Histopathological Effects of Potassium Bromate on Liver Male Rat's and Possible Protective Role of Ruta chalepensis L. (Rutacae) Oil Extract

Authors

  • Ebtesam M. M. Gheth Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya
  • Ibrahim S Eldurssi Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya
  • Abdullah A. H. Algassi Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya
  • Gasem M. A. Abdalla Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya
  • Mabroka A. S. Hamad Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

DOI:

https://doi.org/10.22270/ajprd.v7i2.473

Keywords:

Keywords: Rat, Liver, Potassium Bromate, Ruta chalepensis, Histopathology.

Abstract

Potassium bromate (KBrO3) is an oxidizing agent that has been used as a food additive, mainly in the bread-making process. Ruta chalepensis L. (Family-Rutaceae) is a small shrub, native to the Mediterranean Basin. The present study aimed to investigate the protective and curative effects of R. chalepensis oil extract against KBrO3 toxicity on liver of male rats. Fifty male albino rats were divided into five groups. The first group served as a control group. The second group was administered Rue at an oral daily dose of 0.5 g/Animal for four weeks. The third group received KBrO3 100 mg/kg/b. w. for four weeks. The fourth group (protective group) was initially administered Rue alone for 2 weeks and followed by KBrO3 in association with Rue for 2 weeks. The fifth group (therapeutic group) was first given KBrO3 alone for 2 weeks and was then administered Rue in association with KBrO3 for 2 weeks. At the end of 2nd and 4th weeks of treatment, the liver tissues were dissected out for histopathological studies. Histopathological sections of rats administered with Rue showed the same histological observations as in the liver of control animals. KBrO3 treated rats exhibited marked congestion and dilatation of the blood vessels, the central veins and the portal veins. Additionally, marked infiltrative inflammatory cells were revealed. The occurrence of the cellular necrobiotic lesions and nuclei in these necrotic cells showed pyknosis. They also, showed cellular atrophied and hyaline degeneration of the cytoplasm. Vacuoles of different shapes and sizes were developed in the hepatocytes. Blood vessels being thick walled and fibrotic encircled by an inflammatory area rich in leucocytes. The protective and therapeutic groups showed marked hepatoprotective activity and better improvement than that noticed in the group which was given KBrO3 only. It may be concluded from the results that the hepatotoxic effect of KBrO3 and the ameliorative effect of Rue an effective when administrated as protective and therapeutic measures. 
Keywords: Rat, Liver, Potassium Bromate, Ruta chalepensis, Histopathology.

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Author Biographies

Ebtesam M. M. Gheth, Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Ibrahim S Eldurssi, Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Abdullah A. H. Algassi, Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Gasem M. A. Abdalla, Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Mabroka A. S. Hamad, Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

Zoology Department, Science Faculty, Omar Al-mukhtar University, El-Beida-Libya,P.O.BOX 919 - El-Beida-Libya

