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Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells

Year 2024, Volume: 16 Issue: 3, 283 - 292, 29.10.2024
https://doi.org/10.18521/ktd.1464261

Abstract

Objective: Exposure to perfluorooctanoic acid (PFOA) is linked to adverse health effects, including cancer and hepatic diseases. PFOA induces reactive oxygen species generation in human hepatic cells, causing oxidative stress and cell death. Resveratrol (RSV) has garnered attention for its protective effects against xenobiotic-induced damage, yet its impact on PFOA-induced oxidative stress and ferroptosis in the liver remains understudied. This study investigates RSV's protective mechanisms against oxidative stress and ferroptosis in HepG2 cells exposed to PFOA.
Method: HepG2 cells were cultured in DMEM with 10% FBS and 1% penicillin/streptomycin in a 5% CO2 incubator at 37°C. PFOA was added to the cells at concentrations ranging from 0 to 450 µM and incubated at 37°C for 24 hours. The IC50 was determined to be 457 μM. To examine RSV's protective effects, cells were treated with 60 μM RSV. Following treatment with PFOA, RSV, and the combination of PFOA+RSV, cell lysates were prepared for analysis. Oxidative stress and ferroptosis parameters were measured spectrophotometrically using ELISA.
Results: In the PFOA+RSV group, antioxidant capacity increased, and ferroptosis was suppressed compared to the control. Conversely, the PFOA group showed decreased antioxidant capacity, increased oxidant capacity, and induced ferroptosis compared to the control and RSV-treated groups.
Conclusion: PFOA exposure heightens oxidative stress and ferroptosis, whereas RSV treatment significantly reduces hepatic oxidative stress and protects against ferroptosis during PFOA exposure.

Ethical Statement

Etik kurul onayı gerekli değildir

Supporting Institution

Duzce University,he University of Duzce Scientific Research Unit Rapid Support

Project Number

The funding support for this study was provided by the University of Duzce Scientific Research Unit Rapid Support (Project No: 2022.14.02.1358).

