Department of Pharmacology & Physiology, College of Medicine, Drexel University, Philadelphia, PA, USA.
Department of Pharmacology & Physiology, College of Medicine, Drexel University, Philadelphia, PA, USA.
Brain Behav Immun. 2023 Oct;113:453-475. doi: 10.1016/j.bbi.2023.07.021. Epub 2023 Aug 9.
Human immunodeficiency virus (HIV) remains a persistent public health concern throughout the world. Substance use disorders (SUDs) are a common comorbidity that can worsen treatment outcomes for people living with HIV. The relationship between HIV infection and SUD outcomes is likely bidirectional, making clear interrogation of neurobehavioral outcomes challenging in clinical populations. Importantly, the mechanisms through which HIV and addictive drugs disrupt homeostatic immune and CNS function appear to be highly overlapping and synergistic within HIV-susceptible reward and motivation circuitry in the central nervous system. Decades of animal research have revealed invaluable insights into mechanisms underlying the pathophysiology SUDs and HIV, although translational studies examining comorbid SUDs and HIV are very limited due to the technical challenges of modeling HIV infection preclinically. In this review, we discuss preclinical animal models of HIV and highlight key pathophysiological characteristics of each model, with a particular emphasis on rodent models of HIV. We then review the implementation of these models in preclinical SUD research and identify key gaps in knowledge in the field. Finally, we discuss how cutting-edge behavioral neuroscience tools, which have revealed key insights into the neurobehavioral mechanisms of SUDs, can be applied to preclinical animal models of HIV to reveal potential, novel treatment avenues for comorbid HIV and SUDs. Here, we argue that future preclinical SUD research would benefit from incorporating comorbidities such as HIV into animal models and would facilitate the discovery of more refined, subpopulation-specific mechanisms and effective SUD prevention and treatment targets.
人类免疫缺陷病毒(HIV)仍然是全球持续存在的公共卫生问题。物质使用障碍(SUD)是一种常见的合并症,可能会恶化 HIV 感染者的治疗效果。HIV 感染和 SUD 结果之间的关系可能是双向的,这使得在临床人群中明确检查神经行为结果具有挑战性。重要的是,HIV 和成瘾药物破坏稳态免疫和中枢神经系统功能的机制在 HIV 易感奖励和动机中枢神经系统回路中似乎高度重叠和协同。几十年来的动物研究为理解 SUD 和 HIV 的病理生理学机制提供了宝贵的见解,尽管由于临床前模拟 HIV 感染的技术挑战,检查合并 SUD 和 HIV 的转化研究非常有限。在这篇综述中,我们讨论了 HIV 的临床前动物模型,并强调了每个模型的关键病理生理学特征,特别强调了 HIV 的啮齿动物模型。然后,我们回顾了这些模型在 SUD 研究中的临床前应用,并确定了该领域知识的关键空白。最后,我们讨论了如何将行为神经科学的前沿工具应用于 HIV 的临床前动物模型,以揭示合并 HIV 和 SUD 的潜在新治疗途径,这些工具揭示了 SUD 的神经行为机制的关键见解。在这里,我们认为未来的 SUD 临床前研究将受益于将 HIV 等合并症纳入动物模型,并促进发现更精细、特定于亚群的机制和有效的 SUD 预防和治疗靶点。