Sources of the neurotoxin quinolinic acid in the brain of HIV-1-infected patients and retrovirus-infected macaques

被引:122
作者
Heyes, MP
Saito, K
Lackner, A
Wiley, CA
Achim, CL
Markey, SP
机构
[1] NIMH, Lab Neurotoxicol, Bethesda, MD 20892 USA
[2] Harvard Univ, Sch Med, New England Reg Primate Res Ctr, Southborough, MA 01772 USA
[3] Presbyterian Univ Hosp, Div Neuropathol, Pittsburgh, PA 15213 USA
关键词
macrophages; astrocytes; indoleamine-2,3-dioxygenase; kynurenine-3-hydroxylase; kynureninase; kynurenine aminotransferase; L-tryptophan; L-kynurenine; kynurenic acid; retrovirus; blood-brain barrier; cytokines; nonhuman primates;
D O I
10.1096/fasebj.12.10.881
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
This: study investigated the sources of quinolinic acid, a neurotoxic tryptophan-kynurenine pathway metabolite, in the brain and blood of HIV-infected patients and retrovirus-infected macaques.In brain, quinolinic acid concentrations in HIV-infected patients were elevated by >300-fold to concentrations that exceeded cerebrospinal fluid (CSF) by 8.9-fold. There were no significant correlations between elevated serum quinolinic acid levels with those in CSF and brain parenchyma. Because nonretrovirus-induced encephalitis confounds the interpretation of human postmortem data, rhesus macaques infected with retrovirus were used to examine the mechanisms of increased quinolinic acid accumulations and determine the relationships of quinolinic acid to encephalitits and systemic responses. The largest kynurenine pathway responses in brain were associated with encephalitis and were independent of systemic responses. CSF quinolinic acid levels were also elevated in all infected macaques, but particularly those with retrovirus-induced encephalitis. In contrast to the brain changes, there was no difference in any systemic measure between macaques with encephalitis: vs. those without. Direct measures of the amount of quinolinic acid in brain derived from blood in a macaque with encephalitis showed that almost all quinolinic acid (>98%) was synthesized locally within the brain. These results demonstrate a role for induction of indoleamine-2,3-dioxygenase in accelerating the local formation of quinolinic acid within the brain tissue, particularly in areas of encephalitis, rather than entry of quinolinic acid into the brain from the meninges or blood. Strategies to reduce QUIN production, targeted at intracerebral sites, are potential approaches to therapy.-Heyes, M. P., Saito, K., Lackner, A., Wiley, C. A., Achim, C. L., Markey, S. P. Sources of the neurotoxin quinolinic acid in the brain of HIV-l-infected patients and retrovirus-infected macaques.
引用
收藏
页码:881 / 896
页数:16
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