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Scientific Abuse in Methanol / Formaldehyde Research Related to Aspartame
Table of Contents
Summary of Aspartame Methanol/Formaldehyde Toxicity
Hiding the Blood Plasma Methanol Increase From Aspartame Ingestion
Methanol and Fruit/Tomatos: Convince the World That a Poison is "Natural"
Avoiding the Discussion of Chronic Methanol Toxicity
Convince Scientists & Physicians With Irrelevant and Flawed Formate Measurements
The "It is Found in the Body, so a Proven Poison Must be Safe" Excuse to Eat Poison
Formaldehyde & Formic Acid in Foods: A Final Attempt to Prove a Poison is "Safe"
Formaldehyde Dose: Fabricating Numbers (Updated Oct. 16 2000)
References
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Summary of Aspartame Methanol/Formaldehyde Toxicity
"These are indeed extremely high levels for adducts of formaldehyde, a substance responsible for chronic
deleterious effects that has also been considered carcinogenic.
....
"It is concluded that aspartame consumption may constitute a hazard because of its contribution to the formation
of formaldehyde adducts." (Trocho 1998)
"It was a very interesting paper, that demonstrates that formaldehyde formation from aspartame ingestion is very
common and does indeed accumulate within the cell, reacting with cellular proteins (mostly enzymes) and DNA
(both mitochondrial and nuclear). The fact that it accumulates with each dose, indicates grave consequences
among those who consume diet drinks and foodstuffs on a daily basis." (Blaylock 1998)
Methanol from aspartame is released in the small intestine when the methyl group of aspartame encounters the
enzyme chymotrypsin (Stegink 1984, page 143). A relatively small amount of aspartame (e.g., one can of soda
ingested by a child) can significantly increase plasma methanol levels (Davoli 1986a).
Clinically, chronic, low-level exposure to methanol has been seen to cause headaches, dizziness, nausea, ear
buzzing, GI distiurbances, weakness, vertigo, chills, memory lapses, numbness & shooting pains, behavioral
disturbances, neuritis, misty vision, vision tunneling, blurring of vision, conjunctivitis, insomnia, vision loss,
depression, heart problems (including disease of the heart muscle), and pancreatic inflammation (Kavet 1990,
Monte 1984, Posner 1975).
The methanol from aspartame is converted to formaldehyde and then formic acid (DHHS 1993, Liesivuori 1991),
although some of the formaldehyde appears to accumulate in the body as discussed above. Chronic
formaldehyde exposure at very low doses has been shown to cause immune system and nervous system changes
and damage as well as headaches, general poor health, irreversible genetic damage, and a number of other
serious health problems (Fujimaki 1992, He 1998, John 1994, Liu 1993, Main 1983, Molhave 1986, National
Research Council 1981, Shaham 1996, Srivastava 1992, Vojdani 1992, Wantke 1996). One experiment (Wantke
1996) showed that chronic exposure to formaldehyde caused systemic health problems (i.e., poor health) in
children at an air concentration of only 0.043 - 0.070 parts per million!
Obviously, chronic exposure to an extremely small amount of formaldehyde is to be avoided. Even if formaldehyde
adducts did not build up in the body from aspartame use, the regular exposure to excess levels of formaldehyde
would still be a major concern to independent scientists and physicians familiar with the aspartame toxicity issue.
In addition to chronic formaldehyde poisoning, the excitotoxic amino acid derived from aspartame will almost
certainly worsen the damage caused by the formladehyde. Synergistic effects from aspartame metabolites are
rarely, if ever, mentioned by the manufacturer. Aspartame breaks down into a free-form (unbound to protein)
excitotoxic amino acid which is quickly-absorbed (as long as it is not given in slow-dissolving capsules) and can
raise the blood plasma levels of this excitotoxin (Stegink 1987). It is well known that free-form excitotoxins can
cause irreversible damage to brain cells (in areas such as the retina, hypothalamus, etc.) in rodents and primates
(Olney 1972, Olney 1980, Blaylock 1994, Lipton 1994). In order to remove excess, cell-destroying excitotoxic
amino acids from extracellular space, glial cells surround the neuron and supply them with energy (Blaylock 1994,
page 39, Lipton 1994). This takes large amounts of ATP. However, formate, a formaldehyde metabolite, is an ATP
inhibitor (Liesivuori 1991). Eells (1996b) points out that excitatory amino acid toxicity may be the "mediators of
retinal damage secondary to formate induced energy depletion in methanol-intoxication." The synergistic effects
from the combination of a chronic formaldehyde exposure from aspartame along with a free-form excitotoxic amino
acid is extremely worrisome.
It appears that methanol is converted to formate in the eye (Eells 1996a, Garner 1995, Kini 1961). Eells (1996a)
showed that chronic, low-level methanol exposure in rats led to formate accumulation in the retina of the eye.
More details about chronic Methanol / Formaldehyde poisoning from aspartame can be found on the Internet at
http://www.holisticmed.com/aspartame/aspfaq.html.
How did the manufacturer convince scientists and physicians that it is "safe" to be exposed regularly to low levels
of an exceptionally toxic poison? Answer: Deceptive research and deceptive statements!
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Hiding the Blood Plasma Methanol Increase From Aspartame Ingestion
On February 22, 1984, the acting FDA Commissioner, Mark Novitch stated (Federal Register 1984):
"... aspartame showed no detectable levels of methanol in the blood of human subjects following the ingestion of
aspartame at 34 mg/kg ...."
The American Medical Association repeated this statement one year later (AMA 1985). This statement was
repeated in American Family Physician in 1989 (Yost 1989). Shaywitz (1994) stated that there was no detectable
levels of methanol in the blood after aspartame administration. Puthrasingam (1996) stated that methanol from
aspartame is "undetectable in peripheral blood or even in portal blood."
