Namba Mark D, Xie Qiaowei, Park Kyewon, Jackson Joshua G, Barker Jacqueline M
Department of Pharmacology & Physiology, College of Medicine, Drexel University, PA, USA.
Graduate Program in Pharmacology and Physiology, College of Medicine, Drexel University, PA, USA.
Addict Neurosci. 2025 Jun;15. doi: 10.1016/j.addicn.2025.100208. Epub 2025 Apr 22.
Cocaine use disorders (CUDs) and human immunodeficiency virus (HIV) remain persistent public health dilemmas throughout the world. Cocaine seeking increases over a protracted period of abstinence, an effect known as the incubation of craving. Little is known about how HIV may modulate this process. Thus, we sought to examine the impact of chronic HIV infection on the incubation of cocaine craving and associated changes in the expression levels of central neuroimmune and peripheral immune substrates. Here, male mice were inoculated with EcoHIV, which is a chimeric HIV-1 construct that produces chronic HIV infection in mice. Mice were conditioned with cocaine daily or intermittently in a conditioned place preference (CPP) paradigm, followed by 1 or 21 days of forced abstinence prior to assessing preference for the cocaine-paired chamber. Mice conditioned daily exhibited potentiated incubation of cocaine CPP after 21 days of abstinence, and EcoHIV increased cocaine CPP across the test session at both abstinence timepoints. Conversely, EcoHIV-infected mice conditioned intermittently showed higher cocaine seeking after 1 day of abstinence compared to 21 days. Analysis of corticolimbic CX3CL1-CX3CR1 and glutamate receptor expression revealed a positive relationship between cocaine seeking and medial prefrontal cortex (mPFC) CX3CL1 and GluA1, as well as a nucleus accumbens (NAc) GluN2A expression. Moreover, examination of peripheral immune markers showed that the effect of abstinence and EcoHIV infection on these measures depended on the cocaine exposure regimen. Altogether, these results highlight the importance of cocaine abstinence and exposure pattern as critical variables that modulate HIV-associated neuroimmune outcomes and relapse vulnerability.
可卡因使用障碍(CUDs)和人类免疫缺陷病毒(HIV)仍然是全球持续存在的公共卫生难题。在长期禁欲期间,对可卡因的渴求会增加,这种效应被称为渴求潜伏期。关于HIV如何调节这一过程,人们知之甚少。因此,我们试图研究慢性HIV感染对可卡因渴求潜伏期以及中枢神经免疫和外周免疫底物表达水平相关变化的影响。在这里,雄性小鼠接种了EcoHIV,这是一种嵌合的HIV-1构建体,可在小鼠中产生慢性HIV感染。小鼠在条件性位置偏爱(CPP)范式中每天或间歇性地接受可卡因条件训练,然后在评估对可卡因配对室的偏爱之前进行1天或21天的强制禁欲。每天接受条件训练的小鼠在禁欲21天后表现出可卡因CPP潜伏期增强,并且在两个禁欲时间点的整个测试过程中,EcoHIV均增加了可卡因CPP。相反,与21天相比,间歇性接受条件训练的EcoHIV感染小鼠在禁欲1天后表现出更高的可卡因寻求行为。对皮质边缘CX3CL1-CX3CR1和谷氨酸受体表达的分析表明,可卡因寻求行为与内侧前额叶皮质(mPFC)CX3CL1和GluA1以及伏隔核(NAc)GluN2A表达之间存在正相关。此外,对外周免疫标志物的检查表明,禁欲和EcoHIV感染对这些指标的影响取决于可卡因暴露方案。总之,这些结果突出了可卡因禁欲和暴露模式作为调节HIV相关神经免疫结果和复发易感性的关键变量的重要性。