File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1089/089771503767168528
- Scopus: eid_2-s2.0-0038045085
- PMID: 12906744
- WOS: WOS:000183926900008
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: GDNF and BDNF alter the expression of neuronal NOS, c-Jun, and p75 and prevent motoneuron death following spinal root avulsion in adult rats
Title | GDNF and BDNF alter the expression of neuronal NOS, c-Jun, and p75 and prevent motoneuron death following spinal root avulsion in adult rats |
---|---|
Authors | |
Keywords | Axotomy Neuronal death Neurotrophic factors Nitric oxide synthase Spinal motoneurons |
Issue Date | 2003 |
Publisher | Mary Ann Liebert, Inc Publishers. The Journal's web site is located at http://www.liebertpub.com/neu |
Citation | Journal Of Neurotrauma, 2003, v. 20 n. 6, p. 603-612 How to Cite? |
Abstract | In the present study, we examined the effects of glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), and insulin growth factor (IGF-1) on adult motoneuron survival following spinal root avulsion. The expression of neuronal nitric oxide synthase (nNOS), c-Jun, and the low-affinity neurotrophin receptor (P75) following treatment with these neurotrophic factors was also examined. In control animals, approximately 80% of spinal motoneurons were nNOS positive at 3 weeks following the lesion, whereas in GDNF or BDNF treated animals no nNOS positive motoneurons were found at the same time point. Following injury and treatment with GDNF and BDNF increased numbers of motoneurons were c-Jun and P75 positive. By 6 weeks following the lesion, only approximately 28% of motoneurons persisted in control animals whereas about 90% of motoneurons survived injury following treatment with either GDNF or BDNF. In contrast, CNTF and IGF-1 were ineffective in either inhibiting nNOS expression or preventing motoneuron death. Our results provide in vivo evidence that the survival of injured adult mammalian motoneurons can be promoted by specific neurotrophic factors, and that this effect is associated with inhibition of nNOS expression and up-regulation of c-Jun and P75 expression. |
Persistent Identifier | http://hdl.handle.net/10722/67622 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.483 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wu, W | en_HK |
dc.contributor.author | Li, L | en_HK |
dc.contributor.author | Yick, LW | en_HK |
dc.contributor.author | Chai, H | en_HK |
dc.contributor.author | Xie, Y | en_HK |
dc.contributor.author | Yang, Y | en_HK |
dc.contributor.author | Prevette, DM | en_HK |
dc.contributor.author | Oppenheim, RW | en_HK |
dc.date.accessioned | 2010-09-06T05:56:46Z | - |
dc.date.available | 2010-09-06T05:56:46Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Journal Of Neurotrauma, 2003, v. 20 n. 6, p. 603-612 | en_HK |
dc.identifier.issn | 0897-7151 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/67622 | - |
dc.description.abstract | In the present study, we examined the effects of glial cell line-derived neurotrophic factor (GDNF), brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), and insulin growth factor (IGF-1) on adult motoneuron survival following spinal root avulsion. The expression of neuronal nitric oxide synthase (nNOS), c-Jun, and the low-affinity neurotrophin receptor (P75) following treatment with these neurotrophic factors was also examined. In control animals, approximately 80% of spinal motoneurons were nNOS positive at 3 weeks following the lesion, whereas in GDNF or BDNF treated animals no nNOS positive motoneurons were found at the same time point. Following injury and treatment with GDNF and BDNF increased numbers of motoneurons were c-Jun and P75 positive. By 6 weeks following the lesion, only approximately 28% of motoneurons persisted in control animals whereas about 90% of motoneurons survived injury following treatment with either GDNF or BDNF. In contrast, CNTF and IGF-1 were ineffective in either inhibiting nNOS expression or preventing motoneuron death. Our results provide in vivo evidence that the survival of injured adult mammalian motoneurons can be promoted by specific neurotrophic factors, and that this effect is associated with inhibition of nNOS expression and up-regulation of c-Jun and P75 expression. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Mary Ann Liebert, Inc Publishers. The Journal's web site is located at http://www.liebertpub.com/neu | en_HK |
dc.relation.ispartof | Journal of Neurotrauma | en_HK |
dc.subject | Axotomy | - |
dc.subject | Neuronal death | - |
dc.subject | Neurotrophic factors | - |
dc.subject | Nitric oxide synthase | - |
dc.subject | Spinal motoneurons | - |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Brain-Derived Neurotrophic Factor - pharmacology - therapeutic use | en_HK |
dc.subject.mesh | Cell Death - drug effects - physiology | en_HK |
dc.subject.mesh | Gene Expression Regulation - drug effects - physiology | en_HK |
dc.subject.mesh | Glial Cell Line-Derived Neurotrophic Factor | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Motor Neurons - drug effects - metabolism - pathology | en_HK |
dc.subject.mesh | Nerve Growth Factors - pharmacology - therapeutic use | en_HK |
dc.subject.mesh | Nitric Oxide Synthase - biosynthesis - genetics | en_HK |
dc.subject.mesh | Nitric Oxide Synthase Type I | en_HK |
dc.subject.mesh | Proto-Oncogene Proteins c-jun - biosynthesis - genetics | en_HK |
dc.subject.mesh | Radiculopathy - drug therapy - metabolism - pathology | en_HK |
dc.subject.mesh | Rats | en_HK |
dc.subject.mesh | Rats, Sprague-Dawley | en_HK |
dc.subject.mesh | Receptor, Nerve Growth Factor | en_HK |
dc.subject.mesh | Receptors, Nerve Growth Factor - biosynthesis - genetics | en_HK |
dc.title | GDNF and BDNF alter the expression of neuronal NOS, c-Jun, and p75 and prevent motoneuron death following spinal root avulsion in adult rats | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0897-7151&volume=20 No 6&spage=603&epage=612&date=2003&atitle=GDNF+and+BDNF+alter+the+expression+of+neuronal+NOS,+c-Jun,+and+p75+and+prevent+motoneuron+death+following+spinal+root+avulsion+in+adult+rats | en_HK |
dc.identifier.email | Wu, W:wtwu@hkucc.hku.hk | en_HK |
dc.identifier.authority | Wu, W=rp00419 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1089/089771503767168528 | - |
dc.identifier.pmid | 12906744 | - |
dc.identifier.scopus | eid_2-s2.0-0038045085 | en_HK |
dc.identifier.hkuros | 85075 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0038045085&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 20 | en_HK |
dc.identifier.issue | 6 | en_HK |
dc.identifier.spage | 603 | en_HK |
dc.identifier.epage | 612 | en_HK |
dc.identifier.isi | WOS:000183926900008 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Wu, W=7407081122 | en_HK |
dc.identifier.scopusauthorid | Li, L=9038682000 | en_HK |
dc.identifier.scopusauthorid | Yick, LW=6603414804 | en_HK |
dc.identifier.scopusauthorid | Chai, H=35918658800 | en_HK |
dc.identifier.scopusauthorid | Xie, Y=7403958873 | en_HK |
dc.identifier.scopusauthorid | Yang, Y=8675011000 | en_HK |
dc.identifier.scopusauthorid | Prevette, DM=7003628635 | en_HK |
dc.identifier.scopusauthorid | Oppenheim, RW=7102628195 | en_HK |
dc.identifier.issnl | 0897-7151 | - |