Tuesday, August 5, 2008

The Truth about Neotame, Acesulfame-K, Sucralose and Aspartame

Chemical Sweeteners
The Truth about Neotame, Acesulfame-K, Sucralose and Aspartame


(Please go to http://www.dorway.com/ to read all the research
about the dangers of artificial sweeteners.)

Neotame (Now found in Adkins and Hershey's products)
Neotame
is the technical name for a new sweetener developed by Monsanto Chemical Corp. It is reported to be approximately 8,000 times sweeter than sugar. The chemical formula for neotame was published in the February 10, 1998 Federal Register. It is quite similar in structure to Monsanto's toxic sweetener aspartame. There have not been any legitimate, independent, long-term human studies on neotame. It has now been approved as of July 5, 2002.


Neotame has similar structure to aspartame -- except that, from it's structure, appears to be even more toxic than aspartame. This potential increase in toxicity will make up for the fact that less will be used in diet drinks. Like aspartame, some of the concerns include gradual neurotoxic and immunotoxic damage from the combination of the formaldehyde metabolite (which is toxic at extremely low doses) and the excitotoxic amino acid. Given all of the suffering being caused by Monsanto's aspartame, the prudent course would be to start out with the assumption that it may cause toxic damage or cancer from long-term exposure and conduct many thorough, long-term, and independent human studies to see the effects.


Even Monsanto's own pre-approval studies of neotame revealed adverse reactions. Unfortunately, Monsanto only conducted a few one-day studies in humans rather than encouraging independent researchers to obtain NIH funding to conduct long-term human studies on the effects of neotame. It is obvious to anyone who has thoroughly read the scientific literature on aspartame that


1) nearly 100% of the independent studies found problems with aspartame (Monsanto's studies never showed problems); and


2) that industry-funded studies bordered on fraudulent research (and a Grand Jury was convened because the officials wanted to pursue fraud charges). Much of industry-funded research related to other Monsanto products such as rBGH and toxic carpeting is similarly deceptive and poorly designed. In addition, a "research" organization led by one of Monsanto's close business parters was caught hiding a reaction-causing substance in beverages given to control groups in double-blind studies. (They did this for 13 years!)Given all of the problems with aspartame industry research and scientific abuse, it is clear that any neotame research that Monsanto, industry groups, or consultants or research friends of Monsanto have any part of should be rejected until which time more trustworthy, independent research can be conducted.


Such experiments should include independent animals studies and especially long-term (e.g., 4-5 years+) human studies in various susceptible population groups.What is likely to happen, however, is:Monsanto's subsidiary, the FDA, will accept Monsanto research as if it were legitimate. Monsanto will given money to their research consultants at various institutions (rather than NIH funding of truly independent researchers) to repeat poorly designed tests and "confirm" neotame safety. This is what they did with aspartame so that they could claim safety. The FDA and Monsanto will claim that "comprehensive" research [by Monsanto consultants] at various institutions proves that neotame is safe. There will be alot of press releases, PR statements from their friends in the research community, and from organizations they fund (e.g., IFIC, ADA, etc.). This will be a time of a massive PR blitz.

The FDA will claim to track adverse reaction reports. But they made the same claim when they told people that had received only 16 aspartame toxicity reaction reports in 1996, but refused to tell people that they stopped taking such adverse reaction reports in early 1996.

Acesulfame-K
From the book SAFE FOOD by Michael F. Jacobson, Ph.D, Lisa Lefferts and Anne Garland

"Acesulfame K, sold commercially as Sunette or Sweet One, was approved by the FDA in 1988 as a sugar substitute in packet or tablet form, in chewing gum, dry mixes for beverages, instant coffee and tea, gelatin desserts, puddings and nondairy creamers. The manufacturer has asked the FDA to approve acesulfame K for soft drinks and baked goods. The public is waiting for an artificial sweetener that is unquestionably safe. But this one isn't it. Even compared to aspartame and saccharin (which are afflicted with their own safety publems - see below), acesulfame K is the worst. The additive is inadequately tested, the FDA based its approval on tests of acesulfame K that fell short of the FDA's own standards. But even those tests indicate that the additive causes cancer in animals, which means it may increase cancer risk in humans. In l987, CSPI urged the FDA not to approve acesulfame K, but was ignored. After the FDA gave the chemical its blessing, CSPI urged that it be banned. The FDA hasn't yet ruled on that request."
From CSPI's web page:... acetoacetamide, a breakdown product, has been shown to affect the thyroid in rats, rabbits, and dogs. Administration of 1% and 5% acetoacetamide in the diet for three months caused benign thyroid tumors in rats. The rapid appearance of tumors raises serious questions about the chemicals carcinogenic potency."

