BIO Mary Nash Stoddard on Twitter

PRESENTING: MARY NASH STODDARD - Co-Founder of the massive international anti-aspartame movement in the mid 1980's, following the brain tumor death of her forty two year old husband, Mike. Ms. Stoddard suffered a life threatening aspartame-related blood disorder in 1985, whereupon, The NutraSweet Co. offered her an all-expense paid vacation for two anywhere in the world, if she would agree to be tested by their doctors. She declined, with the blessing of her doctor, and the rest is history. She has conducted multi-national lecture tours and is a popular visiting professor at colleges, universities and medical schools. "Deadly Deception - Story of Aspartame" is a toxicology sourcebook, edited by Ms. Stoddard, documenting the harmful effects of the world's most toxic artificial sweetener. The companion one hour "Deadly Deception" video is further documentation - taped at a prestigious scientific conference. Stoddard's efforts, over more than two decades, led to the present rejection of the sweetener by many of the food and beverage giants of industry, as they rush to distance themselves from the liabilities associated with use of a neuro-toxic substance in their products. She has testified in court as an Expert Medical Witness and like her counterpart, Erin Brokovitch, helped with a number of lawsuits on behalf of consumers. Her powerful message has reached millions around the world through the airwaves on radio and television, in print and through popular personal appearances. Honors, Awards, Societies: • Expert Medical Witness [1992-present] * Guest Presenter Gulf War Veterans Annual Conference - [Las Vegas 1999] * Visiting Professor: U. T. Southwestern Medical School [1997] * Visiting Professor: American University School of Journalism [1999] * Visiting Professor: University of North Texas at Denton Dept. of Science [1990 and 2005] • Visiting Professor: University of Houston Bioneers Conference [2006] * Invited speaker: Hebrew Univ. Jerusalem - [1997] * Keynote speech: Mexican Government's Annual Conference on Sweeteners [1999] * Appointed Judge - State of Texas [1977-1984] * Broadcast Journalist - [1965-present] * President's Council on Food Safety - [1998-1999] * International Lecture Tours - [1996-present] * Testimony Senate Committee Hearing on Safety of Aspartame - Washington [1987] * Panelist at National News Conference Announcing Dr. John Olney's Brain Tumor/Aspartame Connection - Washington D.C. [1998] * Inducted Member Texas Radio Hall of Fame [2002-present] Representative of the Texas Rice Growers Association [Miss Rice] Board member: Irving Symphony Orchestra Board Member: Irving Community Theater Founding Board Member Radio Station KNON [public radio], Dallas Charter member City of Dallas Citizens Safety Committee Board Member Dallas Mayor’s Fee Task Force Vice President Operation Get Involved, [liaison committee of the D.P.D.] Board member Dallas Homeowners League President Save Open Space Texas Steering Committee Presidential Election Award for Public Service - Mexican Government State of Texas Board of Adjustment

Monday, June 27, 2011

Aspartame Effects - At Rec. Daily Maximum Dose

The effect of aspartame administration on oncogene and suppressor gene expressions.

Gombos KVarjas TOrsos ZPolyak E,  Peredi JVarga ZNowrasteh G,

Tettinger A,  Mucsi GEmber I.

Faculty of Medicine, Institute of Public Health University of Pecs, Pecs, Hungary. katalin_gombos@yahoo.comBACKGROUND: Aspartame (L-phenylalanineN-L-alpha-aspartyl-1-methyl ester) is an artificial sweetener with widespread applications. Previously published results have shown that among rats receiving aspartame a significant increase of lymphoreticular neoplasms, brain tumours and transitional cell tumors occurred. The aim of our short-term experiment was to investigate the biological effect of aspartame consumption by determining the expressions of key oncogenes and a tumour suppressor gene.

MATERIALS AND METHODS: After one week per os administration of various doses of aspartame to CBA/CA female mice, p53, c-myc, Ha-ras gene expression alterations were determined in individual organs.

RESULTS: The results showed an increase in gene expressions concerning all the investigated genes especially in organs with a high proliferation rate: 
*lymphoreticular organs 

Aspartame has a biological effect even at the recommended daily maximum dose.

In Vivo. 2007 Jan-Feb;21(1):89-92.

