کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5534185 1550835 2017 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Metabolomics analysis of serum from subjects after occupational exposure to acrylamide using UPLC-MS
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Metabolomics analysis of serum from subjects after occupational exposure to acrylamide using UPLC-MS
چکیده انگلیسی


- Finding potential biomarkers of ACR by metabolomics techniques.
- UPLC-QTOF MS was employed to examine serum samples of occupational crowd.
- 14 biomarkers were found and initially identified.
- Tryptophan and sphingosine may be related to ACR-mediated neurotoxicity.

Since occupational exposure to acrylamide (ACR) may cause nerve damage, sensitive biomarkers to evaluate the early effects of ACR on human health are needed. In the present study, we have compared a group of individuals with occupational exposure to ACR (contact group, n = 65) with a group of individuals with no exposure (non-contact group, n = 60). Serum metabolomics analysis of the contact and non-contact groups was carried out using ultra performance liquid chromatograph/time of flight mass spectrometry, combined with multivariate analysis, to identify potential metabolites. Serum biochemical indexes of the contact and non-contact groups were also determined using an automatic biochemistry analyzer. There was a clear separation between the contact group and the non-contact group; receiver operator characteristic curve analysis suggested that phytosphingosine, 4E,15Z-bilirubin IXa and tryptophan were the best metabolites to use as biomarkers. Liver function was also found to be abnormal in the contact group. Important, ACR-related, metabolic changes were seen in the contact group and new biomarkers for assessing the toxicity of ACR on the central nervous system have been proposed. This study will provide a sound basis for exploring the toxic mechanisms and metabolic pathways of ACR.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular and Cellular Endocrinology - Volume 444, 15 March 2017, Pages 67-75
نویسندگان
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