Inhibition of brain-derived neurotrophic factor and glial cell line-derived neurotrophic factor expression reduces dopaminergic sprouting in the injured striatum

Eur J Neurosci. 2000 Oct;12(10):3462-8. doi: 10.1046/j.1460-9568.2000.00239.x.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Brain Injuries / drug therapy*
  • Brain Injuries / pathology
  • Brain Injuries / physiopathology
  • Brain-Derived Neurotrophic Factor / drug effects
  • Brain-Derived Neurotrophic Factor / genetics*
  • Brain-Derived Neurotrophic Factor / metabolism
  • Dopamine / metabolism*
  • Glial Cell Line-Derived Neurotrophic Factor
  • Growth Cones / drug effects
  • Growth Cones / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Neostriatum / metabolism
  • Neostriatum / physiopathology*
  • Neostriatum / surgery
  • Nerve Growth Factors*
  • Nerve Regeneration / drug effects*
  • Nerve Regeneration / genetics
  • Nerve Tissue Proteins / drug effects
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Neuronal Plasticity / drug effects*
  • Neuronal Plasticity / genetics
  • Oligonucleotides, Antisense / pharmacology
  • RNA, Messenger / metabolism
  • Wound Healing / drug effects
  • Wound Healing / genetics

Substances

  • Brain-Derived Neurotrophic Factor
  • Gdnf protein, mouse
  • Glial Cell Line-Derived Neurotrophic Factor
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Oligonucleotides, Antisense
  • RNA, Messenger
  • Dopamine