| Peer-Reviewed

The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements

Published in Optics (Volume 4, Issue 6)
Received: 6 September 2015     Accepted: 20 October 2015     Published: 30 October 2015
Views:       Downloads:
Abstract

The possibility of constructing a dynamic neurogoniometer based on a rotary mechanotronic system controlled by stepper motors and a number of controlled reflectors on the galvanometric scanners is considered below. The control is performed by a PIC-controller, but there is also another low-cost construction using stepper motors control modules in a CAMAC standard. There are several designs based on a universal Fedorov stage and the apparatus for stereotaxis. The above schemes can be used both for working with the fixed histological slices and for in vivo or in situ analysis, particularly of the living brain slices. An example of application of such devices is described in this paper.

Published in Optics (Volume 4, Issue 6)
DOI 10.11648/j.optics.20150406.11
Page(s) 37-42
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2015. Published by Science Publishing Group

Keywords

Angular Measurements, Neurogoniometry, Indicatrix, Anisotropy, Isotropy, Orientation, Radiation Patterns

References
[1] Cormie P., Robinson K.R. Embryonic zebrafish neuronal growth is not affected by an applied electric field in vitro // Neurosci Lett., Vol. 411, Issue 2, pp. 128–132 (2007).
[2] Li G.N. Hoffman D. Evaluation of neurite outgrowth anisotropy using a novel application of circular analysis // Journ. Neurosci. Methods., Vol. 174, Issue 2, pp. 202-214 (2008)
[3] Brown M.C., Levine J.L. Dendrites of Medial Olivocochlear (MOC) Neurons in Mouse // Neuroscience, Vol. 154, Issue 1, pp. 147–159 (2008).
[4] Radman T., Ramos R.L., Brumberg J.C., Bikson M. Role of Cortical Cell Type and Morphology in Sub- and Suprathreshold Uniform Electric Field Stimulation // Brain Stimul., Vol. 2, Issue 4, pp. 215–228 (2009).
[5] Pashut T., Wolfus S., Friedman A., Lavidor M., Bar-Gad I., Yeshurun Y., Korngreen A. Mechanisms of Magnetic Stimulation of Central Nervous System Neurons // PLoS Comput Biol., Vol. 7, e1002022, Issue 3 (2011).
[6] Mattie F.J., Stackpole M.M., Stone M.C., Clippard J.R., Rudnick D.A., Qiu Y., Tao J., Allender D.L., Parmar M., Rolls M.M. Directed microtubule growth, +TIPs and kinesin-2 are required for uniform microtubule polarity in dendrites // Curr. Biol., Vol. 20, Issue 24, pp. 2169–2177 (2010).
[7] Ward M., McCann C., DeWullf M., Wu J.Y., Rao Y. Distinguishing between Directional Guidance and Motility Regulation in Neuronal Migration // Journ. Neurosci., Vol. 23, Issue 12, pp. 5170–5177 (2003).
[8] Wang D.D., Kriegstein A.R. GABA Regulates Excitatory Synapse Formation in the Neocortex via NMDA Receptor Activation // Journ. Neurosci., Vol. 28, Issue 21, pp. 5547–5558 (2008).
[9] Chen-Huang C., Peterson B.W. Frequency-Dependent Spatiotemporal Tuning Properties of Non–Eye Movement Related Vestibular Neurons to Three-Dimensional Translations in Squirrel Monkeys // Journ. Neurophysiol., Vol. 103, Issue 6, pp. 3219-3237 (2010).
[10] Chow W.N., Simpson D.G., Bigbee J.W., Colello R.J. Evaluating neuronal and glial growth on electrospun polarized matrices: bridging the gap in percussive spinal cord injuries // Neur. Glia Biol., Vol. 3, No. 2, pp. 119–126 (2007).
[11] Alexander J.K., Fuss B., Colello R.J. Electric field-induced astrocyte alignment directs neurite outgrowth // Neur. Glia Biol., Vol. 2, No. 2, pp. 93–103 (2006).
[12] Ikuta C., Uwate Y., Nishio Y. Chaos glial network connected to Multi-Layer Perceptron for Solving Two-Spiral Problem // Proc. of 2010 IEEE International Symposium on Circuits and Systems (ISCAS), pp. 1360-1363, 2010.
[13] Bolt R.A., de Mul F.M. Goniometric instrument for light scattering measurement of biological tissues and phantoms // Rev. Sci. Instrum., Vol. 73, Issue 5, pp. 2211 - 2213 (2002).
[14] Farago F.T., Curtis M.A. Handbook of Dimensional Measurement. 580 p., Industrial Press., 1994.
[15] Shin F.Y. Image Processing and Mathematical Morphology: Fundamentals and Applications, 439 p., CRC Press, 2009.
[16] Hallimond A.F., Taylor E.W. An Improved Polarizing Microscope IV. The Fedorov Stage (Three-Axis) // Mineralogical Magazine, Vol. 29, No. 209, pp. 150-162 (1950)
[17] Naidu P.R.J. 4-Axes Universal Stage. 106 p., Commercial Printing & Publishing House, Madras, 1958.
[18] Berek M. Mikroskopische Mineralbestimmung mit Hilfe der Universaldrehtisch methoden. 168 p. Gebrüder Borntraeger, Berlin, 1924.
