Vertex-recorded, rather than primary somatosensory cortex-recorded, somatosensory-evoked potentials signal unpleasantness of noxious stimuli in the rat

Brain Research Bulletin

Volumn 70, Issue 3, 2006, Pages 203-212

  Stienen, Peter J ^a,d   van Oostrom, Hugo ^a,d   van den Bos, Ruud ^c,d   de Groot, Harry N M ^a   Hellebrekers, Ludo J ^a,b,d  

^a UTRECHT UNIVERSITY   (Netherlands)

^b Faculty of Veterinary Medicine   (Netherlands)

^c UTRECHT UNIVERSITY   (Netherlands)

^d UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Analgesia; Auditory evoked potential; Fentanyl; Nociceptive system; Pain; SEP

Indexed keywords

FENTANYL;

ANIMAL EXPERIMENT; ARTICLE; AUDITORY CORTEX; BEHAVIORAL SCIENCE; CONTROLLED STUDY; DOSE RESPONSE; EVOKED AUDITORY RESPONSE; EVOKED SOMATOSENSORY RESPONSE; FEAR; INSTRUMENTAL CONDITIONING; MALE; NOCICEPTIVE STIMULATION; NONHUMAN; PRIORITY JOURNAL; RAT; SOMATOSENSORY CORTEX; STEADY STATE; UNPLEASANT SENSATION;

ANALGESICS, OPIOID; ANIMALS; CONDITIONING, CLASSICAL; DOSE-RESPONSE RELATIONSHIP, DRUG; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS, AUDITORY; EVOKED POTENTIALS, SOMATOSENSORY; FEAR; FENTANYL; MALE; PAIN; RATS; RATS, WISTAR;

EID: 33746210124     PISSN: 03619230     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainresbull.2006.06.003     Document Type: Article

References (42)

