THYROID STATUS IN MOUSE-LIKE RODENTS UNDER THE INFLUENCE OF SYNTHETIC PYRETHROID CYPERMETHRIN
- Authors: Chigrinski E.A.1
-
Affiliations:
- Omsk State Medical University, Ministry of Healthcare of the Russian Federation
- Issue: No 5 (2019)
- Pages: 54-59
- Section: Ecological Toxicology
- Published: 28.10.2019
- URL: https://rjsocmed.com/0869-7922/article/view/641220
- DOI: https://doi.org/10.36946/0869-7922-2019-5-54-59
- ID: 641220
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Abstract
The aim of this work was to evaluate the thyroid status in mouse-like rodents under the influence of synthetic pyrethroid cypermethrin.
The studies were performed on 168 male rats (Rattus norvegicus) and 112 male red voles (Myodes rutilus). When simulating acute intoxication, cypermethrin was injected once into the stomach at a dose of lA LD50 followed by observation of rats for 30 days and voles for 7 days. When studying chronic intoxication, cypermethrin was administered to rats at a dose of 1/100 LD50, the duration of the experiment was 120 days. Acaricidal treatment of the forest was carried out on a one-hectare site, and the results of the capture of voles and their thyroid status were compared with voles caught on the background site.
Synthetic pyrethroid cypermethrin in acute and chronic experiments causes a change in thyroid status in laboratory rats, which is reflected in a decrease in the level of thyroid hormones in the blood serum. Moreover, there is an increase in the level of thyroid-stimulating hormone in rats. The introduction of a high dose of cypermethrin (A LD50) into male voles under field vivarium conditions also revealed the sensitivity of representatives of this species to the action of synthetic pyrethroids, which was manifested in a decrease in the synthesis of T4 and T3 in their thyroid glands. Acaricidal forest treatment contributes to a temporary change in thyroid status in male red field vole (Myodes rutilus) caught in the treated area, which, apparently, is a consequence of adaptive changes and migration processes in the population of this species.
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About the authors
E. A. Chigrinski
Omsk State Medical University, Ministry of Healthcare of the Russian Federation
Author for correspondence.
Email: chigrinski@list.ru
Chigrinski Eugene Alexandrovich
644099, Omsk
Russian FederationReferences
- HerwigA., RossA.W., Nilaweera K.N., Morgan PJ, Barrett P. Hypothalamic thyroid hormone in energy balance regulation. Obes. Facts. 2008; 1(2): 71-9.
- Nussey S, Whitehead S. Endocrinology: An Integrated Approach. Oxford: BIOS Scientific Publishers; 2001.
- Petri I., Diedrich V., Wilson D., Fernandez-Calleja J., Herwig A., Steinlechner S. et al. Orchestration of gene expression across the seasons: Hypothalamic gene expression in natural photoperiod throughout the year in the Siberian hamster. Sci. Rep. 2016; 6: 29689.
- Scherbarth F., SteinlechnerS. Endocrine mechanisms of seasonal adaptation in small mammals: from early results to present understanding. J. Comp. Physiol. B. 2010; 180(7): 935-52.
- Verma R., Haldar C. Photoperiodic modulation of thyroid hormone receptor, deiodinase-2 and glucose transporters expression in testis of adult golden hamster, Mesocricetus auratus. J Photochem Photobiol B. 2016; 165: 351-8.
- Viguie C., Battaglia D.F., Krasa H.B., Thrun L.A., Karsch F.J. Thyroid hormones act primarily within the brain to promote the seasonal inhibition of luteinizing hormone secretion in the ewe. Endocrinology. 1999; 140(3): 1111-7.
- Yaglova N.V., Yaglov V.V. Changes in thyroid status of rats after prolonged exposure to low dose dichlorodiphenyltrichloroethane. Bull. Exp. Biol. Med. 2014; 156(6): 760-2.
- Movasseghi A.R., Rodriguez-Estival J., Smits J.E.G. Thyroid pathology in deer mice (Peromyscus maniculata) from a reclaimed mine site on the athabasca oil sands. Environ. Pollut. 2017; 222: 42-9.
- Zhang Q., Ji C., Yin X., Yan L., Lu M., Zhao M. Thyroid hormone-disrupting activity and ecological risk assessment of phosphorus-containing flame retardants by in vitro, in vivo and in silico approaches. Environ. Pollut. 2016; 210: 27-33.
- Gi/oux M., Gan J., Schlenk D. The effects of bifenthrin and temperature on the endocrinology of juvenile Chinook salmon. Environ. Toxicol. Chem. 2019; 38(4): 852-61.
- Tu W., Xu C., Jin Y, Lu B., Lin C., Wu Y. et al. Permethrin is a potential thyroid-disrupting chemical: In vivo and in silico envidence. Aquat. Toxicol. 2016; 175: 39-46.
- Al-Amoudi W.M. Toxic effects of Lambdacyhalothrin, on the rat thyroid: Involvement of oxidative stress and ameliorative effect of ginger extract. Toxicol. Rep. 2018; 5: 728-36.
- Sekeroglu V., Sekeroglu Z.A., Demirhan E. Effects of commercial formulations of deltamethrin and/or thiacloprid on thyroid hormone levels in rat serum. Toxicol. Ind. Health. 2014; 30(1): 40-6.
- Karaseva E.V., Telicyna A.Ju., Zhigal'skij O.A. Methods of studying rodents in the field. Moscow: LKI; 2008 (in Russian).
- Gromov I.M., Erbaeva M.A. Mammals of Fauna of Russia and Adjacent Territories. Lagomorphs and Rodents. Saint Petersburg: ZIN RAN; 1995 (in Russian).
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