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methanol (11% of aspartame), made by body into formaldehyde in many vulnerable tissues, causes modern diseases of civilization, summary of a century of research, Woodrow C Monte PhD, Medical Hypotheses journal: Rich Murray 2009.11.15

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  • Rich Murray
    methanol (11% of aspartame), made by body into formaldehyde in many vulnerable tissues, causes modern diseases of civilization, summary of a century of
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      methanol (11% of aspartame), made by body into formaldehyde in many
      vulnerable tissues, causes modern diseases of civilization, summary of a
      century of research, Woodrow C Monte PhD, Medical Hypotheses journal: Rich
      Murray 2009.11.15
      http://rmforall.blogspot.com/2009_11_01_archive.htm
      Sunday, November 15, 2009
      http://groups.yahoo.com/group/aspartameNM/message/1589
      _____________________________________________________


      Methanol: A Chemical Trojan Horse as the Root of the Inscrutable U
      Prepublication Copy; Medical Hypotheses -- 06 November 2009
      (10.1016/j.mehy.2009.09.059)
      http://www.medical-hypotheses.com/article/S0306-9877(09)00693-8/abstract
      Woodrow C. Monte PhD
      Professor of Food Science (retired)
      Arizona State University
      corresponding author : Woodrow C. Monte PhD
      470 South Rainbow Drive
      Page, Arizona 86040
      Key Words:
      food epidemiology; diseases of civilization; methanol; formaldehyde;
      aspartame; autism; multiple sclerosis; Alzheimer's; U-shaped curve.

      Abstract:

      Until 200 years ago, methanol was an extremely rare component of
      the human diet and is still rarely consumed in contemporary hunter
      and gatherer cultures.
      With the invention of canning in the 1800s, canned and bottled
      fruits and vegetables, whose methanol content greatly exceeds that
      of' their fresh counterparts, became far more prevalent.
      The recent dietary introduction of aspartame, an artificial sweetener,
      11% methanol by weight, has also greatly increased methanol
      consumption.
      Moreover, methanol is a major component of cigarette smoke,
      known to be a causative agent of many diseases of civilization
      (DOC).
      Conversion to formaldehyde in organs other than the liver is
      the principal means by which methanol may cause disease.
      The known sites of class I alcohol dehydrogenase (ADH I),
      the only human enzyme capable of metabolizing methanol to
      formaldehyde, correspond to the sites of origin for many DOC.
      Variability in sensitivity to exogenous methanol consumption may be
      accounted for in part by the presence of aldehyde dehydrogenase
      sufficient to reduce the toxic effect of formaldehyde production
      in tissue through its conversion to the much less toxic formic acid.
      The consumption or endogenous production of small amounts of
      ethanol, which acts as a competitive inhibitor of methanol's
      conversion to formaldehyde by ADH I, may afford some individuals
      protection from DOC.

      [ ----- Original Message -----
      From: Woodrow Monte
      To: rmforall@... ; mgold@...
      Sent: Saturday, November 14, 2009 9:22 AM
      Subject: Hi Rich Murray and Mark Gold from Woodrow Monte

      Richard and Mark:

      I hope all is well with you both.
      I finally had the chance to put exactly what I have been thinking
      relative to methanol and its relationship to formaldehyde and
      formate [formic acid] into an article. The paper was accepted by the
      journal Medical Hypothesis and is now on Pub Med in prepublication
      corrected proof form.

      http://www.ncbi.nlm.nih.gov/pubmed/19896282?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1

      I have attached the pre-publication copy of the article.

      The quote that follows is what the journal says that I can do with
      this copy.

      "the right to post a pre-print version of the journal article on
      Internet web sites including electronic pre-print servers, and
      to retain indefinitely such version on such servers or sites."

      Please email me with any questions.

      As you will see I have no faith in Formate or Formic Acid as
      being the toxic agent for methanol.
      The devil is in the aldehyde. [ Formaldehyde ]

      Thanks for all your support in the past.

      Woodrow ]

      Introduction:

      The quest for a small molecule as an etiological cause of the diseases
      of civilization has always ignored one of its smallest and most stealthy
      agents: methanol -- a molecule capable of effortless perivascular
      access.
      A rare component of unprocessed food, methanol has increased
      incrementally in the human diet since the advent of commercialized
      canning in the 1800s and most recently due to the popularity of
      products sweetened with aspartame.
      Although the extreme sensitivity of humans to methanol is well
      established, its conversion to formaldehyde in situ within the vessels
      of the brain and elsewhere is undetectable, making methanol placed
      formaldehyde a paradigm of toxicity that is as compelling in theory
      as it is difficult in practice to study.
      The methanol toxicity literature of the last forty years has been
      overwhelmingly in favor of a benign role for environmental dosages
      of methanol.
      Drawing on scant evidence from arguably inadequate animal models,
      this research denies any significant link to formaldehyde, pointing
      instead to a considerably less toxic and considerably more detectable
      secondary metabolite -- formate. [formic acid]
      Not insignificantly, much of the funding for such studies comes from
      sources with a vested interest in maintaining public confidence in the
      dietary safety of methanol.
      The fact remains, however, that environmental methanol in humans
      allows formaldehyde greater access to regions of the body prone to
      disease, exposing vulnerable protein and DNA to methylation and
      other modifications capable of inducing carcinogenicity,
      mutagenicity, teratogenicity, and direct macrophage phagocytosis.
      Given its many harmful effects, the potentially critical role of dietary
      methanol in the increasing incidence of diseases of civilization needs
      to be reexamined.

      The Hypothesis:

      Formaldehyde produced from dietary and environmental methanol
      metabolized in situ at the non-hepatic sites of class I alcohol
      dehydrogenase (ADH I) may play a role in many diseases of
      civilization (DOC).
      Ethanol may in turn act as a competitive inhibitor of methanol's
      conversion to formaldehyde by ADH I, as reflected in the
      U-shaped curve of alcohol consumption.

      Discussion:

      July 24, 1981, should be a significant date for scientists investigating
      worldwide epidemics of Alzheimer's disease (AD),[#540],[#533]
      multiple sclerosis (MS),[#77],[#214] atherosclerotic cardiovascular
      disease (ACD),[#532] lupus,[#536] skin[#95] and breast cancer,
      [#250],[#193] autism,[#525] and other diseases of civilization
      (DOC).

      On this date the U.S. Food and Drug Administration approved the
      use of aspartame,[#472] a new artificial sweetener.[#473]
      As aspartame eventually became a major source of methanol in the
      civilized human diet,[#1] the incidence of DOC gradually began to
      rise.
      Rarely found in nature and an insignificant component of the diets of
      Pleistocene man and present-day foragers, methanol has been
      increasing incrementally in the diet of civilized humanity since 1806
      when Nicolas Appert commercialized canning, a process that traps
      methanol derived from the heating and storage of plant materials
      containing pectin.[#1]

      In addition to aspartame, and canned vegetables, fruits, and their
      juices,[#28],[#29] a major source of the methanol
      entering the modern civilized human body is cigarette smoke,[#62]
      causatively linked to atherosclerosis, multiple sclerosis,[#68]
      lupus,[#73] Alzheimer's disease,[#535] rheumatoid arthritis,[#332]
      and other DOC.[#345]

      A poison to which humans are particularly sensitive,[#3] methanol
      was responsible for the loss of hundreds of lives at the beginning of
      the twentieth century[#17] when extensive animal testing determined
      it was safer than ethanol, allowing its first use in foods and
      drugs.[#165]
      Because the toxicity of methanol in the human system cannot be
      properly tested in animals, the results of this research were specious.

