-Caveat Lector-

 from ToxLine:  http://www.medscape.com/misc/FormToxlineInfLive.html
 --------------------------------------------------------------------
 Title
      Effect of aspartame loading on plasma and erythrocyte
      free amino acid concentrations in one-year-old infants.
 Author
      Filer LJ Jr; Baker GL; Stegink LD
 Source
      J Nutr; VOL 113, ISS 8, 1983, P1591-9
 Secondary Source ID
      TOXBIB/83/267837;
 Abstract
      Aspartame is a new dipeptide sweetener.  It has been suggested
      that infants metabolize its constituent amino acids (aspartate
      and phenylalanine) less well than adults.  To test this
      hypothesis, 24 1-year-old infants were administered 34, 50 and
      100 mg/kg body weight aspartame in cherry-flavored beverage
      mix.  Plasma amino acid concentrations and the areas under the
      plasma concentration-time curves (AUC) were determined and were
      compared with values in adults administered equivalent doses.
      The doses studied include the 99th percentile of projected
      ingestion for adults (34 mg/kg), a very high use dose (50 mg/kg
      body weight), and a potentially abusive dose (100 mg/kg body
      weight).  Plasma aspartate concentrations did not change
      significantly (P greater than 0.05) at aspartame doses of
      34 and 50 mg/kg body weight, but did increase significantly at
      the 100 mg/kg body weight dose.  The change over base line was
      similar in infants and adults.  Aspartame dosing significantly
      increased both the mean peak plasma phenylalanine concentration
      and the plasma phenylalanine AUC value in proportion to dose.
      Mean (+/- SD) peak plasma phenylalanine concentrations in
      infants were 9.37 +/- 1.44, 11.6 +/- 4.44 and 22.3 +/- 11.5
      mumol/100 ml at aspartame doses of 34, 50 and 100 mg/kg body
      weight, respectively.  Values in infants were similar to those
      noted in adults.  The data do not support the suggestion that
      infants metabolize the amino acids of aspartame less well than
      adults.


 --------------------------------------------------------------------
 Title
      Blood methanol concentrations in one-year-old infants
      administered graded doses of aspartame.
 Author
      Stegink LD; Brummel MC; Filer LJ Jr; Baker GL
 Source
      J Nutr; VOL 113, ISS 8, 1983, P1600-6
 Secondary Source ID
      TOXBIB/83/267838;
 Abstract
      Blood methanol concentrations were measured in 24 1-year-old
      infants administered aspartame, a dipeptide methyl ester
      sweetener.  The doses studied included a dose projected to be
      the 99th percentile of daily ingestion for adults (34 mg/kg
      body weight), a very high use dose (50 mg/kg body weight) and a
      dose considered to be in the abuse range (100 mg/kg body
      weight).  Blood methanol values in infants were compared to
      values observed previously in adults administered equivalent
      doses of aspartame.  Methanol concentrations were below the
      level of detection (0.35 mg/dl) in the blood of 10 infants
      administered aspartame at 34 mg/kg body weight, but were
      significantly elevated (P less than or equal to 0.05) after
      ingestion of aspartame at 50 and 100 mg/kg body weight.
      At the latter doses, mean peak blood methanol concentrations
      and the area under the blood methanol concentration-time curve
      increased in proportion to dose.  Mean (+/- SEM) peak blood
      methanol concentration was 0.30 +/- 0.10 mg/100 ml at a
      50 mg/kg body weight aspartame dose (n = 6) and 1.02
      +/- 0.28 mg/ml at the 100 mg/kg body weight dose (n = 8).
      Blood methanol values in infants were similar to those
      observed in normal adults.


 --------------------------------------------------------------------
 Title
      Use of aspartame in pregnancy.
 Author
      Sturtevant FM
 Source
      Int J Fertil; VOL 30, ISS 1, 1985, P85-7 (REF: 20)
 Secondary Source ID
      TOXBIB/85/260289;
 Abstract
      The low-calorie sweetening agent, aspartame, is broken down in
      the small intestine into three moieties: aspartic acid,
      methanol and phenylalanine.  Acute loading studies have been
      performed in human beings who received up to six times the 99th
      percentile of the projected daily intake (6 X 34 = 200 mg/kg).
      No evidence of risk to the fetus was developed.  Aspartate does
      not readily cross the placenta.  Small elevations of blood
      methanol following such abuse doses of aspartame did not lead
      to measurable increases of blood formic acid, which is the
      product responsible for the acidosis and ocular toxicity in
      methanol poisoning.  Phenylalanine is concentrated on the fetal
      side of the placenta.  Aspartame in abuse doses up to 200 mg/kg
      in normal subjects, or to 100 mg/kg in PKU heterozygotes, did
      not raise blood phenylalanine levels to the range generally
      accepted to be associated with mental retardation in the
      offspring.  It is concluded that, under foreseeable conditions
      of use, aspartame poses no risk for use in pregnancy.


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