The Opioid System and Magnetic Field Perception

References

• Kholodov Y. A. The Bruin in Electromagnetic Fields. Nauka, MOSCOW 1982, in Russian
   Google Scholar
• Becker R. O. Electromagnetic control over biological growth processes. J. Bioelectricity 1984; 3: 105–121
   Web of Science ®Google Scholar
• Lai H., Horita A., Guy A. W. Microwave irradiation affects radial-arm maze performance in the rat. Bioelectromagnetics 1994; 15: 95–104
   PubMed Web of Science ®Google Scholar
• Blackman C. F., Benane S. G., House D. E. Frequency-dependent interference by magnetic-fields of nerve growth factor-induced neurite outgrowth in PC-12 cells. Bioelectromagnetics 1995; 16: 387–395
   PubMed Web of Science ®Google Scholar
• McLeod K. J. The role of cell and tissue calcium in transducing the effects of exposure to low-frequency electromagnetic fields. Adv Chem Series 1995; 250: 349–365
   Google Scholar
• Belyaev I. Y., Alipov Y. D., Polunin V. A., Shcheglov V. S. Evidence for dependence of resonant frequency of millimeter wave interaction with Escherichia coli K12 cells on haploid genome length. Electro Magnetobiol 1993; 12: 39–49
   Web of Science ®Google Scholar
• Blackman C. F., Blanchard J. P., Benane S. G., House D. E. Empirical test of an ion parametric resonance model for magnetic field interactions with PC-12 cells. Bioelectromagnetics IS; 1994; 239–260
   PubMed Web of Science ®Google Scholar
• Lednev V. V. Possible mechanism for the influence of weak magnetic fields on biological systems. Bioelectromagnetics 1991; 12: 71–75
   PubMed Web of Science ®Google Scholar
• Prato F. S., Carson J. J.L., Ossenkopp K.-P., Kavaliers M. Possible mechanism by which extremely low frequency magnetic field affects opioid function. FASEB J 1995; 9: 807–814
   PubMed Web of Science ®Google Scholar
• Wiltschko W., Munro U., Ford H., Wiltschko R. Effect of a magnetic pulse on the orientation of silvereyes, Zosterops I. lateralis, during spring migration. J. Exp. Biol 1998; 10: 3257–3261
   Google Scholar
• Wiltschko W., Wiltschko R. Orientation in birds. Magnetic orientation and celestial cues in migratory orientation. EXS 1991; 60: 16–37
   PubMedGoogle Scholar
• Wiltschko W., Wiltschko R. Magnetic orientation in birds. J. Exp. Biol 1996; 199: 29–38
   PubMed Web of Science ®Google Scholar
• Kenneth J. L. Magnetic compass orientation. Nature 1993; 362: 703
   PubMed Web of Science ®Google Scholar
• Beason R. C., Semm P. Neuroethological aspects of avian orientation. EXS 1991; 60: 106–127
   PubMedGoogle Scholar
• Lohmann K. J., Lohmann C. M.F. Detection of magnetic field intensity by sea turtles. Nature 1996; 380: 59–61
   Web of Science ®Google Scholar
• Sandberg R., Pettersson J. Magnetic orientation of snow buntings (Plectrophenax nivalis), a species breeding in the high Arctic: passage migration through temperate-zone areas. J. Exp. Biol 1996; 199: 1899–1905
   PubMed Web of Science ®Google Scholar
• Walcott C. Magnetic maps in pigeons. EXS 1991; 60: 38–51
   PubMedGoogle Scholar
• Mouritsen H. Redstars, Phoenicurus phoenicurus, can orient in a true–zero magnetic field. Anim. Behav 1998; 55: 1311–1324
   PubMed Web of Science ®Google Scholar
• Del Seppia C., Ghione S., Luschi P., Papi F. Exposure to oscillating magnetic fields influences and sensitivity to electrical stimuli. I. Experiments on pigeons. Bioelectromagnetics 1995; 16: 290–294
   PubMed Web of Science ®Google Scholar
• Kavaliers M., Ossenkopp K.-P. Repeated naloxone treatments and exposures to weak 60-Hz magnetic fields have ‘analgesic’ effects in snails. Brain Res 1993; 620: 159–162
   PubMed Web of Science ®Google Scholar
• Papi F., Luschi P., Limonta P. Orientation-disturbing magnetic treatment affects the pigeon opioid system. J. Exp. Biol 1992; 166: 169–179
   Web of Science ®Google Scholar
• Tysdale D., Lipa S. M., Ossenkopp K.-P., Kavaliers M. Inhibitory effects of 60 Hz magnetic fields on opiate–induced “analgesia” in the land snail, Cepaea nemoralis, under natural conditions. Physiol. Behav 1991; 49: 53–56
   PubMed Web of Science ®Google Scholar
• Ossenkopp K.-P., Kavaliers M. Clinical and applied aspects of magnetic field exposure: a possible role for the endogenous opioid system. J. Bioelectricity 1988; 7: 89–208, 89
   Google Scholar
• Papi F., Meschini E., Baldaccini N. E. Homing behavior of pigeons released after having been placed in an alternating magnetic field. Comp. Biochem. Physiol 1983; 76A: 673–682
   Web of Science ®Google Scholar
