Dopamine Receptors and Microwave Energy Exposure

References

• Frey A. H. Behavioral biophysics. Psychological Bulletin 1965; 63(5)322–377
   PubMed Web of Science ®Google Scholar
• Frey A. H. Biological function as influenced by low‐power modulated RF energy. IEEE Transactions on Microwave Theory and Techniques 1971; 19(2)153–164, MTT‐19(2
   Google Scholar
• Medici R. G. Methods of assaying behavioral changes during exposure to weak electric fields. Proceedings of Conference XI Abnormal Animal Behavior Prior to Earthquakes II. 1980; 114–140, USGS Open Pile Report 80–453
   Google Scholar
• Frey A. H., Feld S. Avoidance by rats of illumination with low power nonionizing electromagnetic energy. Journal of Comparative and Physiological Psychology 1975; 89(2)183–188
   PubMed 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 of Macaca Menestrina. Brain Research 1970; 18: 491–501
   PubMed Web of Science ®Google Scholar
• Gillard J., Servantie B., Bertharion G., Servantie A. M., Obrenovitch J., Perrin J. C. Study of the microwave induced pertubations of the behavior by the open field test into the white rat. Biological Effects of Electromagnetic Waves, C. C. Johnson, M. L. Shore. HEW Publication (FDA). 1977; Vol. I: 77–8010; 175–186
   Google Scholar
• Hjeresen D. L., Phillips R. D. Perception and response to pulsed microwave radiation by rats. Program and Abstracts for URSI Annual Meeting. Amherst, MA 1976; 4
   Google Scholar
• Medici R., Day S. R. Effects of weak ELF electric fields on schedule controlled behavior in monkeys. Biological Effects of Electromagnetic Waves, C. C. Johnson, M. L. Shore. HEW Publication (FDA). 1976; Vol. I: 77–8010; 215–225
   Google Scholar
• Mitchell D. S., Switzer W. G., Bronaugh E. L. Hyperactivity and disruption of operant behavior in rats after multiple exposures in microwave radiation. Radio Science 1977; 12(6S)263–271
   Web of Science ®Google Scholar
• Monahan J. C., Henton W. W. Free operant avoidance and escape from microwave radiation. Proceeding of Symposium on Biological Effects and Measurement of Radio Frequency/Microwaves, D. G. Hazzard. HEW Publication (FDA), 1977; 77–8026; 23–37
   Google Scholar
• Frey A. H., Spector J. Irritability and aggression in mammals as affected by exposure to electromagnetic energy. Program and Abstracts for UHSI Annual Meeting. Amherst, MA 1976; 93
   Google Scholar
• McGeer P. L., McGeer E. G. Chemistry of mood and emotion. Annual Review of Psychology 1980; 31: 273–307
   PubMed Web of Science ®Google Scholar
• Frey A. H., Wesler L. S. Modification of tail pinch consummatory behavior by microwave energy exposure. Program and Abstracts for URSI Annual Meeting. Seattle, WA 1979; 456
   Google Scholar
• Antelman S. M., Seechtman H. Tail pinch induces eating in sated rats which appears to depend on nigrostriatal dopamine. Science 1975; 189: 731–733
   PubMed Web of Science ®Google Scholar
• Antelman S. M., Szechtman H., Chin P., Fisher A. E. Tail pinch induced eating, gnawing, and licking behavior in rats: Dependence on the nigrostriatal dopamine system. Brain Research 1975; 99: 319–337
   PubMed Web of Science ®Google Scholar
• Frey A. H., Gendleman S. Motor coordination of balance degradation during microwave energy exposure. Bulletin of the Psychonomic Society 1979; 14(6)442–444
   Google Scholar
• Frey A. H., Wesler L. S. Modification of the CER in rats living in a 60 Hz electric field. Abstracts of papers presented at the Bioelectromagnetics Society 3rd Annual Conference. Washington, DC 1981; 93
   Google Scholar
• Stith R. D., Erwin D. M. Effect of exposure to microwaves on the neuroendocrine status of the rat. Bioelectromagnetics Journal 1980; 1(2)236
   Google Scholar
• Alper R. H., Demarest K. T., Moore K. E. Morphine differentially alters synthesis and turnover of dopamine in central neuronal systems. Journal of Neural Transmission 1980; 48: 157–165
   PubMed Web of Science ®Google Scholar
• Sparber S. B., Gellert V. F., Fossom L. On the use of operant behavior to study the neuropsychopharmacology of opiates with special reference to morphine and its relationship to dopamine in the central nervous system, In Neurochemical Mechanisms of Opiates and Endorphins (Advances in Biochemistry and Psychopharmacology), Vol. Frontiers in Catecholoamine Research, H. H. Loh, D. H. Ross. Haven Press, NY 1979; 20: 453–491
   Google Scholar
• Pickel V. M., Joh T. H., Reis D. J., Leeman S. E., Miller R. J. Electron microscopic localization of substance P and enkephalin in axon terminals related to dendrites of catecholaminergic neurons. Brain Research 1979; 160: 387–400
   PubMed Web of Science ®Google Scholar
