SnapShot: Optical Control and Imaging of Brain Activity
Author(s) -
Xiaonan Richard Sun,
Andrea Giovannucci,
Allyson E. Sgro,
Samuel S.H. Wang
Publication year - 2012
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2012.06.009
Subject(s) - biology , snapshot (computer storage) , neuroscience , computational biology , computer science , operating system
Optical methods have assumed a leading role in the study of intact nervous system function. In comparison with traditional electrical recordings, optical imaging enables the measurement of activity in many structures at once, including subcellular domains. For observing function at the cellular level, multiphoton fluorescence microscopy allows tracking to be done with spatiotemporal resolution in the micron and millisecond range. Light can also be used to activate brain tissue by using “caged” neurotransmitters and second messengers, and, more recently, by using light-sensitive ion channels, pumps, and receptors to allow optogenetic activation.
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