Literature DB >> 3950689

Responses of neurons in feline trigeminal subnucleus caudalis (medullary dorsal horn) to cutaneous, intraoral, and muscle afferent stimuli.

N Amano, J W Hu, B J Sessle.   

Abstract

The extracellular activity of single neurons was recorded in subnucleus caudalis (medullary dorsal horn) of chloralose-anesthetized cats to test the effects of electrical and natural stimuli that activated afferents supplying the jaw and tongue muscles as well as the face, teeth, and intraoral mucosa. Many caudalis neurons that 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) neurons could be excited by muscle afferent stimuli. Only five neurons were encountered that received muscle afferent inputs and had no demonstrable cutaneous, dental, or mucosal input. The muscle afferent inputs were a particular feature of the cutaneous nociceptive (i.e., WDR and NS) neurons. Approximately two-thirds of this nociceptive neuronal population (n = 109) could be excited by jaw and/or tongue muscle stimulation, whereas only a small proportion of the LTM neuronal population (n = 247) was activated by muscle afferent stimulation. Neurons with a demonstrated direct axonal projection to the contralateral thalamus as well as nonprojection neurons received muscle afferent inputs. The caudalis nociceptive neurons receiving muscle as well as cutaneous afferent inputs had receptive-field properties comparable to those previously described for caudalis cutaneous nociceptive neurons; they were predominantly located in laminae I/II and V/VI, and many also received convergence of tooth pulp afferent inputs. These neurons generally had larger cutaneous receptive fields than neurons unresponsive to muscle afferent stimulation. The muscle afferent inputs were considered to be predominantly of a nociceptive character for several reasons. These included the long latency and high threshold of most neuronal responses evoked by electrical stimulation of the muscle afferents, the predominance of afferents of small diameter in some of the muscle nerves stimulated, the preferential responsiveness to the muscle afferent stimulation of neurons that were functionally identified as cutaneous nociceptive neurons, and the responsiveness of most of the neurons excited by electrical stimulation of the muscle nerves also to noxious mechanical or thermal stimulation of muscle and the injection of two or more algesic chemicals into small arteries supplying the jaw and tongue muscles. Of the algesic chemicals used in this study (7% NaCl, KCl, bradykinin, histamine, 5-HT), the first two were found to be the most effective and to cause the most rapidly induced excitation.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3950689     DOI: 10.1152/jn.1986.55.2.227

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  21 in total

1.  Response behaviour of cat dorsal horn neurones receiving input from skeletal muscle and other deep somatic tissues.

Authors:  U Hoheisel; S Mense
Journal:  J Physiol       Date:  1990-07       Impact factor: 5.182

2.  Role of capsaicin-sensitive primary afferent inputs from the masseter muscle in the C1 spinal neurons responding to tooth-pulp stimulation in rats.

Authors:  M Takeda; T Tanimoto; M Ito; M Nasu; S Matsumoto
Journal:  Exp Brain Res       Date:  2005-01       Impact factor: 1.972

3.  Localization of pain-related brain activation: a meta-analysis of neuroimaging data.

Authors:  Emma G Duerden; Marie-Claire Albanese
Journal:  Hum Brain Mapp       Date:  2011-12-01       Impact factor: 5.038

Review 4.  Basic science issues related to improved diagnoses for chronic orofacial pain.

Authors:  G J Bennett; B J Sessle
Journal:  Anesth Prog       Date:  1990 Mar-Jun

Review 5.  The striatum and pain modulation.

Authors:  Ana C Barceló; Bárbara Filippini; Jorge H Pazo
Journal:  Cell Mol Neurobiol       Date:  2011-07-26       Impact factor: 5.046

6.  Spontaneous discharge and peripherally evoked orofacial responses of trigemino-thalamic tract neurons during wakefulness and sleep.

Authors:  B E Cairns; S A McErlane; M C Fragoso; W G Jia; P J Soja
Journal:  J Neurosci       Date:  1996-12-15       Impact factor: 6.167

7.  Separate functions for responses to oral temperature in thermo-gustatory and trigeminal neurons.

Authors:  Christian H Lemon; Yi Kang; Jinrong Li
Journal:  Chem Senses       Date:  2016-03-14       Impact factor: 3.160

8.  Differential activation of the human trigeminal nuclear complex by noxious and non-noxious orofacial stimulation.

Authors:  Paul G Nash; Vaughan G Macefield; Iven J Klineberg; Greg M Murray; Luke A Henderson
Journal:  Hum Brain Mapp       Date:  2009-11       Impact factor: 5.038

9.  Responses of bradykinin sensitive tooth-pulp driven neurons in cat cerebral cortex.

Authors:  K Iwata; H Itoga; H Muramatsu; K Toda; R Sumino
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

10.  Responses of lateral thalamic neurons to algesic chemical stimulation of the cat knee joint.

Authors:  W D Hutchison; M A Lühn; R F Schmidt
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

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