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Effects of Dihydroquercetin on Behavior of Albino Rat Offspring with Transgenerational Chemical Body Burden

https://doi.org/10.35627/2219-5238/2020-323-2-38-41

Abstract

Introduction. Lead pollution is a common environmental problem. Having no physiological functions, this toxicant has a negative polytropic impact on a body, including neurotoxic, reproductive, and transgenerational effects. The mechanism of lead toxicity is oxidative stress. Flavonoids have active antioxidant properties. They are widely represented in plant foods, are able to restore protective capabilities of cells and have chelating properties with respect to lead. One of the representatives of this group of substances is dihydroquercetin. The objective was to study the effect of dihydroquercetin on behavior of rats with hereditary chemical body burden exposed to lead at 60 mg/ kg during 25 days. Materials and methods. We studied the behavior of rat offspring in an open field and established their blood lead levels by electrothermal atomization atomic absorption spectrometry. For statistical processing the U-Mann - Whitney test was used. Results. In the present experiment, the effect of lead on the offspring of male albino rats exposed to 60 mg/kg of lead for 25 days caused changes in the activity of animals in the open field. The severity of changes was more pronounced in animals with a hereditary chemical body burden. These animals showed a decrease in orientation and physical activity and increased anxiety. In rats with a hereditary burden, changes in behavior were detected when administering dihydroquercetin. The activity of animals demonstrated a positive dynamics: we observed a statistically significant increase in physical activity and orientation. The number and duration of behavioral acts approached control values. Conclusions. The revealed effects of lead on the offspring of albino rats with a transgenerational chemical body burden require further study to understand the mechanism of the phenomenon.

About the Authors

E. A. Kapustina
East-Siberian Institute of Medical and Ecological Research
Russian Federation


L. G. Lisetskaya
East-Siberian Institute of Medical and Ecological Research
Russian Federation


References

1. Hon KL, Fung CK, Leung AK. Childhood lead poisoning: an overview. HKMJ. 2017; 23(6):616-21. DOI: 10.12809/ hkmj176214

2. Sanders T, Liu YM, Tchounwou PB. Cytotoxic, genotoxic, and neurotoxic effects of Mg, Pb, and Fe on pheochromocytoma (PC-12) cells. Environ Toxicol 2015; 30(12):1445-1458. DOI: 10.1002/tox.22014

3. Pant N, Kumar G, Upadhyay AD, et al. Reproductive toxicity of lead, cadmium, and phthalate exposure in men. Environ Sci Pollut Res Int. 2014; 21(18):11066-74. DOI: 10.1007/s11356-014-2986-5

4. Soleimanzadeh A, Kian M, Moradi S, et al. Protective effects of hydro-alcoholic extract of Quercus brantii against lead-induced oxidative stress in the reproductive system of male mice. Avicenna J Phytomed. 2018; 8(5):448-456.

5. Соседова Л.М., Капустина Е.А., Вокина В.А. Влияние интоксикации ацетатом свинца самцов белых крыс на функционирование нервной системы их потомства // Гигиена и санитария. 2018. Т. 97, № 10. С. 972-975

6. Sallmto M, Suvisaari J, Lindbohm ML, et al. Paternal occupational lead exposure and offspring risks for schizophrenia. Schizophr Res. 2016; 176(2-3):560-565. DOI: 10.1016/j.schres.2016.06.004

7. Zimet Z, Bilban M, Fabjan T, et al. Lead exposure and oxidative stress in coal miners. Biomed Environ Sci. 2017; 30(11):841-845. DOI: 10.3967/bes2017.113

8. Peng M, Shi S, Zhang Y. The influence of Cd2+, Hg2+ and Pb2+ on taxifolin binding to bovine serum albumin by spectroscopic methods: With the viewpoint of toxic ions/drug interference. Environ Toxicol Pharmacol. 2012; 33(2):327-33. DOI: 10.1016/j. etap.2011.12.025

9. Ayinde OC, Ogunnowo S, OgedegbeRA. Influence of vitamin C and vitamin E on testicular zinc content and testicular toxicity in lead exposed albino rats. BMC Pharmacol Toxicol. 2012; 13:17. DOI: 10.1186/2050-6511-13-17.

10. Буреш Я., Бурешова О., Хьюстон Д.П. Методики и основные эксперименты по изучению мозга и поведения. М.: Высш. шк., 1991. 399 с.

11. Дорогова В.Б., Лисецкая Л.Г., Журба О.М., и др. Атомно-абсорбционный анализ микроэлементов в биосредах и метрологические основы контроля аналитических работ. Методические указания 4.4.-99. Иркутск. 1999. 25 с.

12. Nelson BK, Moorman WJ, Schrader SM, et al. Paternal exposure of rabbits to lead: behavioral deficits in offspring. Neurotoxicol Teratol. 1997; 19(3):191-8.

13. Al-Juboori B, Hamdan F, Al-Salihi A. Paternal exposure to low-dose lead acetate: effect on implantation rate, pregnancy outcome, and sex ratio in mice. Turk J Med Sci. 2016; 46(3):936-41. DOI: 10.3906/sag-1412-62

14. Levin ED, Hawkey AB, Hall BJ, et al. Paternal THC exposure in rats causes long-lasting neurobehavioral effects in the offspring. Neurotoxicol Teratol. 2019; 74:106806. DOI: 10.1016/j. ntt.2019.04.003

15. Сидорин Г.И., Луковникова Л.В. Об основных механизмах адаптации к действию химических веществ // Медицина труда и промышленная экология. 2017. № 9. С. 172-173


Review

For citations:


Kapustina E.A., Lisetskaya L.G. Effects of Dihydroquercetin on Behavior of Albino Rat Offspring with Transgenerational Chemical Body Burden. Public Health and Life Environment – PH&LE. 2020;(2):38-41. (In Russ.) https://doi.org/10.35627/2219-5238/2020-323-2-38-41

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ISSN 2219-5238 (Print)
ISSN 2619-0788 (Online)