Excitotoxins in processed foods: the best guarded secret of the food and drug industries

Excitotoxicity is the pathological process by which nerve cells are damaged or killed by excessive stimulation by neurotransmitters such as glutamic acid (glutamate).

In 1969 when researcher Dr. John Olney of Washington University in St. Louis observed that process in his laboratory, it should have resulted in sweeping changes in how food additives are regulated. 

He noted that glutamate fed as monosodium glutamate (MSG) to laboratory animals killed brain cells and subsequently caused gross obesity, reproductive dysfunction, and behavior abnormalities.

Before that, the world knew nothing of what Dr. Olney had dubbed “excitotoxins.” And after Olney’s discovery, the existence of free excitotoxic amino acids present in food became the best-guarded secret of the food and drug industries.

Today, excitotoxins present in food remain largely ignored or unknown, mostly because the rich and powerful food and pharmaceutical industries want it that way. A great deal of food industry profit depends on using excitotoxins to “enhance” the taste of cheaply made food. And a great deal of pharmaceutical industry profit depends on selling drugs to “cure” the diseases and disabilities caused by the excitotoxins in the food supply.

What are excitotoxins?

Excitotoxins are often amino acids, but not all amino acids are excitotoxins. The amino acid with the greatest excitotoxic footprint is glutamate. When present in protein or released from protein in a regulated fashion (through routine digestion), glutamate is vital to normal body function. It is the major neurotransmitter in humans, carrying nerve impulses from glutamate stimuli to glutamate receptors throughout the body. Yet, when present outside of protein in amounts that exceed what the healthy human body was designed to accommodate (which can vary widely from person to person), glutamate becomes an excitotoxic neurotransmitter, firing repeatedly, damaging targeted glutamate-receptors and/or causing neuronal and non-neuronal death by over exciting those glutamate receptors until their host cells die.

Technically speaking, neurotransmitters that over-stimulate their receptors to the point of killing the cells that host them are called excitotoxic neurotransmitters, and the resulting condition is referred to as excitotoxicity. Glutamate excitotoxicity is the process that underlies the damage done by MSG and the other ingredients that contain processed free glutamic acid (MfG). 

Glutamate is called a non-essential amino acid because if the body does not have sufficient quantities to function normally, any needed glutamate can be produced from other amino acids. So, there is no need to add glutamate to the human diet. The excitotoxins in MSG and other ingredients that contain MfG are not needed for nutritional purposes. MSG and many other ingredients have been designed to enhance the taste of cheaply made food for the sole purpose of lining the pockets of those who manufacture and sell them.

Glutamate neurotransmitters trigger glutamate receptors both in the central nervous system and in peripheral tissue (heart, lungs, and intestines, for example). After stimulating glutamate receptors, glutamate neurotransmitters may do no damage and simply fade away, so to speak, or they may damage the cells that their receptors cling to, or overexcite their receptors until the cells that host them die.

There’s another possibility. There are a great many glutamate receptors in the brain, so it’s possible that if a few are damaged or wiped out following ingestion of MfG, their loss may not be noticed because there are so many undamaged ones remaining. It is also possible that individuals differ in the numbers of glutamate receptors that they have. If so, people with more glutamate receptors to begin with are less likely to feel the effects of brain damage following ingestion of MfG because even after some cells are killed or damaged, there will still be sufficient numbers of undamaged cells to carry out normal body functions.

That might account for the fact that some people are more sensitive to MfG than others.

Less is known about glutamate receptors outside the brain – in the heart, stomach, and lungs, for example. It would make sense (although that doesn’t make it true) that cells serving a particular function would be grouped together. It would also seem logical that in each location there would be fewer glutamate receptors siting on host cells than found in the brain, and for some individuals there might be so few cells with glutamate receptors to begin with, that ingestion of even small amounts of MfG might trigger asthma, atrial fibrillation, or irritable bowel disease; while persons with more cells hosting glutamate receptors would not notice damage or loss.

