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Evidence for Effects on Neurology and Behavior - BioInitiative Report

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In more recent studies, Blackman explored the effects of different exposure c<strong>on</strong>diti<strong>on</strong>s<br />

[Blackman et al., 1988, 1989, 1991]. Multiple power windows of calcium efflux from chick<br />

brains were reported. Within the power densities studied in this experiment (0.75-14.7 mW/cm 2 ,<br />

SAR 0.36 mW/kg per mW/cm 2 ) narrow ranges of power density with positive effect were<br />

separated by gaps of no significant effect. The temperature in which the experiment was run was<br />

also reported to be an important factor of the efflux effect. A hypothetical model involving the<br />

dynamic properties of cell membrane has been proposed to account <str<strong>on</strong>g>for</str<strong>on</strong>g> these effects [Blackman<br />

et al., 1989].<br />

In additi<strong>on</strong> to calcium i<strong>on</strong>, changes in other trace metal i<strong>on</strong>s in the central nervous system<br />

have also been reported after RFR exposure. Stavinoha et al. [1976] reported an increase in zinc<br />

c<strong>on</strong>centrati<strong>on</strong> in the cerebral cortex of rats exposed to 19-MHz RFR. Increases in the<br />

c<strong>on</strong>centrati<strong>on</strong> of ir<strong>on</strong> in the cerebral cortex, hippocampus, striatum, hypothalamus, midbrain,<br />

medulla, <strong>and</strong> cerebellum; manganese in the cerebral cortex <strong>and</strong> medulla; <strong>and</strong> copper in the<br />

cerebral cortex were reported in the rat after 10 min of exposure to 1600-MHz RFR at 80<br />

mW/cm 2 (SAR 48 W/kg) [Chamness et al., 1976]. The significance of these changes is not<br />

known. The effects could be as a result of hyperthermia, because the col<strong>on</strong>ic temperature of the<br />

animals increased by as much as 4.5 o C after exposure.<br />

RADIOFREQUENCY RADIATION AND THE ACTIONS OF<br />

PSYCHOACTIVE DRUGS<br />

The acti<strong>on</strong>s of psychoactive drugs depend <strong>on</strong> the functi<strong>on</strong>s of the neurotransmitter systems<br />

in the brain. Changes in neurotransmitter functi<strong>on</strong>s after RFR exposure will inevitably lead to<br />

changes in the acti<strong>on</strong>s of psychoactive drugs administered to the animal. On the other h<strong>and</strong>, if<br />

there is no change in the pharmacokinetics of drugs after RFR exposure, observed changes in<br />

psychoactive drug acti<strong>on</strong>s would imply RFR-induced changes in neurotransmitter functi<strong>on</strong>s in<br />

the animal. Pharmacological studies of RFR effects provide an important insight into the neural<br />

mechanisms affected by exposure to RFR.<br />

Psychoactive drugs of various types have been tested in animals after exposure to RFR.<br />

Since an effect of RFR is to increase the body temperature of an animal, special attenti<strong>on</strong> has<br />

been given to study the effects of psychoactive drugs <strong>on</strong> the thermal effect of RFR. Jauchem<br />

[1985] has reviewed the effects of drugs <strong>on</strong> thermal resp<strong>on</strong>ses to RFR. Radiofrequency radiati<strong>on</strong><br />

of high power densities was used in these studies.<br />

Some psychoactive drugs have a profound effect <strong>on</strong> thermoregulati<strong>on</strong> <strong>and</strong>, thus, alter the<br />

body temperature of an animal up<strong>on</strong> administrati<strong>on</strong>. The effect could be due to direct drug<br />

acti<strong>on</strong> <strong>on</strong> the thermoregulatory mechanism within the central nervous system or effects <strong>on</strong><br />

aut<strong>on</strong>omic functi<strong>on</strong>s such as respirati<strong>on</strong>, cardiovascular <strong>and</strong> muscular systems, which lead to<br />

changes in body temperature. Several studies have investigated the neuroleptic (anti-psychotic)<br />

drug, chlorpromazine. Michaels<strong>on</strong> et al. [1961] reported that chlorpromazine enhanced the<br />

thermal effect of RFR in dogs (2800 MHz, pulsed, 165 mW/cm 2 ). Drug-treated animals had a<br />

faster rate of body temperature increase <strong>and</strong> a higher peak temperature when irradiated with<br />

RFR. Similar effects were seen with pentobarbital <strong>and</strong> morphine sulfate. On the other h<strong>and</strong>,<br />

Jauchem et al. [1983, 1985] reported that chlorpromazine attenuated the thermal effect of RFR in<br />

ketamine anesthetized rats. The drug slowed the rate of rise in col<strong>on</strong>ic temperature (from 38.5-<br />

39.5 o C) <strong>and</strong> facilitated the return to base line temperature after exposure to RFR (2800-MHz, 14<br />

44

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