Beason & Sem: Responses of neurons to amplitude modulated microwave RF (11/5/02)
Authors: Robert C.
Beason1 and Peter Semm2
Authors' affiliations: Dept. of Biology, State Univ. of New York, Geneseo, NY 15454 USA
Present address: 1Dept. of Biology, Univ. of Louisiana at Monroe, 700 University Ave., Monroe, LA 71209 USA, 2Fachbereich Biologie, der J. W. Goethe-Universität Frnakfurt a. M., Seismayerstr. 70, 60054 Frankfurt a.M., Germany
Corresponding author: Robert C. Beason, Present address: Dept. of Biology, Univ. of Louisiana at Monroe, 700 University Ave., Monroe, LA 71209; Telephone: 318-342-1790; Fax: 318-342-3312; E-mail: firstname.lastname@example.org
Running head: Neuronal responses to digital signals
Running head: Neuronal responses to digital signals
In this study we investigated the effects of a pulsed RF signal similar to the signal produced by GSM (global system for mobile communication) telephones (900 MHz carrier, modulated at 217 Hz) on neurons of the avian brain. We found that such stimulation resulted in changes in the amount of neural activity by more than half of the brain cells. Most (76%) of the responding cells increased in their rates of firing by an average 3.5-fold. Other cells responded to the stimulus with a decrease in spontaneous activity Such responses indicate a potential health risk for humans using hand-held cellular phones.
words: cellular telephone, magnetic field, health risk, avian, Central
Key words: cellular telephone, magnetic field, health risk, avian, Central Nervous System
The postulated biological effects of electromagnetic fields are highly diverse, ranging from use of natural fields by animals for navigation to thermal cooking that occurs with strong fields such as produced by microwave ovens . Athermal effects have been the most difficult to explain because the mechanism by which they affect biological tissue is usually unknown. It has been shown that fluctuations of Earth-strength magnetic fields influence the electrical activity of neurons and pineal cells and the synthesis of melatonin in birds and mammals [1, 8, 9], including humans . The question arises as to whether there is a particular sensitivity of the neural tissues of the brain to high frequency electromagnetic fields such as is produced by broadcast transmitters.
We tested the effects of electromagnetic radio frequency (RF) signals having a carrier frequency of 900 MHz, unmodulated and pulse modulated at 217 Hz with a duty cycle of 12.5% and a power density of 0.1 mW/cm2 because this signal is similar to that used by the GSM (global system for mobile communication) telephone system. The test subjects were 34 adult zebra finches (Taenopygia guttata), anesthetized with a mixture of ketamine (0.05 mg/g) and xylazine (0.01 mg/g) injected i.m. into the pectoralis major. The anesthetized bird was mounted in a nonconducting plastic holder. The bird and the holder were placed inside a tuned RF cavity (23.5 cm diameter, 100.5 cm long) made of perforated metal. The cavity was fitted with two tuned RF stubs (each 23.5 cm from opposite ends): one for emitting the signal and one for monitoring the frequency and power of the signal within the cavity. To record from neurons in the brain of the bird, a small hole (4 mm diameter) was made through the skull. A glass microelectrode (tip diameter 1–2 µm) filled with a conducting solution physiological saline was slowly advanced into the brain through this hole until a spontaneously active nerve cell was detected. A silver reference electrode was inserted beneath the skin along the back of the head directly behind the glass microelectrode to complete the circuit. Arranging the electrodes along the long axis of the cavity prevented them from acting as an antenna and electrically stimulating the cells. Once a spontaneously active cell was located, it was tested with the stimulus. The protocol for all the testing procedures was a 10 min prestimulus period, a 10 min stimulus period, and a 10 min poststimulus period. The rates of the cell's activity during these three time intervals were compared to detect any effect of the stimulation.
