Title
Author
DOI
Article Type
Special Issue
Volume
Issue
Integration of nociceptive activity from orofacial, cranial and cervical regions in the trigeminocervical nucleus: a scoping review with clinical implications
1Faculty of Economics and Social Sciences, University of Applied Sciences Osnabrück, 49076 Osnabrück, NDS, Germany
2Post-Graduation Program in Oral and Maxillofacial Surgery, Piracicaba Dental School, State University of Campinas, UNICAMP, 13083-857 Piracicaba, SP, Brazil
3Obstetrics and Gynaecology, IWK Health Center, Halifax, NS B3K 6R8, Canada
4Geoffrey and Robyn Sperber Health Sciences Library, University of Alberta, Edmonton, AB T6G 1C9, Canada
5Faculty of Dentistry, National University of Singapore, 119077, Singapore, Singapore
6Department of Physical Therapy, Faculties of Rehabilitation Medicine and Medicine and Dentistry, University of Alberta, Edmonton, AB T6G 2R3, Canada
DOI: 10.22514/jofph.2025.042 Vol.39,Issue 3,September 2025 pp.1-12
Submitted: 30 April 2024 Accepted: 27 August 2024
Published: 12 September 2025
*Corresponding Author(s): Susan Armijo-Olivo E-mail: sla4@ualberta.ca; s.armijo-olivo@hs-osnabrueck.de
† These authors contributed equally.
A connection between orofacial, cranial and cervical regions has been documented through the trigeminocervical nucleus (TCN), but the predominant direction (orofacial/cranial-to-cervical or cervical-to-orofacial/cranio) of this connection still remains unclear. This scoping review was designed to determine the dominant direction of the connection between these two areas. Searches were conducted by combining these concepts: TCN, cervical and face/jaw/head region. Eighty-three studies were included. The most predominant direction was reported to be from the orofacial/cranial to the cervical region, with most of the studies conducted in mammals. The clinical implications of these findings for the spread and referral of pain between these regions are examined and discussed.
Spinal trigeminal nucleus; Trigeminocervical nucleus; Nociception; Pain perception; Neck pain; Facial pain; Headache; Cervicogenic pain; Temporomandibular disorders
Felix Pankrath,Elisa Bizetti Pelai,Ana Izabela Sobral de Oliveira-Souza,Fatemeh Baghbaninaghadehi,Liz Dennett,Peter Svensson,Harry von Piekartz,Susan Armijo-Olivo. Integration of nociceptive activity from orofacial, cranial and cervical regions in the trigeminocervical nucleus: a scoping review with clinical implications. Journal of Oral & Facial Pain and Headache. 2025. 39(3);1-12.
[1] Safiri S, Kolahi AA, Hoy D, Buchbinder R, Mansournia MA, Bettampadi D, et al. Global, regional, and national burden of neck pain in the general population, 1990–2017: systematic analysis of the Global Burden of Disease Study 2017. The BMJ. 2020; 368: m791.
[2] Slade GD, Ohrbach R, Greenspan JD, Fillingim RB, Bair E, Sanders AE, et al. Painful temporomandibular disorder: decade of discovery from OPPERA studies. Journal of Dental Research. 2016; 95: 1084–1092.
[3] Racich MJ. Occlusion, temporomandibular disorders, and orofacial pain: an evidence-based overview and update with recommendations. Journal of Prosthetic Dentistry. 2018; 120: 678–685.
[4] Castien R, De Hertogh W. A neuroscience perspective of physical treatment of headache and neck pain. Frontiers in Neurology. 2019; 10: 276.
[5] De Laat A, Meuleman H, Stevens A, Verbeke G. Correlation between cervical spine and temporomandibular disorders. Clinical Oral Investigations. 1998; 2: 54–57.
[6] Xiong G, Matsushita M. Upper cervical afferents to the motor trigeminal nucleus and the subnucleus oralis of the spinal trigeminal nucleus in the rat: an anterograde and retrograde tracing study. Neuroscience Letters. 2000; 286: 127–130.
