Direct exposure to N-methyl-D-aspartate alters mitochondrial function

被引:2
|
作者
Korde, Amit S. [1 ]
Maragos, William F. [1 ,2 ]
机构
[1] Hunter Holmes McGuire Vet Adm Med Ctr, Richmond, VA 23249 USA
[2] Virginia Commonwealth Univ, Dept Neurol, Med Coll Virginia Campus, Richmond, VA 23298 USA
关键词
Calcium; Cytochrome c; Mitochondria; N-methyl-D-aspartate receptor; Permeability transition; Reactive oxygen species; OXYGEN SPECIES GENERATION; NEURONAL DEATH; CALCIUM; GLUTAMATE; CA2+; APOPTOSIS;
D O I
10.1016/j.neulet.2016.04.054
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
N-methyl-D-aspartate (NMDA) receptors have long been known to be associated with the plasma membrane, providing a channel for the passage of extracellular Ca2+ into the cytosol during synaptic transmission. Recent results from our laboratory indicate that in addition to this classic location, an NMDA-sensitive site (NMDA(m)) may also exist within the inner mitochondrial membrane. We report direct exposure of mitochondrial to NMDA enhances the production of reactive oxygen species and attenuate ROS-induced cytochrome c release, all the while slowing the rate of Ca2+-induced mitochondrial swelling. Treatment with NMDA did not alter the mitochondrial membrane potential. The findings of this study lend further support for the existence of NMDA(m) and suggest that this site may serve to stabilize mitochondrial function. Published by Elsevier Ireland Ltd.
引用
收藏
页码:47 / 51
页数:5
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