Detailed Information on Publication Record
2007
An increased amount of ED-1+ cell profiles in DRG following sciatic nerve ligature and ventral root transection
DUBOVÝ, Petr, Lucie TUČKOVÁ, Ivana SVÍŽENSKÁ, Radim JANČÁLEK, Ilona KLUSÁKOVÁ et. al.Basic information
Original name
An increased amount of ED-1+ cell profiles in DRG following sciatic nerve ligature and ventral root transection
Name in Czech
Zvýšené množství ED1+ makrofágů ve spinálních gangliích po ligatuře sedacího nervu a po transekci ventrálního kořene spinálního nervu
Authors
DUBOVÝ, Petr, Lucie TUČKOVÁ, Ivana SVÍŽENSKÁ, Radim JANČÁLEK and Ilona KLUSÁKOVÁ
Edition
The 2nd Intern. Congress on Neuropathic Pain, 2007
Other information
Language
English
Type of outcome
Prezentace na konferencích
Field of Study
30000 3. Medical and Health Sciences
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Organization unit
Faculty of Medicine
ISBN
1090-3801
Keywords in English
neuropathic pain-experimental model-Wallerian degeneration
Tags
International impact
Změněno: 21/1/2008 09:08, MUDr. Ilona Klusáková, Ph.D.
V originále
A peripheral nerve injury induces cellular and molecular changes in the corresponding (homologous) DRG responsible for ectopic discharge of the primary sensory neurons, factor thought to contribute to the development and maintenance of neuropathic pain. Macrophages increase in number in corresponding DRG following nerve injury, and their activity is referred to be important in initiating of neuropathic pain. Sciatic nerve ligature and ventral root transection are used as experimental models of neuropathic pain with different mechanisms of effect to DRG. Macrophages exhibiting ED-1+ immunostaining were examined quantitatively in the rat L4-L5 DRG from both ipsi- and contralateral side following unilateral sciatic nerve ligature (SNL) or ventral root transection (VRT) under an aseptic condition. An amount of ED-1+ macrophages were found in the interstitial space of naive DRG without intimate location to the neuronal bodies. In comparison to naive DRG, area of ED-1+ cells was significantly enlarged in ipsilateral DRG 2 and 4 weeks from SNL. The ED-1+ macrophages and their cytoplasmic processes were frequently located close to neuronal bodies to become their satellite cells. Contralateral DRG also displayed an increased amount of ED-1+ macrophages, but significant enlargement was found only following 4 weeks when compared with naive DRG or contralateral DRG after 2 weeks. In all cases, contralateral in contrast to ipsilateral DRG contained significantly lower amount of ED-1+ cells. Ventral root transection for 2 and 4 weeks resulted in an increased amount of ED1+ cells in both ipsi- and contralateral DRG in comparison to naive ones. However, the enlargement was similar on both sides after 2 weeks, but greater elevation was observed only in ipsilateral DRG 4 weeks from VRT. The results indicate that SNL stimulated invasion of ED1+ macrophages predominantly into ipsilateral DRG, and later (4 weeks) to contralateral ones. In contrast, VRT induced a higher invasion of ED1+ cells to contralateral DRG already after 2 weeks. Our results suggested that Wallerian degeneration produces signals for invasion of ED1+ macrophages to contralateral DRG.
In Czech
Unilaterální poškození periferního nervu vede k invazi ED1+ makrofágů do spinálních ganglií nejen na ipsilaterální, ale i na kontralaterální straně.
Links
| GA309/07/0121, research and development project |
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| MSM0021622404, plan (intention) |
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