Magnetic fields, brain and immunity: Effect on humoral and cell-mediated immune responses

References

• Adey W. R. Tissue interactions with nonionizing electromagnetic fields. Physiological Reviews 1981; 61: 435–514
   PubMed Web of Science ®Google Scholar
• Arnold W., Steele R., Mueller H. On the magnetic asymmetry of muscle fibers. Proceedings of the National Academy of Sciences (U.S.A.) 1958; 44: 1–4
   PubMed Web of Science ®Google Scholar
• Audus L. J. Magnetotropism: a new plant-growth response. Nature 1960; 185: 132–134
   Web of Science ®Google Scholar
• Baker R. R. Goal orientation by blindfolded humans after long-distance displacement: possible involvement of a magnetic sense. Science 1980; 210: 555–557
   PubMed Web of Science ®Google Scholar
• Bardasano J. L., Meyer A. J., Picazo L. The pineal organ of the hamster and magnetic fields. Proceedings of the Eight European Congress on Electron Microscopy 1984; 3: 1949–1950
   Google Scholar
• Barker A. T., Jalinous R. Non-invasive magnetic stimulation of human motor cortex. The Lancet 1985; 1: 1106–1107
   PubMed Web of Science ®Google Scholar
• Barnothy J. M., Barnothy M. F., Boszormeny-Negy I. Influence of magnetic field upon leucocytes of mouse. Nature 1956; 177: 577–578
   PubMed Web of Science ®Google Scholar
• Besedovsky H. O., Del Ray A., Sorkin E., Da Prada M., Keller H. H. Immunoregulation mediated by the symphatetic nervous system. Cellular Immunology 1979; 48: 346–355
   PubMed Web of Science ®Google Scholar
• Bistolti F. Classification of possible targets of interaction of magnetic fields with living matter. Panminesra Medica 1987; 29: 71–73
   PubMed Web of Science ®Google Scholar
• Biziere K., Renoux M., Renoux G. Modulation of the T-cell lineage by the cerebral cortex. Proceedings of the First International Workshop on Neuroimmunomodulation 1985; 20–22
   Google Scholar
• Blakemore R. P. Magnetotactic bacteria. Science 1975; 190: 377–379
   PubMed Web of Science ®Google Scholar
• Blask F. P. The pineal: an oncostatic gland. The pineal gland, J. Reiter. Raven Press, New York 1968; 253–285
   Google Scholar
• Bowen F. P. Immunological reactions after cortical lesions in rabbits. Archives in Neurology 1968; 19: 398–402
   PubMedGoogle Scholar
• Brinchmann J. E., Vartdal F., Gaudernack G., Markussen G., Funderud S., Ugelstad J., Thorsby E. Direct immunomagnetic quantification of lymphocyte subsets in blood. Clinical and Experimental Immunology 1988; 71: 182–186
   PubMed Web of Science ®Google Scholar
• Brown F. A., Barnwell F. H., Webb H. M. Adaptation of the magneto-receptive mechanism of mud snails to geomagnetic field strength. Biological Bulletin 1964; 127: 221–223
   Web of Science ®Google Scholar
• Brown F. A., Park Y. H. Duration of an after effect in planarians following a reversed horizontal magnetic vector. Biologicall Bulletin 1965; 128: 347–349
   Google Scholar
• Brown F. A., Scow K. M. Magnetic induction of a circadian cycle in hamsters. Journal of Interdisciplinary Cycle Research 1978; 9: 137–145
   Google Scholar
• Carr D. J. J., Klimpel G. R. Enhancement of the generation of cytotoxic T cells by endogenous opiates. Journal of Neuroimmunology 1986; 12: 75–87
   PubMed Web of Science ®Google Scholar
• Chagneux R., Chagneux H., Chalazonitis N. Decrease in magnetic anisotropy of external segments of the retinal rods after a total photolysis. Biophysical Journal 1977; 18: 125–128
   PubMed Web of Science ®Google Scholar
