TY - JOUR
T1 - Human consumption of methyleugenol and its elimination from serum
AU - Schecter, Arnold
AU - Lucier, George W.
AU - Cunningham, Michael L.
AU - Abdo, Kamal M.
AU - Blumenthal, Greg
AU - Silver, Andrew G.
AU - Melnick, Ron
AU - Portier, Christopher
AU - Barr, Dana B.
AU - Barr, John R.
AU - Stanfill, Stephen B.
AU - Patterson, Donald G.
AU - Needham, Larry L.
AU - Stopford, Woodhall
AU - Masten, Scott
AU - Mignogna, Jill
AU - Tung, Kuang Chi
PY - 2004/5
Y1 - 2004/5
N2 - Under a mandate from the U.S. Congress, the National Toxicology Program (NTP) of the U.S. Department of Health and Human Services conducts animal bioassays for carcinogenicity of potentially toxic chemicals to which the U.S. population might be exposed. Methylaugenol, a natural as well as synthesized substance, was nominated for study because it is structurally similar to safrole, a known animal carcinogen. Methyleugenol was found to be a very potent multisite carcinogen in male and femal F344/N rats and B6C3F1 mice at all doses tested in 2-year NTP bioassays using gavage dosing. For this reason, human toxicokinetic studies were added to the traditional NTP protocol. A commercial brand of gingersnaps was found by chemists at die Centers for Disease Control and Prevention to contain a relatively high concentration of methyleugenol. After thorough scientific and clinical review, and approval by a National Institutes of Health institutional review board for the protection of human subjects, a study was conducted with nine healthy adult male and female human volunteers. The volunteers were given 12 gingersnaps for breakfast. Blood was drawn immediately before the meal and at 15, 30, 60, and 120 min afterward. The mean ± SD fasting level of methyleugenol in serum was 16.2 ± 4.0 pg/g wet weight. Peak blood levels were found at 15 min (mean ± SD, 53.9 ± 7.3 pg/g wet weight), followed by a rapid decline; the half-life of elimination was about 90 min. The peak levels were within the range of methyleugenol blood levels in the U.S. population, as measured concurrently in a subset of nonfasting participants in the Third National Health and Nutrition Examination Survey (NHANES III).
AB - Under a mandate from the U.S. Congress, the National Toxicology Program (NTP) of the U.S. Department of Health and Human Services conducts animal bioassays for carcinogenicity of potentially toxic chemicals to which the U.S. population might be exposed. Methylaugenol, a natural as well as synthesized substance, was nominated for study because it is structurally similar to safrole, a known animal carcinogen. Methyleugenol was found to be a very potent multisite carcinogen in male and femal F344/N rats and B6C3F1 mice at all doses tested in 2-year NTP bioassays using gavage dosing. For this reason, human toxicokinetic studies were added to the traditional NTP protocol. A commercial brand of gingersnaps was found by chemists at die Centers for Disease Control and Prevention to contain a relatively high concentration of methyleugenol. After thorough scientific and clinical review, and approval by a National Institutes of Health institutional review board for the protection of human subjects, a study was conducted with nine healthy adult male and female human volunteers. The volunteers were given 12 gingersnaps for breakfast. Blood was drawn immediately before the meal and at 15, 30, 60, and 120 min afterward. The mean ± SD fasting level of methyleugenol in serum was 16.2 ± 4.0 pg/g wet weight. Peak blood levels were found at 15 min (mean ± SD, 53.9 ± 7.3 pg/g wet weight), followed by a rapid decline; the half-life of elimination was about 90 min. The peak levels were within the range of methyleugenol blood levels in the U.S. population, as measured concurrently in a subset of nonfasting participants in the Third National Health and Nutrition Examination Survey (NHANES III).
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U2 - 10.1289/ehp.6766
DO - 10.1289/ehp.6766
M3 - Review article
C2 - 15121510
AN - SCOPUS:2442557311
SN - 0091-6765
VL - 112
SP - 678
EP - 680
JO - Environmental health perspectives
JF - Environmental health perspectives
IS - 6
ER -