The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
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
Abstract
Because of the likely involvement of central convergence of afferent inputs in mechanisms underlying referred pain, the activity of single neurones was recorded in the cat's trigeminal (V) subnucleus caudalis (medullary dorsal horn) to test for the presence and extent of convergent inputs to the neurones. In chloralose-anaesthetized or decerebrate unanaesthetized cats, electrical stimuli were applied to afferents supplying facial skin, oral mucosa, canine and premolar tooth pulp, laryngeal mucosa, cervical skin and muscle, and jaw and tongue muscles, and tactile and noxious mechanical and thermal stimuli were applied to skin and mucosa. Considerable proportions of caudalis neurones which could be functionally classified on the basis of their cutaneous receptive field properties as low-threshold mechanoreceptive (LTM), wide-dynamic-range (WDR), or nociceptive-specific (NS) neurones, could be excited by electrical stimulation of several of these afferent inputs. Extensive convergence of afferent inputs, including inputs from skin or mucosal areas outside the neuronal oral-facial receptive field delineated by natural stimuli, was a particular feature of the units classified as cutaneous nociceptive neurones (i.e., WDR and NS). On the basis of antidromic activation, 15% of these WDR and NS neurones were shown to have a direct projection to the contralateral thalamus. The findings question the use of terminology and classifications of somatosensory neurones based only on the cutaneous receptive field properties of the neurones since distinctions between the different neuronal populations become less obvious when properties other than those related to cutaneous afferent inputs are taken into account. Moreover, the observations of extensive convergence of different types of afferents, which was especially apparent in cutaneous nociceptive neurones, also suggest a role for these neurones in mediating deep pain and in spread and referral of pain.
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Citations
Cites
A stereotaxic atlas of the cat brain
Snider, R. S., & Niemer, W. T. (1987) · U-M-I Out-of-Print Books on Demand · Cited by 1,292
Spinal and Trigeminal Mechanisms of Nociception
Dubner, R., & Bennett, G. J. (1983) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.06.030183.002121 · Cited by 597
The Neural Basis of Oral and Facial Function
Dubner, R., Sessle, B. J., & Storey, A. T. (1978) · Springer eBooks · doi:10.1007/978-1-4757-1682-5 · Cited by 586
Self-citationNeurons that subserve the sensory-discriminative aspects of pain
Price, D. D., & Dubner, R. (1977) · Pain · doi:10.1016/0304-3959(77)90063-x · Cited by 425
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Hagamen, W. D. (1962) · Archives of Neurology · doi:10.1001/archneur.1962.04210060107009 · Cited by 420
ON DISTURBANCES OF SENSATION WITH ESPECIAL REFERENCE TO THE PAIN OF VISCERAL DISEASE
HEAD, H. (1893) · Brain · doi:10.1093/brain/16.1-2.1 · Cited by 398
Price, D. D., Dubner, R., & Hu, J. W. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.5.936 · Cited by 354
Self-citationThe presence of ineffective synapses and the circumstances which unmask them
Wall, P. D., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1977.0048 · Cited by 341
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Cited by
Invited Review: The Neurobiology of Facial and Dental Pain: Present Knowledge, Future Directions
Sessle, B. J. (1987) · Journal of Dental Research · doi:10.1177/00220345870660052201 · Cited by 285
Self-citationAssociations among four modalities of experimental pain in women
Bhalang, K., Sigurdsson, A., Slade, G. D., & Maixner, W. (2005) · The Journal of Pain · doi:10.1016/j.jpain.2005.04.006 · Cited by 89
Temporomandibular Disorder Pain After Whiplash Trauma: A Systematic Review
Häggman-Henrikson, B., List, T., Westergren, H., & Axelsson, S. (2013) · Journal of Orofacial Pain · doi:10.11607/jop.1027 · Cited by 48
Functional anatomy of the vagus system: how does the polyvagal theory comply?
Neuhuber, W. L., & Berthoud, H.-R. (2022) · Biological Psychology · doi:10.1016/j.biopsycho.2022.108425 · Cited by 42
Metadata
- Authors
- Sessle, B. J., Hu, J. W., Amano, N., & Zhong, G.
- Venue
- Pain
- Published
- 1986-11
- Volume
- 27
- Issue
- 2
- Pages
- 219-235
- ISSN
- 0304-3959 (ISSN-L)
- OpenAlex
- W1967064754
- Cited by
- 358
- References
- 31
- FWCI
- 4.85
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: 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. https://app.cochat.ai/papers/10.1016/0304-3959(86)90213-7
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- Sessle, B. J., Hu, J. W., Amano, N., & Zhong, G. (1986). 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. https://doi.org/10.1016/0304-3959(86)90213-7
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