Dopamine-denervation enhances the trophic activity in striatum: evaluation by morphological and electrophysiological development in PC12D cells

Neurosci Res. 1997 Jul;28(3):209-21. doi: 10.1016/s0168-0102(97)00046-1.

Abstract

To evaluate the possibility that dopamine (DA) denervation enhances the trophic activity in striatum, normal or DA-depleted striatal tissue extract (N- or L-extract, respectively) was obtained, and their trophic effects on PC12D cells were investigated from the viewpoints of differentiation using morphological and electrophysiological analyses. Treatment with N- or L-extract induced neurite outgrowth in a concentration-dependent manner, and induced the enlargement of cell size. These effects were stronger in L-extract than in N-extract. Cation currents were investigated in whole cell patch-clamp mode. Development of cation current started with delayed-rectifier type K+ current (IK) and transient type K+ current (IA), followed by Ca2+ current (ICa) and tetrodotoxin-sensitive Na+ current (INa). INa was expressed more frequently in L-extract treated cells than N-extract treated cells at D7-9. The larger IK amplitude in L-extract treatment at D7-9 seemed to be related to the expression of INa. Development of IA was similar at any stage for both treatments. ICa development started at D3-5 after treatments, and the amplitude and current density were similar in both treatments. ICa was strongly blocked by omega-conotoxin GVIA (3 microM), indicating that N-type channels were mainly expressed after treatments. The data suggests that L-extract has stronger effects to hasten the differentiation of PC12D cells than N-extract by promoting the neurite outgrowth, cell enlargement and expression of voltage-dependent cation channels, especially INa and IK.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / drug effects
  • Axons / physiology
  • Calcium Channels / drug effects
  • Cell Size / drug effects
  • Denervation
  • Dopamine / physiology*
  • Electrophysiology
  • Female
  • Fibroblast Growth Factor 2 / pharmacology
  • Ion Channel Gating / drug effects
  • Neostriatum / physiology*
  • Neostriatum / ultrastructure
  • Nerve Growth Factors / pharmacology
  • Neurites / drug effects
  • Neurites / ultrastructure
  • PC12 Cells
  • Patch-Clamp Techniques
  • Potassium Channels / drug effects
  • Rats
  • Rats, Wistar
  • Sodium Channels / drug effects
  • Tissue Extracts / pharmacology

Substances

  • Calcium Channels
  • Nerve Growth Factors
  • Potassium Channels
  • Sodium Channels
  • Tissue Extracts
  • Fibroblast Growth Factor 2
  • Dopamine