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Richard D.
Sauerheber, Ph.D.
(Chemistry, University of California, San Diego, 1976)
Palomar Community College
1140 W. Mission Rd.
San Marcos, CA 92069
Summary
The mechanism by which fluoride's lethal poisoning of man and animals occurs
is presented. "Low" level fluoridation of municipal water exhibits
well known alterations in teeth and bone structure and calcification of
tendons and ligaments. 'Moderate' doses cause spinal deformities and
increased hip fracture tendency and kidney and gall stones. Higher levels
cause death and are responsible for its major industrial use as a
rodenticide. Solubility calculations indicate that fluoride doses required to
decrease calcium below physiological blood levels are comparable to those
present in poisoned victims' tissues and to those causing decreased beat
rates in isolated heart cells in culture. Acute lethal poisoning and many of
the chronic 'low' level effects of fluoride are mediated by calcium binding
by the fluoride ion.
Introduction
An array of scientific findings indicate that the decision made by many
cities as early as 1956 to add fluoride (a rodenticide) to municipal drinking
water, as long as the dose is below a certain level (usually 1 part per
million, 1 milligram fluoride per liter or 0.05 mM) to decrease the incidence
of something as minor as tooth decay, was irrational. We now know that
precipitates of calcium fluoride occur in fluoridated water cities when the
acidity is low (a pH above 7) depending on the fluoride level used. This
causes scaling of water pipes (1) and numerous biological effects in
consumers, the extent determined by the acidity and the amount of calcium in
the water.
Fluoridated
municipal water supplies in the United States have been found to contain
fluoride levels ranging anywhere from 0.012 mM to a record lethal accidental
7.5 mM (8). The biologic effects have been diverse, covering the entire above
range. In spite of lethal poisonings from municipal water fluoridation
programs, the Public Health Service retains its mandate to fluoridate all
U.S. cities as soon as possible and to reach out to other cities throughout
the world in an effort to minimize tooth decay while fluoridating the blood
of the water consumer as though this were an acceptable alternative to
topical fluoride or to addition of fluoride to one's own consumed water.
Unfortunately,
in 1992 at the mouth of the Yukon River in Hooper Bay, Alaska the unthinkable
occurred. In what is considered an accident, an entire village was poisoned
by its own fluoridated water supply when the system malfunctioned. This
represents the first 'experiment' in which human beings were exposed to
lethal doses of fluoride. Blood samples were measured for incorporated
fluoride and calcium ion and provided much pathologic information on the
effects of high doses of fluoride assimilated from municipal drinking water
supplies (8). 296 residents were severely poisoned with one fatality. Most
had heart malfunction-associated symptoms and severe gastrointestinal pain.
It is
now understood that the conversion of fluoride ion into HF, hydrofluoric
acid, occurred in the stomach due to the stomach acid HCl at pH 3 and the HF
caused the intense pain. HF cannot be stored in glass since it dissolves the
container; it also dissolves leather and skin. Also blood calcium levels
dropped to 1/3 of normal in one victim, causing a heart attack and the loss
of his life. Although the authors of the study were uncertain whether the
fluoride itself caused the effect directly or rather was due to its known
ability to precipitate magnesium or calcium ion, our recent computations
indicate that low blood calcium is responsible for the lethal effect of acute
fluoride poisoning, as indicated below.
Precipitation
of calcium fluoride into peoples' bones, tendons and ligaments (9) occurs
depending at typical doses added to municipal water. The condition known
medically as fluorosis is associated as expected with spinal rigidity and bone
fragility (2), the severity depending on the fluoride level present in the
blood and for how long.
If
fluoride exposure is sufficiently high or prolonged, formation of kidney and
gall stones is known to occur, due to the low solubility of calcium fluoride
(0.04 mM at pH 7 at room temperature) (4,6). People with hyperparathyroidism
or osteosclerosis are more susceptible in this regard to chronic consumption
than others since the calcium fluoride deposits in the soft tissues more
efficiently because of lack of sufficient binding sites in bones for it (1).
Interestingly,
in children raised on fluoridated water, teeth themselves are more rigid
while at the same time may be somewhat more resistant to cavities, but no
such effect on adult teeth occurs according to many sources (1, chap. 39, p.
896). Thus fluoridation of adult blood is unnecessary and indeed useless for
this purpose.
The
dean of Tulane University in New Orleans indicated that fluoridated water
consumption at certain doses eventually causes gum disease and for this
reason New Orleans water was not fluoridated at the time Chicago and New York
and other cities approved it (1). Also, in 1960 under oath in Chicago, the
researcher for the Public Health Service who started the fluoridation idea
admitted that his data constituting the scientific basis for fluoridation
were invalid, shattering its foundation (1). The original observation that
people consuming water in Texas that happened to have fluoride into it also
had whiter teeth than usual was insufficient to justify mass fluoride
addition to other public water supplies, since no one was cognizant of the
coexistence of other unhealthful effects that also occurred.
