Literature DB >> 11929909

Responses of spinothalamic lamina I neurons to maintained noxious mechanical stimulation in the cat.

D Andrew1, A D Craig.   

Abstract

Noxious mechanical stimuli that are maintained for minutes produce a continuous sensation of pain in humans that augments during the stimulus. It has recently been shown with systematic force-controlled stimuli that, while all mechanically responsive nociceptors adapt to these stimuli, the basis for such pain can be ascribed to A-fiber rather than C-fiber nociceptors, based on distinctions in their respective response profiles and stimulus-response functions. The present experiments investigated whether similar distinctions could be made in subsets of nociceptive lamina I spinothalamic tract (STT) neurons using similar maintained stimuli. Twenty-eight lamina I STT neurons in the lumbosacral dorsal horn of barbiturate-anesthetized cats were tested with noxious mechanical stimuli applied with a probe of 0.1 mm(2) contact area at forces of 25, 50, and 100 g for 2 min. The neurons were classified as nociceptive-specific (NS, n = 14) or polymodal nociceptive (HPC, n = 14) based on their responses to quantitative thermal stimuli. The NS neurons had greater responses and showed less adaptation than the HPC neurons in response to these stimuli, and they encoded stimulus intensity better. Comparison of the normalized response profiles of all 28 nociceptive lamina I STT neurons, independent of cell classification, revealed 2 subgroups that differed significantly: "Maintained" cells with responses that remained above 50% of the initial peak rate during stimulation and "Adapting" cells with responses that quickly declined to <50%. The Maintained neurons encoded the intensity of the mechanical stimuli better than the Adapting neurons, based on ratiometric functions. A k-means cluster analysis of all 28 cells distinguished the identical two subgroups. These categories corresponded closely to the NS and HPC categories: Maintained cells were mostly NS neurons (10 NS, 3 HPC), and Adapting cells were mostly HPC neurons (4 NS, 11 HPC). Thus the present data are consistent with the distinctions between A-fiber and C-fiber nociceptors observed previously, because A-fiber nociceptors are the predominant input to NS lamina I STT neurons and C-fiber nociceptors are the predominant input to HPC neurons. These findings support the view that NS, but perhaps not HPC, lamina I STT neurons have a role in the pain caused by maintained mechanical stimuli and contribute to the sensations of "first" pain and "sharpness." Nonetheless, none of the units studied showed increasing responses during the stimuli, suggesting a role for other ascending neurons or forebrain integration in the augmenting pain produced by maintained mechanical stimulation.

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Year:  2002        PMID: 11929909     DOI: 10.1152/jn.00577.2001

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


  8 in total

1.  Properties of mouse spinal lamina I GABAergic interneurons.

Authors:  Kimberly J Dougherty; Michael A Sawchuk; Shawn Hochman
Journal:  J Neurophysiol       Date:  2005-07-13       Impact factor: 2.714

2.  Quantitative responses of spinothalamic lamina I neurones to graded mechanical stimulation in the cat.

Authors:  David Andrew; A D Bud Craig
Journal:  J Physiol       Date:  2002-12-15       Impact factor: 5.182

Review 3.  History of Spinal Cord "Pain" Pathways Including the Pathways Not Taken.

Authors:  Allan Basbaum
Journal:  Front Pain Res (Lausanne)       Date:  2022-06-09

Review 4.  Descending control of nociception: Specificity, recruitment and plasticity.

Authors:  M M Heinricher; I Tavares; J L Leith; B M Lumb
Journal:  Brain Res Rev       Date:  2008-12-25

5.  Area 3a neuron response to skin nociceptor afferent drive.

Authors:  Barry L Whitsel; Oleg V Favorov; Yongbiao Li; Miguel Quibrera; Mark Tommerdahl
Journal:  Cereb Cortex       Date:  2008-06-04       Impact factor: 5.357

Review 6.  [Symptoms and pathophysiological mechanisms of neuropathic pain syndromes].

Authors:  S Lanz; C Maihöfner
Journal:  Nervenarzt       Date:  2009-04       Impact factor: 1.214

7.  Reduction of anion reversal potential subverts the inhibitory control of firing rate in spinal lamina I neurons: towards a biophysical basis for neuropathic pain.

Authors:  Steven A Prescott; Terrence J Sejnowski; Yves De Koninck
Journal:  Mol Pain       Date:  2006-10-13       Impact factor: 3.395

8.  Ineffectiveness of tactile gating shows cortical basis of nociceptive signaling in the Thermal Grill Illusion.

Authors:  E R Ferrè; G D Iannetti; J A van Dijk; P Haggard
Journal:  Sci Rep       Date:  2018-04-26       Impact factor: 4.379

  8 in total

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