Protective effect of extracts of Teucrium Polium and Rumex Crispus against cyclophosphamide-induced genotoxic damage in human lymphocytes

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Abstract

Teucrium polium (T. polium) and Rumex crispus (R. crispus) are plant species that grow widely in Anatolia and are thought to have healing effects for many diseases. In this study plant extracts are suggested as alternative agents in repairing cellular damage by using sister chromatid exchange (SCE), micronucleus (MN), mitotic index (MI), replication index (RI) and nuclear abnormalities (NAs), against the genotoxicity of cyclophosphamide (CP) in the human lymphocyte cells. 8 experimental groups were formed in the study. The cell culture medium was supplemented with 0.16 μg/ml CP and the cells were treated with 50, 100 and 250 μM T. polium and R. crispus extracts in the presence and absence of CP. As a result, CP significantly decreased MI frequency while increasing SCE, MN and NAs frequencies in cells. 100 μM T. polium plus CP decreased SCEs when compared with CP alone. In addition, MN frequency was significantly decreased in 100 μM T. poliumplus CP and 250 μM R. crispus plus CP combine groups. Our results suggest that these plant extracts are not genetically damaging and have improving effects at these doses.

About the authors

Sengul Yuksel

Inonu University

Author for correspondence.
Email: sengul.yuksel@inonu.edu.tr
ORCID iD: 0000-0002-7190-431X

