reflex in freely moving rats. Brain Res 614: 155-163.
  • Carter GM, Matthews B (1989) Responses of jaw muscles to electrical stimulation of tooth pulp in rat, cat and man. In: Electromyography of Jaw Reflexes in Man (Van Steenberghe D, De Laat A Eds.). University Press, Leuven, BE, p. 205-256. Chapman CR, Gerlach R, Jacobson R, Buffington V, Kaufmann E (1986) Comparison of short-latency trigeminal evoked potentials elicited by painful dental and gingival stimula­tion. Electroencephalogr Clin Neurophysiol 65: 20-26.
  • Cioni B, Meglio M (2007) Motor cortex stimulation for chronic non-malignant pain: current state and future pros­pects. Acta Neurochir Suppl 97: 45-49.
  • Cox EH, Langemeijer MW, Danhof M, Leiden C (1998) Pharmacokinetic-pharmacodynamic modelling of the anal­gesic effect of alfentanil in the rat using tooth pulp evoked potentials. J Pharmacol Toxicol Methods 39: 19-27.
  • Danneman PJ (1994) Cortical potentials evoked by tooth pulp stimulation differentiate between the analgesic and sedative effects of morphine in awake rats. J Pharmacol Exp Ther 269: 1100-1106.
  • Engstrand P, Shya BC, Andersson SA (1983) Is selective stimulation of the rat incisor tooth pulp possible? Pain 15: 27-34.
  • Falinower S, Willer JC, Junien JL, Le Bars D (1994) A C-Fiber reflex modulated by heterotopic noxious somatic stimuli in the rat. J Neurophysiol 72: 194-213.
  • Gojyo F, Sugiyo S, Kuroda R, Kawabata A, Varathan V, Shigenaga Y, Takemura M (2002) Effects of somatosen- sory cortical stimulation on expression of c-Fos in rat medullary dorsal horn in response to formalin-induced noxious stimulation. J Neurosci Res 68: 479-488.
  • Grass S, Crawley JN, Xu XJ, Wiesenfeld-Hallin Z (2003) Reduced spinal cord sensitization to C-fiber stimulation in mice over-expressing galanin. Eur J Neurosci 17: 1829-1832.
  • Gutiérrez JC, Seijo FJ, Alvarez Vega MA, Fernández González F, Lozano Aragoneses B, Blázquez M (2009) Therapeutic extradural cortical stimulation for Parkinson's Disease: report of six cases and review of the literature. Clin Neurol Neurosurg 111: 703-707.
  • Hayashi H (1980) A problem in electrical stimulation of incisor tooth pulp in rats. Exp Neurol 67: 438-441.
  • Jiffry MM, Matthews B (1977) Conduction velocities of pulpal afferents in the rat. J Dent Res 56: D128-160.
  • Jiffry MM (1981) Afferent innervation of the rat incisor pulp. Exp Neurol 73: 209-218.
  • Kolb B (1990) Animal models for human PFC-related disor­ders. In: The Prefrontal Cortex: Its Structure, Function and Pathology, Progress in Brain Research (Vol. 85) (Uylings HBM, van Eden CG, de Bruin JPC, Corner MA, Feenstra MGP, Eds.). Elsevier, Amsterdam, NL, p. 501-519.
  • Kowler E (1990) The role of visual and cognitive processes in the control of eye movement. In: Eye Movements and Their Role in Visual and Cognitive Processes (Kowler E, Ed.). Elsevier, Amsterdam, NL. p. 486-498.
  • Kuroda R, Kawabata A, Kawao N, Umeda W, Takemura M, Shigenaga Y (2000) Somatosensory cortex stimulation- evoked analgesia in rats: potentiation by NO synthase inhibition. Life Sci 66: 271-276.
  • Kuroda R, Kawao N, Yoshimura H, Umeda W, Takemura M, Shigenaga Y, Kawabata A (2001) Secondary somatosen- sory cortex stimulation facilitates the antinociceptive effect of the NO synthase inhibitor through suppression of spinal nociceptive neurons in the rat. Brain Res 903: 110-116.
