Hahn Yun K, Paris Jason J, Lichtman Aron H, Hauser Kurt F, Sim-Selley Laura J, Selley Dana E, Knapp Pamela E
Department of Anatomy & Neurobiology, Virginia Commonwealth University, Medical College of Virginia (MCV) Campus, Richmond, VA 23298-0709, USA.
Department of Pharmacology & Toxicology, Virginia Commonwealth University, Medical College of Virginia (MCV) Campus, Richmond, VA 23298-0613, USA.
Neurobiol Dis. 2016 Aug;92(Pt B):124-36. doi: 10.1016/j.nbd.2016.01.014. Epub 2016 Feb 1.
Co-exposure to opiates and HIV/HIV proteins results in enhanced CNS morphological and behavioral deficits in HIV(+) individuals and in animal models. Opiates with abuse liability, such as heroin and morphine, bind preferentially to and have pharmacological actions through μ-opioid-receptors (MORs). The mechanisms underlying opiate-HIV interactions are not understood. Exposure to the HIV-1 transactivator of transcription (Tat) protein causes neurodegenerative outcomes that parallel many aspects of the human disease. We have also observed that in vivo exposure to Tat results in apparent changes in morphine efficacy, and thus have hypothesized that HIV proteins might alter MOR activation. To test our hypothesis, MOR-mediated G-protein activation was determined in neuroAIDS-relevant forebrain regions of transgenic mice with inducible CNS expression of HIV-1 Tat. G-protein activation was assessed by MOR agonist-stimulated [(35)S]guanosine-5'-O-(3-thio)triphosphate ([(35)S]GTPγS) autoradiography in brain sections, and in concentration-effect curves of MOR agonist-stimulated [(35)S]GTPγS binding in membranes isolated from specific brain regions. Comparative studies were done using the MOR-selective agonist DAMGO ([D-Ala(2), N-MePhe(4), Gly-ol]-enkephalin) and a more clinically relevant agonist, morphine. Tat exposure reduced MOR-mediated G-protein activation in an agonist, time, and regionally dependent manner. Levels of the GPCR regulatory protein β-arrestin-2, which is involved in MOR desensitization, were found to be elevated in only one affected brain region, the amygdala; amygdalar β-arrestin-2 also showed a significantly increased association with MOR by co-immunoprecipitation, suggesting decreased availability of MOR. Interestingly, this correlated with changes in anxiety and fear-conditioned extinction, behaviors that have substantial amygdalar input. We propose that HIV-1 Tat alters the intrinsic capacity of MOR to signal in response to agonist binding, possibly via a mechanism involving altered expression and/or function of β-arrestin-2.
在HIV阳性个体和动物模型中,同时接触阿片类药物和HIV/HIV蛋白会导致中枢神经系统形态和行为缺陷加剧。具有成瘾性的阿片类药物,如海洛因和吗啡,优先与μ-阿片受体(MORs)结合并通过其产生药理作用。阿片类药物与HIV相互作用的潜在机制尚不清楚。暴露于HIV-1转录激活因子(Tat)蛋白会导致神经退行性病变,这与人类疾病的许多方面相似。我们还观察到,体内暴露于Tat会导致吗啡药效出现明显变化,因此我们推测HIV蛋白可能会改变MOR的激活。为了验证我们的假设,在可诱导中枢神经系统表达HIV-1 Tat的转基因小鼠的神经艾滋病相关前脑区域测定了MOR介导的G蛋白激活。通过MOR激动剂刺激的[(35)S]鸟苷-5'-O-(3-硫代)三磷酸([(35)S]GTPγS)放射自显影术在脑切片中评估G蛋白激活,并在从特定脑区分离的膜中进行MOR激动剂刺激的[(35)S]GTPγS结合的浓度-效应曲线评估。使用MOR选择性激动剂DAMGO([D-丙氨酸(2),N-甲基苯丙氨酸(4),甘氨醇]-脑啡肽)和一种更具临床相关性的激动剂吗啡进行了比较研究。Tat暴露以激动剂、时间和区域依赖性方式降低了MOR介导的G蛋白激活。参与MOR脱敏的G蛋白偶联受体调节蛋白β-抑制蛋白-2的水平仅在一个受影响的脑区杏仁核中升高;杏仁核β-抑制蛋白-2通过共免疫沉淀也显示与MOR的结合显著增加,表明MOR的可用性降低。有趣的是,这与焦虑和恐惧条件性消退的变化相关,这些行为有大量来自杏仁核的输入。我们提出,HIV-1 Tat可能通过涉及β-抑制蛋白-2表达和/或功能改变的机制改变MOR对激动剂结合作出信号反应的内在能力。