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D型逆转录病毒感染的恒河猴脑脊液中喹啉酸与犬尿烯酸比值升高:与临床及病毒状态的关系

Increased ratio of quinolinic acid to kynurenic acid in cerebrospinal fluid of D retrovirus-infected rhesus macaques: relationship to clinical and viral status.

作者信息

Heyes M P, Mefford I N, Quearry B J, Dedhia M, Lackner A

机构信息

Section on Analytical Biochemistry, National Institute of Mental Health, Bethesda, MD 20892.

出版信息

Ann Neurol. 1990 Jun;27(6):666-75. doi: 10.1002/ana.410270614.

Abstract

Increased concentrations of excitotoxin quinolinic acid in cerebrospinal fluid (CSF) are associated with infection with the human immunodeficiency virus (HIV-1) and have been implicated in the pathogenesis of the acquired immune deficiency syndrome (AIDS) dementia complex. In the present study, inoculation of macaques with D/1/California, an immunosuppressive serotype 1 type D retrovirus, was associated with acute and chronic increases in CSF and serum quinolinic acid concentrations in macaques that had developed SAIDS, a simian disease analogous to AIDS in humans--particularly macaques with demonstrable opportunistic infections. Kynurenic acid, an antagonist of excitatory amino acid receptors as well as the excitotoxic effects of quinolinic acid, was also increased in the CSF of SAIDS macaques, but to a significantly lesser degree than was quinolinic acid (kynurenic acid, 1.8-fold; quinolinic acid, 15.6-fold). CSF quinolinic acid, but not kynurenic acid, was also increased in viremic macaques with SAIDS-related complex (2.4-fold) and asymptomatic virus positive carriers (3.4-fold). Macaques that had recovered from D/1/California infection and were antibody positive and virus negative had normal CSF quinolinic acid and kynurenic acid concentrations. Increased activity of indoleamine-2,3-dioxygenase, the first enzyme of the kynurenine pathway, was indicated in the macaques with SAIDS by reduced serum L-tryptophan and elevated serum L-kynurenine concentrations. Macaques infected with D/1/California may provide a primate model for investigation of the mechanisms involved in increases in CSF quinolinic acid in retrovirus and other infectious diseases, including HIV-1. It remains to be determined whether the increased CSF quinolinic acid concentrations and the increased ratio of quinolinic acid to kynurenic acid have neurological significance or are a useful "marker" of infection.

摘要

脑脊液(CSF)中兴奋性毒素喹啉酸浓度的升高与人类免疫缺陷病毒(HIV-1)感染有关,并被认为与获得性免疫缺陷综合征(AIDS)痴呆综合征的发病机制有关。在本研究中,用D/1/加利福尼亚株(一种免疫抑制性D型1型逆转录病毒)接种猕猴,与已发展为SAIDS(一种类似于人类AIDS的猴病)的猕猴脑脊液和血清中喹啉酸浓度的急性和慢性升高有关,特别是那些有明显机会性感染的猕猴。犬尿喹啉酸是兴奋性氨基酸受体的拮抗剂以及喹啉酸的兴奋毒性作用的拮抗剂,在SAIDS猕猴的脑脊液中也有所增加,但程度明显低于喹啉酸(犬尿喹啉酸,1.8倍;喹啉酸,15.6倍)。在患有SAIDS相关综合征的病毒血症猕猴(2.4倍)和无症状病毒阳性携带者(3.4倍)中,脑脊液喹啉酸而非犬尿喹啉酸也有所增加。从D/1/加利福尼亚株感染中恢复且抗体阳性但病毒阴性的猕猴脑脊液喹啉酸和犬尿喹啉酸浓度正常。通过血清L-色氨酸降低和血清L-犬尿氨酸升高表明,患有SAIDS的猕猴中犬尿氨酸途径的第一种酶吲哚胺-2,3-双加氧酶的活性增加。感染D/1/加利福尼亚株的猕猴可能为研究逆转录病毒和其他传染病(包括HIV-1)中脑脊液喹啉酸增加所涉及的机制提供一个灵长类动物模型。脑脊液喹啉酸浓度升高以及喹啉酸与犬尿喹啉酸的比例增加是否具有神经学意义或是否是感染的有用“标志物”仍有待确定。

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