      Searching for the cause of the metabolic anomaly that makes the
      human relationship to methanol distinct from all laboratory animal
      models, including primates,[#116] has always been muddied by
      industrial agendas[#39] with a vested interest in proving that the
      formaldehyde produced from methanol in the human body does no
      harm.[#40],[#121]
      The prevalence of compromised literature and the lack of an
      applicable animal model may explain why methanol, which fits many
      of the criteria of availability and stealth that one would expect of a
      usual suspect, has not yet caught the attention of scientists searching
      for the elusive etiologic agent of DOC.
      The single article that posits methanol as the possible direct cause of
      multiple sclerosis[#8] is never cited in the MS literature.
      A recent series of comprehensive in-vitro studies has also
      convincingly linked Alzheimer's disease to very low concentrations of
      formaldehyde.
      This research mentions methanol as a possible invivo source,[#234],
      [#235] but significantly, it neglects to stress the fact that there is no
      simpler way for formaldehyde to get past the blood brain barrier
      than in the form of this smallest of alcohols.[#367]
      Methanol is itself harmless but is a Trojan horse for formaldehyde,
      a chemical that can pose a severe risk to humans,[#7] who appear
      to be the only mammal exclusively endowed with a hepatic catalase
      enzyme incapable of removing dietary methanol before it can enter
      the general circulation.[#52]

      Once methanol runs the gauntlet of first-pass metabolism, its
      detoxification is no longer exclusive to the liver.
      Formaldehyde, the first metabolite of methanol, can then be
      produced within the arteries and veins,[#220] heart,[#503]
      brain,[#218] lungs,[#221] breast,[#358] bone,[#503]
      and skin.[#221]

      These major organs harbor extra hepatic sites of the only remaining
      human enzyme capable of metabolizing methanol,
      class I alcohol dehydrogenase (ADH I).[#112]

      Methanol transports its potential to become formaldehyde past
      normal biological barriers in the brain and elsewhere that
      environmental formaldehyde itself cannot usually penetrate.[#122]

      That formaldehyde produced in these organs from methanol has
      not been detected directly in humans should not be surprising since
      formaldehyde vanishes within minutes, binding to
      macromolecules[#114] even when a solution of it is injected directly
      into tissue[#122] or spiked into cell-free human serum.[#236]

      Although methylation caused by this toxic process could be
      functionally destructive to the macromolecule so modified, the
      addition of methyl groups to large molecules renders the modification
      and its source invisible to any clinical or histological testing
      procedure.[#122],[#236]

      However, in a study by Trocho et al., a portion of the C14 labeled
      methanol moiety of aspartame was shown to bind to such
      macromolecules via formaldehyde and not pass directly into the
      one-carbon cycle via formate as predicted by the generally accepted
      model of methanol toxicity,[#40] a model developed from studying
      the severe methanol poisoning of monkeys, not the chronic
      environmental exposure of humans.

      Formate derived from methanol metabolism is never measurable in
      human blood when small environmentally reflective doses of methanol
      are administered.[#42]
      During acute methanol poisoning, where the methanol concentration
      of the portal vein far exceeds that of ethanol, liver ADH I would be
      saturated with methanol.

      The liver's ample supply of aldehyde dehydrogenase would assure
      production of formic acid, which is metabolized very slowly,
      causing leakage of formate into the general circulation.
      Formate is not, however, a significant poison to humans and has,
      in fact, been used therapeutically and as a food additive.[#365]

      It certainly would be more convenient to have a stable, measurable
      entity such as formate to predict the danger of exposure to methanol,
      but an iron-clad case for the toxicological significance of this much
      less toxic, secondary metabolite has not yet been made.[#55]

      Moreover, the results of Trocho's elegant study should give one
      pause before accepting the widely held premise that formate and
      not formaldehyde is the toxic component of methanol poisoning.

      Laboratories that publish the most cited works are often financially
      supported by industries with much to lose were the safety of methanol
      disproved.
      This research must be carefully reconsidered before we can dismiss
      the potential threat posed by formaldehyde strategically placed by
      dietary methanol.

      Formaldehyde produced within the cell immediately reacts with water
      to produce formal hydrate,[#27] a strong acid[#114] with twice the
      number of available hydrogen ions as the next methanol metabolite,
      formic acid.
      Formal hydrate produced from methanol by the ADH I sites found in
      the intima, media, and adventitia lining of the circulatory system of the
      heart and brain[#220] would be expected to diffuse into the localized
      tissue, quickly methylating basic molecules such as myelin basic
      protein (MS)[#224] and tau protein (Alzheimer's).[#234]

      Such changes have been shown in these disease states.
      Formaldehyde, also known to uncouple oxidative phosphorylation
      and inhibit phosphorylation within cells,[#113] could contribute to
      these changes reported in MS[#224] and Alzheimer's.[#506]

      The immune system reacts swiftly to methylation of protein by
      formaldehyde -- a phenomenon put to good use by the vaccine
      industry for the last hundred years.[#26]

      Macrophages have activation sites specifically for formaldehyde
      modified protein[#23] and are well known to have a ravenous
      appetite for LDLs reacted with small aldehydes.[#507]

      This induces the esterification of phagocytized LDL cholesterol and
      the subsequent transformation of the macrophages to
      foam cells,[#508] similar to the sequence of events leading to
      atheroma production adjacent to the intima layer of the human aorta,
      rich in ADH I.[#220]

      The potential for antibody production against methylated self-protein
      phagocytized by macrophages has never been investigated.

      Ethanol in low concentrations acts as a powerful competitive
      inhibitor[#439] with a 16:1 preference for ethanol to acetaldehyde
      over the conversion of methanol of formaldehyde by ADH I.[#389]
      For this reason, ethanol is used, without FDA approval, as the
      preferred antidote for accidental methanol poisoning in emergency
      rooms throughout the world.[#253]

      Very low levels of ethanol in the bloodstream would substantively
      prevent all formaldehyde production from dietary methanol
      anywhere in the body.

      Protection from formaldehyde production may account for the yet
      unexplained dose region of apparent improvement in the
      U-shaped curve of alcohol consumption.
      Epidemiologic studies show moderate consumption of alcohol is
      associated with a reduced risk of myocardial infarction,[#485]
      dementia,[#534] lupus,[#73] and other DOC.

      Low doses of ethanol appear to provide a preventative measure
      against the causes of DOC.[#279]
      Recent studies of individuals who consumed at least one alcoholic
      drink per day show subjects had an additional 86 percent
      reduction in risk of myocardial infarction if they were genetically
      endowed with a genotype of ADH I that was 2.5 times slower to
      metabolize ethanol than the control
      These findings were "consistent with the hypothesis that a slower
      rate of clearance of alcohol enhances the beneficial effect of
      moderate alcohol consumption on the risk of cardiovascular
      disease."[#483]

      A compelling explanation of the dose region of adverse effects of
      the U-shaped curve with high ethanol consumption, which shows
      increased risk of these same diseases, could be the mechanism by
      which humans habituate to high consumption of ethanol.