Sucralose
Splenda, also known as sucralose, is artificial sweetener which is a chlorinated sucrose derivative. Facts about this artificial chemical follows:

Pre-Approval Research

Pre-approval research showed that sucralose caused shrunken thymus glands (up to 40% shrinkage) and enlarged liver and kidneys. The manufacturer put forth two arguments in an attempt to claim that sucralose is not toxic:


The dose of sucralose in the experiments was high. However, for chemicals that do not have generations of safe use, the dosage tested must be adjusted for variations in potential toxicity within the human population and between humans and rodents. In order to this, toxicologists estimate a variation of effects in the human population of 10 times. In other words, one person may not have effects until a dose of 10 mg per kg of body weight (10 mg/kg) is reached, while another person may have chronic toxicity effects at 1 mg per kg of body weight (1 mg/kg). In addition, it is well known that many chemicals are much more toxic in humans than in rodents (or even monkeys). For example, the chemicals that the sweetener aspartame breaks down into vary from 5 to 50 times more toxic in humans than in rodents. Therefore, toxicologists estimate a further 10 times the dose for differences between human and rodent toxicity for a total of 100 times (10 * 10). In order to estimate a potential safe dose in humans, one must divide the lowest dose in given to rodents that was seen to have any negative effects on their thymus glands, liver or kidneys by 100. That dose is then known as the maximum Tolerable Daily Intake (TDI) for lifetime use. Keep in mind that the TDI is just an estimate. Some chemicals are much more than 10 times more toxic in humans than in rodents (or will cause cancer in humans in low-dose, long-term exposure and do not cause cancer in rodents at all). A person ingesting the TDI for some chemical may find that it causes cancer or immune system or neurological problems after many years or decades of use. So, if the manufacturer claims that the dose was equivalent to 50 diet sodas, then the TDI would be one half (1/2) of a diet soda, and even that dose may or may not be safe.The manufacturer claimed that the sucralose was unpleasant for the rodents to eat in large doses. They said that starvation caused the shruken thymus glands. From the New Scientist (23 Nov 1991, pg 13):[Toxicologist Judith] Bellin reviewed studies on rats starved under experimental conditions, and concluded that their growth rate could be reduced by as much as a third without the thymus losing a significant amount of weight (less than 7 percent). The changes were much more marked in rats fed on sucralose. While the animals' growth rate was reduced by between 7 and 20 percent, their thymuses shrank by as much as 40 percent.

Recent Research

A possible problem with caecal enlargement and renal mineralization has been seen in post approval animal research.
Sucralose Breaks DownDespite the manufacturer's mis-statements, sucralose does break down into small amounts of 1,6-dichlorofructose, a chemical which has not been adequtely tested in humans.

Independent, Long-Term Human Research None.

Manufacturer's "100's of studies" (some of which show hazards) were clearly inadequate and do not demonstrate safety in long-term use.

Chlorinated Pesticides

The manufacturer claims that the chlorine added to sucralose is similar to the chlorine atom in the salt (NaCl) molecule. That is not the case. Sucralose may be more like ingesting tiny amounts of chlorinated pesticides, but we will never know without long-term, independent human research.

Conclusion

While it is unlikely that sucralose is as toxic as the poisoning people are experiencing from Monsanato's aspartame, it is clear from the hazards seen in pre-approval research and from its chemical structure that years or decades of use may contribute to serious chronic immunological or neurological disorders.

Addendum (October 2, 2000)

Ocassionally, persons emailing ask questions about sucralose research. What follows is a copy of a response one such question. The answer starts by summarizing the aspartame (NutraSweet) issue and then addresses the sucralose issue.
Let me start by saying that, as you may know, there is a quickly growing body of evidence demonstrating the toxicity of aspartame. This includes:
Recent European research showing that ingesting aspartame leads to the accumulation of formaldehyde in the brain, other organs and tissues (Formaldehyde has been shown to damage the nervous system, immune system, and cause irreversible genetic damage in humans.)
An extremely large number of toxicity reactions reported to the FDA and other organizations
A recent report showing that nearly 100% of independent research has found problems with aspartame.Why is this relevent to the sucralose question? Similar to the aspartame situation 15 years ago:
Pre-approval test indicated potential toxicity of sucralose.
There are no *independent* controlled human studies on sucralose (similar to 15 years ago for aspartame).
There are no long-term (12-24 months) human studies of sucralose's effects.
There is no monitoring of health effects. It took government agencies decades to agree that there were countless thousands of deaths from tobacco. Why? Simply because there had been no monitoring or epidemiological studies. Without such monitoring and studies, huge effects can easily go unnoticed. So, without even addressing the pre-approval research showing potential toxicity, it is clear that sucralose has

a) no long history (e.g., decades) of safe use,

b) no independent monitoring of health effects,

c) no long-term human studies, and

d) no independent human studies.


