Posts Tagged ‘FDA’

5 Hidden Health Dangers

November 2nd, 2009

I’ve always said – stay away from foods that are advertised.

The food conglomerates are out to make as much money as possible with little regard to our health. They want us to believe their packaged foods are healthy but that couldn’t be further from the truth.

Here are 5 hidden health dangers found in most of the foods in your local grocery store.

1. BHA and BHT

BHA and BHT are antioxidants, mainly used to stabilize fats and oils in package foods. But they aren’t the good kind of antioxidants…at least not for your body. Food manufacturers use these compounds because oxygen reacts preferentially with BHA or BHT, rather than oxidizing fats or oils, thereby protecting the food from spoilage. As a result, the food can last longer on the shelf.

BHA and BHT are fat-soluble which should set off some alarm bells since any compound (good or bad) that is fat soluble will accumulate in the fat stores within the body. If this accumulation persists over time, toxicity results and serious health problems can arise.

In addition to preserving foods, BHA and BHT are also used to preserve fats and oils in cosmetics and pharmaceuticals.

What Foods Contain BHA and BHT?

BHA is generally used to keep fats from becoming rancid; however, it is also used as a yeast de-foaming agent. BHA is mainly found in butter, meats, cereals, chewing gum, baked goods, snack foods, dehydrated potatoes, and beer. It is also found in animal feed, food packaging, cosmetics, rubber products, and petroleum products.

BHT also prevents oxidative rancidity of fats. It’s main role is to preserve food odor, color, and flavor. Many packaging materials incorporate BHT. You’ll often see “BHT added to preserve freshness” in the ingredient list of many common packaged foods such as shortening, cereals, and other foods containing fats and oils.

Are BHA and BHT Safe?

Of course not! If they were, they probably wouldn’t be included in this list of harmful food additives, would they now? Both BHA and BHT have undergone the additive application and review process required by the US Food and Drug Administration. However, the same chemical properties that make BHA and BHT desired preservatives also implicate them in many negative health side effects.

BHA, especially, is known to have serious detrimental effects in the human body. Both BHA and BHT have been shown to contribute to cancer and tumour growth.

According to a German study “…Specific toxic effects to the lung have only been observed with BHT. However, BHA induces in animals tumours of the forestomach, which are dose dependent, whereas BHT induces liver tumours in long-term experiments. … all published findings agree with the fact that BHA and BHT are tumour promoters.”

There is also evidence that many people have difficulty metabolizing BHA and BHT, resulting in health issues such as:

• liver and kidney damage,
• behavioral problems,
• infertility,
• weakened immune system,
• birth defects,
• cancer (IARC Group 2B)

BHA should definitely be should definitely be avoided by infants, young children, pregnant women and those sensitive to aspirin..

There is less extensive human data on BHT; however, studies show cancer-causing effects in animals. For example, according to the Crisp Data Base National Institutes Of Health 1999:

“…The food additive, butylated hydroxytoluene (BHT), encourages the development of tumors from previously initiated cells…in mice…”

The IARC classes BHT as a Group 3 food additive and interestingly enough, it is banned in England. Why not anywhere else???

So the bottom line is to avoid these harmful food additives. Just another reason to eat more natural whole foods.

2. Sodium Nitrite

As a food additive, the lethal sodium nitrite serves a dual purpose in the food industry since it both alters the color of preserved fish and meats and also prevents growth of Clostridium botulinum, the bacteria which causes botulism.

Thus, food manufacturers mainly use sodium nitrite because of its “beautifying” effect on meat, turning it from an ugly brown to an attractive glowing red! Sodium nitrite is most commonly used in processed meats, such as bacon, ham, hot dogs, bologna, liver pate, and many more.

In Europe, sodium nitrite has the E number E250.

While this chemical will prevent the growth of bacteria, it has been well documented to be highly toxic for humans (and other animals).

Various dangers of ingesting this food additive have been suggested and researched by scientists. A principal concern is the formation of carcinogenic nitrosamines by the reaction of sodium nitrite with amino acids in the presence of an acidic environment such as the human stomach.

Numerous studies have found a link between high processed meat consumption and colon cancer, due to the presence of sodium nitrite. A large review of the literature (comprising 17 studies) dramatically revealed that processed meat intake (including sausages, meat burgers, ham, bacon, salami, nitrite-treated meat and meat products) increases the risk of colorectal cancer by a whopping 49%!

Recent studies have also found a link between frequent ingestion of proceesed meats cured with nitrites and the Chronic Obstructive Pulmonary Disease (COPD) form of lung disease as well as the onset of severe migraine headaches.

If you haven’t been able to tell by now, the presence of sodium nitrite in food is controversial due to the development of cancer-causing nitrosamines, which arise when the cured or processed meat is cooked at high temperatures, as well as, when it is presented to an acidic environment like our stomach.

These nitrosamines are produced when nitrites and secondary amines (usually proteins) react in a strongly acidic environment (such as our stomach) or at high temperatures, as in frying. Heating foods, especially frying them in rancid oils, is by far one of the most dangerous things you can do to your foods and to your body. And it follows that such cooking practices may be significantly linked to thousands of cases of colon cancer per year across the world.

Considering their carcinogenic capability, it’s amazing that nitrosamines are still found in so many types of foods, especially beer, fish (and fish byproducts), processed and cured meat, and cheese products preserved with nitrite pickling salt. However, since nitrosamines are not actually considered a food additive per se (just the by-product of one), the regulation of this chemical has been lax, to say the least.

But there is hope – if you want to call it that. Recently, the U.S. government established limits on the amount of nitrites used in meat products in order to decrease cancer risk in the population. Rules have also been established forcing food manufacturers to add ascorbic acid or related compounds to meat, because they tend to inhibit nitrosamine formation.

Regardless of governmental efforts, the fact still remains that a carcinogenic additive is in our food supply. How can there be a safe or acceptable level of any compound that causes cancer? It only makes sense that, over time, any additive like sodium nitrite will accumulate in the body and wreak havoc when it reaches a threshold amount.