[7] Yin CS, Lee YJ, Lee YJ. Neurological influ-ences of the temporomandibular joint. Journal of Bodywork and Movement Therapies. 2007; 11: 285–294.
[8] Armijo-Olivo S, Magee D. Cervical musculoskeletal impairments and temporomandibular disorders. Journal of Oral & Maxillofacial Research. 2013; 3: e4.
[9] Bogduk N. The clinical anatomy of the cervical dorsal rami. Spine. 1982; 7: 319–330.
[10] Möller M, May A. The unique role of the trigeminal autonomic reflex and its modulation in primary headache disorders. Current Opinion in Neurology. 2019; 32: 438–442.
[11] Henssen A, Zilles K, Palomero-Gallagher N, Schleicher A, Mohlberg H, Gerboga F, et al. Cytoarchitecture and probability maps of the human medial orbitofrontal cortex. Cortex. 2016; 75: 87–112.
[12] Kerr FWL. Structural relation of the trigeminal spinal tract to upper vervical roots and the solitary nucleus in the cat. Experimental Neurology. 1961; 4: 134–148.
[13] Olszewski J. On the anatomical and functional organization of the spinal trigeminal nucleus. Journal of Comparative Neurology. 1950; 92: 401–413.
[14] Bartsch T, Goadsby PJ. The trigeminocervical complex and migraine: current concepts and synthesis. Current Pain and Headache Reports. 2003; 7: 371–376.
[15] Hu JW, Sun KQ, Vernon H, Sessle BJ. Craniofacial inputs to upper cervical dorsal horn: implications for somatosensory information processing. Brain Research. 2005; 1044: 93–106.
[16] Bradnam L, Barry C. The role of the trigeminal sensory nuclear complex in the pathophysiology of craniocervical dystonia. The Journal of Neuroscience. 2013; 33: 18358–18367.
[17] Henssen D, Derks B, van Doorn M, Verhoogt NC, Staats P, Vissers K, et al. Visualizing the trigeminovagal complex in the human medulla by combining ex-vivo ultra-high resolution structural MRI and polarized light imaging microscopy. Scientific Reports. 2019; 9: 11305.
[18] Schueler M, Messlinger K, Dux M, Neuhuber WL, De R. Extracranial projections of meningeal afferents and their impact on meningeal nociception and headache. Pain. 2013; 154: 1622–1631.
[19] Schueler M, Neuhuber W, De Col R, Messlinger K. Innervation of rat and human dura mater and pericranial tissues by meningeal afferents. Headache. 2014; 54: 996–1009.
[20] Armijo-Olivo S, Bravo J, Magee DJ, Thie NM, Major PW, Flores-Mir C. The association between head and cervical posture and temporomandibular disorders: a systematic review. Journal of Oral & Facial Pain and Headache. 2006; 20: 9–23.
[21] Browne PA, Clark GT, Kuboki T, Adachi NY. Concurrent cervical and craniofacial pain. A review of empiric and basic science evidence. Oral Surgery, Oral Medicine, Oral Pathology, and Oral Radiology. 1998; 86: 633–640.
[22] Haldeman S, Dagenais S. Cervicogenic headaches: a critical review. The Spine Journal. 2001; 1: 31–46.
[23] Ashkenazi A, Levin M. Greater occipital nerve block for migraine and other headaches: is it useful? Current Pain & Headache Reports. 2007; 11: 231–235.
[24] Piovesan EJ, Kowacs PA, Oshinsky ML. Convergence of cervical and trigeminal sensory afferents. Current Pain & Headache Reports. 2003; 7: 377–383.
[25] Arksey H, O’Malley L. Scoping studies: towards a methodological framework. International Journal of Social Research Methodology. 2005; 8: 19–32.
[26] Tricco AC, Lillie E, Zarin W, O’Brien KK, Colquhoun H, Levac D, et al. PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Annals of Internal Medicine. 2018; 169: 467–473.