Short-term effects of excitotoxic glutamate (such as asthma and migraine headache) have long been obvious to those not influenced by the rhetoric of the glutamate industry and their friends at the U.S. Food and Drug Administration. Hopefully, researchers will soon begin to correlate the adverse effects of glutamate ingestion with endocrine disturbances such as reproductive disorders and gross obesity. It is well known that glutamate plays an important role in some mental disorders and neurodegenerative diseases, but the fact that ingestion of excitotoxic glutamate might contribute to existing pools of free glutamate that could become excitotoxic, still needs to be considered. Finally, a few have begun to realize the importance of glutamate’s access to the human body through the mouth, nose and skin.

There are three excitotoxic amino acids used in quantity in food, cosmetics, pharmaceuticals, protein drinks and powders, and dietary supplements:

1) Glutamic acid — found in flavor enhancers, infant formula, enteral care products for invalids, protein powders, processed foods, anything that is hydrolyzed, and some pesticides/fertilizers.

2) Aspartic acid — found in low-calorie sweeteners, aspartame and its aliases, infant formula, protein powders, anything that is hydrolyzed, and

3) L-cysteine — found in dough conditioners.

According to Dr. Edward Group, the six most dangerous excitotoxins are: MSG (monosodium glutamate), aspartate, domoic acid, L-BOAA, cysteine, and casein.

Resources

Dr. Edward Group The 6 Most Dangerous Excitotoxins. Global Healing Center.  (accessed 8/20/2016)

Blaylock RL. Excitotoxins: The Taste That Kills. Santa Fe, New Mexico: Health Press; 1994.

Olney JW. Brain Lesions, Obesity, and Other Disturbances in Mice Treated with Monosodium Glutamate; Science. 1969;164:719-21.  

Olney JW, Ho OL. Brain damage in infant mice following oral intake of glutamate, aspartate or cystine. Nature. 1970;227:609-611.

Olney, J.W. Excitatory neurotoxins as food additives: an evaluation of risk. Neurotoxicology 2: 163-192, 1980.

Olney JW. Excitotoxins in foods. Neurotoxicology. 1994 Fall;15(3):535-44.

Gudiño-Cabrera G, Ureña-Guerrero ME, Rivera-Cervantes MC, Feria-Velasco AI, Beas-Zárate C. Excitotoxicity triggered by neonatal monosodium glutamate treatment and blood-brain barrier function. Arch Med Res. 2014 Nov;45(8):653-9.

Verywellhealth.com.  An Overview of Cell Receptors and How They Work https://www.verywellhealth.com/what-is-a-receptor-on-a-cell-562554   (Accessed 5/5/2019)

Fake tuna?!

The ever-expanding market for imitation food has reeled in a host of phony fish dishes, the latest coming from “Good Catch,” with its “fish-free TUNA.”

This product contains more brain damaging MfG ingredients than any other product we’ve previously looked at, including pea protein isolate, soy protein concentrate, faba protein, lentil protein, soy protein isolate, citric acid and yeast extract.

Why the company has not been challenged by the FDA for false and misleading labeling isn’t clear, since the FDA has a long list of what can legally be called tuna, which is limited to actual varieties of real fish. Nestle, which also makes a faux fish product at least calls it “Vuna,” a product that “tastes like tuna.”

That little detail hasn’t stopped “Good Catch” from netting millions of dollars in investment capital, including close to $30 million in its latest round of funding.

A picture is worth a thousand words, especially when the words you are hearing are lies

The Glutes talk a lot about how glutamate is eaten, digested, moved into the blood stream, and from there moved into the brain.  That’s interesting, and it’s kind of impressive sounding, but it isn’t how the brain damage triggered by manufactured free glutamate (MfG) actually works. The brain damage initiated by glutamate ingestion is executed in the nervous system. It has little or nothing to do with digestion. 

The glutamate that causes brain damage is always free. The glutamate in MSG is always free.  When free glutamate is taken into the mouth, it triggers glutamate receptors in the mouth and on the tongue, causing them to fire.

If there’s a moderate amount of free glutamate involved, a glutamate receptor will be activated once and will transmit its chemical message to the next glutamate receptor in line until the goal receptor has been reached.  Some of this free glutamate will very likely activate neurons (nerve cells) that facilitate the sensations of sweet, sour, salty, or bitter in the food consumed with it. These neurons are responsible for communicating the sense of taste to the brain. 

