AI Article Synopsis
- The study investigated how tumor necrosis factor-alpha (TNF) affects pain behavior and histological changes in the dorsal root ganglion (DRG) of rats.
- Researchers applied different concentrations of TNF to the L4 DRG and measured the mechanical and thermal pain thresholds, noting significant changes in response to the higher concentration.
- Histological analysis revealed a larger area of enlargement in the DRG with higher TNF application, suggesting a connection between increased TNF levels, pain sensitivity, and the size of histological changes.
Article Abstract
Study Design: Histologic changes in the dorsal root ganglion (DRG) and the nociceptive stimulation thresholds were studied in rats.
Objective: To examine the effects of tumor necrosis factor-alpha (TNF) with special reference to pain behavior and histology of the DRG.
Summary Of Background Data: Recently, it was reported that local application of nucleus pulposus induces a characteristic tissue reaction at the surface of the DRG. However, to our knowledge, there have been no previous reports about the relationship between the histologic changes and pain behavior caused by cytokines.
Methods: Recombinant TNF was applied to the L4 DRG. Mechanical and thermal nociceptive thresholds were tested. The L4 DRG was sectioned and observed by light microscopy.
Results: After the application of 5 ng/microL TNF, significant differences were observed in mechanical and thermal stimulation thresholds. At the site of application of TNF, a characteristic a semilunar-shaped enlargement was observed. The average width of the part was significantly larger in the 5 ng/microL TNF application, as compared to the 0.5-ng/microL TNF application.
Conclusions: The higher concentration of TNF used induced allodynia and hyperalgesia responses. Because the region showing the histologic changes was significantly larger after application of the higher concentration of TNF, the reaction of the DRG may be related to pain.
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| http://dx.doi.org/10.1097/01.brs.0000201260.10082.23 | DOI Listing |
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