Department of Pathology and Laboratory Medicine, Temple University School of Medicine, Philadelphia, PA 19140, USA.
Brain Behav Immun. 2011 Jun;25 Suppl 1(Suppl 1):S61-70. doi: 10.1016/j.bbi.2011.03.001. Epub 2011 Mar 21.
Clinical studies indicate that alcohol dependence has an additive effect on cognitive deficits associated with HIV-1 infection. Findings in humans and animal models suggest that alcohol, similar to HIV-1, induces inflammatory processes in the brain leading to neurodegeneration. The causes of HIV-1-associated neurotoxicity are comparable to those mediating alcohol-induced neuronal injury. This review aims to present the mechanisms of the combined effects of HIV-1 and alcohol abuse in the brain and to discuss neuroprotective therapies. Oxidative stress, overproduction of pro-inflammatory factors, impairment of blood-brain barrier and glutamate associated neurotoxicity appear to play important roles in alcohol driven neurodegeneration. Diminution of neuroinflammation constitutes a logical approach for prevention of HIV-1 and alcohol mediated neurodegeneration. Agonists of cannabinoid receptor 2 (CB₂) possess potent anti-inflammatory and neuroprotective properties. We address multifaceted beneficial effects of CB₂ activation in the setting of HIV-1 brain infection and alcohol abuse.
临床研究表明,酒精依赖会加剧与 HIV-1 感染相关的认知缺陷。人类和动物模型的研究结果表明,酒精与 HIV-1 类似,会在大脑中引发炎症反应,导致神经退行性变。导致 HIV-1 相关神经毒性的原因与介导酒精诱导的神经元损伤的原因相似。本文旨在介绍 HIV-1 和酒精滥用在大脑中的联合作用机制,并讨论神经保护治疗方法。氧化应激、促炎因子的过度产生、血脑屏障的损害以及谷氨酸相关的神经毒性似乎在酒精驱动的神经退行性变中发挥着重要作用。减轻神经炎症是预防 HIV-1 和酒精介导的神经退行性变的合理方法。大麻素受体 2(CB₂)激动剂具有强大的抗炎和神经保护作用。我们将探讨 CB₂ 激活在 HIV-1 脑感染和酒精滥用情况下的多方面有益作用。