Jensen Kathrine L, Runegaard Annika H, Weikop Pia, Gether Ulrik, Rickhag Mattias
Molecular Neuropharmacology and Genetics Laboratory, Lundbeck Foundation Center for Biomembranes in Nanomedicine, Department of Neuroscience and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen.
Laboratory of Neuropsychiatry, Psychiatric Center Copenhagen and Department of Neuroscience and Pharmacology, University of Copenhagen.
J Vis Exp. 2017 Sep 21(127):56093. doi: 10.3791/56093.
Dopamine (DA) is a modulatory neurotransmitter controlling motor activity, reward processes and cognitive function. Impairment of dopaminergic (DAergic) neurotransmission is strongly associated with several central nervous system-associated diseases such as Parkinson's disease, attention-deficit-hyperactivity disorder and drug addiction. Delineating disease mechanisms involving DA imbalance is critically dependent on animal models to mimic aspects of the diseases, and thus protocols that assess specific parts of the DA homeostasis are important to provide novel insights and possible therapeutic targets for these diseases. Here, we present two useful experimental protocols that when combined provide a functional read-out of the DAergic system in mice. Biochemical and functional parameters on DA homeostasis are obtained through assessment of DA levels and dopamine transporter (DAT) functionality. When investigating the DA system, the ability to reliably measure endogenous levels of DA from adult brain is essential. Therefore, we present how to perform high-performance liquid chromatography (HPLC) on brain tissue from mice to determine levels of DA. We perform the experiment on tissue from dorsal striatum (dStr) and nucleus accumbens (NAc), but the method is also suitable for other DA-innervated brain areas. DAT is essential for reuptake of DA into the presynaptic terminal, thereby controlling the temporal and spatial activity of released DA. Knowing the levels and functionality of DAT in the striatum is of major importance when assessing DA homeostasis. Here, we provide a protocol that allows to simultaneously deduce information on surface levels and function using a synaptosomal DA uptake assay. Current methods combined with standard immunoblotting protocols provide the researcher with relevant tools to characterize the DAergic system.
多巴胺(DA)是一种调节性神经递质,控制运动活动、奖赏过程和认知功能。多巴胺能(DAergic)神经传递受损与多种中枢神经系统相关疾病密切相关,如帕金森病、注意力缺陷多动障碍和药物成瘾。阐明涉及DA失衡的疾病机制严重依赖于模拟疾病各个方面的动物模型,因此评估DA稳态特定部分的实验方案对于为这些疾病提供新的见解和可能的治疗靶点非常重要。在这里,我们介绍两种有用的实验方案,将它们结合起来可以对小鼠的DA能系统进行功能读数。通过评估DA水平和多巴胺转运体(DAT)功能来获得DA稳态的生化和功能参数。在研究DA系统时,可靠测量成年大脑中内源性DA水平的能力至关重要。因此,我们介绍如何对小鼠脑组织进行高效液相色谱(HPLC)以测定DA水平。我们在背侧纹状体(dStr)和伏隔核(NAc)的组织上进行实验,但该方法也适用于其他DA支配的脑区。DAT对于将DA重新摄取到突触前终末至关重要,从而控制释放的DA的时间和空间活性。在评估DA稳态时,了解纹状体中DAT的水平和功能非常重要。在这里,我们提供了一个方案,允许使用突触体DA摄取测定法同时推断表面水平和功能的信息。当前的方法与标准免疫印迹方案相结合,为研究人员提供了表征DA能系统的相关工具。