PMID: 17354619 [PubMed - indexed for MEDLI

Tuesday, June 14, 2011


Dallas - Jun. 14, 2011 -- This morning I was doing some filing and came across this first letter from Sen. Teddy Kennedy to me. He was especially interested in the aspartame issue, since it can affect people with phenylketonuria. His sister, Rose [named after her mother], suffered severe mental retardation, due to intake of phenylalanine in foods. She spent her life in an institutional setting. Her condition was responsible for her family fighting for the 'heel-stick test,' given all newborns today in the hospital as a test for PKU. As a direct result of that Hearing, there is a federal law  requiring the words: Contains "Phenylalanine" to be printed on the label of every product containing aspartame. (Unfortunately, no such law protects the public against damages from the toxic Aspartame super clone: Neotame.)This is a warning to PKU individuals. There is, however, no such warning to the unidentified 20 million Carriers of the PKU gene in the US alone. Since PKU runs in his family, I certainly hope Sen. Kennedy was not ingesting anything containing aspartame, in an effort to lose weight, prior to his traumatic death from Brain Cancer (experienced in the laboratory by lab animals fed Aspartame). My husband, Mike Stoddard, died of Brain Cancer in 1985 and I know firsthand the agony it causes, not only the victim, but the family as well. I have many reports in our files on Aspartame-induced brain tumors and grand mal seizures associated with aspartame use, including those of Military and Airline Pilots and children.

I enjoyed meeting Sen. Kennedy at the Senate Hearing as we worked together to organize Aspartame Consumer Safety Network and Pilot Hotline in 1987. I also gave testimony to the Senate during that hearing, and sent out press releases letting media know of the event. Members of the press had not been contacted by anyone before I called to inform them of the hearing. It ended up being extensively covered, due to our news release. It seems, I turned out to be giving Testimony as well as being the de facto Publicist for the Sen. Hearing on the Safety of Aspartame, Nov. 3, 1987. Many breaking news stories were fed to news agencies and networks that evening, based on our original contacts with the National Media in Washington and the stories continue, 24 years later. Which prompts many to ask, "Why is Aspartame still on the market?" Our answer? "Ask the US FDA."

Hon. Mary Nash Stoddard, Founder
Aspartame Consumer Safety Network and Pilot Hotline (since 1987)
Written on US Senate Letterhead by Sen. Edward Kennedy to Mary Nash Stoddard, Founder of the original Aspartame Awareness Campaign that went international, under the expert guidance of James Turner, Esq. and Hon. Mary Nash Stoddard, in 1987:

Edward M. Kennedy
United States Senate
Washington DC 20510
August 27, 1987

Ms. Mary Nash Stoddard, President
Aspartame Victims and Their Friends
PO Box 780634 - Dallas Texas 75378

Dear Ms. Stoddard:

Thank you for your letter concerning NutraSweet (Aspartame).

I share your concern about recent studies that have shown that Aspartame may be less than totally safe. Senator Metzenbaum has raised serious questions about the safety of Aspartame, and the Senate Committee on Labor and Human Resources will most likely hold hearings in the near future on this subject. In these hearings (actually held Nov. 3, 1987), we would hope to provide an opportunity for concerned citizens, biomedical researchers, and industry representatives to provide testimony on the safety or possible toxic effects of Aspartame.

Thank you for sharing your views on this most important topic.


Edward M. Kennedy


Wednesday, June 8, 2011

MEDICINE IN OUR FOOD? (ASPARTAME NEOTAME) aka: NutraSweet, Equal, Canderel, Sweetos, etc.




Aspartame (L-aspartyl-L-phenylalanine methyl ester), a sweetener marketed under the trade name NutraSweet,* releases into the human bloodstream one molecule of methanol for each molecule of aspartame consumed.

This new methanol source is being added to foods that have considerably reduced caloric content and, thus, may be consumed in large amounts. Generally, none of these foods could be considered dietary methanol sources prior to addition of aspartame. When diet sodas and soft drinks, sweetened with aspartame, are used to replace fluid loss during exercise and physical exertion in hot climates, the intake of methanol can exceed 250 mg/day or 32 times the Environmental Protection Agency's recommended limit of consumption for this cumulative toxin.