Oh…I just about forgot to mention that other epidemiological data also suggests that nitrosamines (via sodium nitrite) in preserved foods cause stomach cancer! As if colon and colorectal cancer were not enough.

It’s no surprise then that the International Agency for Research on Cancer has labeled sodium nitrite as Group 2A food additive, meaning that it is “probably carcinogenic to humans”.

3. Sulfites

If you’re like me – someone who is allergy prone and has asthma – then you will want to pay close attention to this commonly used food additive.

Sulfites, also labeled as sulfur dioxide, sodium bisulfite, potassium bisulfite, potassium metabisulfite, sodium metabisulfite, or sodium sulfite, are preservatives used to prevent discoloration and bacterial growth.

Sulfites are commonly used to prevent discoloration in dried fruit, some “fresh” shrimp, and some potatoes. They are also abundantly found in wines and many beers. Other examples of foods that may contain sulfites include: baked goods, soup mixes, jams, canned vegetables, pickled foods, gravies, dried fruit, potato chips, trail mixes, beer and wine, vegetable juices, sparkling grape juice, apple cider, bottled lemon juice and lime juice, tea, many condiments, molasses, fresh or frozen shrimp, maraschino cherries, and dehydrated, pre-cut or peeled potatoes.

Dried Apricots – Brown or Orange?

One of the more deceiving tactics used by food manufacturers is the use of sulfites in dried fruit to preserve a “more attractive colour”. For instance, organic dried apricots (which don’t contain sulfites) have a deep brown colour. However, non-organic dried apricots (which contain sulfites) remain the yellow-orange colour most of us associate with fresh apricots.

Although the non-organic dried apricots are not nearly as healthy for us, they tend to be better sellers simply because they look more attractive to consumers. Remember, food labeling and packaging comes down to what’s going to sell the most – regardless of its health effects! So choose organic dried fruit whenever possible.

The issue with sulfites is that they can trigger mild to severe allergic reaction in about 1% of the population. In fact, the Food and Drug Administration (FDA) estimates that one out of a hundred people is sulfite-sensitive, and that 5% of those who have asthma, like myself, are also at risk of suffering an adverse reaction to the substance. As with food sensitivity, you can develop sensitivity to sulfites at any time in life, and the cause of sensitivity is unknown.

I can speak from personal experience that consuming foods that have sulfites instantly worsens my asthma, causes my face to go flush, and creates irritability. For that reason, I have limited my wine consumption (and other sulfite-infested foods) to virtually never drinking it, except for on special occasions. Can you relate?

Deadly Reactions Leading to Legislation

To non-sensitive individuals, sulfites are generally safe. But if you think you may be sensitive, avoid all forms of this additive, because it caused at least twelve identifiable deaths in the 1980s and probably many, many more in the preceding decades. Deaths and less severe reactions were linked most commonly to restaurants foods. Sulfite levels in the lettuce and potatoes served at restaurants were often extremely high, because workers would allow the vegetable to sit in a sulfite solution for far too long a time.

From 1980 to 1999, the FDA received 1,132 reports of bad reactions to sulfites. More than 90 percent of them occurred in restaurants or other places outside the home. But the number of reported reactions has averaged only about ten a year since 1996, and no deaths have been recorded since 1990. That steep decline was mainly due to the waged a four-year campaign to get the FDA to ban sulfites from food by the Center for Science in the Public Interest (CSPI), starting in 1982.

The tricky thing is that, by law, adverse reactions to drugs must be reported to the FDA by doctors or pharmaceutical companies, yet with sulfites and other food ingredients, reporting is voluntary, making it difficult to say just how many people may be at risk.

In 1986, as a result of pressure from the Center for Science in the Public Interest (CSPI), a congressional hearing, and media attention, the FDA banned the most dangerous uses of sulfites and required that wine labels list sulfite, when used. Furthermore, the FDA banned the use of sulfites on fruits and vegetables that are eaten raw, such as lettuce or apples. Regulations now also require manufacturers who use sulfites in their processed products to list the compounds on their product labels.

But the FDA has yet to act on CSPI’s request to require restaurants to disclose which of their foods contain sulfites.

Complicating matters, scientists have not pinpointed the smallest concentration of sulfites needed to provoke a reaction in sensitive or allergic persons. The FDA requires food manufacturers and processors to disclose the presence of sulfiting agents in concentrations of at least 10 parts per million (that’s 1 part sulfite to 100,000 parts of food–the equivalent of a drop of water in a bathtub), but the threshold may be even lower.

But how much of a poison should be allowed in the body? In mind, none!

Doctors believe that asthmatics develop difficulty breathing by inhaling sulfite fumes from treated foods. In a severe reaction, an overwhelming degree of bronchial constriction occurs, causing breathing to stop. This can lead to lack of oxygen reaching the brain, heart, and other organs and tissues and, possibly, a fatal heart rhythm irregularity. Yet it is not known which comes first, the asthma or the sulfite sensitivity.

Avoiding foods that contain or are likely to contain sulfites is the only way to prevent a reaction. If you are sensitive to sulfites, be sure to read the labels on all food items. When eating out, ask the chef or server if sulfites are used or added to food before or during preparation. If they don’t know, then ask to see the packaging of any foods that are not fresh.

4. Monosodium Glutamate (MSG)

What if I were to tell you that an addictive chemical added to your food could cause brain damage, migraine headaches, obesity, numbness, tingling, tightness of the chest, asthmatic attacks, hives, skin rashes, dizziness, heart palpitations, weakness, nausea/vomiting, abdominal cramps, chills, diarrhea, heartburn, unusual thirst, unusual perspiration, flushing sensation in the face or chest, seizures, tachycardia, and depression, and that this chemical could effect how your children’s nervous systems formed during development so that in later years they may have learning or emotional difficulties?

