Effects of mitochondrial dysfunction on glutamate receptor-mediated neurotoxicity in cultured rat spinal motor neurons

Kanki, R; Nakamizo, T; Yamashita, H; Kihara, T; Sawada, H; Uemura, K; Kawamata, J; Shibasaki, H; Akaike, A; Shimohama, S

HERO ID

4926318

Reference Type

Journal Article

Year

2004

Language

English

PMID

15223368

HERO ID 4926318
In Press No
Year 2004
Title Effects of mitochondrial dysfunction on glutamate receptor-mediated neurotoxicity in cultured rat spinal motor neurons
Authors Kanki, R; Nakamizo, T; Yamashita, H; Kihara, T; Sawada, H; Uemura, K; Kawamata, J; Shibasaki, H; Akaike, A; Shimohama, S
Journal Brain Research
Volume 1015
Issue 1-2
Page Numbers 73-81
Abstract Glutamate-induced excitotoxicity is implicated as playing a key role in the pathogenesis of amyotrophic lateral sclerosis (ALS), and mitochondrial dysfunction is also found in ALS patients. We investigated the relationship between glutamate excitotoxicity and mitochondrial dysfunction elicited by rotenone (a complex I inhibitor), malonate (a complex II inhibitor), or antimycin (a complex III inhibitor), in primary cultures of the embryonic rat spinal cord. Rotenone and malonate induced relatively selective toxicity against motor neurons as compared to non-motor neurons, whereas antimycin caused non-selective toxicity. The toxicity of rotenone was prevented by a non-N-methyl-D-aspartate (NMDA) receptor antagonist, 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) but not by an NMDA receptor antagonist, 5-methyl-10, 11-dihydro-5H-dibenzo[a,d]cyclohepten-5,10-imine hydrogen maleate (MK-801). The toxicity of malonate was blocked by both CNQX and MK-801. The toxicity of antimycin was affected by neither CNQX nor MK-801. When mitochondrial complex I was mildly inhibited by a sub-lethal concentration of rotenone, AMPA-induced motor neuron death was significantly exacerbated. A sub-lethal concentration of malonate exacerbated both NMDA- and AMPA-induced motor neuron death. These data suggest that mitochondrial dysfunction predisposes motor neurons to ionotropic glutamate receptor-mediated excitotoxicity.
Doi 10.1016/j.brainres.2004.04.044
Pmid 15223368
Wosid WOS:000222879500009
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English