[19] Fedorov E.S. Eine neue Methode der optischen Untersuchung von Krystallplatten in parallelem Lichte // Tschermak's Mineralogische und Petrographische Mittheilungen, Vol. 12, pp. 505-509 (1892).
[20] Fedorov E.S. Universal- (Theodolith-) Methode in der Mineralogie und Petrographie // Zeitschrift für Kristallographie und Mineralogie, Vol. 22, pp. 229-268 (1894).
[21] Notchenko A.V., Gradov O.V. A Five-Axis Arm-Manipulator Laser System & an Algorithm for Digital Processing of Output Data for Recording and Morpho-Topological Identification of Cells and Tissue Structures // Visualization, Image Processing and Computation in Biomedicine Vol. 2 (2013) DOI: 10.1615/VisualizImageProcComputatBiomed.2013005967.
[22] Oganesian V. А., Notchenko А. V., Gradov О. V. Mechanotronic neurogoniometer for in vivo & in situ measurements on living brain slices and operating with a stereotaxic apparatus. Preliminary report // Biotechnosphere, no. 33, pp. 32-34, Jun. 2014 [in Russian].
[23] Gradov O.V., Notchenko A.V., Oganessian V.А. Mechano-tronic Neurogoniometry For in vivo & in situ Measurements on Neuroblast Cultures, Neurosphere-Like Stem Cell Clusters, Embryonic Brain Tissues & Living Brain Slices. MIT – Skoltech Biomed. Conf.: “Towards Therapies of the Future”, 2014, DOI: 10.13140/2.1.2616.1281 (May 26-28, 2014).
[24] Oganessian V., Notchenko A., Gradov O. Mechanotronic Neurogoniometer for in vivo & in situ Measurements on Living Brain Slices and Operating with a Stereotactic Apparatus. Х RGC on Biomedical Engineering, SPSEU, Bld. 5, Section: Mechatronics And Biomedical Engineering; DOI: 10.13140/2.1.2255.6809, 4 p. (2014).
[25] Gradov O.V. Shaking-rotating cultivation neurogoniometry: synchronous technique for gradient cultivation of fish neural tissues and cell cultures on the five-axis mechanized stage and direct time-lapse morphometry of differentiation and proliferation of neural cells // Proc. Conf. “The Cell Cultures of Marine and Freshwater Animals”, Vladivostok, Institute of Marine Biology (IMB FEB RAS), 2015, Sept. 8 – 10, p. 12. DOI: 10.13140/RG.2.1.4297.9682.
[26] Gradov O. et al. Mechanotronic Neurogoniometry For in vivo & in situ Measurements on Neuroblast Cultures, Neurosphere-Like Stem Cell Clusters, Embryonic Brain Tissues and Living Brain Slices. Moscow Science Week – 2014, Poster A7. [URL: http://moscowscienceweek.ru/ru/program/poster-talks]
[27] Oganessian V.A., Notchenko A.V., Gradov O.V Multispectral topological laser speckle analyzers of proliferation and differentiation activity during morphogenesis based on tunable laser diodes and spectrometric fingerprinting of the cell cycle stages. Journal of Physical Chemistry & Biophysics, 2015, 5(3): 75.
[28] Gradov O.V., Notchenko A.V., Oganesssian V.A. Microrefractometric and goniometric tomography based on multiaxis robotized Feodorov stage hybridized with pushintegrator and integrating Andine platform controled by stepper motors based on modified Harvard architecure microcontroller and CAMAC modules // 3rd International Conference “Practical microtomography”. pp. 41-44, 2014.
[29] Gradov O.V., Gradova M.A. Cryoelectron microscopy as a functional instrument for system biology, structural analysis and experimental manipulations with living cells // Problems of Cryobiology and Cryomedicine, Vol. 24, No. 3, pp. 193-210 (2014).
[30] Notchenko A.V., Gradov O.V. Laser barcoding methods for identification and decoding of neurophysiological information. VIII Russian-German Conf. Biomed. Eng., Section: “Micro- & nano- technologies in Biomedical Engineering”, pp. 175-180, SPSEU, 2012 [in Russian].
[31] Gradov O.V. Experimental Setups for Ozonometric Microscopy. Biomedical Engineering, Vol. 46, Issue 6, pp. 260-264 (2013).
[32] Notchenko A.V., Gradov O.V. Elementary Morphometric Labs-On-a-Chip Based on Hemocytometric Chambers With Radiofrequency Culture Identification and Relay of Spectrozonal Histochemical Monitoring. Visualization, Image Processing and Computation in Biomedicine, Vol. 2, DOI: 10.1615/VisualizImageProcComputatBiomed.2013005968 (2013)
[33] Alexandrov P.L., Gradov O.V. Conventional Patch-Clamp Techniques For Multi-channel Lab-On-A-Chip Signal Registration Using Real Time Target Machine Interfaces and in situ Real-Time Digital Signal Processing and Modeling. X RGC on Biomedical Engineering, SPSEU, Bld.5; Section: Processing and Analysis of Biomedical Signals and Data; DOI: 10.13140/2.1.4025.1528, 4 p. (2014).
Cite This Article
  • APA Style

