Lelyveld Victor S, Atanasijevic Tatjana, Jasanoff Alan
Department of Biological Engineering, Massachusetts Institute of Technology, NW14-2213, Cambridge, MA 02139.
Int J Imaging Syst Technol. 2010 Mar;20(1):71-79. doi: 10.1002/ima.20221.
Magnetic resonance (MRI)-based molecular imaging methods are beginning to have impact in neuroscience. A growing number of molecular imaging agents have been synthesized and tested in vitro, but so far relatively few have been validated in the brains of live animals. Here, we discuss key challenges associated with expanding the repertoire of successful molecular neuroimaging approaches. The difficulty of delivering agents past the blood-brain barrier (BBB) is a particular obstacle to molecular imaging in the central nervous system. We review established and emerging techniques for trans-BBB delivery, including intracranial infusion, BBB disruption, and transporter-related methods. Improving the sensitivity with which MRI-based molecular agents can be detected is a second major challenge. Better sensitivity would in turn reduce the requirements for delivery and alleviate potential side effects. We discuss recent efforts to enhance relaxivity of conventional longitudinal relaxation time (T(1)) and transverse relaxation time (T(2)) MRI contrast agents, as well as strategies that involve amplifying molecular signals or reducing endogenous background influences. With ongoing refinement of imaging approaches and brain delivery methods, MRI-based techniques for molecular-level neuroscientific investigation will fall increasingly within reach.
基于磁共振成像(MRI)的分子成像方法正开始在神经科学领域产生影响。越来越多的分子成像剂已在体外合成并进行了测试,但到目前为止,在活体动物大脑中得到验证的相对较少。在此,我们讨论与扩大成功的分子神经成像方法库相关的关键挑战。将试剂递送至血脑屏障(BBB)之外存在困难,这是中枢神经系统分子成像的一个特殊障碍。我们回顾了已有的和新兴的跨血脑屏障递送技术,包括颅内输注、血脑屏障破坏和转运体相关方法。提高基于MRI的分子试剂的检测灵敏度是第二个主要挑战。更高的灵敏度反过来会降低递送要求并减轻潜在的副作用。我们讨论了近期为提高传统纵向弛豫时间(T(1))和横向弛豫时间(T(2))MRI造影剂的弛豫率所做的努力,以及涉及放大分子信号或减少内源性背景影响的策略。随着成像方法和脑递送方法的不断完善,基于MRI的分子水平神经科学研究技术将越来越容易实现。