I would hope that the Precautionary Principal, now commonly used in Europe, would be a guiding force for people who are interested in health. Otherwise, we might as well just use any poorly-tested, artificial (lab-created) chemical that has shown potential for long-term toxicity.

As far as the pre-approval research related to sucralose.... As you probably know, pre-approval research is rarely published. It is only available from the FDA by filing a Freedom of Information Act request. However, you can see a very short summary regarding sucralose and shrunken thymus glands in the "New Scientist" (23 November 1991, page 13).
It is very important that people who have any interest in their health stay aware from the highly toxic sweetener, aspartame and other dangerous sweeteners such as sucralose (Splenda), and acesulfame-k (Sunette, Sweet & Safe, Sweet One).

Aspartame
In 1997 there was an increase in aspartame users reporting severe toxicity reactions and damage such as seizures, eye damage and vision loss, confusion, severe migraines, tremors, depression, anxiety attacks, insomnia, etc. In the same years, Ralph Walton, MD, Chairman, The Center for Behavioral Medicine showed that the only studies which didn't find problems with aspartame where those funded by the manufacturer (Monsanto). Given the agreement amongst independent scientists about the toxicity of aspartame, the only question was whether the formaldehyde exposure from aspartame caused the toxicity. That question has now been largely answered because of research in the late 1990s.The following facts shown by recent scientific research:Aspartame (nutrasweet) breaks down into methanol (wood alcohol).
Methanol quickly converts to formadehyde in the body.
Formaldehyde causes gradual and eventually severe damage to the neurological system, immune system and causes permanent genetic damage at extremely low doses.
Methanol from alcoholic beverages and from fruit and juices does not convert to formaldehyde and cause damage because there are protective chemicals in these traditionally ingested beverages.
The most recent independent research in Europe demonstrates that ingestion of small amounts of aspartame leads to the accumulation of significant levels of formaldehyde (bound to protein) in organs (liver, kidneys, brain) and tissues.
Excitotoxic amino acids such as the one which is immediately released from aspartame likely increases the damage caused by the formaldehyde.
Readers are urged to followup by printing and reading the extensive and heavily-referenced discussion related to aspartame and methanol/formaldehyde poisoning (suitable for scientists and laypersons) at: http://www.holisticmed.com/aspartame/abuse/. This document details the research showing formaldehyde toxicity from aspartame and demonstrates the techniques the manufacturer used to help hide these facts.

Toxicity Effects of Aspartame Use
Selection of adverse effects from short-term and/or long-Term use
Note: It often takes at least sixty days without *any* aspartame or nutrasweet to see a significant improvement. Improvement in health is also often accompanied by weight loss. Check all labels very carefully (including vitamins and pharmaceuticals). Look for the word "aspartame" on the label and avoid it. (Also, it is a good idea to avoid "acesulfame-k" or "sunette.") Finally, avoid getting nutrition information from junk food industry PR organizations such as IFIC or organizations that accept large sums of money from the junk and chemical food industry such as the American Dietetic Association.

seizures and convulsions
dizziness
tremors
migraines and severe headaches (Trigger or Cause From Chronic Intake)
memory loss (common toxicity effects)
slurring of speech
confusion
numbness or tingling of extremities
chronic fatigue
depression
insomnia
irritability
panic attacks (common aspartame toxicity reaction)
marked personality changes
phobias
rapid heart beat, tachycardia (another frequent reaction)
asthma
chest pains
hypertension (high blood pressure)
nausea or vomitting
diarrhea
abdominal pain
swallowing pain
itching
hives / urticaria
other allergic reactions
blood sugar control problems (e.g., hypoglycemia or hyperglycemia)
menstrual cramps and other menstraul problems or changes
impotency and sexual problems
food cravings
weight gain
hair loss / baldness or thinning of hair
burning urination & other urination problems
excessive thirst or excessive hunger
bloating, edema (fluid retention)
infection susceptibility
joint pain
brain cancer (Pre-approval studies in animals)
death

Aspartame Disease Mimmicks Symptoms or Worsens the Following Diseases
fibromyalgia
arthritis
multiple sclerosis (MS)
parkinson's disease
lupus
multiple chemical sensitivities (MCS)
diabetes and diabetic Complications
epilepsy
alzheimer's disease
birth defects
chronic fatigue syndrome
lymphoma
lyme disease
attention deficit disorder (ADD and ADHD)
panic disorder
depression and other psychological disorders

*Note: These statements have not been evaluated by the U.S. Federal Drug Administration ("FDA"). These products are not intended to diagnose, treat, cure or prevent any disease.

