Up-regulation of glutamate concentration in the putamen and in the prefrontal cortex of asymptomatic SIVmac251-infected macaques without major brain involvement

被引:12
作者
Bossuet, C
Vaufrey, F
Condé, F
Chrétien, F
Pichon, J
Hantraye, P
Le Grand, R
Dormont, D
Gras, G
机构
[1] Univ Paris Sud, Ctr Rech, Ecole Prat Hautes Etud, Serv Sante Armees,Inst Paris Sud Cytokines,CEA,UM, Fontenay Aux Roses, France
[2] CEA, Serv Hosp Frederic Joliot, DRM, DSV,UIIBP, F-91406 Orsay, France
[3] CEA, Serv Hosp Frederic Joliot, CNRS, URA 2210, F-91406 Orsay, France
[4] Univ Orleans, Dept Biol, UPRES, EA 2633, Orleans, France
[5] Univ Paris 12, Fac Med, INSERM, EMI 0011, Creteil, France
关键词
high performance liquid chromatography; immunohistochemistry; magnetic resonance spectroscopy; pathogenesis; primate; simian immunodeficiency virus;
D O I
10.1046/j.1471-4159.2003.02237.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We quantified putamen and prefrontal cortex metabolites in macaques with simian immunodeficiency virus infection and searched for virological and histological correlates. Fourteen asymptomatic macaques infected since 8-78 months (median: 38) were compared with eight uninfected ones. Absolute concentrations of acetate, alanine, aspartate, choline, creatine, GABA, glutamate, glutamine, lactate, myo-inositol, N-acetylaspartate, taurine and valine were determined by ex vivo proton magnetic resonance spectroscopy. Glutamate concentration in the CSF was determined by HPLC. Gliosis was assessed, by glial fibrillary acidic protein and CD68 immunohistochemistry. Glutamate concentration was slightly increased in the prefrontal cortex (119%, p = 0.0152, Hest) and putamen (13%, p = 0.0354, t-test) of the infected macaques, and was unaffected in the CSF. Myo-inositol concentration was increased in the prefrontal cortex only (27%, p = 0.0136). The concentrations of glutamate and myoinositol in the prefrontal cortex were higher in the animals with marked or intense microgliosis (p = 0.0114). The other studied metabolites, including N-acetylaspartate, were not altered. Glutamate concentration may thus increase in the cerebral parenchyma in asymptomatic animals, but is not accompanied by a detectable. decrease in N-acetylaspartate concentration (neuronal dysfunction). Thus, there are probably compensatory mechanisms that may limit glutamate increase and/or counterbalance its effects.
引用
收藏
页码:928 / 938
页数:11
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