• Cremer-Bartels G., Krause K., Kuchle H. J. Influence of low magnetic-field-strength variations on the retina and pineal gland of quail and humans. Graefe's Archives of Clinical and Experimental Ophthalmology 1983; 220: 248–252
   PubMed Web of Science ®Google Scholar
• Cross R. S., Markesberry W. R., Brooks W. H., Roszman T. L. Hypothalamic-immune interactions. I. The acute effect of anterior hypothalamic lesions on the immune response. Brain Research 1985; 196: 79–88
   Google Scholar
• Czerski P. Microwave effects on the blood-forming system with particular reference to the lymphocyte. Annals of the New York Academy of Sciences 1975; 247: 232–242
   PubMed Web of Science ®Google Scholar
• Delorenzi E. Influence of a magnetic field on the multiplication of cells activated in vitro. Increase in the frequency of mitoses and anomalics of the mitotic process. Biolletino della Societa Italiana di Biologia Sperimentale (Milano) 1935; 10: 702–704
   Google Scholar
• Geacintov N. E., Van Nostrand F., Pope M., Tinkel J. B. Magnetic field effects on the chlorophyll fluorescence in Chorella. Biochimica et Biophysica Acta 1971; 336: 486–491
   Google Scholar
• Gilman S. C., Schwartz J. M., Milner R. J., Bloom F. E., Feldman J. D. Beta-endorphin enhances lymphocyte proliferative responses. Proceedings of the National Academy of Sciences (U.S.A.) 1982; 79: 4226–4230
   PubMed Web of Science ®Google Scholar
• Goetzl E. J., Chernov T., Renold F., Payan D. G. Neuropeptide regulation of the expression of immediate hypersensitivity. Journal of Immunology (Supplement) 1985; 135: 802s–805s
   Web of Science ®Google Scholar
• Gould J. L. The case for magnetic sensitivity in birds and bees (such as it is). American Science 1980; 68: 256–258
   Web of Science ®Google Scholar
• Gould J. L. Magnetic field sensitivity in animals. Annual Review of Physiology 1983; 46: 585–598
   Web of Science ®Google Scholar
• Gould J. L., Able K. P. Human homing: an elusive phenomenon. Science 1981; 212: 1061–1063
   PubMed Web of Science ®Google Scholar
• Gungor M., Gene E., Sagduyu H., Eroglu L., Koyuncuoglu H. Effect of chronic administration of morphine on primary immune response in mice. Experientia 1980; 36: 1309–1310
   PubMedGoogle Scholar
• Haberditzl W. Enzyme activity in high magnetic fields. Nature 1967; 213: 72–73
   Web of Science ®Google Scholar
• Halberg F., Cutkomp L., Nelson W., Southern R. Circadian rhythms in plants, insects and mammals exposed to ELF magnetic and/or electric fields and currents. National Technology Information Service, Springfield, VA 1975
   Google Scholar
• Hoff A. J. Magnetic field effects on photosynthetic reactions. Quarterly Reviews of Biophysics 1981; 14: 599–665
   PubMed Web of Science ®Google Scholar
• Huang A. T., Engle M. E., Elder J. A., Kinn J. B., Ward T. R. The effect of microwave radiation (2450MHz) on the morphology and chromosomes of lymphocytes. Radio Science 1977; 12: 173–177
   Web of Science ®Google Scholar
• Janković B. D., Isaković K., Petrovi S. Effect of pinealectomy on immune reactions in the rat. Immunology 1970; 18: 1–16
   PubMed Web of Science ®Google Scholar
• Janković B. D., Isaković K. Neuro-endocrine correlation of immune response. I. Effects of brain lesions on antibody production. Arthus reactivity and delayed hypersensitivity in the rat. International Archives of Allergy 1973; 45: 360–372
   PubMedGoogle Scholar
