The Influences of Extremely Low Frequency Magnetic Fields on Drug-Induced Convulsion in Mouse

  • Sung, Ji-Hyun (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Jeong, Ji-Hoon (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Kim, Jeong-Soo (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Choi, Tai-Sik (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Park, Joon-Hong (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Kang, Hee-Yun (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Kim, Young-Sil (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Kim, Dong-Suk (Department of Pharmacology, College of Pharmacy, Chung-Ang University) ;
  • Sohn, Uy-Dong (Department of Pharmacology, College of Pharmacy, Chung-Ang University)
  • Published : 2003.06.01

Abstract

This study investigated the effects of extremely low frequency magnetic fields (ELF-MFs) on the sensitivity of seizure response to bicuculline, picrotoxin and NMDA in mice. The mice were exposed to either a sham or 20 G ELF-MFs for 24 hours. Convulsants were then administered i.p. at various doses. The seizure induction time and duration were measured and lethal dose ($LD_{50$}) and convulsant dose ($CD_{50}$) of the clonic and tonic convulsion were calculated. The analysis of glutamate, glycine, taurine and GABA of mouse brain was accomplished by HPLC. The mice exposed to ELF-MFs showed moderately higher $CD_{50}.{\;}LD_{50}$ and onset time on the bicuculline-induced seizure. However, the ELF-MFs did not influence them in the NMDA and picrotoxin-induced seizures. After the exposure to MFs exposure, the glutamate level was increased and GABA was decreased significantly in NMDA and picrotoxin-induced seizure. The level of glutamate and GABA were not changed by MFs in bicuculline-induced seizure. These results suggest that ELF-MFs may alter the convulsion susceptibility through GABAergic mechanism with the involvement of the level of glutamate and GABA.

