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Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord

Limited information is available regarding the role of endogenous Glial cell line-derived neurotrophic factor (GDNF) in the spinal cord following transection injury. The present study investigated the possible role of GDNF in injured spinal cords following transection injury (T(9)–T(10)) in adult ra...

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Autores principales: Zhou, Hao-Li, Yang, Hui-Juan, Li, Yong-Mei, Wang, Ying, Yan, Ling, Guo, Xi-Liang, Ba, Ying-Chun, Liu, Su, Wang, Ting-Hua
Formato: Texto
Lenguaje:English
Publicado: Springer US 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270371/
https://www.ncbi.nlm.nih.gov/pubmed/18095158
http://dx.doi.org/10.1007/s11064-007-9536-1
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author Zhou, Hao-Li
Yang, Hui-Juan
Li, Yong-Mei
Wang, Ying
Yan, Ling
Guo, Xi-Liang
Ba, Ying-Chun
Liu, Su
Wang, Ting-Hua
author_facet Zhou, Hao-Li
Yang, Hui-Juan
Li, Yong-Mei
Wang, Ying
Yan, Ling
Guo, Xi-Liang
Ba, Ying-Chun
Liu, Su
Wang, Ting-Hua
author_sort Zhou, Hao-Li
collection PubMed
description Limited information is available regarding the role of endogenous Glial cell line-derived neurotrophic factor (GDNF) in the spinal cord following transection injury. The present study investigated the possible role of GDNF in injured spinal cords following transection injury (T(9)–T(10)) in adult rats. The locomotor function recovery of animals by the BBB (Basso, Beattie, Bresnahan) scale score showed that hindlimb support and stepping function increased gradually from 7 days post operation (dpo) to 21 dpo. However, the locomotion function in the hindlimbs decreased effectively in GDNF-antibody treated rats. GDNF immunoreactivty in neurons in the ventral horn of the rostral stump was stained strongly at 3 and 7 dpo, and in the caudal stump at 14 dpo, while immunostaining in astrocytes was also seen at all time-points after transection injury. Western blot showed that the level of GDNF protein underwent a rapid decrease at 7 dpo in both stumps, and was followed by a partial recovery at a later time-point, when compared with the sham-operated group. GDNF mRNA-positive signals were detected in neurons of the ventral horn, especially in lamina IX. No regenerative fibers from corticospinal tract can be seen in the caudal segment near the injury site using BDA tracing technique. No somatosensory evoked potentials (SEP) could be recorded throughout the experimental period as well. These findings suggested that intrinsic GDNF in the spinal cord could play an essential role in neuroplasticity. The mechanism may be that GDNF is involved in the regulation of local circuitry in transected spinal cords of adult rats.
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spelling pubmed-22703712008-03-21 Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord Zhou, Hao-Li Yang, Hui-Juan Li, Yong-Mei Wang, Ying Yan, Ling Guo, Xi-Liang Ba, Ying-Chun Liu, Su Wang, Ting-Hua Neurochem Res Original Paper Limited information is available regarding the role of endogenous Glial cell line-derived neurotrophic factor (GDNF) in the spinal cord following transection injury. The present study investigated the possible role of GDNF in injured spinal cords following transection injury (T(9)–T(10)) in adult rats. The locomotor function recovery of animals by the BBB (Basso, Beattie, Bresnahan) scale score showed that hindlimb support and stepping function increased gradually from 7 days post operation (dpo) to 21 dpo. However, the locomotion function in the hindlimbs decreased effectively in GDNF-antibody treated rats. GDNF immunoreactivty in neurons in the ventral horn of the rostral stump was stained strongly at 3 and 7 dpo, and in the caudal stump at 14 dpo, while immunostaining in astrocytes was also seen at all time-points after transection injury. Western blot showed that the level of GDNF protein underwent a rapid decrease at 7 dpo in both stumps, and was followed by a partial recovery at a later time-point, when compared with the sham-operated group. GDNF mRNA-positive signals were detected in neurons of the ventral horn, especially in lamina IX. No regenerative fibers from corticospinal tract can be seen in the caudal segment near the injury site using BDA tracing technique. No somatosensory evoked potentials (SEP) could be recorded throughout the experimental period as well. These findings suggested that intrinsic GDNF in the spinal cord could play an essential role in neuroplasticity. The mechanism may be that GDNF is involved in the regulation of local circuitry in transected spinal cords of adult rats. Springer US 2007-12-20 2008-05 /pmc/articles/PMC2270371/ /pubmed/18095158 http://dx.doi.org/10.1007/s11064-007-9536-1 Text en © The Author(s) 2007
spellingShingle Original Paper
Zhou, Hao-Li
Yang, Hui-Juan
Li, Yong-Mei
Wang, Ying
Yan, Ling
Guo, Xi-Liang
Ba, Ying-Chun
Liu, Su
Wang, Ting-Hua
Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title_full Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title_fullStr Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title_full_unstemmed Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title_short Changes in Glial Cell Line-derived Neurotrophic Factor Expression in the Rostral and Caudal Stumps of the Transected Adult Rat Spinal Cord
title_sort changes in glial cell line-derived neurotrophic factor expression in the rostral and caudal stumps of the transected adult rat spinal cord
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2270371/
https://www.ncbi.nlm.nih.gov/pubmed/18095158
http://dx.doi.org/10.1007/s11064-007-9536-1
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