References

  • 1. Qi Q, Niture S, Gadi S, Arthur E, Moore J, Levine KE, et al. Per‐ and polyfluoroalkyl substances activate UPR pathway, induce steatosis and fibrosis in liver cells. Environ Toxicol. 2023;38(1):225-242.
  • 2. Li K, Gao P, Xiang P, Zhang X, Cui X, Ma LQ. Molecular mechanisms of PFOA-induced toxicity in animals and humans: Implications for health risks. Environ Int. 2017;99:43-54.
  • 3. Kudo N, Kawashima Y. Toxicity and toxicokinetics of perfluorooctanoic acid in humans and animals. J Toxicol Sci. 2003;28(2):49-57.
  • 4. Mahapatra CT, Damayanti NP, Guffey SC, Serafin JS, Irudayaraj J, Sepúlveda MS. Comparative in vitro toxicity assessment of perfluorinated carboxylic acids. J Appl Toxicol. 2017;37(6):699-708.
  • 5. Suja F, Pramanik B, Zain S. Contamination, bioaccumulation and toxic effects of perfluorinated chemicals (PFCs) in the water environment: A review paper. Water Sci Technol. 2009;60:1533-44.
  • 6. Olsen GW, Mair DC, Lange CC, Harrington LM, Church TR, Goldberg CL, et al. Per- and polyfluoroalkyl substances (PFAS) in American Red Cross adult blood donors, 2000–2015. Environ Res. 2017;157:87-95.
  • 7. Seals R, Bartell SM, Steenland K. Accumulation and clearance of perfluorooctanoic acid (PFOA) in current and former residents of an exposed community. Environ Health Perspect. 2011;119(1):119-24.
  • 8. Abudayyak M, Öztaş E, Özhan G. Determination of Perfluorooctanoic Acid Toxicity in a Human Hepatocarcinoma Cell Line. J Health Pollut. 2021;11(31):210909.
  • 9. Wen LL, Lin CY, Chou HC, Chang CC, Lo HY, Juan SH. Perfluorooctanesulfonate mediates renal tubular cell apoptosis through PPARgamma inactivation. PLoS One. 2016;11(5):e0155190.
  • 10. Gallo V, Leonardi G, Genser B, Lopez-Espinosa M-J, Frisbee SJ, Karlsson L, et al. Serum Perfluorooctanoate (PFOA) and Perfluorooctane Sulfonate (PFOS) concentrations and liver function biomarkers in a population with elevated PFOA exposure. Environ Health Perspect. 2012;120(5):655-60.
  • 11. Xu M, Wan J, Niu Q, Liu R. PFOA and PFOS interact with superoxide dismutase and induce cytotoxicity in mouse primary hepatocytes: A combined cellular and molecular methods. Environ Res. 2019;175:63-70.
  • 12. Yang Y, Xie L, Zhu Y, Sheng Y, Wang J, Zhou X, et al. Perfluorooctane sulfonate (PFOS), a novel environmental pollutant, induces liver injury in mice by activating hepatocyte ferroptosis. Ecotoxicol Environ Saf. 2023;267:115.
  • 13. Faghihzadeh F, Hekmatdoost A, Adibi P. Resveratrol and liver: A systematic review. J Res Med Sci. 2015;20(8):797.
  • 14. Gornall AG, Bardawill CJ, David MM. Determination of serum proteins by means of the biuret reaction. J Biolog Chem. 1949;177:751-66.
  • 15. Eriksen KT, Raaschou-Nielsen O, Sørensen M, Roursgaard M, Loft S, Møller P. Genotoxic potential of the perfluorinated chemicals PFOA, PFOS, PFBS, PFNA, and PFHxA in human HepG2 cells. Mutat Res. 2010;700(1):39-43.
  • 16. Liu D, Yan S, Wang P, Chen Q, Liu Y, Cui J, et al. Perfluorooctanoic acid (PFOA) exposure in relation to the kidneys: A review of current available literature. Front Physiol. 2023;14:1103141.
  • 17. U.S. Environmental Protection Agency (EPA). Basic information on PFOA, 2006. Available: http://www.epa.gov/oppt/pfoa/index.
  • 18. Signorelli P, Ghidoni R. Resveratrol as an anticancer nutrient: Molecular basis, open questions and promises. J Nutr Biochem. 2005;16(8):449-66.
  • 19. Naderi M, Seyedabadi M, Talebpour Amiri F, Akbari S, Shaki F. Rutin mitigates perfluorooctanoic acid-induced liver injury via modulation of oxidative stress, apoptosis, and inflammation. Iran J Basic Med Sci. 2023;26(11):1291-7.
  • 20. Franco R, Sánchez-Olea R, Reyes-Reyes EM, Panayiotidis MI. Environmental toxicity, oxidative stress and apoptosis: Ménage à Trois. Mutat Res. 2009;674(1-2):3-22.
  • 21. Shabalina IG, Panaretakis T, Bergstrand A, DePierre JW. Effects of the rodent peroxisome proliferator and hepatocarcinogen, perfluorooctanoic acid, on apoptosis in human hepatoma HepG2 cells. Carcinogenesis. 1999;20(12):2237-46.
  • 22. Wang P, Yao Q, Zhu D, Yang X, Chen Q, Lu Q, et al. Resveratrol protects against deoxynivalenol-induced ferroptosis in HepG2 cells. Toxicology. 2023;494:153589.

PFOA Maruziyetinde Resveratrol’ün Oksidatif Stres ve Ferroptosis Üzerindeki Olası Koruyucu Etkilerinin HepG2 Hücrelerinde Araştırılması

Year 2024, Volume: 16 Issue: 3, 283 - 292, 29.10.2024
https://doi.org/10.18521/ktd.1464261

Abstract

Amaç: Perflorooktanoik asit (PFOA) maruziyeti, kanser ve karaciğer hastalıkları dahil olmak üzere çeşitli olumsuz sağlık etkileri ile ilişkilendirilmiştir. PFOA, insan karaciğer hücrelerinde reaktif oksijen türlerinin oluşumunu indükleyerek oksidatif strese ve hücre ölümüne neden olur. Son yıllarda, Resveratrolün (RSV) ksenobiyotiklerin neden olduğu hasarlara karşı koruyucu etkisi üzerine çalışmalar önem kazanmıştır. Ancak, RSV'nin karaciğerde PFOA'nın neden olduğu oksidatif stres ve ferroptozis üzerindeki koruyucu etkileri hakkında yeterli çalışma bulunmamaktadır. Bu çalışmada, PFOA maruziyeti sonucu HepG2 hücrelerinde oluşabilecek oksidatif stres ve ferroptozis üzerine RSV'nin koruyucu etki mekanizmalarını araştırmayı amaçladık.
Metod: HepG2 hücreleri, %5 CO2 inkübatöründe 37°C'de %10 FBS ve %1 penisilin/streptomisin içeren DMEM'de kültürlendi. PFOA, 0-450 µM konsantrasyonlarında hücrelere eklendi ve 37°C'de 24 saat inkübe edildi. IC50, 457 μM olarak belirlendi. RSV'nin koruyucu etkilerini değerlendirmek için hücreler 60 μM RSV ile muamele edildi. PFOA, RSV ve PFOA+RSV ile muamele sonrasında, hücre lizatı hazırlandı ve analizler için kullanıldı. Oksidatif stres ve ferroptozis parametreleri, ELISA yöntemiyle spektrofotometrik olarak belirlendi.
Bulgular: PFOA+RSV grubunda, kontrol grubuna kıyasla antioksidan kapasite artmış ve ferroptozis baskılanmıştır. Buna karşılık, PFOA grubunda antioksidan kapasite azalmış, oksidan kapasite artmış ve kontrol ve RSV ile muamele edilen gruplara kıyasla ferroptozis indüklenmiştir.
Sonuç: PFOA maruziyeti oksidatif stresi ve ferroptozisi artırırken, RSV tedavisi karaciğer oksidatif stresini önemli ölçüde azaltır ve PFOA maruziyeti sırasında ferroptozise karşı korur.

