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Measurement and analysis of static magnetic fields that block action potentials in cultured neurons
Author(s) -
Cavopol A. V.,
Wamil A. W.,
Holcomb R. R.,
McLean M. J.
Publication year - 1995
Publication title -
bioelectromagnetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.435
H-Index - 81
eISSN - 1521-186X
pISSN - 0197-8462
DOI - 10.1002/bem.2250160308
Subject(s) - magnetic field , field strength , physics , magnet , nuclear magnetic resonance , chemistry , quantum mechanics
To characterize the properties of static magnetic fields on firing of action potentials (AP) by sensory neurons in cell culture, we developed a mathematical formalism based on the expression for the magnetic field of a single circular current loop. The calculated fields fit closely the field measurements taken with a Hall effect gaussmeter. The biological effect induced by different arrays of permanent magnets depended principally on the spatial variation of the fields, quantified by the value of the gradient of the field magnitude. Magnetic arrays of different sizes (macroarray: four center‐charged neodymium magnets of ˜14 mm diameter; microarray: four micromagnets of the same material but of ˜0.4 mm diameter) allowed comparison of fields with similar gradients but different intensities at the cell position. These two arrays had a common gradient value of ˜1 mT/mm and blocked >70% of AP. Alternatively, cells placed in a field strength of ˜0.2 mT and a gradient of ˜0.02 mT/mm produced by the macroarray resulted in no significant reduction of firing; a microarray field of the same strength but with a higher gradient of ˜1.5 mT/mm caused ˜80% AP blockade. The experimental threshold gradient and the calculated threshold field intensity for blockade of action potentials by these arrays were estimated to be ˜0.02 mT/mm and −0.02 mT, respectively. In conclusion, these findings suggest that spatial variation of the magnetic field is the principal cause of AP blockade in dorsal root ganglia in vitro. © 1995 Wiley‐Liss, Inc.