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Evaluation of the cytotoxic and membrane damaging effects of mountain tea (Sideritis stricta Boiss & Heldr.) essential oil on parental and epirubicin-HCl resistant H1299 cells

Year 2018, Volume: 43 Issue: 3, 669 - 677, 30.09.2018
https://doi.org/10.17826/cumj.340273

Abstract

Purpose: In this study, we evaluated Sideritis stricta (S. stricta), as potential-oxidative agents against parental and epirubicin-HCl resistant H1299 cells. 

Material and Methods: Oxidative stress biomarkers such as malondialdehyde level determined in cell lysates. Assessment of cell viability was made by CellTiter-Blue® Cell Viability Assay and 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazoliumbromide (MTT) assay after 20-600 μg/mL essential oil concentrations treated to parental and epirubicin-HCl (drug) resistant H1299 cells for 24, 48 and 72 h. Malondialdehyde levels were assayed for determining the membrane damaging effects. 

Results: Parental H1299 cells were found to be more sensitive to cytotoxic effect of the essential oil. Essential oil showed cytotoxic and more selective effects depend on time and concentration. Essential oil caused increasing malondialdehyde level on both parental and drug resistant H1299 cells. The highest concentration of the essential oil (IC70) treatment caused the highest membrane damage on both parental and drug resistant H1299 cells.

Conclusions: Parental and epirubicin-HCl resistant H1299 cells showed different cellular response against potential antitumour and pro-oxidative effects of essential oil.


