Literature DB >> 9300563

Chronic central pain after spinal cord injury.

M D Christensen1, C E Hulsebosch.   

Abstract

Spinal cord injury (SCI) frequently results in dysesthesias that have remained refractory to clinical treatments despite a variety of interventions. The failure of therapeutic strategies to treat dysesthesias after SCI is due to the lack of attention given to mechanisms that elicit chronic pain following SCI. An overview of the literature with respect to the development of chronic pain in the SCI patient population will be given. In addition, a mammalian model of chronic central pain following spinal cord trauma will be presented. The model is characterized by the development of mechanical and thermal allodynia, as demonstrated by measuring the thresholds of accepted nociceptive tests, the paw withdrawal responses accompanied by changes in behavior consistent with the experience of noxious stimuli. In addition, vocalization responses that are accompanied by postural and behavioral changes consistent with the receipt of a noxious stimulus and involving supraspinal pathways are measured. Locomotor function was also tested and scored using the Basso, Beattie, and Bresnahan (BBB) open field test scale. Our data indicate that somatosensory thresholds for both mechanical and thermal stimuli that elicit paw withdrawal (flexor reflex) or vocalizations, accompanied by complex changes in behavior, are significantly different following SCI. These changes represent the development of mechanical and thermal allodynia. To determine the underlying mechanism for the altered sensory responses, we used electrophysiological techniques to determine if nociceptive dorsal horn neurons demonstrated increased excitability to peripheral stimulation as evidenced by increased responses to natural somatosensory stimuli. The data presented support the development of central sensitization of dorsal horn neurons after spinal cord hemisection. This provides a mechanism for the development of mechanical and thermal allodynia after SCI. Hypotheses that account for the development of the central pain state after SCI, as well as therapeutic interventions to ameliorate the pain state, are discussed.

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Mesh:

Year:  1997        PMID: 9300563     DOI: 10.1089/neu.1997.14.517

Source DB:  PubMed          Journal:  J Neurotrauma        ISSN: 0897-7151            Impact factor:   5.269


  70 in total

1.  Locomotor recovery in spinal cord-injured rats treated with an antibody neutralizing the myelin-associated neurite growth inhibitor Nogo-A.

Authors:  D Merkler; G A Metz; O Raineteau; V Dietz; M E Schwab; K Fouad
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

2.  Conditioned place preference reveals tonic pain in an animal model of central pain.

Authors:  Leyla Davoody; Raimi L Quiton; Jessica M Lucas; Yadong Ji; Asaf Keller; Radi Masri
Journal:  J Pain       Date:  2011-04-23       Impact factor: 5.820

Review 3.  The dark side of neuroplasticity.

Authors:  Arthur Brown; Lynne C Weaver
Journal:  Exp Neurol       Date:  2011-11-12       Impact factor: 5.330

4.  Role of microglia and astrocyte in central pain syndrome following electrolytic lesion at the spinothalamic tract in rats.

Authors:  Kobra Naseri; Elham Saghaei; Fatemeh Abbaszadeh; Mina Afhami; Ali Haeri; Farzaneh Rahimi; Masoumeh Jorjani
Journal:  J Mol Neurosci       Date:  2012-06-22       Impact factor: 3.444

5.  Herpes simplex virus vector-mediated expression of interleukin-10 reduces below-level central neuropathic pain after spinal cord injury.

Authors:  Darryl Lau; Steven E Harte; Thomas J Morrow; Shiyong Wang; Marina Mata; David J Fink
Journal:  Neurorehabil Neural Repair       Date:  2012-05-15       Impact factor: 3.919

Review 6.  Neuropathic Pain After Spinal Cord Injury: Challenges and Research Perspectives.

Authors:  Rani Shiao; Corinne A Lee-Kubli
Journal:  Neurotherapeutics       Date:  2018-07       Impact factor: 7.620

7.  Metabolomics uncovers dietary omega-3 fatty acid-derived metabolites implicated in anti-nociceptive responses after experimental spinal cord injury.

Authors:  J D Figueroa; K Cordero; M Serrano-Illan; A Almeyda; K Baldeosingh; F G Almaguel; M De Leon
Journal:  Neuroscience       Date:  2013-09-14       Impact factor: 3.590

8.  Gabapentin alleviates facet-mediated pain in the rat through reduced neuronal hyperexcitability and astrocytic activation in the spinal cord.

Authors:  Ling Dong; Nathan D Crosby; Beth A Winkelstein
Journal:  J Pain       Date:  2013-10-04       Impact factor: 5.820

9.  Acute and chronic changes in aquaporin 4 expression after spinal cord injury.

Authors:  O Nesic; J Lee; Z Ye; G C Unabia; D Rafati; C E Hulsebosch; J R Perez-Polo
Journal:  Neuroscience       Date:  2006-10-30       Impact factor: 3.590

10.  Intraspinal sprouting of unmyelinated pelvic afferents after complete spinal cord injury is correlated with autonomic dysreflexia induced by visceral pain.

Authors:  S Hou; H Duale; A G Rabchevsky
Journal:  Neuroscience       Date:  2008-12-24       Impact factor: 3.590

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