Article Data

  • Views 276
  • Dowloads 49

Original Research

Open Access

Evidence for Up-regulated Central Nociceptive Processing in Patients with Masticatory Myofascial Pain

  • Eleni Sarlani1,2,*,
  • Edward G. Grace3
  • Mark A. Reynolds4
  • Joel D. Greenspan2

1Departments Comprehensive Care and Therapeutics, Research Center for Neuroendocrine Influences on Pain, Brotman Facial Pain Center, Dental School, University of Maryland at Baltimore, Baltimore, USA

2Departments Biomedical Sciences, Research Center for Neuroendocrine Influences on Pain, Brotman Facial Pain Center, Dental School, University of Maryland at Baltimore, Baltimore, USA

3Department of Health Promotion and Policy, Research Center for Neuroendocrine Influences on Pain, Brotman Facial Pain Center, University of Maryland at Baltimore, Baltimore, USA

4Department of Periodontics, Research Center for Neuroendocrine, Influences on Pain, Dental School, University of Maryland at Baltimore, Baltimore, USA

DOI: 10.11607/jofph.1841 Vol.18,Issue 1,March 2004 pp.41-55

Published: 30 March 2004

*Corresponding Author(s): Eleni Sarlani E-mail: ens002@dental.umaryland.edu

Abstract

Aims: Previous work suggests that hyperexcitability of central nociceptive neurons may play a role in the pain of temporo-mandibular disorders (TMD). The aim of this study was to test this theory by assessing differences, between myalgic TMD patients and pain-free controls, in temporal summation of mechanically evoked pain and aftersensations following repetitive noxious stimulation. Methods: Sixteen series of 10 repetitive, mildly noxious mechanical stimuli were applied to the fingers of 25 female TMD patients with masticatory myofascial pain and 25 age-matched, pain-free female subjects. All subjects rated the pain intensity and unpleasantness evoked by the first, fifth, and tenth stimuli in the series and their aftersensations at 15 seconds and 1 minute following the last stimulus. Data were analyzed by 3-way repeated-measures analysis of variance. Results: Pain and unpleas-antness ratings increased with repetition of the stimulation (P .0001). In addition, there was a significant trial number × group interaction for the pain intensity ratings, such that TMD patients provided higher ratings than controls for the tenth stimulus (P .001). The increase in unpleasantness ratings with repetitive stimu-lation was also higher for the patient group (P .0001). Moreover, TMD patients rated the intensity of aftersensations as higher (P .005) and reported painful aftersensations at signifi-cantly greater frequency (P .05). Conclusion: A generalized hyperexcitability of central nociceptive processing in this TMD patient group is indicated by their more pronounced temporal summation of pain and greater aftersensations following repetitive noxious digital stimulation versus controls. Such hyperexcitability may contribute to the pathophysiology of TMD pain.

Keywords

myofascial pain syndromes; pain thresholds; temporal summation; temporomandibular disorders; wind-up

Cite and Share

Eleni Sarlani,Edward G. Grace,Mark A. Reynolds,Joel D. Greenspan. Evidence for Up-regulated Central Nociceptive Processing in Patients with Masticatory Myofascial Pain. Journal of Oral & Facial Pain and Headache. 2004. 18(1);41-55.

References

1. Dworkin SF. Personal and societal impact of orofacial pain. In: Fricton JR, Dubner R (eds). Orofacial Pain and Temporomandibular Disorders. New York: Raven Press, 1995:15–32.

2. Okeson JP. Differential diagnosis and management considerations of temporomandibular disorders. In: Okeson JP (ed). Orofacial Pain: Guidelines for Assessment, Diagnosis, and Management. The American Academy of Orofacial Pain. Chicago: Quintessence, 1996:113–184.

3. Dworkin SF, LeResche L. Research diagnostic criteria for temporomandibular disorders: Review, criteria, examinations and specifications, critique. J Craniomandib Disord Facial Oral Pain 1992;6:301–355.

4. Dworkin SF. Perspectives on the interaction of biological, psychological and social factors in TMD. J Am Dent Assoc 1994;125:856–863.

5. Ohrbach R, Dworkin SF. Five-year outcomes in TMD: Relationship of changes in pain to changes in physical and psychological variables. Pain 1998;74:315–326.

6. Ohrbach R, Gale EN. Pressure pain thresholds, clinical assessment, and differential diagnosis: Reliability and validity in patients with myogenic pain. Pain 1989;39: 157–169.