Further, what if it could cause or precipitate Alzheimer’s, Parkinson’s Disease, ALS, and Huntington’s Disease?

Pretty scary, right? Well, welcome to the wonderful world of monosodium glutamate (or MSG)! What you’re about to discover are some of the most horrific displays of humanity, and all because of the all mighty dollar!

What is MSG?

MSG is a chemical that is added to food to enhance its flavour. It is also highly regarded by food manufacturers as it creates addictive qualities in the foods in which it is present. This means consumers keep coming back for more because they just can’t get enough. As Pringles potato chips slogan says “Once you pop, you can’t stop!”

MSG is present in almost every single packaged and processed food! And why wouldn’t it? Big food conglomerates know that adding MSG to foods makes them more “tasty” and addictive. Ultimately, this means repeat sales and a sweeter bottom line for these corrupt food peddlers.

MSG is manufactured through a process of protein hydrolysis (which means separation with water). Manufactured free glutamic acid (MSG) is glutamic acid that has been freed from protein through a manufacturing process, or glutamic acid that has been grown from selected bacteria that secrete glutamic acid through their cell walls.

The important thing to remember is that this form of glutamic acid is NOT THE SAME as the L-glutamic acid which is a naturally occurring amino acid within our body and in nature. Food manufacturers claim that MSG couldn’t possibly harm you because it is “naturally occurring,” (not really as we just mentioned) but even if it were so too are arsenic and hydrochloric acid. You don’t see us consuming those “natural” products.

MSG is made up of L-glutamic acid and D-glutamic acid, and may bring with it pyroglutamic acid, mono and dichloro propanols (which are carcinogenic), heterocyclic amines (which are also carcinogenic), and other harmful contaminants (more on this later).

When a product is 99% pure MSG, the product is called “monosodium glutamate” by the FDA and must be labeled as such. However, when a hydrolyzed protein contains less than 99% MSG, the FDA does not require that the MSG be identified.

Therefore, MSG is easily and often masked and commonly found in other ingredients such as hydrolyzed vegetable protein, malt extract, hydrolyzed protein, malt flavouring, hydrolyzed plant protein, bouillon, plant protein extract, broth, sodium caseinate, stock, calcium caseinate, flavouring, and yeast extract.

Toxic Reactions to MSG

The first published report of a reaction to MSG appeared in 1968 when Robert Ho Man Kwok, M.D., who had emigrated from China, reported that although he never had the problem in China, about 20 minutes into a meal at certain Chinese restaurants, he suffered numbness, tingling, and tightness of the chest that lasted for approximately 2 hours. This became known as the “Chinese-Restaurant Syndrome”.

The following year, John W. Olney, M.D. reported that laboratory animals suffered brain lesions and neuroendocrine disorders after being exposed to MSG.

At the same time, scientists studying retinal degeneration in mice treated with MSG had noted that these mice became grotesquely obese. Olney, who speculated that the obesity might be a sign of damage to the hypothalamus (the area of the brain that regulates a number of endocrine functions, including weight control), found that infant laboratory animals given MSG suffered brain damage immediately, and presented neuroendocrine disorders later in life.

In the years that followed, neuroscientists replicated the work of Olney, and Olney spoke out repeatedly about the toxic potential of MSG, causing manufacturers of baby foods (ie. Gerber) to voluntarily remove MSG from their products. However, these companies cleverly replaced the monosodium glutamate with MSG-containing ingredients such as autolyzed yeast and hydrolyzed vegetable protein until the late 1970s when finally manufacturers voluntarily removed all obvious MSG-containing ingredients from baby food.

It has been well established that MSG poses the greatest danger to children. Hundreds of studies have shown that MSG kills brain cells and causes neuroendocrine disorders in laboratory animals and humans (especially in young ones).

Scientists also know that the blood brain barrier, once thought to prevent glutamate (amino acid in MSG) from entering the brain, is not fully developed until puberty and becomes more permeable with age. As a result, scientists have regarded MSG (and its resulting “glutamate cascade”) to be highly dangerous to children, as well as, a contributing factor to a number of age-related disease conditions such as ALS, Alzheimer’s disease, seizures, and stroke.

Scientists also understand that MSG is simply processed free glutamic acid, and that glutamic acid is a neurotransmitter that causes nerves to fire; and when present in excess quantities, causes nerves to fire until they die. This is one of the reasons that MSG has such detrimental effects on the brain and nervous system.

Considering that more than 25% of the population is known to be sensitive to MSG, its presence in our foods is a frightening reality. However, its effects varies greatly from one person to the next.

For instance, some people eat MSG and react immediately, while some others can react as late as 48 hours (or even 72 hours) after ingesting MSG. However, it is helpful to know that each person typically reacts within one predictable time frame after ingesting MSG. In my case, I experience tightness in my breathing with subsequent wheezing within just a few hours after eating ingesting foods with MSG. For me, this is pretty consistent observation.

Reactions to MSG are also dose related. Some people cannot tolerate even the smallest amount of MSG without having a reaction, whereas others tolerate single small amounts, but react to MSG when they ingest a gram or more in any one meal. Other people can ingest five grams or more without experiencing a reaction but may eventually fall prey to the adverse effects of cumulative MSG consumption.

The obvious goal is to minimize and eliminate MSG from your diet as best as possible!

5. Artificial Colourings (Food Dyes)

Most artificial colourings are synthetic chemicals that do not occur in nature. The use of coloring simply indicates that fruit or another natural ingredient has not been used. Because of this, as well as the fact that colourings are used almost solely in foods of low nutritional value (candy, soda pop, gelatin desserts, etc.), you should simply avoid all artificially coloured foods.

The main role of artificial colourings is to render foods more acceptable and attractive to food consumers. However, the use of colour can conceal the “true identity” of a food that may be damaged or inferior to another product. Colours can help make a food look better than it really is. Take for example the numerous rainbow coloured kids cereals, sugar filled energy drinks, and countless candies on the market that offer little to no nutritional value.

