Study the Effect of Selenium Supplementations on the Liver, Kidney and Thyroid Gland Activities in Male Rats

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Hamzah H. Kzar
Rawaa S. A. AL-Azawi
Suhad J. Hadi
Ahmed F. Farhood

Abstract

The liver, kidney, and thyroid glands are main vital in biochemical and physiological activities in animals and humans.  In this study, we examined the effects of adding selenium supplementation on the improvement activity of many glands such as the liver, kidney, and thyroid after cadmium chloride administration (induced toxicity) in male rabbits. This study included 16 male rabbits divided into four groups, the 1st group (CON) was control and administration normal fed and drinking water, the 2nd group (NC ) was negative control group that administration of 1ml of cadmium chloride (100ppm) with normal fed, the 3rd group (S1) was administration of 1ml of sodium selenite, and 4th group (S2) was administration of 5ml of selenium and all groups continuous for same style up to 8th week of experiment. Antioxidant and oxidative stress status was investigated by measuring the levels of T-AOC and MDA. The liver was assessed  by estimation of ALT, AST, TP, and TB while kidney was assessed by calculation of blood CRI and UR and the thyroid gland assessed by measurement of serum T3 and T4. The levels of selenoprotein (SeP) mg/l were assessed by HPLC for standard and S2 group. The results of present study shows highly statistical differences between four group when compare the mean±SD of the levels of ALT,AST,TP,TB,CRI,UR,T3, and T4 (p-value <0.005). In conclusion,  this study showing highly ability of selenium supplementation to lowering the levels of the markers of liver, kidney, and thyroid gland and work as protective factor from toxicity induced by cadmium in  male rabbits.

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How to Cite
Hamzah H. Kzar, Rawaa S. A. AL-Azawi, Suhad J. Hadi, & Ahmed F. Farhood. (2023). Study the Effect of Selenium Supplementations on the Liver, Kidney and Thyroid Gland Activities in Male Rats. International Journal of Pharmaceutical and Bio Medical Science, 3(07), 328–334. https://doi.org/10.47191/ijpbms/v3-i7-03
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References

I. Saxena R, Theise ND, Crawford JM. Microanatomy of the human liver-exploring the hidden interfaces. Hepatology. 1999 Dec;30(6):1339-46.

II. Si-Tayeb K, Lemaigre FP, Duncan SA. Organogenesis and development of the liver. Dev Cell. 2010 Feb 16;18(2):175-89.]

III. Almazroo OA, Miah MK, Venkataramanan R. Drug Metabolism in the Liver. Clin Liver Dis. 2017 Feb;21(1):1-20.

IV. O'Brien L, Hosick PA, John K, Stec DE, Hinds TD. Biliverdin reductase isozymes in metabolism. Trends Endocrinol Metab. 2015 Apr;26(4):212-20.

V. Zhang JL, Rusinek H, Chandarana H, Lee VS. Functional MRI of the kidneys. J Magn Reson Imaging. 2013 Feb;37(2):282-93.

VI. McMahon RS, Penfold D, Bashir K. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Jul 25, 2022. Anatomy, Abdomen and Pelvis, Kidney Collecting Ducts.

VII. 23- Coste AH, Lofgren DH, Shermetaro C. StatPearls [Internet]. StatPearls Publishing; Treasure Island (FL): Sep 12, 2022. Branchial Cleft Cyst.

VIII. Kieliszek, M. Selenium−fascinating microelement, properties and sources in food. Molecules 2019, 24 (7), 1298−1311.

IX. Al-Dossari M.H., Fadda L.M., Attia H.A., Hasan I.H., Mahmoud A.M. Curcumin and Selenium Prevent Lipopolysaccharide/Diclofenac-Induced Liver Injury by Suppressing Inflammation and Oxidative Stress. Biol. Trace Elem. Res. 2020;196:173–183.

X. Nangliya V., Sharma A., Yadav D., Sunder S., Nijhawan S., Mishra S. Study of trace elements in liver cirrhosis patients and their role in prognosis of disease. Biol. Trace Elem. Res. 2015;165:35–40.

XI. Zhang M., Song G., Minuk G.Y. Effects of hepatic stimulator substance, herbal medicine, selenium/vitamin E, and ciprofloxacin on cirrhosis in the rat. Gastroenterology. 1996;110:1150–1155.

XII. ong Y., Dong F., Geng Y., Zhuang H., Ma Z., Zhou Z., Huang B., Sun Z., Hou B. Selenium concentration, dietary intake and risk of hepatocellular carcinoma—A systematic review with meta-analysis. Nutr. Hosp. 2019;36:1430–1437.

XIII. Vaidya VS, Ramirez V, Ichimura T, Bobadilla NA, Bonventre JV. Urinary kidney injury molecule-1: a sensitive quantitative biomarker for early detection of kidney tubular injury. Am J Physiol Renal Physiol. 2006;290:F517–29.

XIV. Hagiwara S, Koga H, Iwasaka H, Kudo K, Hasegawa A, Kusaka J. et al. ETS-GS, a New Antioxidant, Ameliorates Renal Ischemia-Reperfusion Injury in a Rodent Model. J Surg Res. 2011;171:226–33.

XV. Avlan D, Erdougan K, Cimen B, Dusmez Apa D, Cinel I, Aksoyek S. The protective effect of selenium on ipsilateral and contralateral testes in testicular reperfusion injury. Pediatr Surg Int. 2005;21:274–8.

XVI. Mills, G. C. (1959) The purification and properties of glutathione peroxidase of erythrocytes. J. Biol. Chem. 234:502–506.

XVII. Danforth, E., Jr & Burger, A. G. (1989) The impact of nutrition on thyroid hormone physiology and action. Annu. Rev. Nutr. 9:201–207.

XVIII. Shen, H. M., Yang, C. F. & Ong, C. N. (1999) Sodium selenite-induced oxidative stress and apoptosis in human hepatoma HepG(2) cells. Int. J. Cancer 81:820–828