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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Stranger Things Star Winona Ryder Tackled Spicy Tofu On ‘Hot Ones’
on November 26, 2025
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Sweet Cranberry Glazed BBQ Ribs
on November 26, 2025
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PETA Founder Says ‘I Don’t Think We Went Far Enough’
on November 26, 2025
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Vegan Mini Flank Galettes With Caramelized Onion & Pear
on November 25, 2025
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Sprout Power: Boost Digestion, Protein, and Energy with Homemade Lentils
on November 25, 2025
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Lidl Calls For Mandatory Plant-Based Targets To ‘Level The Playing Field’
on November 25, 2025
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Vegetarian Society Reports ‘Significant Rise’ In Brands Adopting Plant-Based Certification
on November 24, 2025
Top Health News — ScienceDaily
- New study shows rheumatoid arthritis begins long before symptomson November 26, 2025
Rheumatoid arthritis begins years before pain ever appears, and scientists have now mapped the hidden immune battle that unfolds long before symptoms. By studying people with RA-linked antibodies over seven years, researchers discovered sweeping inflammation, malfunctioning immune cells, and even epigenetic reprogramming in cells that had never encountered a threat. These changes show that the body is preparing for autoimmune attack long before joints become damaged.
- Stanford’s new cell therapy cures type 1 diabetes in miceon November 26, 2025
Researchers at Stanford found a way to cure or prevent Type 1 diabetes in mice using a combined blood stem cell and islet cell transplant. The procedure creates a hybrid immune system that stops autoimmune attacks and eliminates the need for immune-suppressing drugs. The method uses tools already common in clinical practice, putting human trials within reach. Scientists think the same strategy could transform treatments for autoimmune conditions and organ transplantation.
- A hidden brain energy signal drives depression and anxietyon November 26, 2025
Scientists discovered that lowered brain energy signaling in the hippocampus can lead to both depression- and anxiety-like behaviors in mice. Stress reduced ATP, a molecule important for cell energy and communication. Altering a protein called connexin 43, which helps release ATP, caused similar symptoms even without stress. Restoring this protein improved mood-related behavior.
- The body trait that helps keep your brain youngon November 25, 2025
Scientists discovered that more muscle and less hidden abdominal fat are linked to a younger biological brain age. Deep visceral fat appeared to accelerate brain aging, while muscle mass offered a protective effect.
- How personalized algorithms trick your brain into wrong answerson November 25, 2025
Personalized algorithms may quietly sabotage how people learn, nudging them into narrow tunnels of information even when they start with zero prior knowledge. In the study, participants using algorithm-curated clues explored less, absorbed a distorted version of the truth, and became oddly confident in their wrong conclusions. The research suggests that this kind of digital steering doesn’t just shape opinions—it can reshape the very foundation of what someone believes they understand.
- Scientists reveal a hidden alarm system inside your cellson November 25, 2025
Ribosomes don’t just make proteins—they can sense when something’s wrong. When they collide, they send out stress signals that activate a molecule called ZAK. Researchers uncovered how ZAK recognizes these collisions and turns them into protective responses. The discovery shows how cells quickly spot trouble.
- Cocoa and tea may protect your heart from the hidden damage of sittingon November 25, 2025
Scientists found that high-flavanol foods can prevent the decline in blood vessel function that occurs after prolonged sitting. Even physically fit men weren’t protected unless they had consumed flavanols beforehand. A cocoa drink rich in these compounds kept arteries functioning normally. Everyday foods like berries, apples, tea, and certain cocoa products could offer a simple way to protect long-term vascular health.
PubMed, #vegan-diet –
- The German LAKE-score reliably predicts urinary and dietary potential renal acid load: a three-armed translational studyon November 25, 2025
CONCLUSION: The German version of the LAKE score is a rapid, inexpensive and feasible tool for an initial PRAL evaluation in a clinical context, characterized by a good validity and reliability. Results suggest that the German LAKE score could be suitable as an estimate for an individual’s PRAL, and could also guide clinicians to make dietary recommendations and monitor PRAL-relevant changes in individual patients.
