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      Toxico-metabolomics study of a deep eutectic solvent comprising choline chloride and urea suggests in vivo toxicity involving oxidative stress and ammonia stress

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          Abstract

          The in vitro and in vivo studies suggest that choline chloride-based deep eutectic solvents may not be considered as pure, safe mixtures even if they consist of safe compounds.

          Abstract

          Deep eutectic solvents (DESs) comprising safe constituents are generally considered green and nontoxic without careful assessment. Here, eight different DESs were prepared from edible components including choline chloride (ChCl) as the hydrogen bond acceptor and were tested for in vitro cytotoxicity. Both DESs and simple aqueous mixtures of DES constituents showed different cytotoxicities depending on the cell line and often had elevated toxicities compared to their individual constituents. Moreover, several DESs were more cytotoxic than their aqueous mixtures. An in vivo toxico-metabolomic study was applied for the first time to CU (1 : 2), a commonly used DES, comprising ChCl and urea at 1 : 2 molar ratio. Mice were acutely exposed to CU (1 : 2) (1.5 g kg −1) via oral administration; its effects were investigated in comparison with those of ChCl, urea, an aqueous mixture of ChCl and urea, and saline. Metabolomic analyses of the liver, kidney, and serum revealed disturbances in the metabolism of glutathione, nicotinamide, taurine, pyruvate, lactate, and lysophosphatidylcholines, suggesting that CU (1 : 2) treatment induced oxidative stress. The levels of branched-chain amino acids and taurocholic acid were perturbed, suggesting that the CU (1 : 2)-treated mice underwent ammonia stress and intestinal dysbiosis, respectively. The DES-induced oxidative stress was confirmed by biochemical assays to measure superoxide dismutase activity, catalase activity, the ratio of reduced to oxidized glutathione, and malondialdehyde levels. Ammonia stress was confirmed because the blood of the DES-treated mice had significantly elevated ammonia levels. Ammonia assay revealed that ammonia could be produced from ChCl and urea during the DES preparation both with and without heat, and ammonia was also detected in the DESs comprising ChCl and organic acids. Thus, ChCl-based DESs, especially those containing urea should be used with caution because they may contain ammonia, which is putatively responsible for toxic effects of DESs different from simple mixtures. The in vitro and in vivo studies together suggest that ChCl-based DESs may not be considered as pure, safe mixtures even if they consist of safe compounds.

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          Occurrence of the potent mutagens 2- nitrobenzanthrone and 3-nitrobenzanthrone in fine airborne particles

          Polycyclic aromatic compounds (PACs) are known due to their mutagenic activity. Among them, 2-nitrobenzanthrone (2-NBA) and 3-nitrobenzanthrone (3-NBA) are considered as two of the most potent mutagens found in atmospheric particles. In the present study 2-NBA, 3-NBA and selected PAHs and Nitro-PAHs were determined in fine particle samples (PM 2.5) collected in a bus station and an outdoor site. The fuel used by buses was a diesel-biodiesel (96:4) blend and light-duty vehicles run with any ethanol-to-gasoline proportion. The concentrations of 2-NBA and 3-NBA were, on average, under 14.8 µg g−1 and 4.39 µg g−1, respectively. In order to access the main sources and formation routes of these compounds, we performed ternary correlations and multivariate statistical analyses. The main sources for the studied compounds in the bus station were diesel/biodiesel exhaust followed by floor resuspension. In the coastal site, vehicular emission, photochemical formation and wood combustion were the main sources for 2-NBA and 3-NBA as well as the other PACs. Incremental lifetime cancer risk (ILCR) were calculated for both places, which presented low values, showing low cancer risk incidence although the ILCR values for the bus station were around 2.5 times higher than the ILCR from the coastal site.
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            A simple practice guide for dose conversion between animals and human

            Understanding the concept of extrapolation of dose between species is important for pharmaceutical researchers when initiating new animal or human experiments. Interspecies allometric scaling for dose conversion from animal to human studies is one of the most controversial areas in clinical pharmacology. Allometric approach considers the differences in body surface area, which is associated with animal weight while extrapolating the doses of therapeutic agents among the species. This review provides basic information about translation of doses between species and estimation of starting dose for clinical trials using allometric scaling. The method of calculation of injection volume for parenteral formulation based on human equivalent dose is also briefed.
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              Glutathione metabolism and its implications for health.

              Glutathione (gamma-glutamyl-cysteinyl-glycine; GSH) is the most abundant low-molecular-weight thiol, and GSH/glutathione disulfide is the major redox couple in animal cells. The synthesis of GSH from glutamate, cysteine, and glycine is catalyzed sequentially by two cytosolic enzymes, gamma-glutamylcysteine synthetase and GSH synthetase. Compelling evidence shows that GSH synthesis is regulated primarily by gamma-glutamylcysteine synthetase activity, cysteine availability, and GSH feedback inhibition. Animal and human studies demonstrate that adequate protein nutrition is crucial for the maintenance of GSH homeostasis. In addition, enteral or parenteral cystine, methionine, N-acetyl-cysteine, and L-2-oxothiazolidine-4-carboxylate are effective precursors of cysteine for tissue GSH synthesis. Glutathione plays important roles in antioxidant defense, nutrient metabolism, and regulation of cellular events (including gene expression, DNA and protein synthesis, cell proliferation and apoptosis, signal transduction, cytokine production and immune response, and protein glutathionylation). Glutathione deficiency contributes to oxidative stress, which plays a key role in aging and the pathogenesis of many diseases (including kwashiorkor, seizure, Alzheimer's disease, Parkinson's disease, liver disease, cystic fibrosis, sickle cell anemia, HIV, AIDS, cancer, heart attack, stroke, and diabetes). New knowledge of the nutritional regulation of GSH metabolism is critical for the development of effective strategies to improve health and to treat these diseases.
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                Author and article information

                Contributors
                Journal
                GRCHFJ
                Green Chemistry
                Green Chem.
                Royal Society of Chemistry (RSC)
                1463-9262
                1463-9270
                2021
                2021
                Affiliations
                [1 ]School of Pharmacy
                [2 ]Sungkyunkwan University
                [3 ]Suwon
                [4 ]Republic of Korea
                Article
                10.1039/D0GC03927F
                de93c61d-0fcd-45c0-a6c6-e5b9b958b114
                © 2021

                http://rsc.li/journals-terms-of-use

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