References

  • 1. Marete EN., Jacquier JC, O’Riordan D. Feverfew as a source of bioactives for functional foods: Storage stability in model beverages. J Funct Foods 2011; 3: 38-43.
  • 2. Atoui AK, Mansouri A, Boskou G, Kefalas P. Tea and herbal infusions: Their antioxidant activity and phenolic profile. Food Chem 2005; 89: 27–36.
  • 3. Rodriguez Vaquer MJ, Tomassini Serravalle LR, Manca de Narda MC, Strasser de Saad AM. Antioxidant capacity and antibacterial activity of phenolic compounds from Argentinean herb infusions. Food Control 2010; 21: 779–785.
  • 4. Guimara˜es R, Barros L, Carvalho AM, Ferreira CFR. Infusions and decoctions of mixed herbs used in folk medicine: Synergism in antioxidant potential. Phytother Res 2011; 25: 1209–1214.
  • 5. Raal A, Orav A, Pu¨ssa T, Valner C, Malmiste B, Arak E. Content of essential oil, terpenoids and polyphenols in commercial chamomile (Chamomilla recutita L. Rauschert) teas from different countries. Food Chem 2012; 131: 632–638.
  • 6. Kırımer N, Baser KHC, Demirci B, Duman H. Essential oils of Sideritis species of Turkey belonging to the section. Empedoclia Chem Nat Compd 2004; 40: 19-23.
  • 7. Küpeli E, Şahin FP, Çaliş İ, Yeşilada E, Ezer N. Phenolic compounds of Sideritis ozturkii and their in vivo anti-inflammatory and antinociceptive activities. J Ethnopharmacol 2007; 112: 356-360.
  • 8. Mill M. In Flora of Turkey and East Aegean Islands 1982; Vol. 7; Davis P. H., Ed.; Edinburgh University Press, Edinburgh, UK.
  • 9. Huber-Morath A. In Flora of Turkey and East Aegean Islands 1988; Vol. 10 ; Davis P. H., Mill R. R., Tan K., Eds.;Edinburgh University Press, Edinburgh, UK,.
  • 10. Güneş F, Özhatay N Lathyrus L. in: Güner A, Özhatay N, Ekim T & Başer KHC (eds.) Flora of Turkey and the East Aegean Islands (Suppl. 2) 2000; Vol. 11. pp. 92-94. Edinburgh: Edinburgh University Press.
  • 11. Topçu G, Gören AC. Biological activity of diterpenoids isolated from Anatolian Lamiaceae plants. Rec Nat Prod 2007; 1: 1-16.
  • 12. Halfon B, Goren AC, Ertas A, Topcu G. Complete 13C NMR assignments for Ent-Kaurene diterpenoids from Sideritis species. Magn Reson Chem 2011; 49: 291-294.
  • 13. Topçu G, Ertaş A, Öztürk M, Dinçel D, Kılıç T, Halfon B. Ent-kaurane diterpenoids isolated from Sideritis congesta. Phytochem Lett 2011; 4: 436-439.
  • 14. Fraga BM. Phytochemistry and chemotaxonomy of Sideritis species from the Mediterranean region. Phytochemistry 2012; 76: 7-24.
  • 15. Şahin FP, Ezer N, Alis IC. Terpenic and phenolic compounds from Sideritis stricta. Turk J Chem 2006; 30: 495-504.
  • 16. Kırmızıbekmez H, Ariburnu E, Masullo M, Festa M, Capasso A, Yesilada E, Piacente S. Iridoid, phenylethanoid and flavonoid glycosides from Sideritis trojana. Fitoterapia 2012; 8: 130-136.
  • 17. Gonz´alez-Burgos E, Carretero ME, G´omez-Serranillos MP. Sideritis spp.: uses, chemical composition and pharmacological activities – a review. J Ethnopharmacol 2011; 135: 209–225.
  • 18. Tadi´c VM, Jeremic I, Dobric S, Isakovic A, Markovic I, Trajkovic V, Bojovic D, Arsic I. Anti-inflammatory, gastroprotective, and cytotoxic effects of Sideritis scardica extracts. Planta Med 2012; 78: 415–427.
  • 19. Özcan M, Chalchat JC, Akgül A. Essential oil composition of Turkish mountain tea (Sideritis spp.). Food Chem 2001; 75: 459-463.
  • 20. Küpeli E, Şahin FP, Çaliş İ, Yeşilada E, Ezer N. Phenolic compounds of Sideritis ozturkii and their in vivo anti-inflammatory and antinociceptive activities. J Ethnopharmacol 2007; 112: 356-360.
  • 21. Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 2007; 39: 44–84.
  • 22. Erdogan A, Ozkan A. A comparative study of cytotoxic, membrane and DNA damaging effects of Origanum majorana’s essential oil and its oxygenated monoterpene component linalool on parental and epirubicin-resistant H1299 cells. Biologia 2013; 68: 754-761.
