Ca2+ channel blockers attenuate beta-amyloid peptide toxicity to cortical neurons in culture

J Neurochem. 1994 Jan;62(1):372-5. doi: 10.1046/j.1471-4159.1994.62010372.x.

Abstract

Deposit of beta-amyloid protein (A beta) in Alzheimer's disease brain may contribute to the associated neurodegeneration. We have studied the neurotoxicity of A beta in primary cultures of murine cortical neurons, with the aim of identifying pharmacologic ways of attenuating the injury. Exposure of cultures to A beta (25-35 fragment; 3-25 microM) generally triggers slow, concentration-dependent neurodegeneration (over 24-72 h). With submaximal A beta-(25-35) exposure (10 microM), substantial (> 40% within 48 h) degeneration often occurs and is markedly attenuated by the presence of the Ca2+ channel blockers nimodipine (1-20 microM) and Co2+ (100 microM) during the A beta exposure. However, A beta neurotoxicity is not affected by the presence of glutamate receptor antagonists. We suggest that Ca2+ influx through voltage-gated Ca2+ channels may contribute to A beta-induced neuronal injury and that nimodipine and Co2+, by attenuating such influx, are able to attenuate A beta neurotoxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amyloid beta-Peptides / antagonists & inhibitors
  • Amyloid beta-Peptides / toxicity*
  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Cells, Cultured
  • Cerebral Cortex / cytology*
  • Dizocilpine Maleate / pharmacology
  • Fetus
  • Mice
  • Neurons / cytology
  • Neurons / drug effects*
  • Neurotoxins / antagonists & inhibitors
  • Neurotoxins / toxicity*
  • Nimodipine / pharmacology*
  • Quinoxalines / pharmacology

Substances

  • Amyloid beta-Peptides
  • Calcium Channel Blockers
  • Neurotoxins
  • Quinoxalines
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Nimodipine
  • Dizocilpine Maleate