Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University New York, NY, USA.
Front Neural Circuits. 2009 Jul 6;3:6. doi: 10.3389/neuro.04.006.2009. eCollection 2009.
Two-photon imaging has become a useful tool for optical monitoring of neural circuits, but it requires high laser power and serial scanning of each pixel in a sample. This results in slow imaging rates, limiting the measurements of fast signals such as neuronal activity. To improve the speed and signal-to-noise ratio of two-photon imaging, we introduce a simple modification of a two-photon microscope, using a diffractive optical element (DOE) which splits the laser beam into several beamlets that can simultaneously scan the sample. We demonstrate the advantages of DOE scanning by enhancing the speed and sensitivity of two-photon calcium imaging of action potentials in neurons from neocortical brain slices. DOE scanning can easily improve the detection of time-varying signals in two-photon and other non-linear microscopic techniques.
双光子成像已成为光学监测神经回路的有用工具,但它需要高激光功率和对样品中每个像素进行串行扫描。这导致成像速度较慢,限制了对神经元活动等快速信号的测量。为了提高双光子成像的速度和信噪比,我们对双光子显微镜进行了简单的修改,使用了一个衍射光学元件(DOE),将激光束分成几个可以同时扫描样品的光束。我们通过提高新皮层脑片神经元动作电位的双光子钙成像的速度和灵敏度来证明 DOE 扫描的优势。DOE 扫描可以轻松提高双光子和其他非线性显微镜技术中时变信号的检测能力。