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Optical recording of action potentials with second-harmonic generation microscopy.利用二次谐波产生显微镜对动作电位进行光学记录。
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克服二次谐波产生显微镜中的光损伤:神经元动作电位的实时光学记录。

Overcoming photodamage in second-harmonic generation microscopy: real-time optical recording of neuronal action potentials.

作者信息

Sacconi L, Dombeck D A, Webb W W

机构信息

School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.

出版信息

Proc Natl Acad Sci U S A. 2006 Feb 28;103(9):3124-9. doi: 10.1073/pnas.0511338103. Epub 2006 Feb 17.

DOI:10.1073/pnas.0511338103
PMID:16488972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1413939/
Abstract

Second-harmonic generation (SHG) has proven essential for the highest-resolution optical recording of membrane potential (Vm) in intact specimens. Here, we demonstrate single-trial SHG recordings of neuronal somatic action potentials and quantitative recordings of their decay with averaging at multiple sites during propagation along branched neurites at distances up to 350 mum from the soma. We realized these advances by quantifying, analyzing, and thereby minimizing the dynamics of photodamage (PD), a frequent limiting factor in the optical imaging of biological preparations. The optical signal and the PD during SHG imaging of stained cultured Aplysia neurons were examined with intracellular electrode recordings monitoring the resting Vm variations induced by laser-scanning illumination. We found that the PD increased linearly with the dye concentration but grew with the cube of illumination intensity, leading to unanticipated optimization procedures to minimize PD. The addition of appropriate antioxidants in conjunction with an observed Vm recovery after termination of laser scanning further refined the imaging criteria for minimization and control of PD during SHG recording of action potentials. With these advances, the potential of SHG as an effective optical tool for neuroscience investigations is being realized.

摘要

二次谐波产生(SHG)已被证明对于完整标本中膜电位(Vm)的最高分辨率光学记录至关重要。在此,我们展示了神经元体细胞动作电位的单次试验SHG记录,以及在沿分支神经突从胞体传播至距离达350μm的多个位点处对其衰减进行平均的定量记录。我们通过量化、分析并由此最小化光损伤(PD)的动态变化实现了这些进展,光损伤是生物制剂光学成像中常见的限制因素。利用细胞内电极记录监测激光扫描照明诱导的静息Vm变化,对染色培养的海兔神经元进行SHG成像期间的光信号和PD进行了检测。我们发现,PD随染料浓度呈线性增加,但随照明强度的立方增长,这导致了意想不到的优化程序以最小化PD。在激光扫描终止后添加适当的抗氧化剂并结合观察到的Vm恢复,进一步完善了动作电位SHG记录期间最小化和控制PD的成像标准。随着这些进展,SHG作为神经科学研究有效光学工具的潜力正在得到实现。