The
effects of fluoride are subtle enough to go unnoticed for most people at the
levels of fluoridation used currently in Southern California (0.012
mM)(Vallecitos Municipal Water district handouts) and at the increased levels
proposed to be used. But since fluoride is converted completely in the
stomach to hydrofluoric acid (5), the most corrosive substance known to man,
it is likely that consumption of fluoride at levels used in some cities is
associated with ulceration of gastric and duodenal tissue (where the pH has
yet to return to basic values that occur in the middle intestine). And many report
evidence in rats that it eventually causes cancer (1),.
Some
argue these effects are unimportant if the municipal water supply maintains
very low levels of fluoridation; but the longer the consumption occurs for an
individual and the more elderly the person with less cell division occurring
in the gastric mucosa, the more overt symptoms become. Individuals with
ulcers or heartburn are not good candidates for the long term consumption of
water containing fluoride, particularly at doses allowed by the Public Health
Service (2-4 mg/L, 0.1-0.2 mM)(VWD handouts). These high doses can be
dangerous depending on the amount of water consumed, the individual's own
body chemistry, and the ionic composition and pH of the particular cities'
water that would be fluoridated to this level.
We
here determine whether and to what extent blood levels of calcium may be
affected by various fluoride doses that are known to occur in the blood of
fluoridated water consumers to attempt to determine its modes of action. Our
calculations are consistent with the notion that fluoride's lethal effects on
the heart are due to low blood calcium subsequent to saturation of body
fluids with fluoride at its known low solubility in the presence of
physiologic levels of calcium.
Analytical Results and Discussion
Sublethal poisoning occurs at 0.1-0.2 mM fluoride in blood (3,7) and lethal
poisoning occurs in the 0.2 to 0.6 mM range due to heart failure (3). We
investigate the possibility that the margin of safety is so slight between
unnoticed effects (0.02-0.05 mM) to sublethal (0.1-0.2 mM) and lethal
poisoning (0.2-0.6 mM) is because below the critical concentration of
fluoride in the blood that causes precipitation of calcium fluoride only
chronic, often unnoticed effects would occur. Much like being near a hot
electrical wire, one can coexist next to it for lifetimes without any
difficulties. But one false movement too close to the wire would be a
disaster.
With
this in mind, we calculated the concentration of fluoride that would cause
calcium fluoride precipitates to first form from the known solubility product
constant (Ksp) for calcium fluoride (Ksp = 3.4 x 10-11 (6)) and the known
concentration of calcium ion in normal human blood (3 mM) (5). The computed
dose is 0.1 mM. Here the concentration of fluoride is: [F-] = (Ksp/[Ca2+])1/2
from the definition of the solubility product constant for insoluble salts
where CaF2 Ca2+ + 2 F- and Ksp = [Ca2+][F-]2 (see Table I). The concentration
of fluoride where the blood calcium level would be lowered to the lethal low
level of about 1 mM is 0.2 mM fluoride.
In
Table I the calculated calcium levels that would coexist in fluid with a
given fluoride level from solubility considerations are compared with actual
measurements of blood levels of calcium and fluoride ion in the lethal
poisoned human victim from Hooper Bay, Alaska. Note the good agreement
between theoretically calculated fluoride levels, that should lower blood
calcium ion to levels below normal, with the actual calcium and fluoride ion
levels measured in the blood of this human victim poisoned with fluoridated
municipal water in Hooper Bay.
Also
note the below-normal calculated calcium ion level that would coexist with
fluoride doses found to slow heart cell beat rates in detailed in vitro experiments
(10). Isolated beating heart cell preparations from mammals exhibit beat
rates that are proportional to the calcium ion level in the incubation medium
from .3 - 3 mM. Calcium chelating agents EGTA and EDTA and the calcium
binding site competitor La3+ ion completely block excitation-contraction
coupling in intact beating hearts and in isolated cell preparations (11).
Further, addition of fluoride to beating heart cell preparations slows beat
rates in a dose-dependent manner that Ksp calculations indicate would lower
calcium ion levels in the incubation medium (see Table I).
These
calculated doses are fully consistent with other published data indicating
that tissue levels of fluoride in poisoned people are in the 0.2 - 0.4 mM
range (5). Also the known human lethal dose is 1-5 grams per adult taken at
one time acutely (3,5). Since the average adult contains about 43 liters of
body fluid this corresponds to a concentration of fluoride of 0.5 mM in such
a case of instant acute poisoning.
