Literature DB >> 15290408

The effects of epidural application of allografted nucleus pulposus in rats on cytokine expression, limb withdrawal and nerve root discharge.

Srinivasu Kallakuri1, Tsuneo Takebayashi, A Cuneyt Ozaktay, Chaoyang Chen, Shangyou Yang, Paul H Wooley, John M Cavanaugh.   

Abstract

This study investigated cytokine expression, behavioral and neurophysiologic changes in Lewis rats whose lumbar nerve roots were exposed to nucleus pulposus (NP). Allografted NP or fat was implanted over the left L5 nerve root. Sham rats had no NP or fat implantation. Control rats had no surgery. Rats were allowed to survive for 7 days and were tested daily for hind-paw mechanical and thermal withdrawal response (TWR). Granulation tissue was processed by immunohistochemistry for cytokines--interleukin 1 beta (IL-1beta), interleukin 6 (IL-6) and tumor necrosis factor (TNF). Neurophysiological response from the L5 nerve roots was also characterized after 7 days. Significant staining density for IL-1beta, IL-6 and TNF was observed in NP granulation tissue compared with fat and sham (p<0.05). However, there were no significant thermal and mechanical behavioral changes. TWR data computed as percentage-difference scores indicated no significant changes in withdrawal response between the four groups, although NP-treated group showed a trend of decreasing withdrawal latency. Comparison of combined percentage-difference scores revealed increased sensitivity in the NP group on days 4, 5 and 6, 7 when compared with control rats only, with no significant changes in the percentage-difference scores of fat and sham rats when compared to control. Neurophysiologically, the percentage increase in discharge rate in NP-treated rats was higher than control (p<0.05) but not higher than fat and sham rats. These results support the inflammatory nature of NP but offer limited support to NP-mediated thermal behavioral changes.

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Year:  2004        PMID: 15290408     DOI: 10.1007/s00586-004-0773-6

Source DB:  PubMed          Journal:  Eur Spine J        ISSN: 0940-6719            Impact factor:   3.134


  34 in total

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3.  Pathogenesis of sciatic pain: role of herniated nucleus pulposus and deformation of spinal nerve root and dorsal root ganglion.

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4.  Pathomechanism of pain-related behavior produced by allografts of intervertebral disc in the rat.

Authors:  M Kawakami; T Tamaki; J N Weinstein; H Hashizume; H Nishi; S T Meller
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6.  Herniated lumbar intervertebral discs spontaneously produce matrix metalloproteinases, nitric oxide, interleukin-6, and prostaglandin E2.

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7.  Methylprednisolone reduces the early vascular permeability increase in spinal nerve roots induced by epidural nucleus pulposus application.

Authors:  G Byröd; K Otani; H Brisby; B Rydevik; K Olmarker
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8.  Mechanical compression of the lumbar nerve root alters pain-related behaviors induced by the nucleus pulposus in the rat.

Authors:  M Kawakami; T Tamaki; N Hayashi; H Hashizume; T Matsumoto; A Minamide; T Kihira
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10.  Tumor necrosis factor alpha and nucleus-pulposus-induced nerve root injury.

Authors:  K Olmarker; K Larsson
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  14 in total

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5.  Effects of interleukin-1 beta, interleukin-6, and tumor necrosis factor on sensitivity of dorsal root ganglion and peripheral receptive fields in rats.

Authors:  A Cüneyt Ozaktay; Srinivasu Kallakuri; Tsuneo Takebayashi; John M Cavanaugh; Ibrahim Asik; Joyce A DeLeo; James N Weinstein
Journal:  Eur Spine J       Date:  2006-02-11       Impact factor: 3.134

6.  A rat model for chronic spinal nerve root compression.

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Journal:  Eur Spine J       Date:  2013-10-19       Impact factor: 3.134

7.  Gait abnormalities and inflammatory cytokines in an autologous nucleus pulposus model of radiculopathy.

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8.  The effect of hyaluronidase in interlaminar lumbar epidural injection for failed back surgery syndrome.

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9.  Mechanical compression and nucleus pulposus application on dorsal root Ganglia differentially modify evoked neuronal activity in the thalamus.

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10.  Changes in midbrain pain receptor expression, gait and behavioral sensitivity in a rat model of radiculopathy.

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