Methemoglobin Forming Effect of Dimethyl Trisulfide in Mice

References

• Oser BL, Hall RL. Recent progress in the consideration of flavoring ingredients under the Food Additives Amendment: 5. GRAS Substances. Food Technol-Chicago. 1972;26(5)35–42.
   Google Scholar
• Zuo C, Zhang W, Chen Z, et al. RNA sequencing reveals that endoplasmic reticulum stress and disruption of membrane integrity underlie dimethyl trisulfide toxicity against Fusarium oxysporum f. sp. cubense tropical race 4. Front Microbiol. 2017;8:1365–1376.
   PubMed Web of Science ®Google Scholar
• Pozsgai G, Payrits M, Sághy É, et al. Analgesic effect of dimethyl trisulfide in mice is mediated by TRPA1 and sst4 receptors. Nitric Oxide. 2017;65:10–21.
   PubMed Web of Science ®Google Scholar
• Wu M, Cui Y, Bhargav A, et al. Organotrisulfide: a high capacity cathode material for rechargeable lithium batteries. Angew Chem Int Ed Engl. 2016;55(34):10027–10031.
   PubMed Web of Science ®Google Scholar
• Rockwood GA, Thompson DE, Petrikovics I. Dimethyl trisulfide: a novel cyanide countermeasure. Toxicol Ind Health. 2016;32(12):2009–2016.
   PubMed Web of Science ®Google Scholar
• DeLeon SM, Downey JD, Hildenberger DM, et al. DMTS is an effective treatment in both inhalation and injection models for cyanide poisoning using unanesthetized mice. Clin Toxicol. 2017;56(5):1–10.
   Web of Science ®Google Scholar
• Way JL. Cyanide intoxication and its mechanism of antagonism. Annu Rev Pharmacol Toxicol. 1984;24(1):451–481.
   PubMedGoogle Scholar
• Kovacs K, Jayanna PK, Duke A, et al. A lipid base formulation for intramuscular administration of a novel sulfur donor for cyanide antagonism. Curr Drug Deliv. 2016;13(8):1351–1357.
   PubMed Web of Science ®Google Scholar
• Kovacs K, Duke AC, Shifflet M, et al. Parenteral dosage form development and testing of dimethyl trisulfide, as an antidote candidate to combat cyanide intoxication. Pharm Dev Technol. 2017;22(8):958–963.
   PubMed Web of Science ®Google Scholar
• Bartling CM, Andre JC, Howland CA, et al. Stability characterization of a polysorbate 80-dimethyl trisulfide formulation, a cyanide antidote candidate. Drugs R D. 2016;16(1):109–127.
   PubMed Web of Science ®Google Scholar
• Kiss L, Duke A, Kovacs K, et al. Sealing effects on the storage stability of the cyanide antidotal candidate, dimethyl trisulfide. Drugs R D. 2018;18(1):45–49.
   PubMed Web of Science ®Google Scholar
• Kiss L, Bocsik A, Walter FR, et al. In vitro and in vivo blood-brain barrier penetration studies with the novel cyanide antidote candidate dimethyl trisulfide in mice. Toxicol Sci. 2017;160(2):398–407.
   PubMed Web of Science ®Google Scholar
• Kiss L, Holmes S, Chou CE, et al. Method development for detecting the novel cyanide antidote dimethyl trisulfide from blood and brain, and its interaction with blood. J Chromatogr B. 2017;1044:149–157.
   PubMed Web of Science ®Google Scholar
• De Silva D, Lee S, Duke A, et al. Intravascular residence time determination for the cyanide antidote dimethyl trisulfide in rat by using liquid-liquid extraction coupled with high performance liquid chromatography. J Anal Methods Chem. 2016;2016:6546475. doi: 10.1155/2016/6546475.
   PubMedGoogle Scholar
• Dong X, Kiss L, Petrikovics I, et al. Reaction of dimethyl trisulfide with hemoglobin. Chem Res Toxicol. 2017;30(9):1661–1663.
   PubMed Web of Science ®Google Scholar
• Voet D, Voet JG, Pratt CW. Protein function: myoglobin and hemoglobin, muscle contraction, and antibodies. Fundamentals of Biochemistry: Life at the Molecular Level, 5th ed. Hoboken (NJ, USA): Wiley & Sons. 2016:190–196.
   Google Scholar
• Price DP. Methemoglobin inducers. In: Hoffman RS, Howland MA, Lewin NA, et al., Editors. Goldfrank’s Toxicologic Emergencies. New York (NY, USA); McGraw-Hill Publishers. 2015:1622–1631.
   Google Scholar
• Rechetzki KF, Henneberg R, da Silva PH, et al. Reference values for methemoglobin concentrations in children. Rev Bras Hematol Hemoter. 2012;34(1):14–16.
   PubMedGoogle Scholar
• Smith RP, Alkaitis AA, Shafer PR. Chemically induced methemoglobinemias in the mouse. Biochem Pharmacol. 1967;16(2):317–328.
   PubMed Web of Science ®Google Scholar
• Cortazzo JA, Lichtman AD. Methemoglobinemia: a review and recommendations for management. J Cardiothorac Vasc Anesth. 2014;28(4):1043–1047.
   PubMed Web of Science ®Google Scholar
• Groeper K, Katcher K, Tobias JD. Anesthetic management of a patient with methemoglobinemia. South Med J. 2003;96(5):504–509.
   PubMedGoogle Scholar
• Evelyn KA, Malloy HT. Microdetermination of oxyhemoglobin, methemoglobin, and sulfhemoglobin in a single sample of blood. J Biol Chem. 1938;126:655–662.
   Google Scholar
• Horecker BL, Brackett FS. A rapid spectrophotometric method for the determination of methemoglobin and carbonylhemoglobin in blood. J Biol Chem. 1944;152:669–677.
   Google Scholar
• National Research Council, 2011. Guide for the Care and Use of Laboratory Animals, 8th ed. Washington (DC, USA): National Academies Press; 2010 (https://doi.org/10.17226/12910).
   Google Scholar
• Underwood W, Anthony R, Gwaltney-Brant S, et al. AVMA Guidelines for the Euthanasia of Animals, 2013 ed. Schaumburg (IL, USA): American Veterinary Medical Association; 2013.
   Google Scholar
• Richterich R. Clinical Chemistry: Theory, Practice and Interpretation. Chichester (West Sussex, UK): John Wiley & Sons Ltd. 1981. ISBN: 978-0471278092.
   Google Scholar
• Zwart A, van Kampen EJ, Zijlstra WG. Results of routine determination of clinically significant hemoglobin derivatives by multicomponent analysis. Clin Chem. 1986;32(6):972–978.
   PubMed Web of Science ®Google Scholar
• Zijistra WG, Buursma A. Rapid multicomponent analysis of hemoglobin derivatives for controlled antidotal use of methemoglobin-forming agents in cyanide poisoning. Clin Chem. 1993;39(8):1685–1689.
   PubMed Web of Science ®Google Scholar