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Am. J. Biomed. Sci. 2014, 6(1), 32-40; doi: 10.5099/aj140100032
Received: 26 February 2014; | Revised: 16 March 2014; | Accepted: 22 March 2014

 

Evaluation of Toxicological Profile of Ibuprofen in Wistar Albino Rats

 

Jonah Sydney Aprioku1*, Lucky Legbosi Nwidu2, Cecilia Nwadiuto Amadi3

1Department of Pharmacology, Faculty of Basic Medical Sciences, University of Port Harcourt, Port Harcourt, Nigeria

2 Department of Pharmacology and Toxicology, Faculty of Pharmacy, Niger Delta University, Wilberforce Island, Yenagoa, Bayelsa State, Nigeria.

3Department of Clinical Pharmacy and Management, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria

*Corresponding Author

Jonah Sydney Aprioku

Department of Pharmacology

Faculty of Basic Medical Sciences

University of Port Harcourt

Port Harcourt, Nigeria

Phone: +234(0) 8035082379

Email: sydaprio@yahoo.com

 

Abstract

Ibuprofen is an effective, cheap, and frequently used non-steroidal anti-inflammatory drug. The present study investigated the dose- and time-dependent effects of ibuprofen on hepatic, renal, and hematological functions in rats. Groups of rats (n=6) were given ibuprofen (20, 40 mgkg-1day-1) for 7, 14 or 28 days; or vehicle (control), orally. Blood samples were obtained, and hematological indices and biochemical markers of hepatic and renal functions were measured. Ibuprofen significantly increased, P < 0.001 serum alkaline phosphatase level at all doses and durations of exposure. Serum uric acid level was dose- and time-dependently decreased by ibuprofen, but alanine transaminase was increased, P < 0.05 by ibuprofen, only at 40 mgkg-1 and following subchronic (28 days) exposure. In addition, at 40 mgkg-1, ibuprofen increased creatinine and urea levels at all durations of exposure; but at 20 mgkg-1, creatinine and urea were increased only in rats that were exposed for 28 days. Furthermore, subchronic exposure of 40 mgkg-1 ibuprofen increased, P < 0.01 WBC count, but it caused no significant effect on WBC at the lower durations of exposure and dose. Also, while RBC and hematocrit were not affected, ibuprofen significantly, P < 0.01,P < 0.001 decreased platelet counts in all treated rats except those that were exposed for 7 days. The implication of this research is that chronic use of ibuprofen could affect hepatic, renal and hematological functions in the rat; and duration of exposure may promote ibuprofen toxicity relative to dose.

Keywords: Aminotransferases, ibuprofen, platelets, renal toxicity, subchronic.

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