One chemical made industry so happy. It is chemical that does all the things that excitotoxins do but unlike MSG is sweet to the taste. It is chemical known as aspartame (Nutra Sweet).
Milos Pokimica
Written By: Milos Pokimica
Medically Reviewed by: Dr. Xiùying Wáng, M.D.
Updated September 30, 2023When the industry removes fat from the product, it has to add something to make that product tasty again. What they do if they remove fat is that there is nothing in the product so the solution is to add something back to increase the taste, usually sugar. If the product is not sweet, then sugar is no option. Then what they do is they will add MSG and salt. The response in the brain from excitotoxins will compensate for missing sugar. However, then the problem arises.
What will you add back if a product needs to be sweet?
What if the product needs to be without added calories or just without added sugar but still sweet? In that case, they can add other artificial sweeteners, but that will not trigger the brain in the same manner as sugar will so they have a problem. Adding regular artificial sweeteners will lead to unsatisfying results for various reasons I already disguised here (Artificial sweeteners- Understanding the basics). They need something to truly activate dopamine signaling in the brain as sugar does so the taste is just half of the equation.
The problem that sweet-tasting excitotoxin will solve.

Think of aspartame as a sweet MSG substitute. In cases when they need to have both sugar and fat removed they can add excitotoxins to have the desired effect. That is why MSG soup is tasty without any calories. That is why diet Coke is tasty without any calories. They will add stimulants to it like caffeine and excitotoxins like aspartame that have a sweet taste and will stimulate the brain at the same time, so the response from the brain will be like you have eaten something that actually contains sugar. Drinking diet sodas can be addictive because of this simulative effect.
When we use a stimulant, we become excited. By reacting with our dopamine system, the stimulant provides us with pleasure and euphoria which motivates us to consume the same stimulant again in order to experience a repeated feeling of reward (a process identified as positive re-enforcement).

Another side of this, known as negative re-enforcement, is the sudden discontinuation of addictive stimulants that can result in cravings, which is essentially the feeling of wanting to avoid the discomfort that develops once the artificial high of the stimulant has gone.

Within both of these processes, we are left wanting more. In fact, the memory for cocaine addiction resides within the glutamate receptor (Mao et al., 2013). In response to drug exposure, these receptors in neurons show marked and dynamic changes in expression. Emerging evidence ties them to the remodeling of excitatory synapses and persistent drug seeking. The high level of expression of mGluR7 glutamate receptors in the limbic reward circuitry implies its role in drug addiction. In fact, evidence associates this receptor with the addictive effects of psychostimulants, alcohol, and opiates. It is glutamate as same as glutamate in MSG.
In response to operant administration of common addictive drugs, such as psychostimulants (cocaine and amphetamine), alcohol, and opiates, limbic group III mGluRs undergo drastic adaptations to contribute to the enduring remodeling of excitatory synapses and usually suppress drug-seeking behavior. As a result, a loss-of-function mutation (knockout) of individual group III receptor subtypes often promotes drug seeking (Mao et al., 2013).

This is exactly why aspartame, a chemical with very unique properties, is used even if it is one of the most toxic and neurotoxic chemical around. It is very unique in its form which is both sweet and has excitotoxicity characteristics at the same time so for time being it is unreplaceable. The side effects down the line that this chemical can have on our health are impossible to legally correlate to companies that use it. It has a dopamine-inducing effect on the brain and combined with caffeine that has the same effect can successfully trigger addicting behavior, especially in children. That is why coke zero used it for example and not something healthier like erythritol. All companies today know about this and they will do whatever it takes to keep aspartame around knowing very well that you or let’s say most of the population, 99% never ever read labels nonetheless read articles like this one. And this includes pregnant women, children, people with cancer, and so on. Even the history of the substance is so telling to understand what is, in reality, going on behind the marketing and propaganda.
Back in 1965 while working on an ulcer drug, James Schlatter, a chemist at G.D. Searle (a subsidiary of Pfizer), accidentally discovered aspartame, a substance that is 180 times sweeter than sugar yet has no calories. He was recrystallizing aspartame from ethanol. The compound spilled on the outside of the flask, and some of it stuck to his fingers. He forgot about it and licked his fingers to pick up a piece of paper and noticed an overpowering sweet taste.

