Callaway Edward M, Yuste Rafael
The Salk Institute for Biological Studies, Systems Neurobiology Laboratories, 10010 North Torrey Pines Road, La Jolla, California 92037, USA.
Curr Opin Neurobiol. 2002 Oct;12(5):587-92. doi: 10.1016/s0959-4388(02)00364-1.
Recent technological advances have enabled the use of different optical methods to activate neurons, including 'caged' glutamate, photoactivation of genetically engineered cascades, and direct two-photon excitation. The ability to use light as a stimulation tool provides, in principle, a non-invasive method for the temporally and spatially precise activation of any neuron or any part of a neuron. When combined with two-photon excitation, excellent spatial control can be achieved even in complex and highly scattering preparations, such as living nervous tissue. Different methods that have been developed in the last several decades have been used to probe neuronal sensitivity, mimic synaptic input, and elucidate patterns of neural connectivity.
最近的技术进步使得利用不同的光学方法来激活神经元成为可能,包括“笼锁”型谷氨酸、基因工程级联反应的光激活以及直接双光子激发。将光用作刺激工具的能力原则上提供了一种对任何神经元或神经元的任何部分进行时空精确激活的非侵入性方法。当与双光子激发相结合时,即使在复杂且高度散射的标本(如活体神经组织)中也能实现出色的空间控制。在过去几十年中开发的不同方法已被用于探究神经元敏感性、模拟突触输入以及阐明神经连接模式。