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DNA Damage in the Tissues of White Rats Exposed to Wildfire Smoke. P. 335–342

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Section: Medical and biological sciences

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Authors

Ekaterina A. Kapustina* ORCID: https://orcid.org/0000-0002-2803-4048
Vera A. Vokina* ORCID: https://orcid.org/0000-0002-8165-8052
Elizaveta S. Andreeva* ORCID: https://orcid.org/0000-0002-3709-8676
*East-Siberian Institute of Medical and Ecological Research (Angarsk, Irkutsk Region, Russian Federation)
Corresponding author: Ekaterina Kapustina, address: mkr. 12A, 3, Angarsk, 664003, Irkutskaya obl., Russian Federation; e-mail: kapustinkae@yandex.ru

Abstract

Wildfire smoke affects the health of the population of the entire planet and each year the situation is getting worse. Fire smoke has mutagenic, carcinogenic and other long-term effects. The aim of this paper was to study the genotoxic effect of wildfire smoke on male white rats and the transgenerational effect of wildfire smoke on their offspring. Smoke exposure simulation was performed on 40 male white rats in 200-litre exposure chambers. Forest litter, branches, fallen bark, and the upper layer of soil served as a combustible substrate. The exposure was carried out for 4 hours 5 days a week in the course of 4 weeks. Offspring of both sexes were obtained from the exposed animals and intact females. We analysed DNA fragmentation and global DNA methylation in the gonadal tissue and blood cells of the exposed animals immediately after the exposure and global DNA methylation in the blood cells of the offspring upon reaching sexual maturity. The research was performed using the comet assay with modifications to study global DNA methylation with MspI and HpaII restriction enzymes. The exposed animals showed an increased level of global DNA methylation in their blood cells. In male offspring, a decrease in the level of global DNA methylation in the blood cells was revealed, compared with the controls, while females showed no differences from the controls. The established facts of changes in global DNA methylation after exposure to wildfire smoke require further in-depth research, since the mechanism of the development of this phenomenon remains rather unclear.
For citation: Kapustina E.A., Vokina V.A., Andreeva E.S. DNA Damage in the Tissues of White Rats Exposed to Wildfire Smoke. Journal of Medical and Biological Research, 2021, vol. 9, no. 3, pp. 335–342. DOI: 10.37482/2687-1491-Z071

Keywords

wildfire smoke, genotoxic effect of smoke, transgenerational effect of smoke, DNA fragmentation, global DNA methylation, comet assay, white rats

