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未经治疗的无症状 HIV 患者中多巴胺能神经传递的增加与多巴胺能突触的适应性变化无关。

Increased dopaminergic neurotransmission in therapy-naïve asymptomatic HIV patients is not associated with adaptive changes at the dopaminergic synapses.

机构信息

Institute of Virology and Immunobiology, University of Würzburg, Versbacherstr. 7, 97078 Würzburg, Germany.

出版信息

J Neural Transm (Vienna). 2010 Jun;117(6):699-705. doi: 10.1007/s00702-010-0415-6. Epub 2010 May 9.

Abstract

Central dopaminergic (DA) systems are affected during human immunodeficiency virus (HIV) infection. So far, it is believed that they degenerate with progression of HIV disease because deterioration of DA systems is evident in advanced stages of infection. In this manuscript we found that (a) DA levels are increased and DA turnover is decreased in CSF of therapy-naïve HIV patients in asymptomatic infection, (b) DA increase does not modulate the availability of DA transporters and D2-receptors, (c) DA correlates inversely with CD4+ numbers in blood. These findings show activation of central DA systems without development of adaptive responses at DA synapses in asymptomatic HIV infection. It is probable that DA deterioration in advanced stages of HIV infection may derive from increased DA availability in early infection, resulting in DA neurotoxicity. Our findings provide a clue to the synergism between DA medication or drugs of abuse and HIV infection to exacerbate and accelerate HIV neuropsychiatric disease, a central issue in the neurobiology of HIV.

摘要

中枢多巴胺(DA)系统在人类免疫缺陷病毒(HIV)感染期间受到影响。到目前为止,人们认为随着 HIV 疾病的进展,它们会退化,因为在感染的晚期,DA 系统的恶化是明显的。在本文中,我们发现:(a)在无症状感染的未经治疗的 HIV 患者的 CSF 中,DA 水平升高,DA 周转率降低;(b)DA 增加不会调节 DA 转运体和 D2 受体的可用性;(c)DA 与血液中的 CD4+数量呈负相关。这些发现表明,在无症状 HIV 感染中,中枢 DA 系统在没有适应反应的情况下被激活。在 HIV 感染的晚期,DA 的恶化可能源于早期感染中 DA 可用性的增加,导致 DA 神经毒性。我们的发现为 DA 药物或滥用药物与 HIV 感染之间的协同作用提供了线索,这种协同作用会加剧和加速 HIV 神经精神疾病,这是 HIV 神经生物学中的一个核心问题。

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