• Janković B. D., Nesi K., Markovi B. M. Neuroimmunomodulation: electrical stimulations of the hypothalamus and cortex potentiate the immune response. Neuroscience Letters 1983; 14: S180
   Google Scholar
• Janković B. D., Marić D. Modulation of in vivo immune responses by enkephalins. Clinical Neuropharmacology 1986; 9: 476–478
   PubMed Web of Science ®Google Scholar
• Janković B. D., Marić D. Enkephalins and immunity. I. In vivo suppression and potentiation of humoral immune response. Annals of the New York Academy of Sciences 1987a; 496: 115–125
   PubMed Web of Science ®Google Scholar
• Janković B. D., Marić D. Enkephalins and anaphylactic shock: modulation and prevention of shock in the rat. Immunology Letters 1987b; 15: 153–160
   PubMed Web of Science ®Google Scholar
• Janković B. D., Marić D. Enkephalins and autoimmunity: differential effect of methionineenkephalin on experimental allergic encephalomyelitis in Wistar and Lewis rats. Journal of Neuroscience Research 1987c; 18: 88–94
   PubMed Web of Science ®Google Scholar
• Neuroimmune interactions: Proceedings of the second international workshop on neuroimmunodulation, B. D. Janković, B. M. Markovi, N. H. Spector. The New York Academy of Sciences, New York 1987
   Google Scholar
• Janković B. D., Maric D. Enkephalins modulate in vivo immune reactions through delta- and mu-opioid receptors. Annals of the New York Academy of Sciences 1988; 540: 691–693
   PubMedGoogle Scholar
• Janković B. D., Marić D. Methionine-enkephalin inhibits adoptive transfer of experimental allergic encephalomyelitis in the rat. International Journal of Neuroscience 1990; 51: 197–199
   PubMed Web of Science ®Google Scholar
• Janković B. D., Marić D., Veljić J. Cerebrally mediated modulation of anaphylactic shock by methionine-enkephalin. International Journal of Neuroscience 1990; 51: 193–194
   PubMed Web of Science ®Google Scholar
• Janković B. D., Veljić J. Brain, enkephalins and immunity: modulation of immune responses by methionine enkephalin injected into lateral ventricles of the rat brain. Neuro-Psycho-Immunology: Recent Research. (in press), B. D. Janković, B. M. Markovi. Gordon and Breach Publishers, Inc, Philadelphia 1991
   Google Scholar
• Jitariu P., Lascu N., Topala N., Lazar M. The influence of magnetic fields on the antitoxicantitetanic immunity in guinea pigs. Revue Roumaine de Biologie-Zoologie 1965; 10: 33–38
   Google Scholar
• Johnson H. M., Smith E. M., Torres B. A., Blalock J. E. Regulation of in vitro antibody response by neuroendoctrine hormones. Proceedings of the National Academy of Sciences (U.S.A.) 1982; 79: 4171–4174
   PubMed Web of Science ®Google Scholar
• Nuclear magnetic resonance imaging in medicine, L. Kaufman, L. E. Crooks, A. R. Margulis. Igaku-Shoin, New York 1982
   Google Scholar
• Kavaliers M., Ossenkopp K.-P. Tolerance to morphine-induced analgesia in mice: magnetic fields function as environmental specific cues and reduce tolerance development. Life Sciences 1985a; 37: 1125–1135
   PubMed Web of Science ®Google Scholar
• Kavaliers M., Ossenkopp K.-P. Exposure to rotating magnetic fields alters morphine-induced behavioral responses in two strains of mice. Neuropharmacology 1985b; 24: 337–340
   PubMed Web of Science ®Google Scholar
• Kavaliers M., Ossenkopp K.-P. Magnic fields differentially inhibit mu, delta, kappa and sigma opiate-induced analgesia in mice. Peptides 1986; 7: 449–453
   PubMed Web of Science ®Google Scholar