[27] Peters MDJ, Marnie C, Tricco AC, Pollock D, Munn Z, Alexander L, et al. Updated methodological guidance for the conduct of scoping reviews. JBI Evidence Synthesis. 2020; 18: 2119–2126.
[28] Stannard CF, Kalso E, Ballantyne J. Evidence-based chronic pain management. 5th edn. Wiley-Blackwell/BMJ: Chichester, UK/Hoboken, NJ. 2010.
[29] Vadivelu N, Vadivelu A, Kaye AD. Orofacial pain. 1st edn. Springer International Publishing: Cham. 2014.
[30] Becher B, Lozano-López C, Castro-Carletti EM, Hoffmann M, Becher C, Mesa-Jimenez J, et al. Effectiveness of therapeutic exercise for the management of cervicogenic headache: a systematic review. Musculoskeletal Science & Practice. 2023; 66: 102822.
[31] Guzman J, Hurwitz EL, Carroll LJ, Haldeman S, Côté P, Carragee EJ, et al. A new conceptual model of neck pain: linking onset, course, and care: the bone and joint decade 2000–2010 task force on neck pain and its associated disorders. Spine. 2008; 33: S14–S23.
[32] Bogduk N. The anatomy and pathophysiology of neck pain. Physical Medicine and Rehabilitation Clinics of North America. 2011; 22: 367–382, vii.
[33] Chibuzo GA, Cummings JF. The origins of the afferent fibers to the lingual muscles of the dog, a retrograde labelling study with horseradish peroxidase. The Anatomical Record. 1981; 200: 95–101.
[34] Chudler EH, Foote WE, Poletti CE. Responses of cat C 1 spinal cord dorsal and ventral horn neurons to noxious and non-noxious stimulation of the head and face. Brain Research. 1991; 555: 181–192.
[35] Classey JD, Knight YE, Goadsby PJ. The NMDA receptor antagonist MK-801 reduces Fos-like immunoreactivity within the trigeminocervical complex following superior sagittal sinus stimulation in the cat. Brain Research. 2001; 907: 117–124.
[36] Hirata H, Takeshita S, Hu JW, Bereiter DA. Cornea-responsive medullary dorsal horn neurons: modulation by local opioids and projections to thalamus and brain stem. Journal of Neurophysiology. 2000; 84: 1050–1061.
[37] Goadsby PJ, Zagami AS. Stimulation of the superior sagittal sinus increases metabolic activity and blood flow in certain regions of the brainstem and upper cervical spinal cord of the cat. Brain. 1991; 114: 1001–1011.
[38] Hu JW, Sessle BJ, Raboisson P, Dallel R, Woda A. Stimulation of craniofacial muscle afferents induces prolonged facilitatory effects in trigeminal nociceptive brain-stem neurones. Pain. 1992; 48: 53–60.
[39] Kubo A, Sugawara S, Iwata K, Yamaguchi S, Mizumura K. Masseter muscle contraction and cervical muscle sensitization by nerve growth factor cause mechanical hyperalgesia in masticatory muscle with activation of the trigemino-lateral parabrachial nucleus system in female rats. Headache. 2022; 62: 1365–1375.
[40] Marfurt CF, Rajchert DM. Trigeminal primary afferent projections to “non-trigeminal” areas of the rat central nervous system. Journal of Comparative Neurology. 1991; 303: 489–511.
[41] Luo P, Wong R, Dessem D. Projection of jaw-muscle spindle afferents to the caudal brainstem in rats demonstrated using intracellular biotinamide. The Journal of Comparative Neurology. 1995; 358: 63–78.
[42] Panneton WM. Primary afferent projections from the upper respiratory tract in the muskrat. Journal of Comparative Neurology. 1991; 308: 51–65.
[43] Nishimori T, Sera M, Suemune S, Yoshida A, Tsuru K, Tsuiki Y, et al. The distribution of muscle primary afferents from the masseter nerve to the trigeminal sensory nuclei. Brain Research. 1986; 372: 375–381.
