Monosodium Glutamate vs Olestra: which is worse?
Quick answer: Olestra carries the heavier risk profile. Monosodium Glutamate is — in the EU and — in the US; Olestra is — in the EU and — in the US.
| Property | Monosodium Glutamate | Olestra |
|---|---|---|
| EU status | — | — |
| US status | — | — |
| Risk level | — | — |
| Banned in | — | United Kingdom, Canada |
| Restricted in | Australia/New Zealand (required labeling), European Union (required declaration as 'flavor enhancer MSG (E621)') | European Union (not approved for food use) |
| Category | additive | additive |
| Where it hides | — | — |
What is Monosodium Glutamate?
Monosodium glutamate (MSG) is the sodium salt of glutamic acid, a naturally occurring non-essential amino acid found in many proteins. It is used as a flavor enhancer to intensify umami (savory) taste. MSG was first isolated from seaweed in 1908 by Japanese chemist Kikunae Ikeda and has been used commercially since then.
What is Olestra?
Olestra (brand name Olean) is a synthetic fat substitute made from sucrose and fatty acids. Unlike regular fats, olestra is not absorbed by the digestive system — it passes through the body unchanged, providing zero calories while mimicking fat's texture and taste in food. It was developed by Procter & Gamble and FDA-approved in 1996.
Documented risks
Monosodium Glutamate: MSG safety has been one of the most extensively debated food additive questions in the past 50 years. The 'Chinese Restaurant Syndrome' — a cluster of symptoms (headache, flushing, sweating, chest tightness) reported after eating Chinese food — was attributed to MSG in a 1968 letter in the New England Journal of Medicine. This set off decades of controversy. Multiple rigorous double-blind, placebo-controlled trials have failed to consistently demonstrate that MSG at doses present in food causes these symptoms when participants do not know whether they received MSG or a placebo. A comprehensive 1993 review by the FDA-commissioned Federation of American Societies for Experimental Biology (FASEB) found that while some sensitive individuals may experience symptoms at high doses (>3g of pure MSG on an empty stomach), the doses in typical food servings do not consistently produce symptoms in double-blind conditions. The FDA classifies MSG as GRAS (generally recognized as safe). EFSA's 2017 re-evaluation set an ADI of 30 mg/kg body weight per day, acknowledging that very high doses could affect neurological function but concluding typical dietary exposure is safe. Critics including Dr. Russell Blaylock and advocacy groups have argued that MSG is an 'excitotoxin' — a compound that overstimulates glutamate receptors in the brain and could cause neuronal damage. While glutamate is indeed a neurotransmitter and high-dose glutamate can cause neurotoxicity in animal models, the blood-brain barrier and normal metabolic regulation are generally considered sufficient to prevent dietary MSG from affecting brain glutamate levels. A 2018 EFSA re-evaluation noted that combined exposure to glutamates from all sources (including naturally occurring glutamate in protein-rich foods and other added glutamates E621-E625) could approach the new lower ADI in high consumers — a concern particularly for children with high processed food intake.
Olestra: Olestra caused significant gastrointestinal side effects that were prominently noted on mandatory warning labels: 'This Product Contains Olestra. Olestra may cause abdominal cramping and loose stools. Olestra inhibits the absorption of some vitamins and other nutrients. Vitamins A, D, E, and K have been added.' Reported gastrointestinal effects included diarrhea, abdominal cramping, oily anal leakage ('anal leakage' or 'rectal leakage'), and fatty stools. These effects were often embarrassing and uncomfortable. Multiple consumer complaints documented GI distress from Olean chips. Beyond GI effects, olestra significantly inhibits the absorption of fat-soluble vitamins (A, D, E, K) and fat-soluble carotenoids (lycopene, lutein, beta-carotene). Since fat-soluble vitamins require fat for absorption, and olestra passes through without being absorbed, it 'captures' these vitamins and carries them out of the body. Studies found olestra consumption reduced serum carotenoid levels, prompting Frito-Lay to fortify olestra products with fat-soluble vitamins to compensate. The FDA removed the mandatory GI warning requirement in 2003 after Frito-Lay argued the warning was overstated, though olestra's use had already declined dramatically due to consumer avoidance.
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