Curcumin Attenuates Cytotoxic Effect of Bisphenol A in the Liver of Adult Wister Rats

Authors

  • Sunday Okon Elijah Department of Anatomy, Faculty of Basic Medical Sciences, College of Medicine and Allied health Sciences, Bingham University, Karu, Nasarawa State https://orcid.org/0000-0003-3739-304X
  • Moses Ibrahim Auza Department of Anatomy, Faculty of Basic Medical Sciences, College of Medicine and Allied health Sciences, Bingham University, Karu, Nasarawa State https://orcid.org/0000-0002-8830-6471
  • Abigail Abraham Department of Anatomy, Faculty of Basic Medical Sciences, College of Medicine and Allied health Sciences, Bingham University, Karu, Nasarawa State
  • Charles O. Ayara Department of Anatomy, Faculty of Basic Medical Sciences, College of Medicine and Allied health Sciences, Bingham University, Karu, Nasarawa State

DOI:

https://doi.org/10.55006/biolsciences.2024.4210

Keywords:

Bisphenol A, Cytotoxic, Liver, Curcumin, Wistar Rats

Abstract

This study investigates the effect of curcumin on bisphenol A induced cytotoxicity in the liver of adult Wister rats. Twenty adult Wistar rats (weight = 190±10g) were placed into four groups (N=4). Group 1 (control) received vital feed, water and sunflower oil only throughout the research, group 2 (BPA) received vital feed, water and 65mg/kg of bisphenol A, group 3 (BPA and Curcumin) received vital feed, water and 65ml/kg of bisphenol A and 100mg/kg of Curcumin, and group 4 (Curcumin) received vital feed, water and 100mg/kg of curcumin for a total 28 days. Rats exposed to BPA for 28 days demonstrated liver damages as evidence by increased concentration of Alkaline phosphatase (ALP) in blood, increase in Malondialdehyde (MDA) concentration and decrease in Glutathione (GSH) level. In regard to histological analysis, curcumin had positive effects on the liver except for group 2 (BPA) which showed degenerative changes due to the administration of bisphenol A only. This study reveals that curcumin has ameliorative and cytoprotective effect on bisphenol A cytotoxocity on the liver.

Downloads

Download data is not yet available.

References

1. Ashfaq, M., Sun, Q. and Zhang, H., et al. (2018). Occurrence and fate of bisphenol Atransformation products, bisphenol A monomethyl ether and bisphenol A dimethyl ether, in wastewater treatment plants and surface water. Journal of Hazardous Materials, 357:401–407. doi: 10.1016/j.jhazmat.2018.06.022.

2. Vogel, S. A, (2009). The politics of plastics: The making and unmaking of bisphenol a "safety". Am J Public Health, 99: S559-566. DOI: 10.2105/AJPH.2008.159228

3. Murakami, K., Ohashi, A., and Hori, H., et al. (2007). Accumulation of bisphenol A in hemodialysis patients. Blood Purification, 25(3):290–294. doi: 10.1159/000104869.

4. Andra, S. S., Charisiadis, P., Arora, M., van Vliet-Ostaptchouk, J. V. and Makris, K. C. (2015). Biomonitoring of human exposures to chlorinated derivatives and structural analogs of bisphenol A. Environment international, 85:352–379. doi: 10.1016/j.envint.2015.09.011.

5. Ke, Z. H., Pan J, X., and Jin, L. Y., et al. (2016) Bisphenol A exposure may induce hepatic lipid accumulation via reprogramming the DNA methylation patterns of genes involved in lipid metabolism. Scientific Reports, 6(1) doi: 10.1038/srep31331.

6. vom Saal, F. S., and Hughes, C. (2005). An extensive new literature concerning low-dose effects of bisphenol a shows the need for a new risk assessment. Environ Health Perspect 113(8): 926-933, DOI: 10.1289/ehp.7713.

7. Aggarwal, B. B., Kumar, A., and Bharti, A. C. (2003). Anticancer potential of curcumin: Preclinical and clinical studies. Anticancer Res, 23, 363–398

8. Gupta, S.C., Patchva, S., and Aggarwal, B. B. (2013). Therapeutic Roles of Curcumin: Lessons Learned from Clinical Trials. AAPS J, 15, 195–218.

9. Aggarwal, B. B., and Harikumar, K. B. (2009). Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases. Int. J. Biochem. Cell Biol, 41, 40–59.

10. Kuptniratsaikul, V., Dajpratham, P., Taechaarpornkul, W., Buntragulpoontawee, M., Lukkanapichonchut, P., Chootip, C., Saengsuwan, J., Tantayakom, K., and Laongpech, S. (2014). Efficacy and safety of Curcuma domestica extracts compared with ibuprofen in patients with knee osteoarthritis: A multicenter study. Clin. Interv. Aging, 9, 451–458.

11. Mazzolani, F., and Togni, S. (2013). Oral administration of a curcumin-phospholipid delivery system for the treatment of central serous chorioretinopathy: A 12-month follow-up study. Clin. Ophthalmol, 7, 939–945.

12. Allegri, P., Mastromarino, A., and Neri, P. (2010). Management of chronic anterior uveitis relapses: Efficacy of oral phospholipidic curcumin treatment. Long-term follow-up. Clin. Ophthalmol, 4, 1201–1206.

13. Anand, P., Kunnumakkara, A. B., Newman, R. A., and Aggarwal, B. B. (2007). Bioavailability of curcumin: Problems and promises. Mol. Pharm, 4, 807–818

14. Hewling, S., and Kalman, D. (2017). Curcumin: A Rview of its effect on Human Health. Foods, 6 (10),92. https://doi.org/10.3390/foods6100092.

