Literature DB >> 25757395

Monitoring urinary mercapturic acids as biomarkers of human dietary exposure to acrylamide in combination with acrylamide uptake assessment based on duplicate diets.

Meike Ruenz1, Tamara Bakuradze1, Gerhard Eisenbrand1, Elke Richling2.   

Abstract

The present human intervention study investigated the relation between the intake of acrylamide (AA) in diets with minimized, low, and high AA contents and the levels of urinary exposure biomarkers. As biomarkers, the mercapturic acids, N-acetyl-S-(carbamoylethyl)-L-cysteine (AAMA), and N-acetyl-S-(1-carbamoyl-2-hydroxyethyl)-L-cysteine (GAMA) were monitored. The study was performed with 14 healthy male volunteers over a period of 9 days, under controlled conditions excluding any inadvertent AA exposure. Dietary exposure to AA was measured by determining AA contents in duplicates of all meals consumed by the volunteers. The study design included an initial washout period of 3 days on AA-minimized diet, resulting in dietary AA exposure not exceeding 41 ng/kg bw/d. Identical washout periods of 2 days each followed the AA exposure days (day 4, low exposure, and day 7, high exposure). At the respective AA intake days, volunteers ingested 0.6-0.8 (low exposure) or 1.3-1.8 (high exposure) μg AA/kg bw/d with their food. Both low and high AA intakes resulted in an AAMA output within 72 h corresponding to 58 % of the respective AA intake. At the end of the initial 3-day washout period, an AAMA baseline level of 93 ± 31 nmol/d was recorded, suggestive for an assumed net AA baseline exposure level of 0.2-0.3 μg AA/kg bw/d.

Entities:  

Keywords:  Acrylamide exposure; Biomarkers; Duplicate diets; Human intervention study

Mesh:

Substances:

Year:  2015        PMID: 25757395     DOI: 10.1007/s00204-015-1494-9

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  8 in total

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Journal:  Arch Toxicol       Date:  2020-06-15       Impact factor: 5.153

Review 2.  The role of endogenous versus exogenous sources in the exposome of putative genotoxins and consequences for risk assessment.

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3.  Assessment of the genotoxicity of acrylamide.

Authors:  Diane Benford; Margherita Bignami; James Kevin Chipman; Luisa Ramos Bordajandi
Journal:  EFSA J       Date:  2022-05-05

4.  Harmonization of acronyms for volatile organic compound metabolites using a standardized naming system.

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Journal:  Int J Hyg Environ Health       Date:  2021-05-04       Impact factor: 7.401

Review 5.  Exposure assessment of process-related contaminants in food by biomarker monitoring.

Authors:  Ivonne M C M Rietjens; P Dussort; Helmut Günther; Paul Hanlon; Hiroshi Honda; Angela Mally; Sue O'Hagan; Gabriele Scholz; Albrecht Seidel; James Swenberg; Justin Teeguarden; Gerhard Eisenbrand
Journal:  Arch Toxicol       Date:  2018-01-04       Impact factor: 5.153

6.  Biomarker monitoring of controlled dietary acrylamide exposure indicates consistent human endogenous background.

Authors:  Katharina Goempel; Laura Tedsen; Meike Ruenz; Tamara Bakuradze; Dorothea Schipp; Jens Galan; Gerhard Eisenbrand; Elke Richling
Journal:  Arch Toxicol       Date:  2017-05-22       Impact factor: 5.153

Review 7.  Revisiting the evidence for genotoxicity of acrylamide (AA), key to risk assessment of dietary AA exposure.

Authors:  Gerhard Eisenbrand
Journal:  Arch Toxicol       Date:  2020-06-03       Impact factor: 5.153

8.  Nrf2 Activation Attenuates Acrylamide-Induced Neuropathy in Mice.

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Journal:  Int J Mol Sci       Date:  2021-06-01       Impact factor: 5.923

  8 in total

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