MEASUREMENT AND ANALYSIS OF STATIC MAGNETIC-FIELDS THAT BLOCK ACTION-POTENTIALS IN CULTURED NEURONS

Citation
Av. Cavopol et al., MEASUREMENT AND ANALYSIS OF STATIC MAGNETIC-FIELDS THAT BLOCK ACTION-POTENTIALS IN CULTURED NEURONS, Bioelectromagnetics, 16(3), 1995, pp. 197-206
Citations number
6
Categorie Soggetti
Biophysics
Journal title
ISSN journal
01978462
Volume
16
Issue
3
Year of publication
1995
Pages
197 - 206
Database
ISI
SICI code
0197-8462(1995)16:3<197:MAAOSM>2.0.ZU;2-R
Abstract
To characterize the properties of static magnetic fields on firing of action potentials (AP) by sensory neurons in cell culture, we develope d a mathematical formalism based on the expression for the magnetic fi eld of a single circular current loop. The calculated fields fit close ly the field measurements taken with a Hall effect gaussmeter. The bio logical effect induced by different arrays of permanent magnets depend ed principally on the spatial variation of the fields, quantified by t he value of the gradient of the field magnitude. Magnetic arrays of di fferent sizes (macroarray: four center-charged neodymium magnets of si milar to 14 mm diameter; microarray: four micromagnets of the same mat erial but of similar to 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 similar to 1 mT/mm an d blocked >70% of AP. Alternatively, cells placed in a field strength of similar to 0.2 mT and a gradient of similar to 0.02 mT/mm produced by the macroarray resulted in no significant reduction of firing; a mi croarray field of the same strength but with a higher gradient of simi lar to 1.5 mT/mm caused similar to 80% AP blockade. The experimental t hreshold gradient and the calculated threshold field intensity for blo ckade of action potentials by these arrays were estimated to be simila r to 0.02 mT/mm and similar to 0.02 mT, respectively. In conclusion, t hese findings suggest that spatial variation of the magnetic field is the principal cause of AP blockade in dorsal root ganglia in vitro. (C ) 1995 Wiley-Liss, Inc.