β-Amyloid neurotoxicity is mediated by a glutamate-triggered excitotoxic cascade in rat nucleus basalis

T. Harkany, I. Ábrahám, W. Timmerman, G. Laskay, B. Tóth, M. Sasvári, C. Kónya, J. B. Sebens, J. Korf, C. Nyakas, M. Zarándi, K. Soós, B. Penke, P. G M Luiten

Research output: Contribution to journalArticle

215 Citations (Scopus)

Abstract

Whereas a cardinal role for β-amyloid protein (Aβ) has been postulated as a major trigger of neuronal injury in Alzheimer's disease, the pathogenic mechanism by which Aβ deranges nerve cells remains largely elusive. Here we report correlative in vitro and in vivo evidence that an excitotoxic cascade mediates Aβ neurotoxicity in the rat magnocellular nucleus basalis (MBN). In vitro application of Aβ to astrocytes elicits rapid depolarization of astroglial membranes with a concomitant inhibition of glutamate uptake. In vivo Aβ infusion by way of microdialysis in the MBN revealed peak extracellular concentrations of excitatory amino acid neurotransmitters within 20-30 min. Aβ-triggered extracellular elevation of excitatory amino acids coincided with a significantly enhanced intracellular accumulation of Ca2+ in the Aβ injection area, as was demonstrated by 45Ca2+ autoradiography. In consequence of these acute processes delayed cell death in the MBN and persistent loss of cholinergic fibre projections to the neocortex appear as early as 3 days following the Aβ-induced toxic insult. Such a sequence of Aβ toxicity was effectively antagonized by the N-methyl-D-aspartate (NMDA) receptor ligand dizocilpine maleate (MK-801). Moreover, Aβ toxicity in the MBN decreases with advancing age that may be associated with the age-related loss of NMDA receptor expression in rats. In summary, the present results indicate that Aβ compromises neurons of the rat MBN via an excitotoxic pathway including astroglial depolarization, extracellular glutamate accumulation, NMDA receptor activation and an intracellular Ca2+ overload leading to cell death.

Original languageEnglish
Pages (from-to)2735-2745
Number of pages11
JournalEuropean Journal of Neuroscience
Volume12
Issue number8
DOIs
Publication statusPublished - 2000

Fingerprint

N-Methyl-D-Aspartate Receptors
Amyloid
Glutamic Acid
Excitatory Amino Acids
Dizocilpine Maleate
Cell Death
Cholinergic Fibers
Neurons
Serum Amyloid A Protein
Poisons
Neocortex
Microdialysis
Autoradiography
Astrocytes
Neurotransmitter Agents
Alzheimer Disease
Ligands
Injections
Membranes
Wounds and Injuries

Keywords

  • Alzheimer's disease
  • Calcium
  • Excitotoxicity
  • N-methyl-D-aspartate receptor

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

β-Amyloid neurotoxicity is mediated by a glutamate-triggered excitotoxic cascade in rat nucleus basalis. / Harkany, T.; Ábrahám, I.; Timmerman, W.; Laskay, G.; Tóth, B.; Sasvári, M.; Kónya, C.; Sebens, J. B.; Korf, J.; Nyakas, C.; Zarándi, M.; Soós, K.; Penke, B.; Luiten, P. G M.

In: European Journal of Neuroscience, Vol. 12, No. 8, 2000, p. 2735-2745.

Research output: Contribution to journalArticle

Harkany, T. ; Ábrahám, I. ; Timmerman, W. ; Laskay, G. ; Tóth, B. ; Sasvári, M. ; Kónya, C. ; Sebens, J. B. ; Korf, J. ; Nyakas, C. ; Zarándi, M. ; Soós, K. ; Penke, B. ; Luiten, P. G M. / β-Amyloid neurotoxicity is mediated by a glutamate-triggered excitotoxic cascade in rat nucleus basalis. In: European Journal of Neuroscience. 2000 ; Vol. 12, No. 8. pp. 2735-2745.
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AU - Harkany, T.

AU - Ábrahám, I.

AU - Timmerman, W.

AU - Laskay, G.

AU - Tóth, B.

AU - Sasvári, M.

AU - Kónya, C.

AU - Sebens, J. B.

AU - Korf, J.

AU - Nyakas, C.

AU - Zarándi, M.

AU - Soós, K.

AU - Penke, B.

AU - Luiten, P. G M

PY - 2000

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N2 - Whereas a cardinal role for β-amyloid protein (Aβ) has been postulated as a major trigger of neuronal injury in Alzheimer's disease, the pathogenic mechanism by which Aβ deranges nerve cells remains largely elusive. Here we report correlative in vitro and in vivo evidence that an excitotoxic cascade mediates Aβ neurotoxicity in the rat magnocellular nucleus basalis (MBN). In vitro application of Aβ to astrocytes elicits rapid depolarization of astroglial membranes with a concomitant inhibition of glutamate uptake. In vivo Aβ infusion by way of microdialysis in the MBN revealed peak extracellular concentrations of excitatory amino acid neurotransmitters within 20-30 min. Aβ-triggered extracellular elevation of excitatory amino acids coincided with a significantly enhanced intracellular accumulation of Ca2+ in the Aβ injection area, as was demonstrated by 45Ca2+ autoradiography. In consequence of these acute processes delayed cell death in the MBN and persistent loss of cholinergic fibre projections to the neocortex appear as early as 3 days following the Aβ-induced toxic insult. Such a sequence of Aβ toxicity was effectively antagonized by the N-methyl-D-aspartate (NMDA) receptor ligand dizocilpine maleate (MK-801). Moreover, Aβ toxicity in the MBN decreases with advancing age that may be associated with the age-related loss of NMDA receptor expression in rats. In summary, the present results indicate that Aβ compromises neurons of the rat MBN via an excitotoxic pathway including astroglial depolarization, extracellular glutamate accumulation, NMDA receptor activation and an intracellular Ca2+ overload leading to cell death.

AB - Whereas a cardinal role for β-amyloid protein (Aβ) has been postulated as a major trigger of neuronal injury in Alzheimer's disease, the pathogenic mechanism by which Aβ deranges nerve cells remains largely elusive. Here we report correlative in vitro and in vivo evidence that an excitotoxic cascade mediates Aβ neurotoxicity in the rat magnocellular nucleus basalis (MBN). In vitro application of Aβ to astrocytes elicits rapid depolarization of astroglial membranes with a concomitant inhibition of glutamate uptake. In vivo Aβ infusion by way of microdialysis in the MBN revealed peak extracellular concentrations of excitatory amino acid neurotransmitters within 20-30 min. Aβ-triggered extracellular elevation of excitatory amino acids coincided with a significantly enhanced intracellular accumulation of Ca2+ in the Aβ injection area, as was demonstrated by 45Ca2+ autoradiography. In consequence of these acute processes delayed cell death in the MBN and persistent loss of cholinergic fibre projections to the neocortex appear as early as 3 days following the Aβ-induced toxic insult. Such a sequence of Aβ toxicity was effectively antagonized by the N-methyl-D-aspartate (NMDA) receptor ligand dizocilpine maleate (MK-801). Moreover, Aβ toxicity in the MBN decreases with advancing age that may be associated with the age-related loss of NMDA receptor expression in rats. In summary, the present results indicate that Aβ compromises neurons of the rat MBN via an excitotoxic pathway including astroglial depolarization, extracellular glutamate accumulation, NMDA receptor activation and an intracellular Ca2+ overload leading to cell death.

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