Literature DB >> 11580892

A miniature head-mounted two-photon microscope. high-resolution brain imaging in freely moving animals.

F Helmchen1, M S Fee, D W Tank, W Denk.   

Abstract

Two-photon microscopy has enabled anatomical and functional fluorescence imaging in the intact brain of rats. Here, we extend two-photon imaging from anesthetized, head-stabilized to awake, freely moving animals by using a miniaturized head-mounted microscope. Excitation light is conducted to the microscope in a single-mode optical fiber, and images are scanned using vibrations of the fiber tip. Microscope performance was first characterized in the neocortex of anesthetized rats. We readily obtained images of vasculature filled with fluorescently labeled blood and of layer 2/3 pyramidal neurons filled with a calcium indicator. Capillary blood flow and dendritic calcium transients were measured with high time resolution using line scans. In awake, freely moving rats, stable imaging was possible except during sudden head movements.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11580892     DOI: 10.1016/s0896-6273(01)00421-4

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  157 in total

Review 1.  Natural patterns of neural activity: how physiological mechanisms are orchestrated to cope with real life.

Authors:  Rafael Kurtz; Martin Egelhaaf
Journal:  Mol Neurobiol       Date:  2003-02       Impact factor: 5.590

2.  In vivo mammalian brain imaging using one- and two-photon fluorescence microendoscopy.

Authors:  Juergen C Jung; Amit D Mehta; Emre Aksay; Raymond Stepnoski; Mark J Schnitzer
Journal:  J Neurophysiol       Date:  2004-05-05       Impact factor: 2.714

Review 3.  Fiber optic in vivo imaging in the mammalian nervous system.

Authors:  Amit D Mehta; Juergen C Jung; Benjamin A Flusberg; Mark J Schnitzer
Journal:  Curr Opin Neurobiol       Date:  2004-10       Impact factor: 6.627

4.  Friction-based stabilization of juxtacellular recordings in freely moving rats.

Authors:  Lucas Herfst; Andrea Burgalossi; Kurt Haskic; John J Tukker; Martin Schmidt; Michael Brecht
Journal:  J Neurophysiol       Date:  2012-04-18       Impact factor: 2.714

5.  Increased illumination uniformity and reduced photodamage offered by the Lissajous scanning in fiber-optic two-photon endomicroscopy.

Authors:  Wenxuan Liang; Kartikeya Murari; Yuying Zhang; Yongping Chen; Ming-Jun Li; Xingde Li
Journal:  J Biomed Opt       Date:  2012-02       Impact factor: 3.170

6.  Compact and flexible raster scanning multiphoton endoscope capable of imaging unstained tissue.

Authors:  David R Rivera; Christopher M Brown; Dimitre G Ouzounov; Ina Pavlova; Demirhan Kobat; Watt W Webb; Chris Xu
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-17       Impact factor: 11.205

Review 7.  Imaging calcium signals in vivo: a powerful tool in physiology and pharmacology.

Authors:  James T Russell
Journal:  Br J Pharmacol       Date:  2011-08       Impact factor: 8.739

8.  Micromirror-scanned dual-axis confocal microscope utilizing a gradient-index relay lens for image guidance during brain surgery.

Authors:  Jonathan T C Liu; Michael J Mandella; Nathan O Loewke; Henry Haeberle; Hyejun Ra; Wibool Piyawattanametha; Olav Solgaard; Gordon S Kino; Christopher H Contag
Journal:  J Biomed Opt       Date:  2010 Mar-Apr       Impact factor: 3.170

Review 9.  Mechanisms of neural and behavioral dysfunction in Alzheimer's disease.

Authors:  Daniel W Wesson; Ralph A Nixon; Efrat Levy; Donald A Wilson
Journal:  Mol Neurobiol       Date:  2011-03-22       Impact factor: 5.590

10.  Imaging Cortical Dynamics in GCaMP Transgenic Rats with a Head-Mounted Widefield Macroscope.

Authors:  Benjamin B Scott; Stephan Y Thiberge; Caiying Guo; D Gowanlock R Tervo; Carlos D Brody; Alla Y Karpova; David W Tank
Journal:  Neuron       Date:  2018-10-25       Impact factor: 17.173

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.