In 1960, the U.S. government ordered retesting of all food colourings on the market. At the time there were 140 such colours. Today there are only 9 that are deemed as safe for human consumption! As you are about to learn, some of these colourings are still from safe if consumed on a regular basis.

Below is a list, description, and word of caution of the some of the most commonly used artificial colourings found in our food supply.

FD and C Blue NO. 1

This “Briliant Blue” colouring, a derivative of coal-tar, is frequently used in bottle soft drinks, gelatin desserts, ice cream, candy, confections, cereals, baked goods, and puddings.

It may cause allergic reactions in hypersensitive individuals and was shown to produce malignant tumours when ingested by and injected into rats. In 2003, the FDA warned of several reports of toxicity, including death, associated with FD and C Blue No.1 (aka. Blue 1).

Considering these findings, it is amazing that Blue 1 is still allowed in so many foods. I often see athletes guzzling down liters of “antifreeze-coloured” sports drinks. They may be replenishing their fuel stores but at what cost? Apparently, the WHO does not mind as it classifies this food dye as “completely acceptable” for food use. It is even a permanent fixture on the FDA’s list of colour additives.

FD and C Blue NO. 2

Another derivative of coal-tar, this indigo or royal blue colouring is used in bottled soft drinks, baked goods, cereals, candy, confection, and dry drink powders. Like Blue 1, it can cause allergic reactions in sensitive individuals and has shown to produce malignant tumours in rats.

The largest study on Blue 2 suggested, but did not prove, that this dye caused brain tumors in male mice. The FDA concluded that there is “reasonable certainty of no harm.” And, the WHO’s toxicology rating indicates that the data on Blue 2 is not entirely sufficient to meet requirements acceptable for food use. Interesting, though, that it is still in so many foods!

FD and C Citrus Red No. 2

For beautifying purposes, this food dye has been permitted to colour the skin of oranges.
This, despite findings in 1960 that Citrus Red 2 damages internal organs and acts as a weak carcinogenic additive. Since most oranges are picked before they are fully ripe, this dye is added to enhance their orange-red glow! After all, who would want to buy a green skinned, unripe orange?

The WHO claims that the Citrus Red 2 can cause cancer and that the toxicological data previously available has been inadequate to determine a safe intake level. As such, it recommends that Citrus Red 2 not be used as a food colouring. Nevertheless, the FDA has approved its use despite several rodent studies showing potential for inducing bladder and urinary cancers.

It has been said that this dye does not seep through the orange skin into the pulp and that there is no risk of Citrus Red 2 intake except for when eating the peel. Knowing full well that many pesticides can indeed penetrate the peel and skin of many fruits, I prefer not to believe what the “experts” deem as safe when it comes to the penetrating potential of such food colourings.

The frustrating part is that where on an orange do you find a label noting the presence of this food dye?

FD and C Red No. 3

One of the most harmful food colourings; found in maraschino cherries, bubble gum, snack foods, candy, baked goods, hot dogs, barbecue potato chips, cereals, cherry pie mix, toothpaste, and oral medications.

Red 3 has been determined a carcinogen. The evidence that this dye caused thyroid tumors in rats is “convincing,” according to a 1983 review committee report requested by FDA. The FDA’s recommendation that the dye be banned was overruled by pressure from the Reagan Administration.

Other reports by the National Institutes of Health (NIH) revealed that Red 3 may interfere with the transmission of nerve impulses in the brain.

Eventhough it was banned from cosmetic use in 1990, Red 3 is still permitted for use in foods and oral medications, by the FDA. Shocking really, considering the 1996 findings of researchers at Northeastern Illinois University who showed that Red 3 causes and promotes the proliferation of human breast cancer cells, even at very low doses.

FD and C Red No. 40

This is the newest and most widely used food dye. While this is one of the most-tested food dyes, the key tests on mice have been flawed and inconclusive. However, many scientists urge interpreting these “flawed” results with a grain of salt since all the tests on Red 40 were conducted by the manufacturer! An FDA review committee acknowledged problems, but said evidence of harm was not “consistent” or “substantial.” Like other dyes, Red 40 is used mainly in junk foods, drug, and cosmetics.

The National Cancer Institute reported that p-credine, a chemical used in the preparation of Red 40 is carcinogenic in animals and at high doses causes adverse reproductive effects.

Nonetheless, Red 40 is a permanent resident on the FDA’s “approved” additives for food list.

FD and C Yellow No. 5

The second most widely used coloring, also known as Tartrazine, is a lemon yellow coal-tar derivative, and is used in many breakfast cereals, jellies, bottled soft drinks, gelatin desserts, ice cream, candy, confections, baked goods, spaghetti, and puddings.

Yellow 5 is also used in more than 60% of both over-the-counter and prescription drugs. An ironic, yet scary, truth considering Yellow 5 can trigger severe allergic reactions such as life threatening asthmatic symptoms in individuals sensitive to aspirin and close to 100,000 other people in North America.

Yellow 5 became a permanently listed colour additive without restrictions after “interested parties” (ie. the colour industry) objected to the FDA’s 300 ppm in food limit in 1966. However, since 1981, Yellow 5 is required to be listed on any labels in which it is found.

The WHO also lists this food colour as “acceptable in food”.

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Coke Zero Gets a Big ZERO!

August 20th, 2009

coke_2I’m sure by now everyone in the world has been subjected the comical Coke Zero commercials with the talking eyeball and tongues, right?

But is it really that funny?

Not when you think of the health consequences of their newest product – Coke Zero.

Coke Zero is sweetened with aspartame and acesulfame potassium (ace-k) and has zero calories. The only chemical difference between Coke Zero and Diet Coke is that Coke Zero has about half the aspartame but has more acesfulfame potassium.