    Oleg Gradov, Alexander Notchenko, Vahagn Oganessian. (2015). The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements. Optics, 4(6), 37-42. https://doi.org/10.11648/j.optics.20150406.11

    Copy | Download

    ACS Style

    Oleg Gradov; Alexander Notchenko; Vahagn Oganessian. The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements. Optics. 2015, 4(6), 37-42. doi: 10.11648/j.optics.20150406.11

    Copy | Download

    AMA Style

    Oleg Gradov, Alexander Notchenko, Vahagn Oganessian. The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements. Optics. 2015;4(6):37-42. doi: 10.11648/j.optics.20150406.11

    Copy | Download

  • @article{10.11648/j.optics.20150406.11,
      author = {Oleg Gradov and Alexander Notchenko and Vahagn Oganessian},
      title = {The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements},
      journal = {Optics},
      volume = {4},
      number = {6},
      pages = {37-42},
      doi = {10.11648/j.optics.20150406.11},
      url = {https://doi.org/10.11648/j.optics.20150406.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.optics.20150406.11},
      abstract = {The possibility of constructing a dynamic neurogoniometer based on a rotary mechanotronic system controlled by stepper motors and a number of controlled reflectors on the galvanometric scanners is considered below. The control is performed by a PIC-controller, but there is also another low-cost construction using stepper motors control modules in a CAMAC standard. There are several designs based on a universal Fedorov stage and the apparatus for stereotaxis. The above schemes can be used both for working with the fixed histological slices and for in vivo or in situ analysis, particularly of the living brain slices. An example of application of such devices is described in this paper.},
     year = {2015}
    }
    

    Copy | Download

  • TY  - JOUR
    T1  - The Neurogoniometry: Applied Optical Analysis for Neural Structure Directogramm / Radiation Pattern Measurements
    AU  - Oleg Gradov
    AU  - Alexander Notchenko
    AU  - Vahagn Oganessian
    Y1  - 2015/10/30
    PY  - 2015
    N1  - https://doi.org/10.11648/j.optics.20150406.11
    DO  - 10.11648/j.optics.20150406.11
    T2  - Optics
    JF  - Optics
    JO  - Optics
    SP  - 37
    EP  - 42
    PB  - Science Publishing Group
    SN  - 2328-7810
    UR  - https://doi.org/10.11648/j.optics.20150406.11
    AB  - The possibility of constructing a dynamic neurogoniometer based on a rotary mechanotronic system controlled by stepper motors and a number of controlled reflectors on the galvanometric scanners is considered below. The control is performed by a PIC-controller, but there is also another low-cost construction using stepper motors control modules in a CAMAC standard. There are several designs based on a universal Fedorov stage and the apparatus for stereotaxis. The above schemes can be used both for working with the fixed histological slices and for in vivo or in situ analysis, particularly of the living brain slices. An example of application of such devices is described in this paper.
    VL  - 4
    IS  - 6
    ER  - 

    Copy | Download

Author Information
  • Talrose Institute for Energy Problems of Chemical Physics, Russian Academy of Sciences, Moscow, Russia

  • Institute for Information Transmission Problems, Russian Academy of Ssiences, Moscow, Russia

  • Bauman Moscow State Technical University, Robototechnics (graduate), Moscow, Russia

  • Sections