All of these statements were very convincing ... and very wrong! The statements were based on aspartame
industry research which used an outdated plasma methanol measuring test (Baker 1969). The test they used had
a limit of methanol detection of 4 mg/l. However, Cook (1991) measured an average baseline (unexposed)
methanol level of ~0.6 mg/l. Others (Davoli 1986, d'Alessandro 1994, Osterloh 1996) have measured an average
baseline methanol level of close to 1 mg/l. This means that a person's methanol levels would have to rise 350% to
600% before an increase would have been noticed by the industry researchers using this outdated test! An
increase of less than 350% to 600% appeared as no increase at all!
Probably only a handful of people in the world would have noticed that by using a plasma methanol measuring
test with limits of 4 mg/l, they avoided seeing an methanol level increase -- even though there was a large
increase. Below are some of the experiments which used the inappropriate methanol measuring technique.
Note: 10 mg/kg is approximately a one liter bottle of diet soda for a 60 kg adult and 1.5 cans of diet soda for a 30
kg child. Children with aspartame freely-available can ingest between 27 mg/kg - 77 mg/kg (Frey 1976) and adults
dieters have been shown to ingest between 8 mg/kg and 36 mg/kg (Porikos 1984).
In 1986, Davoli (1986a) published a study which showed that 6 mg/kg to 8.7 mg/kg of aspartame could
significantly raise the plasma methanol levels. The methanol levels nearly doubled in some cases. While there
were some logical errors in Davoli's conclusion (discussed below), the study proved that by using a reasonable
methanol testing method, plasma methanol levels will increase from a relatively low dose of aspartame ingestion.
The methanol measuring technique used by Davoli was published in 1985 (Davoli 1986b) and was sensitive to
0.012 mg/l.
Other researchers have used sensitive plasma methanol measurement techniques. d'Alessandro (1994)
measured plasma methanol levels in humans well below 1 mg/l. Cook (1991) used a methanol test developed in
1981 to measure methanol plasma methanol levels in humans below 0.5 mg/l.
What did industry scientists know or should have known?
They knew and admitted that their methanol testing procedure developed in 1969 was not sensitive enough to
detect the large increases of plasma methanol levels when aspartame was given at doses of 34 mg/kg (Stegink
1984b).
They must have been aware that Davoli found methanol levels increase significantly when aspartame was given
at doses of 6 mg/kg to 8.7 mg/kg. To believe that they were not aware of this, one has to believe that none of the
researchers choose to or knew how to conduct a simple Medline database search.
They should have known that there were several legitimate plasma methanol measurement techniques developed
since 1969. Given that they admitted their technique was not appropriate for aspartame doses of less than 34
mg/kg (Stegink 1984b), they should have at least looked to find an appropriate test.
Given that Leon (1989) was aware enough to test for formate levels, he must have been aware that all of the
methanol from aspartame would have already converted to formaldehyde after a 12-hour fast.
I believe that Monsanto/NutraSweet and the aspartame industry are clearly taking advantage physicians and
scientists who lack the time to carefully investigate each number in a study to see if there is deception. While
these actions may not amount to "scientific fraud," it does amount to an abuse of the scientific method in my
opinion.
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Methanol and Fruit/Tomatos: Convince the World That a Poison is "Natural"
Monsanto/NutraSweet's all time favorite aspartame fairy tale is:
"In addition, exposure to methanol from many fruits, vegetables, and juices in the normal diet is several times
greater than that from beverages sweetened with APM [aspartame]." (Butchko 1991)
This statement from NutraSweet scientists has been repeated countless times (AMA 1985, FDA 1984, Hertelendy
1993, Lajtha 1994, Monsanto 1999, Nelson 1996, Stegink 1981, Stegink 1983, Yost 1989, etc.). This is very
convincing ... but deceptive and irrelevant!
It is well known that alcoholic beverages such a wine contain a large amount of ethanol, a protective factor which
prevents methanol poisoning by preventing the conversion of methanol to the highly toxic formaldehyde (Leaf
1952, Liesivuori 1991, Roe 1982). Because alcoholic beverages contain protective factors which prevent chronic
poisoning from methanol metabolites (formaldehyde, formate), comparisons between the methanol derived from
aspartame and the methanol derived from alcoholic beverages are inappropriate.
Clinical reports and a small number of epidemiological studies appear to demonstrate that prolonged exposure to
methanol air concentrations (in the workplace) of > 260 mg/m3 (200 ppm) can cause chronic methanol toxicity
(Kavet 1990, Frederick 1984, Kingsley 1954-55). The weekly amount of methanol absorbed from a 260 mg/m3
workday exposure is (formula in Kavet 1990):
(260 mg/m3 * 6.67 m3/workday * 5 workdays * 60% absorption rate) / 70 kg adult
= 75 mg/kg weekly methanol
Note: While this seems like a high weekly methanol dose, please keep in mind that 1) much lower levels may
cause toxicity in some individuals; and 2) that aspartame breaks down into an excitotoxin which will likely enhance
the toxicity of methanol metabolites as described above.
However, the ingestion of a moderate amount of apples or oranges (or juice equivalent) per week leads to a
similar exposure to methanol (Lindinger 1997):
(750 mg methanol (1.5 kg fruit) * 7 days) / 70 kg adult
= 74 mg/kg weekly methanol
Keep in mind that tomatoes may have more than five times the amount of methanol as that found in oranges
(Kazeniac 1970, Nisperos-Carriedo 1990), so exposure to regular ingestion of tomatoes and tomato juice may
produce very large amounts of methanol.
Lindinger (1997) points out that the amount of methanol released in the human body from a few apples or
oranges is equivalent to:
"...0.3 liters of brandy (40% ethanol) containing 0.5% of methanol (compared with ethanol), which would qualify as
significantly methanol-contaminated liquor."
Because of the high amounts of methanol in fruits/tomatoes, enough that would clearly cause chronic methanol
poisoning, these foods must contain protective factors (as does alcoholic beverages). If they did not contain
protective factors, we would be seeing widespread methanol poisoning for persons who ingestion fruits and
tomatoes regularly.
