117 BioelectroBioenerg1996
117 BioelectroBioenerg1996
117 BioelectroBioenerg1996
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Abstract
Melatonin secretion by the pineal gland has been reported to be affected by exposure to electromagnetic fields (EMFs). In an initial investigation to
determine if calcifications commonly found in the pineal gland could respond to EMFs by a transducer mechanism, studies were conducted to ascertain if
pineal tissues were piezoelectric. Second harmonic generation (SHG) measurements showed that pineal tissues contained noncentrosymmetric crystals, thus
proving the presence of piezoelectricity. Both mulberry-like and faceted crystalline calcifications were observed by scanning electron microscopy (SEM).
Some of the calcifications had compositions similar to that of hydroxyapatite; others contained a high concentration of aluminum.
Keywords: Aluminum; Calcification; Crystals; Electromagnetic fields; Scanning electron microscopy (SEM); Second harmonic generation (SHG)
A positive SHG response is proof of the presence of tional cadavers were fixed in buffered formalin and then
piezoelectric crystals. ashed at 2000C for 2 h. The resulting material (about 50
mg) was analyzed by SHG, X-ray diffraction, and SEM.
Because the samples were opaque or only slightly
2. Experimental methods translucent, SHG measurements were made in a reflection
mode (at approximately 45° incidence). No detectable SHG
In the technique of SHG, a sufficiently intense light was observed from the glass cover slides, as evidenced by
wave of frequency ω is focused on a crystal. If the crystal is blank measurements without a sample. In an experiment,
noncentrosymmetric, the electric field of the light wave the laser was focused at an arbitrary point on the surface of
induces a polarization at twice the incident frequency a sample with the monochromator window at one of the
causing the crystal to emit light at double the frequency or settings, 532 nm, above 532 nm (540—550) or below 532
half the wavelength. Kurtz and Dougherty [11] have pre- nm (510—520). Sets of 200 laser pulses were produced
sented a statistical analysis for the sensitivity of SHG in several times for each window setting. Then the laser beam
determination of noncentrosymmetry in powders. impingement point was moved to another arbitrary
The SHG detection technique used in our studies was as location.
follows. The beam from a pulsed neodymium YAG laser After the SHG measurements, a conductive gold coating
emitting 15 ns pulses of approximately 4 mJ energy at a was evaporated on some of the samples and they were
wavelength of 1064 nm was focused to a diameter of about examined by a scanning electron microscope (SEM) using
500 µm on the sample. An absorption filter was used to a 25 kV beam voltage. Crystals and crystal-like regions
remove the 1064 nm component from the radiation re- were studied. Energy dispersive X-ray spectroscopy (EDS)
flected from the sample. The remaining radiation passed was used for a quantitative analysis of chemical elements
through a monochromator and then was analyzed by a high with an atomic number of 11 or greater.
gain photomultiplier with photon counting sensitivity. Inci- X-ray diffraction and atomic absorption studies were
dent photons were counted for 200 pulses of the laser. carried out using conventional techniques.
When the monochromator was set with a 532-nm window,
both SHG and any spurious background signal (which may
originate from instrument noise, luminescence, or ther- 3. Results
mally excited processes) would be measured. The back-
ground contribution was determined by measurement with The results of the SHG measurements on the tissues
the monochromator set at a wavelength either 15—20 nm from Subject 1 are illustrated in Fig. 1, and the results on
above or below the SHG wavelength. Thus the ratio of the tissues from all of the subjects are shown in Fig. 2. The
photon counts at 532 nm to that at nearby wavelengths following criteria were used to determine if SHG was
formed a signal-to-noise ratio. In addition, signals propor- observed at a specific location in a sample: (1) the number
tional to the intensity of both the incident 1064-nm radia- of photon counts for 200 laser pulses was greater than 10
tion and the detected radiation were displayed on a dual- and, (2) the number of photon counts with the monochro-
beam oscilloscope. If the detected radiation was not coinci- mator set at 532 nm was statistically significant compared
dent in time with the incident radiation (with resolution of
approximately 10 ns), it was assumed that thermal pro-
cesses, which were significantly slower than those due to
SHG, were being observed. The functioning of the SHG
system was checked prior to each set of experiments using
a sample of powdered urea which gives a very large SHG
signal (measured at about 3 x l05 photon counts per 200
laser pulses).
All SHG measurements were made on pineal glands
from six human cadavers of both sexes, 45—78 years of
age. In most instances, regions of the pituitary gland, the
cortex and the cerebellum were also measured as controls.
The tissues were fixed in absolute alcohol (except in
buffered formalin, in one case), sliced using a scalpel,
placed on glass slides with a cover slip, and air-dried under
slight pressure. The resulting preparations were 100—300
µm thick. For atomic absorption determinations of alu-
minum, the tissues from four cadavers were frozen at Fig. 1. SHG measurements on tissues from Subject I. Different measure-
ment locations are designated by letters in the abscissa. The ordinates give
—700C until analyzed. To determine the thermal stability
the number of photon counts detected by the photomultiplier during the
of pineal crystals, the entire pineal glands from five addi operating period of the laser.
SB. Lang et al./Bioelectrochemistry and Bioenergetics 41(1996)191—195 193
during the operating period of the laser. The bars show the Fig. 4. SEM photograph of the faceted crystalline structures in pineal
mean + standard deviation (SD) of the photon counts on glands.
194 SB. Lang et al./Bioelectrochemistry and Bioenergetics 41(1996)191—195
4. Discussion