Your Nails As Evidence Of Your Health

Nail Your Health!


Lengthwise grooves of ridges
May indicate a kidney disorder and is associated with aging.
An iron deficiency may also cause ridges.


Brittle nails
Signify possible iron deficiency and thyroid problems, impaired kidney function, and circulatory problems.


Yellow nails
Can indicate internal disorders long before other symptoms appear.
Some of these problems with the lymphatic system, respiratory disorders, diabetes, and liver disorders.


Nails that chip, peel, crack, or break easily
Show a nutritional deficiency and insufficient hydrochloric acid and protein.
Minerals are also needed.


Brittle, soft, shiny nails without a moon
May indicate an overactive thyroid.


White lines across the nail
May indicate a liver disease.


White lines length wise
Show possible heart disease, high fever, or arsenic poisoning.


Nails separated from the nail bed
May signify a thyroid disorder.


Nails raised at the base ("clubbing") with small white ends
Show a respiratory disorder such as emphysema or chronic bronchitis.
("Clubbing" with lung disorders is one condition of the nails that is recognized by Standard Medicine.)


Downward curved nail ends
May denote heart, liver, or respiratory problems.


Ridges running up and down the nails
Indicate a tendency to develop arthritis.


Lack of vitamin A and calcium causes dryness and brittleness.


Vitamin B deficiency causes fragility, with horizontal and vertical ridges.


Insufficient intake of vitamin B 12 leads to excessive dryness, very rounded and curved nail ends, and darkened nails.


White bands can indicate protein deficiency.
Call Nutritional Living at 1-800-620-9975 today!


*Note: These statements have not been evaluated by the U.S. Federal Drug Administration ("FDA"). These products are not intended to diagnose, treat, cure or prevent any disease.

Natural Immune System Nutrients

A. Proteolytic Enzymes
Refers to enzymes that digest protein.
Long history in cancer treatment.
Increases the manufacture of cancer-blocking antiproteases.
Inhibits angiogenesis and metastasis.
Enhance the immune response.
Modest increases of life expectancy.
Fights against viral infections as a result of chemo-induced immune suppression.
Breast, lung, stomach, head & neck, ovaries, cervix, colon, lyphomas and multiple myeloma.
Safe and effective.
Do not use 2 – 3 days before and after surgery, may increase the risk of bleeding.

B. Curcumin
Yellow pigment of Turmeric.
Significant anti-inflammatory and anticancer effects.
Research states curcumin causes cancer to regress, means to grow smaller.
Inhibits the formation of cancer-causing nitrosamines.
Enhances the body’s production of cancer-fighting compounds such as glutathione.
Promotes the liver’s proper detoxification of cancer-causing compounds.
Prevents overproduction of cyclooxygenase 2 (COX-2), an enzyme that can contribute to the development of tumors.
Inhibits cancer cells from growing.
Inhibits angiogenesis – means it stops the formation of new blood vessels to feed a growing tumor.
Inhibits nuclear factor kappa beta – A protein that many cancers produce to block the signals commanding it to stop growing.
Increases the expression of the nuclear p53 protein. This protein is essential for apoptosis, the normal process of cell suicide.
Inhibits growth-promoting enzymes.
Fights against prostate, breast, skin, colon, stomach and liver cancer.
Can be used during chemotherapy and radiation.

C. Quercetin
Most common flavonoid in the human diet.
Most effective flavonoid to inhibit tumor formation.
Keeps cancer cells from dividing. In human breast cancer cells, the presence of mutant p53 protein – a common cancer mutation – leads to uncontrolled cell growth and cancer. Quercetin suppresses the production of mutant p53 protein to nearly undetectable levels.
Inhibits enzymes known as tyrosine kinases. When activated, tyrosine kinases send powerful signals to the nucleus telling cancer cells it’s time to divide.
Inhibits cancer cell growth, but they don’t usually kill cancer cells.
The first tyrosine kinases-inhibiting compound ever tested in a human trial.
Further research is needed to determine which types of cancer are most likely to benefit from its use.
May treat breast cancer, lung, skin, ovaries, colon, rectum, and brain.
Enhances the effects of chemotherapy while reducing its side effects. May be helpful in leukemia.
Take with proteolytic enzymes to enhance absorption.