I spent a good deal of time dissecting the dangers of consuming aspartame in 2 previous posts so in this post we’re going to look at Coke Zero’s other deadly ingredient…

Acesulfame Potassium

Acesulfame potassium is a calorie-free artificial sweetener, also known as Acesulfame K or Ace K (K being the symbol for potassium). It more commonly known, and marketed, as Sunett and Sweet One and manufactured by Hoechst, a giant German chemical company. In the European Union, it is known under the E number (additive code) E950.

Acesulfame K is 180-200 times sweeter than table sugar, as sweet as aspartame, about half as sweet as saccharin, and one-quarter as sweet as sucralose. Like saccharin, it has a slightly bitter aftertaste, especially at high concentrations. However, clever marketers at Kraft Foods have patented the use of sodium ferulate to mask acesulfame’s aftertaste.

To make our taste buds sizzle even more, Acesulfame K is often blended with other sweeteners (usually sucralose or aspartame). These blends are reputed to give a more sugar-like taste whereby each sweetener masks the other’s aftertaste, and/or exhibits a synergistic effect by which the blend is sweeter than its components.

The reason food manufacturers love using acesulfame K is that, unlike aspartame, it is stable under heat and in moderately acidic or basic conditions, allowing it to be used in baked goods, chewing gum, gelatin dessets, and in other products that require a long shelf life. In July 1998, the FDA allowed this chemical to be used in soft drinks, thereby greatly increasing consumer exposure. In these carbonated drinks, it is almost always used in conjunction with another sweetener, such as aspartame or sucralose.

Flawed FDA Studies and Cancer Concerns

A blog post (July 1, 2008) by the nutrition expert at About.com claimed that this sweetener is not toxic and has no detrimental effects on the body! WOW…I couldn’t believe what I was reading! Although her rationale was that about 90 FDA studies have shown acesulfame K to be safe, there is plenty of evidence to the contrary.

For instance, food watchdog agency, Center for Science in the Public Interest (CSPI), has repeatedly expressed concern that acesulfame K is a potential carcinogen and questions the safety of exposure to one of its components – methylene chloride, a known cancer-causing chemical.

In June 1995, the CSPI filed a protest with the FDA, saying that the sweetener’s carcinogenicity had not been properly tested in long-term animal feeding tests.

According to CSPI, the numerous tests done on acesulfame K “followed inadequate protocols, which are greatly at variance with current standards for test design, execution and reporting required for the National Toxicology Program’s bioassays.”

Furthermore, the CSPI notes that acetoacetamide, a breakdown product of acesulfame K, has been shown to cause tumor growth in the thyroid gland in rats, rabbits, and dogs after administration of only 1% acetoacetamide in the diet for three months.

CSPI also charged that the FDA has failed to require the manufacturer to conduct high-quality tests of the artificial sweetener.

The only known manufacturer of acesulfame K is Hoechst Food Ingredients in Germany. CSPI claims the protocols in Hoeschst’s tests on rats and mice done in 1988 are seriously flawed. This isn’t surprising though considering this “unethical” pharmaceutical and chemical company also pleaded guilty in 1999 to a 17-year conspiracy to fix prices of sorbates, a type of food preservative, which affected $1 billion in commerce in the United States alone!

While the National Toxicology Program requires long-term studies on rats and mice to be done for 104 weeks, the Hoechst study on mice lasted only 80 weeks, while the studies on rats featured doses of acesulfame K that were “questionably” low, leading to adequate enough results to allow the sweetener to be approved for mass consumption.

However, two rat studies suggested that the additive might cause cancer, causing the CSPI to urge the FDA to seriously reconsider allowing acesulfame K into soft drinks. Obviously, if you look on most diet sodas, you’ll see that nothing has been done to remove this hazardous chemical from our foods.

Other safety tests of acesulfame K were conducted in the 1970s and were of mediocre quality to say the least. For instance, tests conducted on rats were afflicted by disease in the animal colonies, as well as dosages that were suspiciously low to cause any potential harm.

My verdict is that acesulfame K should not be consumed. Perhaps it won’t present any problems at low dosages but when consumed over a period of years there’s no denying the potential harmful effects it may have on your body!

If you’re drinking Coke Zero to prevent weight gain or to lose weight fast then you should probably not be drinking soft drinks in the first place, working your butt off in the gym, and eating a healthy whole foods diet.

Dangers of Aspartame | Diet Sodas – PART 2

August 14th, 2009

Yesterday, in the first part of this Aspartame series, we uncovered a comprehensive list of many of the Aspartame-related symptoms that have been reported to the FDA. In this section, we’re going to look at some of the reasons why Aspartame has been proven to be dangerous to the human (and animal) health.

How Aspartame Affects the Body

Aspartame is a neurotoxin whose by-products (explained below) can bind to specific receptors within the brain and nervous system. Because of this, Aspartame appears to cause slow, silent damage, especially in the brain and nervous system, in those unfortunate enough to not have immediate reactions to it. For such people, it may take one year, 5 years, 10 years, or 40 years, but it seems to cause some reversible and some irreversible changes in health over long-term use.

The real danger with Aspartame consumption, it now seems, pertains to pregnant women and the developing fetus. A startling 2007 animal study in the journal Environmental Health Perspectives showed that rats fed roughly twice the “acceptable daily intake” (ADI) amount of aspartame from the 12th day of fetal life until their natural death had significant increases in malignant lymphomas/leukemias and mammary tumours!

Although the study was conducted on rats (not humans) and at a dosage higher than the FDA’s ADI levels, it is the second study from the same researchers to show Aspartame’s cancer-causing potential, especially when administered during fetal development.

In their previous study from 2006, Dr. Morando Soffriti and his team showed that Aspartame is a multipotential carcinogenic agent, even at a daily dose of 20 mg/kg of bodweight (milligrams per kilograms per body weight), much less than the current ADI for humans in Europe (40 mg/kg of bodyweight) and in the United States (50 mg/kg bodyweight).