There is extreme variation in the human response to acute methanol poisoning, the lowest recorded lethal oral dose being 100 mg/kg with one individual surviving a dose over ninety times this level. Humans, due perhaps to the loss of two enzymes during evolution, are more sensitive to methanol than any laboratory animal; even the monkey is not generally accepted as a suitable animal model. There are no human or mammalian studies to evaluate the possible mutagenic, teratogenic, or carcinogenic effects of chronic administration of methyl alcohol.

The average intake of methanol from natural sources varies but limited data suggests an average intake of considerably less than 10 mg/day 8. Alcoholics may average much more, with a potential range of between 0 and 600 mg/day, depending on the source and in some cases the quality of their beverages.

Ethanol, the classic antidote for methanol toxicity, is found in natural food sources of methanol at concentrations 5 to 500,000 times that of the toxin (Table 1). Ethanol inhibits metabolism of methanol and allows the body time for clearance of the toxin through the lungs and kidneys.

The question asked is whether uncontrolled consumption of this new sweetener might increase the methanol intake of certain individuals to a point beyond which our limited knowledge of acute and chronic human methanol toxicity can be extrapolated to predict safety.


Aspartame (L-aspartyl-L-phenylalanine methyl ester) has recently been approved as a sweetener for liquid carbonated beverages. It has had wide acceptance as an additive in many dry food applications after Food and drug Administration approval on July 24, 1981.

The Food and Drug Administration, Dr. Richard Wurtman and I have received well over a thousand written complaints relative to aspartame consumption. By far, the most numerous of these include dizziness, visual impairment, disorientation, ear buzzing, high SGOT, tunnel vision, loss of equilibrium, severe muscle aches, numbing of extremities, pancreatitis, episodes of high blood pressure, retinal hemorrhaging, menstrual flow changes, and depression. The validity of these complaints has yet to be scientifically evaluated. However, a thorough knowledge of just what makes this new sweetener stand apart from other nutritional substances might aid physicians in making dietary recommendations for their patients.

Aspartame (NutraSweet)* is a small molecule made up of three components: Phenylalanine, aspartic acid, and methanol (wood alcohol)47. When digested, these components are released into the bloodstream.

Phenylalanine and aspartic acid are both amino acids which are found in natural proteins, and under normal circumstances are beneficial, if not essential, for health. Proteins are complex molecules which contain many chemically bonded amino acids. it takes several enzymes to break these bonds and liberate the amino acids. This is a slow process and the amino acids area released gradually into the bloodstream. The quaternary structure of protein also slows the digestion of these amino acids: the amino acids in the center of the protein molecule aren't released until the outer layers of amino acids on the surface have been swept away. This natural time release process saves the body form large numbers of any one of the 21 amino acids being released into the bloodstream at any one time.

Aspartame requires the breaking of only two bonds for absorption. This happens very quickly with the potential to raise component blood levels rapidly. The methyl ester bond of phenylalanine is the first to cleave due to its susceptibility to pancreatic enzymes. This is highly unusual; the methyl esters associated with pectin for instance are completely impervious to all human digestive enzymes.


Phenylalanine is an essential amino acid, the daily consumption of which is required to maintain life. However, Dr. Richard J. Wurtman, Professor of Neuroendocrine Regulation at the Massachusetts Institute of Technology, presented data to the FDA demonstrating that in humans the feeding of a carbohydrate with aspartame significantly enhances aspartame's positive effect on plasma and brain phenylalanine and tyrosine levels (48 Federal Register at 31379). There are sound scientific reasons to believe that increasing the brain levels of these large neutral amino acids could affect the synthesis of neurotransmitters and in turn affect bodily functions controlled by the autonomic nervous system (e.g., blood pressure). The proven ability of aspartame to inhibit the glucose-induced release of serotonin within the brain may also affect behaviors, such as satiety and sleep.

Aspartic acid

Aspartic acid, is not an essential amino acid but is normally easily utilized for human metabolism. However, under conditions of excess absorption it has caused endocrine disorders in mammals with markedly elevated plasma levels of luteinizing hormone and testosterone in the rat and release of pituitary gonadotropins and prolactin in the rhesus monkey. The amount of luteinizing hormone in the blood is a major determinant of menstrual cycling in the human female.