• Kronick P. L., Campbell G. L., Joseph K. Magnetic microspheres prepared by redox polymerization used in a cell separation based on gangliosides. Science 1978; 200: 1074–1076
   PubMed Web of Science ®Google Scholar
• Labes M. M. A possible explanation for the effect of magnetic fields on biological systems. Nature 1966; 211: 968
   PubMed Web of Science ®Google Scholar
• Liboff A. R., Williams T., Strong D. M., Wistar R. Time-varying magnetic fields: effect on DNA synthesis. Science 1984; 233: 818–819
   Google Scholar
• Lobel D., Halc J. R., Montgomery D. B. A new magnetic technique for the treatment of giant retinal tears. American Journal of Ophthalmology 1978; 85: 699–701
   PubMed Web of Science ®Google Scholar
• DeLorge J. Effects of magnetic fields on behavior in nonhuman primates. Magnetic field effects in biological systems, T. Tenforde. Plenum Press, New York 1979; 32
   Google Scholar
• Maestroni G. J. M., Conti A., Pierpaoli W. Role of the pineal gland in immunity: circadian synthesis and release of melatonin modulates the antibody response and antagonizes the immunosuppressive effect of corticosterone. Journal of Neuroimmunology 1986; 13: 19–30
   PubMed Web of Science ®Google Scholar
• Maestroni G. J. M., Conti A., Pierpaoli W. The pineal gland and the circadian, opiatergic, immunomodulatory role of melatonin. Annals of the New York Academy of Sciences 1987; 496: 67–77
   PubMed Web of Science ®Google Scholar
• Mahlum D. D., Sikov M. R., Decker J. R. Dominant lethal studies in mice exposed to direct current magnetic fields. Biological effects of extremely low frequency electromagnetic fields, R. D. Phillips, M. F. Gillis. US Department of Energy. 1979; 474, Conf. 781016
   Google Scholar
• Malinin G. I., Gregory W. D., Morelli L. Evidence of morphological and physiological transformation of mammalian cells by strong magnetic fields. Science 1976; 194: 844–846
   PubMed Web of Science ®Google Scholar
• Mandler R. N., Biddison W. E., Mandler S., Serate S. A. Beta-endorphin augments the cytolitic activity and interferon production of natural killer cells. Journal of Immunology 1986; 136: 934–939
   PubMed Web of Science ®Google Scholar
• Maret G., Dransfield K. Macromolecules and membranes in high magnetic fields. Physica 1977; 86–88 B: 1077
   Google Scholar
• Marić D., Janković B. D. Enkephalins and immunity. II. In vivo modulation of cell mediated immunity. Annals of the New York Academy of Sciences 1987a; 496: 126–136
   PubMed Web of Science ®Google Scholar
• Marić D., Janković B. D. Methionine-enkephalin acts via delta receptors on humoral immune response in mice. Federation Proceedings 1987b; 46: 1446
   Google Scholar
• Melvile D., Paul F., Roath S. Direct separation of red cells from whole blood. Nature 1975; 255: 706
   PubMed Web of Science ®Google Scholar
• McCain H. V., Lanster I. B., Bilotta J. Modulation of human T-cell suppressor activity by beta-endorphin and glycyl-L-glutamine. International Journal of Immunopharmacology 1986; 8: 443–446
   PubMed Web of Science ®Google Scholar
• Miller D. B., Blackman C. F., Ali J. S. Behavioral responses to morphine-treated mice to ELF magnetic fields. Abstracts of the Bioelectromagnetology Society 1985; 54
   Google Scholar
• Murayama M. Orientation of sicled erythrocytes in a magnetic field. Nature 1965; 206: 420–422
   PubMed Web of Science ®Google Scholar
• Neugebauer D. C., Blaurock A. E., Worcester D. L. Magnetic orientation of purple membranes demonstrated by optical measurements and neutron scattering. Federation of European Biochemical Societies Letters 1977; 78: 31–35
