New biomarkers for 1,1-dimethylhydrazine

Author:

Ukolov Anton Igorevich1ORCID,Laptev Denis Sergeevich1ORCID,Karmanov Evgeny Yurievich1,Karakashev Georgy Vasilyevich1,Krivorotov Denis Viktorovich1ORCID,Bogachenkov A. S.1,Nechaikina Olga Valeryevna1ORCID,Bobkov Dmitry Vladimirovich1ORCID,Petunov Sergey Gervasievich1ORCID

Affiliation:

1. FSUE «Research Institute of Hygiene, Occupational Pathology and Human Ecology» FMBA of Russia

Abstract

Introduction. Despite the large-scale use of asymmetric dimethylhydrazine (UDMH) in the domestic rocket and space industry, its biomarkers of exposure in blood plasma and urine, as well as biomarkers of cardiotoxic effects, have not yet been described. Material and methods. The study of blood and urine samples of rats after a single injection of 10 mg/kg UDMH (1/16 LD50) was carried out by HPLC-MS. The determination of the non-metabolized form of UDMH was also carried out using the method of gas chromatography with mass-selective detection with preliminary derivatization with 4-pyridinecarboxyaldehyde. The cardiotoxic effect of UDMH was assessed on a model of an isolated rat heart with subchronic intragastric administration for 28 days at doses of 0,02; 0,2; 2,0 mg/kg. Results. It has been established that the main metabolites of UDMH are dimethylhydrazones of pyridoxal (vitamin B6) and pyruvic acid (pyruvate). The possibility of determining the non-metabolized form of UDMH in blood and urine by HPLC-MS was shown, concentrations reach 10-60 ng/ml of blood plasma and 200-2000 ng/ml. The use of UDMH leads to an increase in the mass coefficient of the heart at a dose of 2,0 mg/kg. In ex vivo experiments on the rat heart, the cardiotoxic effect of UDMH was shown at subchronic use at a dose of 0,2 mg/kg and above, expressed in significant dilatation of the coronary bloodstream and left ventricle, the development of pronounced negative inotropic and chronotropic effects, and a decrease in the maximum rate of contraction and relaxation of the left ventricle. ventricle, reflecting the inhibition of myocardial energy metabolism. Limitations of the study. In the work, biomarkers were detected after a single intragastric injection of NDMG, the toxicokinetic characteristics of biomarkers and their retrospectivity were not evaluated. Conclusion. The main metabolites of UDMH with intravenous administration of 1/16 DL50 are dimethylhydrazones of pyridoxal (vitamin B6) and pyruvic acid (pyruvate). With subchronic administration, UDMH has cardiotoxicity at a dose of 0,02 mg/kg and above.

Publisher

Federal Scientific Center for Hygiene F.F.Erisman

Reference13 articles.

1. Ivanov S.D., Kolbasov S.E., Yamshanov V.A., Kovan’ko E.G., Monahov A.S., Melihova M.V. et al. Express assessment of toxicogenomic effects of asymmetric dimethylhydrazine. Toksikologicheskij vestnik. 2009; 3(96): 11–7. (in Russian)

2. Bugaev P.A., Antushevich A.E., Rejnyuk V.L., Basharin V.A., Zacepin V.V. Hydrazine and its derivatives: toxicological characteristics. Sovremennye problemy nauki i obrazovaniya. 2017; 4: 31. (in Russian)

3. U.S. Environmental Protection Agency. Health and Environmental Effects Profile for 1,1-Dimethylhydrazine. Environmental Criteria and Assessment Office, Office of Health and Environmental Assessment, Office of Research and Development, Cincinnati, OH. EPA/600/x-84/134.1984.

4. Antushevich A.E., Basharin V.A., Rejnyuk V.L., Bugaev P.A. Efficacy of inosine glycyl-cysteinyl-glutamate disodium and pyridoxine hydrochloride in acute poisoning with asymmetric dimethylhydrazine. Vestnik Rossijskoj Voenno-medicinskoj akademii. 2018; 1(61): 164–7. (in Russian).

5. Environmental health criteria 155. Biomarkers and Risk Assessment: Concepts and Principles. Moscow; 1996.

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