Fine-wire electromyography of the transverse head of adductor hallucis during locomotion

2021 ◽  
Vol 85 ◽  
pp. 7-13
Author(s):  
Kelly A. Robb ◽  
Hope D. Melady ◽  
Stephen D. Perry
Keyword(s):  
2005 ◽  
Vol 289 (6) ◽  
pp. H2468-H2477 ◽  
Author(s):  
J. James Wiley ◽  
Raymond E. Ideker ◽  
William M. Smith ◽  
Andrew E. Pollard

This study was designed to test the feasibility of using microfabricated electrodes to record surface potentials with sufficiently fine spatial resolution to measure the potential gradients necessary for improved computation of transmembrane current density. To assess that feasibility, we recorded unipolar electrograms from perfused rabbit right ventricular free wall epicardium ( n = 6) using electrode arrays that included 25-μm sensors fabricated onto a flexible substrate with 75-μm interelectrode spacing. Electrode spacing was therefore on the size scale of an individual myocyte. Signal conditioning adjacent to the sensors to control lead noise was achieved by routing traces from the electrodes to the back side of the substrate where buffer amplifiers were located. For comparison, recordings were also made using arrays built from chloridized silver wire electrodes of either 50-μm (fine wire) or 250-μm (coarse wire) diameters. Electrode separations were necessarily wider than with microfabricated arrays. Comparable signal-to-noise ratios (SNRs) of 21.2 ± 2.2, 32.5 ± 4.1, and 22.9 ± 0.7 for electrograms recorded using microfabricated sensors ( n = 78), fine wires ( n = 78), and coarse wires ( n = 78), respectively, were found. High SNRs were maintained in bipolar electrograms assembled using spatial combinations of the unipolar electrograms necessary for the potential gradient measurements and in second-difference electrograms assembled using spatial combinations of the bipolar electrograms necessary for surface Laplacian (SL) measurements. Simulations incorporating a bidomain representation of tissue structure and a two-dimensional network of guinea pig myocytes prescribed following the Luo and Rudy dynamic membrane equations were completed using 12.5-μm spatial resolution to assess contributions of electrode spacing to the potential gradient and SL measurements. In those simulations, increases in electrode separation from 12.5 to 75.0, 237.5, and 875.0 μm, which were separations comparable to the finest available with our microfabricated, fine wire, and coarse wire arrays, led to 10%, 42%, and 81% reductions in maximum potential gradients and 33%, 76%, and 96% reductions in peak-to-peak SLs. Maintenance of comparable SNRs for source electrograms was therefore important because microfabrication provides a highly attractive methods to achieve spatial resolutions necessary for improved computation of transmembrane current density.


2007 ◽  
Vol 340-341 ◽  
pp. 525-530 ◽  
Author(s):  
Satoshi Kajino ◽  
Motoo Asakawa

The mechanical and electrical applications of fine wires (D = 0.1 mm) has become more widely spread. In general, it is well known that fine drawn wires have high tensile strength while maintaining ductility. It has been determined that a hardened layer of around 0.04 mm in depth, referred to as the “additional shear strain layer,” is generated beneath the surface layer of the wire, and this additional shear strain layer affected the tensile strength of the fine wire. As an origin of this phenomenon, it was ascertained that the microstructure of surface layer was finer than that of center layer. The purpose of this paper is to investigate the effect of die angle on the microstructure and the tensile strength of the additional shear strain layer. The tensile test was performed as the surface layer was thinned by electro-polishing, and the crystal orientation and the crystal grain were measured via EBSD. As a result, it was ascertained that die angle affected the tensile strength and crystal grain refinement of the additional shear stray layer.


1961 ◽  
Vol 10 (4) ◽  
pp. 577-587 ◽  
Author(s):  
M. H. Silk ◽  
A. O. Hawtrey ◽  
I. M. Spence ◽  
J. H. S. Gear

A technic is described for high resolution intracellular autoradiography in the electron microscope. Cultures of LLC-MK2 monkey kidney cells were incubated for 72 hours in a medium containing 0.4 µcurie per ml of thymidine-H3. After labeling, the cells were fixed with osmium tetroxide and embedded in methacrylate. Ultrathin sections of the labeled tissue were taken up on Formvar-coated and carbon-stabilized electron microscope grids. A 150 to 450 A layer of silver metal was then evaporated onto the tissue. The coated grids were exposed to bromine vapor for 1.5 to 2 minutes under red light, allowed to dry for 1 minute, and then covered with a thin film of 1 per cent aqueous gelatin applied by means of a fine wire loop lowered over the grid supported on a glass peg. For autoradiographic exposure, the grids were stored 50 days in a light-proof container at 4°C with calcium chloride desiccant. Development was carried out for 5 minutes at 20°C in Promicrol (May and Baker, England) diluted 1:1 with water, followed by a 1 minute water wash and fixation for 2.5 minutes in 15 per cent aqueous sodium thiosulphate. After removal of the gelatin by immersion for 16 hours in water at 37°C, the autoradiograms were dried and examined in the electron microscope. Ultrastructural detail was fairly well defined and the cytoplasm of each labeled cell was covered with an electron opaque deposit of silver, suggesting that a polynucleotide containing thymidine may be synthesized in the cytoplasm. The matter is discussed.


Physiotherapy ◽  
2011 ◽  
Vol 97 (4) ◽  
pp. 357-359 ◽  
Author(s):  
Craig A. Wassinger ◽  
Hamish Osborne ◽  
Daniel Cury Ribeiro

2021 ◽  
Vol 2021.59 (0) ◽  
pp. 04b2
Author(s):  
Yu MIYAZAKI ◽  
Masato MIYOSHI ◽  
Akira OKADA
Keyword(s):  
Wire Edm ◽  

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