Department of Biomedical Engineering, Vanderbilt University, Nashville, TN, USA.
Sci Rep. 2013;3:2600. doi: 10.1038/srep02600.
Analysis and control of neural circuitry requires the ability to selectively activate or inhibit neurons. Previous work showed that infrared laser light selectively excited neural activity in endogenous unmyelinated and myelinated axons. However, inhibition of neuronal firing with infrared light was only observed in limited cases, is not well understood and was not precisely controlled. Using an experimentally tractable unmyelinated preparation for detailed investigation and a myelinated preparation for validation, we report that it is possible to selectively and transiently inhibit electrically-initiated axonal activation, as well as to both block or enhance the propagation of action potentials of specific motor neurons. Thus, in addition to previously shown excitation, we demonstrate an optical method of suppressing components of the nervous system with functional spatiotemporal precision. We believe this technique is well-suited for non-invasive investigations of diverse excitable tissues and may ultimately be applied for treating neurological disorders.
分析和控制神经回路需要能够选择性地激活或抑制神经元。以前的工作表明,红外激光光选择性地激发内源性未髓鞘化和髓鞘化轴突中的神经活动。然而,用红外光抑制神经元放电仅在有限的情况下观察到,其机制尚不清楚,也无法精确控制。我们使用一种实验上易于处理的未髓鞘化制剂进行详细研究,并用一种有髓鞘化制剂进行验证,报告说有可能选择性地和短暂地抑制电引发的轴突激活,以及阻断或增强特定运动神经元的动作电位的传播。因此,除了之前显示的兴奋之外,我们还展示了一种用光抑制神经系统成分的方法,具有功能上的时空精度。我们相信这种技术非常适合对各种可兴奋组织进行非侵入性研究,最终可能用于治疗神经疾病。