| Literature DB >> 28966846 |
Masaaki Sato1,2,3,4, Yuki Motegi1,2, Shogo Yagi5, Keiko Gengyo-Ando1,2,3, Masamichi Ohkura1,2, Junichi Nakai1,2,6.
Abstract
Fluorescence microendoscopy is becoming a promising approach for deep brain imaging, but the current technology for visualizing neurons on a single focal plane limits the experimental efficiency and the pursuit of three-dimensional functional neural circuit architectures. Here we present a novel fast varifocal two-photon microendoscope system equipped with a gradient refractive index (GRIN) lens and an electrically tunable lens (ETL). This microendoscope enables quasi-simultaneous imaging of the neuronal network activity of deep brain areas at multiple focal planes separated by 85-120 µm at a fast scan rate of 7.5-15 frames per second per plane, as demonstrated in calcium imaging of the mouse dorsal CA1 hippocampus and amygdala in vivo.Entities:
Keywords: (110.2760) Gradient-index lenses; (170.2150) Endoscopic imaging; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy; (180.6900) Three-dimensional microscopy
Year: 2017 PMID: 28966846 PMCID: PMC5611922 DOI: 10.1364/BOE.8.004049
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732