The manufacturer showed that the protective factor in fruits cannot be ethanol by itself (Sturtevant 1985), but
there are a myriad of chemicals in fruits which might serve as protective factors.
What did industry scientists know or should have known?
They knew that alcoholic beverages contain protective factors which prevent chronic methanol poisoning
(Sturtevant 1985).
Because industry scientists regularly announced that certain fruits contain extremely high levels of methanol, they
should have taken the time to find out that fruits have protective factors which help prevent chronic poisoning
from methanol metabolites.
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Avoiding the Discussion of Chronic Methanol Toxicity
A number of Monsanto/NutraSweet public relations statements as well as statements from government officials
imply that the amount of methanol obtained from aspartame is not toxic:
"From estimates based on blood levels in methanol poisonings, it appears that the ingestion of methanol on the
order of 200 to 500 mg/kg body weight is required to produce a significant accumulation of formate in the blood
which may produce visual and central nervous system toxicity" (Federal Register 1984)
Lajtha (1994) claimed that "blood methanol concentrations greater than 200 to 100 mg/L are required for clinical
neurotoxicity or for measurable formate formation." Non-scientists on the Internet often make similar claims.
Shahangian (1984) claimed that the amount of formate (methanol and formaldehyde metabolite) is not enough to
cause toxicity.
This sounds very convincing until one realizes that the doses they are referirng to are the single doses required
for death or near death in humans! Monsanto/NutraSweet and persons promoting aspartame will avoiding
discussing chronic, low-level methanol or formaldehyde poisoning because once this issue is raised it becomes
apparent that the manufacturer did not conduct or even cite any legitimate studies on chronic, low-level methanol
exposure in humans!
Only on very rare occasion will the manufacturer mention chronic methanol toxicity (Nelson 1996, Sturtevant
1985). When they do this, they always cite a study of infant monkeys (a species closely related to rhesus
monkeys) (Reynolds 1984). A dose of 3,000 mg/kg of aspartame was given to the monkeys for nine months. This
amounts to a daily methanol dose of 300 mg/kg -- a huge dose.
What Monsanto/NutraSweet fails to mention is 300 mg/kg of methanol has been estimated as the minimum single
dose which can cause death in humans (Kavet 1991). If such a study were conducted on humans, nine months of
daily ingestion of the minimum lethal single dose of methanol would clearly kill everyone in the study!. As pointed
out by Roe (1982), methanol is significantly more toxic in humans than in monkeys or rodents. It is important to
note that the free-form excitotoxin derived from aspartame and which will likely increase the formaldehyde/formate
damage from aspartame, appears to be approximately twenty times more toxic in humans than in monkeys due to
differences in excitotoxin metabolism (Olney 1988, Stegink 1979, page 90).
What did industry scientists know or should have known?
They knew that there was never a controlled, long-term study of methanol exposure in humans. Given that the
manufacturer was expecting to dose the human population with aspartame for a lifetime and even generations,
some might consider it criminal to sell a poison under these circumstances.
They should have known that an excitotoxin will likely increase the toxicity of the formaldehyde/formate based
upon the way these chemicals produce cell damage and cell death. At the very least, the manufacturer should
have exhausted all reasonable possibilities of synergistic reactions as opposed to using flawed research and
flawed logic to explain away the countless cases of aspartame poisoning.
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Convince Scientists & Physicians With Irrelevant and Flawed Formate Measurements
The FDA Commissioner has claimed (Federal Register 1984):
"In the Searle [manufacturer] clinical study using abuse doses of aspartame equivalent to 20 mg/kg body weight
of methanol, no significant increases were observed in plasma concentrations of formate, suggesting that the rate
of formate production does not exceed its rate of urinary excretion."
The AMA (1985) claimed that abuse doses of aspartame have not been shown to increase blood formate levels.
Stegink (1989, 1990) claimed that large doses of aspartame did not raise blood and urine formate levels
significantly. Leon (1989) claimed to show no increase in urinary formate from a daily dose of 75 mg/kg of
aspartame. Hertelendy (1993) claimed that there was not increase in urine or plasma formate levels from 15
mg/kg aspartame ingestion.
Since methanol metabolizes into formaldehyde and formaldehyde metabolizes into formate, all of these
statements appear to point to safety ... at first glance. But what the manufacturer does not tell you is that these
tests are now known to be irrelevant and flawed!
Formate (formic acid) measurement of the urine is not an appropriate test for low-level formaldehyde poisoning.
(Keep in mind that extremely low doses of formaldehyde have been shown to cause chronic poisoning symptoms
as discussed above.) Triebig (1989) states that formic acid excretion in the urine is a "unspecific and insensitive
biological indicator for monitoring low-dose formaldehyde exposure." Schmid (1994) found that neither a single
significant exposure to formaldehyde nor a week-long exposure to formaldehyde correlated with urine formic acid
measurements. After testing subjects exposed to formaldehyde, Heinzow (1992) stated:
"Excretion [of formic acid] in the general population is determined by endogenous metabolism of amino acids,
purine- and pyrimidine-bases rather than the uptake and metabolism of precursors like formaldehyde. Hence in
contrast to recent recommendations in environmental medicine, formic acid in urine is not an appropriate
parameter for biological-monitoring of low level exposure to formaldehyde."
Therefore, all of the aspartame industry's urine formate measurements are useless for chronic
methanol/formaldehyde poisoning from aspartame.
Blood formate measurements also appear to be inadequate for chronic, low-level methanol or formaldehyde
poisoning. d'Alessandro (1994) stated:
"While exposure to several different levels of methanol above the threshold limit [200 ppm] might demonstrate
slight increases in formate concentrations, it seems doubtful that this measure would be useful for monitoring
individual low-level exposure."
And after further study, Osterloh (1996) stated:
"Previously, we reviewed exposure studies (both occupational and experimental) in which formate concentrations
were measures, along with these data, as a basis for the conclusion that methanol, not formate, in serum can be
used as a biological marker of exposures."