In 1967 Searle begins the safety tests on aspartame that are necessary for applying for FDA approval of food additives. Seven infant monkeys were administered aspartame mixed in milk. One died after 300 days. Five others (out of seven total) had grand mal seizures. The results were withheld from the FDA when G.D. Searle submitted its initial applications. Why did they mix aspartame with milk? Because milk will slow down its digestion to some extent in the hope that it would not overwhelm the brain in a short time and cause damage. The bigger problem was that tried to hide the results. A couple of years later Searle Company executives had created the internal policy memo in which they were describing different psychological tactics the company should use to bring the FDA into a “subconscious spirit of participation” with them on aspartame and get FDA regulators into the “habit of saying, Yes.” By that time there were more not industry-funded studies.
Neuroscientist Dr. John Olney (that pioneering research with monosodium glutamate was responsible for having it removed from baby foods) did a couple of them and by that time already informed the Searle Company that his studies showed that aspartic acid (one of the ingredients of aspartame) is causing holes in the brains of infant mice. But by 1973 after spending tens of millions of dollars conducting safety tests, Searle Company applied for FDA approval and submitted 11 pivotal studies, and did 113 studies in support of aspartame’s safety in following years. One year later the FDA grants aspartame its first approval for restricted use in dry foods.
The same year two men Jim Turner and Dr. John Olney filed the first objections against aspartame’s approval. Two years later their petition triggered an FDA investigation of the laboratory practices of aspartame’s manufacturer, G.D. Searle. The investigation found that Searle’s testing procedures were unscientific, full of errors, and “manipulated” data. The researchers report they “had never seen anything as bad as Searle’s testing.” G.D. Searle company in the crusade to get approval conducted a line of studies on animals. When they submitted this to the FDA, there was some question about the studies.
One way they tried to manipulate the data was that they showed in the studies that there are no significantly more tumors in the test group than in the control group. When some of the neuroscientists that work for the FDA looked at the data, they saw that this is correct, but then there were other problems. Both groups had significantly higher tumor rates than the normal average, especially for brain tumors. This can happen when someone tries to manipulate data and represent some of the control rats with tumors as a part of the control group. This will lower the tumor rate in a test group, it will rise it in the control group, and at the end, they can say that it does not cause any tumor or what so ever but then both the control group and the test group will have significantly higher tumor rates than the normal average.
So they requested research to be done by the Bureau of foods which was the precursor to the FDA. Dr. Jerome Bressler was in charge of the group that looked through the research that had been done by Searle. In his report, he stated that there were misinterpretations of the data and that it was the world’s worst research. The record notices that 98 of the 196 animals died during one of Searle’s studies and weren’t autopsied until later dates. Numerous errors and discrepancies are noted. For instance, a rat was recorded alive, then dead, then alive, then dead again. They found that some of the animals that died after aspartame Searle scientists did not autopsy until a full year later. After that period the flesh was petrified, and there was no possible way to do an autopsy. However, they represented that they had done autopsies and that animals are normal. They were cutting tumors out and saying that animals are healthy. They had animal tissue that had obvious tumors in it that were reported normal. Testicular atrophy was not noted. There where an effort to cover up the negative effects to get approval. If they did normal science aspartame would not be approved.
The FDA formally requested the U.S. Attorney’s office to begin grand jury procedures to review whether charges should be filed against Searle for deliberately misleading conclusions and “concealing material facts and making false statements” in aspartame safety tests.
That was the first time in the FDA’s history that they asked for a criminal investigation of a manufacturer.
While the grand jury inquiry is undertaken, Sidley & Austin, the law firm representing Searle, had begun the job of negotiations with the U.S. Attorney in charge of the investigation, Samuel Skinner. Samuel Skinner will leave the U.S. Attorney’s office later that year and will take a job with Searle’s law firm Sidley and Ostin. At the same time, G. D. Searle is going to hire the prominent Washington insider Donald Rumsfeld as the new CEO. A former Member of Congress and Secretary of Defense in the Ford Administration. Yes, that Donald Rumsfeld. Rumsfeld was appointed Secretary of Defense for a second time in January 2001 by President George W. Bush.

