2010
DOI: 10.2478/v10039-010-0020-9
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Synergistic effects of NGF, CNTF and GDNF on functional recovery following sciatic nerve injury in rats

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Cited by 41 publications
(21 citation statements)
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“…NT-3 facilitates axonal regeneration and the degree of histomorphologic or electrophysiologic limitation according to the nervous injury (Chen et al 2010). It has an important role in axonal extension, survival and maintenance of neurons, myelination and regeneration of neural fibers (Li et al 2006).…”
Section: Discussionmentioning
confidence: 98%
“…NT-3 facilitates axonal regeneration and the degree of histomorphologic or electrophysiologic limitation according to the nervous injury (Chen et al 2010). It has an important role in axonal extension, survival and maintenance of neurons, myelination and regeneration of neural fibers (Li et al 2006).…”
Section: Discussionmentioning
confidence: 98%
“…[15][16][17][18] NGF also can promote regeneration of the peripheral nerve. [19][20][21] However, despite extensive previous research, the clinical application of NGF for IAN damage has been impeded, primarily because of its very short in vivo half-life. 22 Hence, NGF should be applied directly to the damaged site to maintain the effective dose for as long as needed.…”
mentioning
confidence: 99%
“…Viability assays confirmed that the motoneuron outgrowth and branching effects were independent of changes in motoneuron viability. This suggests that CN X-derived motoneurons are not influenced by paired NFs in a fashion similar to peripheral and embryonic neurons, [17][18][19][20] supporting unique in vitro behavior of CN X motoneurons.…”
Section: Summary Of Main Findingsmentioning
confidence: 89%
“…While dissociated cultures from dorsal root ganglia, peripheral, and embryonic motoneurons have been critical in contributing to the panoply of knowledge that exists today on NFs and neuropathic conditions, neuronal responses to NFs differ in a myriad of ways depending on motoneuron site, developmental stage, timing of initial therapy, and NF concentration. [17][18][19][20][21] Thus, establishing a model specific to the study of CN X motoneurons in culture is essential if the unique pathophysiology associated with CN X regeneration is to be unveiled. While the model ultimately may be used to investigate the molecular mechanisms of CN X motoneuron regeneration, this study's identification of CNTF as a promoter of CN X outgrowth may treatment groups showed no significant effect on mean motoneuron branching when compared to saline controls.…”
Section: Implications For Future Research or Clinical Practicementioning
confidence: 99%