[44] Sugimoto T, Fujiyoshi Y, Xiao C, He YF, Ichikawa H. Central projection of calcitonin gene-related peptide (CGRP)- and substance P (SP)-immunoreactive trigeminal primary neurons in the rat. The Journal of Comparative Neurology. 1997; 378: 425–442.
[45] Vos BP, Strassman AM. Fos expression in the medullary dorsal horn of the rat after chronic constriction injury to the infraorbital nerve. The Journal of Comparative Neurology. 1995; 357: 362–375.
[46] Adachi K, Shimizu K, Hu JW, Suzuki I, Sakagami H, Koshikawa N, et al. Purinergic receptors are involved in tooth-pulp evoked nocifensive behavior and brainstem neuronal activity. Molecular Pain. 2010; 6: 59.
[47] Bereiter DA, Bereiter DF, Ramos M. Vagotomy prevents morphine-induced reduction in Fos-like immunoreactivity in trigeminal spinal nucleus produced after TMJ injury in a sex-dependent manner. Pain. 2002; 96: 205–213.
[48] Bereiter DA. Sex differences in brainstem neural activation after injury to the TMJ region. Cells Tissues Organs. 2001; 169: 226–237.
[49] Busch V, Jakob W, Juergens T, Schulte-Mattler W, Kaube H, May A. Functional connectivity between trigeminal and occipital nerves revealed by occipital nerve blockade and nociceptive blink reflexes. Cephalalgia. 2006; 26: 50–55.
[50] Casatti CA, Frigo L, Bauer JA. Origin of sensory and autonomic innervation of the rat temporomandibular joint: a retrograde axonal tracing study with the fluorescent dye fast blue. Journal of Dental Research. 1999; 78: 776–783.
[51] Chiaia NL, Hess PR, Hosoi M, Rhoades RW. Morphological characteristics of low-threshold primary afferents in the trigeminal subnuclei interpolaris and caudalis (the medullary dorsal horn) of the golden hamster. Journal of Comparative Neurology. 1987; 264: 527–546.
[52] Demartini C, Tassorelli C, Zanaboni AM, Tonsi G, Francesconi O, Nativi C, et al. The role of the transient receptor potential ankyrin type-1 (TRPA1) channel in migraine pain: evaluation in an animal model. Journal of Headache & Pain. 2017; 18: 94.
[53] Du BL, Li JN, Guo HM, Li S, Liu B. The effect of functional mandibular shift on the muscle spindle systems in head-neck muscles and the related neurotransmitter histamine. Journal of Craniofacial Surgery. 2017; 28: 1628–1634.
[54] Hathaway CB, Hu JW, Bereiter DA. Distribution of Fos-like immunoreactivity in the caudal brainstem of the rat following noxious chemical stimulation of the temporomandibular joint. Journal of Comparative Neurology. 1995; 356: 444–456.
[55] Honda K, Kitagawa J, Sessle BJ, Kondo M, Tsuboi Y, Yonehara Y, et al. Mechanisms involved in an increment of multimodal excitability of medullary and upper cervical dorsal horn neurons following cutaneous capsaicin treatment. Molecular Pain. 2008; 4: 59.
[56] Honda K, Noma N, Shinoda M, Miyamoto M, Katagiri A, Kita D, et al. Involvement of peripheral ionotropic glutamate receptors in orofacial thermal hyperalgesia in rats. Molecular Pain. 2011; 7: 75.
[57] Imbe H, Ren K. Orofacial deep and cutaneous tissue inflammation differentially upregulates preprodynorphin mRNA in the trigeminal and paratrigeminal nuclei of the rat. Brain Research Molecular Brain Research. 1999; 67: 87–97.
[58] Jacquin MF, Renehan WE, Mooney RD, Rhoades RW. Structure-function relationships in rat medullary and cervical dorsal horns. I. Trigeminal primary afferents. Journal of Neurophysiology. 1986; 55: 1153–1186.