The medal that Rumsfeld received in 2004 was the Presidential Medal of Freedom. “Freedom” proposes the right to use your influential associates in Washington to support your company’s hazardous substance for human consumption and make a fat bonus on the way out the door. It also means you can drop bombs on other countries. It also means you can bribe the U.S. Attorney in charge of the investigation.
After U.S. Attorney Skinner’s withdrawal and resignation, there were significant stalls in the Searle grand jury investigation for so long that the statute of limitations on the aspartame charges had run out.
Assistant US attorney William Conlon who was assigned to the grand jury investigation let the statute of limitations run out. He was hired fifteen months later by the same Searl law firm Sidley & Austin.
The grand jury investigation was dropped.
Two years later in 1979, the FDA established a Public Board of Inquiry to rule on safety issues surrounding NutraSweet. The Public Board of Inquiry’s conclusion was that aspartame should not be approved until further research is done. The board stated that:
“It has not been presented with proof of reasonable certainty that aspartame is safe for use as a food additive.”
By 1980 the FDA outlaws aspartame from use after having three autonomous scientific studies of the sweetener.
When someone wants to say that all of this is just conspiracy, remind him that FDA already outlawed the substance even with all of the lobbying behind it. That will say a lot about the toxicity of aspartame. It was concluded that one primary health effects were that it had a high chance of inducing brain tumors. We also need to keep in mind that back in that time there was no requirement for the FDA to examine the effects on the brain from food additives. There were never any studies done to examine the effect of aspartame on long-term or even short-term neurological effects. Cancer studies turned into brain tumors, but that is cancer studies, not brain studies. Cancer studies were the primary and the only ones that they ever investigated. Despite all of this at this it was clear that aspartame was not fit to be used in foods and banned stayed in place, but not for long.
In 1981 Ronald Reagan was sworn in as President of the United States. His transition team included Donald Rumsfeld, CEO of G. D. Searle. Rumsfeld appointed Dr. Arthur Hull Hayes Jr. to be the new FDA Commissioner. Even before that the first thing that Ronald Reagan did when he was sworn in as president was to suspend the authority of the FDA commissioner to take any actions.
The first thing that Regan did, not the second or third, but the first thing was to push for approval for this chemical. There was obviously a fear that Commissioner was going to do something about aspartame before he leaves office. That will make things more difficult for them so Regan suspended the authority of the FDA commissioner until they can elect a new one in a month or so.
In that month the old FDA commissioner was prevented from taking any actions. It did not take long for the new FDA Commissioner handpicked by Donald Rumsfeld, CEO of G. D. Searle to approve the chemical substance that is made by G. D. Searle.
The new FDA commissioner selected a 5-person Scientific Commission to evaluate the board of inquiry’s decision. It took just a couple of weeks when presented with all of the toxic effects of the substance for the panel to decide 3-2 in favor of supporting the ban of aspartame.
Hull then resolved to a different tactic. He appointed a 6th member to the board, which created a tie in the voting, 3-3. Then Hull himself decided to break the tie and approve aspartame for use personally. Hull later left the FDA under several allegations, served briefly at New York Medical College as a cover, and then took a position as a consultant (1000$ per day) basically to do nothing with Burston-Marsteller. Burston-Marsteller is the main public relations firm for both Monsanto and GD Searle. Since that time he disappeared and has never spoken publicly about aspartame. Seven of the key people that made decisions in this entire process that made aspartame go through the entire process ended up living and getting a new jobs for some of the Nutra Sweet using industries. In 1985, Monsanto decided to purchase the aspartame patent from G.D. Searle.
Also beginning in the middle 1980s, the FDA dissuaded and actually prevented the National Toxicology Program from doing any long-term cancer research on aspartame. What was left is hundreds of industry-founded studies that showed nothing, a 100% safe rate, and over 90 independently done studies more than 90% of them showed increased cancer risk and many other adverse effects. Scientific studies have been carried out with conclusions ranging from “safe under all conditions” to “unsafe at any dose.”

There is a well-documented increase in incident rates of brain tumors in the year 1985 that remained elevated to this day. National Cancer Institute recorded an impressive increase in the primary brain cancer rate since 1985. At that time this trend was singularly attributed to more innovative scanning and diagnostic procedures. The problem is that adequate brain scanning devices were widely available for at least ten years prior to 1985. Also, incidents of other forms of cancers outside of the brain remained the same and in some cases declined. Aspartame was fully marketed by 1983. Already by 1984, there were a 10% increase in brain cancer rate in the U.S. and the incidence of brain lymphoma, a type of aggressive brain tumor jumped by 60%.