When excessive amounts of free glutamate are taken into the mouth, the nerves that are triggered fire repeatedly until the glutamate receptors at which the firing glutamate neurotransmitters are aimed, become overstimulated and die. And the nerve cells that are obliterated in this way, are not replaced with neurons (nerve cells).  And the functions those obliterated cells would have regulated had they not been destroyed — like controlling appetite and satiety involved in obesity and controlling reproductive function for example — will never be replaced.

Basic to understanding how this works, is the fact that only free glutamate, meaning glutamate outside of protein when it is ingested, is potentially harmful.  Glutamate must be free in order to take up its role as a neurotransmitter, triggering the nerves that will start the neurotransmission of glutamate stimuli to glutamate receptors.  That explains why a tomato, which has lots of glutamate in it (glutamate that is bound to other amino acids), does not cause brain damage or adverse reactions when ingested as an unprocessed tomato.

Reaction to an “excessive” amount of MSG/MfG is a reaction caused by an excitotoxic neurotransmitter in the central, or possibly the peripheral, nervous system, not by anything related to blood circulation or digestion.

What transpires when free glutamate enters the mouth can be visualized as follows:

Failure to tell the entire story of what happens when MSG/MfG is ingested, lies at the root of the web of distraction the Glutes spin about the alleged safety of MSG/MfG.  Not a lie in one sense of the word, but omission of a material fact seemingly designed to draw attention away from the truth — a strategy that delivers greater impact than any simple lie.

Something to think about: Industry’s FDA

Article Nine of the Bill of Rights refers to the rights retained by the people — and that it is the right of the people to know everything going on in the government.  It is therefore unlawful for the FDA to fail to respond to a Freedom of Information request for copies of data used by the FDA for determining to give GRAS (generally recognized as safe) status to free glutamic acid used in food.

It seems reasonable to conclude that in filling the request for data, the FDA would have to admit that 1) there are no data that demonstrate that free glutamate can be safely used in food, and 2) that the only studies that claim to have demonstrated the safety of free glutamate have been double-blind studies where excitotoxic aspartic acid (in aspartame) has been used in placebos.

Aspartic acid (in aspartame) and glutamic acid (in MSG) both cause brain damage and identical adverse reactions.

Something to think about

As the glutamate industry pumps out ever increasing amounts of excitotoxic free glutamate to be used in food, the incidence of glutamate-induced disease and disability has been growing.

Check it out.  You’ll find the numbers in market reports and at the national library of medicine’s PubMed.gov.

And don’t be put off by the fact that there are other toxins in the environment that surely contribute.  That doesn’t make glutamate’s harmful role any less a factor.

MSG: a double whammy to your liver

When Dr. Russell Blaylock came out with his eye-opening book in 1994, “Excitotoxins: the Taste that Kills,” he forecast an ongoing obesity epidemic based on the sheer amount of MSG and other excitotoxins dumped into processed foods and beverages.

Now, almost three decades later he says, “Unfortunately, my prediction has come true. Obesity is now a national epidemic – not just among adults, but also among children, even the very young.”

But the damage caused by our national obesity epidemic didn’t stop with extreme weight gain. It has helped to foster another widespread condition (even called a “pandemic” by some doctors and researchers), known as non-alcoholic fatty liver disease, or NAFLD. This chronic liver condition was a rare occurrence only a few decades ago. Now it’s not only rampant among adults but being diagnosed more and more in kids, some just toddlers.

As the name implies, NAFLD is a buildup of fat in the liver, something that can progress to a life-threatening condition called non-alcoholic steatohepatitis (NASH), which can lead to liver failure and liver cancer.

MSG has the distinction of contributing to NAFLD and NASH is two ways. As Blaylock revealed in Excitotoxins, it had been decisively shown in research that baby mice fed MSG became “grossly obese,” and that their “obesity was very difficult to reverse.” (Today, researchers turn to MSG as a tool to fatten up their lab animals for obesity studies.)

The other way MSG is helping to create this pandemic of liver disease was found in a study showing how low doses of MSG (extremely easy to consume if you eat any kind of processed food), combined with the ever-popular sweetener high fructose corn syrup, “greatly increased the risk” of both liver conditions, Blaylock recently reported.

HFCS, a cheap genetically modified sugar substitute, is extremely toxic to the liver. Study after study has found a significant connection between ingesting all forms of processed fructose and liver damage.