Methanol (methyl alcohol, wood alcohol), a poisonous substance, is added as a component during the manufacture of aspartame. This methanol is subsequently released within hours of consumption after hydrolysis of the methyl group of the dipeptide by chymotrypsin in the small intestine as it occurs in soft drinks after decomposition of aspartame during storage or in other foods after being heated. Regardless of whether the aspartame-derived methanol exists in food in its free form or still esterified to phenylalanine, 10% of the weight of aspartame intake of an individual will be absorbed by the bloodstream as methanol within hours after consumption.

Methanol has no therapeutic properties and is considered only as a toxicant. The ingestion of two teaspoons is considered lethal in humans.

Methyl alcohol produces the Methyl alcohol syndrome, consistently, only in humans and no other test animal, including monkeys. There is a clear difference between "toxicity", which can be produced in every living thing, and the "toxic syndrome."


Birth defects in laboratory animals. Even the staunchest critic of formaldehyde involvement in methanol toxicity admits:

"It is not possible to completely eliminate formaldehyde as a toxic intermediate because formaldehyde could be formed slowly within cells and interfere with normal cellular function without ever obtaining levels that are detectable in body fluid or tissues."34

Acute Toxicity in man "Toxic Syndrome"

A striking feature of methyl alcohol syndrome the asymptomatic interval (latent period) which usually lasts 12 to 18 hours after consumption. This is followed by a rapid and severe acidosis caused partially by the production of formic acid. Insufficient formic acid is generated to account for the severity of metabolic acidosis produced and, therefore, other organic acids may be involved.

Patients may complain of lethargy, confusion, and impairment of articulation, all frequently encountered signs in moderate central nervous system (CNS) intoxication resulting from other toxic compounds.

Patients may also suffer leg cramps, back pain, severe headache, abdominal pain, labored breathing, vertigo and visual loss, the latter being a very important clue to making a diagnosis of methanol poisoning. Other striking clinical features associated only with the oral administration of methanol are elevated serum amylase or the finding of pancreatitis or pancreatic necrosis on autopsy.

In fatal cases, liver, kidneys and heart may show parenchymatous degeneration. the lungs show desquamation of epithelium, emphysema, edema, congestion and bronchial pneumonia.

Chronic Human Exposure

This is the most important aspect of methanol toxicity to those who are interested in observing the effect of increased methanol consumption on a population.

The data presented here were compiled by the Public Health Service. The individuals studied were working in methanol contaminated environments. It is interesting to note that the visual signs always associated with acute toxicity often do not surface under chronic conditions.

Many of the signs and symptoms of intoxication due to methanol ingestion are not specific to methyl alcohol. For example, headaches, ear buzzing, dizziness, nausea and unsteady gait (inebriation), gastrointestinal disturbances, weakness, vertigo, chills, memory lapses, numbness and shooting pains in the lower extremities . . .  hands and forearms, behavioral disturbances, and neuritis. The most characteristic signs and symptoms of methyl alcohol poisoning in humans are the various visual disturbances which can occur without acidosis although they unfortunately do not always appear. Some of these symptoms are the following: misty vision, progressive contraction of visual fields (vision tunneling), mist before the eyes, blurring of vision, and obscuration of vision.


Alcoholics in general, but particularly those who consume large quantities of wine or fruit liqueur, would seem, from the available evidence, to be the only population thus far exposed to consistently high levels of methanol ingestion (Table 1). The high ethanol/methanol ratio of alcoholic beverages must have a very significant protective effect, though enzyme kinetics mandate some constant but low level of methanol metabolism. One could speculate that the delicate balance which maintains this defense might be jeopardized by the general nutritional neglect and specifically the folic acid deficiency associated with the meager food intake of some alcoholics. Alcoholics have a much higher incidence of cancer and other degenerative diseases, none of which can be attributed to ethanol alone. The fascinating similarities linking unusual clinical features of methanol toxicity and alcoholism are worth noting.


Chronic occupational exposure to methanol often produces human complaints of neuritis with paresthesia, numbing, prickling and shooting pains in the extremities.