1. Arendt-Nielsen L. Characteristics, detection, and modulation of laser-evoked vertex potentials. Acta Anaesthesiol. Scand. Suppl. 101 (1994) 7-44
2. Banoub M., Tetzlaff J.E., and Schubert A. Pharmacologic and physiologic influences affecting sensory evoked potentials: implications for perioperative monitoring. Anesthesiology 99 (2003) 716-737
3. Barth D.S., and Di S. Three-dimensional analysis of auditory-evoked potentials in rat neocortex. J. Neurophysiol. 64 (1990) 1527-1536
4. Bjerring P., and Arendt-Nielsen L. Argon laser induced single cortical responses: a new method to quantify pre-pain and pain perceptions. J. Neurol. Neurosurg. Psychiatry 51 (1988) 43-49
5. Bromm B., and Lorenz J. Neurophysiological evaluation of pain. Electroencephalogr. Clin. Neurophysiol. 107 (1998) 227-253
6. Casey K.L., Svensson P., Morrow T.J., Raz J., Jone C., and Minoshima S. Selective opiate modulation of nociceptive processing in the human brain. J. Neurophysiol. 84 (2000) 525-533
7. Chapin J.K., and Lin C.S. Mapping the body representation in the SI cortex of anesthetized and awake rats. J. Comp. Neurol. 229 (1984) 199-213
8. de Ribaupierre F. Acoustical information processing in the auditory thalamus and cerebral cortex. In: Ehret G., and Romand R. (Eds). The Central Auditory System (1997), Oxford University Press, New York 317-397
9. Fanselow M.S., and Bolles R.C. Naloxone and shock-elicited freezing in the rat. J. Comp. Physiol. Psychol. 93 (1979) 736-744
10. Garcia-Rill E., Homma Y., and Skinner R.D. Arousal mechanisms related to posture and locomotion: 1. Descending modulation. Prog. Brain Res. 143 (2004) 283-290
11. Haberham Z.L., van den Brom W.E., Venker-van Haagen A.J., Baumans V., de Groot H.N., and Hellebrekers L.J. EEG evaluation of reflex testing as assessment of depth of pentobarbital anaesthesia in the rat. Lab. Anim. 33 (1999) 47-57
12. Haberham Z.L., van den Brom W.E., Venker-van Haagen A.J., de Groot H.N., Baumans V., and Hellebrekers L.J. The rat vertex-middle latency auditory-evoked potential as indicator of anaesthetic depth: a comparison with evoked-reflex testing. Brain Res. 873 (2000) 287-290
13. Heppelmann B., Pawlak M., Just S., and Schmidt R.F. Cortical projection of the rat knee joint innervation and its processing in the somatosensory areas SI and SII. Exp. Brain Res. 141 (2001) 501-506
14. Iannetti G.D., Leandri M., Truini A., Zambreanu L., Cruccu G., and Tracey I. Adelta nociceptor response to laser stimuli: selective effect of stimulus duration on skin temperature, brain potentials and pain perception. Clin. Neurophysiol. 115 (2004) 2629-2637
15. Kakigi R., Watanabe S., and Yamasaki H. Pain-related somatosensory evoked potentials. J. Clin. Neurophysiol. 17 (2000) 295-308
16. Kalliomaki J., Luo X.L., Yu Y.B., and Schouenborg J. Intrathecally applied morphine inhibits nociceptive C fiber input to the primary somatosensory cortex (SI) of the rat. Pain 77 (1998) 323-329
17. Kolpakov V.G., Borodin P.M., and Barykina N.N. Catatonic behaviour in the Norway rat. Behaviour 62 (1977) 190-208
18. LeDoux J. The emotional brain, fear, and the amygdala. Cell Mol. Neurobiol. 23 (2003) 727-738
19. Maes J.H., and Vossen J.M. State-dependency of conditioning and extinction of an appetitive response with amphetamine and midazolam. Pharmacol. Biochem. Behav. 58 (1997) 305-310
20. Maren S. Neurobiology of Pavlovian fear conditioning. Annu. Rev. Neurosci. 24 (2001) 897-931
21. Millan M.J. The induction of pain: an integrative review. Prog. Neurobiol. 57 (1999) 1-164
22. Miyazato H., Skinner R.D., Crews T., Williams K., and Garcia-Rill E. Serotonergic modulation of the P13 midlatency auditory evoked potential in the rat. Brain Res. Bull. 51 (2000) 387-391
23. Miyazato H., Skinner R.D., and Garcia-Rill E. Neurochemical modulation of the P13 midlatency auditory evoked potential in the rat. Neuroscience 92 (1999) 911-920
24. Miyazato H., Skinner R.D., Reese N.B., Boop F.A., and Garcia-Rill E. A middle-latency auditory-evoked potential in the rat. Brain Res. 37 (1995) 247-255
25. Ohara S., Crone N.E., Weiss N., Treede R.D., and Lenz F.A. Amplitudes of laser evoked potential recorded from primary somatosensory, parasylvian and medial frontal cortex are graded with stimulus intensity. Pain 110 (2004) 318-328
26. Overton D. Contextual stimulus effects of drugs and internal states. In: Balsam P.D., and Tomie A. (Eds). Context and Learning (1985), Lawrence Erlbaum, Hillsdale, NJ 357-384
27. Price D.D. Psychological and neural mechanisms of the affective dimension of pain. Science 288 (2000) 1769-1772
28. Reese N.B., Garcia-Rill E., and Skinner R.D. Auditory input to the pedunculopontine nucleus: I. Evoked potentials. Brain Res. Bull. 37 (1995) 257-264
29. Reese N.B., Garcia-Rill E., and Skinner R.D. Auditory input to the pedunculopontine nucleus: II. Unit responses. Brain Res. Bull. 37 (1995) 265-273
30. Schnitzler A., and Ploner M. Neurophysiology and functional neuroanatomy of pain perception. J. Clin. Neurophysiol. 17 (2000) 592-603
31. Schouenborg J., Kalliomaki J., Gustavsson P., and Rosen I. Field potentials evoked in rat primary somatosensory cortex (SI) by impulses in cutaneous A beta- and C-fibres. Brain Res. 397 (1986) 86-92
32. Sewards T.V., and Sewards M.A. The medial pain system: neural representations of the motivational aspect of pain. Brain Res. Bull. 59 (2002) 163-180
33. Shaw F.Z., Chen R.F., Tsao H.W., and Yen C.T. Comparison of touch- and laser heat-evoked cortical field potentials in conscious rats. Brain Res. 824 (1999) 183-196
34. Silbert S.C., Beacham D.W., and McCleskey E.W. Quantitative single-cell differences in mu-opioid receptor mRNA distinguish myelinated and unmyelinated nociceptors. J. Neurosci. 23 (2003) 34-42
35. Skinner R.D., Homma Y., and Garcia-Rill E. Arousal mechanisms related to posture and locomotion: 2. Ascending modulation. Prog. Brain Res. 143 (2004) 291-298
36. Stienen P.J., de Groot H.N.M., Venker-van Haagen A.J., van den Brom W.E., and Hellebrekers L.J. Differences between somatosensory-evoked potentials recorded from the ventral posterolateral thalamic nucleus, primary somatosensory cortex and vertex in the rat. Brain Res. Bull. 67 (2005) 269-280
37. Stienen P.J., Haberham Z.L., van den Brom W.E., de Groot H.N.M., Venker-Van Haagen A.J., and Hellebrekers L.J. Evaluation of methods for eliciting somatosensory-evoked potentials in the awake, freely moving rat. J. Neurosci. Methods 126 (2003) 79-90
38. Stienen P.J., van den Brom W.E., de Groot H.N.M., Venker-van Haagen A.J., and Hellebrekers L.J. Differences between primary somatosensory cortex- and vertex-derived somatosensory-evoked potentials in the rat. Brain Res. 1030 (2004) 256-266
39. Teneud L., Miyazato H., Skinner R.D., and Garcia-Rill E. Cholinergic modulation of the sleep state-dependent P13 midlatency auditory evoked potential in the rat. Brain Res. 884 (2000) 196-200
40. van Oostrom H., Stienen P.J., van den Bos R., de Groot H.N.M., and Hellebrekers L.J. Development of a rat model to assess the efficacy of the somatosensory-evoked potential as indicator of analgesia. Brain Res. Brain Res. Protoc. 15 (2005) 14-20
41. Yeomans D.C., Cooper B.Y., and Vierck C.J. Effects of systemic morphine on responses of primates to first or second pain sensations. Pain 66 (1996) 253-263
42. Yeomans D.C., Pirec V., and Proudfit H.K. Nociceptive responses to high and low rates of noxious cutaneous heating are mediated by different nociceptors in the rat: behavioral evidence. Pain 68 (1996) 133-140