Simple and cost-effective hardware and software for functional brain mapping using intrinsic optical signal imaging

被引:44
作者
Harrison, Thomas C. [1 ,2 ]
Sigler, Albrecht [1 ,2 ]
Murphy, Timothy H. [1 ,2 ,3 ,4 ]
机构
[1] Univ British Columbia, Dept Psychiat, Kinsmen Lab, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Brain Res Ctr, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Cellular & Physiol Sci, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, In Vivo Imaging Ctr, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
In vivo imaging; Brain mapping; LED light sources; Sensory cortex; Mouse; Cranial surgery; IN-VIVO; NEURONAL-ACTIVITY; VISUAL-CORTEX; MICROSCOPY; STROKE; MICROCIRCULATION; ORGANIZATION; ARCHITECTURE; ACTIVATION; EXCITATION;
D O I
10.1016/j.jneumeth.2009.06.021
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a simple and low-cost system for intrinsic optical signal (IOS) imaging using stable LED light sources, basic microscopes, and commonly available CCD cameras. JOS imaging measures activity-dependent changes in the light reflectance of brain tissue, and can be performed with a minimum of specialized equipment. Our system uses LED ring lights that can be mounted on standard microscope objectives or video lenses to provide a homogeneous and stable light source, with less than 0.003% fluctuation across images averaged from 40 trials. We describe the equipment and surgical techniques necessary for both acute and chronic mouse preparations, and provide software that can create maps of sensory representations from images captured by inexpensive 8-bit cameras or by 12-bit cameras. The JOS imaging system can be adapted to commercial upright microscopes or custom macroscopes, eliminating the need for dedicated equipment or complex optical paths. This method can be combined with parallel high resolution imaging techniques such as two-photon microscopy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 218
页数:8
相关论文
共 31 条
  • [1] LED Arrays as Cost Effective and Efficient Light Sources for Widefield Microscopy
    Albeanu, Dinu F.
    Soucy, Edward
    Sato, Tomokazu F.
    Meister, Markus
    Murthy, Venkatesh N.
    [J]. PLOS ONE, 2008, 3 (05):
  • [2] IMAGING CELL-VOLUME CHANGES AND NEURONAL EXCITATION IN THE HIPPOCAMPAL SLICE
    ANDREW, RD
    MACVICAR, BA
    [J]. NEUROSCIENCE, 1994, 62 (02) : 371 - 383
  • [3] Suprathreshold auditory cortex activation visualized by intrinsic signal optical imaging
    Bakin, JS
    Kwon, MC
    Masino, SA
    Weinberger, NM
    Frostig, RD
    [J]. CEREBRAL CORTEX, 1996, 6 (02) : 120 - 130
  • [4] A LIGHT-EMITTING DIODE LIGHT STANDARD FOR PHOTO-MICROSCOPY AND VIDEOMICROSCOPY
    BEACH, JM
    DULING, BR
    [J]. JOURNAL OF MICROSCOPY, 1993, 172 : 41 - 48
  • [5] BONHOEFFER T, 1993, J NEUROSCI, V13, P4157
  • [6] Extensive turnover of dendritic spines and vascular remodeling in cortical tissues recovering from stroke
    Brown, Craig E.
    Li, Ping
    Boyd, Jamie D.
    Delaney, Kerry R.
    Murphy, Timothy H.
    [J]. JOURNAL OF NEUROSCIENCE, 2007, 27 (15) : 4101 - 4109
  • [7] Simultaneous multiwavelength laminar optical tomography
    Burgess, Sean A.
    Bouchard, Matthew B.
    Yuan, Baohong
    Hillman, Elizabeth M. C.
    [J]. OPTICS LETTERS, 2008, 33 (22) : 2710 - 2712
  • [8] Two-dimensional spatial distribution of surface mechanomyographical response to single motor unit activity
    Cescon, Corrado
    Madeleine, Pascal
    Graven-Nielsen, Thomas
    Merletti, Roberto
    Farina, Dario
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 2007, 159 (01) : 19 - 25
  • [9] CHEN B, 2004, LONG TERM HIGH RESOL, P423
  • [10] COHEN LB, 1973, PHYSIOL REV, V53, P373