  • 23. Dobbs NA, Twelwes CJ, Rizzi P, Warvick JD, Metivier EM, Williams R, Johnson PJ EPI in hepatocellular carcinoma: Pharmacokinetics and clinical activity. Cancer. Chemother Pharmacol 1994; 34: 405-410.
  • 24. Rihova B, Strohalm J, Kobackova K. Acquired and specific immunological mechanisms co-responsile for efficacy of polymer-bound drugs. J Control Release 2002; 78: 97-114.
  • 25. Ozkan A. Lymphokine-activated killer cell susceptibility in epirubicin resistant and parental human non-small cell lung cancer (NSCLC). Biologia 2007; 62: 232-237.
  • 26. Jansson O, Motlagh PB, Persson M, Henrikson R, Grankvist K Increase in doxorubicin cytotoxicity by carvedilol inhibition of P-glycoprotein activity. Biochemical Pharmacol 1999; 58: 1801-1806.
  • 27. Gloeckner H, Jonuleit T, Lemke HD. Monitoring of cell viability and cell growth in a hollow-fiber bioreactor by use of the dye Alamar Blue (TM). J Immunol Methods 2001; 252: 131-138.
  • 28. Mosmann T. Rapid Colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65: 55-63.
  • 29. Wasowicz W, Neve J, Peretz A. Optimized steps in fluorometric determination of thiobarbitiric acid-reactive substances in serum; importance of extraction pH and influence of sample preservation and storage. Clin Chem 1993; 39: 2522-2526. 30. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 1976; 72: 248-254.
  • 31. Kirkman TW. Statistics to use [Online]. 1996 Available:http://www.physics.csbsju.edu/stats/1996 [17 August 2008].
  • 32. Hong L, Piao Y, Han Y, Wang J, Zhang X, Du Y, Cao S, Qiao T, Chen Z, Fan D. Zinc ribbon domain containing 1 (ZNRD1) mediates multidrug resistance of leukemia cells through regulation of P-glycoprotein and Bcl-2. Mol Cancer Ther 2005; 4: 1936-1942.
  • 33. Ozkan A, Erdogan A. Membrane and DNA damaging/protective effects of eugenol, eucalyptol, terpinen-4-ol and camphor at various concentrations on parental and drug resistant H1299 cells. Turk J Biol 2012; 37: 405-413.
  • 34. Ozkan A, Erdogan A. A comparative study of the antioxidant/prooxidant effects of carvacrol and thymol at various concentrations on membrane and DNA of parental and drug resistant H1299 cells. Nat Prod Commun 2012; 7: 1557-1560. 35. Ozkan A, Erdogan A, Sokmen M, Tugrulay S, Unal O. Antitumoral and antioxidant effect of essential oils and in vitro antioxidant properties of essential oils and aqueous extracts from Salvia pisidica. Biologia 2010; 65: 990-996.
  • 36. Ozkan A, Erdogan A. Antioxidant and anticancer activity of fresh corm extract from Romulea tempskyana (Iridaceae). Nat Prod Res 2012; 26: 2126-2128.
  • 37. Erdogan A, Ozkan A. Effects of Thymus revolutus Célak essential oil and its two major components on Hep G2 cells membrane. Biologia 2013; 68: 105-111.
  • 38. Ozkan A, Erdogan A. A comparative evaluation of antioxidant and anticancer activity of essential oil from Origanum onites (Lamiaceae) and its two major phenolic components. Turk J Biol 2011; 35: 735-742.
  • 39. Bakkali F, Averbeck S, Averbeck D, Idaomar M. Biological effects of essential oils – A review. Food Chem Toxicol 2008; 46: 446-475.
  • 40. Richter C, Schlegel J. Mitochondrial calcium release induced by prooxidants. Toxicol Lett 1993; 67: 119-127. 41. Novgorodov SA, Gudz TI. Permeability transition pore of the inner mitochondrial membrane can operate in two open states with different selectivities. J Bioenerg Biomembr 1996; 28: 139-146.
  • 42. Vercesi AE, Kowaltowski AJ, Grijalba MT, Meinicke AR, Castilho R.F. The role of reactive oxygen species in mitochondrial permeability transition. Biosci Rep 1997; 17: 43-52.
  • 43. Yoon HS, Moon SC, Kim ND, Park BS, Jeong MH, Yoo YH. Genistein induces apoptosis of RPE-J cells by opening mitochondrial PTP. Biochem Biophys Res Commun 2000; 276: 151-156.
  • 44. Armstrong JS. Mitochondrial membrane permeabilization: The sine qua non for cell death. BioEssays 2006; 28: 253-260.

