Assessment of zinc acetate on hepatic histology and liver enzymes in rats

The effect of Zinc acetate on Rat's liver

Authors

  • Mahmood A. Hussein College of Dentistry, University of Mosul, Iraq,
  • Maha T. AL-Saffar Dental Basic Sciences Department, College of Dentistry, University of Mosul, Iraq
  • Karam H. AL-mallah Pathology and Poultry Diseases Department, College of Veterinary Medicine, University of Mosul, Iraq

DOI:

https://doi.org/10.60988/p.v36i2.11

Keywords:

Zinc, Liver enzyme, Liver histology

Abstract

Background: Overconsumption of dietary Zn supplements is one of the most common causes of acute Zn poisoning. Zinc is commonly found in commercially available minerals and nutritional supplements. Aims: to look into the histopathological and biochemical toxic effects of zinc acetate on the liver. Materials and Methods: Twenty-five healthy male Albino rats with an age range of (2-3) months and weights of (250-360 g) were bought from Animal House. The rodents were separated into five equal groups (5 rats each): the control group received normal saline intraperitoneally once every other day for 3 weeks, groups 2,3,4, and 5 received zinc acetate (4,8, 12, and 24mg/kg) respectively, intraperitoneally once every other day for 3 weeks. All the experimental animals of all groups were euthanized on day 22 for biochemical serum assessment and histopathological assessment of the liver. Results: Liver enzymes significantly elevated in a dose-dependent manner particularly in group 5 compared to control and other groups. Histopathological examination of the liver revealed the architectural changes and modulation of liver histological parameters, these changes were dose-dependent and more apparent in group 5 compared to control and other groups. In conclusion: subacute toxic effects of zinc acetate produce significant effects on liver biochemical parameterAlkaline Phosphatase, Aspartate Aminotransferase, and Alanine Aminotransferase in all treated groups corresponding with dose and significant effects on liver revealed by histological examination like congestion of portal and central veins, focal lymphocytic infiltration and capsular fibrosis at all treated groups and more severe at 4th and 5th groups.

References

Althanoon ZA, Merkhan MM. Effects of zinc supplementation on metabolic status in patients with metabolic syndrome. Acta Poloniae Pharmaceutica. 2021 Jul 1;78(4).

Ivanova ID, Pal A, Simonelli I, et al. Evaluation of zinc, copper, and Cu: Zn ratio in serum, and their implications in the course of COVID-19. Journal of Trace Elements in Medicine and Biology. 2022 May 1;71:126944. https://doi.org/10.1016/j.jtemb.2022.126944

Aoki C, Imai K, Owaki T, et al. The possible effects of zinc supplementation on postpartum depression and anemia. Medicina. 2022 May 29;58(6):731. https://doi.org/10.3390/medicina58060731

Richards CD, Burke R. Local and systemic effects of targeted zinc redistribution in Drosophila neuronal and gastrointestinal tissues. Biometals. 2015 Dec;28:967-74. https://doi.org/10.1007/s10534-015-9881-5

Merkhan MM, Abdulrazzaq GM, Al-Taii HA. Coronavirus (COVID-19): preventive measures and potential interventions. European Journal of Molecular & Clinical Medicine. 2021 Jan 13;7(10):1388-99.

Darweesh O, Abdulrazzaq GM, Al-Zidan RN, et al. Evaluation of the pharmacologic treatment of COVID-19 pandemic in Iraq. Current Pharmacology Reports. 2021 Sep;7:171-8. https://doi.org/10.1007/s40495-021-00262-9

Younis HY, Imad A. Effect of zinc as an add on to metformin therapy on serum lipid profile and uric acid in type 2 diabetes mellitus patients. Curr topics in Pharmacology. 2021;25..

Younis HY, Thanoon IA, Fadhil NN, et al. Effect of zinc as an add-on to metformin therapy on glycemic control, serum insulin, and c-peptide levels and insulin resistance in type 2 diabetes mellitus patient. Research Journal of Pharmacy and Technology. 2022;15(3):1184-8. Article DOI : 10.52711/0974-360X.2022.00198

Grissinger M. A fatal zinc overdose in a neonate: confusion of micrograms with milligrams. Pharmacy and Therapeutics. 2011 Jul;36(7):393.

Claverie C, Corbella R, Martin D, et al. Protective effects of zinc on cadmium toxicity in rodents. Biological Trace Element Research. 2000 Jun;75:1-9. https://doi.org/10.1385/BTER:75:1-3:1

Barceloux DG. Zinc. Journal of Toxicology: Clinical Toxicology. 1999 37(2), 279-292.

Cassel GH. Zinc: a review of current trends in therapy and our knowledge of its toxicity. Delaware medical journal. 1978 Jun;50(6):323-8.

Scott MA, Stockham SL. Fundamentals of veterinary clinical pathology. John Wiley & Sons; 2013 May 31.