We recorded 133 spontaneously active units from 34 anesthetized adult zebra finches; 91 units (69%) showed some response to the stimulation: 69 (52%) responded with excitation (Fig. 1A) and 22 (17%) responded with inhibition (Fig. 1B). The remaining 42 (31%) cells showed no discernible response. The cells showing excitation responded with increases in their rate of firing to the stimulation (mean rate during stimulation = 3.5 ± 0.30 [SE] times prestimulus rate). Most of the inhibitory responses were small (mean rate during stimulation = 0.4 ± 0.07 times prestimulus rate), in part because the cells were firing slowly before the stimulation. Two of the cells showing inhibition exhibited marked depression in their rates of spontaneous activity (Fig. 1B). All responses we recorded were to power densities of 0.1 mW/cm2 and stronger (up to 0.5 mW/cm2). The mean latency from the initiation of the stimulus to the start of the response was 104 (± 197) sec, with the response lasting beyond the end of the stimulus period in half of the responding cells. The mean persistence beyond the end of stimulation was 308 (± 68) sec, but there was no correlation (r = 0.489, P > 0.05) between the latency of the response and how long the cell continued responding beyond the end of the stimulus.
Three cells that responded to the modulated carrier were also tested with an unmodulated signal of the same carrier frequency. The power of the unmodulated signal was tested at two densities that equaled the peak power and the average power of the modulated stimulus. None of these cells exhibited a response to the unmodulated carrier. In addition to responses to the nominal stimulus, we also tested four cells that did not respond to the 0.1 mW/cm2 pulsed signal with higher power densities (up to 0.5 mW/cm2). Three cells did not respond to the stronger intensities, but one cell that did not respond to the 0.1 mW/cm2 stimulus responded to an intensity of 0.3 mW/cm2 with depression of its rate of activity.
One concern is that the electrodes themselves were acting as an antenna and stimulating the cells electrically. The arrangement of the active and reference electrode along the long axis of the waveguide chamber prevented them from serving as a loop antenna. In preliminary experiments we varied the positions of the electrodes to determine whether they could, in fact, act as an antenna. When the electrodes were not aligned, the stimulus artifact was detected directly and observed on the oscilloscope display. Whether such a stimulus was strong enough to stimulate the cells is unknown. A second factor that supports the idea that the cells were not stimulated electrically is that not all cells responded to the stimulus, even those in the close neighbourhood of a responding cell. This speaks clearly against an artifact..
These high frequency RF fields produced a response in many types of neurons in the avian Central Nervous System (in both cerebellum and cerebrum) and did not appear to be limited to any specialized receptor. Similar responses (long latency and ongoing higher activity after cessation of the fields) also were reported to a 52 GHz carriar, 16Hz modulated signal (Semm er al., unpubl. data). Thus, the effect does not appear to be limited to magnetic sensory cells , but may occur in any part of the brain. The stimulus might mimic a natural mechanism involved in cell communication, producing responses from many different types of neurons. It is unlikely that the effects we observed are the result of thermal excitation caused by the RF radiation because the power densities we applied were 2 to 3 orders of magnitude below what is required (10 mW/cm2) to produce heating of even 0.5° C (Bernhardt 1992). Consequently, we conclude that the effects we observed are not the result of thermal agitation but at this point we cannot offer an athermal mechanism to account for the observations.
Although individual neurons in the zebra finch brain responded to the pulsed RF stimulus, we do not know whether these responses by the nervous system are manifested in the bird's behavior or its health. Bruderer and coworkers [4, 5] reported no behavioral responses of birds to pulsed or continuous RF microwave signals, but their studies involved different frequencies and lower power densities of the stimulus. Whether similar neuronal responses occur in mammals, including humans, requires further investigation. Borbély and coworkers  reported that exposure to a RF signal similar to the one we used influenced sleep and sleep electroencephalogram in humans. Their results and the responses we recorded clearly indicate the potential for effects on the human nervous system.
We gratefully acknowledge financial support of the Deutsche Telekom and the Geneseo Foundation. Technical assistance and the loan of equipment were provided by the Deutche Telekom.
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Fig. 1. Examples of neuronal responses in the zebra finch brain to stimulation of a 217 Hz, 12.5% duty cycle square wave modulated 900 MHz carrier signal: A. simulation and B. inhibition. The solid bar above each graph indicates the presence of the stimulating RF signal.