Parental ve epirubicin-HCl dirençli H1299 hücrelerinde dağ çayı (Sideritis stricta Boiss & Heldr.) uçucu yağının sitotoksik ve membran hasar verici etkilerinin değerlendirilmesi

Year 2018, Volume: 43 Issue: 3, 669 - 677, 30.09.2018
https://doi.org/10.17826/cumj.340273

Abstract

Amaç:. Bu çalışmada, Sideritis stricta (S. stricta) parental ve epirubicin-HCl dirençli H1299 hücrelerine karşı potansiyel oksidatif ajan olarak değerlendirilmiştir. 

Gereç ve Yöntem: Hücre lisatlarında malondialdehit seviyesi gibi oksidatif stres biyobelirteçleri saptanmıştır. Hücre sitotoksisitesinin değerlendirilmesi, 20-600 μg/mL konsantrasyonlarında 24, 48 ve 72 saat parental ve epirubicin-HCl (ilaç) dirençli H1299 hücrelerine uçucu yağ uygulamasından sonra CellTiter-Blue® Hücre Canlılık Testi ve 3- (4,5-dimetil-2-tiazolil) -2,5-difenil-2H-tetrazolyumbromid (MTT) testi ile yapılmıştır. Malondialdehid seviyeleri membran hasar etkisini ortaya koymak için belirlenmiştir.

Bulgular:  Parental H1299 hücreleri uçucu yağın sitotoksik etkisine karşı daha duyarlı bulunmuştur. Uçucu yağ, zaman ve konsantrasyona bağlı olarak sitotoksik ve daha seçici etkiler göstermiştir. Uçucu yağ, hem parental hem de ilaca dirençli H1299 hücrelerinde malondialdehit seviyesinde artışa neden olmuştur. Uçucu yağın (IC70) en yüksek konsantrasyonu, hem parental hem de ilaca dirençli H1299 hücrelerinde en yüksek membran hasarına neden olmuştur.

Sonuç: Parental ve epirubicin-HCl dirençli H1299 hücreleri uçucu yağın potansiyel antitümör ve pro-oksidatif etkilerine karşı farklı hücresel tepkiler göstermiştir.