Three other reasons why aspartame industry formate measurements can be considered useless include:
Trocho (1998) showed a significant amount of formaldehyde from aspartame binding with proteins and
accumulating in tissues rather than metabolizing into formate.
The average baseline (pre-exposure) measurements of formate in the aspartame industry research (e.g., Stegink
1981, 1989, 1990) is unexplicabally 1.5 to 3 times higher than any other independent researcher (d'Alessandro
1994, Baumann 1979, Buttery 1988, Heinrich 1982, Osterloh 1986, Osterloh 1996). As pointed out by Kavet
(1990), high pre-exposure blood formate levels "may have masked any subtle increases that the aspartame may
have caused."
A respected formaldehyde and formic acid exposure researcher has pointed out that several formate
measurement techniques including the one used by aspartame industry researchers (Makar 1982) are
"notoriously inaccurate." (Liesivuori 1986).
Unfortunately, there are still researchers who cite old tests of formate levels related to aspartame ingestion even
though these tests have proven to be meaningless and flawed.
What did industry scientists know or should have known?
The industry researchers should have keep up-to-date on formate measurement research. Had they done that,
they would have known that such measurements are inappropriate for chronic, low-level methanol and
formaldehyde exposure.
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The "It is Found in the Body, so a Proven Poison Must be Safe" Excuse to Eat Poison
From time to time, it will be implied that because methanol and formaldehyde are in the body, it is perfectly safe to
add more. Acting FDA Commissioner Mark Novitch stated the following (Federal Register 1984):
"Normal metabolic processes such as purine and pyrimidine biosynthesis and amino acid metabolism require
methyl groups from compounds like methanol. It also appears that either methanol or formaldehyde may serve as
precursors for the methyl groups in choline synthesis."
On the Internet, this is a popular technique used to try to convince people that methanol and formaldehyde
exposure is safe. What the FDA Commissioner and other persons unfamiliar with this issue did not point out is
that chronic poisoning from low-level methanol and formaldehyde exposure is already accepted in the medical
community. In fact, children who were chronically-exposed to formaldehyde in the air at concetrations of 0.05
parts per million (ppm) developed systemic health problems after several months (Wantke 1996). This is
equivalent to a daily exposure of only 0.75 mg of formaldehyde (or less if 100% of the formaldehyde is not
absorbed):
0.05 ppm formaldehyde ~= 0.075 mg/m3
0.075 mg/m3 * 10 m3/workday = 0.75 mg/day (for a workday/schoolday)
Other researchers have noted formaldehyde toxicity symptoms appearing at chronic, low-level exposure
(Srivastava 1992):
"Complaints pertaining to gastrointestinal, musculoskeletal and cardiovascular systems were also more frequent
in exposed subjects. In spite of formaldehyde concentrations being well within the prescribed ACGIH [American
Conference of Governmental Industrial Hygienists] limits of 1 ppm...."
This proves that formaldehyde levels in the body must be very tightly-controlled since a very low daily exposure
leads to health problems. Even a very small, regular increase can lead to chronic, low-level poisoning.
Davoli (1986) showed that aspartame significantly increases plasma methanol levels. However, he mistakenly
concluded that because the post-aspartame administration methanol levels did not rise above the baseline
methanol levels of every other human being, those levels might not be toxic. What Davoli failed to consider,
however, is that 1) we know that methanol and formaldehyde levels in the body must be tightly controlled because
exposure to very low levels of these chemicals have been shown to lead to chronic toxicity; and 2) that people
have their own individual metabolism so that a slight addition of formaldehyde to the current tightly-controlled level
in one individual could cause toxicity even though it might not rise above the baseline level of another individual's
formaldehyde level. As one can see from the Davoli (1986) study, the administration of aspartame lead to a fairly
sudden and significant increase in plasma methanol levels and would be expected to cause a significant
formaldehyde exposure.
--------------------------------------------------------------------------------
Formaldehyde & Formic Acid in Foods: A Final Attempt to Prove a Poison is "Safe"
"... formaldehyde [exposure from aspartame is] comparable to a serving of fresh broccoli." (Weber 1999)
Every once in a while there will be a statement pointing out that some foods have relatively high levels of
formaldehyde and formic acid. What is not pointed out is that formaldehyde in food is much less toxic than
formaldehyde from air exposure or formaldehyde from aspartame exposure due to the way the body metabolizes it.
Restani (1991) points out that formaldehyde can be found in seafood, honey, fruits, vegetables, etc. Restani
(1991) points to a human study showing where 200 mg of formaldehyde per day was ingested for 13 weeks
without showing adverse effects. This would be equivalent to an daily air exposure of:
200 mg/day / 10 m3/workday = 20.0 mg/m3 = 13.3 ppm
13.3 ppm daily air exposure is many times over the 0.05 levels which caused chronic toxicity in Wantke (1996)
and many times over the American Conference of Governmental Industrial Hygienists limit of 1 ppm which was
shown to cause chronic toxicity in Srivastava (1992).
This proves that formaldehyde found in foods is either not absorbed well:
"Ingestion represents a minor route of [formaldehyde] exposure because the dilution factor and the binding to the
macromolecules present in food reduce substantially the [formaldehyde] concentration that enters into contact
with the gastrointestinal mucosa" (Restani 1991)
Or formaldehyde may be broken down by the digestive system. With aspartame, however, the methanol has been
proven to be absorbed and then after it is already in the bloodstream, it is converted to formaldehyde (or directly
to formate in certain tissues such as the retina).