7. Reid KI, Gracely RH, Dubner R. The influence of time, facial side, and location on pain-pressure thresholds in chronic myogenous temporomandibular disorder. J Orofac Pain 1994;8:258–265.

8. Farella M, Michelotti A, Steenks M, Romeo R, Cimino R, Bosman F. The diagnostic value of pressure algometry in myofascial pain of the jaw muscles. J Oral Rehabil 2000; 27:9–14.

9. Sarlani E, Greenspan JD. Evidence for generalized hyper-algesia in temporomandibular disorders patients. Pain 2003;102:221–226.

10. Maixner W, Fillingim R, Sigurdsson A, Kincaid S, Silva S. Sensitivity of patients with painful temporomandibular disorders to experimentally evoked pain: Evidence for altered temporal summation of pain. Pain 1998;76:71–81.

11. Ren K. Wind-up and the NMDA receptor: From animal studies to humans. Pain 1994;59:157–158.

12. Mendell LM, Wall PD. Responses of single dorsal horn cells to peripheral cutaneous unmyelinated fibers. Nature 1965;206:97–99.

13. Mendell LM. Physiology properties of unmyelinated fiber projection to the spinal cord. Exp Neurol 1966;16: 316–332.

14. Price DD, Hu JW, Dubner R, Gracely RH. Peripheral suppression of first pain and central summation of second pain evoked by noxious heat pulses. Pain 1977;3:57–68.

15. Davies SN, Lodge D. Evidence for involvement of N-methyl-aspartate receptors in “wind-up” of class 2 neurones in the dorsal horn of the rat. Brain Res 1987;424: 402–406.

16. Dickenson AH, Sullivan AF. Evidence for a role of the NMDA receptor in the frequency dependent potentiation of deep rat dorsal horn nociceptive neurones following C fibre stimulation. Neuropharmacology 1987;26:1235–1238.

17. Price DD, Mao J, Frenk H, Mayer DJ. The N-methyl-D-aspartate receptor antagonist dextromethorphan selectively reduces temporal summation of second pain in man. Pain 1994;59:165–174.

18. Arendt-Nielsen L, Petersen-Felix S, Fischer M, Bak P, Bjerring P, Zbinden AM. The effect of N-methyl-D-aspar-tate antagonist (ketamine) on single and repeated nociceptive stimuli: A placebo-controlled experimental human study. Anesth Analg 1995;81:63–68.

19. Vierck CJ Jr, Cannon RL, Fry G, Maixner W, Whitsel BL. Characteristics of temporal summation of second pain sensations elicited by brief contact of glabrous skin by a preheated thermode. J Neurophysiol 1997;78:992–1002.

20. Riley JL III, Robinson ME, Wise EA, Price DD. A meta-analytic review of pain perception across the menstrual cycle. Pain 1999;81:225–235.

21. Greenspan JD, McGillis SLB. Stimulus features relevant to the perception of sharpness and mechanically evoked cutaneous pain. Somatosens Motor Res 1991;8:137–147.

22. Gescheider GA. The classical psychophysical methods. In: Gescheider GA (ed). Psychophysics: The Fundamentals. Mahwah, NJ: Lawrence Erlbaum Associates, 1997:45–72.

23. Slugg RM, Meyer RA, Campbell JN. Response of cutaneous A- and C-fiber nociceptors in the monkey to controlled-force stimuli. J Neurophysiol 2000;83:2179–2191.

24. Raja SN, Meyer RA, Ringkamp M, Campbell JN. Peripheral neural mechanisms of nociception. In: Wall PD, Melzack R (eds). Textbook of Pain. Edinburgh: Churchill Livingstone, 1999:11–57.

25. Price DD, McGrath PA, Rafii A, Buckingham B. The validation of visual analogue scales as ratio scale measures for chronic and experimental pain. Pain 1983;17:45–56.

26. Maixner W, Fillingim R, Booker D, Sigurdsson A. Sensitivity of patients with painful temporomandibular disorders to experimentally evoked pain. Pain 1995; 63:341–351.

27. Svensson P, List T, Hector G. Analysis of stimulus-evoked pain in patients with myofascial temporomandibular pain disorders. Pain 2001;92:399–409.

28. Malow RM, Grimm L, Olson RE. Differences in pain perception between myofascial pain dysfunction patients and normal subjects: A signal detection analysis. J Psychosom Res 1980;24:303–309.

29. Molin C, Edman G, Schalling D. Psychological studies of patients with mandibular pain dysfunction syndrome. 2. Tolerance for experimentally induced pain. Sven Tandlak Tidskr 1973;66:15–23.