Alcoholic polyneuropathy or multiple peripheral neuritis 21 differs symptomatically from the methanol induced syndrome only in its first and often exclusive affinity for legs. The unpleasant sensations of intolerable pain associated with slight tactile stimulation is not an uncommon anecdotal consumer complaint following long term consumption of aspartame. In one such case reported to me, my interpretation of an electromyogram indicated the signs of denervation indicative of alcoholic polyneuropathy. The individual's ischemic lactate pyruvate curve, before and after fasting, was flat. Less that six weeks after aspartame consumption ceased the major symptoms subsided and repetition of these tests produced normal responses, although the individual still experienced intermittent pain.


Methanol is one of the few etiologic factors associated with acute pancreatic inflammation. Microscopic findings of pancreatic necrosis on autopsy have been reported after acute oral methanol poisoning. In fact, pancreatic injury probably accounts for almost universal violent epigastric pain and occasional elevated serum amylase levels which marks the end of the latent period.

There is a generally accepted association between alcoholism and pancreatitis. Most patients, however, give a history of 5 to 10 years of heavy drinking before the onset of the first attack. The fact that 40% of all cases of acute pancreatitis complaints are attributable to alcoholics, however, must be taken into consideration to avoid artifactual association. Pancreatitis has been a complaint associated with aspartame consumption.

Methanol and the Heart:

A 21-year-old non-drinking male who had been exposed daily to the fine dust of aspartame at the packaging plant he had worked in for over a year, was complaining of blurred vision, headaches, dizziness, and severe depression before his sudden death. An autopsy revealed (aside from the organ involvement one might expect from methanol toxicity) myocardial hypertrophy and dilatation with the myocardiopathy and left ventricle involvement reminiscent of alcoholic cardiomyopathy. Alcoholic cardiomyopathy however typically occurs in 30-55 year old men who have a history of alcohol intake in quantities comprising 30 to 50 percent of their daily caloric requirement over a 10 to 15 year period.

It has been suggested that alcohol is the etiologic factor in at least 50 percent of the cases of congestive cardiomyopathy. The significantly lower hospitalization incidence for coronary disease among moderate drinkers than among nondrinkers and protection to coronary risk afforded the moderate drinker (less than two drinks a day) over the nondrinker seems contradictory. However, if we implicate methanol as the etiologic factor, then clearly the nondrinker is at a disadvantage with a much lower ethanol to methanol ratio (Table 1) when consuming naturally occurring methanol in a diet otherwise equivalent to the drinkers. The chronic alcoholic for reasons already proposed might sacrifice this protection.

As mentioned below, high temperature canning as developed late in the 19th century should increase significantly the methanol content of fruits and vegetables. The increased availability and consumption of these food products in various countries over the years may parallel better than most other dietary factors the increase in incidence of coronary disease in their populations. Cigarette smoke, a known coronary risk factor, contains four times as much methanol as formaldehyde and only traces of ethanol.


The importance of ethanol as an antidote to methanol toxicity in humans is very well established in the literature. The timely administration of ethanol is still considered a vital part of methanol poisoning management. Ethanol slows the rate of methanol's conversion to formaldehyde and formate, allowing the body time to excrete methanol in the breath and urine. Inhibition is seen in vitro even when the concentration of ethyl alcohol was only 1/16th that of methanol. The inhibitory effect is a linear function of the log of the ethyl alcohol concentration, with a 72% inhibition rate at only a 0.01 molar concentration of ethanol.

Oxidation of methanol, like that of ethanol, proceeds independently of the blood concentration, but a rate only one seventh to one fifth that of ethanol.

Folacin may play an important role in the metabolism of methanol by catalyzing the elimination of formic acid. If this process proves to be as protective for humans as has been shown in other organisms, it may account, in part for the tremendous variability of human responses to acute methanol toxicity. Folacin is a nutrient often found lacking in the normal human diet, particularly during pregnancy and lactation.


An average aspartame-sweetened beverage would have a conservative aspartame content of a bout 555 mg/liter, and therefore, a methanol equivalent of 56 mg/liter (56 ppm). For example, if a 25 kg child consumed on a warm day, after exercising, two-thirds of a two-liter bottle of soft drink sweetened with aspartame, that child would be consuming over 732 mg of aspartame (29 mg/kg). This alone exceeds what the Food and drug Administration considers the 99 - percentile daily consumption level of aspartame. The child would also absorb over 70 mg of methanol from that soft drink. This is almost ten times the Environmental Protection Agency's recommended daily limit of consumption for methanol.