In the gut, aspartame is broken down to release methanol and two amino acids phenylalanine, and aspartate. About 50% of it is aspartic acid, 40% of it is phenylalanine, and 10% of it is wood alcohol or methanol.
Methanol is further metabolized into formaldehyde.
You might know formaldehyde as an embalming fluid. The body cannot get rid of formaldehyde. Any amount of it the body stores. The industry has made a big deal about how there is a methyl group that is found in all fruits and vegetables. Anything that we eat has methyl groups so eating methanol in aspartame is no big deal and concentrations of formaldehyde in comparison are minuscule. The amount of formaldehyde we eat from fruit is much more than the amount we could get from aspartame. You will hear this with any doctor or research that is designed to defend the use of aspartame. But again they don’t tell the whole truth.
When the body metabolizes aspartame, you end up with a small amount of formaldehyde, but that formaldehyde is in free form.
When you eat fruit, you take more methanol, but that methanol is bound to pectin. Humans lack the enzyme to break down pectin. We are unable to split methanol from pectin. It goes through the body without doing any damage whatsoever. Even if there is more methanol in fruit and vegetables in reality that methanol is irrelevant. In aspartame, the free methanol and then free formaldehyde even in minute amounts are dangerous because of the accumulative toxic effect of it. Besides methanol, in nature, we are eating the same amount of ethanol in fruit or vegetables. There are methanol and ethanol in fruits, and they counteract each other.
When G. D. Searle did an experiment with monkeys, aspartame give those monkeys grand mal seizures. Monkeys have a higher reaction to ethanol than humans. Regular alcohol like wine. On the other hand, they have really high resistance to methanol. Much higher than humans. Even with high resistance, and even though they were fed aspartame with milk, they still had seizures, and one died from cardiac arrest caused by overstimulation of the nervous system.
Besides methanol aspartic acid is an excitotoxin and phenylalanine had been shown to cross the blood-brain barrier, and it is a precursor of norepinephrine (adrenalin in the brain).
Phenylalanine occurs naturally in the brain. It is not that bad but if we have an unnaturally high level it can be very bad. There is a medical disorder that affects 1 in 10,000 people known as PKU (Phenylketonuria). It is an overabundance of Phenylalanine in the brain because of the body’s inability to process it. If you add phenylalanine to someone that does not have PKU you can trigger a very bad response. Excess amounts of phenylalanine are linked to a reduction in serotonin production. Phenylalanine can trigger for example manic attacks in people who are suffering from manic depression.
It is being known for a long time, and there are also studies that when you take aspartame with carbohydrates, you will decrease the availability of l-tryptophan in the brain which is a building block for serotonin. It can also trigger regular depletion in susceptible individuals. In one study (Walton et al., 1993) they even had to stop the experiment. Although the protocol required the recruitment of 40 patients with unipolar depression and 40 without any psychiatric history, the project was halted by the Institutional Review Board after a total of 13 individuals had completed the study because of the severity of the reactions in a group of subjects with a history of depression. It was concluded that it was unethical to continue the study. In this case also the Nutra Sweet company refused to provide the product for testing and even refused to sell it to them. Researchers had to find it in the third-party vendors.
In one of the new studies on the effect of aspartame on mood disorders done back in 2014 (Lindseth et al., 2014) they took regular healthy people and put them on a high aspartame diet. Healthy adults who consumed a study-prepared high-aspartame diet (25 mg/kg body weight/day) for 8 days and a low-aspartame diet (10 mg/kg body weight/day) for 8 days, with a 2-week washout between the diets, were examined for within-subject differences in cognition, depression, mood, and headache. When consuming high-aspartame diets, participants had a more irritable mood, exhibited more depression, and performed worse on spatial orientation tests. These were all healthy people with no history of mental illness.
Now, how much high a dose of 25 mg/kg body weight/day in actuality is? Well FDA put the safe upper limit at 50 mg/kg body weight/day. The high consumption level examined here was well under the maximum acceptable daily intake level of 40-50 mg. And this is just eight days.