[59] Jacquin MF, Rhoades RW. Central projections of the normal and ‘regenerate’ infraorbital nerve in adult rats subjected to neonatal unilateral infraorbital lesions: a transganglionic horseradish peroxidase study. Brain Research. 1983; 269: 137–144.
[60] Kamimura R, Hossain MZ, Unno S, Ando H, Masuda Y, Takahashi K, et al. Inhibition of 2-arachydonoylgycerol degradation attenuates orofacial neuropathic pain in trigeminal nerve-injured mice. Journal of Oral Science. 2018; 60: 37–44.
[61] Kato S, Papuashvili N, Okada YC. Identification and functional characterization of the trigeminal ventral cervical reflex pathway in the swine. Clinical Neurophysiology. 2003; 114: 263–271.
[62] Kaube H, Keay KA, Hoskin KL, Bandler R, Goadsby PJ. Expression of c-Fos-like immunoreactivity in the caudal medulla and upper cervical spinal cord following stimulation of the superior sagittal sinus in the cat. Brain Research. 1993; 629: 95–102.
[63] Kiyomoto M, Shinoda M, Honda K, Nakaya Y, Dezawa K, Katagiri A, et al. p38 phosphorylation in medullary microglia mediates ectopic orofacial inflammatory pain in rats. Molecular Pain. 2015; 11: 48.
[64] Kiyomoto M, Shinoda M, Okada-Ogawa A, Noma N, Shibuta K, Tsuboi Y, et al. Fractalkine signaling in microglia contributes to ectopic orofacial pain following trapezius muscle inflammation. Journal of Neuroscience. 2013; 33: 7667–7680.
[65] Kobayashi A, Shinoda M, Sessle BJ, Honda K, Imamura Y, Hitomi S, et al. Mechanisms involved in extraterritorial facial pain following cervical spinal nerve injury in rats. Molecular Pain. 2011; 7: 12.
[66] Kramer PR, Bellinger LL. Reduced GABAA receptor a6 expression in the trigeminal ganglion enhanced myofascial nociceptive response. Neuroscience. 2013; 245: 1–11.
[67] Kramer PR, Bellinger LL. Infusion of Gabra6 siRNA into the trigeminal ganglia increased the myogenic orofacial nociceptive response of ovariectomized rats treated with 17b-estradiol. Neuroscience. 2014; 278: 144–153.
[68] Kurose M, Imbe H, Nakatani Y, Hasegawa M, Fujii N, Takagi R, et al. Bilateral increases in ERK activation at the spinomedullary junction region by acute masseter muscle injury during temporomandibular joint inflammation in the rats. Experimental Brain Research. 2017; 235: 913–921.
[69] Lam DK, Sessle BJ, Hu JW. Surgical incision can alter capsaicin-induced central sensitization in rat brainstem nociceptive neurons. Neuroscience. 2008; 156: 737–747.
[70] Lam DK, Sessle BJ, Hu JW. Glutamate and capsaicin effects on trigeminal nociception II: activation and central sensitization in brainstem neurons with deep craniofacial afferent input. Brain Research. 2009; 1253: 48–59.
[71] Li CX, Yang Q, Vemulapalli S, Waters RS. Forelimb amputation-induced reorganization in the cuneate nucleus (CN) is not reflected in large-scale reorganization in rat forepaw barrel subfield cortex (FBS). Brain Research. 2013; 1526: 26–43.
[72] Li KW, Yu YP, Zhou C, Kim DS, Lin B, Sharp K, et al. Calcium channel a2δ1 proteins mediate trigeminal neuropathic pain states associated with aberrant excitatory synaptogenesis. Journal of Biological Chemistry. 2014; 289: 7025–7037.
[73] Liu MG, Matsuura S, Shinoda M, Honda K, Suzuki I, Shibuta K, et al. Metabotropic glutamate receptor 5 contributes to inflammatory tongue pain via extracellular signal-regulated kinase signaling in the trigeminal spinal subnucleus caudalis and upper cervical spinal cord. Journal of Neuroinflammation. 2012; 9: 258.