      The induction of the P450 hepatic microsomal ethanol oxidizing
      system[#175] results in a considerably higher clearance rate of
      ethanol from the bloodstream for an extended period of time, thus
      accounting for more consumption leading to statistically less time
      of protection.
      Small amounts of supplemental alcohol not sufficient to induce
      P450 might be expected to prolong the residence time and avoid
      gaps in the protection afforded by ethanol in preventing methanol
      placed formaldehyde.

      It appears that the average person, whether or not an imbiber,
      may typically have endogenous ethanol in the blood[#174]
      produced by gut fermentation.[#363]
      This ethanol must pass through the liver via the hepatic portal vein
      coincidently with dietary methanol absorbed from the gut contents.
      The liver has the highest concentration of ADH I in the body.

      Even traces of ethanol in the blood, however, would seem to
      indicate the absence of available sites remaining for the oxidation
      of the much less competitive methanol, allowing most dietary
      methanol to pass freely into the general circulation.

      What follows is a biochemical game of musical chairs as methanol
      travels round and round the circulation, waiting for the ethanol levels
      to reach zero and the music to stop.
      The closest ADH I free to service the methanol will convert it to
      formaldehyde. If this happens in the liver, where there are ample
      supplies of aldehyde dehydrogenase, metabolism to carbon dioxide
      will proceed safely.

      In mammary epithelium, however,
      where human class I alcohol dehydrogenase is highly expressed[#358]
      but active aldehyde dehydrogenase[#216] is scarce, methanol placed
      formaldehyde could become a problem.

      Formaldehyde is a class I carcinogen[#11] and mutagen[#449]
      with methanol providing its only easy avenue into this tissue.
      In the vasculature of the brain[#218] and other ADH I positive
      organs, the consequences may be similarly troublesome.
      The obvious way to prevent formaldehyde from damaging this
      sensitive tissue is to keep the music playing, a solution dependent
      on our ability to answer the following questions:
      Just how much ethanol is essential in this seemingly inscrutable
      U-shaped curve?
      What measures should we take to combat this chemical Trojan horse,
      thereby reducing the methanol contamination in the diet of civilization
      and making it more like the diet of our ancient ancestors?

      Both research areas present intriguing inquiries, but as a food
      scientist, I would stress the relative ease and greater benefits of
      investigating the latter.

      Proposed test of the hypothesis:

      Under strict medical supervision this hypothesis would best be tested
      on experimental subjects suffering from relapsing multiple sclerosis.
      Without here getting into great detail, the preferred mode of
      administration of small amounts of ethanol would be via gaseous
      administration at sufficient, carefully controlled, atmospheric
      concentration to maintain a constant 1-2 parts per million ethanol
      concentrations in the test subjects bloodstream.
      At such low levels, well below the ambient concentrations of ethanol
      in the average pub environment, ethanol is quite safe and not
      detectable in the air via the olfactory system of most people.
      A water vaporization control would work well and be conducive to
      a double blind study.
      Vaporous administration of ethanol is well covered in the literature,
      and is used frequently to induce alcohol intoxication of test animals
      for toxicity testing purposes.

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      Science 1981;213(28):986-87.

      473. Dickson D.
      Aspartame sugar substitute. New court overruled.
      Nature 292:283 1981;292(July 23):283.

      483. Hines LM., Meir S, Stampfer J, Jingma H, Gaziano M.
      Genetic Variation in Alcohol Dehydrogenase and the Beneficial
      Effect of Moderate Alcohol Consumption on Myocardial
      Infarction.
      N Engl J Med 2001;344(8):549-55.

      485. Klatsky A.
      Alcohol, wine, and vascular diseases -- an abundance of paradoxes.
      Am J Physiol Heart Circ Physiol 2008;294:582-83.

      503. Estonius M, Svensson S, Höög J.
      Alcohol dehydrogenase in human tissues: localisation of transcripts
      coding for five classes of the enzyme.
      FEBS Lett. 1996;397:338-42.

      506. Luo Y, Ingram V.
      Uncoupling of mitochondria activates protein phosphatases and
      inactivates MBP protein kinases.
      J Alzheimers Dis 2001;3(6):593-98.

      507. Kawamura M, Heinecke J, Chait A.
      Increased uptake of alpha-hydroxy aldehyde-modified
      low density lipoprotein by macrophage scavenger receptors.
      J Lipid Res. 41(7):1054 2000;41(7):1054-59.

      508. Fogelman A, Shechter I, Seager J, Hokom M, Child J,
      Edwards P.
      Malondialdehyde alteration of low density lipoproteins leads to
      cholesteryl ester accumulation in human monocyte-macrophages.
      Proc Natl Acad Sci. 1980;77(4):2214-8.

      525. Blaxill M.
      What's going on? The question of time trends in autism.
      Public Health 2004;119(6):536-51.

      532. Yusuf S, Ounpuu S, Anand S.
      The global epidemic of atherosclerotic cardiovascular disease.
      Med Princ Pract 2002;11(Suppl 2):3-8.

      533. Waldman M.
      Are We Experiencing an Alzheimer's Epidemic?
      Presentation (Abstract 90)
      [AD/PD 2009: 9th International Conference on Alzheimer's
      and Parkinson's Diseases:] ; 2009.
      http://www.medscape.com/viewarticle/590106

      534. Sink K.
      Moderate Alcohol Consumption May Lower Dementia Risk in
      Cognitively Normal Elderly.
      Presentation. Alzheimer's Association
      2009 International Conference on Alzheimer's Disease (ICAD),
      Vienna. www.medscape.com

      535. Mehlig K, Skoog I, Guo X, Schütze M, Gustafson D,
      Waern M, et al.
      Alcoholic Beverages and Incidence of Dementia: 34-Year Follow-up
      of the Prospective Population Study of Women in Göteborg.
      Am J Epidemiol 2008;167(6):684-91.

      536. Uramoto K, Michet C, Thumboo J, Sunku J, O'Fallon W,
      Gabriel S.
      Trends in the incidence and mortality of systemic lupus
      erythematosus, 1950-1992.
      Arthritis Rheum 1999;42(1):46-50.

