Hepatic Impact of Different Concentrations of Hibiscus rosa Zinc Oxide Nanoparticles on Rats

Document Type : Original Articles

Author

Department of Pharmacology and Toxicology, College of Pharmacy, University of Al-Muthana, Samawah, Iraq

Abstract

Nanomaterial, especially zinc oxide nanoparticles, has entered the manufacture of many materials used in daily lives. The current study aimed to assess the impact of three concentrations of hibiscus rosa zinc oxide nanoparticles (HrZnONPs) and hibiscus rosa extract (Hre) on the liver tissue and DNA fragmentation of liver cells. A total of 35 adult male Wistar rats were grouped as follows: The first group which was the control (n=7) did not receive any treatment. The remaining 28 animals were randomly assigned to four groups. Group 1 (n=7) were subcutaneously injected with 100mg\kg BW of Hibiscus rosa extract for 60 days; the rats in group 2 were subcutaneouslyinjected with 25 mg\kg BW of HrZnONPs for 60 days; rats in group 3 were subcutaneouslyinjected with 75mg\kg BW of HrZnONPs for 60 days; rats in group 4 were subcutaneously injected with 100mg\kg BW of HrZnONPs for 60 days.  The liver biomarkers, aspartate aminotransferase (AST), alkaline phosphatase (ALP), and alanine aminotransferase (ALT) have been assessed in serum at zero time, after one month, and after two months of the experiment. At the end of the experiment, all animals were euthanized, the liver was dissected, the specimen underwent a pathohistological investigation, and the percentage of DNA fragmentation was evaluated. The results pointed out that the rats which were treated with HrZnONPs at concentrations of 75 and 100 mg\kg B.W. demonstrated a salient elevation in serum AST, ALT, or ALP activity, a modulation in hepatic tissue architecture, and an elevated percentage of high DNA damage, as compared to those treated with HrZnONPs at a concentration of 25 mg\kg B.W. On the other hand, the recorded data indicated that the administration of Hre has some ameliorative effects on AST, ALP, and ALT levels, histological cross-section, and the value of comet assay for liver cells due to the role of Hre antioxidant. In conclusion, the results of the current study demonstrated that high doses of HrZnONPs had exerted more adverse effects, compared to low doses. Moreover, the findings confirmed the ameliorative impact of Hre on liver biomarkers, a histological cross-section of the liver, and DNA damage.