References

  • 1. Marete EN., Jacquier JC, O’Riordan D. Feverfew as a source of bioactives for functional foods: Storage stability in model beverages. J Funct Foods 2011; 3: 38-43.
  • 2. Atoui AK, Mansouri A, Boskou G, Kefalas P. Tea and herbal infusions: Their antioxidant activity and phenolic profile. Food Chem 2005; 89: 27–36.
  • 3. Rodriguez Vaquer MJ, Tomassini Serravalle LR, Manca de Narda MC, Strasser de Saad AM. Antioxidant capacity and antibacterial activity of phenolic compounds from Argentinean herb infusions. Food Control 2010; 21: 779–785.
  • 4. Guimara˜es R, Barros L, Carvalho AM, Ferreira CFR. Infusions and decoctions of mixed herbs used in folk medicine: Synergism in antioxidant potential. Phytother Res 2011; 25: 1209–1214.
  • 5. Raal A, Orav A, Pu¨ssa T, Valner C, Malmiste B, Arak E. Content of essential oil, terpenoids and polyphenols in commercial chamomile (Chamomilla recutita L. Rauschert) teas from different countries. Food Chem 2012; 131: 632–638.
  • 6. Kırımer N, Baser KHC, Demirci B, Duman H. Essential oils of Sideritis species of Turkey belonging to the section. Empedoclia Chem Nat Compd 2004; 40: 19-23.
  • 7. Küpeli E, Şahin FP, Çaliş İ, Yeşilada E, Ezer N. Phenolic compounds of Sideritis ozturkii and their in vivo anti-inflammatory and antinociceptive activities. J Ethnopharmacol 2007; 112: 356-360.
  • 8. Mill M. In Flora of Turkey and East Aegean Islands 1982; Vol. 7; Davis P. H., Ed.; Edinburgh University Press, Edinburgh, UK.
  • 9. Huber-Morath A. In Flora of Turkey and East Aegean Islands 1988; Vol. 10 ; Davis P. H., Mill R. R., Tan K., Eds.;Edinburgh University Press, Edinburgh, UK,.
  • 10. Güneş F, Özhatay N Lathyrus L. in: Güner A, Özhatay N, Ekim T & Başer KHC (eds.) Flora of Turkey and the East Aegean Islands (Suppl. 2) 2000; Vol. 11. pp. 92-94. Edinburgh: Edinburgh University Press.
  • 11. Topçu G, Gören AC. Biological activity of diterpenoids isolated from Anatolian Lamiaceae plants. Rec Nat Prod 2007; 1: 1-16.
  • 12. Halfon B, Goren AC, Ertas A, Topcu G. Complete 13C NMR assignments for Ent-Kaurene diterpenoids from Sideritis species. Magn Reson Chem 2011; 49: 291-294.
  • 13. Topçu G, Ertaş A, Öztürk M, Dinçel D, Kılıç T, Halfon B. Ent-kaurane diterpenoids isolated from Sideritis congesta. Phytochem Lett 2011; 4: 436-439.
  • 14. Fraga BM. Phytochemistry and chemotaxonomy of Sideritis species from the Mediterranean region. Phytochemistry 2012; 76: 7-24.
  • 15. Şahin FP, Ezer N, Alis IC. Terpenic and phenolic compounds from Sideritis stricta. Turk J Chem 2006; 30: 495-504.
  • 16. Kırmızıbekmez H, Ariburnu E, Masullo M, Festa M, Capasso A, Yesilada E, Piacente S. Iridoid, phenylethanoid and flavonoid glycosides from Sideritis trojana. Fitoterapia 2012; 8: 130-136.
  • 17. Gonz´alez-Burgos E, Carretero ME, G´omez-Serranillos MP. Sideritis spp.: uses, chemical composition and pharmacological activities – a review. J Ethnopharmacol 2011; 135: 209–225.
  • 18. Tadi´c VM, Jeremic I, Dobric S, Isakovic A, Markovic I, Trajkovic V, Bojovic D, Arsic I. Anti-inflammatory, gastroprotective, and cytotoxic effects of Sideritis scardica extracts. Planta Med 2012; 78: 415–427.
  • 19. Özcan M, Chalchat JC, Akgül A. Essential oil composition of Turkish mountain tea (Sideritis spp.). Food Chem 2001; 75: 459-463.
  • 20. Küpeli E, Şahin FP, Çaliş İ, Yeşilada E, Ezer N. Phenolic compounds of Sideritis ozturkii and their in vivo anti-inflammatory and antinociceptive activities. J Ethnopharmacol 2007; 112: 356-360.
  • 21. Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 2007; 39: 44–84.
  • 22. Erdogan A, Ozkan A. A comparative study of cytotoxic, membrane and DNA damaging effects of Origanum majorana’s essential oil and its oxygenated monoterpene component linalool on parental and epirubicin-resistant H1299 cells. Biologia 2013; 68: 754-761.
  • 23. Dobbs NA, Twelwes CJ, Rizzi P, Warvick JD, Metivier EM, Williams R, Johnson PJ EPI in hepatocellular carcinoma: Pharmacokinetics and clinical activity. Cancer. Chemother Pharmacol 1994; 34: 405-410.
  • 24. Rihova B, Strohalm J, Kobackova K. Acquired and specific immunological mechanisms co-responsile for efficacy of polymer-bound drugs. J Control Release 2002; 78: 97-114.