      540. Casserly I, Topol E.
      Convergence of atherosclerosis and Alzheimer's disease:
      inflammation, cholesterol, and misfolded proteins.
      Lancet 2004;363(9415):1139-46.
      _____________________________________________________


      old tiger roars -- Woodrow C Monte, PhD -- aspartame causes
      many breast cancers, as ADH enzyme in breasts makes methanol
      from diet soda into carcinogenic formaldehyde -- same in dark
      wines and liquors, Fitness Life 2008 Jan.: Murray 2008.02.11
      http://rmforall.blogspot.com/2008_02_01_archive.htm
      Monday, February 11, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1517

      role of formaldehyde, made by body from methanol from foods
      and aspartame, in steep increases in fetal alcohol syndrome,
      autism, multiple sclerosis, lupus, teen suicide, breast cancer,
      Nutrition Prof. Woodrow C. Monte, retired, Arizona State U.,
      two reviews, 190 references supplied, Fitness Life,
      New Zealand 2007 Nov, Dec: Murray 2007.12.26
      http://rmforall.blogspot.com/2007_12_01_archive.htm
      Wednesday, December 26 2007
      http://groups.yahoo.com/group/aspartameNM/message/1498

      Monte WC., Is your Diet Sweetener killing you?
      Fitness Life. 2007 Nov; 33: 31-33.
      Monte WC., A Deadly Experiment.
      Fitness Life. 2007 Dec; 34: 38-42.
      Monte WC., Bittersweet: Aspartame Breast Cancer Link.
      Fitness Life. 2008 Feb; 34: 21-22.

      Article 1 http://www.thetruthaboutstuff.com/review1.shtml
      Article 2 http://www.thetruthaboutstuff.com/review2.shtml
      Article 3 http://www.thetruthaboutstuff.com/review3.shtml

      http://www.thetruthaboutstuff.com/articles.shtml
      223 references with abstracts or full and partial texts


      http://groups.yahoo.com/group/aspartameNM/message/870
      Aspartame: Methanol and the Public Interest 1984: Monte:
      Murray 2002.09.23 rmforall

      Dr. Woodrow C. Monte Aspartame: methanol, and the public health.
      Journal of Applied Nutrition 1984; 36 (1): 42-54.
      (62 references) Professsor of Food Science [retired 1992]
      Arizona State University, Tempe, Arizona 85287
      woodymonte@...; woodymonte@...;
      The methanol from 2 L of diet soda, 5.6 12-oz cans, 20 mg/can, is
      112 mg, 10% of the aspartame.
      The EPA limit for water is 7.8 mg daily for methanol (wood alcohol),
      a deadly cumulative poison.
      Many users drink 1-2 L daily.
      The reported symptoms are entirely consistent with chronic methanol
      toxicity. (Fresh orange juice has 34 mg/L, but, like all juices, has 16
      times more ethanol, which strongly protects against methanol.)

      "The greater toxicity of methanol to man is deeply rooted in the
      limited biochemical pathways available to humans for detoxification.
      The loss of uricase (EC 1.7.3.3.),
      formyl-tetrahydrofolate synthetase (EC 6.3.4.3.) (42)
      and other enzymes (18) during evolution sets man apart from all
      laboratory animals including the monkey (42).

      There is no generally accepted animal model
      for methanol toxicity (42, 59).

      Humans suffer "toxic syndrome" (54) at a minimum lethal dose
      of <1 gm/kg, much less than that of monkeys, 3-6 g/kg (42, 59).

      The minimum lethal dose of methanol
      in the rat, rabbit, and dog is 9.5, 7.0 , and 8.0 g/kg, respectively (43);
      ethyl alcohol is more toxic than methanol to these test animals (43)."

      Recent research [see links at end of post] supports his focus on the
      methanol to formaldehyde toxic process:

      "The United States Environmental Protection Agency in their
      Multimedia Environmental Goals for Environmental Assessment
      recommends a minimum acute toxicity concentration
      of methanol in drinking water at 3.9 parts per million,
      with a recommended limit of consumption below 7.8 mg/day (8).

      This report clearly indicates that methanol:

      "...is considered a cumulative poison due to the low rate of excretion
      once it is absorbed. In the body, methanol is oxidized to
      formaldehyde and formic acid; both of these metabolites are
      toxic." (8)...

      Recently the toxic role of formaldehyde (in methanol toxicity) has
      been questioned (34).
      No skeptic can overlook the fact that, metabolically, formaldehyde
      must be formed as an intermediate to formic acid production (54).

      Formaldehyde has a high reactivity which may be why it has not been
      found in humans or other primates during methanol poisoning (59)....

      If formaldehyde is produced from methanol and does have a
      reasonable half life within certain cells in the poisoned organism
      he chronic toxicological ramifications could be grave.

      Formaldehyde is a known carcinogen (57) producing squanous-cell
      carcinomas by inhalation exposure in experimental animals (22).
      The available epidemiological studies do not provide adequate data
      for assessing the carcinogenicity of formaldehyde in man (22, 24, 57).

      However, reaction of formaldehyde with deoxyribonucleic acid
      (DNA) has resulted in irreversible denaturation that could interfere
      with DNA replication and result in mutation (37)..."


      It is certain that high levels of aspartame use,
      above 2 liters daily for months and years,
      must lead to chronic formaldehyde-formic acid toxicity.

      Fully 11 % of aspartame is methanol -- 1,120 mg aspartame
      in 2 L diet soda, almost six 12-oz cans, gives 123 mg methanol
      (wood alcohol). The methanol is immediately released
      into the body after drinking .
      Within hours, the liver turns much of the methanol into formaldehyde,
      and then much of that into formic acid, both of which in time
      are partially eliminated as carbon dioxide and water.

      However, about 30 % of the methanol remains in the body
      as cumulative durable toxic metabolites of formaldehyde
      and formic acid -- 37 mg daily,
      a gram every month, accumulating in and affecting every tissue.

      If only 10 % of the methanol is retained daily as formaldehyde,
      that would give 12 mg daily formaldehyde accumulation -- about
      60 times more than the 0.2 mg from 10 % retention
      of the 2 mg EPA daily limit for formaldehyde in drinking water.

      Bear in mind that the EPA limit for formaldehyde in drinking water is
      1 ppm, or 2 mg daily for a typical daily consumption of 2 L of water.

      http://groups.yahoo.com/group/aspartameNM/message/835
      ATSDR: EPA limit 1 ppm formaldehyde in drinking water July 1999:
      Murray 2002.05.30

      This long-term low-level chronic toxic exposure leads to typical
      patterns of increasingly severe complex symptoms,
      starting with headache, fatigue, joint pain, irritability, memory loss,
      rashes, and leading to vision and eye problems, and even seizures.
      In many cases there is addiction. Probably there are immune system
      disorders, with a hypersensitivity to these toxins and other chemicals.