To look at the issue from another perspective, the literature reveals death from consumption of the equivalent of 6 gm of methanol. It would take 200 12 oz. cans of soda to yield the lethal equivalent of 6 gm of methanol According to FDA regulations, compounds added to foods that are found to cause some adverse health effect at a particular usage level are actually permitted in foods only at much lower levels. The FDA has established these requirements so that an adequate margin of safety exists to protect particularly sensitive people and heavy consumers of the chemical. Section 170.22 of Title 21 of the Code of Federal Regulations mandates that this margin of safety be 100-fold below the "highest no-effect" level has tragically not been determined for methanol, but assuming very conservatively that the level is one tenth of the lethal dose, the FDA regulations should have limited consumption to approximately 2.4 ounces of aspartame sweetened soft drink per day,

The FDA allows a lower safety margin only when "evidence is submitted which justifies use of a different safety factor." (21.C.F.R. 170.22) No such evidence has been submitted to the FDA for methanol. Thus, not only have the FDA's requirements for acute toxicity not been met, but also, no demonstration of chronic safety has been made. The fact that methyl alcohol appears in other natural food products increases greatly the danger of chronic toxicity developing by adding another unnatural source of this dangerous cumulative toxin to the food system.


Methanol does appear in nature.

To determine what impact the addition of a toxin will have on an environment it is very helpful to accurately determine the background levels of consumption.

Fruit and vegetables contain pectin with variable methyl ester content. However, the human has no digestive enzymes for pectin, particularly the pectin esterase required for its hydrolysis to methanol. Fermentation in the gut may cause disappearance of pectin but the production of free methanol is not guaranteed by fermentation. In fact, bacteria in the colon probably reduce methanol directly to formic acid or carbon dioxide (aspartame is completely absorbed before reaching the colon). Heating of pectins has been shown to cause virtually no demethoxylation: even temperatures of 120 C produced only traces of methanol. Methanol evolved during cooking of high pectin foods 7 has been accounted for in the volatile fraction during boiling and is quickly lost to the atmosphere. Entrapment of these volatiles probably accounts for the elevation in methanol levels of certain fruit and vegetable products during canning.

In the recent denial by the food and drug Administration of my request for a public hearing on this issue, the claim is made by them that methanol occurs in fruit juice at an average of 140 parts per million (a range of between 15-640 parts per million). This often used average originates from an informative table in a conference paper presented by Francot and Geoffroy. The authors explain that the data presented in the table "may not" represent their work but "other author's." There is no methodology given nor is the original source cited and only the identity of the lowest methanol source, grape juice (12 ppm), and the highest, black currant (680 ppm), are revealed. The other 22 samples used to generate this disarmingly high average are left completely to the imagination. The authors conclude their paper by insisting that "the content of methanol in fermented or non-fermented beverages should not be of concern to the fields of human physiology and public health." They imply that wines "do not present any toxicity" due to the presence of certain natural protective substances. When they present their original data relating to the methanol content of French wines (range 14-265 ppm) or when the methanol content of any alcoholic beverage is given, the ratio of methanol to ethanol is also presented. Of the wines they tested, the ratio associated with the highest methanol content (265 ppm) indicates over 262 times as much ethanol present as methanol. The scientific literature indicates that a fair estimate of methanol content of commonly consumed fruit juices is on the order of 40 parts per million (Table 1). Stegink, et al. points out that some neutral spirits contain as much as 1.5 grams/liter of methanol. What is not mentioned is the fact that if these spirits are at least 60 proof (30% ethanol) this still represents the presence of over 200 molecules of ethanol for every molecule of methanol that is digested. An exhaustive search of the present literature indicates that no testing of natural substances has ever shown methanol appearing alone. In every case ethanol is also present, usually, in much higher concentrations. Fresh orange juices can have very little methanol (0.8 mg/liter), and have a concomitant ethyl alcohol content of 380 mg/liter. Long term storage in cans has a tendency to cause an increase in these levels, but even after three years of storage, testing has revealed only 62 mg/liter of methanol, with an ethanol content of 484 mg/liter. This is a ratio of almost eight times ethanol/methanol. Testing done recently in Spain showed orange juice with 33 mg/liter methanol and 651 mg/liter ethanol (20/1 ratio). The range for grapefruit juices are similar, ranging from 0.2 mg methanol/liter to 43 mg methanol/liter. The lowest ratio of any food item was found in canned grapefruit sections with 50- 70 mg/liter methanol and 200-400 mg/liter ethanol, thus averaging six molecules ethanol for every molecule of methanol.