References

1. Kurokawa Y, Mackawa A, Takahashi N , Hayeshi Y,Toxicity and carcinogenicity of potassium bromate - a new renal carcinogen. Environ. Health Perspect, 1990; 87:309-355.
2. Ahmad MK, Mahmood R, Oral administration of potassium bromate, a major water disinfection by-product, induces oxidative stress and impairs the antioxidant power of rat blood. Chemosphere, 2012; 87(7):750-756.
3. Akanji MA, Nafiu M O, Yakubu MT, Enzyme activities and histopathology of selected tissues in rats treated with potassium bromate. Afr. J. Biomed. Res, 2018; 11:87-95.
4. Abuelgasim A, Omer R, Elmahdi B, Serrobiochemical Effects of Potassium Bromate on Wistar Albino Rats. Am. J. Food Technol., 2008; 3:303-309.
5. Gibreel HM, (2008). Toxicity of Potassium Bromate to Nubian Goat Kids. M V Sc. Thesis, Faculty of Veterinary Medicine, University of Khartoum.
6. Bayomy NA, Soliman GM, Abdelaziz, EZ, Effect of Potassium Bromate on the Liver of Adult Male Albino Rat and A Possible Protective Role of Vitamin C: Histological, Immunohistochemical, and Biochemical Study. Anat. Rec., 2016; 299:12560-1269.
7. Kong YC, Ng KH, Wat KH, Wong A, Saxena IF, Cheng KF, But PP, Chang HT, Yuehchukene, a Novel Anti-implantation Indole Alkaloid from Murraya paniculata. Planta Med, 1985; 51(4):304-307.
8. Shah AH, Qureshi S, Ageel AM, Toxicity studies in mice of ethanol extracts of Foeniculum vulgare fruit and Ruta chalepensis aerial parts, J. Ethnopharmacol,1991; 34:167-172.
9. Ratheesh M, Shyni GL, Helen A, Methanolic extract of Ruta graveolens L. inhibits inflammation and oxidative stress in adjuvant induced model of arthritis in rats. Inflammopharmacol,2009; 17(2):100-105.
10. Acquaviva R, Iauk L, Sorrenti V, Lanteri R, Santangelo R, Licata A, Licata F, Vanella A, Malaguarnera M, Ragusa S, Di Giacomo C, Oxidative profile in patients with colon cancer: effects of Ruta chalepensis L. Eur. Rev. Med. Pharmacol. Sci., 2011; 15)2(:181-191.
11. Kanadea R, Bhatkhandeb DS, Extraction of ginger oil using different methods and effect of solvents, time, temperature to maximize yield. Inter. J. Adv. Sci. Eng. Technol., 2016; 4(2):241-244.
12. Ukoha UU, Umeasalugo KE, Okafor J I, Udemezue OO, Ndukwe GU, Udenwogu CJ, (2014). The Histological Effect of Potassium Bromate on the Cerebellum of Adult Wistar Rats. Inter. J. Health Sci. Res., 2014; 4(9):114-118.
13. Al Qarawi AA, Stimulatory Effect of the Aqueous Extract of Ruta chalepensis on the Sex Organs and Hormones of Male Rats. J. Appl. Res., 2005; 5(1):206-211.
14. Lillie RD, (1954). Histopathological Techniques and Practical Histochemistry, McGraw-Hill, U. S. A.
15. Harris HF, (1900). After Bruce Casselman W. C. (1959). Histochemical Technique, by Methuen and Co. Ltd.
16. Fujii M, Oikawa K, Saito H, Fukuhara C, Onosaka S, Tanaka T, Metabolism of potassium bromate in rats II. In vitro studies. Chemosphere1984; 13(11):1213–1219.
17. Raghav SK, Gupta B, Agrawal C, Goswami K, Das HR, Anti-inflammatory effect of Ruta graveolens L. in murine macrophage cells. J. Ethnopharmacol., 2006; 104(1-2):234-239.
18. Adam Sh IY, Ahmed NN A, Eltayeb AM, Saad H, Taha KA, Toxicity of Ruta graveolens Seeds’ Extracts on Male Wistar Rats. Int. J. Anim. Veter. Adv., 2014; 6(3):92-96.
19. Abdel Gadir, EH, Abdel Gadir, WS, Adam SEI, Effects of Various Levels of Dietary Potassium Bromate on Wistar Rats. J. Pharmacol. Toxicol., 2007; 2(7):672-676.
20. Abuelgasim A, Omer R, Elmahdi B, Serrobiochemical Effects of Potassium Bromate on Wistar Albino Rats. Am. J. Food Technol., 2008; 3:303-309.
21. Oyewo OO, Onyije FM, Awoniran PO, Hepatotoxic effect of potassium bromate on the liver of wistar rats. J. Morphol. Sci., 2013; 30(2):107-114.
22. El-Sherif FG, Gobri MS, Zahran WM, Abdel-Hamid TF, Histological, histochemical studies and ATP-ase localization in the rat liver after morphine sulphates induction. J. Egypt. Ger. Soc. Zool.,2002; 39:175-187.
23. Cotran, RS, Kumar V, Collins T, (1999). The Liver and the Biliary Tract. In: Pathologic Basis of Disease. 6th ed., London, W. B. Saunders, pp.: 846-901.
24. Shimizu, S., Eguchi, Y., Kamiike, W., Waguri, S., Uchiyama, Y., Matsuda, H. and Tsujimoto, Y. (1996). Retardation of chemical hypoxia induced necrotic cell death by Bcl-2 and ICE inhibitors: Possible involvement of common mediators in apoptotic and necrotic signal transductions. Oncogene., 12: 2045-2050.
25. Tavill, AS, Intracellular pathways of protein synthesis and secretion in the hepatocytes. Semin Liver Dis., 1985; 5:95-109.
26. Phillips, MI, Poucell S, Patterson J, Valencia P, (1987). The liver. An Atlas and Text of Ultrastructural Pathology. Raven Press, New York, p. 398.
27. Bopanna, KN, Balaraman R, Nadig RS,. Organotropic ultrastructural changes produced by monosodium glutamate in rats on Atherogenic diet: effect of S-allyl cysteine sulphoxide. Ind. J. Pharmacol., 1999; 31(4):266-274.
28. ElAgouza, IMA, El Nashar, DE,Eissa S.S, The possible ultra structural ameliorative effect of taurine in rat’s liver treated with monosodium glutamate (MSG). The Open Hepato. J, 2010; 2:1-9.
29. Ahmad MK, Mahmood R. Oral administration of potassium bromate, a major water disinfection by-product, induces oxidative stress and impairs the antioxidant power of rat blood. Chemosphere, 2012; 87(7): 750-756.
30. Ben Sghaier M, Louhichi T, Hakem A, Ammari Y, Chemical investigation of polar extracts from Ruta chalpensis L. growing in Tunisia: Correlation with their antioxidant activities. Agri. Biotech., 2017; 49 (4): 2971-2978.

Published

2019-04-15

How to Cite

Gheth, E. M. M., Eldurssi, I. S., Algassi, A. A. H., Abdalla, G. M. . A., & Hamad, M. A. S. (2019). Histopathological Effects of Potassium Bromate on Liver Male Rat’s and Possible Protective Role of Ruta chalepensis L. (Rutacae) Oil Extract. Asian Journal of Pharmaceutical Research and Development, 7(2), 93–97. https://doi.org/10.22270/ajprd.v7i2.473