  • 25. Ozkan A. Lymphokine-activated killer cell susceptibility in epirubicin resistant and parental human non-small cell lung cancer (NSCLC). Biologia 2007; 62: 232-237.
  • 26. Jansson O, Motlagh PB, Persson M, Henrikson R, Grankvist K Increase in doxorubicin cytotoxicity by carvedilol inhibition of P-glycoprotein activity. Biochemical Pharmacol 1999; 58: 1801-1806.
  • 27. Gloeckner H, Jonuleit T, Lemke HD. Monitoring of cell viability and cell growth in a hollow-fiber bioreactor by use of the dye Alamar Blue (TM). J Immunol Methods 2001; 252: 131-138.
  • 28. Mosmann T. Rapid Colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65: 55-63.
  • 29. Wasowicz W, Neve J, Peretz A. Optimized steps in fluorometric determination of thiobarbitiric acid-reactive substances in serum; importance of extraction pH and influence of sample preservation and storage. Clin Chem 1993; 39: 2522-2526. 30. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 1976; 72: 248-254.
  • 31. Kirkman TW. Statistics to use [Online]. 1996 Available:http://www.physics.csbsju.edu/stats/1996 [17 August 2008].
  • 32. Hong L, Piao Y, Han Y, Wang J, Zhang X, Du Y, Cao S, Qiao T, Chen Z, Fan D. Zinc ribbon domain containing 1 (ZNRD1) mediates multidrug resistance of leukemia cells through regulation of P-glycoprotein and Bcl-2. Mol Cancer Ther 2005; 4: 1936-1942.
  • 33. Ozkan A, Erdogan A. Membrane and DNA damaging/protective effects of eugenol, eucalyptol, terpinen-4-ol and camphor at various concentrations on parental and drug resistant H1299 cells. Turk J Biol 2012; 37: 405-413.
  • 34. Ozkan A, Erdogan A. A comparative study of the antioxidant/prooxidant effects of carvacrol and thymol at various concentrations on membrane and DNA of parental and drug resistant H1299 cells. Nat Prod Commun 2012; 7: 1557-1560. 35. Ozkan A, Erdogan A, Sokmen M, Tugrulay S, Unal O. Antitumoral and antioxidant effect of essential oils and in vitro antioxidant properties of essential oils and aqueous extracts from Salvia pisidica. Biologia 2010; 65: 990-996.
  • 36. Ozkan A, Erdogan A. Antioxidant and anticancer activity of fresh corm extract from Romulea tempskyana (Iridaceae). Nat Prod Res 2012; 26: 2126-2128.
  • 37. Erdogan A, Ozkan A. Effects of Thymus revolutus Célak essential oil and its two major components on Hep G2 cells membrane. Biologia 2013; 68: 105-111.
  • 38. Ozkan A, Erdogan A. A comparative evaluation of antioxidant and anticancer activity of essential oil from Origanum onites (Lamiaceae) and its two major phenolic components. Turk J Biol 2011; 35: 735-742.
  • 39. Bakkali F, Averbeck S, Averbeck D, Idaomar M. Biological effects of essential oils – A review. Food Chem Toxicol 2008; 46: 446-475.
  • 40. Richter C, Schlegel J. Mitochondrial calcium release induced by prooxidants. Toxicol Lett 1993; 67: 119-127. 41. Novgorodov SA, Gudz TI. Permeability transition pore of the inner mitochondrial membrane can operate in two open states with different selectivities. J Bioenerg Biomembr 1996; 28: 139-146.
  • 42. Vercesi AE, Kowaltowski AJ, Grijalba MT, Meinicke AR, Castilho R.F. The role of reactive oxygen species in mitochondrial permeability transition. Biosci Rep 1997; 17: 43-52.
  • 43. Yoon HS, Moon SC, Kim ND, Park BS, Jeong MH, Yoo YH. Genistein induces apoptosis of RPE-J cells by opening mitochondrial PTP. Biochem Biophys Res Commun 2000; 276: 151-156.
  • 44. Armstrong JS. Mitochondrial membrane permeabilization: The sine qua non for cell death. BioEssays 2006; 28: 253-260.
There are 41 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Research
Authors

Ayşe Erdoğan This is me

Aysun Özkan

Orhan Ünal

Canan Dülgeroğlu

Publication Date September 30, 2018
Acceptance Date December 8, 2017
Published in Issue Year 2018 Volume: 43 Issue: 3

Cite

MLA Erdoğan, Ayşe et al. “Evaluation of the Cytotoxic and Membrane Damaging Effects of Mountain Tea (Sideritis Stricta Boiss & Heldr.) Essential Oil on Parental and Epirubicin-HCl Resistant H1299 Cells”. Cukurova Medical Journal, vol. 43, no. 3, 2018, pp. 669-77, doi:10.17826/cumj.340273.