This high ethanol to methanol ratio, even at these low ethanol concentrations, may have some protective effect. As stated previously, ethanol slows the rate of methanol's conversion to formaldehyde and formate allowing the body time to excrete methanol in the breath and urine. Inhibition is seen in vitro even when the concentration of ethyl alcohol was only 1/16th that of methanol. The inhibitory effect is a linear function of the log of the ethyl alcohol concentration, with a 72% inhibition rate at only a 0.01 molar concentration of ethanol. Therefore if a liter of a high methanol content orange juice is consumed, with 33 mg/liter of methanol and a 20/1 ratio of ethanol/methanol, only one molecule of methanol in 180 will be metabolized into dangerous metabolites until the majority of the ethanol has been cleared from the bloodstream. If a similar amount of methanol equivalent from aspartame were consumed, there would be no competition.

Another factor reducing the potential danger associated with methanol from natural juices is that they have an average caloric density of 500 K cal/liter and high osmolarity which places very definite limits to their consumption level and rate.TABLE 1


METHANOL mg/liter METHANOL (MG.) CALORIC DENSITY Calories/Liter RATIO Consumed per 1,000 Calories *Methanol (mg.) Ethanol (wt.) Methanol (wt.) Consumption per day Juices *Orange, fresh28 1 470 2 475 1 *Orange, fresh45 33470 70206 mg *Orange, fresh31 34470 72166 mg *Orange, canned2831470 66156 mg *Grapefruit, fresh27 1 400 1 2000 1 mg *Grapefruit31 43400 108 5 7 mg Grapefruit, Canned31 27400 689 5 mg Grape15 12660 18---- Alcoholic Beverages Beer (4.5%) 0 400 ------ Grain Alcohol55 1 2950 1 500000 -- Bourbon, 100 proof55 552950 199090 -- Rum, 80 proof15 732300 325000 -- Wines

(French)15 White 32800 442500 -- Rose 78800 981000 -- Red 128 800 160 667 -- Pear 188 1370 137 250 -- Cherry 276 1370 201 294 -- Wines (American)30 Low 50800 622500 -- High 325 800 406 385 -- Aspartame Sweetened Beverages 48 2 liters 5 liters Uncarbonated Drinks48 558 6875 0 110 mg 275 mg Cola (Carbonated)48 568 7000 0 112 mg 280 mg Orange (Carbonated)48 918 11375 0 182 mg 455 mg Aspartame, pure25000 *17.6% of U.S. Population consume an average of 185.5 gm of Orange juice a day1 *1.1% of the U.S. Population consume an average of 173.9 gm of Grapefruit Juice a day1

Data obtained in a Department of Agriculture survey of the food intake of a statistically sampled group of over 17,000 consumers nationwide, indicate that the 17.6% of the population that consume orange juice daily take in an average of 185.5 gm of that juice. these statistics indicated that 1.1% of the population consume an average of 173.9 gm of grapefruit juice while only 1.8% drink approximately 201 gm of tomato juice daily. Table 1 shows that under normal conditions these individuals would only be expected to consume between 1 and 7 mg of methanol a day from the sources. Even if an individual consumed two juices in the same day or a more exotic juice such as black currant, there would still be some protection afforded by the ethanol present in these natural juices. Consumption of aspartame sweetened drinks at levels commonly used to replace lost fluid during exercise yields methanol intake between 15 and 100 times these normal intakes (Table 1). This is comparable to that of "winos" but without the metabolic reprieve afforded by ethanol. An alcoholic consuming 1500 calories a day from alcoholic sources alone may consume between 0 and 600 mg of methanol each day depending on his choice of beverages (Table 1).