Project Number

The funding support for this study was provided by the University of Duzce Scientific Research Unit Rapid Support (Project No: 2022.14.02.1358).

References

  • 1. Qi Q, Niture S, Gadi S, Arthur E, Moore J, Levine KE, et al. Per‐ and polyfluoroalkyl substances activate UPR pathway, induce steatosis and fibrosis in liver cells. Environ Toxicol. 2023;38(1):225-242.
  • 2. Li K, Gao P, Xiang P, Zhang X, Cui X, Ma LQ. Molecular mechanisms of PFOA-induced toxicity in animals and humans: Implications for health risks. Environ Int. 2017;99:43-54.
  • 3. Kudo N, Kawashima Y. Toxicity and toxicokinetics of perfluorooctanoic acid in humans and animals. J Toxicol Sci. 2003;28(2):49-57.
  • 4. Mahapatra CT, Damayanti NP, Guffey SC, Serafin JS, Irudayaraj J, Sepúlveda MS. Comparative in vitro toxicity assessment of perfluorinated carboxylic acids. J Appl Toxicol. 2017;37(6):699-708.
  • 5. Suja F, Pramanik B, Zain S. Contamination, bioaccumulation and toxic effects of perfluorinated chemicals (PFCs) in the water environment: A review paper. Water Sci Technol. 2009;60:1533-44.
  • 6. Olsen GW, Mair DC, Lange CC, Harrington LM, Church TR, Goldberg CL, et al. Per- and polyfluoroalkyl substances (PFAS) in American Red Cross adult blood donors, 2000–2015. Environ Res. 2017;157:87-95.
  • 7. Seals R, Bartell SM, Steenland K. Accumulation and clearance of perfluorooctanoic acid (PFOA) in current and former residents of an exposed community. Environ Health Perspect. 2011;119(1):119-24.
  • 8. Abudayyak M, Öztaş E, Özhan G. Determination of Perfluorooctanoic Acid Toxicity in a Human Hepatocarcinoma Cell Line. J Health Pollut. 2021;11(31):210909.
  • 9. Wen LL, Lin CY, Chou HC, Chang CC, Lo HY, Juan SH. Perfluorooctanesulfonate mediates renal tubular cell apoptosis through PPARgamma inactivation. PLoS One. 2016;11(5):e0155190.
  • 10. Gallo V, Leonardi G, Genser B, Lopez-Espinosa M-J, Frisbee SJ, Karlsson L, et al. Serum Perfluorooctanoate (PFOA) and Perfluorooctane Sulfonate (PFOS) concentrations and liver function biomarkers in a population with elevated PFOA exposure. Environ Health Perspect. 2012;120(5):655-60.
  • 11. Xu M, Wan J, Niu Q, Liu R. PFOA and PFOS interact with superoxide dismutase and induce cytotoxicity in mouse primary hepatocytes: A combined cellular and molecular methods. Environ Res. 2019;175:63-70.
  • 12. Yang Y, Xie L, Zhu Y, Sheng Y, Wang J, Zhou X, et al. Perfluorooctane sulfonate (PFOS), a novel environmental pollutant, induces liver injury in mice by activating hepatocyte ferroptosis. Ecotoxicol Environ Saf. 2023;267:115.
  • 13. Faghihzadeh F, Hekmatdoost A, Adibi P. Resveratrol and liver: A systematic review. J Res Med Sci. 2015;20(8):797.
  • 14. Gornall AG, Bardawill CJ, David MM. Determination of serum proteins by means of the biuret reaction. J Biolog Chem. 1949;177:751-66.
  • 15. Eriksen KT, Raaschou-Nielsen O, Sørensen M, Roursgaard M, Loft S, Møller P. Genotoxic potential of the perfluorinated chemicals PFOA, PFOS, PFBS, PFNA, and PFHxA in human HepG2 cells. Mutat Res. 2010;700(1):39-43.
  • 16. Liu D, Yan S, Wang P, Chen Q, Liu Y, Cui J, et al. Perfluorooctanoic acid (PFOA) exposure in relation to the kidneys: A review of current available literature. Front Physiol. 2023;14:1103141.
  • 17. U.S. Environmental Protection Agency (EPA). Basic information on PFOA, 2006. Available: http://www.epa.gov/oppt/pfoa/index.
  • 18. Signorelli P, Ghidoni R. Resveratrol as an anticancer nutrient: Molecular basis, open questions and promises. J Nutr Biochem. 2005;16(8):449-66.
  • 19. Naderi M, Seyedabadi M, Talebpour Amiri F, Akbari S, Shaki F. Rutin mitigates perfluorooctanoic acid-induced liver injury via modulation of oxidative stress, apoptosis, and inflammation. Iran J Basic Med Sci. 2023;26(11):1291-7.
  • 20. Franco R, Sánchez-Olea R, Reyes-Reyes EM, Panayiotidis MI. Environmental toxicity, oxidative stress and apoptosis: Ménage à Trois. Mutat Res. 2009;674(1-2):3-22.
  • 21. Shabalina IG, Panaretakis T, Bergstrand A, DePierre JW. Effects of the rodent peroxisome proliferator and hepatocarcinogen, perfluorooctanoic acid, on apoptosis in human hepatoma HepG2 cells. Carcinogenesis. 1999;20(12):2237-46.
  • 22. Wang P, Yao Q, Zhu D, Yang X, Chen Q, Lu Q, et al. Resveratrol protects against deoxynivalenol-induced ferroptosis in HepG2 cells. Toxicology. 2023;494:153589.
There are 22 citations in total.

