Environment International · 2020 · 62 citations · 28 references
PharmacyEnvironmental SciencesToxicologyAquatic ToxicologyBiochemical ToxicologyEnvironmental ToxicologyDrinking Water SafetyGenotoxicity In Aquatic OrganismsWater ChemistryWater ManagementWater PollutionWater QualityChlorinationChlorination By-productsChlorination ByproductsConcentrationDrinking Water ContaminantsHealth-promoting PropertiesWater Contaminant ToxicityWater Quality Hazards
Metformin (MET), a worldwide used drug for type 2 diabetes, has been found with the largest amount by weight among all drugs in aquatic environment, including the drinking water systems where this emerging micropollutant is inevitably transformed during chlorination process. Whether MET chlorination byproducts Y (C4H6ClN5) and C (C4H6ClN3) exist in drinking water remains unknown. Although MET has health-promoting properties, whether or how its chlorination byproducts affect health is still uncharacterized. Here we reveal that MET and byproduct C are present in worldwide drinking water with the highest doses detected for MET and C as 1203.5 ng/L and 9.7 ng/L respectively. Under simulated chlorination conditions, we also demonstrate that both byproducts can be increasingly produced with increment of MET concentration, suggesting a hidden threat on the safety and sustainability of global water supply. Through systematic evaluations, we demonstrate that MET chlorination byproducts Y and C exhibit toxicities instead of genotoxicity to live worms and human HepG2 cells at millimolar doses. Moreover, both byproducts are harmful to mice and particularly Y at 250 ng/L destroys the mouse small intestine integrity. Unprecedentedly, we unveil boiling and activated carbon adsorption as effective alternative solutions that may be in urgent demand globally for removing these byproducts from drinking water.
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Metformin Retards Aging in C. elegans by Altering Microbial Folate and Methionine Metabolism
Filipe Cabreiro, Catherine Au, Kit‐Yi Leung et al. · Cell · 2013 · 965 citations · Full text
Metformin, Independent of AMPK, Inhibits mTORC1 in a Rag GTPase-Dependent Manner
Adem Kalender, Anand Selvaraj, So Young Kim et al. · Cell Metabolism · 2010 · 874 citations · Full text
Helga H.J. Gerets, Karen Tilmant, Brigitte Gerin et al. · Cell Biology and Toxicology · 2012 · 679 citations · Full text
Pharmacy, Pharmacology, Toxicology +17