   PubMed Web of Science ®Google Scholar
• Neurath P. W. High gradient magnetic field inhibits embryonic development of frogs. Nature 1968; 219: 1358–1359
   PubMed Web of Science ®Google Scholar
• Neveu P. J., Barneoud P., Vitiello S., Betancur C., Le Moal M. Brain modulation of the immune system: association between lymphocyte responsiveness and paw preference in mice. Brain Research 1988; 457: 392–394
   PubMed Web of Science ®Google Scholar
• Okada Y. C., Lauritzen M., Nicholson C. Magnetic field associated with neural activities in an isolated cerebellum. Brain Research 1987; 412: 151–155
   PubMed Web of Science ®Google Scholar
• Olcese J., Reuss S., Vollrath L. Evidence for the involvement of the visual system in mediating magnetic field effects on pineal melatonin synthesis in the rat. Brain Research 1985; 333: 382–384
   PubMed Web of Science ®Google Scholar
• Olcese J., Reuss S. Magnetic field effects on pineal gland melatonin synthesis: comparative studies on albino and pigmented rodents. Brain Research 1986; 369: 365–368
   PubMed Web of Science ®Google Scholar
• Olcese J., Reuss S., Semm P. Minireview: geomagnetic field detection in rodents. Life Science 1988; 42: 605–613
   PubMed Web of Science ®Google Scholar
• Ossenkopp K. P., Kavaliers M., Hirst M. Reduced nocturnal morphine-analgesia in mice following geomagnetic disturbance. Neuroscience Letters 1983; 40: 321–325
   PubMed Web of Science ®Google Scholar
• Owen C. S. High gradient magnetic capture of cells and ferritin-bound particles. Institute of Electrical and Electronic Engineers Transaction and Magnetism 1982; 18: 1514–1516
   Google Scholar
• Phillips J. B. Use of the earth's magnetic field by orienting cave salamander (Eurycea lucifuga). Journal of Comparative Physiology 1977; 121: 273A
   Web of Science ®Google Scholar
• Plotnikoff N. P., Miller G. C. Enkephalins as immunomodulators. International Journal of Immunopharmacology 1983; 5: 437–441
   PubMed Web of Science ®Google Scholar
• Plotnikoff N. P., Miller G. C., Solomon S. K. T., Faith R. E., Edwards L. D., Murgo A. J. Methionine-enkephalin: immunomodulator in normal volunteers (in vivo). Psychopharmacology Bulletin 1986; 22: 1097–1100
   PubMedGoogle Scholar
• CRC Handbook of biological effects of electromagnetic fields, C. Polk, E. Postow. CRC Press, Inc, Bora Raton, Florida 1986
   Google Scholar
• Prato F. S., Ossenkopp K. P., Kavaliers M., Sestini E. Magnetic resonance imaging and morphine-induced analgesia: some temporal effects of the time varying magnetic fields. Society of Neuroscience Abstracts 1985; 23: 1280
   Google Scholar
• Quinn T. P. Evidence for celestial and magnetic compass orientation in lake migrating sockeye salmon fry. Journal of Comparative Physiology 1980; 137: 243–245
   Web of Science ®Google Scholar
• Radosevi-Stasi B., Jonji S., Poli L., Rukavina D. Immune response of rats after pharmacologic pinealectomy. Periodicum Biologorum 1983; 85: 119–121
   Web of Science ®Google Scholar
• Renoux G., Biziere K., Renoux M., Guillaumin J. M. The production of T-cell inducing factors in mice is controlled by the brain neocortex. Scandinavian Journal of Immunology 1983; 17: 45–50
   PubMed Web of Science ®Google Scholar
• Reuss S., Semm P., Vollrath L. Different types of magnetically sensitive cells in the rat pineal gland. Neuroscience Letters 1983; 40: 23–26
