Jiang Bin, Hou Wensheng, Xia Nan, Peng Fei, Wang Xing, Chen Chunye, Zhou Yi, Zheng Xiaolin, Wu Xiaoying
Chongqing University, Ministry of Education, Key Laboratory of Biorheological Science and Technology, Chongqing, China.
Chongqing University, Chongqing Collaborative Innovation Center for Brain Science, China.
Neurophotonics. 2019 Jul;6(3):035009. doi: 10.1117/1.NPh.6.3.035009. Epub 2019 Aug 27.
Near-infrared radiation (NIR) has been described as one of the highest-resolution tools for neuromodulation. However, the poor tissue penetration depth of NIR has limited its further application on some of the deeper layer neurons . A 980-nm short-wavelength NIR (SW-NIR) with high penetration depth was employed, and its inhibitory effect on neurons was investigated . In experiments, SW-NIR was implemented on the rat's cochlear nucleus (CN), the auditory pathway was activated by pure-tones through the rat's external auditory canal, and the neural responses were recorded in the inferior colliculus by a multichannel electrode array. Neural firing rate (FR) and the first spike latency (FSL) were analyzed to evaluate the optically induced neural inhibition. Meanwhile, a two-layered finite element, consisting of a fluid layer and a gray matter layer, was established to model the optically induced temperature changes in CN; different stimulation paradigms were used to compare the inhibitory efficiency of SW-NIR. Results showed that SW-NIR could reversibly inhibit acoustically induced CN neural activities: with the increase of laser radiant exposures energy, neural FR decreased significantly and FSL lengthened steadily. Significant inhibition occurred when the optical pulse stimulated prior to the acoustic stimulus. Results indicated that the inhibition relies on the establishment time of the temperature field. Moreover, our preliminary results suggest that short-wavelength infrared could regulate the activities of neurons beyond the neural tissues laser irradiated through neural networks and conduction . These findings may provide a method for accurate neuromodulation .
近红外辐射(NIR)已被描述为神经调节的最高分辨率工具之一。然而,近红外辐射较差的组织穿透深度限制了其在一些深层神经元上的进一步应用。采用了具有高穿透深度的980纳米短波近红外(SW-NIR),并研究了其对神经元的抑制作用。在实验中,将SW-NIR作用于大鼠的耳蜗核(CN),通过大鼠外耳道用纯音激活听觉通路,并通过多通道电极阵列在下丘记录神经反应。分析神经放电率(FR)和首次放电潜伏期(FSL)以评估光诱导的神经抑制。同时,建立了由流体层和灰质层组成的双层有限元模型,以模拟CN中的光诱导温度变化;使用不同的刺激模式来比较SW-NIR的抑制效率。结果表明,SW-NIR可以可逆地抑制声诱导的CN神经活动:随着激光辐射暴露能量的增加,神经FR显著降低,FSL稳步延长。当光脉冲在声刺激之前刺激时,会出现显著抑制。结果表明,这种抑制依赖于温度场的建立时间。此外,我们的初步结果表明,短波红外可以通过神经网络和传导调节激光照射的神经组织之外的神经元活动。这些发现可能为精确的神经调节提供一种方法。