Departments of Chemistry and Pharmacology, University of Michigan, Ann Arbor, MI, United States.
Curr Opin Chem Biol. 2013 Oct;17(5):860-7. doi: 10.1016/j.cbpa.2013.06.012. Epub 2013 Jul 12.
Mapping chemical dynamics in the brain of live subjects is a challenging but highly rewarding goal because it allows neurotransmitter fluctuations to be related to behavior, drug effects, and disease states. A popular method for such measurements is microdialysis sampling coupled to analytical measurements. This method has become well-established for monitoring low molecular weight neurotransmitters, metabolites, and drugs, especially in pharmacological and pharmacokinetic studies. Recent technological developments which improve the temporal and spatial resolution of the methods will enable it to be used for studying behavior and small brain nuclei. Better assays allow monitoring more neurotransmitters simultaneously. Extension to analysis of aggregating proteins like amyloid β is proving extremely useful for uncovering the roles of these molecules and how they contribute to neurodegenerative diseases.
在活体研究对象的大脑中进行化学动力学映射是一个具有挑战性但极具回报的目标,因为它可以使神经递质波动与行为、药物作用和疾病状态相关联。一种用于此类测量的流行方法是与分析测量相结合的微透析采样。该方法已广泛用于监测低分子量神经递质、代谢物和药物,特别是在药理学和药代动力学研究中。最近的技术发展提高了方法的时空分辨率,这将使其能够用于研究行为和小的脑核。更好的检测方法可以同时监测更多的神经递质。对聚集蛋白(如淀粉样β)的分析扩展证明对于揭示这些分子的作用以及它们如何导致神经退行性疾病非常有用。