[74] Luz LL, Fernandes EC, Dora F, Lukoyanov NV, Szucs P, Safronov BV. Trigeminal Aδ- and C-afferent supply of lamina I neurons in the trigeminocervical complex. Pain. 2019; 160: 2612–2623.
[75] Lyubashina OA, Panteleev SS, Sokolov AY. Inhibitory effect of high-frequency greater occipital nerve electrical stimulation on trigeminovascular nociceptive processing in rats. Journal of Neural Transmission. 2017; 124: 171–183.
[76] Lyubashina OA, Sokolov AY, Panteleev SS. Vagal afferent modulation of spinal trigeminal neuronal responses to dural electrical stimulation in rats. Neuroscience. 2012; 222: 29–37.
[77] Marfurt CF, Turner DF. The central projections of tooth pulp afferent neurons in the rat as determined by the transganglionic transport of horseradish peroxidase. Journal of Comparative Neurology. 1984; 223: 535–547.
[78] Margolis TP, LaVail JH, Setzer PY, Dawson CR. Selective spread of herpes simplex virus in the central nervous system after ocular inoculation. Journal of Virology. 1989; 63: 4756–4761.
[79] Matsumoto S, Takeda M, Tanimoto T. Effects of electrical stimulation of the tooth pulp and phrenic nerve fibers on C-1 spinal neurons in the rat. Experimental Brain Research. 1999; 126: 351–358.
[80] Miyamoto M, Tsuboi Y, Takamiya K, Huganir RL, Kondo M, Shinoda M, et al. Involvement of GluR2 and GluR3 subunit C-termini in the trigeminal spinal subnucleus caudalis and C1-C2 neurons in trigeminal neuropathic pain. Neuroscience Letters. 2011; 491: 8–12.
[81] Morch CD, Hu JW, Arendt-Nielsen L, Sessle BJ. Convergence of cutaneous, musculoskeletal, dural and visceral afferents onto nociceptive neurons in the first cervical dorsal horn. European Journal of Neuroscience. 2007; 26: 142–154.
[82] Nakajima A, Tsuboi Y, Suzuki I, Honda K, Shinoda M, Kondo M, et al. PKCgamma in Vc and C1/C2 is involved in trigeminal neuropathic pain. Journal of Dental Research. 2011; 90: 777–781.
[83] Noma N, Tsuboi Y, Kondo M, Matsumoto M, Sessle BJ, Kitagawa J, et al. Organization of pERK-immunoreactive cells in trigeminal spinal nucleus caudalis and upper cervical cord following capsaicin injection into oral and craniofacial regions in rats. Journal of Comparative Neurology. 2008; 507: 1428–1440.
[84] Noma N, Watanabe K, Sato Y, Imamura Y, Yamamoto Y, Ito R, et al. Botulinum neurotoxin type A alleviates mechanical hypersensitivity associated with infraorbital nerve constriction injury in rats. Neuroscience Letters. 2017; 637: 96–101.
[85] Nomura H, Ogawa A, Tashiro A, Morimoto T, Hu JW, Iwata K. Induction of Fos protein-like immunoreactivity in the trigeminal spinal nucleus caudalis and upper cervical cord following noxious and non-noxious mechanical stimulation of the whisker pad of the rat with an inferior alveolar nerve transection. Pain. 2002; 95: 225–238.
[86] Ogawa A, Meng ID, Ren K, Imamura Y, Iwata K. Differential responses of rostral subnucleus caudalis and upper cervical dorsal horn neurons to mechanical and chemical stimulation of the parotid gland in rats. Brain Research. 2006; 1106: 123–133.
[87] Ogawa A, Ren K, Tsuboi Y, Morimoto T, Sato T, Iwata K. A new model of experimental parotitis in rats and its implication for trigeminal nociception. Experimental Brain Research. 2003; 152: 307–316.
[88] Okamoto K, Kimura A, Donishi T, Imbe H, Senba E, Tamai Y. Central serotonin 3 receptors play an important role in the modulation of nociceptive neural activity of trigeminal subnucleus caudalis and nocifensive orofacial behavior in rats with persistent temporomandibular joint inflammation. Neuroscience. 2005; 135: 569–581.