As for MSG and the manufactured free glutamate (MfG) it contains, it not only is a major cause of obesity that leads to NAFLD, but has been linked to numerous other conditions including many incapacitating neurological disorders.

Ironically, many processed foods labeled as “low-cal,” which are pitched to those hoping to lose weight, contain the worst additives when it comes to weight loss, as well as liver health. For example, HFCS-90, with a whopping 90 percent fructose, is often added to diet dishes, as only a small amount is needed for sweetening. And since lower-calorie processed foods are typically made from cheap, tasteless ingredients, MSG and other forms of MfG are added liberally.

While Dr. Blaylock has made a significant contribution to our understanding of the toxic nature of MSG and other excitotoxins — warning for decades about the dangers of consuming them – unfortunately, you still don’t have to look very hard to find them in our food supply.

But perhaps as even more children sadly fall victim to suffering the consequences of the widespread use of such additives, more people will join those already demanding change in how processed foods are made and regulated.

Protein powders: healthy additions or brain-damaging toxin?

Adding a scoop of a protein powder to a shake or smoothie sure sounds like a good idea. After all, proteins are essential nutrients for the human body. They are one of the building blocks of body tissue and can also serve as fuel sources.

But there’s a very important distinction to be made between the protein in meat, fish, poultry (and other whole-food sources) and the powder that comes out of that box, bag, or jar. Read this post carefully before you touch another protein-fortified drink, snack bar or supplement. Your brain will thank you!

Amino acids

Proteins are polymer chains made of amino acids linked together by peptide bonds. During human digestion, proteins are broken down in the stomach to smaller polypeptide chains via hydrochloric acid and protease enzyme actions.   

When protein is ingested and then broken into individual amino acids, those individual amino acids proceed slowly through the human digestion processes. Unless one is allergic or sensitive to the food that contains the protein, its amino acids continue along to be digested without adverse effect.

But if protein is broken into individual amino acids before it is ingested, those free amino acids take on a toxic potential that they would never have ingested as part of a whole protein.

Take glutamic acid (glutamate).  When released from protein during digestion, glutamate is vital to normal body function. Often referred to as “a building block of protein,” it is the major neurotransmitter in the human body, carrying nerve impulses from glutamate stimuli to glutamate receptors throughout the body.

Yet, when freed from its protein source (be it from milk, peas, soy, etc.) and then consumed in amounts that exceed what the healthy human body was designed to accommodate, glutamate takes on “excitotoxic” properties. What was a normally functioning neurotransmitter turns hostile, firing repeatedly and damaging receptor cells in the brain and elsewhere until they die.

Excitotoxins 

The U.S. Food and Drug Administration (FDA) makes a labeling distinction between whole protein foods and potentially excitotoxic processed protein products that are made up of individual amino acids.

FDA rules say that an unadulterated tomato is to be called a “tomato.” A “pea” is required to be called a “pea” and whey is called “whey.” Those are their common or usual names. No reference is made to the fact that these protein-containing foods contain protein.  

In contrast, when amino acids are freed from proteins such as peas, the resulting ingredients will be called “pea protein,” or “isolated pea protein,” “pea protein concentrate,” or “hydrolyzed pea protein.” And you’ll find these ingredients in all kinds of food products, including a popular dairy-free drink called Ripple.

Other food ingredients that have the same excitotoxic properties have names that include the words “hydrolyzed,” “autolyzed,” “amino acid,” “L-glutamate,” “glutamic acid,” and “L-glutamic acid.”

So, why haven’t you come across this information before? Why are products containing these brain-damaging excitotoxins even allowed on the market?   

The answers lie in the dark history of an unregulated industry – “policed” by an FDA that chooses to look the other way. That history can be read in The Toxicity/Safety of Processed Free Glutamic Acid (MSG): A study in Suppression of InformationAccountability in Research. 1999(6):259-310; by A. Samuels.

To learn more about how the FDA cooperates with Ajinomoto, the world’s largest producer of monosodium glutamate, check out this page at our website.  