Wang,
Zhang and Wang also found the heart cell beat rate in cultured cells in
well-controlled experiments progressively slows with increasing fluoride
levels in a regular, concentration-dependent manner (10). Unlike skeletal
muscle, cardiac muscle requires extracellular calcium ion from the
bloodstream to couple electrical excitation of the cell membrane with
contraction of cardiac muscle fibers (11). Each time the heart contracts,
calcium fluxes into the heart cells from the extracellular fluid (at 3 mM
calcium ion normally). When the heart relaxes, the calcium is pumped back out
of the cell, allowing the fibrils to relax. Lowered extracellular calcium ion
levels block contraction of the heart.
These
data together suggest that the mechanism by which fluoride ingestion is lethal
is by causing hypocalcemia and blockage of heart contractions. Fluoride
levels in blood below 0.1 mM do not lower calcium ion below normal as no
precipitate yet forms in the blood at this or lower doses. But the instant
fluoride exceeds this amount to any degree, calcium ion precipitates and the
blood level is lowered, unable to support normal heart function.
Fluoride
acts as an enzyme inhibitor for all enzymes requiring calcium for function by
binding the ion and is used routinely to block sugar metabolism in red blood
cells for clinical laboratory analyses of blood specimens. Fluoride also
attaches to calcium anywhere this ion is concentrated throughout the body,
including teeth, bones, ligaments, skeletal muscle and brain. But the most
crucial function requiring calcium that is fluoride-sensitive is the
mechanism of contraction in normal beating hearts.
That
extracellular calcium is an obligatory requirement for heart cells to undergo
contraction after electrical excitation is well known. Heart cells do not
have well-developed sarcoplasmic reticulum to store calcium for this purpose
as does all skeletal muscle, which does not exhibit this extreme sensitivity
to changes in blood calcium level. The cellular uptake of calcium occurs
during the plateau phase of the cardiac action potential and extracellular
calcium is necessary for the development of contractile force (11). The
strength of contraction (inotropic state) of the heart depends on calcium,
where half maximal contractility occurs at 0.5 mM calcium outside cells (12).
It is
also possible that chronic 'low' level biologic effects of fluoride are also
mediated exclusively by binding and sequestration of calcium. Prior to levels
of calcium in the blood being lowered (below 0.1 mm fluoride), regions in the
body enriched in calcium would still precipitate calcium fluoride, as in
bone, teeth, ligaments and brain. The usual physiologic response to such an
insult is to increase levels of hormones such as calcitonin to mobilize
calcium from bone to fight the sequestration. At higher fluoride doses,
precipitates may be directly responsible for the known formation of gall and
kidney stones in fluoridated consumers.
The
current level of fluoride in Southern California drinking water is 0.25 mg
per liter or 0.012 mM. The blood level is typically in consumers about 1/5 to
1/8 the water level. This is below the solubility for calcium fluoride at
normal body pH, temperature and prevailing body fluid calcium levels, and it
is easy for many to assume the information in this manuscript is irrelevant.
But some cities use up to 1 or 1/5 mg/L (0.05-0.075 mM) or the Federal
allowed ceiling of 2-4 mg/L (0.1-0.2 mM) and are near or at the maximum level
that would just begin precipitation of calcium, with hypocalcemia, unless the
city water happened to have so much calcium in it that it precipitated as the
fluoride preventing the fluoride added from entering one's blood at that
level. The finding that fluoridated cities generally have increased per
capita heart attack rates is consistent with this discussion.
The
fluoride level that would precipitate calcium from Southern California water
(where calcium ion is about 2 mM) would be 0.14 mM fluoride. So before we
could reach fluoride levels approaching the Federal ceiling in water it would
precipitate calcium from our drinking water first. To maintain a higher level
of fluoride than 0.14 mM would be expensive, requiring addition of enough to
precipitate the calcium in the water first. More would be required on top of
that amount to increase fluoride to a higher desired level. Fortunately this
would be very difficult.
Adding
sodium fluoride to public water is paid for by taxpayer adults who will not
reap any measurable benefits from it. It takes resources, time, chemicals and
machinery to continue to add it to drinking water. It is putting the water
district in charge of drugging the public and for something as innocuous as a
cavity rather than for serious effects such as infectious illness for which
we have properly chosen chlorination, with the much less electronegative
halogen.
