Neurodegeneration of substantia nigra accompanied with macrophage/microglia infiltration after intrastriatal hemorrhage

Neurosci Res. 2003 Jul;46(3):289-98. doi: 10.1016/s0168-0102(03)00065-8.

Abstract

Intrastriatal hemorrhage in rats causes neurodegenaration of the substantia nigra (SN) followed by the appearance of ED1(+) cells (macrophage/microglia). ED1(+) cells were observed for at least 8 weeks after hemorrhage. Phosphorylation of p38 mitogen-activated protein kinase (MAPK) was shown in ED1(+) cells with the expression of both brain-derived neurotrophic factor (BDNF) mRNA and BDNF, suggesting that activated-p38 MAPK(+)/ED1(+) cells would produce BDNF and may exhibit trophic effect on the degenerating neurons in the SN. However, in ELISA, BDNF protein decreased significantly in ipsilateral SN at 7 days after hemorrhage, which may be due to a dramatic decrease of BDNF immunoreactive neurons in pars compacta. Data suggest that activation of p38 MAPK in ED1(+) cells infiltrating in ipsilateral SN after hemorrhage may produce BDNF, but that the amount of BDNF produced from ED1(+) cells is insufficient for the rescue of degenerating neurons.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apomorphine / pharmacology
  • Behavior, Animal
  • Brain-Derived Neurotrophic Factor / biosynthesis
  • Brain-Derived Neurotrophic Factor / genetics
  • Central Nervous System Stimulants / pharmacology
  • Cerebral Hemorrhage / chemically induced
  • Cerebral Hemorrhage / complications*
  • Cerebral Hemorrhage / metabolism
  • Cerebral Hemorrhage / pathology
  • Collagenases / toxicity
  • Disease Models, Animal
  • Dopamine Agonists / pharmacology
  • Ectodysplasins
  • Enzyme-Linked Immunosorbent Assay
  • Functional Laterality
  • Immunohistochemistry
  • In Situ Hybridization
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Male
  • Membrane Proteins / metabolism
  • Methamphetamine / pharmacology
  • Microglia / metabolism*
  • Microglia / pathology
  • Mitogen-Activated Protein Kinases / biosynthesis
  • Nerve Degeneration / etiology*
  • Nerve Degeneration / metabolism
  • Nerve Degeneration / pathology
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Rotation
  • Substantia Nigra / metabolism
  • Substantia Nigra / pathology*
  • Time Factors
  • Tyrosine 3-Monooxygenase / metabolism
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Brain-Derived Neurotrophic Factor
  • Central Nervous System Stimulants
  • Dopamine Agonists
  • Ectodysplasins
  • Membrane Proteins
  • RNA, Messenger
  • Methamphetamine
  • Tyrosine 3-Monooxygenase
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Collagenases
  • Apomorphine