On the basis of these research results, the Italian research team recommended a re-evaluation of the present guidelines on the use and consumption of Aspartame as “urgent and cannot be delayed.”

These studies provide alarming findings on Aspartame, even if they were conducted on rats. Their merit lies in the fact that the dosages used were similar to what most humans would normally consume and that they studied the rats for the entirety of their lives, not just for 1 or 2 years like many flawed studies showing Aspartame’s safety have used.

Aspartame is a compound molecule and its effects on the body can be studied on numerous levels. To that point, it is helpful to understand that upon ingestion, Aspartame breaks down into 3 components: methanol, phenylalanine, and aspartic acid.

Methanol…Formaldehyde…and Formic Acid

Methanol, also known as wood alcohol, comprises 10% of Aspartame and is considered toxic if consumed frequently.

Most of the methanol in Aspartame is absorbed and quickly converted into formaldehyde, and then to formic acid. While some scientists (and interested companies such as Monsanto and Ajinomoto) believe that the metabolism of aspartame into methanol does not damage the body, other experts disagree.

Their disagreement stems from the fact that Aspartame-containing beverages have no ethanol to prevent the conversion to the lethal methanol. In natural products, methanol never appears alone. In every case, it is balanced by the presence of ethanol, which helps to block the body’s enzymes from converting methanol into formic acid.

The researchers also believe that even low levels of methanol (and its by-products formaldehyde and formic acid) can accumulate in the brain, liver, and kidneys of rats while also proving toxic to humans.

Once in the body, methanol is converted to formaldehyde, and then to formic acid. These 2 final by-products of methanol metabolism are well-known toxins! Along these lines, the Environmental Protection Agency (EPA) has stated that methanol:

“…is considered a cumulative poison due to the low rate of excretion once it is absorbed. In the body, methanol is oxidized to formaldehyde and formic acid; both of these metabolites are toxic.”

Formaldehyde is a deadly neurotoxin and a known cancer-causing substance. It causes damage to the retina of the eyes, interferes with DNA replication, and can lead to birth defects.

Formic acid is toxic because it inhibits a key mitochondrial enzyme, depriving the body’s cells from oxygen, resulting in metabolic acidosis (which is associated with bone density loss, kidney problems, and cancer), among a variety of other metabolic disturbances.

According to the EPA, the recommended limit of methanol consumption is 7.8 mg/day. But really, how much of a poison is safe to ingest?? A 1-litre Aspartame-sweetened beverage contains about 56 mg of methanol – that’s about 7 times the EPA’s recommended limit! Maybe 1-litre is excessive for most. So why not consider that a single 12 oz. can of diet coke contains 20 mg of methanol. So either way, you lose!

Phenylalanine and Aspartic Acid

Phenylalanine and aspartic acid, which comprise 90% of aspartame, are amino acids normally used by the body’s cells when supplied by the foods we eat. Phenylalanine is an essential amino acid that is needed for normal growth and tissue maintenance, but sustained high blood levels of phenylalanine can lead to brain damage.

This is of particular concern to roughly one out of 20,000 children born with phenylketonuria or PKU. These children cannot metabolize phenylalanine properly, so it builds up to dangerous levels in their brains.

For this reason, it is law in the United States for Aspartame-containing products to contain a warning of the presence of phenylalanine.

Aspartic acid belongs to a class of chemicals that in high concentrations act as an excitotoxin, inflicting damage on brain and nerve cells. Aspartatic acid does not normally cross the blood-brain barrier in most parts of the brain without active uptake by specific transporters, yet high levels of this excitotoxin has been shown in numerous animal studies to cause damage to areas of the brain unprotected by the blood-brain barrier, leading to variety of degenerative diseases.

While some experts agree that typical use of aspartame does not spike aspartic acid to extremely high levels in adults, they are particularly concerned with its potential effects in infants and young children, as they have undeveloped blood-brain barriers.

It’s a far stretch to think that small children will consume diet sodas because they want to lose weight, but parents should pay attention to infant formulas and other infant foods that may contain Aspartame, even at small doses. More importantly, mothers-to-be should seriously refrain from putting any Aspartame in their bodies in light of the startling “fetal” study alluded to earlier.

Summing Up

Without a doubt, the three breakdown products of Aspartame are all toxic at high doses. But even at small doses, why would you put a poison into your body? Would you put even a small dash of paint thinner (a deadly toxin) into your morning smoothie if it tasted sweet? Of course not!

Counter-arguments have been put forth by experts such as Joe Schwarcz, author of “An Apple a Day”, who claim that the typical Aspartame user consumes far less than the FDA’s “acceptable daily intake” (ADI) rendering Aspartame more or less harmless. But let’s not forget about the corruption inherent in the FDA that led to the approval of Aspartame in the first place or the fact that roughly 100 studies have demonstrated serious detrimental neurological effects from frequent use of Aspartame, even at a lower than ADI levels!

Any chemical that is chronically ingested will accumulate over time. Whether the body can properly metabolize it or not will depend on the health of the body and its major filtering (ie. the liver) and enzyme systems.

Unfortunately, based on most peoples’ current state of poor health, their compromised liver, kidney, and immune function, and their depleted enzyme levels from eating dead foods, it is highly unlikely that, in the long run, their bodies will not show the effects of chronic contamination!

In the case of Aspartame, it has been said that roughly 60 days are required for its by-products to be eliminated from the human body! That’s quite the decay time for a chemical that is often consumed on a daily basis by millions of dieting individuals.

There’s the information. Now, the choice is yours. I hope you make the right one!

 

References:

Soffriti, et al. (2007). Lifespan Exposure to Low Doses of Aspartame Beginning During Prenatal Life Increases Cancer Effects in Rats Environment Health Perspectives 115: 1293-1297.

Soffritti, et al. (2006). Aspartame induces lymphomas and leukemias in rats. European Journal of Oncology, 10(2): 107-116.