D. Maitake MD-Fraction
Effective taken by mouth. Reishi is effective only by injection.
30% more active than D-Fraction.
Consist of polysaccharides known as beta glucans. An ideal beta glucan source. Beta glucans from a yeast source may not be well absorbed.
The beta glucan activity of MD-Fraction is like a key inserted into a lock, they turn on the white blood cells, thus increasing the immune system.
Protects healthy cells from becoming cancerous.
Enhances the immune system’s ability to seek out and destroy cancer cells.
Helps the cell regain control of cell division and programmed cell death (apoptosis).
Helps to prevent the spreading (metastasis) of cancer.
Has greater effect on inhibiting tumor growth and white blood cells.
Can be used during chemo and radiation, treatments which destroy white blood cell production.
Inhibits tumors in colon, lungs, stomach, liver, prostate, cervix, bladder, and brain. Leukemia.
In a 1994, Chinese scientists showed the regression of tumors in 73% of breast cancer patients; 67% of lung cancer, 47% of liver cancer.
In 1998, the FDA approved a detailed pilot study on maitake D-fraction’s effects on advanced breast and prostate cancers.

E. Graviola
Significant anti-tumor properties
Toxic to cancer cells without harming healthy cells
8 published clinical studies
Anti-cancerous, anti-tumorous, antiviral
Inhibits enzyme processes that are only found in the membranes of cancerous tumor cells. This is why they are toxic to cancer cells.
The National Cancer Institute has funded research on Graviola.
Purdue University has filed at least nine patents on the properties of Graviola.
Has shown to kill tumors which were resistant to other anti-cancer agents.
Cancer cells that survive chemotherapy develop a resistant to the chemo. 2% of the cancer cells will become resistant and these are the ones which become multi-drug resistant.
Graviola has shown to kill these cells which become multi-drug resistant.
For cancer (all types)
As a broad-spectrum internal and external antimicrobial to treat bacterial and fungal infections
For internal parasites and worms
For high blood pressure
For depression, stress, and nervous disorders

F. PSK/PSP
Known as Krestin.
PSK/PSP are closely related protein-bound polysaccharides from the cloud fungus mushroom (Coriolus veriscolor).
Contains active beta glucans to enhance immune function.
Not necessary to take both PSK/PSP and MD-Fraction. Take one or the other.
Inhibits the growth of virtually every type of cancer.
Enhances the positive effects of chemo while reducing side effects.

G. Polyerga (Polyerga Plus)
Highly purified extracts of peptides from the spleens of pigs.
Found by accident. In WWII, there was a shortage of pigs to extract insulin from their pancreases, including spleens. Walter Kuhlmey found that pig spleen extract had insulin-like activity, but it also increased energy. He started to sell it under the name of Polyerga.
In 1951, an oncologist started to treat a terminally ill patient who was diagnosed with pancreatic cancer, a cancer which is rarely overcome. The doctor gave her injections of Polyerga to ease her suffering. The results shocked the physician. Her pain was reduced, she had energy, she felt live again. She lived for another three years and died from causes unrelated to the cancer. At the autopsy, pathologists discovered the pancreatic tumor, once the size of an egg was completely gone.
Increases white blood cell count. Take during chemo to prevent suppression of white blood cell formation.
Prevents chemotherapy side effects.
Enhances the effectiveness of chemotherapy and radiation.
Prevents metastasis.
Enhances general well-being, improving energy levels and preventing weight loss.
Increases the quality of life and the survival time of cancer patients.
Use for breast, colon, carcinomas. Lung cancer patients didn’t responds well.
Start as soon as possible upon diagnosis of cancer.

H. Modified Citrus Pectin
Obtained from the peel and pulp of citrus fruits.
Reduces the risk of metastasis.
Blocks the cancer cell’s ability to clump and spread.
No direct anticancer effect, but should be used to prevent the spread of cancer.
Ideal to use when a biopsy or cancer surgery is recommended. This prevents metastasis caused by these procedures.
Prevents metastasis of breast, prostate, lung, and melanoma.

I. IP6
Experts recommend a high fiber. IP6 is possibly responsible for the protective effects against cancer.
Found mainly in the fiber from whole grains and legumes.
Converts into IP3. When IP3 is low in cancer cells, they replicate our of control. But when the levels of IP3 are increased, the cancer cells turn themselves off.
Stimulates the activity of the white blood cells known as natural killer cells. NK cells literally kill cancer cells, viruses.
Fights against breast, prostate, lung, skin, brain, lymphomas and leukemia.
Can be used in conjunction with chemo and radiation.
Shown to enhance these therapies.