Peng Fu, Yin Liu, Liang Zhu, Mengqi Wang, Yuan Yu, Fen Yang, Weijie Zhang, Hequn Zhang, Shy Shoham, Anna Wang Roe, Wang Xi
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引用次数: 0
摘要
意义重大:脉冲红外线神经刺激(INS,1875 nm)是一种新兴的神经刺激技术,它通过提供局灶脉冲热量来激活特定功能的中尺度网络,并有望应用于临床。然而,人们对其对大脑皮层兴奋性和抑制性细胞类型的影响知之甚少。目的:对群体神经元反应时间过程总和的估计为其他研究中描述的神经和血液动力学信号提供了潜在依据:利用小鼠躯体感觉皮层的双光子钙成像技术,我们研究了 INS 脉冲串应用对 hSyn 神经元和标记有 GCaMP6s 的 mDlx 神经元的影响:结果:我们发现,在麻醉小鼠体内,每一列 INS 脉冲都能可靠地诱导 hSyn 神经元产生强健的反应,并表现出积极的去向反应。令人惊讶的是,mDlx 神经元表现出负向反应。利用相关性指数进行的定量分析表明,反应具有可重复性、强度依赖性和局灶性。此外,当应用 INS 时,可观察到对侧激活:总之,INS 刺激的神经元群包括 hSyn 和 mDlx 神经元;在一定的刺激强度范围内,这会导致受刺激神经元群的整体兴奋,从而导致之前观察到的远处突触后位点的激活。
Two-photon imaging of excitatory and inhibitory neural response to infrared neural stimulation.
Significance: Pulsed infrared neural stimulation (INS, 1875 nm) is an emerging neurostimulation technology that delivers focal pulsed heat to activate functionally specific mesoscale networks and holds promise for clinical application. However, little is known about its effect on excitatory and inhibitory cell types in cerebral cortex.
Aim: Estimates of summed population neuronal response time courses provide a potential basis for neural and hemodynamic signals described in other studies.
Approach: Using two-photon calcium imaging in mouse somatosensory cortex, we have examined the effect of INS pulse train application on hSyn neurons and mDlx neurons tagged with GCaMP6s.
Results: We find that, in anesthetized mice, each INS pulse train reliably induces robust response in hSyn neurons exhibiting positive going responses. Surprisingly, mDlx neurons exhibit negative going responses. Quantification using the index of correlation illustrates responses are reproducible, intensity-dependent, and focal. Also, a contralateral activation is observed when INS applied.
Conclusions: In sum, the population of neurons stimulated by INS includes both hSyn and mDlx neurons; within a range of stimulation intensities, this leads to overall excitation in the stimulated population, leading to the previously observed activations at distant post-synaptic sites.
期刊介绍:
At the interface of optics and neuroscience, Neurophotonics is a peer-reviewed journal that covers advances in optical technology applicable to study of the brain and their impact on the basic and clinical neuroscience applications.