[89] Okamoto K, Bereiter DF, Thompson R, Tashiro A, Bereiter DA. Estradiol replacement modifies c-fos expression at the spinomedullary junction evoked by temporomandibular joint stimulation in ovariectomized female rats. Neuroscience. 2008; 156: 729–736.
[90] Okamoto K, Imbe H, Kimura A, Donishi T, Tamai Y, Senba E. Activation of central 5HT2A receptors reduces the craniofacial nociception of rats. Neuroscience. 2007; 147: 1090–1102.
[91] Park J, Trinh VN, Sears-Kraxberger I, Li KW, Steward O, Luo ZD. Synaptic ultrastructure changes in trigeminocervical complex posttrigeminal nerve injury. Journal of Comparative Neurology. 2016; 524: 309–322.
[92] Puri J, Bellinger LL, Kramer PR. Estrogen in cycling rats alters gene expression in the temporomandibular joint, trigeminal ganglia and trigeminal subnucleus caudalis/upper cervical cord junction. Journal of Cellular Physiology. 2011; 226: 3169–3180.
[93] Qu ZY, Liu L, Zhao LP, Xu X, Li Z, Zhu Y, et al. Prophylactic electroacupuncture on the upper cervical segments decreases neuronal discharges of the trigeminocervical complex in migraine-affected rats: an in vivo extracellular electrophysiological experiment. Journal of Pain Research. 2020; 13: 25–37.
[94] Sabino MA, Honore P, Rogers SD, Mach DB, Luger NM, Mantyh PW. Tooth extraction-induced internalization of the substance P receptor in trigeminal nucleus and spinal cord neurons: imaging the neurochemistry of dental pain. Pain. 2002; 95: 175–186.
[95] Sato T, Kitagawa J, Ren K, Tanaka H, Tanabe A, Watanabe T, et al. Activation of trigeminal intranuclear pathway in rats with temporomandibular joint inflammation. Journal of Oral Science. 2005; 47: 65–69.
[96] 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.
[97] Shibuta K, Suzuki I, Shinoda M, Tsuboi Y, Honda K, Shimizu N, et al. Organization of hyperactive microglial cells in trigeminal spinal subnucleus caudalis and upper cervical spinal cord associated with orofacial neuropathic pain. Brain Research. 2012; 1451: 74–86.
[98] Shigenaga Y, Sera M, Nishimori T, Suemune S, Nishimura M, Yoshida A, et al. The central projection of masticatory afferent fibers to the trigeminal sensory nuclear complex and upper cervical spinal cord. Journal of Comparative Neurology. 1988; 268: 489–507.
[99] Shigenaga Y, Chen IC, Suemune S, Nishimori T, Nasution ID, Yoshida A, et al. Oral and facial representation within the medullary and upper cervical dorsal horns in the cat. Journal of Comparative Neurology. 1986; 243: 388–408.
[100] Shimizu K, Asano M, Kitagawa J, Ogiso B, Ren K, Oki H, et al. Phosphorylation of Extracellular Signal-Regulated Kinase in medullary and upper cervical cord neurons following noxious tooth pulp stimulation. Brain Research. 2006; 1072: 99–109.
[101] Strassman AM, Mineta Y, Vos BP. Distribution of fos-like immunoreactivity in the medullary and upper cervical dorsal horn produced by stimulation of dural blood vessels in the rat. Journal of Neuroscience. 1994; 14: 3725–3735.
[102] Strassman AM, Vos BP. Somatotopic and laminar organization of fos-like immunoreactivity in the medullary and upper cervical dorsal horn induced by noxious facial stimulation in the rat. Journal of Comparative Neurology. 1993; 331: 495–516.
[103] Sugimoto T, Hara T, Shirai H, Abe T, Ichikawa H, Sato T. c-fos induction in the subnucleus caudalis following noxious mechanical stimulation of the oral mucous membrane. Experimental Neurology. 1994; 129: 251–256.