Jung WC, Kim S, Lee HJ. Acute Toxicity of Nano-Scale Zinc Oxide Powder in ICR Mice. Journal of Biomedical Research. 2010 Dec;11(4):219-24.

Ben-Slama I, Mrad I, Rihane N, et al. Sub-acute oral toxicity of zinc oxide nanoparticles in male rats. Journal of Nanomedicine & Nanotechnology. 2015 May 1;6(3):1.

Wang B, Feng WY, Wang TC, et al. Acute toxicity of nano-and micro-scale zinc powder in healthy adult mice. Toxicology letters. 2006 Feb 20;161(2):115-23. https://doi.org/10.1016/j.toxlet.2005.08.007

Sharma V, Singh P, Pandey AK, et al. Induction of oxidative stress, DNA damage and apoptosis in mouse liver after sub-acute oral exposure to zinc oxide nanoparticles. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 2012 Jun 14;745(1-2):84-91. https://doi.org/10.1016/j.mrgentox.2011.12.009

Ibrahim NM, Eweis EA, El-Beltagi HS, et al. Effect of lead acetate toxicity on experimental male albino rat. Asian Pacific journal of tropical biomedicine. 2012 Jan 1;2(1):41-6. https://doi.org/10.1016/S2221-1691(11)60187-1

Farida T, Salawu OA, Tijani AY, et al. Pharmacological evaluation of Ipomoea asarifolia (Desr.) against carbon tetrachloride-induced hepatotoxicity in rats. Journal of ethnopharmacology. 2012 Aug 1;142(3):642-6. https://doi.org/10.1016/j.jep.2012.05.029

Surekha P, Kishore AS, Srinivas A, et al. Repeated dose dermal toxicity study of nano zinc oxide with Sprague-Dawley rats. Cutaneous and ocular toxicology. 2012 Mar 1;31(1):26-32. https://doi.org/10.3109/15569527.2011.595750

Ding H, Peng R, Chen J. Effects of high dietary zinc on liver function, hepatic drug metabolism enzymes and membrane fluidity in mice. Wei Sheng yan jiu= Journal of Hygiene Research. 1998 May 1;27(3):180-2.

Karnakar RY, Saritha CH, Sridhar Y, et al. Naringenin prevents the zinc oxide nanoparticles induced toxicity in swiss albino mice. J. Pharmacol. Clin. Toxicol. 2014;2:1021.

Mansouri E, Khorsandi L, Orazizadeh M, et al. Dose-dependent hepatotoxicity effects of zinc oxide nanoparticles. Nanomedicine Journal 2(4): 273–282. DOI:10.7508/nmj.2015.04.005

Abdel-Warith AA, Younis EM, Al-Asgah NA, et al. Effect of zinc toxicity on liver histology of Nile tilapia, Oreochromis niloticus. Scientific Research and Essays. 2011 Aug 26;6(17):3760-9.

Moatamed ER, Hussein AA, El-Desoky MM, et al. Comparative study of zinc oxide nanoparticles and its bulk form on liver function of Wistar rat. Toxicology and Industrial Health. 2019 Oct;35(10):627-37. https://doi.org/10.1177/0748233719878970

AL-Hamdani SK. Pathological study of lethal concentration of N-ZnO in common carp cyprinus carpio l. Basrah Journal of Veterinary Research. 2013;12(1).

Almansour MI, Alferah MA, Shraideh ZA, et al. Zinc oxide nanoparticles hepatotoxicity: histological and histochemical study. Environmental Toxicology and Pharmacology. 2017 Apr 1;51:124-30. https://doi.org/10.1016/j.etap.2017.02.015

Meyer K, Rajanahalli P, Ahamed M, et al. ZnO nanoparticles induce apoptosis in human dermal fibroblasts via p53 and p38 pathways. Toxicology in vitro. 2011 Dec 1;25(8):1721-6. https://doi.org/10.1016/j.tiv.2011.08.011

Landsiedel R, Ma-Hock L, Van Ravenzwaay B, et al. Gene toxicity studies on titanium dioxide and zinc oxide nanomaterials used for UV-protection in cosmetic formulations. Nanotoxicology. 2010 Dec 1;4(4):364-81. https://doi.org/10.3109/17435390.2010.506694

John E, Laskow TC, Buchser WJ, et al. Zinc in innate and adaptive tumor immunity. Journal of translational medicine. 2010 Dec;8(1):1-6. https://doi.org/10.1186/1479-5876-8-118

Merkhan MM, Shephard MT, Forsyth NR. Physoxia alters human mesenchymal stem cell secretome. Journal of Tissue Engineering. 2021 Oct;12:20417314211056132. https://doi.org/10.1177/20417314211056132

Shephard MT, Merkhan MM, Forsyth NR. Human Mesenchymal Stem Cell Secretome Driven T Cell Immunomodulation Is IL-10 Dependent. International Journal of Molecular Sciences. 2022 Nov 6;23(21):13596. https://doi.org/10.3390/ijms232113596

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Published

19-07-2024

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Research Articles