Department of Pathology and Anatomical Sciences, 206 Farber Hall, State University of New York at Buffalo, Buffalo, NY, 14214, USA.
J Neuroimmune Pharmacol. 2015 Mar;10(1):136-52. doi: 10.1007/s11481-015-9585-1. Epub 2015 Jan 22.
Opiates act on the dopaminergic system of the brain and perturb 32 kDa dopamine and adenosine 3', 5'-monophosphate-regulated phosphoprotein (DARPP-32) function. The DARPP-32 mediated inhibition of protein phosphatase-1 (PP-1) and modulation of transcriptional factor CREB is critical to the changes in neuronal plasticity that result in behavioral responses during drug abuse. To investigate the role of DARPP-32 mediated signaling on withdrawal behavior in a rat model of opiate addiction, we used intracerebral administration of gold nanorods (GNR) complexed to DARPP-32 siRNA to silence DARPP-32 gene expression and measure its effects on the opiate withdrawal syndrome. We hypothesized that DARPP-32 siRNA will suppress the neurochemical changes underlying the withdrawal syndrome and therefore prevent conditioned place aversion by suppressing or removing the constellation of negative effects associated with withdrawal, during the conditioning procedure. Our results showed that opiate addicted animals treated with GNR-DARPP-32 siRNA nanoplex showed lack of condition place aversive behavior consequent to the downregulation of secondary effectors such as PP-1 and CREB which modify transcriptional gene regulation and consequently neuronal plasticity. Thus, nanotechnology based delivery systems could allow sustained knockdown of DARPP-32 gene expression which could be developed into a therapeutic intervention for treating drug addiction by altering reward and motivational systems and interfere with conditioned responses.
阿片类药物作用于大脑的多巴胺能系统,并扰乱 32 kDa 多巴胺和腺苷 3',5'-单磷酸调节的磷蛋白(DARPP-32)功能。DARPP-32 介导的蛋白磷酸酶-1(PP-1)抑制和转录因子 CREB 的调节对于导致药物滥用期间行为反应的神经元可塑性变化至关重要。为了研究 DARPP-32 介导的信号在阿片类药物成瘾大鼠模型中的戒断行为中的作用,我们使用金纳米棒(GNR)与 DARPP-32 siRNA 复合物脑内给药,沉默 DARPP-32 基因表达,并测量其对阿片类戒断综合征的影响。我们假设 DARPP-32 siRNA 将抑制戒断综合征的神经化学变化,从而通过抑制或消除与戒断相关的负面效应的组合,在调节过程中预防条件性位置厌恶。我们的结果表明,用 GNR-DARPP-32 siRNA 纳米复合物治疗的阿片类成瘾动物表现出缺乏条件性位置厌恶行为,这是由于次要效应物如 PP-1 和 CREB 的下调所致,这些效应物调节转录基因调节,从而调节神经元可塑性。因此,基于纳米技术的递药系统可以允许持续下调 DARPP-32 基因表达,这可以通过改变奖励和动机系统并干扰条件反应来开发成治疗药物成瘾的治疗干预措施。