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感染HIV的小鼠对可卡因寻求行为的消退受损,同时伴有外周和中枢免疫失调。

Impaired extinction of cocaine seeking in HIV-infected mice is accompanied by peripheral and central immune dysregulation.

作者信息

Barker Jacqueline, Buck Lauren, Xie Qiaowei, Willis Michelle, Side Christine, Giacometti Laura, Gaskill Peter, Park Kyewon, Shaheen Farida, Guo Lili, Gorantla Santhi

机构信息

Drexel University.

出版信息

Res Sq. 2023 Sep 28:rs.3.rs-3276379. doi: 10.21203/rs.3.rs-3276379/v1.

Abstract

Substance use disorders (SUDs) are highly comorbid with HIV infection, necessitating an understanding of the interactive effects of drug exposure and HIV. The relationship between HIV infection and cocaine use disorder is likely bidirectional, with cocaine use directly impacting immune function while HIV infection alters addiction-related behavior. To better characterize the neurobehavioral and immune consequences of HIV infection and cocaine exposure, this study utilized a humanized mouse model to investigate the outcomes of HIV-1 infection on cocaine-related behaviors in a conditioned place preference (CPP) model, and the interactive effects of cocaine and HIV infection on peripheral and central nervous system inflammation. HIV infection selectively impaired cocaine CPP extinction without effecting reinstatement or cocaine seeking under conflict were observed. Behavioral alterations were accompanied by immune changes in HIV infected mice, including increased prefrontal cortex astrocyte immunoreactivity and brain-region specific effects on microglia number and reactivity. Peripheral immune system changes were observed in both mouse and human cytokines, including HIV-induced reductions in mouse IL-1α and G-CSF and human TNFα, and cocaine induced alterations in mouse GM-CSF. Together these data provide new insights into the unique neurobehavioral outcomes of HIV infection and cocaine exposure and how they interact to effect immune responses.

摘要

物质使用障碍(SUDs)与HIV感染高度共病,因此有必要了解药物暴露与HIV的交互作用。HIV感染与可卡因使用障碍之间的关系可能是双向的,可卡因使用直接影响免疫功能,而HIV感染则改变与成瘾相关的行为。为了更好地表征HIV感染和可卡因暴露对神经行为和免疫的影响,本研究利用人源化小鼠模型,在条件性位置偏爱(CPP)模型中研究HIV-1感染对可卡因相关行为的影响,以及可卡因和HIV感染对周围和中枢神经系统炎症的交互作用。观察到HIV感染选择性地损害了可卡因CPP消退,而在冲突情况下对恢复或寻求可卡因没有影响。行为改变伴随着HIV感染小鼠的免疫变化,包括前额叶皮质星形胶质细胞免疫反应性增加以及对小胶质细胞数量和反应性的脑区特异性影响。在小鼠和人类细胞因子中均观察到外周免疫系统变化,包括HIV诱导的小鼠IL-1α和G-CSF减少以及人类TNFα减少,以及可卡因诱导的小鼠GM-CSF改变。这些数据共同为HIV感染和可卡因暴露的独特神经行为结果以及它们如何相互作用影响免疫反应提供了新的见解。

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