Department of Neurobiology and Anatomy, University of Texas Medical School at Houston, Houston, TX, USA.
Brain Res. 2010 Feb 2;1312:89-100. doi: 10.1016/j.brainres.2009.11.035. Epub 2009 Nov 22.
Psychostimulants like amphetamine and methylphenidate (MPD) are used to treat attention deficit hyperactivity disorder (ADHD), which is marked by developmentally inappropriate inattention, hyperactivity, and impulsivity. Neuropsychological analyses indicate that ADHD patients are impaired on tasks of behavioral inhibition, reward reversal, and working memory, which are functions of the prefrontal cortex (PFC) and are modulated by the mesocortical dopamine (DA) system. Non-specific electrical lesioning of PFC eliminated the expression of behavioral sensitization elicited by chronic MPD administration. Behavioral sensitization is the progressive augmentation of locomotor activity as a result of repetitive (chronic) exposure to the drug. It is believed that the sensitization to chronic drug treatment is caused due to an increase in DA in the mesocorticolimbic DA system, which includes the PFC. Therefore, this study investigated the role of PFC DA in mediating the behavioral sensitization to repeated administration of MPD in adult male Sprague-Dawley rats. On experimental day (ED) 1, the behavior was recorded post-saline injection. On ED 2, the rats were divided into three groups--control, sham and bilateral 6-OHDA treated group; and the sham and 6-OHDA treated groups underwent respective surgeries. After 5 days of rest following surgery, the post-surgery baseline was recorded on ED 8 following a saline injection. All three groups received 2.5 mg/kg MPD for 6 days (from ED 9 to ED 14), followed by a 3-day washout period (ED 15 to ED 18). On ED 19, a rechallenge injection of 2.5 mg/kg MPD was given and locomotor activity was recorded. It was found that the 6-OHDA lesion group failed to exhibit behavioral sensitization to MPD. The involvement of the dopaminergic afferents of PFC in behavioral sensitization to MPD is discussed.
兴奋剂,如安非他命和哌醋甲酯(MPD),被用于治疗注意缺陷多动障碍(ADHD),其特征是发育过程中注意力不集中、过度活跃和冲动。神经心理学分析表明,ADHD 患者在行为抑制、奖励逆转和工作记忆任务上存在障碍,而这些功能是前额叶皮层(PFC)的作用,并且由中皮质多巴胺(DA)系统调节。PFC 的非特异性电损伤消除了慢性 MPD 给药引起的行为敏感化的表达。行为敏感化是由于药物的重复(慢性)暴露而导致运动活动的逐渐增强。据信,对慢性药物治疗的敏感是由于中皮质边缘 DA 系统(包括 PFC)中的 DA 增加引起的。因此,本研究在成年雄性 Sprague-Dawley 大鼠中研究了 PFC DA 在介导对重复给予 MPD 的行为敏感化中的作用。在实验日(ED)1,注射盐水后记录行为。在 ED2,大鼠分为三组——对照组、假手术组和双侧 6-OHDA 处理组;假手术组和 6-OHDA 处理组分别进行手术。手术后休息 5 天后,在 ED8 注射盐水后记录术后基线。所有三组均接受 2.5mg/kgMPD 治疗 6 天(从 ED9 至 ED14),随后进行 3 天的洗脱期(ED15 至 ED18)。在 ED19,给予 2.5mg/kgMPD 的再挑战注射,并记录运动活动。结果发现,6-OHDA 损伤组未能表现出对 MPD 的行为敏感化。讨论了 PFC 中多巴胺能传入在 MPD 行为敏感化中的作用。