The consumption of aspartame sweetened soft drinks or other beverages is not limited by either calories or osmolarity, and can equal the daily water loss of an individual (which for active people in a state like Arizona can exceed 5 liters). The resultant daily methanol intake might then rise to unprecedented levels. Methanol is a cumulative toxin 8 and for some clinical manifestations it may be a human-specific toxin.


Simply because methanol is found "naturally" in foods, we can not dismiss the need for carefully documented safety testing in appropriate animal models before allowing a dramatic increase in its consumption.

We know nothing of the mutagenic, teratogenic or carcinogenic effect of methyl alcohol on man or mammal5. Yet, if predictions are correct 5 it won't be long before an additional 2,000,000 pounds of it will be added to the food supply yearly.

Must this, then, constitute our test of its safety?


1. Agricultural Research Service, U.S. Department of Agriculture, portion sizes and days intakes of selected foods. ARS-NE-67 (1975) 

2. Bartlett, G.R., Inhibition of Methanol Oxidation by Ethanol in the Rat. Am. J. Physiol., 163:619-621 (1950). 

3. Braverman, J. B. S. and Lifshitz, A., Pectin Hydrolysis in Certain Fruits During Alcoholic Fermentation. Food Tech., 356-358. July, (1957). 

4. Browing, E., Toxicity and Metabolism of Industrial Solvents. New your: Elsevier Publishing Company, (1965). 

5. Bylinsky, G., The Battle for America's Sweet Tooth. Fortune. 28-32, July (1982). 

6. Campbell, L.A., Palmer G.H., Pectin in topics in Dietary Fiber Research, Edited Spiller, G.A. and Amen. R.J. Plenum Press, NY (1978).

follow: marystod on
Mary Nash Stoddard, Founder
Aspartame Consumer Safety Network and Pilot Hotline 
[Promoting FDA Recall of Aspartame - since 1987]
P.O. Box 2001 - Frisco, TX 75034 - U.S.
phone: 1-214-387-4001

Wednesday, June 1, 2011

Neotame NutraSweet Product Info Press Rel. (Made w/Phenylalanine Cultured in E.Coli)

NutraSweet Expects Higher Neotame Sales in 2011

Spiking sugar prices are key factor in volume growth
CHICAGO--(BUSINESS WIRE)--The NutraSweet Company said today that it expects sales volume for neotame, its most powerful sweetener ingredient, to continue to grow in 2011. According to CEO Craig R. Petray, the current imbalance in the supply and demand cycle for sugar is a key factor in the company's outlook.
"In fact, when we work on sweetener blends with customers in our SweetSpot beverage lab, we find that neotame actually enhances many flavors"
Neotame enjoyed sharply higher sales in 2010 as sugar prices rose more than 70 percent to a 30-year high. Consequently, neotame sales jumped 20 percent as manufacturers moved to find economical sugar substitutes. Sales also were aided by neotame ingredient approvals from authorities in the European Union, Norway, Turkey, Hong Kong, Vietnam and Israel. NutraSweet sells neotame in Europe through its distribution partners, Brenntag (Western & Central Eastern Europe) and Disproquima (Iberia).
Neotame has developed an important niche in the sweetener market as an ingredient that can be blended with lesser amounts of sugar in many food products. The blends yield lower ingredient costs for food and beverage makers and offer important consumer benefits such as lower sugar content and reduced calories. Neotame is 8,000 times sweeter than sugar.
As important, according to Petray, neotame can be substituted without altering the taste characteristics of favorite foods and beverages. "In fact, when we work on sweetener blends with customers in our SweetSpot beverage lab, we find that neotame actually enhances many flavors," Petray said.
Many sources say that sugar supplies are expected to be short of demand again in 2011, producing yet another period of increased price pressure. Already this year, supplies of raw sugar from Australia, the world's third largest exporter, have been hard hit by weather problems. Output from Brazil, the world's No. 1 exporter, also has experienced weather related shortfalls in recent months.
About The NutraSweet Company
The NutraSweet Company, headquartered in Chicago, produces and markets sweeteners in more than 100 countries. Its sweeteners are used in over 5,000 food and beverage products and are consumed by 250 million people worldwide. The company is owned by J.W. Childs Associates, a leading private investment firm located in Boston with substantial experience in the food, beverage and food ingredient business.


Beacon Advisors, Inc.
Hud Englehart, 773-281-1100