Consuming this stuff for a prolonged period can have even more severe effects. Especially in children and pregnant women. Problem is that today aspartame and other excitotoxins are added everywhere. There is no real possibility that anyone who eats anything made by the food industry would be able to avoid eating them. And these chemicals are just the tip of the iceberg.
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Milos Pokimica is a doctor of natural medicine, clinical nutritionist, medical health and nutrition writer, and nutritional science advisor. Author of the book series Go Vegan? Review of Science, he also operates the natural health website GoVeganWay.com
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Milos Pokimica is a health and nutrition writer and nutritional science advisor. Author of the book series Go Vegan? Review of Science, he also operates the natural health website GoVeganWay.com
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- Omega-3 fish oil supplements cut heart attacks and strokes by 43% in dialysis patientson March 11, 2026
A major international trial has found that daily fish oil supplements significantly reduced life-threatening cardiovascular events in dialysis patients. People who took four grams per day had a 43% lower risk of heart attack, stroke, cardiac death, or vascular-related amputations compared with those on placebo. The findings stand out because few treatments have successfully lowered heart risk in this high-risk group.
- AI finally tests a century old theory about how cancer beginson March 10, 2026
Cancer often begins when the genetic instructions that guide our cells become scrambled, allowing cells to grow uncontrollably. Now, scientists at EMBL have developed an AI-powered system called MAGIC that can automatically spot and tag cells showing early signs of chromosomal trouble—tiny DNA-filled structures known as micronuclei that are linked to future cancer development.
- Scientists discover molecule that stops aggressive breast cancer in its trackson March 10, 2026
Scientists at Oregon Health & Science University have developed a new molecule that could open the door to treating triple-negative breast cancer, one of the most aggressive and difficult-to-treat forms of the disease. The compound, called SU212, targets and disables a key enzyme that cancer cells rely on to fuel their growth. In tests using humanized mouse models, the molecule caused tumors to shrink and slowed the spread of cancer by forcing the enzyme to break down.
- Stanford scientists say colorblindness may hide a deadly bladder cancer warningon March 10, 2026
Colorblindness may be doing more than making traffic lights confusing — it could also be hiding a life-threatening warning sign. Researchers analyzing millions of medical records found that people with bladder cancer who are also colorblind have a 52% higher mortality rate over 20 years compared to those with normal vision. The likely reason: many people with color vision deficiency struggle to see red, making it harder to notice blood in urine, the most common early sign of bladder cancer.
- Researchers find alarming Alzheimer’s pattern in rural Americaon March 10, 2026
A new analysis of more than 422,000 patients reveals a stark Alzheimer’s care gap between Maryland’s urban and rural communities. Rural regions often lack hospitals and dementia specialists, forcing older patients to travel farther for diagnosis and treatment. Researchers found areas with high Alzheimer’s death rates but surprisingly low diagnosis rates, suggesting many cases may never be identified.
- Hidden metabolism found operating inside the cell nucleuson March 9, 2026
Researchers have found hundreds of metabolic enzymes attached to human DNA inside the cell nucleus. Different tissues and cancers show unique patterns of these enzymes, forming a “nuclear metabolic fingerprint.” Some of the enzymes gather around damaged DNA to assist with repair. The discovery reveals an unexpected link between metabolism and gene regulation that could influence how cancers grow and respond to treatment.
- Scientists found a surprising way to make exercise work betteron March 9, 2026
Exercise normally boosts the body’s ability to use oxygen, a key marker of health and longevity — but high blood sugar can block that benefit. Researchers found that a ketogenic diet helped mice normalize blood sugar and dramatically improved how their muscles responded to exercise. Their muscles became better at using oxygen and built more endurance fibers. The results suggest diet and exercise may work together in surprising ways to improve metabolic health.
PubMed, #vegan-diet –
- Sleeping green: an Italian survey for the assessment of the relationship between sleep and vegetarian dieton March 10, 2026
CONCLUSION: Our findings suggest that an utterly veg diet can affect several sleep variables differently, mainly reducing the risk of OSA and increasing the frequency of hypnic jerks. We highlight the relevance of a thorough assessment of sleep measures associated with the veg diet and the importance of controlling for other confounding factors to reach a more nuanced understanding of the relationship between dietary patterns and sleep.
