Article Data

  • Views 318
  • Dowloads 42

Original Research

Open Access

Jaw Clenching Modulates Sensory Perception in High- But Not In Low-Hypnotizable Subjects

  • Michael Tal1,2,*,
  • Yair Sharav2,3

1Department of Anatomy and Cell Biology, Schools of Dental Medicine and Medicine, Hebrew University, Jerusalem, Israel

2Hadassah Medical Center, Center for Research on Pain, Jerusalem, Israel

3Department of Oral Medicine, School of Dental Medicine, Hebrew University

DOI: 10.11607/jofph.1976 Vol.19,Issue 1,March 2005 pp.76-81

Published: 30 March 2005

*Corresponding Author(s): Michael Tal E-mail: talm@cc.huji.ac.il

Abstract

Aims: To investigate the effect of jaw clenching on the sensations evoked at segmental and nonsegmental levels by painful and non-painful stimuli and in relation to hypnotic susceptibility. Methods: The effect of jaw clenching on painful and nonpainful sensations on the face and leg was studied in high-hypnotizable (HH) and low-hypnotizable (LH) subjects. Sixteen healthy subjects were selected and assigned to either the HH group (n = 8) or the LH group (n = 8). Painful and nonpainful electrical stimuli were deliv-ered in random order to the face and leg. The subjects rated the intensity of the evoked sensation on a visual analog scale (VAS) while clenching or not clenching their jaw. Results: Jaw clenching significantly attenuated the VAS sensory ratings of all the subjects under various conditions (F1-31 = 6.15, P < .02). When the HH and LH subjects were analyzed separately, jaw clenching was found to be effective in reducing sensations only in the HH sub-jects (F1–15 = 8.30, P = .01), only those evoked in the face (segmen-tal level), and only those evoked by nonpainful stimuli (tied Z = 2.52, tied P < .02). Conclusion: Sensory modulation produced by jaw clenching may be related to hypnotic susceptibility. On the whole, jaw clenching had a weak, local effect in modulating sensa-tion, in contrast to its known widespread effect on motor behav-ior.

Keywords

heterotopic stimulation; hypnotic susceptibility; jaw clenching; pain modulation; sensory modulation

Cite and Share

Michael Tal,Yair Sharav. Jaw Clenching Modulates Sensory Perception in High- But Not In Low-Hypnotizable Subjects . Journal of Oral & Facial Pain and Headache. 2005. 19(1);76-81.

References

1. Miyahara T, Hagiya N, Ohyama T, Nakamura Y. Modulation of human soleus H reflex in association with voluntary clenching of the teeth. J Neurophysiol 1996;76: 2033–2041.

2. Sugawara K, Kasai T. Facilitation of motor evoked potentials and H-reflexes of flexor carpi radialis muscle induced by voluntary teeth clenching. Hum Mov Sci 2002;21: 203–212.

3. Kemppainen P, Leppanen H, Waltimo A, Pertovaara A. Effects of jaw clenching, jaw movement and static jaw position on facial skin sensitivity to non-painful electrical stimulation in man. Arch Oral Biol 1993;38:303–308.

4. Hardy JD, Wolff HG, Goodell H. Studies on pain. A new method for measuring pain threshold: Observation on spatial summation of pain. J Clin Investig 1940;19: 649–657.

5. Willer JC, Boureau F, Albe-Fessard D. Supraspinal influences on nociceptive flexion reflex and pain sensation in man. Brain Res 1979;179:61–68.

6. Pertovaara A, Kemppainen P, Johansson G, Karonen SL. Ischemic pain nonsegmentally produces a predominant reduction of pain and thermal sensitivity in man: A selective role for endogenous opioids. Brain Res 1982;251: 83–92.

7. Price DD, McHaffie JG. Effects of heterotopic conditioning stimuli on first and second pain: A psychophysical evaluation in humans. Pain 1988;34:245–252.

8. Plaghki L, Delisle D, Godfraind JM. Heterotopic nociceptive conditioning stimuli and mental task modulate differentially the perception and physiological correlates of short CO2 laser stimuli. Pain 1994;57:181–192.

9. Cadden SW, van der Glas HW, Lobbezoo F, van der Bilt A. Effects of remote noxious stimulation on exteroceptive reflexes in human jaw-closing muscles. Brain Res 1996;726:189–197.

10. Le Bars D, Dickenson AH, Besson JM. Diffuse noxious inhibitory controls (DNIC). I. Effects on dorsal horn convergent neurons in the rat. Pain 1979;6:283–304.

11. Dickenson AH, Le Bars D, Besson JM. Diffuse noxious inhibitory controls (DNIC). Effects on trigeminal nucleus caudalis neurons in the rat. Brain Res 1980;200:293–305.

12. Gerhart KD, Yezierski RP, Giesler GJ Jr, Willis WD. Inhibitory receptive fields of primate spinothalamic tract cells. J Neurophysiol 1981;46:1309–1325.