• Papi F., Luschi P. Pigeon navigation: naloxone injection and magnetic disturbance have a similar effect in initial orientation. Rend. Fis. Ass. Licei s. IX 1990; 1: 473–477
   Google Scholar
• Del Seppia C., Luschi P., Papi F. Further studies on the nature of effect of magnetic treatment on the orientation of homing pigeon (Columba livia). Boll. Zool 1994; 61: 88
   Google Scholar
• Lai H. Spatial learning deficit in rat after exposure to a 60 Hz magnetic field. Bioelectromagnetics 1996; 17: 494–496
   PubMed Web of Science ®Google Scholar
• Easley S. P., Coelho A. M., Rogers W. R. Effects of a 30 kV/m, 60 Hz electric field on the social behavior of baboons: a crossover experiment. Bioelectromagnetics 1992; 13: 395–400
   PubMed Web of Science ®Google Scholar
• Pich E. M., Solfrini V., Agnati L. F., Savoldi F. Exposure to strong static magnetic fields induces hypoactivity in weaning mice. J. Bioelectricity 1991; 10: 53–64
   Web of Science ®Google Scholar
• Gavalas R. J., Walter D. O., Hamer J., Adey W. R. Effect of low-level, low-frequency electric fields on EEG and behavior in Macaca nemestrina. Brain Res 1970; 18: 491–501
   PubMed Web of Science ®Google Scholar
• National Council on Radiation Protection and Measurements. Biological Effects and Exposure Criteria for Radiofrequency Magnetic Fields. NCRP Report No. 86. NCRP, Bethesda, MD 1986
   Google Scholar
• Stem S., Laties V. G. 60 Hz magnetic field on activity levels of mice. Radio Sci 1985; 12/6S: 279–286
   Google Scholar
• Stem S., Laties V. G., Stancampiano C. V., Cox C., de Lorge J. O. Behavioral detection of 60 Hz electric fields by rats. Bioelectromagnetics 1983; 4: 215–247
   PubMed Web of Science ®Google Scholar
• Sagan P. M., Stell M. E., Bryan G. K., Adey W. R. Detection of 60 Hz vertical electric fields by rats. Bioelectromagnetics 1987; 8: 303–313
   PubMed Web of Science ®Google Scholar
• Smith R. F., Clarke R. L., Justesen D. R. Behavioral sensitivity of rats to extremely low–frequency magnetic fields. Bioelectromagnetics 1994; 15: 411–426
   PubMed Web of Science ®Google Scholar
• Wiltschko R., Wiltschko W. Magnetoreception: why is conditioning so seldom successful?. Naturwissenschaften 1996; 83: 241–247
   PubMed Web of Science ®Google Scholar
• Lai H., Carino M. A., Horita A., Guy A. D. Effects of a 60 Hz magnetic field on central cholinergic systems of the rat. Bioelectromagnetics 1993; 14: 5–15
   PubMed Web of Science ®Google Scholar
• Thomas A. W., Persinger M. A. Daily post-training exposure to pulsed magnetic fields that evoke morphine-like analgesia affects consequent motivation but not proficiency in maze learning in rats. Electro- Magnetobiol 1997; 16: 33–41
   Web of Science ®Google Scholar
• Zadina J. E., Banks W. A., Kastin A. J. Central nervous system effects of peptides, 1980–1985: a cross listing of peptides and their central actions from the first six years of the journal “Peptides”. Peptides 1986; 7: 497–537
   PubMed Web of Science ®Google Scholar
• Wied D., Jolles J. Neuropeptides derived from pro-opiocortin: behavioral, physiological and neurochemical effects. Physiol Rev 1982; 62: 976–1041
   PubMed Web of Science ®Google Scholar
• Hudges J., Smith T. W., Kosterlitz H. W. Identification of two related pentapeptides from the brain with potient opiate agonist activity. Nature 1975; 258: 577–579
   PubMed Web of Science ®Google Scholar
• Olson G. A., Olson R. D., Kastin A. J. Endogenous opiates: 1995. Peptides 1986; 7: 907–933
   PubMed Web of Science ®Google Scholar
• Gallagher M., Rapp P. R., Fanelli R. J. Opiate antagonist facilitation of time-dependent memory processes: dependence upon intact norepinephrine function. Brain Res 1985; 347: 284–290
   PubMed Web of Science ®Google Scholar
• Fanelli R. J., Rosenberg R. A., Gallagher M. Role of noradrenergic function in the opiate antagonist facilitation of spatial memory. Behav. Neurosci 1985; 99: 751–755
   PubMed Web of Science ®Google Scholar
• DelCerro S., Borrel J. Naloxone influences retention behavior depending on the degree of novelty inherent to the training situation. Physiol. Behav 1985; 35: 667–671
   PubMed Web of Science ®Google Scholar
• Nikolskaya K., Shtemler V., Yeschenko O., Savonenko A., Osipov A., Nikolsky S. The sensitivity of cognitive processes to the inhomogeneity of natural magnetic fields. Electro-Magnetobiol 1996; 15: 163–174
   Web of Science ®Google Scholar
• Robinson R. The Genetics of the Norway Rat. Pergamon Press, Oxford 1965
   Google Scholar
• Presman A. S. Electromagnetic Fields and Life. Plenum Press, New York 1970
   Google Scholar