Hepatoprotective effect of Tetracarpidium conophorum oil in diclofenac sodium induced hepatotoxicity in rats

Authors

  • Kenneth Maduabuchi Ezealisiji Department of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria.
  • Chika John Mbah Department of Pharmaceutical and Medicinal Chemistry, Faculty of Pharmaceutical sciences, University of Nigeria, Nsukka, Nigeria.

DOI:

https://doi.org/10.30574/gscbps.2019.6.2.0018

Keywords:

Omega-3, Tetracarpidium conophorum, Diclofenac sodium, Rheumatoid arthritis, Omega-9, Histological

Abstract

Western dietary lifestyle has gained lots of attention globally with high level of patronage hence generating human health concern. This calls for dietary balance and supplementation with vegetables, fish and nuts which are known to contain Omega-3, Omega-6 and Omega-9 fatty acids. Plant based oils such as Walnut (Tetracarpidium conophorum), are known to be rich in Omega-fatty acids, which can help lower pathological conditions such as heart diseases. Therefore, the study investigated the effects of pre-treatment with Tetracarpidium conophorum oil (Oil of African Walnut) in adult male Wistar rats exposed to diclofenac sodium (DFS). Twenty four male rats were randomly divided into four groups of six rats each, this includes: Group 1-Normal control; Group 2- DFS control; Group 3- low dose Tc oil + DFS; and Group 4- high dose Tc oil + DFS. The rats in group 2 received intramuscular dose of DFS (10 mg/kg body weight/day during the last 7 days of T. conophorum oil treatment. Rats in treatment groups 3 and 4 were pre-treated with T. Conophorum oil at 5.0 and 10 ml/kg b.w/day per oral for 21 days, afterwards they were administered DFS at 10 mg/kg b.w/day respectively for 7 days. The result showed that, DFS increased significantly biochemical and pro-inflammatory markers. Pre-treatment with oil of T. conophrum significantly prevented the pathological conditions due to diclofenac. In conclusion, pre-treatment dosing with oil of T. Conophorum could be suggested as a novel adjuvant in long term management of rheumatoid arthritis in man using diclofenac sodium.

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References

Andrea H, Roland L, Robert G, Michaela B, Thomas H, Werner A, Lothar V, Walther S, Fatima F, and Martin H. (2010). Diclofenac hypersensitivity: Antibody responses to the parent drug and relevant metabolites. PLoS One, 5(10), e13707.

Ngui JS, Tang W, Stearns RA, Shou M, Miller RR, Zhang Y, Lin JH and Baillie TA. (2000). Cytochrome P450 3A4-mediated interaction of diclofenac and quinidine. Drug Metabolism and Disposition, 28(9), 1043-50.

Rajeshwary G, Sumanta KG, Luis Felipe BBF, Bruce H and Aldrin VG. (2016). Diclofenac induces proteasome and mitochondrial dysfunction in murine cardiomyocytes and hearts. International Journal of Cardiology, 223(1), 923–935.

Haritha C, Reddy A, Gopala YA, Kalakumar B and Reddy GD. (2010). Oxidative stress induced by diclofenac alone and under the influence of certain variables in broilers. Toxicology International, 17(1), 27–29.

Fernando B. (2010). Non-steroidal anti-inflammatory drugs: What is the actual risk of liver damage? World Journal of Gastroenterology, 16(45), 5651–5661.

Kenneth ME and Emmanuel AN. (2015). Investigation of anti-ulcerogenic properties of fixed oil of African walnut (Tetracapidium conophorum) against gastric ulcers in albino wistar rats. Nigerian Journal of Pharmaceutical and Applied Science Research, 4(2), 7-11.

Ezealisiji KM and Agbo MO. (2016). Phytochemical analysis of N-Hexane nut extract of Tetracarpidium conophorum (Euphorbiaceae) using ultraviolet-visible, fourier transform infrared and gas chromatography mass spectrometry techniques. Journal of Pharmacognosy and Phytochemistry, 5(6), 332-336.

Galarraga B, Ho M, Youssef HM, Hill A, McMahon H, Hall C, Ogston S, Nuki G and Belch JJ. (2008). Cod liver oil (n-3 fatty acids) as an non-steroidal anti-inflammatory drug sparing agent in rheumatoid arthritis. Rheumatology (Oxford); 47(5), 665-9.

Freund M and Carol B. (1064). Factors affecting haemocytometer counts of sperm concentration in human semen. Journal of Reproduction and Fertility, 8(1), 149-155.

Lars KN, Gordon KS and Paul FG. (1991). Hemacytometer cell count distributions: Implications of non‐poisson behavior. Biotechnology Progress, 7(1), 560-563.

Shaima MA, Amr KE, Hala EH. (2016). Ultrastructure and histomorphometric analysis of human umbilical cord vessels in preeclampsia: a potential role of VEGF, VEGFR-1 and VEGFR-2. Romanian Journal of Morphology and Embryology, 57(2), 681–689.

Wade LS, John GH, Karl H, and Henry MR. (2015). VarBase: A platform for the storage and clinical interpretation of next generation sequencing data. Journal of Pathology Informatics, 6, 24-32.

Gaafar R, Mohsen E, and Thomas B. (2017). Gout: An old disease in new perspective – A review. Journal of Advanced Research, 8(5), 495–511.

Changyi C, Jian-Ming L and Qizhi Y. (2016). Hyperuricemia-Related Diseases and Xanthine Oxidoreductase (XOR) Inhibitors: An Overview. Medical Science Monitor, 22, 2501–2512.

Xiaoni S, Wenjie L, Fabao G, Dandan L, Jing H, Yan L, Zeping Z, Hui J, Yinglan Z and Xiaobo C. (2016). Uric acid induces cognitive dysfunction through hippocampal inflammation in rodents and humans. Journal of Neuroscience, 36 (43), 10990-11005.

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Published

2019-02-28

How to Cite

Ezealisiji, K. M., & Mbah, C. J. (2019). Hepatoprotective effect of Tetracarpidium conophorum oil in diclofenac sodium induced hepatotoxicity in rats. GSC Biological and Pharmaceutical Sciences, 6(2), 084–089. https://doi.org/10.30574/gscbps.2019.6.2.0018

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Original Article