Keywords

References

  1. Adey, W. R., Tissue interactions with nonionizing electromagnetic fields. Physiol. Rev., 61, 435-514 (1981) https://doi.org/10.1152/physrev.1981.61.2.435
  2. Anninos, P. A., Tsagas, N., Sandyk, R., and Derpapas, K., Magnetic stimulation in the treatment of partial seizures. Int. J. Neurosci., 60, 141-171 (1991) https://doi.org/10.3109/00207459109167029
  3. Bowery, N. G., GABAB receptor pharmacology. Annu. Rev. Pharmacol. Toxicol., 33, 109-147 (1993) https://doi.org/10.1146/annurev.pa.33.040193.000545
  4. Ferraz, A. C., Anselmo_Franci, J. A., Perosa, S. R., De_Castro_Neto, E. F., Bellissimo, M. I., De_Oliveira, B. H., Cavalheiro, E. A., Naffah_Mazzacoratti, M. D. A. G., and Da_Cunha, C., Amino acid and monoamine alterations in the cerebral cortex and hippocampus of mice submitted to ricinine-induced seizures. Pharmacol. Biochem. Behav., 72, 779-786 (2002) https://doi.org/10.1016/S0091-3057(02)00750-5
  5. Ferreira, J., Santos, A. R. , and Calixto, J. B., The role of systemic, spinal and supraspinal L-argininenitric oxidecGMP pathway in thermal hyperalgesia caused by intrathecal injection of glutamate in mice. Neuropharmacol., 38, 835-842. (1999) https://doi.org/10.1016/S0028-3908(99)00006-4
  6. Frey, A. H., Electromagnetic field interactions with biological systems. FASEB J., 7, 272-281 (1993) https://doi.org/10.1096/fasebj.7.2.8440406
  7. Goto, T., Matsuo, N., and Takahashi, T., CSF glutamate/GABA concentrations in pyridoxine-dependent seizures: etiology of pyridoxine-dependent seizures and the mechanisms of pyridoxine action in seizure control. Brain Dev., 23, 24-29 (2001) https://doi.org/10.1016/S0387-7604(00)00193-5
  8. Gould, J. L., Magnetic field sensitivity in animals. Ann. Rev. Physiol., 46, 585-598 (1984) https://doi.org/10.1146/annurev.ph.46.030184.003101
  9. Jeong, J. H., Choi, K. B., Yi, B. C., Chun, C. H., Sung, K. Y., Sung, J. Y., Gimm, Y. M., Huh, I. H., and Sohn, U. D., Effects of extremely low frequency magnetic fields on pain thresholds in mice: roles of melatonin and opioids. J. Auton. Pharmacol., 20, 259-264 (2000) https://doi.org/10.1046/j.1365-2680.2000.00189.x
  10. Juutilainen, J., Bjork, E., and Saali, K., Epilepsy and electromagnetic fields: effects of simulated atmospherics and 100-Hz magnetic fields on audiogenic seizure in rats. Intl. J. Biometeorol., 32, 17-20 (1988) https://doi.org/10.1007/BF01623987
  11. Keskil, I. S., Keskil, Z. A., Canseven, A. G., and Seyhan, N., No effect of 50 Hz magnetic field observed in a pilot study on pentylenetetrazol-induced seizures and mortality in mice. Epilepsy Res., 44, 27-32 (2001) https://doi.org/10.1016/S0920-1211(00)00193-5
  12. Kondziella, D., Bidar, A., Urfjell, B., Sletvold, O., and Sonnewald, U., The pentylenetetrazole-kindling model of epilepsy in SAMP8 mice: behavior and metabolism. Neurochem. Int., 40, 413-418 (2002) https://doi.org/10.1016/S0197-0186(01)00104-8
  13. Korpi, E. R., Grunder, G., and Luddens, H., Drug interactions at GABA(A) receptors. Prog. Neurobiol., 67, 113-159 (2002) https://doi.org/10.1016/S0301-0082(02)00013-8
  14. Lott, I. T., Coulombe, T., Di_Paolo, R. V., Richardson, E. P., and Levy, H. L., Vitamin B6-dependent seizures: pathology and chemical findings in brain. Neurology, 28, 47-54 (1978) https://doi.org/10.1212/WNL.28.1.47
  15. Macdonald, R. L. and Olsen, R. W., GABAA receptor channels. Annu. Rev. Neurosci., 17, 569-602 (1994) https://doi.org/10.1146/annurev.ne.17.030194.003033
  16. Min, Y. S., Jeong, J. H., Choi, Y. M., Lee, B. C., Huh, I. H., Lee, S. Y., and Sohn, U. D., The influences of extremely low frequency magnetic fields on clonidine-induced sleep in 2-day-old chicks. J. Auton. Pharmacol., 21, 197-203 (2001) https://doi.org/10.1046/j.1365-2680.2001.00227.x
  17. Morrisett, R. A., Mott, D. D., Lewis, D. V., Swartzwelder, H. S., and Wilson, W. A., GABAB-receptor-mediated inhibition of the N-methyl-D-aspartate component of synaptic transmission in the rat hippocampus. J. Neurosci., 11, 203-209 (1991)
  18. Ossenkopp, K. P. and Cain, D. P., Inhibitory effects of acute exposure to low-intensity 60-Hz magnetic fields on electrically kindled seizures in rats. Brain Res., 442, 255-260 (1988) https://doi.org/10.1016/0006-8993(88)91510-7
  19. Pende, M., Lanza, M., Bonanno, G., and Raiteri, M., Release of endogenous glutamic and aspartic acids from cerebrocortex synaptosomes and its modulation through activation of a gamma-aminobutyric acid B (GABAB) receptor subtype. Brain Res., 604, 325-330 (1993) https://doi.org/10.1016/0006-8993(93)90384-Y
  20. Piredda, S., Lim, C. R., and Gale, K., Intracerebral site of convulsant action of bicuculline. Life Sci., 36, 1295-1298 (1985) https://doi.org/10.1016/0024-3205(85)90275-9
  21. Pittaluga, A., Asaro, D., Pellegrini, G., and Raiteri, M., Studies on [3H]GABA and endogenous GABA release in rat cerebral cortex suggest the presence of autoreceptors of the GABAB type. Eur. J. Pharmacol., 144, 45-52 (1987) https://doi.org/10.1016/0014-2999(87)90007-0
  22. Potschka, H., Thun-Battersby, S., and Loscher, W., Effect of low-intensity 50-Hz magnetic fields on kindling acquisition and fully kindled seizures in rats. Brain Res., 809, 269-276 (1998) https://doi.org/10.1016/S0006-8993(98)00919-6
  23. Ruhenstroth-Bauer, G., Vogl, S., Baumer, H., Moritz, C., and Weinmann, H. M., Natural atmospherics and occurrence of seizures in six adolescents with epilepsy: a cross correlation study. Seizure, 4, 303-306 (1995) https://doi.org/10.1016/S1059-1311(95)80008-5
  24. Sejima, H., Ito, M., Kishi, K., Tsuda, H., and Shiraishi, H., Regional excitatory and inhibitory amino acid concentrations in pentylenetetrazol kindling and kindled rat brain. Brain Dev., 19, 171-175 (1997) https://doi.org/10.1016/S0387-7604(96)00492-5
  25. Sperber, E. F., Wurpel, J. N., Zhao, D. Y., and Moshe, S. L., Evidence for the involvement of nigral GABAA receptors in seizures of adult rats. Brain Res., 480, 378-382 (1989) https://doi.org/10.1016/0006-8993(89)90211-4