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Formaldehyde Dose: Fabricating Numbers
One way to convince at least a few people that it is 'safe' to be poisoned with aspartame is to simply make up
numbers that appear to show that formaldehyde exposure from aspartame is low. One author claimed that
formaldehyde exposure was only 30 micrograms -- a figure off by a factor of over 400,000 for the aspartame dose
that was used! The following web page calculates and discusses the dose of formaldehyde exposure and
accumulation due to aspartame ingestion:
Source:http://www.holisticmed.com/aspartame/abuse/methanol.html
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Summary of Aspartame Methanol/Formaldehyde Toxicity
Hiding the Blood Plasma Methanol Increase From Aspartame Ingestion
Methanol and Fruit/Tomatos: Convince the World That a Poison is "Natural"
Avoiding the Discussion of Chronic Methanol Toxicity
Convince Scientists & Physicians With Irrelevant and Flawed Formate Measurements
The "It is Found in the Body, so a Proven Poison Must be Safe" Excuse to Eat Poison
Formaldehyde & Formic Acid in Foods: A Final Attempt to Prove a Poison is "Safe"
Formaldehyde Dose: Fabricating Numbers (Updated Oct. 16 2000)
References
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Summary of Aspartame Methanol/Formaldehyde Toxicity
"These are indeed extremely high levels for adducts of formaldehyde, a substance responsible for chronic
deleterious effects that has also been considered carcinogenic.
....
"It is concluded that aspartame consumption may constitute a hazard because of its contribution to the formation
of formaldehyde adducts." (Trocho 1998)
"It was a very interesting paper, that demonstrates that formaldehyde formation from aspartame ingestion is very
common and does indeed accumulate within the cell, reacting with cellular proteins (mostly enzymes) and DNA
(both mitochondrial and nuclear). The fact that it accumulates with each dose, indicates grave consequences
among those who consume diet drinks and foodstuffs on a daily basis." (Blaylock 1998)
Methanol from aspartame is released in the small intestine when the methyl group of aspartame encounters the
enzyme chymotrypsin (Stegink 1984, page 143). A relatively small amount of aspartame (e.g., one can of soda
ingested by a child) can significantly increase plasma methanol levels (Davoli 1986a).
Clinically, chronic, low-level exposure to methanol has been seen to cause headaches, dizziness, nausea, ear
buzzing, GI distiurbances, weakness, vertigo, chills, memory lapses, numbness & shooting pains, behavioral
disturbances, neuritis, misty vision, vision tunneling, blurring of vision, conjunctivitis, insomnia, vision loss,
depression, heart problems (including disease of the heart muscle), and pancreatic inflammation (Kavet 1990,
Monte 1984, Posner 1975).
The methanol from aspartame is converted to formaldehyde and then formic acid (DHHS 1993, Liesivuori 1991),
although some of the formaldehyde appears to accumulate in the body as discussed above. Chronic
formaldehyde exposure at very low doses has been shown to cause immune system and nervous system changes
and damage as well as headaches, general poor health, irreversible genetic damage, and a number of other
serious health problems (Fujimaki 1992, He 1998, John 1994, Liu 1993, Main 1983, Molhave 1986, National
Research Council 1981, Shaham 1996, Srivastava 1992, Vojdani 1992, Wantke 1996). One experiment (Wantke
1996) showed that chronic exposure to formaldehyde caused systemic health problems (i.e., poor health) in
children at an air concentration of only 0.043 - 0.070 parts per million!
Obviously, chronic exposure to an extremely small amount of formaldehyde is to be avoided. Even if formaldehyde
adducts did not build up in the body from aspartame use, the regular exposure to excess levels of formaldehyde
would still be a major concern to independent scientists and physicians familiar with the aspartame toxicity issue.
In addition to chronic formaldehyde poisoning, the excitotoxic amino acid derived from aspartame will almost
certainly worsen the damage caused by the formladehyde. Synergistic effects from aspartame metabolites are
rarely, if ever, mentioned by the manufacturer. Aspartame breaks down into a free-form (unbound to protein)
excitotoxic amino acid which is quickly-absorbed (as long as it is not given in slow-dissolving capsules) and can
raise the blood plasma levels of this excitotoxin (Stegink 1987). It is well known that free-form excitotoxins can
cause irreversible damage to brain cells (in areas such as the retina, hypothalamus, etc.) in rodents and primates
(Olney 1972, Olney 1980, Blaylock 1994, Lipton 1994). In order to remove excess, cell-destroying excitotoxic
amino acids from extracellular space, glial cells surround the neuron and supply them with energy (Blaylock 1994,
page 39, Lipton 1994). This takes large amounts of ATP. However, formate, a formaldehyde metabolite, is an ATP
inhibitor (Liesivuori 1991). Eells (1996b) points out that excitatory amino acid toxicity may be the "mediators of
retinal damage secondary to formate induced energy depletion in methanol-intoxication." The synergistic effects
from the combination of a chronic formaldehyde exposure from aspartame along with a free-form excitotoxic amino
acid is extremely worrisome.
It appears that methanol is converted to formate in the eye (Eells 1996a, Garner 1995, Kini 1961). Eells (1996a)
showed that chronic, low-level methanol exposure in rats led to formate accumulation in the retina of the eye.
More details about chronic Methanol / Formaldehyde poisoning from aspartame can be found on the Internet at
http://www.holisticmed.com/aspartame/aspfaq.html.
How did the manufacturer convince scientists and physicians that it is "safe" to be exposed regularly to low levels
of an exceptionally toxic poison? Answer: Deceptive research and deceptive statements!
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Hiding the Blood Plasma Methanol Increase From Aspartame Ingestion
On February 22, 1984, the acting FDA Commissioner, Mark Novitch stated (Federal Register 1984):
"... aspartame showed no detectable levels of methanol in the blood of human subjects following the ingestion of
aspartame at 34 mg/kg ...."
The American Medical Association repeated this statement one year later (AMA 1985). This statement was
repeated in American Family Physician in 1989 (Yost 1989). Shaywitz (1994) stated that there was no detectable
levels of methanol in the blood after aspartame administration. Puthrasingam (1996) stated that methanol from
aspartame is "undetectable in peripheral blood or even in portal blood."
