Biochemical and histomorphological changes in liver and kidney of Rattus norvegicus domestica rats following tetracycline administration
DOI:
https://doi.org/10.30574/gscbps.2020.12.2.0200Keywords:
Biochemical changes, Histomorphological changes, Liver, Kidney, Rattus norvegicus domestica, Tetracycline administrationAbstract
This study was aimed on assessing the biochemical and histomorphological changes in liver and kidney of Rattus norvegicus domestica rats following tetracycline administration. Five ml blood specimen was collected from twenty one rats weighing 0.2072-0.3062 kg into lithium heparin bottles with seven of them each administered with 0.12 mg/0.2072 kg of tetracycline for two weeks (short term toxicity study) and four weeks (long term toxicity study) respectively, while the remaining seven which served as control group were not administered with tetracycline. The following biochemical parameters: alanine aminotransferase, aspartate aminotransferase, urea and creatinine were measured quantitatively. The mean values of all the measured biochemical parameters in the short term toxicity study were not statistically significant (p≥0.05) as compared to the control group and these values were also in conformity to the histomorphological study of the liver and kidney organs while that of the long term toxicity study showed statistically significant differences (p≤0.05) in all the measured biochemical parameters as compared to the control group and also in conformity to the histomorphological study of the liver and kidney organs. In conclusion, administration of 0.12 mg/0.2072 kg of tetracycline for four weeks may induce changes in the biochemical and histomorphological study of liver and kidney of Rattus norvegicus domestica rats, while that of two weeks may not. It is therefore recommended that tetracycline capsule should not be used indiscriminately for a long period. Besides, routine estimation of these biochemical parameters should be carried out in long term administration of tetracycline in humans.
Metrics
References
Bastos LFS, Merlo LA and Rocha Coecho MM. (2007). Characterization of the antinociceptive and anti-inflammatory activities of doxycycline and minocycline in different experimental models. European Journal of Pharmacology, 576, 171-179.
Chopra I and Roberts M. (2001). Tetracycline antibiotics mode of action, applications, molecular biology and epidemiology of bacteria resistance. Microbiology and Molecular Biology Reviews, 65(2), 232-260.
Yin HQ, Kim M, Kim JH, Kong G, Lee MO, Kang KS, Yoon BI, Kim HL and Lee BH. (2006). Hepatic gene expression profiling and lipid homeostasis in mice exposed to steatogenic drug, tetracycline. Toxicological Sciences, 62(3), 222 -239.
Casarett and Doulls. (1986). Toxicology the basis science of poisons. Klaasen C.D, Amdur M.O., Doull, J., 3rd edition, Macmillan Publishing, 501-611.
Uges DRA. (1996). Therapeutic and toxic drug concentrations. The TIAF Bulletin, 26, 1-34.
Emmanuel T, Friday Okaka ANC, Ibiam Udu A and Sonni M. (2017).The toxicological effects of cement dust on hepatic and renal functions of cement factory workers. Int. J. Life Scs. Research, 5(3), 37-45.
George GS, Wankasi MM and Egoro ET. (2014). Creatinine and urea levels as critical markers in end sytage renal failure. Research and Reviews: Journal of Medical and Health Sciences, 3(1), 41-44.
Avwioro OG. (2014). Histochemistry and tissue pathology, principles and tecniques. 3rd edition, Claverianum Press Big Limited. ISBN 978-35627-9-7.
Kikkawa R, Fujikawa M, Yamamoto T, Hamada Y, Yamada H and Horii I. (2006). In-vivo hepatotoxicity study of rats in comparism with in vitro hepatotoxicity screening system. Journal of Toxicology Sciences, 31, 23-24.
Miller CS and McGarity GJ. (2009). Tetracycline-induced renal failure after dental treatment. Journal of the American Dental Association, 140(1), 56-60.
Downloads
Published
How to Cite
Issue
Section
License
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.