  • Lefaucheur JP, Drouot X, Menard-Lefaucheur I, Nguyen JP (2004) Neuropathic pain controlled for more than a year by monthly session of repetitive transcranial magnetic stimulation. Clin Neurophysiol 34: 91-95.
  • Logginidou HG, Li BH, Li DP, Lohmann JS, Schuler HG, DiVittore NA, Kreiser S, Cronin AJ (2003) Propofol sup­presses the cortical somatosensory evoked potential in rats. Anesth Analg 97: 1784-788.
  • Meyerson BA, Lindblom U, Linderoth B, Lind G, Herregots P (1993) Motor cortex stimulation as treatment of trigem­inal neuropathic pain. Acta Neurochir Suppl (Wien) 58: 150-153.
  • Morita N, Tamai Y, Tsujimoto T (1977) Unit response acti­vated by tooth pulp stimulation in lateral hypothalamic area of rat. Brain Res 134: 158-160.
  • Nguyen JP, Keravel Y, Fève A, Uchiyama T, Cesaro P, Le Guerinel C, Pollin B (1997) Treatment of deafferentation pain by chronic stimulation of the motor cortex: report of a series of 20 cases. Acta Neurochir Suppl 68: 54-60.
  • Nguyen JP, Lefaucheur JP, Decq P, Lohmann JS, Schuler HG, DiVittore NA, Kreiser S, Cronin C (1999) Chronic motor cortex stimulation in the treatment of central and neuropathic pain. Correlations between clinical, electrophysiological and anatomical data. Pain 82: 245-251.
  • Paxinos G, Watson C (2007) The Rat Brain in Stereotaxic Coordinates (6th ed.). Academic Press, New York, NY.
  • Rusina R, Vaculin S, Yamamotova A, Barek S, Dvorakova H, Rokyta R (2005) The effect of motor cortex stimula­tion in deafferentated rats. Neuro Endocrinol Lett 26: 283-288.
  • Senapati AK, Huntington PJ, LaGraize SC, Wilson HD, Fuchs PN, Peng ZB (2005) Electrical stimulation of the primary somatosensory cortex inhibits spinal dorsal horn neuron activity. Brain Res 1057: 134-140.
  • Shigenaga Y, Matano S, Kusuyama M, Sakai A (1974) Cortical neurons responding to electrical stimulation of the rats incisor pulp. Brain Res 67: 153-156.
  • Starr R, Kristeva D, Cheyne G, Lindinger L, Deecke L (1991) Localization of brain activity during auditory ver­bal short-term memory derived from magnetic record­ings. Brain Res 558: 181-190.
  • Sugimoto T, Takemura M, Wakisaka S (1988) Cell size analysis of primary neurons innervating the cornea and tooth pulp of the rat. Pain 32: 375-381.
  • Suri ML, Kaltenbach BL, Grundy H, Derendorf E (1996) Pharmacodynamic evaluation of codeine using tooth pulp evoked potentials J Clin Pharmacol 36: 1126-1131.
  • Toda K, Iriki A (1980) Quantitative relations between nox­ious stimulus intensity and magnitude of central afferent evoked responses in rat. Neurosci Lett 17: 313-316.
  • Toda K, Iriki A, Ichioka M (1981) Selective stimulation of intrapulpar nerve of rat lower incisor using a bi-polar electrod method. Physiol Behav 26: 307-311.
  • Tsubokawa T, Katayama Y, Yamamoto T, Hirayama T, Koyama S (1991) Chronic motor cortex stimulation for the treatment of central pain. Acta Neurochir Suppl (Wien) 52: 137-139.
  • Vaculin S, Franek M, Yamamotova A, Rokyta R (2008) Motor cortex stimulation in rats with chronic constriction injury. Exp Brain Res 185: 331-335.
  • You HJ, Morch CD, Chen J, Arendt-Nielsen L (2003) Role of central NMDA versus non NMDA receptor in spinal withdrawal reflex in spinal anesthetized rats under normal and hyperexcitable conditions. Brain Res 981: 12-22.
  • Zimmermann M (1983) Ethical guidelines for investigations of experimental pain in conscious animals. Pain 16: 109-110.

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