All of these statements were very convincing ... and very wrong! The statements were based on aspartame
industry research which used an outdated plasma methanol measuring test (Baker 1969). The test they used had
a limit of methanol detection of 4 mg/l. However, Cook (1991) measured an average baseline (unexposed)
methanol level of ~0.6 mg/l. Others (Davoli 1986, d'Alessandro 1994, Osterloh 1996) have measured an average
baseline methanol level of close to 1 mg/l. This means that a person's methanol levels would have to rise 350% to
600% before an increase would have been noticed by the industry researchers using this outdated test! An
increase of less than 350% to 600% appeared as no increase at all!
Probably only a handful of people in the world would have noticed that by using a plasma methanol measuring
test with limits of 4 mg/l, they avoided seeing an methanol level increase -- even though there was a large
increase. Below are some of the experiments which used the inappropriate methanol measuring technique.
Note: 10 mg/kg is approximately a one liter bottle of diet soda for a 60 kg adult and 1.5 cans of diet soda for a 30
kg child. Children with aspartame freely-available can ingest between 27 mg/kg - 77 mg/kg (Frey 1976) and adults
dieters have been shown to ingest between 8 mg/kg and 36 mg/kg (Porikos 1984).
In 1986, Davoli (1986a) published a study which showed that 6 mg/kg to 8.7 mg/kg of aspartame could
significantly raise the plasma methanol levels. The methanol levels nearly doubled in some cases. While there
were some logical errors in Davoli's conclusion (discussed below), the study proved that by using a reasonable
methanol testing method, plasma methanol levels will increase from a relatively low dose of aspartame ingestion.
The methanol measuring technique used by Davoli was published in 1985 (Davoli 1986b) and was sensitive to
0.012 mg/l.
Other researchers have used sensitive plasma methanol measurement techniques. d'Alessandro (1994)
measured plasma methanol levels in humans well below 1 mg/l. Cook (1991) used a methanol test developed in
1981 to measure methanol plasma methanol levels in humans below 0.5 mg/l.
What did industry scientists know or should have known?
They knew and admitted that their methanol testing procedure developed in 1969 was not sensitive enough to
detect the large increases of plasma methanol levels when aspartame was given at doses of 34 mg/kg (Stegink
1984b).
They must have been aware that Davoli found methanol levels increase significantly when aspartame was given
at doses of 6 mg/kg to 8.7 mg/kg. To believe that they were not aware of this, one has to believe that none of the
researchers choose to or knew how to conduct a simple Medline database search.
They should have known that there were several legitimate plasma methanol measurement techniques developed
since 1969. Given that they admitted their technique was not appropriate for aspartame doses of less than 34
mg/kg (Stegink 1984b), they should have at least looked to find an appropriate test.
Given that Leon (1989) was aware enough to test for formate levels, he must have been aware that all of the
methanol from aspartame would have already converted to formaldehyde after a 12-hour fast.
I believe that Monsanto/NutraSweet and the aspartame industry are clearly taking advantage physicians and
scientists who lack the time to carefully investigate each number in a study to see if there is deception. While
these actions may not amount to "scientific fraud," it does amount to an abuse of the scientific method in my
opinion.
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Methanol and Fruit/Tomatos: Convince the World That a Poison is "Natural"
Monsanto/NutraSweet's all time favorite aspartame fairy tale is:
"In addition, exposure to methanol from many fruits, vegetables, and juices in the normal diet is several times
greater than that from beverages sweetened with APM [aspartame]." (Butchko 1991)
This statement from NutraSweet scientists has been repeated countless times (AMA 1985, FDA 1984, Hertelendy
1993, Lajtha 1994, Monsanto 1999, Nelson 1996, Stegink 1981, Stegink 1983, Yost 1989, etc.). This is very
convincing ... but deceptive and irrelevant!
It is well known that alcoholic beverages such a wine contain a large amount of ethanol, a protective factor which
prevents methanol poisoning by preventing the conversion of methanol to the highly toxic formaldehyde (Leaf
1952, Liesivuori 1991, Roe 1982). Because alcoholic beverages contain protective factors which prevent chronic
poisoning from methanol metabolites (formaldehyde, formate), comparisons between the methanol derived from
aspartame and the methanol derived from alcoholic beverages are inappropriate.
Clinical reports and a small number of epidemiological studies appear to demonstrate that prolonged exposure to
methanol air concentrations (in the workplace) of > 260 mg/m3 (200 ppm) can cause chronic methanol toxicity
(Kavet 1990, Frederick 1984, Kingsley 1954-55). The weekly amount of methanol absorbed from a 260 mg/m3
workday exposure is (formula in Kavet 1990):
(260 mg/m3 * 6.67 m3/workday * 5 workdays * 60% absorption rate) / 70 kg adult
= 75 mg/kg weekly methanol
Note: While this seems like a high weekly methanol dose, please keep in mind that 1) much lower levels may
cause toxicity in some individuals; and 2) that aspartame breaks down into an excitotoxin which will likely enhance
the toxicity of methanol metabolites as described above.
However, the ingestion of a moderate amount of apples or oranges (or juice equivalent) per week leads to a
similar exposure to methanol (Lindinger 1997):
(750 mg methanol (1.5 kg fruit) * 7 days) / 70 kg adult
= 74 mg/kg weekly methanol
Keep in mind that tomatoes may have more than five times the amount of methanol as that found in oranges
(Kazeniac 1970, Nisperos-Carriedo 1990), so exposure to regular ingestion of tomatoes and tomato juice may
produce very large amounts of methanol.
Lindinger (1997) points out that the amount of methanol released in the human body from a few apples or
oranges is equivalent to:
"...0.3 liters of brandy (40% ethanol) containing 0.5% of methanol (compared with ethanol), which would qualify as
significantly methanol-contaminated liquor."
Because of the high amounts of methanol in fruits/tomatoes, enough that would clearly cause chronic methanol
poisoning, these foods must contain protective factors (as does alcoholic beverages). If they did not contain
protective factors, we would be seeing widespread methanol poisoning for persons who ingestion fruits and
tomatoes regularly.
The manufacturer showed that the protective factor in fruits cannot be ethanol by itself (Sturtevant 1985), but
there are a myriad of chemicals in fruits which might serve as protective factors.