Trocho, C. et al. (1998). Formaldehyde derived from dietary aspartame binds to tissue components in vivo. Life Sci, 63(5):337-49.

http://www.epa.gov/

Liesivuori J, Savolainen H (September 1991). “Methanol and formic acid toxicity: biochemical mechanisms”. Pharmacol. Toxicol. 69 (3): 157–63.

Olney, J. (1994). “Excitotoxins in Foods”. Neurotoxicology 15 (3): 535–544.


Aspartame and Why You Shouldn’t Drink Diet Coke – PART 1

August 13th, 2009

The creation, and subsequent introduction, of the man-made “poison” called Aspartame is one of the greatest downfalls of mankind over the last 50 years! That is quite a bold statement but it’s true.

I wanted to share this “whistle blower” information with you because it is a subject that has negatively impacted many people I know. Aspartame is deadly and highly political and you’re about to find out why…

Similar to MSG, Aspartame has been pushed onto the market to satisfy the wallets of key individuals and organizations with a vested interest in its success. 

It is the hallmark ingredient of many diet sodas including Diet Coke. After this 2-part series on Aspartame’s side effects you may reconsider ever drinking another diet soda. It definitely has no place in a healthy diet.

Aspartame is an artificial sweetener that is marketed under a number of trademark names, including Tropicana Slim, Equal, NutraSweet, Spoonful, and Canderel. In the European Union, it is also known under the E number (additive code) E951.

Millions of people have reported symptoms and ill effects after ingesting Aspartame. In fact, in 1995, FDA Epidemiology Branch Chief Thomas Wilcox reported that Aspartame complaints represented 75% of all reports of adverse reactions to substances in the food supply from 1981 to 1995.

Aspartame Side Effects

Here are some of the wonderful symptoms that have been reported: seizures and convulsions, dizziness, tremors, migraines and severe, headaches, memory loss, slurred of speech, confusion, numbness or tingling of extremities, chronic fatigue, depression, insomnia, irritability, panic attacks, rapid heart beat, tachycardia, asthma, chest pains, hypertension, nausea or vomiting, diarrhea, abdominal pain, swallowing pain, itching, hives, allergic reactions, menstrual problems, impotency and sexual problems, food cravings and weight gain, hair loss / baldness or thinning of hair, burning urination & other urination problems, bloating, joint pain and brain tumours.

But wait, there’s more! Keep reading to discover the scary ones.

Considering Aspartame’s detrimental effects on the body, it is shockingly still found in more than 6,000 consumer foods and beverages sold worldwide; including, sugar-free chewing gums, some brands of chewable vitamins, and many table condiments.

Most commonly, though, it is the acclaimed artificial sweetener in diet soft drinks, originally gaining mass appeal because its caloric yield is negligible, while still providing a great deal of sweetness. Aspartame is 180 times sweeter than sugar, without the high energy value of sugar. Food manufacturers instantly saw this as an opportunity to put traditional sugar on the backburner and jump on the “low sugar” bandwagon in response to the growing obesity epidemic beginning in the 1980s. Aspartame is, unfortunately, also one of the sugar substitutes used by people with diabetes.

Shady Science

It should be noted that not all scientific studies have shown Aspartame to be dangerous to humans. Of 164 Aspartame studies relevant to human safety, 74 have had aspartame industry-related sponsorship, while 90 have been funded without any industry money.

Not surprisingly, of the 90 non-industry-sponsored studies, 83 (92%) have identified one or more problems with Aspartame, with 6 of the studies that showed no problems being conducted by the FDA. Shortly, you will learn why even FDA-conducted studies should be considered with caution.

Ironically, of the 74 Aspartame industry-sponsored studies, all 74 (100%) claimed that no problems were found with Aspartame!

The Birth of a Monster

Aspartame was discovered accidentally in 1965 by James M. Schlatter, a chemist working for pharmaceutical giant G.D. Searle & Company (now Pfizer, Inc.). Schlatter had synthesized Aspartame in the course of producing an anti-ulcer drug and discovered its sweet taste mistakenly when he licked his finger, which had accidentally become tainted with a touch of the new chemical.

However, it wasn’t until several years later, in 1981, that Aspartame was approved for use in dry foods. For several years, the FDA refused to approve it because of the seizures and brain tumors the harmful sugar substitute was producing in lab animals.

In 1980, the FDA convened a Public Board of Inquiry (PBOI) consisting of independent advisors whose responsibility it was to examine the reported relationship between Aspartame and brain cancer. The PBOI concluded that Aspartame does not cause brain damage, but it did recommend against approving aspartame at that time, citing unanswered questions about cancer in laboratory rats.

Shortly after, The Bressler Report, which compared all the available raw data and summary data on Aspartame against the manufacturer’s FDA submission, found missing raw data, numerous errors, and discrepancies in the available data. Regardless, the FDA chose to ignore Bressler’s report.

Wow, what a surprise!

Amazingly, at that point in time, there was no requirement in place in FDA regulations to include brain research in the approval process! Only cancer research was deemed important enough to be considered by the FDA during the approval process.

Prior to 1981, then FDA commissioner, Jere E. Goyan would not approve the use of aspartame due to several studies documenting increase cancers in rats. However, his reign quickly ended on the first day of Ronald Reagan’s presidency in 1981.

Here’s What Happened…

Upon Reagan’s introduction to the White House, Donald Rumsfeld (former congressman, former White House chief of staff, and former secretary of defense) joined the Reagan transition team. At that time, and from 1977 to 1985, Rumsfeld was the president and CEO of G.D. Searle, mainly because of his influence within the White House!

In January 1981, Rumsfeld expressed that his mission was to get Aspartame approved by the end of the year. On January 25th, the day the new president took office, the previous FDA commissioner’s authority was suspended, and the next month, the commissioner’s job went to Dr. Arthur Hull Hayes.

Hayes was a medical doctor, a professor, and a Defense Department contract researcher.
In July 1981, Hayes approved Aspartame as a food additive despite a strong recommendation from an FDA Public Board of Inquiry (PBOI) to do otherwise.