PhD., Medical Faculty, Department of Medical Biology & Genetics

Turkey, Malatya, 44100

Selcen Korkmaz Sezer

Inonu University

Email: selcenkorkmaz@hotmail.com

PhD., Medical Faculty, Department of Medical Biology & Genetics

Turkey, Malatya, 44100

Elcin Latife Kurtoglu

Lokman Hekim University

Email: elcinkurtoglu@hotmail.com

PhD, Medical Faculty, Department of Medical Biology

Turkey, Ankara, 06100

Harika Gozukara Bag

Inonu University

Email: harika.gozukara@inonu.edu.tr

PhD, Medical Faculty, Department of Biostatistics and Medical Informatics

Turkey, Malatya, 44100

References

  1. Celik TA. Potential Genotoxic and Cytotoxic Effects of Plant Extracts. IntechOpen. 2012. https://doi.org/10.5772/28488.
  2. Ozkan G, Kamiloglu S, Ozdal T, et al. Potential Use of Turkish Medicinal Plants in the Treatment of Various Diseases. Molecules. 2016;21(3):257. https://doi.org/10.3390/molecules21030257.
  3. Gontijo VS, Dos Santos MH, Viegas C, Jr. Biological and Chemical Aspects of Natural Biflavonoids from Plants: A Brief Review. Mini Rev Med Chem. 2017;17(10):834-862. https://doi.org/10.2174/1389557517666161104130026.
  4. Bozkurt-Guzel C, Serbetci T, Kultur S. Cytotoxic activities of some Turkish medicinal plants against HeLa cells in vitro. Indian J Traditional Knowledge. 2018;17(1):43-49.
  5. Dinç M, Doğu S, Bilgili B, Duran A. Comparative anatomical and micromorphological studies on Teucrium creticum and Teucrium orientale var. orientale (T. sect. Teucrium, Lamiaceae). Nord J Bot. 2009;27(3):251-256. https://doi.org/10.1111/j.1756-1051.2008.00323.x.
  6. Hasani P, Yasa N, Vosough-Ghanbari S, et al. In vivo antioxidant potential of Teucrium polium, as compared to α-tocopherol. Acta Pharm. 2007;57(1):123-129. https://doi.org/10.2478/v10007-007-0010-z.
  7. Sharififar F, Dehghn-Nudeh G, Mirtajaldini M. Major flavonoids with antioxidant activity from Teucrium polium L. Food Chemistry. 2009;112(4):885-888. https://doi.org/10.1016/j.foodchem.2008.06.064.
  8. Bahramikia S, Yazdanparast R. Phytochemistry and medicinal properties of Teucrium polium L. (Lamiaceae). Phytother Res. 2012;26(11):1581-1593. https://doi.org/10.1002/ptr.4617.
  9. Milosevic-Djordjevic O, Radovic Jakovljevic M, Markovic A, et al. Polyphenolic contents of Teucrium polium L. and Teucrium scordium L. associated with their protective effects against MMC-induced chromosomal damage in cultured human peripheral blood lymphocytes. Turk J Biol. 2018;42(2):152-162. https://doi.org/10.3906/biy-1707-36.
  10. Rajabalian S. Methanolic extract of Teucrium polium L. potentiates the cytotoxic and apoptotic effects of anticancer drugs of vincristine, vinblastine and doxorubicin against a panel of cancerous cell lines. Exp Oncol. 2008;30(2):133-138.
  11. Sghaier MB, Ismail MB, Bouhlel I, et al. Leaf extracts from Teucrium ramosissimum protect against DNA damage in human lymphoblast cell K562 and enhance antioxidant, antigenotoxic and antiproliferative activity. Environ Toxicol Pharmacol. 2016;44:44-52. https://doi.org/10.1016/j.etap.2016.04.006.
  12. Yıldırım A, Mavi A, Kara AA. Determination of Antioxidant and Antimicrobial Activities of Rumex crispus L. Extracts. J Agric Food Chem. 2001;49(8):4083-4089. https://doi.org/10.1021/jf0103572.
  13. Idris OA, Wintola OA, Afolayan AJ. Phytochemical and antioxidant activities of Rumex crispus L. in treatment of gastrointestinal helminths in Eastern Cape Province, South Africa. Asian Pac J Trop Biomed. 2017;7(12):1071-1078. https://doi.org/10.1016/j.apjtb.2017.10.008.
  14. Shim KS, Lee B, Ma JY. Water extract of Rumex crispus prevents bone loss by inhibiting osteoclastogenesis and inducing osteoblast mineralization. BMC Complement Altern Med. 2017;17(1):483. https://doi.org/10.1186/s12906-017-1986-7.
  15. Coruh I, Gormez A, Ercisli S, Sengul M. Total Phenolic Content, Antioxidant, and Antibacterial Activity of Rumex crispus Grown Wild in Turkey. Pharm Biol. 2008;46(9):634-638. https://doi.org/10.1080/13880200802182240.
  16. Shiwani S, Singh NK, Wang MH. Carbohydrase inhibition and anti-cancerous and free radical scavenging properties along with DNA and protein protection ability of methanolic root extracts of Rumex crispus. Nutr Res Pract. 2012;6(5):389-395. https://doi.org/10.4162/nrp.2012.6.5.389.
  17. Uren N, Yuksel S, Onal Y. Genotoxic effects of sulfur dioxide in human lymphocytes. Toxicol Ind Health. 2014;30(4):311-315. https://doi.org/10.1177/0748233712457441.
  18. Yuksel S, Tasdemir S, Korkmaz S. Protective effect of thymoquinone against cyclophosphamide-induced genotoxic damage in human lymphocytes. Bratisl Lek Listy. 2017;118(4):208-211. https://doi.org/10.4149/BLL_2017_041.
  19. Tolbert PE, Shy CM, Allen JW. Micronuclei and other nuclear anomalies in buccal smears: methods development. Mutat Res. 1992;271(1):69-77. https://doi.org/10.1016/0165-1161(92)90033-i.
  20. AL-Dulaimi, DW, Faisal SF, Baharetha HM, et al. Cytogenetic an experimental monitoring test for plant extracts. IOSR J Pharm Biol Sci. 2017;12(1):100-105.
  21. Speit G, Haupter S. On the mechanism of differential Giemsa staining of bromodeoxyuridine-substituted chromosomes. Hum Genet. 1985;70(2). https://doi.org/10.1007/bf00273070.
  22. Yuksel S, Yesilada E, Gulbay G, et al. Protective effect of myricetin against estradiol-17β-induced genotoxic damage in human lymphocytes. Fresenius Environmental Bulletin. 2012;21(4):1022-1026.
  23. Zulkipli IN, David SR, Rajabalaya R, Idris A. Medicinal Plants: A Potential Source of Compounds for Targeting Cell Division. Drug Target Insights. 2015;9:9-19. https://doi.org/10.4137/DTI.S24946.
  24. Rahmouni F, Saoudi M, Amri N, et al. Protective effect of Teucrium polium on carbon tetrachloride induced genotoxicity and oxidative stress in rats. Arch Physiol Biochem. 2018;124(1):1-9. https://doi.org/10.1080/13813455.2017.1347795.
  25. Zhang J, Tian Q, Zhou S-F. Clinical Pharmacology of Cyclophosphamide and Ifosfamide. Curr Drug Ther. 2006;1(1):55-84. https://doi.org/10.2174/157488506775268515.
  26. Kurtoglu EL, Yuksel S. Genotoxic effects of tacrolimus on human lymphocyte cells. Russian Journal of Genetics. 2012;48(6):651-655. https://doi.org/10.1134/s1022795412050134.
  27. Kocaman AY, Istifli ES, Buyukleyla M, et al. In vitro evaluation of the protective effects of 4-thujanol against mitomycin-C and cyclophosphamide-induced genotoxic damage in human peripheral lymphocytes. Toxicol Ind Health. 2013;29(1):23-37. https://doi.org/10.1177/0748233712436640.
  28. Cho EJ, Um SI, Han JH, et al. The cytoprotective effect of Rumex Aquaticus Herba extract against hydrogen peroxide-induced oxidative stress in AGS cells. Arch Pharm Res. 2016;39(12):1739-1747. https://doi.org/10.1007/s12272-016-0863-0.
  29. Wang Q, Wang Y, Xing Y, et al. Physcion 8-O-beta-glucopyranoside induces apoptosis, suppresses invasion and inhibits epithelial to mesenchymal transition of hepatocellular carcinoma HepG2 cells. Biomed Pharmacother. 2016;83:372-380. https://doi.org/10.1016/j.biopha.2016.06.045.
  30. Tepe B, Degerli S, Arslan S, et al. Determination of chemical profile, antioxidant, DNA damage protection and antiamoebic activities of Teucrium polium and Stachys iberica. Fitoterapia. 2011;82(2):237-246. https://doi.org/10.1016/j.fitote.2010.10.006.
  31. Ozer Z, Kiliç T, Çarikçi S, et al. Investigation of phenolic compounds and antioxidant activity of Teucrium polium L. decoction and infusion. J BAUN Inst Sci Technol. 2018;20(1):212-218. https://doi.org/10.25092/baunfbed.370594.
  32. Ljubuncic P, Dakwar S, Portnaya I, et al. Aqueous extracts of Teucrium polium possess remarkable antioxidant activity in vitro. Evid Based Complement Alternat Med. 2006;3(3):329-338. https://doi.org/10.1093/ecam/nel028.
  33. Wegiera M, Smolarz HD, Bogucka-Kocka A. Rumex L. species induce apoptosis in 1301, EOL-1 and H-9 cell lines. Acta Pol Pharm. 2012;69(3):487-499.

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Copyright (c) 2019 Yuksel S., Sezer S., Kurtoglu E., Bag H.

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