It is
not in keeping with a free society or with proper health care practice to
impose these risks associated with fluoridating the blood of people,
livestock, and pets, and also all agricultural products, not to mention our
lawns and gardens, compared to the less significant problem of perhaps having
tooth decay. Tooth decay should be minimized more efficiently and safely if
desired with addition of fluoride products to children's teeth carefully
without swallowing or better yet by simply brushing more vigorously and
regularly. After the death of the Brooklyn, New York boy in the dentist chair
when fluoride gel was swallowed, and after the Hooper Bay, Alaska incident,
it is clear that our blood is more important than concern for cavities. Teeth
are replaceable but lives are not. In keeping with the Hippocratic oath, no
physician reserves the right to medicate anyone without their permission, and
all patients must remain free to withdraw from drug or other treatment
programs at any time. Forced fluoridation in public water supplies ironically
constitutes a reversal of these Public Health Service policies. The easy way
- fluoridate through the bloodstream by drinking - is unnecessary (since
topical application is possible) and criminal (in light of the above
findings). Proper dental hygiene is much safer and achieves the desired
result anyway. The notion recently publicized that 'antifluoridationists' are
similar to earlier critics of smallpox vaccination is inconsistent with the
facts that 1) smallpox is lethal and could not be prevented without blood
vaccination, but 2) cavities are not lethal and can be prevented with proper
hygiene and if necessary the bacteria that cause caries in the first place
can be quickly destroyed with simple methods such as hydrogen peroxide
washings, etc. without loss of life.
References
1. The Grim Truth about Fluoridation, Robert M. Buck, G.P. Putnam & Son,
New York, 1964.
2. Blakiston's Medical Dictionary, 1960, 3rd edition.
3. The Merck Index, 9th edition, Merck and Co., Inc., Rahway, New Jersey,
1976.
4. The Handbook of Chemistry and Physics, 50th edition, Chemical Rubber Co.,
Cleveland, Ohio, 1976.
5. Teitz, N., Clinical Chemistry, W.B. Saunders, Philadelphia, 1976.
6. Ebbing, D. , General Chemistry, Houghton Mifflin Co, Inc., Boston, 1990
7. Clinical Toxicology of Commercial Products, Gleason, M., ed. Williams and
Wilkins, Baltimore, 3rd edition, 1969.
8. Gessner, B., New England Journal of Medicine 330 p. 95, 1994
9. Goodman, L.S. and Gilman, A. The Pharmacological Basis of Therapeutics,
5th edition, MacMillan Publishing Co., New York
10. Wang F., Zhang, D., and Wang, R. "Toxic effects of fluoride on
beating myocardial cells cultured in vitro", Fluoride 31(1) pp. 26-32,
1998.
11. Langer, G. A., Federation Proceedings, 35, p.1274, 1976.
12. Williamson, J. R., Woodrow, M. L., Scarpa, A. in: Fleckenstein, A.,
Dhalla, N.S., eds., "Recent Advances in Cardiac Structure and
Metabolism", vol. 5, Baltimore, University Park Press, p. 61, 1975.
Table
I
Effects
of F- on Blood Ca2+ Concentrations*
Blood
[Ca2+] Blood [F-] (mM)
3.0
0.10 (F- , calculated from Ksp, for 1st precipitation of normal blood Ca2+)
1.3
0.48 (human blood measurements, Hooper Bay, Alaska from lethal dose victim)
1.1
0.15 (Ca2+ calculated from Ksp for F- dose lowering heart cell beat rate 17%)
1.0 0.20 (F- calculated from Ksp to lower blood Ca2+ to 1 mM)
0.4
0.30 (Ca2+ calculated from Ksp for F- dose lowering heart cell beat rate 27%)
*Some
cities recommend 01. - 0.2 mM fluoride be added to drinking water. Typically
1/5 or so of the water fluoride level is the consumers' blood fluoride level
(as long as there are no accidents, equipment malfunction as in Hooper Bay
disaster, or miscalculated doses added).
As for
any insoluble precipitate, the Ksp solubility product constant determines the
concentration in solution of the ions that dissolve from the salt. For
calcium fluoride where CaF2 Ca2+ + 2F-, Ksp = [Ca2+][F-]2 = 3.4 x 10-11. This
relation was used to calculate F- levels for a given Ca2+ level or Ca2+
levels for a known F- level. Other measurements in the table were from actual
blood samples drawn from Hooper Bay, Alaska victims where fluoridated
municipal water for which machinery malfunctioned poisoned 296 residents. Not
mentioned is the increased thirst associated with heavily fluoridated water,
a biologic response to this insult that was up to that time unknown.
The
solubility of calcium fluoride changes somewhat with temperature and pH. It
is slightly more soluble at body temperature (37oC) than room temperature but
since it also decreases in solubility with increasing basicity, we here
estimate the solubility in blood at about the published value at pH 7 for
water at room temperature because the slight increase it actually has is
offset by the higher pH of blood, at 7.4.
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