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https://ahro.austin.org.au/austinjspui/handle/1/9264
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Batchelor, Peter Egerton | en |
dc.contributor.author | Liberatore, G T | en |
dc.contributor.author | Porritt, Michelle J | en |
dc.contributor.author | Donnan, Geoffrey A | en |
dc.contributor.author | Howells, David William | en |
dc.date.accessioned | 2015-05-15T22:17:24Z | |
dc.date.available | 2015-05-15T22:17:24Z | |
dc.date.issued | 2000-10-01 | en |
dc.identifier.citation | The European Journal of Neuroscience; 12(10): 3462-8 | en |
dc.identifier.govdoc | 11029615 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/9264 | en |
dc.description.abstract | After striatal injury, sprouting dopaminergic fibres grow towards and intimately surround wound macrophages which, together with microglia, express the dopaminergic neurotrophic factors glial cell line-derived neurotrophic factor (GDNF) and brain derived neurotrophic factor (BDNF). To evaluate the importance of these endogenously secreted neurotrophic factors in generating striatal peri-wound dopaminergic sprouting, the peri-wound expression of BDNF or GDNF was inhibited by intrastriatal infusion of antisense oligonucleotides for 2 weeks in mice. Knock-down of both BDNF and GDNF mRNA and protein levels in the wounded striatum were confirmed by in situ hybridization and enzyme-linked immunosorbent assay, respectively. Dopamine transporter immunohisto-chemistry revealed that inhibition of either BDNF or GDNF expression resulted in a marked decrease in the intensity of peri-wound sprouting. Quantification of this effect using [H3]-mazindol autoradiography confirmed that peri-wound sprouting was significantly reduced in mice receiving BDNF or GDNF antisense infusions whilst control infusions of buffered saline or sense oligonucleotides resulted in the pronounced peri-wound sprouting response normally associated with striatal injury. BDNF and GDNF thus appear to be important neurotrophic factors inducing dopaminergic sprouting after striatal injury. | en |
dc.language.iso | en | en |
dc.subject.other | Animals | en |
dc.subject.other | Brain Injuries.drug therapy.pathology.physiopathology | en |
dc.subject.other | Brain-Derived Neurotrophic Factor.drug effects.genetics.metabolism | en |
dc.subject.other | Dopamine.metabolism | en |
dc.subject.other | Glial Cell Line-Derived Neurotrophic Factor | en |
dc.subject.other | Growth Cones.drug effects.metabolism | en |
dc.subject.other | Male | en |
dc.subject.other | Mice | en |
dc.subject.other | Mice, Inbred C57BL | en |
dc.subject.other | Neostriatum.metabolism.physiopathology.surgery | en |
dc.subject.other | Nerve Growth Factors | en |
dc.subject.other | Nerve Regeneration.drug effects.genetics | en |
dc.subject.other | Nerve Tissue Proteins.drug effects.genetics.metabolism | en |
dc.subject.other | Neuronal Plasticity.drug effects.genetics | en |
dc.subject.other | Oligonucleotides, Antisense.pharmacology | en |
dc.subject.other | RNA, Messenger.metabolism | en |
dc.subject.other | Wound Healing.drug effects.genetics | en |
dc.title | Inhibition of brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression reduces dopaminergic sprouting in the injured striatum. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | The European journal of neuroscience | en |
dc.identifier.affiliation | Department of Medicine, University of Melbourne, Austin, Australia | en |
dc.description.pages | 3462-8 | en |
dc.relation.url | https://pubmed.ncbi.nlm.nih.gov/11029615 | en |
dc.type.austin | Journal Article | en |
local.name.researcher | Donnan, Geoffrey A | |
item.languageiso639-1 | en | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.openairetype | Journal Article | - |
crisitem.author.dept | The Florey Institute of Neuroscience and Mental Health | - |
Appears in Collections: | Journal articles |
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