13. Morgan MM, Gogas KR, Basbaum AI. Diffuse noxious inhibitory controls reduce the expression of noxious stimulus-evoked Fos-like immunoreactivity in the superficial and deep laminae of the rat spinal cord. Pain 1994;56: 347–352.

14. Hernandez N, Dmitrieva N, Vanegas H. Medullary on-cell activity during tail-flick inhibition produced by hetero-topic noxious stimulation. Pain 1994;58:393–401.

15. Morgan MM, Whitney PK. Behavioral analysis of diffuse noxious inhibitory controls (DNIC): Antinociception and escape reactions. Pain 1996;66:307–312.

16. Pitcher GM, Yashpal K, Coderre TJ, Henry JL. Mechanisms underlying antinociception provoked by heteroseg-mental noxious stimulation in the rat tail-flick test. Neuroscience 1995;65:273–281.

17. Yashpal K, Pitcher GM, Henry JL. Noxious peripheral stimulation produces antinociception mediated via substance P and opioid mechanisms in the rat tail-flick test. Brain Res 1995;674:97–103.

18. Sandrini G, Milanov I, Malaguti S, Nigrelli MP, Moglia A, Nappi G. Effects of hypnosis on diffuse noxious inhibitory controls. Physiol Behav 2000;69:295–300.

19. Kiernan BD, Dane JR, Phillips LH, Price DD. Hypnotic analgesia reduces R-III nociceptive reflex: Further evidence concerning the multifactorial nature of hypnotic analgesia. Pain 1995;60:39–47.

20. Danziger N, Fournier E, Bouhassira D, et al. Different strategies of modulation can be operative during hypnotic analgesia:A neurophysiological study. Pain 1998;75: 85–92.

21. Price D. Psychological Mechanisms of Pain and Analgesia. Progress in Pain Research and Management, vol 15. Seattle: IASP Press, 1999:198–199.

22. Miron D, Duncan GH, Bushnell MC. Effects of attention on the intensity and unpleasantness of thermal pain. Pain 1989;39:345–352.

23. Hodes RL, Howland EW, Lightfoot N, Cleeland CS. The effects of distraction on responses to cold pressor pain. Pain 1990;41:109–114.

24. van der Glas HW, Cadden SW, van der Bilt A. Mechanisms underlying the effects of remote noxious stimulation and mental activities on exteroceptive jaw reflexes in man. Pain 2000;84:193–202.

25. Petrovic P, Petersson KM, Ghatan PH, Stone-Elander S, Ingvar M. Pain-related cerebral activation is altered by a distracting cognitive task. Pain 2000;85:19–30.

26. Bantick SJ, Wise RG, Ploghaus A, Clare S, Smith SM, Tracey I. Imaging how attention modulates pain in humans using functional MRI. Brain 2002;125:310–319.

27. Friederich M, Trippe RH, Ozcan M, Weiss T, Hecht H, Miltner WH. Laser-evoked potentials to noxious stimulation during hypnotic analgesia and distraction of attention suggest different brain mechanisms of pain control. Psychophysiology 2001;38:768–776.

28. Freeman R, Barabasz A, Barabasz M, Warner D. Hypnosis and distraction differ in their effects on cold pressor pain. Am J Clin Hypn 2000;43:137–148.

29. Hilgard ER, Hilgard JR. Hypnosis in the Relief of Pain. Los Altos, California: W. Kaufmann, 1983:63–82.

30. Hilgard ER, Crawford HJ, Wert A. The Stanford Hypnotic Arm Levitation Induction and Test (SHALIT): A six-minute hypnotic induction and measurement scale. Int J Clin Exp Hypn 1979;27:111–124.

31. Sharav Y, Tal M. Masseter inhibitory periods and sensations evoked by electrical tooth-pulp stimulation in subjects under hypnotic anesthesia. Brain Res 1989;479: 247–254.

32. Sharav Y, Tal M. Focused analgesia and generalized relaxation produce differential hypnotic analgesia in response to ascending stimulus intensity. Int J Psychophysiol 2004;52:187–196.

33. De Pascalis V, Chiaradia C, Carotenuto E. The contribution of suggestibility and expectation to placebo analgesia phenomenon in an experimental setting. Pain 2002;96: 393–402.

34. Feine JS, Chapman CE, Lund JP, Duncan GH, Bushnell MC. The perception of painful and nonpainful stimuli during voluntary motor activity in man. Somatosens Mot Res 1990;7:113–124.

35. Lund JP, Rossignol S. Modulation of the amplitude of the digastric jaw opening reflex during the masticatory cycle. Neuroscience 1981;6:95–98.

36. Lund JP, Enomoto S, Hayashi H, et al. Phase-linked variations in the amplitude of the digastric nerve jaw-opening reflex response during fictive mastication in the rabbit. Can J Physiol Pharmacol 1983;61:1122–1128.

Abstracted / indexed in

Science Citation Index (SCI)

Science Citation Index Expanded (SCIE)

BIOSIS Previews

Scopus

Cumulative Index to Nursing and Allied Health Literature (CINAHL)

Submission Turnaround Time

Conferences

Top