      J. Nutrition 1973 Oct; 103(10): 1454-1459.
      Metabolism of aspartame in monkeys.
      Oppermann JA, Muldoon E, Ranney RE.
      Dept. of Biochemistry, Searle Laboratories,
      Division of G.D. Searle and Co. Box 5110, Chicago, IL 60680
      They found that about 70 % of the radioactive methanol in aspartame
      put into the stomachs of 3 to 7 kg monkeys
      was eliminated within 8 hours, with little additional elimination,
      as carbon dioxide in exhaled air and as water in the urine.
      They did not mention that this meant that about 30 % of the methanol
      must transform into formaldehyde and then into formic acid,
      both of which must remain as toxic products in all parts of the body.
      They did not report any studies on the distribution of radioactivity
      in body tissues, except that blood plasma proteins after 4 days
      held 4 % of the initial methanol.
      This study did not monitor long-term use of aspartame.

      http://groups.yahoo.com/group/aspartameNM/message/1373
      aspartame rat brain toxicity re cytochrome P450 enzymes,
      especially CYP2E1, Vences-Mejia A, Espinosa-Aguirre JJ et al,
      2006 Aug, Hum Exp Toxicol: relevant abstracts re formaldehyde
      from methanol in alcohol drinks: Murray 2006.09.29

      http://groups.yahoo.com/group/aspartameNM/message/1463
      Direct and indirect cellular effects of aspartame on the brain,
      Humphries P, Pretorius E, Naude H, U. Pretoria, South Africa,
      Eur J Clin Nutr. 2007 Aug 8: Murray 2007.08.12

      http://groups.yahoo.com/group/aspartameNM/message/1340
      aspartame groups and books: updated research review
      of 2004.07.16: Murray 2006.05.11

      details on 6 epidemiological studies since 2004 on diet soda
      (mainly aspartame) correlations, as well as 14 other mainstream
      studies on aspartame toxicity since summer 2005:
      Murray 2007.11.18
      http://rmforall.blogspot.com/2007_11_01_archive.htm
      Wednesday, November 14, 2007
      http://groups.yahoo.com/group/aspartameNM/message/1490

      older women drinking over 2 aspartame beverages daily had 30%
      decline kidney function in 11 years, Nurses Health Study, Julie Lin,
      Gary C Curhan, Brigham and Women's Hospital, Boston:
      Rich Murray 2009.11.02
      http://rmforall.blogspot.com/2009_11_01_archive.htm
      Monday, November 2, 2009
      http://groups.yahoo.com/group/aspartameNM/message/1588

      consider co-factors (methanol, formaldehyde, and protective folic
      acid), re UK FSA test of aspartame in candy bars on 50 reactors,
      Stephen L Atkin, Hull York Medical School:
      Rich Murray 2009.09.29
      http://rmforall.blogspot.com/2009_09_01_archive.htm
      Tuesday, September 29, 2009
      http://groups.yahoo.com/group/aspartameNM/message/1587

      Included herein is substantial mainstream evidence that the natural
      conversion in humans of orally ingested methanol into formaldehyde
      and then formic acid results in substantial, durable, cumulative
      retention of toxic reaction products.

      Adequate folic acid levels expedite the safe metabolism of methanol
      in most people.

      Ethyl alcohol and folic acid in vegetables and fruits are sufficient
      to protect most people from conversion of their methanol into
      formaldehyde.

      Many common agents interfere with folic acid (folic acid antagonists).

      Additionally, genetic variations are potent.

      About 3/4 of reactors are female.

      Those who rarely have alcohol hangovers may be substantially immune
      to methanol and formaldehyde.

      Recent exposure to alcohol beverages, tobacco and wood smoke,
      and a large variety of formaldehyde sources may compromise the
      clarity of aspartame reaction tests.

      Aspartame reactors often report allergies to many agents, with similar
      symptoms: mercury (amalgams and fish), MSG and free glutamate in
      foods (for instance, hydrolyzed vegetable or yeast protein), carbon
      monoxide, molds, many foods, etc. -- up to Multiple Chemical
      Sensitivity.

      Aspartame reactors often take many steps to exercise, reduce stress,
      lower salt, emphasize organic plant foods, reduce drug and chemical
      exposures, limit protein and fat intake, use vitamin and mineral
      supplements, limit processed foods -- thus complicating attempts to
      create a matching control group, and introducing uncertainty about
      whether the reactors are as vulnerable now as in the past, when they
      may have had more negative factors for years.

      So, genetic background, age, sex, obesity, existing illnesses, diet,
      exercise, environmental toxins, medicines and drugs, parental
      exposure to all these factors, and more may corrode the "gold
      standard" of a single exposure double-blind experimental test,
      especially for a rather modest test group of 50.

      Perhaps, a more productive research strategy would be to test 10
      reactors, one at a time, for 24 hours each, using a wide range of
      tests, recording the enormous individual variations that are usually
      swamped by taking group data averages.

      Computerized tests facilitate fast, affordable measures of cognitive
      and memory effects.

      Full audio and video recording is now available.

      Dimethyl dicarbonate, an approved additive for reducing fungi in
      wines, perhaps with a neutral taste, quickly releases about the same
      level of methanol upon ingestion as aspartame drinks, making
      possible studies free of any possible "excitotoxic" effects of
      aspartic acid and phenylalanine, while allowing a third beverage
      to be a control substance.

      This approach would also contribute to the meager research literature
      about the role of methanol in alcohol hangovers.

      aspartame reactors may send detailed feedback to Andrew Wadge,
      UK Food Standards Agency to guide new pilot study re bad
      reactions: Rich Murray 2009.06.22
      http://rmforall.blogspot.com/2009_06_01_archive.htm
      Monday, June 22, 2009
      http://groups.yahoo.com/group/aspartameNM/message/1577

      unexamined cofactors re folic acid antagonist research include
      methanol (quickly turns into formaldehyde and then formic acid in
      humans) from tobacco and wood smoke, alcohol beverages,
      aspartame, demethylation of caffeine: Rich Murray
      2008.12.01
      http://rmforall.blogspot.com/2008_10_01_archive.htm
      Monday, December 1, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1569

      http://www.dorway.com/products.txt

      [ rearranged, 11% methanol added ]
      From the Nutrasweet Web Site: (amounts in various "foods")

      Product Category -- Serving Size -- aspartame -- 11% methanol

      Gelatin Dessert ----------- 8 ounces -----190 mg ---- 21 mg
      Carbonated Beverage --- 12 ounces ----- 180 ------- 20
      " ------------------------ 48 ounces ----- 720 ------- 79
      Powdered Drink -------- 12 ounces ----- 180 -------- 20
      Fruit Drink (10% juice) -- 12 ounces ----- 140 -------15.4
      Hot Chocolate ----------- 12 ounces ----- 100 -------11
      Yogurt ------------------- 8 ounces ----- 124 --------13.6
      Ice Cream ---------------- 8 ounces ----- 100 ------- 11
      Pudding Dessert ---------- 8 ounces ------ 50 --------- 5.5
      Frozen Novelty ----------- 2-3 ounces ---- 50 --------- 5.5
      Gum ----------------------- 1 stick -------- 6-8 -------- 0.7-0.9
      Vitamins ------------------ 1 vitamin ------ 4 ---------- 0.44
      Breath mint ---------------- 1 mint --------- 1.5 -------- 0.17



      http://groups.yahoo.com/group/aspartameNM/message/846
      aspartame in Merck Maxalt-MLT worsens migraine,
      AstraZeneca Zomig, Eli Lilly Zyprexa,
      J&J Merck Pepcid AC (Famotidine 10mg) Chewable Tab,
      Pfizer Cool Mint Listerine Pocketpaks: Murray 2002.07.16

      Migraine MLT-Down: an unusual presentation of migraine
      in patients with aspartame-triggered headaches.
      Newman LC, Lipton RB Headache 2001 Oct; 41(9): 899-901.
      [ Merck 10-mg Maxalt-MLT, for migraine, has 3.75 mg aspartame,
      while 12 oz diet soda has 200 mg. ]
      Headache Institute, St. Lukes-Roosevelt Hospital Center,
      New York, NY
      Department of Neurology newmanache@...
      Albert Einstein College of Medicine, Bronx, NY
      Innovative Medical Research RLipton@...


