Prevention from hypoxia-induced apoptosis by pre-conditioning: a mechanistic approach in cultured neurons from fetal rat forebrain

Brain Res Mol Brain Res. 1998 Jul 15;58(1-2):237-9. doi: 10.1016/s0169-328x(98)00123-5.

Abstract

Molecular effects of pre-conditioning by 1-h hypoxia were investigated in cultured neurons from fetal rat forebrain, submitted the following day to a 6-h hypoxia that induces apoptosis. While preventing from apoptosis, pre-conditioning led to increased number of living neurons, DNA synthesis, with persistent overexpression of Bcl-2 and proliferating cell nuclear antigen (PCNA). Adaptative mechanisms would involve anti-apoptotic proteins and regulators of the cell cycle, to finally promote neuronal proliferation.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology*
  • Cell Cycle
  • Cell Division
  • Cell Hypoxia*
  • Cells, Cultured
  • Culture Media, Serum-Free
  • DNA / biosynthesis
  • Epidermal Growth Factor / pharmacology
  • Fetus
  • Fibroblast Growth Factor 2 / pharmacology
  • Mitosis
  • Necrosis
  • Neurons / cytology*
  • Neurons / physiology*
  • Proliferating Cell Nuclear Antigen / biosynthesis
  • Prosencephalon / cytology*
  • Prosencephalon / physiology*
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • Rats
  • Time Factors

Substances

  • Culture Media, Serum-Free
  • Proliferating Cell Nuclear Antigen
  • Proto-Oncogene Proteins c-bcl-2
  • Fibroblast Growth Factor 2
  • Epidermal Growth Factor
  • DNA