Multi-Fiber Photometry to Record Neural Activity in Freely-Moving Animals

被引:77
作者
Martianova, Ekaterina [1 ]
Aronson, Sage [2 ,3 ,4 ]
Proulx, Christophe D. [1 ]
机构
[1] Univ Laval, Dept Psychiat & Neurosci, CERVO Brain Res Ctr, Quebec City, PQ, Canada
[2] Univ Calif San Diego, Ctr Neural Circuits & Behav, Dept Neurosci, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Sect Neurobiol, Div Biol, La Jolla, CA 92093 USA
[4] Neurophotometrics Ltd, San Diego, CA USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2019年 / 152期
基金
加拿大自然科学与工程研究理事会;
关键词
Behavior; Issue; 152; genetically encoded calcium indicator; GCaMP; fiber photometry; behavior; neural pathways; freely-moving animals; LATERAL HABENULA; NEURONS; DYNAMICS; DOPAMINE;
D O I
10.3791/60278
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recording the activity of a group of neurons in a freely-moving animal is a challenging undertaking. Moreover, as the brain is dissected into smaller and smaller functional subgroups, it becomes paramount to record from projections and/or genetically-defined subpopulations of neurons. Fiber photometry is an accessible and powerful approach that can overcome these challenges. By combining optical and genetic methodologies, neural activity can be measured in deep brain structures by expressing genetically-encoded calcium indicators, which translate neural activity into an optical signal that can be easily measured. The current protocol details the components of a multi-fiber photometry system, how to access deep brain structures to deliver and collect light, a method to account for motion artifacts, and how to process and analyze fluorescent signals. The protocol details experimental considerations when performing single and dual color imaging, from either single or multiple implanted optic fibers.
引用
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页数:9
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