Using Metabolomics to Investigate Biomarkers of Drug Addiction

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Using Metabolomics to Investigate Biomarkers of Drug Addiction Reza Ghanbari, Susan Sumner  Trends in Molecular Medicine  Volume 24, Issue 2, Pages 197-205 (February 2018) DOI: 10.1016/j.molmed.2017.12.005 Copyright © 2017 Terms and Conditions

Figure 1 Effects of Human Alcohol Consumption and Smoking on Folate and Choline Metabolism. The use of tobacco products may reduce serum concentrations of choline, and ethanol use can inhibit methionine synthase and regeneration of methionine, as well as divert acetylcholine to acetyl Co-A, which impairs choline utilization, perturbing the conversion of betaine to dimethylglycine [43–47]. Methionine is essential for the methylation of proteins, lipids, and other small molecules, and for the regulation of DNA and RNA expression. Folate is an essential nutrient for the one-carbon transfer pathway, protein synthesis, DNA repair, and the synthesis of new DNA and RNA. In countries that do not fortify foods with folic acid, disturbances to folate metabolism and choline-related metabolites may contribute to increased cancer risks associated with drug use, although this remains to be further investigated. Abbreviations: BHMT, betaine-homocysteine S-methyltransferase; DHFR, dihydrofolate reductase; MS, methionine synthase; MTHFR, methylenetetrahydrofolate reductase. Trends in Molecular Medicine 2018 24, 197-205DOI: (10.1016/j.molmed.2017.12.005) Copyright © 2017 Terms and Conditions