Attenuation of N-methyl-D-aspartate-mediated cytoplasmic vacuolization in primary rat hippocampal neurons by mood stabilizers

被引:33
作者
Bown, CD [1 ]
Wang, JF [1 ]
Young, LT [1 ]
机构
[1] McMaster Univ, Mood Disorders Program, Dept Psychiat & Behav Neurosci, Hamilton, ON L8N 3Z5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
vacuolization; lithium; valproate; carbamazepine; neuroprotection; transmission electron microscopy;
D O I
10.1016/S0306-4522(02)00743-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent post-mortem and brain imaging studies suggest that decreased neuronal and glial densities may account for cell loss in vulnerable brain regions such as the hippocampus and the frontal cortex in patients with bipolar disorder. Investigations into the mechanisms of action of mood stabilizers suggest that these drugs may regulate the expression of neuroprotective genes and protect against excitotoxicity. In this study, we characterized the ultrastructural appearance of rat hippocampal neurons pretreated with mood stabilizers and then exposed to the glutamate receptor agonist N-methyl-D-aspartate. Using transmission electron microscopy we found that rat hippocampal neurons exposed to 0.5 mM N-methyl-D-aspartate for 10 min produced more cytoplasmic vacuolization than in control neurons. Chronic treatment with mood stabilizers, lithium, valproate or carbamazepine for 7 days at therapeutically relevant concentrations fully attenuated N-methyl-D-aspartate-mediated cytoplasmic vacuolization. These results suggest that inhibition of neurotoxicity may be involved in the action of mood stabilizers. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:949 / 955
页数:7
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