- A gradient risk of cognitive impairment with vegetarian diets in older adults: highest for vegan and potential benefit for pescatarianon February 28, 2026
CONCLUSION: Strict vegetarian diets are associated with elevated cognitive impairment risk in older adults, especially in rural areas. These findings highlight the need for careful consideration of dietary patterns in ageing populations and suggest that less restrictive vegetarian diets may be preferable for cognitive health.
- Precision Nutrition in Type 2 Diabetes Prevention Through Molecular Nutrigenomic and Epigenetic Modulation of Insulin Signaling and Glucose Metabolismon February 27, 2026
Precision nutrition has emerged as a promising strategy for the prevention of type 2 diabetes mellitus (T2DM) by targeting molecular pathways underlying insulin resistance and impaired glucose metabolism. Accumulating evidence indicates that dietary patterns, caloric intake, and specific nutrients can modulate gene expression and epigenetic mechanisms involved in insulin signaling, inflammation, and energy homeostasis. This narrative review synthesizes recent human and experimental studies…
- Simulated Gastrointestinal Digestion Modulates Anticholinesterase, Antioxidant, and Anti-Inflammatory Activities of Vegan Soups Rich in Natural Cholinesterase Inhibitorson February 27, 2026
CONCLUSIONS: Overall, gastrointestinal digestion and microbial activity markedly reshape the bioactivity of plant-based soups, indicating that the colonic phase is critical for realistic evaluation of functional food potential and supporting digestion-aware assessment of dietary strategies relevant to cognitive and inflammatory health.
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Latest from PubMed, #plant-based diet –
- Sleeping green: an Italian survey for the assessment of the relationship between sleep and vegetarian dietby Maurizio Gorgoni on March 10, 2026
CONCLUSION: Our findings suggest that an utterly veg diet can affect several sleep variables differently, mainly reducing the risk of OSA and increasing the frequency of hypnic jerks. We highlight the relevance of a thorough assessment of sleep measures associated with the veg diet and the importance of controlling for other confounding factors to reach a more nuanced understanding of the relationship between dietary patterns and sleep.
- The active plant compounds demonstrated positive activity on mouse intestinal organoids as an inflammation model systemby Selinay Şenkal-Turhan on March 10, 2026
Diet has an important impact on intestinal homeostasis, and the establishment of appropriate experimental models to study the effect of food compounds is of interest. The organoid model can be used to check the positive protective role of active food compounds on intestinal tissue. In the current study, mouse intestinal organoids were used to model air-liquid interface (ALI), lipopolysaccharide (LPS)-induced inflammation, and macrophage co-culture-based inflammation modelling. The activity of…
- Food sources of macro- and micronutrients in young children and adults following vegan, vegetarian, and omnivorous dietsby Venla Tilli on March 9, 2026
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- Diet, Gut Microbiota, and Intestinal Permeability: Emerging Mechanisms in Hypertension Pathogenesisby Esha Vashisht on March 9, 2026
Hypertension is a leading contributor to global morbidity and mortality, arising from the interplay of genetic and environmental risk factors together with the dysregulation of multiple physiological systems involved in blood pressure control. Recent advances have established the gut as a central regulator, implicating the intestinal microbiota and barrier integrity in the modulation of blood pressure. Alterations in the gut microbial consortium, along with changes in levels of metabolites…
- Are European diets healthy and sustainable? Evidence from nine countries using the planetary health diet frameworkby Agustin R Miranda on March 7, 2026
CONCLUSION: European diets show systematic deviations from the PHD. Targeted and multilevel policies are needed to promote healthy and sustainable diets.
- Broccoli and Other Botanicals in the Prevention and Treatment of Premenstrual Syndromeby Amin Gasmi on March 6, 2026
Pre-menstrual syndrome (PMS) consists of a range of physical, mental, and behavioral changes that can affect women at various stages during their menstrual cycle. These changes are caused by fluctuations in hormone levels, which play a significant role in PMS. Diet, along with other practices, can help reduce the symptoms related to PMS. Even small dietary changes like increased intake of certain foods and less caffeine consumption may help to mitigate or regulate PMS symptoms. This study […]



























