Evaluation of the Effect of Ginger Zingiber Officinale Extract on Liver of Albino Rat Administered with Graded Doses of Piroxicam

Authors

  • Uwuigbe Mathew Ambrose Alli University Ekpoma
  • Ohiwerei Wisdom Omogbai Ohilux Global Research and Training Institute, Edo State
  • Edebiri O E Ambrose Alli University Ekpoma
  • Ajanwachukwu Ogbonna Wilson Benson Idahosa University, Benin, Edo State
  • Obeagu E I Imo State University, Owerri, Imo State

DOI:

https://doi.org/10.59890/ijaamr.v3i3.498

Keywords:

Zingiber Officinale, Piroxicam, Liver Histology, Albino Rats, Immunohistochemistry

Abstract

This study aimed to evaluate the effects of Zingiber officinale (ginger) extract on the liver when administered with graded doses of piroxicam. Fifty albino rats were divided into five groups (A–E) of ten each. Group A served as the control, while Group B received 2.7 mg/kg of piroxicam, Group C was given 400 mg/kg of ginger, Group D received 2.7 mg/kg of piroxicam and 100 mg/kg of ginger, and Group E was administered 2.7 mg/kg of piroxicam along with 400 mg/kg of ginger. Substances were administered daily for 21 days, and the weights of both test and control animals were monitored. After treatment, the rats were anesthetized with chloroform, and their livers were harvested for immunohistochemistry processing. ANOVA was used for statistical analysis, with significance set at P < 0.05. Data were expressed as Mean ± SEM, with control group weight values recorded as 247.00 ± 3.35 at baseline, 219 ± 9.36 after acclimatization, and 219 ± 6.40 before sacrifice. No significant differences (p < 0.05) were found between the test groups and the control. Histological analysis revealed leukocyte infiltration in the liver of Group B (piroxicam 2.7 mg/kg) and leukocyte deposition in Group C (ginger 400 mg/kg). Group D (piroxicam 2.7 mg/kg + ginger 100 mg/kg) exhibited cellular changes and tissue damage, while Group E (piroxicam 2.7 mg/kg + ginger 400 mg/kg) showed neoplastic changes. Further research is recommended to accurately determine the effects of varying doses of Zingiber officinale on piroxicam-induced liver alterations

References

Ahmad, J., & Odin, J. A. (2017). Epidemiology and genetic risk factors of drug hepatotoxicity. Clinics in Liver Disease, 21(1), 55–72.

Danan, G., & Benichou, C. (2003). Causality assessment of adverse reactions to drugs-I. A novel method based on the conclusions of international consensus meetings: Application to drug-induced liver injuries. The British Journal of Nutrition, 46(11), 1323–1330.

Gonzalez, H. C., Jafri, S.-M., & Gordon, S. C. (2017). Management of acute hepatotoxicity including medical agents and liver support systems. Clinics in Liver Disease, 21(1), 163–180.

Goodman, Z. D. (2017). Phenotypes and pathology of drug-induced liver disease. Clinics in Liver Disease, 21(1), 89–101.

Habib, S. H. M., Makpol, S., Abdul Hamid, N. A., Das, S., Ngah, W. Z. W., & Yusof, Y. A. M. (2008). Ginger extract (Zingiber officinale) has anti-cancer and anti-inflammatory effects on ethionine-induced hepatoma rats. Clinics (Sao Paulo, Brazil), 63(6), 807–813.

Haniadka, R., Saldanha, E., Sunita, V., Palatty, P. L., Fayad, R., & Baliga, M. S. (2013). A review of the gastroprotective effects of ginger (Zingiber officinale Roscoe). Food & Function, 4(6), 845–855.

Jiang, Y., Gu, L., Zhang, R., Zhang, Y., Zhang, L., Ju, P., … Chen, X. (2014). Evaluation of the indicative roles of seven potential biomarkers on hepato-nephrotoxicity induced by Genkwa Flos. Journal of Ethnopharmacology, 158 Pt A, 317–324.

Kumar, P., & Wang, C. C. (2005). Depletion of anaphase-promoting complex or cyclosome (APC/C) subunit homolog APC1 or CDC27 of Trypanosoma brucei arrests the procyclic form in metaphase but the bloodstream form in anaphase. The Journal of Biological Chemistry, 280(36), 31783–31791.

Lu, T. T., Makishima, M., Repa, J. J., Schoonjans, K., Kerr, T. A., Auwerx, J., & Mangelsdorf, D. J. (2000). Molecular basis for feedback regulation of bile acid synthesis by nuclear receptors. Molecular Cell, 6(3), 507–515.

Mansour, M. A., Bekheet, S. A., Al-Rejaie, S. S., Al-Shabanah, O. A., Al-Howiriny, T. A., Al-Rikabi, A. C., & Abdo, A. A. (2010). Ginger ingredients inhibit the development of diethylnitrosoamine induced premalignant phenotype in rat chemical hepatocarcinogenesis model. BioFactors (Oxford, England), 36(6), 483–490.

Möller, B., Pruijm, M., Adler, S., Scherer, A., Villiger, P. M., Finckh, A., & Swiss Clinical Quality Management in Rheumatic Diseases (SCQM) Foundation, CH-8048 Zurich, Switzerland. (2015). Chronic NSAID use and long-term decline of renal function in a prospective rheumatoid arthritis cohort study. Annals of the Rheumatic Diseases, 74(4), 718–723.

Ravindran, P. N. (2016). Botany and crop improvement of ginger. In Ginger (pp. 35–106). CRC Press.

Trivedi, M. (2015). Spectroscopic characterization of disulfiram and nicotinic acid after biofield treatment. The British Journal of Nutrition, 6(265).

Xu, S., Rouzer, C. A., & Marnett, L. J. (2014). Oxicams, a class of nonsteroidal anti‐inflammatory drugs and beyond. IUBMB life, 66(12), 803-811.

Yemitan, O. K., & Izegbu, M. C. (2006). Protective effects of Zingiber officinale (Zingiberaceae) against carbon tetrachloride and acetaminophen-induced hepatotoxicity in rats. Phytotherapy Research: PTR, 20(11), 997–1002.

Zakhari, S. (2006). Overview: how is alcohol metabolized by the body? Alcohol Research & Health: The Journal of the National Institute on Alcohol Abuse and Alcoholism, 29(4), 245–254.

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Published

2025-03-28

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