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  1. Tsekhmistrenko S, Bityutskyy V, Tsekhmistrenko O, Horalskyi L, Tymoshok N, Spivak M. Bacterial synthesis of nanoparticles: A green approach. Biosyst Divers. 2020;28(1):9-17.
  2. Wiesmann N, Gieringer R, Viel M, Eckrich J, Tremel W, Brieger J. Zinc Oxide Nanoparticles Can Intervene in Radiation-Induced Senescence and Eradicate Residual Tumor Cells. Cancers. 2021;13(12):2989.
  3. Lee C-C, Lin Y-H, Hou W-C, Li M-H, Chang J-W. Exposure to ZnO/TiO2 nanoparticles affects health outcomes in cosmetics salesclerks. Int J Environ Res. 2020;17(17):6088.
  4. Bera D, Pal K, Mondal D, Karmakar P, Das S, Nandy P. Gum acacia capped ZnO nanoparticles, a smart biomaterial for cell imaging and therapeutic applications. Advances in Natural Sciences: Nanoscience and Nanotechnology. 2020;11(3):035015.
  5. Zhu W, Hu C, Ren Y, Lu Y, Song Y, Ji Y, et al. Green synthesis of zinc oxide nanoparticles using Cinnamomum camphora (L.) Presl leaf extracts and its antifungal activity. J Environ Chem Eng. 2021;9(6):106659.
  6. Rajendiran M, Trivedi HM, Chen D, Gajendrareddy P, Chen L. Recent Development of Active Ingredients in Mouthwashes and Toothpastes for Periodontal Diseases. Molecules. 2021;26(7):2001.
  7. Canta M, Cauda V. The investigation of the parameters affecting the ZnO nanoparticle cytotoxicity behaviour: A tutorial review. Biomater Sci. 2020;8(22):6157-74.
  8. Singh TA, Das J, Sil PC. Zinc oxide nanoparticles: A comprehensive review on its synthesis, anticancer and drug delivery applications as well as health risks. Adv Colloid Interface Sci. 2020:102317.
  9. Nagarajan M, Maadurshni GB, Tharani GK, Udhayakumar I, Kumar G, Mani KP, et al. Exposure to zinc oxide nanoparticles (ZnO-NPs) induces cardiovascular toxicity and exacerbates pathogenesis–Role of oxidative stress and MAPK signaling. Chem Biol Interact. 2022;351:109719.
  10. Yu Z, Li Q, Wang J, Yu Y, Wang Y, Zhou Q, et al. Reactive oxygen species-related nanoparticle toxicity in the biomedical field. Nanoscale Res Lett. 2020;15:1-14.
  11. Boey A, Ho HK. All roads lead to the liver: metal nanoparticles and their implications for liver health. Small. 2020;16(21):2000153.
  12. Sruthi S, Ashtami J, Mohanan P. Biomedical application and hidden toxicity of Zinc oxide nanoparticles. Mater Today Chem. 2018;10:175-86.
  13. Ali ZS, Khudair KK. Synthesis, Characterization of Silver Nanoparticles Using Nigella sativa Seeds and Study Their Effects on the Serum Lipid Profile and DNA Damage on the Rats’ Blood Treated with Hydrogen Peroxide: Zainab Sattar Ali and Khalisa Khadim Khudair. Iraqi J Vet Sci. 2019;43(2):23-37.
  14. Devi RS, Gayathri R. Green synthesis of zinc oxide nanoparticles by using Hibiscus rosa-sinensis. Int J Curr Eng Technol. 2014;4(4):2444-6.
  15. Reitman S, Frankel S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am J Clin Pathol. 1957;28(1):56-63.
  16. Kaplan MM. Alkaline phosphatase. Gastroenterology. 1972;62(3):452-68.
  17. Olive PL, Banáth JP, Durand RE. Heterogeneity in radiation-induced DNA damage and repair in tumor and normal cells measured using the" comet" assay. Radiat Res. 1990;122(1):86-94.
  18. Luna LG. Manual of histologic staining methods of the Armed Forces Institute of Pathology. 1968.
  19. Snedecor GW, Cochran WG. Statistical methods, 8thEdn. Ames: Iowa State Univ Press Iowa. 1989;54:71-82.
  20. Aboulhoda BE, Abdeltawab DA, Rashed LA, Abd Alla MF, Yassa HD. Hepatotoxic Effect of Oral Zinc Oxide Nanoparticles and the Ameliorating Role of Selenium in Rats: A histological, immunohistochemical and molecular study. Tissue Cell. 2020;67:101441.
  21. Sudhakaran S, Athira S, Varma H, Mohanan P. Determination of the bioavailability of zinc oxide nanoparticles using ICP-AES and associated toxicity. Colloids Surf B. 2020;188:110767.
  22. Yousef MI, Mutar TF, Kamel MAE-N. Hepato-renal toxicity of oral sub-chronic exposure to aluminum oxide and/or zinc oxide nanoparticles in rats. Toxicol Rep. 2019;6:336-46.
  23. Guo Z, Luo Y, Zhang P, Chetwynd AJ, Xie HQ, Monikh FA, et al. Deciphering the particle specific effects on metabolism in rat liver and plasma from ZnO nanoparticles versus ionic Zn exposure. Environ Int. 2020;136:105437.
  24. Attia H, Nounou H, Shalaby M. Zinc oxide nanoparticles induced oxidative DNA damage, inflammation and apoptosis in rat’s brain after oral exposure. Toxics. 2018;6(2):29.
  25. Liang X, Zhang D, Liu W, Yan Y, Zhou F, Wu W, et al. Reactive oxygen species trigger NF-κB-mediated NLRP3 inflammasome activation induced by zinc oxide nanoparticles in A549 cells. Toxicol Ind Health. 2017;33(10):737-45.
  1. Piperigkou Z, Karamanou K, Engin AB, Gialeli C, Docea AO, Vynios DH, et al. Emerging aspects of nanotoxicology in health and disease: from agriculture and food sector to cancer therapeutics. Food Chem Toxicol. 2016;91:42-57.
  2. Lam P-L, Wong R-M, Lam K-H, Hung L-K, Wong M-M, Yung L-H, et al. The role of reactive oxygen species in the biological activity of antimicrobial agents: An updated mini review. Chem Biol Interact. 2020;320:109023.
  3. Hamza RZ, Al-Salmi FA, El-Shenawy NS. Evaluation of the effects of the green nanoparticles zinc oxide on monosodium glutamate-induced toxicity in the brain of rats. PeerJ. 2019;7:7460.
  4. Abdel-Halim KY, Osman SR, Abdou GY. In vivo evaluation of oxidative stress and biochemical alteration as biomarkers in glass clover snail, Monacha cartusiana exposed to zinc oxide nanoparticles. Environ Pollut. 2020;257:113120.
  5. Hao L, Chen L. Oxidative stress responses in different organs of carp (Cyprinus carpio) with exposure to ZnO nanoparticles. Ecotoxicol Environ Saf. 2012;80:103-10.
  6. Schattauer SS, Bedini A, Summers F, Reilly-Treat A, Andrews MM, Land BB, et al. Reactive oxygen species (ROS) generation is stimulated by κ opioid receptor activation through phosphorylated c-Jun N-terminal kinase and inhibited by p38 mitogen-activated protein kinase (MAPK) activation. Biol Chem. 2019;294(45):16884-96.
  7. Danabas D, Ates M, Tastan BE, Cimen ICC, Unal I, Aksu O, et al. Effects of Zn and ZnO Nanoparticles on Artemia salina and Daphnia magna organisms: Toxicity, accumulation and elimination. Science of The Total Environment. 2020;711:134869.
  8. De Angelis I, Barone F, Zijno A, Bizzarri L, Russo MT, Pozzi R, et al. Comparative study of ZnO and TiO2 nanoparticles: physicochemical characterisation and toxicological effects on human colon carcinoma cells. Nanotoxicology. 2013;7(8):1361-72.
  9. Elje E, Mariussen E, Moriones OH, Bastús NG, Puntes V, Kohl Y, et al. Hepato (Geno) Toxicity assessment of nanoparticles in a HepG2 liver spheroid model. Nanomaterials. 2020;10(3):545.
  10. Jeffery TD, Richardson ML. A review of the effectiveness of hibiscus for treatment of metabolic syndrome. J Ethnopharmacol. 2021;270:113762.