Two years later, Hayes’ last decision was the approval of Aspartame for soft drinks and carbonated beverages.

As a Congressional Record, Senate, S5497, May 7, l985 states:

“Hayes’ decisions to approve Aspartame for use in dry foods such as cereals in l981 and soft drinks in l983 does not square with the role the FDA is supposed to play. The FDA is the government agency that reviews and approves all tests submitted by companies before allowing food additives on the market. The law requires a manufacturer – in this case Searle – to prove to the satisfaction of the FDA that there is a “reasonable certainty” that a food additive is safe. The government does not have to prove that it is harmful – an important distinction. If tests are inconclusive, an additive is not supposed to be approved by the FDA.”

Following the approval of Aspartame in soft drinks and after being under fire for accepting corporate gifts, Hayes left the FDA and went to Searle’s public relations firm (Burston-Marsteller) as senior medical advisor where he was allegedly paid $1,000 per day!

Shortly after the FDA soft-drink approval (1983), Searle began test marketing aspartame, and complaints began to arrive at the FDA of such reactions as dizziness, blurred vision, headaches, and seizures. The complaints were more numerous and more serious than the agency had ever received on any food additive.

In 1985, the FDA asked the Centers for Disease Control (CDC) to review the first 650 complaints (there are now over 10,000). The CDC found that the more than 92 symptoms in approximately 25% of the complainants had stopped and then restarted, corresponding with a respective stop and then restart, either purposely or by accident, of Aspartame consumption.

Considering Aspartame’s economic potential (more than $1 billion/year in profit), Monsanto, the world’s largest conventional seed and agricultural biotechnology company, purchased Searle late in 1985 (although later selling it in 2000). In this merger, Searle’s Aspartame business became a separate Monsanto subsidiary, the NutraSweet Company – a name coined by Searle lawyer, Robert Shapiro, who subsequently became president and CEO of Monsanto.

Donald Rumsfeld reportedly earned $12 million from increased stock value when G. D. Searle & Company was sold to Monsanto!

By 1993, Aspartame had outrageously been approved for use in other beverages, baked goods, and confectionary goods. In 1996, the FDA removed all restrictions from Aspartame allowing it to be used in all foods!

Amazingly, Aspartame has also been investigated and approved by the Joint Expert Committee on Food Additives of the United Nations Food and Agricultural Organization and by the World Health Organization.

STAY TUNED FOR PART 2 (coming tomorrow) where we’ll look at the dangers of aspartame. You won’t want miss it!

 

References:

Food Chemical News, June 12, 1995, Page 27.

http://presidiotex.com/bressler/

http://www.fda.gov/bbs/topics/answers/ans00772.html

http://www.wnho.net/aspartame_interacts.htm

Mark Mazzetti; Richard J. Newman; Kenneth T. Walsh; Kevin Whitelaw; Jeff Glasser (2001-12-17). “Rumsfeld Way”, U.S. News & World Report, p. 20.

Debunking the “Official Aspartame Myth, http://www.dorway.com/offasprt.html


Food Additives – One More Reason to Eat More Raw Foods

August 12th, 2009

If you need another reason to eat more raw foods then this could be it. Keep reading to find out the chilling facts about our westernized “non-whole foods diet”

Non-foods. Faux foods. Dead foods. These are just some of the names I use to refer to packaged and processed foods “created” by big food conglomerates such as Kraft, General Mills, and McDonald’s. Part of what makes these foods so deadly is that they are laden with food additives.

Big Business

The total U.S. market for food additives is an estimated $5.8 billion, a huge increase from $1.3 billion in 1978. Food sellers are very clever that most consumers are more likely to buy products that contain additives that render their foods more appealing, in one way or another. They spend, therefore, more than $1.4 billion annually to introduce 10,000 new food products into the market.

Most recently, we’ve witnessed the unfortunate introduction of “functional foods” such as Wonder Bread with DHA, Tropicana Orange with Omega-3s, and many more foods that add one healthy element to make it more appealing to the masses without providing any additional nutritional value.

The chilling reality is that it takes many years of research and unfortunate trial and error for governing bodies to realize the true effects of many of the food additives in our food supply. As an example, in 1978, there were 35 widely used additives that had been approved as safe for food but have since been removed as unsafe, most because they were found be carcinogenic.

Generally Recognized As Safe (GRAS)

But just how are such substances established as safe for human consumption?

Foods approved for human consumption need to be deemed as “Generally Recognized As Safe” or GRAS. Such foods are placed on the GRAS list and then ready for our bittersweet enjoyment.

The GRAS list was established in 1958. However, substances added to food before that time were exempt from the Food Additives Amendment, which created the GRAS list. Therefore, additives like saccharin and many of the later banned food additives were, at the time, deemed safe because a handful of scientists simply decided they were.

Needless to say, over the past 50 years new research has brought awareness to the need for proper food additive testing. In fact, many of the food additives added to the GRAS list early on did not even have adequate testing. As a result of these shortcomings, in 1969, U.S. President Richard Nixon ordered the FDA to re-test all 415 pre-1958 substances on the GRAS list.

Unfortunately, under new rule, decades later the federal government weakened the GRAS additive requirements. As of the late 1990s, food manufacturers simply had to notify the FDA of their additives GRAS and provide minimal evidence to support their claims.

This easier approval process was put in place to save the FDA money, since they believed that passing the buck to the manufacturers would allow the FDA to gain increased awareness of new ingredients in the nation’s food supply.

Before this time, food manufacturers were required to go through a stricter petitioning process before their additives could be approved for mass consumption.

A step in the wrong direction to the say the least!

This is just a brief introduction to the nonsense that goes on in our food supply. And I’ll be giving you more of the gritty details over the coming weeks. For now, do yourself a favour and avoid foods that come in a package or box.

Stick to a natural whole foods diet and live with vitality!