• Lindvall O., Stenevi U. Dopamine and noradrenaline neurons projecting to the septal area in the rat. Cell and Tissue Research 1978; 190: 383–407
   PubMed Web of Science ®Google Scholar
• Marshall H. W., Stoner H. B. The effect of dopamine on shivering in the rat. Journal of Physiology 1979; 288: 393–399
   PubMed Web of Science ®Google Scholar
• Waldmeier P. C., Delini‐Stula A. A. Serotonin dopamine interactions in the nigrostriatal system. European Journal of Pharmacology 1979; 55: 363–373
   PubMed Web of Science ®Google Scholar
• Margolin D. I., Moon B. H. Naloxone blockade of apomorphine induced stereotyped behavior. Journal of the Neurological Sciences 1979; 43: 13–17
   PubMed Web of Science ®Google Scholar
• Fog K. Behavioral effects in rats of morphine and amphetamine and a combination of the two drugs. Psychopharmacologia 1970; 16: 305–312
   PubMedGoogle Scholar
• Puri S. K., Reddy C., Lal H. Blockade of central dopaminergic receptors by morphine – Effect of haloperidol, apomorphine, or benztropine. Research Communications in Chemical Pathology and Pharmacology 1977; 5: 389–401
   Google Scholar
• McKenzie G. M., Sadoff M. Effect of morphine and chlorpromazine on apomorphine induced stereotyped behavior. Journal of Pharmacy and Pharmacology 1974; 26: 280–282
   PubMed Web of Science ®Google Scholar
• Brase D. A. Pre‐ and postsynaptic striatal dopamine receptors: Differential sensitivity to apomorphine inhibition of ‘3H’ dopamine and ‘14C’ CABA release In Vitro, Communications. Journal of Pharmacy and Pharmacology 1980; 32: 432–433
   PubMed Web of Science ®Google Scholar
• Aghajanian G., Bunney B. S. S. H. Snyder, E. Urdin. Pergamon, Oxford 1973; 443–648
   Google Scholar
• Groves P. M., Wilson C. J., Young S. J., Rebec G. V. Self‐inhibition by dopaminergic neurons. Science 1975; 190: 522–529
   PubMed Web of Science ®Google Scholar
• Extein I., Lo C., Goodwin F. K., Schoenfeld R. I. Dopamine‐mediated behavior produced by the enkephalin analogue FK 33–824. Psychiatry Research 1979; 1: 333–339
   PubMed Web of Science ®Google Scholar
• Biggio G., Casu M., Corda M. G., DiBello C., Gessa G. L. Stimulation of dopamine synthesis in caudate nucleus by intrastriatal enkephalins and antagonism by naloxone. Science 1978; 200: 552–554
   PubMed Web of Science ®Google Scholar
• Costa E., Cheney D. L., Mao C. C., Moroni F. Action of antischizophrenic drugs on the metabolism of g‐aminobutyric acid and acetylcholine in globus pallidus, striatum and n. accumbens. Federation Proceedings 1978; 37(10)2408–2414
   PubMedGoogle Scholar
• Volavka J., Davis L. G., Ehrlich Y. H. Endorphins, dopamine, and schizophrenia. Schizophrenia Bulletin 1979; 5(2)227–239
   PubMed Web of Science ®Google Scholar
• Jacquet Y. F. Excitatory and inhibitory effects of opiates in the rat Vas Deferens: A dual mechanism of opiate action. Science 1980; 210: 95–97
   PubMed Web of Science ®Google Scholar
• VanderWende C., Spoerlein M. T. Antagonism by dopa of morphine analgesia ‐ A hypothesis for morphine tolerance. Research Communications in Chemical Pathology and Pharmacology 1972; 3: 37, AND Role of dopaminergic receptors in morphine analgesia and tolerance, Research Communications in Chemical Pathology and Pharmacology 5, 35, 1973
   PubMedGoogle Scholar
• Pleuvry B. J., Tobias M. A. Comparison of the antinociceptive activities of physostigmine, oxotremorine and morphine in the mouse. British Journal of Pharmacology 1971; 43: 706
   PubMed Web of Science ®Google Scholar
• Major C. T., Pleuvry B. J. Effects of a‐methyl‐p‐tyrosine, p‐chlorophenylalanine, L‐b‐(3,4‐dihydroxyphenyl)‐alanine. 5‐hydroxytryptophan and diethyldithiocarbamate on the analgesic activity of morphine and methylamphetamine in the mouse. British Journal of Pharmacology 1971; 42: 512
   PubMed Web of Science ®Google Scholar
• Tulunay F. C., Sparber S. B., Takemori A. E. The effect of dopaminergic stimulation and blockade on the nociceptive and antinociceptive responses of mice. European Journal of Pharmacology 1975; 33: 65–70
   PubMed Web of Science ®Google Scholar
• D'Amour F. E., Smith D. L. A method for determining loss of pain sensation. Journal of Pharmacology and Experimental Therapeutics 1941; 72: 74–79
   Google Scholar
• Wesler L. S., Frey A. H. Microwave energy interaction with the dopamine and opiate systems of the brain. Bioelectromagnetics Society 3rd Annual Conference Abstracts. Washington, DC 1981
   Google Scholar
• Frey A. H. Biological mediators and mechanisms for low intensity electromagnetic effects. Bioelectromagnetics Society 3rd Annual Conference Program. Washington, DC 1981
   Google Scholar