[104] Suzuki I, Kitagawa J, Noma N, Tsuboi Y, Kondo M, Honda K, et al. Attenuation of naloxone-induced Vc pERK hyper-expression following capsaicin stimulation of the face in aged rat. Neuroscience Letters. 2008; 442: 39–43.
[105] Takemura M, Sugimoto T, Sakai A. Topographic organization of central terminal region of different sensory branches of the rat mandibular nerve. Experimental Neurology. 1987; 96: 540–557.
[106] Takeshita S, Hirata H, Bereiter DA. Intensity coding by TMJ-responsive neurons in superficial laminae of caudal medullary dorsal horn of the rat. Journal of Neurophysiology. 2001; 86: 2393–2404.
[107] Tanimoto T, Takeda M, Matsumoto S. Suppressive effect of vagal afferents on cervical dorsal horn neurons responding to tooth pulp electrical stimulation in the rat. Experimental Brain Research. 2002; 145: 468–479.
[108] Tanimoto T, Takeda M, Nishikawa T, Matsumoto S. The role of 5-hydroxytryptamine3 receptors in the vagal afferent activation-induced inhibition of the first cervical dorsal horn spinal neurons projected from tooth pulp in the rat. Journal of Pharmacology and Experimental Therapeutics. 2004; 311: 803–810.
[109] Yasuda K, Furusawa K, Tanaka M, Yamaoka M. The distribution of afferent neurons in the trigeminal mesencephalic nucleus and the central projection of afferent fibers of the mylohyoid nerve in the rat. Somatosensory & Motor Research. 1995; 12: 309–315.
[110] Young RF, Perryman KM. Pathways for orofacial pain sensation in the trigeminal brain-stem nuclear complex of the Macaque monkey. Journal of Neurosurgery. 1984; 61: 563–568.
[111] Zerari-Mailly F, Dauvergne C, Buisseret P, Buisseret-Delmas C. Localization of trigeminal, spinal, and reticular neurons involved in the rat blink reflex. Journal of Comparative Neurology. 2003; 467: 173–184.
[112] Zhou Q, Imbe H, Dubner R, Ren K. Persistent Fos protein expression after orofacial deep or cutaneous tissue inflammation in rats: implications for persistent orofacial pain. Journal of Comparative Neurology. 1999; 412: 276–291.
[113] Westberg KG, Olsson KA. Integration in trigeminal premotor interneurones in the cat. 1. Functional characteristics of neurones in the subnucleus-gamma of the oral nucleus of the spinal trigeminal tract. Experimental Brain Research. 1991; 84: 102–114.
[114] Chudler EH, Foote WE, Poletti CE. Topography of C1 nerve- and trigeminal-evoked potentials in the ventrobasal complex of the cat thalamus. Neuroscience Letters. 1991; 132: 33–36.
[115] Arrowsmith J. Trial watch: phase III and submission failures: 2007–2010. Nature Reviews Drug Discovery. 2011; 10: 87.
[116] Kucharczuk CR, Ganetsky A, Vozniak JM. Drug-drug interactions, safety, and pharmacokinetics of EGFR tyrosine kinase inhibitors for the treatment of non-small cell lung cancer. Journal of the Advanced Practitioner in Oncology. 2018; 9: 189–200.
[117] Li Y, Tang W, Guo M. The cell as matter: connecting molecular biology to cellular functions. Matter. 2021; 4: 1863–1891.
[118] Bursac N. Cardiac tissue engineering using stem cells. IEEE Engineering in Medicine and Biology Magazine. 2009; 28: 80, 82, 84–86, 88–89.
[119] Berridge MJ, Lipp P, Bootman MD. The versatility and universality of calcium signalling. Nature Reviews Molecular Cell Biology. 2000; 1: 11–21.
[120] Davis K, Drey N, Gould D. What are scoping studies? A review of the nursing literature. International Journal of Nursing Studies. 2009; 46: 1386–1400.
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