      http://groups.yahoo.com/group/aspartameNM/message/855
      Blumenthall & Vance: aspartame chewing gum headaches
      Nov 1997: Murray 2002.07.28

      Harvey J. Blumenthal, MD, Dwight A Vance, RPh
      Chewing Gum Headaches. Headache 1997 Nov; 37(10): 665-6.
      Department of Neurology, University of Oklahoma College of
      Medicine, Tulsa, USA. neurotulsa@...
      Aspartame, a popular dietetic sweetener, may provoke headache in
      some susceptible individuals. Herein, we describe three cases of
      young women with migraine who reported their headaches could be
      provoked by chewing gum sweetened with aspartame.
      [ 6-8 mg aspartame per stick chewing gum ]


      http://groups.yahoo.com/group/aspartameNM/message/1143
      antiseptic? antifungal? antiviral? methanol (formaldehyde, formic
      acid) disposition: Bouchard M et al, full plain text, 2001:
      substantial
      sources are degradation of fruit pectins, liquors, aspartame, smoke:
      Murray 2005.01.05 rmforall

      http://www.toxsci.oupjournals.org/cgi/content/full/64/2/169
      free full text

      A Biologically Based Dynamic Model for Predicting the Disposition
      of Methanol and Its Metabolites in Animals and Humans.
      Michèle Bouchard,
      Robert C. Brunet,
      Pierre-Olivier Droz,
      and Gaétan Carrier.
      Toxicological Sciences 64, 169-184 (2001)
      Copyright © 2001 by the Society of Toxicology
      [ extracts ]

      "Exposure to methanol also results from the consumption of certain
      foodstuffs (fruits, fruit juices, certain vegetables, aspartame
      sweetener, roasted coffee, honey) and alcoholic beverages (Health
      Effects Institute, 1987; Jacobsen et al., 1988).
      [ It's unusual for a mainstream journal article to mention "fruits,
      fruit juices, certain vegetables, aspartame sweetener" and "alcoholic
      beverages" to be methanol sources.]
      ... little is known about the chronic effects of low exposure doses...
      Systemic methanol is extensively metabolized by liver alcohol
      dehydrogenase [ ADH ] and catalase-peroxidase enzymes to
      formaldehyde, which is in turn rapidly oxidized to formic acid by
      formaldehyde dehydrogenase enzymes...
      Formaldehyde, as it is highly reactive, forms relatively stable
      adducts with cellular constituents...
      Primates and humans appear to be more susceptible to the acute
      toxicity of methanol than rodents...
      Although methanol has been reported to be metabolized mainly in
      the liver, pulmonary metabolism is also likely to occur. Indeed,
      the catalase-peroxidase system responsible for a major fraction of
      methanol metabolism in rats is widely distributed in mammalian
      tissues...
      The model included a constant background whole body methanol
      burden of 2.133 mmol, which corresponds to the mean blood
      concentration of 0.5 mg/L of methanol measured by Osterloh et al.
      (1996) in control subjects at the end of an 8-h frequent blood
      sampling period...
      ... once formed, a substantial fraction of formaldehyde is converted
      to unobserved forms. This pathway contributes to a long-term
      unobserved compartment. The latter, most plausibly, represents
      either the formaldehyde that ( directly or after oxidation to
      formate )
      binds to various endogenous molecules (Heck et al., 1983; Roe,
      1982)...
      That substantial amounts of methanol metabolites or by-products
      are retained for a long time is verified by Horton et al. (1992)
      who estimated that 18 h following an iv injection of 100 mg/kg
      of 14C-methanol in male Fischer-344 rats, only 57% of the
      dose was eliminated from the body. From the data of Dorman
      et al. (1994) and Medinsky et al. (1997), it can further be
      calculated that 48 h following the start of a 2-h inhalation
      exposure to 900 ppm of 14C-methanol vapors in female
      cynomolgus monkeys, only 23% of the absorbed 14C-methanol
      was eliminated from the body. These findings are corroborated by
      the data of Heck et al. (1983) showing that 40% of a
      14C-formaldehyde inhalation dose remained in the body 70 h
      postexposure...
      Experimental studies on the detailed time profiles following
      controlled repeated exposures to methanol are lacking...
      Thus, in monkeys and plausibly humans, a much larger fraction of
      body formaldehyde is rapidly converted to unobserved forms
      rather than passed on to formate and eventually CO2."

      If we assume 30% retention of durable cumulative toxic products of
      formaldehyde and formic acid, then a 12-oz can diet drink gives 200
      mg aspartame, 22 mg methanol, and 7 mg formaldehyde and formic
      acid at 30% cumulative retention. We may add that well known
      sources of formaldehyde include both wood and tobacco smoke,
      and, notoriously, mobile homes. Two teams give evidence that
      formaldehyde and formic acid from methanol in ethanol drinks
      (often far above the 100 mg/L methanol in red wines, two times the
      level in aspartame drinks) are the main cause of the many symptoms
      of "morning after" hangovers.

      http://groups.yahoo.com/group/aspartameNM/message/1495
      folic acid prevents neurotoxicity from formic acid, made by body
      from methanol impurity in alcohol drinks [ also 11 % of aspartame ],
      BM Kapur, PL Carlen, DC Lehotay, AC Vandenbroucke,
      Y Adamchik, U. of Toronto, 2007 Dec., Alcoholism Cl. Exp. Res.:
      Murray 2007.11.27

      Furthermore, BM Kapur et al, 2007 give evidence that formic acid
      from methanol in ethanol drinks is a major cause of Fetal Alcohol
      Syndrome, readily preventable by adequate levels of folic acid,
      which expedites the safe metabolism of formaldehyde, in most
      people.
      "Methanol is endogenously formed in the brain and is present as a
      congener in most alcoholic beverages.
      Because ethanol is preferentially metabolized over methanol
      (MeOH) by alcohol dehydrogenase, it is not surprising that
      MeOH accumulates in the alcohol-abusing population.
      This suggests that the alcohol-drinking population will have higher
      levels of MeOH's neurotoxic metabolite, formic acid (FA).
      FA elimination is mediated by folic acid.
      Neurotoxicity is a common result of chronic alcoholism.
      This study shows for the first time that FA, found in chronic
      alcoholics, is neurotoxic and this toxicity can be .mitigated by
      folic acid administration." ...
      "MeOH concentrations between 4 and 4500 mg/l can be present
      in various alcoholic beverages (Sprung et al., 1988)."