What did industry scientists know or should have known?
They knew that alcoholic beverages contain protective factors which prevent chronic methanol poisoning
(Sturtevant 1985).
Because industry scientists regularly announced that certain fruits contain extremely high levels of methanol, they
should have taken the time to find out that fruits have protective factors which help prevent chronic poisoning
from methanol metabolites.
--------------------------------------------------------------------------------
Avoiding the Discussion of Chronic Methanol Toxicity
A number of Monsanto/NutraSweet public relations statements as well as statements from government officials
imply that the amount of methanol obtained from aspartame is not toxic:
"From estimates based on blood levels in methanol poisonings, it appears that the ingestion of methanol on the
order of 200 to 500 mg/kg body weight is required to produce a significant accumulation of formate in the blood
which may produce visual and central nervous system toxicity" (Federal Register 1984)
Lajtha (1994) claimed that "blood methanol concentrations greater than 200 to 100 mg/L are required for clinical
neurotoxicity or for measurable formate formation." Non-scientists on the Internet often make similar claims.
Shahangian (1984) claimed that the amount of formate (methanol and formaldehyde metabolite) is not enough to
cause toxicity.
This sounds very convincing until one realizes that the doses they are referirng to are the single doses required
for death or near death in humans! Monsanto/NutraSweet and persons promoting aspartame will avoiding
discussing chronic, low-level methanol or formaldehyde poisoning because once this issue is raised it becomes
apparent that the manufacturer did not conduct or even cite any legitimate studies on chronic, low-level methanol
exposure in humans!
Only on very rare occasion will the manufacturer mention chronic methanol toxicity (Nelson 1996, Sturtevant
1985). When they do this, they always cite a study of infant monkeys (a species closely related to rhesus
monkeys) (Reynolds 1984). A dose of 3,000 mg/kg of aspartame was given to the monkeys for nine months. This
amounts to a daily methanol dose of 300 mg/kg -- a huge dose.
What Monsanto/NutraSweet fails to mention is 300 mg/kg of methanol has been estimated as the minimum single
dose which can cause death in humans (Kavet 1991). If such a study were conducted on humans, nine months of
daily ingestion of the minimum lethal single dose of methanol would clearly kill everyone in the study!. As pointed
out by Roe (1982), methanol is significantly more toxic in humans than in monkeys or rodents. It is important to
note that the free-form excitotoxin derived from aspartame and which will likely increase the formaldehyde/formate
damage from aspartame, appears to be approximately twenty times more toxic in humans than in monkeys due to
differences in excitotoxin metabolism (Olney 1988, Stegink 1979, page 90).
What did industry scientists know or should have known?
They knew that there was never a controlled, long-term study of methanol exposure in humans. Given that the
manufacturer was expecting to dose the human population with aspartame for a lifetime and even generations,
some might consider it criminal to sell a poison under these circumstances.
They should have known that an excitotoxin will likely increase the toxicity of the formaldehyde/formate based
upon the way these chemicals produce cell damage and cell death. At the very least, the manufacturer should
have exhausted all reasonable possibilities of synergistic reactions as opposed to using flawed research and
flawed logic to explain away the countless cases of aspartame poisoning.
--------------------------------------------------------------------------------
Convince Scientists & Physicians With Irrelevant and Flawed Formate Measurements
The FDA Commissioner has claimed (Federal Register 1984):
"In the Searle [manufacturer] clinical study using abuse doses of aspartame equivalent to 20 mg/kg body weight
of methanol, no significant increases were observed in plasma concentrations of formate, suggesting that the rate
of formate production does not exceed its rate of urinary excretion."
The AMA (1985) claimed that abuse doses of aspartame have not been shown to increase blood formate levels.
Stegink (1989, 1990) claimed that large doses of aspartame did not raise blood and urine formate levels
significantly. Leon (1989) claimed to show no increase in urinary formate from a daily dose of 75 mg/kg of
aspartame. Hertelendy (1993) claimed that there was not increase in urine or plasma formate levels from 15
mg/kg aspartame ingestion.
Since methanol metabolizes into formaldehyde and formaldehyde metabolizes into formate, all of these
statements appear to point to safety ... at first glance. But what the manufacturer does not tell you is that these
tests are now known to be irrelevant and flawed!
Formate (formic acid) measurement of the urine is not an appropriate test for low-level formaldehyde poisoning.
(Keep in mind that extremely low doses of formaldehyde have been shown to cause chronic poisoning symptoms
as discussed above.) Triebig (1989) states that formic acid excretion in the urine is a "unspecific and insensitive
biological indicator for monitoring low-dose formaldehyde exposure." Schmid (1994) found that neither a single
significant exposure to formaldehyde nor a week-long exposure to formaldehyde correlated with urine formic acid
measurements. After testing subjects exposed to formaldehyde, Heinzow (1992) stated:
"Excretion [of formic acid] in the general population is determined by endogenous metabolism of amino acids,
purine- and pyrimidine-bases rather than the uptake and metabolism of precursors like formaldehyde. Hence in
contrast to recent recommendations in environmental medicine, formic acid in urine is not an appropriate
parameter for biological-monitoring of low level exposure to formaldehyde."
Therefore, all of the aspartame industry's urine formate measurements are useless for chronic
methanol/formaldehyde poisoning from aspartame.
Blood formate measurements also appear to be inadequate for chronic, low-level methanol or formaldehyde
poisoning. d'Alessandro (1994) stated:
"While exposure to several different levels of methanol above the threshold limit [200 ppm] might demonstrate
slight increases in formate concentrations, it seems doubtful that this measure would be useful for monitoring
individual low-level exposure."
And after further study, Osterloh (1996) stated:
"Previously, we reviewed exposure studies (both occupational and experimental) in which formate concentrations
were measures, along with these data, as a basis for the conclusion that methanol, not formate, in serum can be
used as a biological marker of exposures."