30. Maixner W, Fillingim R, Kincaid S, Sigurdsson A, Harris MB. Relationship between pain sensitivity and resting arterial blood pressure in patients with painful temporo-mandibular disorders. Psychosom Med 1997;59:503–511.

31. Kashima K, Rahman O, Sakoda S, Shiba R. Increased pain sensitivity of the upper extremities of TMD patients with myalgia to experimentally-evoked noxious stimulation: possibility of worsened endogenous opioid systems. Cranio 1999;17:241–246.

32. Sharav Y, McGrath PA, Dubner R. Masseter inhibitory periods and sensations evoked by electrical tooth pulp stimulation in patients with oralfacial pain and mandibular dysfunction. Arch Oral Biol 1982;27:305–310.

33. Davidson R, Gale EN. Cutaneous sensory thresholds from skin overlying masseter and forearm in MPD patients and controls. J Dent Res 1983;62:555–558.

34. Svensson P, Arendt-Nielsen L, Nielsen H, Larsen JK. Effect of chronic and experimental jaw muscle pain on pain-pressure thresholds and stimulusresponse curves. J Orofac Pain 1995;9:347–356.

35. Curran SL, Carlson CR, Okeson JP. Emotional and physiologic responses to laboratory challenges: Patients with temporomandibular disorders versus matched control subjects. J Orofac Pain 1996;10:141–150.

36. Carlson CR, Reid KI, Curran SL, et al. Psychological and physiological parameters of masticatory muscle pain. Pain 1998;76:297–307.

37. Bragdon EE, Light KC, Costello NL, Sigurdsson A, Bunting S, Bhalang K. Group differences in pain modula-tion: Pain-free women compared to pain-free men and to women with TMD. Pain 2002;96:227–237.

38. Hagberg C, Hellsing G, Hagberg M. Perception of cutaneous electrical stimulation in patients with craniomandibular disorders. J Craniomandib Disord Facial Oral Pain 1990;4:120–125.

39. Dubner R. Neuronal plasticity and pain following peripheral tissue inflammation or nerve injury. In: Bond MR, Charlton JE, Woolf CJ (eds). Pain Research and Clinical Management. Vol 4: Proceedings of the VIth World Congress on Pain. Amsterdam: Elsevier, 1991:263–276.

40. Coderre TJ, Katz J, Vaccarino AL, Melzack R. Contri-bution of central neuroplasticity to pathological pain: Review of clinical and experimental evidence. Pain 1993;52:259–285.

41. Ren K, Hylden JLK, Williams GM, Ruda MA, Dubner R. The effects of a non-competitive NMDA receptor antagonist, MK-801, on behavioral hyperalgesia and dorsal horn neuronal activity in rats with unilateral inflammation. Pain 1992;50:331–344.

42. Huber M, Hall E. A comparison of the signs of temporo-mandibular joint dysfunction and occlusal discrepancies in a symptom-free population of men and women. Oral Surg Oral Med Oral Pathol 1990;70:180–183.

43. Turp JC, Kowalski CJ, Stohler CS. Temporomandibular disorders—Pain outside the head and face is rarely acknowledged in the chief complaint. J Prosthet Dent 1997;78:592–595.

44. Turp JC, Kowalski CJ, O’Leary N, Stohler CS. Pain maps from facial pain patients indicate a broad pain geography. J Dent Res 1998;77:1465–1472.

45. Yap A, Tan K, Chua E, Tan H. Depression and somatization in patients with temporomandibular disorders. J Prosthet Dent 2002;88:479–484.

46. Von Korff M, Ormel J, Keefe FJ, Dworkin SF. Grading the severity of chronic pain. Pain 1992;50:133–149.

47. Lautenbacher S, Rollman GB, McCain GA. Multi-method assessment of experimental and clinical pain in patients with fibromyalgia. Pain 1994;59:45–53.

48. Kosek E, Ekholm J, Hansson P. Modulation of pressure pain thresholds during and following isometric contraction in patients with fibromyalgia and in healthy controls. Pain 1996;64:415–423.

49. Vierck CJ Jr, Staud R, Price DD, Cannon RL, Mauderli AP, Martin A. The effect of maximal exercise on temporal summation of second pain (windup) in patients with fibromyalgia syndrome. J Pain 2001;2:334–344.

50. Sorensen J, Graven-Nielsen T, Henriksson KG, Bengtsson M, Arendt-Nielsen L. Hyperexcitability in fibromyalgia. J Rheumatol 1998;25:152–155.