- Biological versus Technical Reliability of Epigenetic Clocks and Implications for Disease Prognosis and Intervention Responseon November 24, 2025
DNA methylation-based aging biomarkers, or epigenetic clocks, are increasingly used to estimate biological age and predict health outcomes. Their translational utility, however, depends not only on predictive accuracy but also on reliability, the ability to provide consistent results across technical replicates and repeated biological measures. Here, we leveraged the TranslAGE platform to comprehensively evaluate the technical and biological reliability of 18 Epigenetic clocks, including…
- Learning molecular fingerprints of foods to decode dietary intakeon November 24, 2025
Assessing dietary intake from biological samples provides critical objective insights into nutrition and health. We present a reference-based strategy using untargeted metabolomics to estimate relative dietary composition. The approach learns food-specific molecular ion features first – both annotated and unannotated – via supervised classification and discriminant analysis. These features then guide extraction of corresponding MS1 intensities from unknown samples, enabling proportional,…
- Eating within planetary boundaries – a cross-country analysis of iodine provision from the EAT-Lancet dieton November 24, 2025
The EAT-Lancet Commission’s 2019 reference diet promotes health and environmental sustainability through predominantly plant-based foods, raising concerns about micronutrient adequacy, particularly iodine. This study evaluated the iodine content of the EAT-Lancet diet across sixteen countries using national food composition data. Iodine intake was modelled under three scenarios: (1) strict adherence to specified food items; (2) inclusion of a broader range of foods within each group; and (3) […]
- Vegetarian and Vegan Diets and the Risk of Hip Fracture in Adults: A Systematic Review and Meta-analysison November 23, 2025
CONCLUSION: These findings emphasize the importance of incorporating dietary patterns into strategies for promoting bone health, especially among individuals following plant-based diets. Healthcare providers should offer guidance to individuals adopting vegetarian or vegan diets to ensure adequate nutrient intake and support bone health.
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Latest from PubMed, #plant-based diet –
- Fertilization fallout and fish fertility in low-silt ponds: studying the impacts on soil properties, water quality, immune-physiological response, and reproductive performance in red tilapia…by Ghada R Sallam on November 26, 2025
A 210-day reproduction trial tested the effect of organic fertilizer composed of fish sludge + compost of Beta vulgaris leaves (FS + BVL) on water quality, soil properties and fertility of red tilapia Oreochromis sp. fed a plant-based diet under varying salinities in low-silt ponds. A 1:3 sex ratio (500♂: 1500♀) was stocked into 32 hapas (24.3 m³ each) placed in 8 earthen ponds (150 m² each). Four ponds held 18‰ saltwater (2 fertilized, 2 unfertilized) and four ponds held 36‰ […]
- Impact of Healthy Diet Shifts on Soil Greenhouse Gas Emissions Across Europeby Vasilis Michailidis on November 25, 2025
Shifting towards healthy, plant-based diets is widely recognized as a strategy to reduce greenhouse gas emissions (GHG) from food systems, primarily through reduced methane emissions from livestock. However, the implications of this transition for soil-based GHG emissions, a major contributor to climate change, remain uncertain. We used the MAGNET economic model and the DayCent biogeochemical model to assess the impacts of dietary shifts aligned with the EAT-Lancet guidelines on soil organic…
- Plant-based diets especially healthy ones are negatively associated with depression: a cross-sectional studyby Bao Zhang on November 25, 2025
CONCLUSIONS: Plant-based diets, especially when they are enriched with healthier plant foods, may be beneficial for primary prevention of depression. However, plant-based diets that emphasize less healthy plant foods are associated with higher depression levels among US adults.
- The German LAKE-score reliably predicts urinary and dietary potential renal acid load: a three-armed translational studyby Maximilian Andreas Storz on November 25, 2025
CONCLUSION: The German version of the LAKE score is a rapid, inexpensive and feasible tool for an initial PRAL evaluation in a clinical context, characterized by a good validity and reliability. Results suggest that the German LAKE score could be suitable as an estimate for an individual’s PRAL, and could also guide clinicians to make dietary recommendations and monitor PRAL-relevant changes in individual patients.
- Dietary n-3 Polyunsaturated Fatty Acids From Fish Are Associated With Better Healthy Aging Indicators: Results of the DIAPELH Studyby Alexandra Foscolou on November 24, 2025
CONCLUSION: The results underscore the significance of nutrition in older adults, highlighting the possible protective impact of n-3 PUFAs on maintaining functionality. Future prospective studies may validate these associations and contribute to the development of targeted nutritional strategies for older adults.
- Taxonomic and functional shifts in the rumen microbiome of buffalo calves under long-term strategic supplementation of phyto-feed additivesby Pramod Kumar Soni on November 24, 2025
INTRODUCTION: The present study aimed to understand the shift in the rumen microbiome of buffaloes fed diets with and without phyto-additives. The rationale was based on the hypothesis that plant-based additives can modulate the microbial population in the rumen, potentially reducing methane production and enhancing fiber degradation. Given the possibility that prolonged use of the same additives may lead to microbial adaptation and diminished efficacy, the study also investigated the effects […]






