   PubMed Web of Science ®Google Scholar
• Rosen A. D., Lubowsky J. Magnetic field influence on the central nervous system function. Experimental Neurology 1987; 95: 679–687
   PubMed Web of Science ®Google Scholar
• Rudolph K., Witz-Justic A., Krauchi K., Feer H. Static magnetic fields decrease nocturnal pineal cAMP in the rat. Brain Research 1988; 446: 159–160
   PubMed Web of Science ®Google Scholar
• Salles-Chuna S. X., Battocletti J. H., Sances A. Steady magnetic fields in noninvasive electromagnetic flowmetry. Proceedings of the Institute of Electrical and Electronic Engineers 1980; 68: 149–151
   Web of Science ®Google Scholar
• Semm P., Schneider T., Vollrath L. Effects of an earth-strength magnetic field on electrical activity of pineal cells. Nature 1980; 288: 607–608
   PubMed Web of Science ®Google Scholar
• Semm P., Schneider T., Vollrath L., Wiltschko W. Magnetic sensitive cells in pigeons. Avian Navigation, F. Papi, H. G. Wallruff. Springer, Berlin 1982; 329–377
   Google Scholar
• Smialowicz R. J., Kinin J. B., Weil C. M., Ward T. R. Chronic exposure of rats to 425 or 2450 MHz microwave radiation. Proceedings of International Union Radio Science Symposium on Biological Effects of Electromagnetic Waves, Airlie, VA, 1977, 140
   Google Scholar
• Sperber D., Dransfield K., Maret G., Weisenseel M. H. Oriented growth of pollen tubes in strong magnetic field. Naturwissenschaften 1981; 68: 40–43
   Web of Science ®Google Scholar
• Magnetic field effects on biological systems, T. S. Tenforde. Plenum Press, New York 1979
   Google Scholar
• Torbert J., Maret G. Fibers of highly oriented Pfl bacteriophage produced in a strong magnetic field. Journal of Molecular Biology 1979; 134: 843–845
   PubMed Web of Science ®Google Scholar
• Torbet J., Freyssinet J. M., Hudry-Clergon G. Orriented fibrin gels formed by polymertahon in strong magnetic fields. Nature 1981; 289: 91–93
   PubMed Web of Science ®Google Scholar
• Tubaro E., Borelli G., Croce C., Cavallo G., Santiangeli C. Effect of morphine on resistance to infection. Journal of Infectious Diseases 1983; 148: 656–666
   PubMed Web of Science ®Google Scholar
• Walcott C. Magnetic orientation in homing pigeons. Institute of Electrical and Electronic Engineers transaction and Magnetism 1980; 16: 1008–1010
   Google Scholar
• Welker H. A., Semm P., Willig R. P., Commentz J. C., Wiltschko W., Vollarth L. Effects of an artificial magnetic field on serotonin N-acetyltransferase activity and melatonin content of the rat pineal gland. Experimental Brain Research 1983; 50: 426–432
   PubMed Web of Science ®Google Scholar
• Wever R. Einfluss schwacher elektro-magnetischer Felder auf die circadiane Periodik des Menschen. Naturwissenshaften 1968; 55: 29–33
   PubMed Web of Science ®Google Scholar
• Widder K. J., Senyei A. E., Sears B. Experimental methods in cancer therapeutics. Journal of Pharmacological Science 1982; 71: 379–387
   PubMed Web of Science ®Google Scholar
• Wiktor-Jedrzejczak W., Ahmed A., Czerski P., Leach W. M., Sell K. W. Immune response of mice to 2450 MHz microwave radiation: overview of immunology and empirical studies of lymphoid splenic cells. Radio Science 1977; 12: 209–210
   Web of Science ®Google Scholar
• Wybran J., Apelboom T., Famaey J. P., Govaerts A. Suggestive evidence for receptors for morphine and methionine-enkephalin on normal human blood T lymphocytes. Journal of Immunology 1979; 123: 1068–1070
   PubMed Web of Science ®Google Scholar