References

1. Cascio W.E. Wildland Fire Smoke and Human Health. Sci. Total Environ., 2018, vol. 15, no. 624, pp. 586–595. DOI: 10.1016/j.scitotenv.2017.12.086
2. Liu J.C., Wilson A., Mickley L.J., Ebisu K., Sulprizio M.P., Wang Y., Peng R.D., Yue X., Dominici F., Bell M.L. Who Among the Elderly Is Most Vulnerable to Exposure to and Health Risks of Fine Particulate Matter from Wildfire Smoke? Am. J. Epidemiol., 2017, vol. 186, no. 6, pp. 730–735. DOI: 10.1093/aje/kwx141
3. Reid C.E., Considine E.M., Watson G.L., Telesca D., Pfister G.G., Jerrett M. Associations Between Respiratory Health and Ozone and Fine Particulate Matter During a Wildfire Event. Environ. Int., 2019, vol. 129, pp. 291–298. DOI: 10.1016/j.envint.2019.04.033
4. Lewtas J., Claxton L., Mumford J., Lofroth G. Bioassay of Complex Mixtures of Indoor Air Pollutants. IARC Sci. Publ., 1993, vol. 109, pp. 85–95.
5. Kim Y.H., Warren S.H., Krantz Q.T., King C., Jaskot R., Preston W.T., George B.J., Hays M.D., Landis M.S., Higuchi M., DeMarini D. M., Gilmour M.I. Mutagenicity and Lung Toxicity of Smoldering vs. Flaming Emissions from Various Biomass Fuels: Implications for Health Effects from Wildland Fires. Environ. Health Perspect., 2018, vol. 126, no. 1. Art. no. 017011. DOI: 10.1289/EHP2200
6. Vokina V.A., Novikov M.A., Alekseenko A.N., Sosedova L.M., Kapustina E.A., Bogomolova E.S., Elfimova T.A. Experimental Evaluation of Effect of Wildfire Smoke Exposure on Reproductive Function of Small Mammals and Their Offspring. Bull. Irkutsk State Univ. Ser. Biol. Ecol., 2019, vol. 29, pp. 88–98. DOI: 10.26516/2073-3372.2019.29.88 (in Russ.).
7. Zhanataev A.K., Anisina E.A., Chayka Z.V., Miroshkina I.A., Durnev A.D. The Phenomenon of Atypical DNA Comets. Cell Tissue Biol., 2017, vol. 11, no. 4, pp. 286–292. DOI: 10.1134/S1990519X17040113
8. Wentzel J.F., Gouws C., Huysamen C., van Dyk E., Koekemoer G., Pretorius P.J. Assessing the DNA Methylation Status of Single Cells with the Comet Assay. Anal. Biochem., 2010, vol. 400, no. 2, pp. 190–194. DOI: 10.1016/j.ab.2010.02.008
9. Ewa B., Danuta M.Š. Polycyclic Aromatic Hydrocarbons and PAH-Related DNA Adducts. J. Appl. Genet., 2017, vol. 58, no. 3, pp. 321–330. DOI: 10.1007/s13353-016-0380-3
10. Muthusamy S., Peng C., Ng J.C. Genotoxicity Evaluation of Multi-Component Mixtures of Polyaromatic Hydrocarbons (PAHs), Arsenic, Cadmium, and Lead Using Flow Cytometry Based Micronucleus Test in HepG2 Cells. Mutat. Res. Genet. Toxicol. Environ. Mutagen., 2018, vol. 827, pp. 9–18. DOI: 10.1016/j.mrgentox.2018.01.002
11. Miller S.R., Cherrington N.J. Transepithelial Transport Across the Blood-Testis Barrier. Reproduction, 2018, vol. 156, no. 6, pp. 187–194. DOI: 10.1530/REP-18-0338
12. DeFlorio-Barker S., Crooks J., Reyes J., Rappold A.G. Cardiopulmonary Effects of Fine Particulate Matter Exposure Among Older Adults, During Wildfire and Non-Wildfire Periods, in the United States 2008–2010. Environ. Health Perspect., 2019, vol. 127, no. 3. Art. no. 37006. DOI: 10.1289/EHP3860
13. Krejcova L., Richtera L., Hynek D., Labuda J., Adam V. Current Trends in Electrochemical Sensing and Biosensing of DNA Methylation. Biosens. Bioelectron., 2017, vol. 97, pp. 384–399. DOI: 10.1016/j.bios.2017.06.004
14. Fernández-Santiago R., Merkel A., Castellano G., Heath S., Raya A., Tolosa E., Martí M.-J., Consiglio A., Ezquerra M. Whole-Genome DNA Hyper-Methylation in iPSC-Derived Dopaminergic Neurons from Parkinson’s Disease Patients. Clin. Epigenetics, 2019, vol. 11, no. 1. Art. no. 108. DOI: 10.1186/s13148-019-0701-6
15. Thalheim T., Herberg M., Galle J. Linking DNA Damage and Age-Related Promoter DNA Hyper-Methylation in the Intestine. Genes (Basel), 2018, vol. 9, no. 1. Art. no. 17. DOI: 10.3390/genes9010017
16. Taleat Z., Mathwig K., Sudhölter E.J.R., Rassaei L. Detection Strategies for Methylated and Hypermethylated DNA. TrAC Trends Anal. Chem., 2015, vol. 66, pp. 80–89. DOI: 10.1016/j.trac.2014.11.013
17. Potabattula R., Dittrich M., Schorsch M., Hahn T., Haaf T., El Hajj N. Male Obesity Effects on Sperm and Next-Generation Cord Blood DNA Methylation. PLoS One, 2019, vol. 14, no. 6. Art. no. e0218615. DOI: 10.1371/journal.pone.0218615
18. Watkins A.J., Dias I., Tsuro H., Allen D., Emes R.D., Moreton J., Wilson R., Ingram R.J.M., Sinclair K.D. Paternal Diet Programs Offspring Health Through Sperm- and Seminal Plasma-Specific Pathways in Mice. Proc. Natl. Acad. Sci. USA, 2018, vol. 115, no. 40, pp. 10064–10069. DOI: 10.1073/pnas.1806333115
19. Pogribny I., Koturbash I., Tryndyak V., Hudson D., Stevenson S.M.L., Sedelnikova O., Bonner W., Kovalchuk O. Fractionated Low-Dose Radiation Exposure Leads to Accumulation of DNA Damage and Profound Alterations in DNA and Histone Methylation in the Murine Thymus. Mol. Cancer Res., 2005, vol. 3, no. 10, pp. 553–561. DOI: 10.1158/1541-7786.MCR-05-0074
20. Chan J.C., Nugent B.M., Bale T.L. Parental Advisory: Maternal and Paternal Stress Can Impact Offspring Neurodevelopment. Biol. Psychiatry, 2018, vol. 83, no. 10, pp. 886–894. DOI: 10.1016/j.biopsych.2017.10.005
21. Elmhiri G., Gloaguen C., Grison S., Kereselidze D., Elie C., Tack K., Benderitter M., Lestaevel P., Legendre A., Souidi M. DNA Methylation and Potential Multigenerational Epigenetic Effects Linked to Uranium Chronic Low-Dose Exposure in Gonads of Males and Females Rats. Toxicol. Lett., 2018, vol. 282, pp. 64–70. DOI: 10.1016/j. toxlet.2017.10.004



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