Details

Primary Language English
Subjects Health Services and Systems (Other)
Journal Section Articles
Authors

Didem Oral 0000-0002-7025-6576

Ceyhan Hacıoğlu 0000-0002-0993-6118

Project Number The funding support for this study was provided by the University of Duzce Scientific Research Unit Rapid Support (Project No: 2022.14.02.1358).
Publication Date October 29, 2024
Submission Date April 5, 2024
Acceptance Date September 10, 2024
Published in Issue Year 2024 Volume: 16 Issue: 3

Cite

APA Oral, D., & Hacıoğlu, C. (2024). Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells. Konuralp Medical Journal, 16(3), 283-292. https://doi.org/10.18521/ktd.1464261
AMA Oral D, Hacıoğlu C. Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells. Konuralp Medical Journal. October 2024;16(3):283-292. doi:10.18521/ktd.1464261
Chicago Oral, Didem, and Ceyhan Hacıoğlu. “Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells”. Konuralp Medical Journal 16, no. 3 (October 2024): 283-92. https://doi.org/10.18521/ktd.1464261.
EndNote Oral D, Hacıoğlu C (October 1, 2024) Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells. Konuralp Medical Journal 16 3 283–292.
IEEE D. Oral and C. Hacıoğlu, “Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells”, Konuralp Medical Journal, vol. 16, no. 3, pp. 283–292, 2024, doi: 10.18521/ktd.1464261.
ISNAD Oral, Didem - Hacıoğlu, Ceyhan. “Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells”. Konuralp Medical Journal 16/3 (October 2024), 283-292. https://doi.org/10.18521/ktd.1464261.
JAMA Oral D, Hacıoğlu C. Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells. Konuralp Medical Journal. 2024;16:283–292.
MLA Oral, Didem and Ceyhan Hacıoğlu. “Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells”. Konuralp Medical Journal, vol. 16, no. 3, 2024, pp. 283-92, doi:10.18521/ktd.1464261.
Vancouver Oral D, Hacıoğlu C. Investigation of Possible Protective Effects of Resveratrol on Oxidative Stress and Ferroptosis in PFOA Exposure in HepG-2 Cells. Konuralp Medical Journal. 2024;16(3):283-92.