Yeast extract, now with more toxic, brain damaging ‘food flavor enhancement’

Yeast extract might well be called the darling of the processed food industry, and the straw that breaks the camel’s back for MSG-sensitive people. Like MSG it’s manufactured (not “natural”), and also like MSG it contains toxic manufactured free glutamic acid (MfG).

Yeast extract is one of those “clean label” ingredients, often used in products such as soups and fake proteins that state “No added MSG” on the label (which is actually against FDA regulations, but enforcing that rule is no longer bothered with by the FDA). Also qualifying as a “clean label” ingredient would be any ingredient other than MSG that contains MfG. (Check out over 40 ingredient names that contain varying amounts of MfG here.)

Now we’re learning of a recent invention, a method for “large scale” production of a yeast extract product with nearly triple the brain damaging “glutamic acid content” of other yeast extracts. Its patent describes how this new and improved yeast extract “possesses more delicious flavor and improved capability for food flavor enhancement.” Glutamic acid, the patent states, in free form can “strengthen the delicate flavour of food.” We’re being told in this official document that the more MfG an ingredient contains, the more flavor it will impart to any food it’s added to.

The patent was applied for and owned by Angel Yeast Co., which calls itself a “high-tech yeast company in China” with 10 “advanced” manufacturing facilities in China, Egypt and Russia. Angel provides yeast extract to food manufacturers for use in everything from soup to snacks, promising its product provides a “magic flavor explosion.”

It’s a “magic flavor explosion” that comes with brain-damaging — excitotoxic — glutamate.

When consumed in excess (which differs from person to person), free glutamate becomes excitotoxic, with the capacity to overstimulate glutamate receptors in the body, causing them to fire rapidly and die. In simple terms, it causes brain damage.

We know that the new and improved yeast extract will contribute to the accumulation of toxic free glutamate.

What we don’t know is how much it will take to cause an excitotoxic “explosion.”

Questions and answers: What’s causing the obesity epidemic?

What’s causing the obesity epidemic?

They’re called excitotoxins.

These are Jekyll and Hyde amino acids.

On the one hand, they’re absolutely necessary for human
health.

On the other hand, they turn toxic/poisonous when more are
eaten than needed.

What damage do they do?

They damage the brains of vulnerable people.

People who have had head injuries,

People whose brains are not yet mature,

A newborn child,

A child in the womb: a fetus.

How can excitotoxins get to the immature brains of newborns and
fetuses?

Excitotoxins are eaten by pregnant women.

Pregnant women pass what they eat to their unborn offspring
(fetuses) through the umbilical cord and the placenta.

Nursing mothers pass what they eat to their babies through mother’s
milk.

Exactly what damage do these excitotoxins do to the brains of fetuses and newborns that brings about obesity?

They obliterate (wipe out) the neurons (nerve cells) in that part of the
arcuate nucleus of the hypothalamus that would have played a role in
weight control, had they not been destroyed.

And although the empty space left in the brain when the neurons are
destroyed is filled in with other cells, the neurons are not replaced.

What excitotoxins do this?

The one known best from research done in the 1970s is glutamic acid
(a.k.a. glutamate).

Glutamate is essential for normal body function. There has always
been glutamate in food. Why haven’t more people always been
obese?

Until 1957, the glutamate in food (and there is glutamate in
essentially all food) was almost always part of something larger than
itself. It was a part of protein. Scientists who wanted to examine
glutamate had to break the protein apart before they could examine it.
(They speak of glutamate being “bound up” in protein: tied to other
amino acids in long chains. That’s still true.)

Glutamate bound in protein is not excitotoxic. Only glutamate outside
of protein causes brain damage.

In 1957, the U.S. manufacturer of excitotoxic glutamate (for use in
monosodium glutamate) revised its manufacturing process, and from
that point on, virtually unlimited amounts of excitotoxic manufactured
free glutamate (MfG) were produced. After 1957, there was sufficient
MfG in ultra-processed food (at least in the U.S.) to provide the
“excess” amounts of MfG needed to cause brain damage.

Then why didn’t the “obesity epidemic” happen in 1957?

1957 was the year that the new and improved method for fabricating
virtually unlimited amounts of the excitotoxic – brain damaging – MfG
was put into production. But 1960 was the year that increased
obesity began to be noticed. 1960-62 saw the first statistics kept on
numbers of overweight people.