      A variety of mutations, as well as aspirin and many painkillers,
      impede folic acid. However, fruits and vegetables give enough folic
      acid to mitigate harm from their methanol. Then again, formaldehyde
      may in many people treat infections by fungi, bacteria, and virusus.
      All these unexamined co-factors have confused attempts to study
      aspartame toxicity for three decades.


      http://groups.yahoo.com/group/aspartameNM/message/1141
      Nurses Health Study can quickly reveal the extent of aspartame
      (methanol, formaldehyde, formic acid) toxicity: Murray 2004.11.21

      The Nurses Health Study is a bonanza of information about the health
      of probably hundreds of nurses who use 6 or more cans daily of diet
      soft drinks -- they have also stored blood and tissue samples from
      their immense pool of subjects, over 100,000 for decades.

      http://groups.yahoo.com/group/aspartameNM/message/1490
      details on 6 epidemiological studies since 2004 on diet soda
      (mainly aspartame) correlations, as well as 14 other mainstream
      studies on aspartame toxicity since summer 2005:
      Murray 2007.11.27

      A widely proclaimed NIH-AARP mass survey by U Lim et al. 2006,
      while failing to show specific cancers with feeble diet drink
      consumption data for a year for seniors, did find that 4% of a
      half-million seniors drank 3 and more cans daily diet soda
      [ 12-oz can gives 200 mg aspartame, 22 mg methanol,
      7 mg formaldehyde and formic acid at 30% cumulative retention ]

      aspartame mg/d
      0 ---- under 100 - 100-200 - 200-400 - 400-600 - 600-1200 -
      cohort %
      46 ------- 25 ------ 13 ------- 7 --------- 5 ------ about 3 ----

      over 1200 mg/d
      under 1%

      This is the first good data about the percentage of aspartame users
      who use over 3 cans daily, averaging 5 cans daily at 200 mg per 12
      oz can diet soda.
      About 4% of 473,984 is 19,000 people, with a peak intake of 17
      cans daily, and average 5 cans daily.
      It would be worthwhile to investigate a wide variety of symptoms for
      the 0.1 % of highest level users, about 500 people.
      For about 200 million USA aspartame users, this would be 200,000
      people.

      The highest level 3400 mg aspartame [ 17 12-oz cans ] gives
      11% = 374 mg methanol, 48 times the recommended daily limit of
      consumption of 7.8 mg as recommended by the
      Environmental Protection Agency (EPA).3

      At 30% retention of cumulative toxic products of formaldehyde and
      formic acid, these would be 125 mg, 60 times higher than the 1999
      EPA alarm level for formaldehyde in daily drinking water of
      1 ppm = 2 mg for average daily drinking water of 2 L daily.

      Since no adequate data has ever been published on the
      exact disposition of toxic metabolites in specific tissues in humans
      of the 11 % methanol component of aspartame,
      the many studies on morning-after hangover from the methanol
      impurity in alcohol drinks are the main available resource to date.

      http://groups.yahoo.com/group/aspartameNM/message/1469
      highly toxic formaldehyde, the cause of alcohol hangovers, is
      made by the body from 100 mg doses of methanol from
      dark wines and liquors, dimethyl dicarbonate, and aspartame:
      Murray 2007.08.31

      http://groups.yahoo.com/group/aspartameNM/message/1052
      DMDC: Dimethyl dicarbonate 200mg/L in drinks
      adds methanol 98 mg/L ( becomes formaldehyde in body ):
      EU Scientific Committee on Foods 2001.07.12:
      Murray 2004.01.22

      http://europa.eu.int/comm/food/fs/sc/scf/out96_en.pdf

      "...DMDC was evaluated by the SCF in 1990
      and considered acceptable for the cold sterilization of soft drinks
      and fruit juices at levels of addition up to 250 mg/L (1)
      ...DMDC decomposes primarily to CO2 and methanol ...

      [ Note: Sterilization of bacteria and fungi is a toxic process,
      probably due to the inevitable conversion in the body of methanol
      into highly toxic formaldehyde and then formic acid. ]

      The use of 200 mg DMDC per liter would add 98 mg/L of
      methanol to wine which already contains an average of about
      40 mg/L from natural sources.

      http://groups.yahoo.com/group/aspartameNM/message/1286
      methanol products (formaldehyde and formic acid) are main
      cause of alcohol hangover symptoms [same as from similar
      amounts of methanol, the 11% part of aspartame]:
      YS Woo et al, 2005 Dec: Murray 2006.01.20

      Addict Biol. 2005 Dec;10(4): 351-5.
      Concentration changes of methanol in blood samples during
      an experimentally induced alcohol hangover state.
      Woo YS, Yoon SJ, Lee HK, Lee CU, Chae JH, Lee CT,
      Kim DJ.
      Chuncheon National Hospital, Department of Psychiatry,
      The Catholic University of Korea, Seoul, Korea.
      http://www.cuk.ac.kr/eng/ sysop@...
      Songsin Campus: 02-740-9714
      Songsim Campus: 02-2164-4116
      Songeui Campus: 02-2164-4114
      http://www.cuk.ac.kr/eng/sub055.htm eight hospitals

      [ Han-Kyu Lee ]

      A hangover is characterized by the unpleasant physical and
      mental symptoms that occur between 8 and 16 hours after
      drinking alcohol.

      After inducing experimental hangover in normal individuals,
      we measured the methanol concentration prior to
      and after alcohol consumption
      and we assessed the association between the hangover
      condition and the blood methanol level.

      A total of 18 normal adult males participated in this study.

      They did not have any previous histories of psychiatric
      or medical disorders.

      The blood ethanol concentration prior to the alcohol intake
      (2.26+/-2.08) was not significantly different from that
      13 hours after the alcohol consumption (3.12+/-2.38).

      However, the difference of methanol concentration
      between the day of experiment (prior to the alcohol intake)
      and the next day (13 hours after the alcohol intake)
      was significant (2.62+/-1.33/l vs. 3.88+/-2.10/l, respectively).

      A significant positive correlation was observed
      between the changes of blood methanol concentration
      and hangover subjective scale score increment when covarying
      for the changes of blood ethanol level (r=0.498, p<0.05).

      This result suggests the possible correlation of methanol
      as well as its toxic metabolite to hangover. PMID: 16318957

      [ The toxic metabolite of methanol is formaldehyde, which in turn
      partially becomes formic acid -- both potent cumulative toxins
      that are the actual cause of the toxicity of methanol.]

      This study by Jones AW (1987) found next-morning hangover
      from red wine with 100 to 150 mg methanol
      (9.5 % w/v ethanol, 100 mg/l methanol, 0.01 %).
      Fully 11% of aspartame is methanol --
      1,120 mg aspartame in 2 L diet soda,
      almost six 12-oz cans, gives 123 mg methanol (wood alcohol).

      Pharmacol Toxicol. 1987 Mar; 60(3): 217-20.
      Elimination half-life of methanol during hangover.
      Jones AW. wayne.jones@...;
      Department of Forensic Toxicology,
      University Hospital, SE-581 85 Linkoping, Sweden.

