Fogorvosi szemle, 2005 (98. évfolyam, 1-6. szám)

2005-10-01 / 5. szám

192 FOGORVOSI SZEMLE ■ 98. évf. 5. sz. 2005. 30. Mchaffie JG, Larson MA, Stein BE: Response properties of noci­ceptive and low-threshold neurons in rat trigeminal pars caudalis. J Comp Neurol 1994;15:409-425. 31. Nähri M, Jyvasjarvi E, Virtanen A, Huopaniemi T, Ngassapa D, Hirvonen T: Role of intradental A- and C-type nerve fibres in dental pain mechanisms. Proc Finn Dent Soc 1992;88 Suppl: 507-516. 32. Nähri MVO: The Characteristics of Intradental Sensory Units and Their Responses to Stimulation. J Dent Res 1985; 64: 564-571. 33. Nord SG, Young RF: Projection of tooth pulp afferents to the cat trigeminal nucleus caudais. Brain Res 1975;90:195-204. 34. Nord SG: Electrical stimulation of the tooth pulp in the study of pain. Brain Res Bull 1976;1: 251-254. 35-Palestini M, Mariottoi M, Velasco JM, Formenti A, Mancia M: Medialis dorsalis thalamic unitary response to tooth pulp stimulation and its conditioning by brainstem and limbic activation. Neurosci Lett 1987;78: 161-165. 36. Park SJ, Chiang CY, Hu JW, Sessle BJ: Neuroplasticity induced by tooth pulp stimulation in trigeminus subnucleus oralis involves NMDA receptor mechanisms. J Neurophysiol 2001 ;85:1836-1846. 37. Pertovaara A, Huopaniemi T, Carlson S, Jyvasjarvi E: Response characteristics of tooth pulp-driven postsynaptic neurons in the spinal trigeminal subnucleus interpolaris of the cat: comparison with primary afferent fiber, subnucleus caudalis, reflex, and sensory responses. Brain Res 1987;422: 205-217. 38. Poggio GF, Mountcastle VB: A study of the functional contribu­tions of the lemniscal and spinothalamic systems to somatic sensibi­lity. Central nervous mechanisms in pain. Bull Johns Hopkins Hosp 1960;106:266-316. 39. Raab WHM: Akuter und chronischer Zahnschmerz. Dtsch Zahn­­ärzf/Z1991;46:101-108. 40. Sessle BJ, Hu JW, Amano N, Zhong G: Convergence of Cutaneous, Tooth Pulp, Visceral, Neck and Muscle Afferents onto Nociceptive and Non-nociceptive Neurones in Trigeminal Subnucleus Caudalis (Medullary dorsal Horn) and its Implications for Referred Pain. Pain 1986;27:219-235. 41. Sessle BJ: The neurobiology of facial and dental pain: present knowledge, future directions. J Dent Res 1987;66: 962-981. 42. Taiwo U, Fabian A, Pazoles C, Fields HL: Further studies on the mechanism of the potentiation of morphine antinociception of the monoamine uptake inhibitors. Pain 1985;21: 329-338. 43. TAKEMURA M, Nagase Y, Yoshida A, Yasuda K, Kitamura S, Shige­­naga Y, Matano S: The central projections of the monkey tooth pulp afferent neurons. Somatosens Mot Res 1993;10: 217-227. 44. Von Knorring L, Almay BG, Haggendal J, Johansson F, Oreland L, Wetterberg L: Discrimination of idiopathic pain syndromes from neurogenic pain syndromes and healthy volunteers by means of cli­nical rating, personality traits, monoamine metabolites in CSF, serum cortisol, platelet MAO and urinary melatonin. Eur Arch Psychiatry Neurol Sei 1986;236: 131-138. 45. Walker JM, Bowen WD, Thompson LA, Frascella J, LehmkuhleS, Hughes HC: Distribution of opiate receptors within visual structures of the cat brain. Exp Brain Res 1988;73: 523-532. 46. WodaA: Pain in the Trigeminal System: from orofacial Nociception to neuronal Network Modeling. J Dent Res 2003;82: 764-768. 47. Yonerhara N, ShibutaniT, Imai Y, Inoki R: Involvement of descen­ding monoaminergic systems in the transmission of dental pain in the trigeminal nucleus caudalis of the rabbit. Brain Res. 1990;508: 234-240. 48. Young RF, Perryman KM: Pathways for orofacial pain sensation in the trigeminal brain-stem nuclear complex of the Macaque monkey. J Neurosurg 1984;61: 563-568. 49. ZELLES T: A fogak érző tevékenysége. In: Zelles T (ed.): Orálbio­­iógiai Előadások. Budapest, 135-140. Perényi J, Fazekas A, Benedek Gy: Neurophysiological Background of Pain in the Orofacial Area Review of the literature The article presents an overview on the peripheral and central neural mechanisms underlying pain in the orofacial area. First a definition of pain and a description of general aspects of orofacial pain are presented. Characteristics of acute and chronic pain are also described. The study highlights the sense organs, the molecular mechanisms and categories of pri­mary afferents involved in peripheral events of orofacial pain. After describing the brain-stem nuclei participating in trigem­inal pain and their functional role, primary afferents involved in nociceptive sensation from the tooth pulp, explanations of dentinal sensitivity and differences between the brain-stem endings of primary afferents among different species are discussed in details. The role of higher brain centres, with a special emphasis on the thalamus and somatosensory cor­tex in the development of orofacial pain sensation is considered. The last section provides a review about how the activ­ities of nociceptive neurons are controlled by higher brain centres and neurochemicals involved in pain transmission. Key words: orofacial pain, dentinal sensitivity, trigeminal nociceptive sensation, modulation of pain, neural aspects of pain

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