51. Staud R, Vierck CJ, Cannon RL, Mauderli AP, Price DD. Abnormal sensitization and temporal summation of second pain (wind-up) in patients with fibromyalgia syn-drome. Pain 2001;91:165–175.

52. Price DD, Staud R, Robinson ME, Mauderli AP, Cannon R, Vierck CJ. Enhanced temporal summation of second pain and its central modulation in fibromyalgia patients. Pain 2002;99:49–59.

53. Staud R, Cannon RC, Mauderli AP, Robinson ME, Price DD, Vierck CJ. Temporal summation of pain from mechanical stimulation of muscle tissue in normal controls and subjects with fibromyalgia syndrome. Pain 2003; 102:87–95.

54. Langemark M, Jensen K, Jensen TS, Olesen J. Pressure pain thresholds and thermal nociceptive thresholds in chronic tension-type headache. Pain 1989;38:203–210.

55. Bendtsen L, Jensen R, Olesen J. Decreased pain detection and tolerance thresholds in chronic tension-type headache. Arch Neurol 1996;53:373–376.

56. Fusco BM, Colantoni O, Giacovazzo M. Alteration of central excitation circuits in chronic headache and analgesic misuse. Headache 1997;37:486–491.

57. Kleinbohl D, Holzl R, Moltner A, Rommel C, Weber C, Osswald PM. Psychophysical measures of sensitization to tonic heat discriminate chronic pain patients. Pain 1999; 81:35–43.

58. Curatolo M, Petersen-Felix S, Arendt-Nielsen L, Giani C, Zbinden AM, Radanov BP. Central hyperexcitability in chronic pain after whiplash injury. Clin J Pain 2001;17: 306–315.

59. Koelbaek Johansen M, Graven-Nielsen T, Schou Olesen A, Arendt-Nielsen L. Generalised muscular hyperalgesia in chronic whiplash syndrome. Pain 1999;83:229–234.

60. Sharav Y, Singer E, Schmidt E, Dionne RA, Dubner R. The analgesic effect of amitriptyline on chronic facial pain. Pain 1987;31:199–209.

61. Herrero JF, Cervero F. Changes in nociceptive reflex facil-itation during carrageenan-induced arthritis. Brain Res 1996;717:62–68.

62. Traub RJ. Spinal modulation of the induction of central sensitization. Brain Res 1997;778:34–42.

63. Ren K, Dubner R. Central nervous system plasticity and persistent pain. J Orofac Pain 1999;13:155–163.

64. Sessle BJ. Acute and chronic craniofacial pain: Brain stem mechanisms of nociceptive transmission and neuroplasticity, and their clinical correlates. Crit Rev Oral Biol Med 2000;11:57–91.

65. McMillan AS, Blasberg B. Pain-pressure threshold in painful jaw muscles following trigger point injection. J Orofac Pain 1994;8:384–390.

66. Okeson JP. Etiology of functional disturbances in the masticatory system. In: Okeson JP (ed). Management of Temporomandibular Disorders and Occlusion, ed 4. St Louis: Mosby, 2003:149–179.

67. Fillingim RB, Maixner W, Kincaid S, Silva S. Sex differ-ences in temporal summation but not sensory-discriminative processing of thermal pain. Pain 1998;75:121–127.

68. Sarlani E, Greenspan JD. Gender differences in temporal summation of mechanically evoked pain. Pain 2002;97: 163–169.

69. Staud R, Robinson ME, Vierck CJ Jr, Price DD. Diffuse noxious inhibitory controls (DNIC) attenuate temporal summation of second pain in normal males but not in normal females or fibromyalgia patients. Pain 2003;101: 167–174.

70. Unruh AM. Gender variations in clinical pain experience. Pain 1996;65:123–167.

71. Drangsholg M, LeResche L. Temporomandibular disorder pain. In: Crombie IK (ed). Epidemiology of Pain. Seattle: IASP Press, 1999:203–233.

72. Fillingim RB, Maixner W, Kincaid S, Sigurdsson A, Harris MB. Pain sensitivity in patients with temporomandibular disorders: Relationship to clinical and psychosocial fac-tors. Clin J Pain 1996;12:260–269.

73. Cornwall A, Donderi DC. The effect of experimentally induced anxiety on the experience of pressure pain. Pain 1988;35:105–113.

74. Rhudy JL, Meagher MW. Fear and anxiety: Divergent effects on human pain thresholds. Pain 2000;84:65–75.

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