      This paper reports the elimination half-life of methanol in human
      volunteers.
      Experiments were made during the morning after the subjects had
      consumed 1000-1500 ml red wine
      (9.5 % w/v ethanol, 100 mg/l methanol)
      the previous evening. [ 100 to 150 mg methanol ]
      The washout of methanol from the body
      coincided with the onset of hangover.
      The concentrations of ethanol and methanol in blood were
      determined indirectly by analysis of end-expired alveolar air.
      In the morning when blood-ethanol dropped
      below the Km of liver alcohol dehydrogenase (ADH)
      of about 100 mg/l (2.2 mM),
      the disappearance half-life of ethanol was 21, 22, 18 and 15 min.
      in 4 test subjects respectively.
      The corresponding elimination half-lives of methanol
      were 213, 110, 133 and 142 min. in these same individuals.
      The experimental design outlined in this paper can be used
      to obtain useful data on elimination kinetics of methanol
      in human volunteers without undue ethical limitations.
      Circumstantial evidence is presented to link methanol
      or its toxic metabolic products, formaldehyde and formic acid,
      with the pathogenesis of hangover. PMID: 3588516


      four Murray AspartameNM reviews in SE Jacob & SA
      Stechschulte debate with EG Abegaz & RG Bursey of
      Ajinomoto re migraines from formaldehyde from aspartame,
      Dermatitis 2009 May: TE Hugli -- folic acid with V-C
      protects: Rich Murray 2009.08.12
      http://rmforall.blogspot.com/2009_08_01_archive.htm
      Wednesday, August 12, 2009
      http://groups.yahoo.com/group/aspartameNM/message/1582
      [ extracts ]

      Formaldehyde, aspartame, migraines: a possible connection.
      Abegaz EG, Bursey RG.
      Dermatitis. 2009 May-Jun;20(3):176-7; author reply 177-9.
      No abstract available. PMID: 19470307

      Eyassu G. Abegaz *
      Robert G. Bursey
      Ajinomoto Corporate Services LLC, Scientific & Regulatory
      Affairs, 1120 Connecticut Ave., N.W., Suite 1010,
      Washington, DC 20036
      * Corresponding author. Tel.: +1 202 457 0284;
      fax: +1 202 457 0107.
      abegazee@... (E.G. Abegaz),
      burseyb@... (R.G. Bursey)

      "For example, fruit juices, coffee, and alcoholic beverages produce
      significantly greater quantities of formaldehyde than aspartame-
      containing products. [6]"

      "[6] Magnuson BA, Burdock GA, Doull J, et al. Aspartame: a
      safety evaluation based on current use levels, regulations, and
      toxicological and epidemiological studies.
      Crit Rev Toxicol 2007;37:629-727"

      [ two detailed critiques of industry affiliations and biased science
      in 99 page review with 415 references by BA Magnuson,
      GA Burdock and 8 more, Critical Reviews in Toxicology,
      2007 Sept.: Mark D Gold 13 page:
      also Rich Murray 2007.09.15: 2008.03.24
      http://rmforall.blogspot.com/2008_03_01_archive.htm
      Monday, March 24, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1531

      "Nearly every section of the Magnuson (2007) review has
      research that is misrepresented
      and/or crucial pieces of information are left out.

      In addition to the misrepresentation of the research,
      readers (including medical professionals) are often not told that
      this review was funded by the aspartame manufacturer, Ajinomoto,
      and the reviewers had enormous conflicts of interest." ]

      http://www.medscape.com/viewarticle/579335

      Dermatitis. 2008; 19(3): E10-E11.
      © 2008 American Contact Dermatitis Society
      Formaldehyde, Aspartame, and Migraines: A Possible Connection
      Sharon E. Jacob; Sarah Stechschulte
      Published: 09/17/2008
      [ Extract ]

      Abstract

      Aspartame is a widely used artificial sweetener that has been linked
      to pediatric and adolescent migraines.
      Upon ingestion, aspartame is broken, converted, and oxidized into
      formaldehyde in various tissues.
      We present the first case series of aspartame-associated migraines
      related to clinically relevant positive reactions to formaldehyde
      on patch testing.

      Case Series

      Six patients (ages 16 to 75 years) were referred for evaluation of
      recalcitrant dermatitis. By history, five of the patients were noted
      to have developed migraines following aspartame consumption; the
      sixth reported dermatitis flares associated with diet cola
      consumption of >2 liters/day.

      All six patients had current environmental exposures to formaldehyde
      or formaldehyde-releasing preservatives in their personal hygiene
      products and/or regular consumption of "sugar-free food" artificially
      sweetened with aspartame.

      Based on their histories and clinical presentations, these patients
      were patch-tested with the North American Contact Dermatitis
      Group 65-allergen Standard Screening Series and selected
      chemicals from the University of Miami vehicle, fragrance, bakery,
      and textile trays.

      All six patients had positive reactions to formaldehyde, and four had
      additional positive reactions to formaldehyde-releasing preservatives
      (FRPs). Expert counseling on allergen avoidance (including
      avoidance of formaldehyde, FRPs, and aspartame) and alternative
      product recommendations were provided to the patients.

      At their follow-up appointments (between 8 and 12 weeks), all the
      patients showed clearance of their dermatitis. Four patients (two
      inadvertently) resumed their consumption of aspartame and
      subsequently returned for an additional follow-up visit. Three of the
      first five patients had recurrences of both their migraines and their
      dermatitis; the sixth patient (who had no migraines) had a positive
      rechallenge dermatitis. These four patients were again counseled on
      avoidance regimen.

      formaldehyde, aspartame, and migraines, the first case series,
      Sharon E Jacob-Soo, Sarah A Stechschulte, UCSD, Dermatitis
      2008 May: Rich Murray 2008.07.18
      http://rmforall.blogspot.com/2008_07_01_archive.htm
      Friday, July 18, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1553


      formaldehyde from many sources, including aspartame, is major
      cause of Allergic Contact Dermatitis, SE Jacob, T Steele, G
      Rodriguez, Skin and Aging 2005 Dec.: Murray 2008.03.27
      http://rmforall.blogspot.com/2008_03_01_archive.htm
      Thursday, March 27, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1533

      "For example, diet soda and yogurt containing aspartame
      (Nutrasweet), release formaldehyde in their natural biological
      degradation.

      One of aspartame's metabolites, aspartic acid methyl ester, is
      converted to methanol in the body, which is oxidized to
      formaldehyde in all organs, including the liver and eyes. 22

      Patients with a contact dermatitis to formaldehyde have been seen
      to improve once aspartame is avoided. 22

      Notably, the case that Hill and Belsito reported had a 6-month
      history of eyelid dermatitis that subsided after 1 week of avoiding
      diet soda. 22"


      Avoiding formaldehyde allergic reactions in children, aspartame,
      vitamins, shampoo, conditioners, hair gel, baby wipes, Sharon E
      Jacob, MD, Tace Steele, U. Miami, Pediatric Annals 2007 Jan.:
      eyelid contact dermatitis, AM Hill, DV Belsito, 2003 Nov.:
      Murray 2008.03.27
      http://rmforall.blogspot.com/2008_03_01_archive.htm
      Thursday, March 27, 2008
      http://groups.yahoo.com/group/aspartameNM/message/1532

      Sharon E. Jacob, MD, Assistant Professor of Medicine
      (Dermatology)
      University of California, San Diego 200 W. Arbor Drive #8420,
      San Diego, CA 92103-8420 Tel: 858-552-8585 ×3504
      Fax: 305-675-8317 sjacob@...;
      Sarah A. Stechschulte, BA sstechschulte@...
      _____________________________________________________


      Rich Murray, MA
      Boston University Graduate School 1967 psychology,
      BS MIT 1964, history and physics,
      1943 Otowi Road, Santa Fe, New Mexico 87505
      505-501-2298 rmforall@...

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