15. Panahi, Y., Hosseini, M. S., Khalili, N., Naimi, E., Simental-Mendia, L. E., Majeed, M., and Sahebkar, A. (2016). Effects of curcumin on serum cytokine concentrations in subjects with metabolic syndrome: A post-hoc analysis of a randomized controlled trial. Biomed. Pharmacother, 82, 578–582.

16. Memon, V. P and Sudheer, A. R. (2007). Antioxidant and anti-inflammatory properties of curcumin. Adv. Exp. Biol. 595: 105 – 125. Doi:10.1007/978-0-387-46401-5_3.

17. Prins, G. S., Tang W. Y., Belmonte, J., and Ho, S.M. (2008). Developmental exposure to bisphenol A increases prostate cancer susceptibility in adult rats: epigenetic mode of action is implicated. Fertil. Steril, 89, 41.

18. Pupo, M., Pisano, A., Lappano, R., Santolla, M. F., De Francesco, E.M., Abonante, S., Rosano, C., and Maggiolini, M. (2012). Bisphenol A induces gene expression changes and proliferative effects through GPER in breast cancer cells and cancer -associated fibroblasts. Environ. Health Perspect, 120, 1177-1182

19. Hiroi, H., Tsutsumi, O., Momoeda, M., Takai, Y., Osuga, Y., and Taketani, Y. (1999). Differential interactions of bisphenol A and 17beta -estradiol with estrogen receptor alpha (ERalpha) and ERbeta. End. J, 46, 773-778

20. Kurosawa, T., Hiroi, H., Tsutsumi, O., Ishikawa, T., Osuga, Y., Fujiwara, T., Inoue, S., Muramatsu, M., Momoeda, M., and Taketani, Y. (2002). The activity of bisphenol A depends on both the estrogen receptor subtype and the cell type. End. J, 49, 465-471

21. Wetherill, Y. B., Akingbemi, B. T., Kanno, J., McLachlan, J. A., Nadal, A., Sonnenschein, C., Watson, C. S., Zoeller, R.T., and Belcher, S.M. (2007). In vitro molecular mechanisms of bisphenol A action. Reprod. Toxicol, 24; 178-198

22. Benzer, F.; Kandemir, F.M.; Kucukler, S.; Comaklı, S. and Caglayan, C. (2018) Chemoprotective effects of curcumin on doxorubicin-induced nephrotoxicity in wistar rats: By modulating inflammatory cytokines, apoptosis, oxidative stress and oxidative DNA damage. Arch. Physiol. Biochem, 124, 448–457.

23. Xia, W., Jiang, Y., Li, Y., Wan, Y., Liu, J., and Ma Y, et al. (2014) Early-Life Exposure to Bisphenol A Induces Liver Injury in Rats Involvement of Mitochondria-Mediated Apoptosis. PLoS One, 9. doi:10.1371

24. Elbarkry, L.M.M.M., Mansour, S.Z., Helal, H. and Ahmed, E.S.E. (2022). Nattokinase Attenuates Bisphenol A or Gamma Irradiation-Mediated Hepatic and Neural Toxicity by Activation of Nrf2 and Suppression of Inflammatory Mediators in Rats. Environmental Science and Pollution Research.29, 75086-75100.

25. Sharma, U., Pal, D., and Prasad, R. (2014). Alkaline Phosphatase: and Overview. Indian Journal of Clinical Biochemistry, 29(3):269-278. https://doi.org/101007/s12291-013-0408-y.

26. Abarikwu, S. O., Akiri O. F., Durojaiye M.A and Alabi, A. (2014), combined administration of curcumin and galic acid-induced suppression of steroidogenesis, sperm output, antioxidant defenses and inflammatory responsive genes. The Journal of steroid biochemistry and molecular biology, 143: 49-60. doi.org/10.1016/j.jsbmb.2014.02.008

27. Yuanyuan, Z., Fajun, L., Fangbin, Y., Rufang, M., Yanhua, Z., Shuquan, M., Bin, H., Guohong, M., and Yongan, Z. (2021). Study of dietary curcumin on the restorative effect of liver injury induced by carbon tetrachloride in common carp, cyprinus carpio, Aquaculture Reports, 21. https;//doi.org/10.1016/j.aqrep.2021.100825.

28. Baker, K, R., and Rice, L. (2012). The amyloidosis; clinical features, diagnosis and treatment. Methodist DeBakey cardiovascular journal, 8(3), 3-7. http;//doi.org/10.14797/mdcj-8-3-3.

29. Dai, J., Li, Y., Kametani, F., Cui, X., Igarashi, Y., Huo, J., Miyahara, H., Mori, M., and Higuchi, K. (2021). Curcumin promotes AApoAII amyloidosis and peroxisome proliferation in mice by activating the PPARa signaling pathway. Elife,10, e63538. https;//doi.org/10.7554/elife.63538.

30. Heger, M., van Golen, R.F., Broekgaarden, M. and Michel, M.C. (2013). The Molecular Basis for the Pharmacokinetics and Pharmacodynamics of curcumin and its metabolites in Relation to Cancer. Pharmacological Reviews. https://doi.org/10.1124/pr.110.004044.

31. Messner, D. J., Sivam, G., and Kowdley, K. V. (2008). Curcumin reduces the toxic effects of iron loading in rat liver epithelial cells. Liver International, 29(1): 63-72.

Downloads

Published

18-06-2024
CITATION

How to Cite

Elijah, S. O., Auza, M. I., Abraham , A., & Ayara , C. O. (2024). Curcumin Attenuates Cytotoxic Effect of Bisphenol A in the Liver of Adult Wister Rats. Biological Sciences, 4(2), 650–656. https://doi.org/10.55006/biolsciences.2024.4210