Three other reasons why aspartame industry formate measurements can be considered useless include:
Trocho (1998) showed a significant amount of formaldehyde from aspartame binding with proteins and
accumulating in tissues rather than metabolizing into formate.
The average baseline (pre-exposure) measurements of formate in the aspartame industry research (e.g., Stegink
1981, 1989, 1990) is unexplicabally 1.5 to 3 times higher than any other independent researcher (d'Alessandro
1994, Baumann 1979, Buttery 1988, Heinrich 1982, Osterloh 1986, Osterloh 1996). As pointed out by Kavet
(1990), high pre-exposure blood formate levels "may have masked any subtle increases that the aspartame may
have caused."
A respected formaldehyde and formic acid exposure researcher has pointed out that several formate
measurement techniques including the one used by aspartame industry researchers (Makar 1982) are
"notoriously inaccurate." (Liesivuori 1986).
Unfortunately, there are still researchers who cite old tests of formate levels related to aspartame ingestion even
though these tests have proven to be meaningless and flawed.
What did industry scientists know or should have known?
The industry researchers should have keep up-to-date on formate measurement research. Had they done that,
they would have known that such measurements are inappropriate for chronic, low-level methanol and
formaldehyde exposure.
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The "It is Found in the Body, so a Proven Poison Must be Safe" Excuse to Eat Poison
From time to time, it will be implied that because methanol and formaldehyde are in the body, it is perfectly safe to
add more. Acting FDA Commissioner Mark Novitch stated the following (Federal Register 1984):
"Normal metabolic processes such as purine and pyrimidine biosynthesis and amino acid metabolism require
methyl groups from compounds like methanol. It also appears that either methanol or formaldehyde may serve as
precursors for the methyl groups in choline synthesis."
On the Internet, this is a popular technique used to try to convince people that methanol and formaldehyde
exposure is safe. What the FDA Commissioner and other persons unfamiliar with this issue did not point out is
that chronic poisoning from low-level methanol and formaldehyde exposure is already accepted in the medical
community. In fact, children who were chronically-exposed to formaldehyde in the air at concetrations of 0.05
parts per million (ppm) developed systemic health problems after several months (Wantke 1996). This is
equivalent to a daily exposure of only 0.75 mg of formaldehyde (or less if 100% of the formaldehyde is not
absorbed):
0.05 ppm formaldehyde ~= 0.075 mg/m3
0.075 mg/m3 * 10 m3/workday = 0.75 mg/day (for a workday/schoolday)
Other researchers have noted formaldehyde toxicity symptoms appearing at chronic, low-level exposure
(Srivastava 1992):
"Complaints pertaining to gastrointestinal, musculoskeletal and cardiovascular systems were also more frequent
in exposed subjects. In spite of formaldehyde concentrations being well within the prescribed ACGIH [American
Conference of Governmental Industrial Hygienists] limits of 1 ppm...."
This proves that formaldehyde levels in the body must be very tightly-controlled since a very low daily exposure
leads to health problems. Even a very small, regular increase can lead to chronic, low-level poisoning.
Davoli (1986) showed that aspartame significantly increases plasma methanol levels. However, he mistakenly
concluded that because the post-aspartame administration methanol levels did not rise above the baseline
methanol levels of every other human being, those levels might not be toxic. What Davoli failed to consider,
however, is that 1) we know that methanol and formaldehyde levels in the body must be tightly controlled because
exposure to very low levels of these chemicals have been shown to lead to chronic toxicity; and 2) that people
have their own individual metabolism so that a slight addition of formaldehyde to the current tightly-controlled level
in one individual could cause toxicity even though it might not rise above the baseline level of another individual's
formaldehyde level. As one can see from the Davoli (1986) study, the administration of aspartame lead to a fairly
sudden and significant increase in plasma methanol levels and would be expected to cause a significant
formaldehyde exposure.
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Formaldehyde & Formic Acid in Foods: A Final Attempt to Prove a Poison is "Safe"
"... formaldehyde [exposure from aspartame is] comparable to a serving of fresh broccoli." (Weber 1999)
Every once in a while there will be a statement pointing out that some foods have relatively high levels of
formaldehyde and formic acid. What is not pointed out is that formaldehyde in food is much less toxic than
formaldehyde from air exposure or formaldehyde from aspartame exposure due to the way the body metabolizes it.
Restani (1991) points out that formaldehyde can be found in seafood, honey, fruits, vegetables, etc. Restani
(1991) points to a human study showing where 200 mg of formaldehyde per day was ingested for 13 weeks
without showing adverse effects. This would be equivalent to an daily air exposure of:
200 mg/day / 10 m3/workday = 20.0 mg/m3 = 13.3 ppm
13.3 ppm daily air exposure is many times over the 0.05 levels which caused chronic toxicity in Wantke (1996)
and many times over the American Conference of Governmental Industrial Hygienists limit of 1 ppm which was
shown to cause chronic toxicity in Srivastava (1992).
This proves that formaldehyde found in foods is either not absorbed well:
"Ingestion represents a minor route of [formaldehyde] exposure because the dilution factor and the binding to the
macromolecules present in food reduce substantially the [formaldehyde] concentration that enters into contact
with the gastrointestinal mucosa" (Restani 1991)
Or formaldehyde may be broken down by the digestive system. With aspartame, however, the methanol has been
proven to be absorbed and then after it is already in the bloodstream, it is converted to formaldehyde (or directly
to formate in certain tissues such as the retina).
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Formaldehyde Dose: Fabricating Numbers
One way to convince at least a few people that it is 'safe' to be poisoned with aspartame is to simply make up
numbers that appear to show that formaldehyde exposure from aspartame is low. One author claimed that
formaldehyde exposure was only 30 micrograms -- a figure off by a factor of over 400,000 for the aspartame dose
that was used! The following web page calculates and discusses the dose of formaldehyde exposure and
accumulation due to aspartame ingestion:
Source:http://www.holisticmed.com/aspartame/abuse/methanol.html
--------------------------------------------------------------------------------
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