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Am. J. Biomed. Sci. 2014, 6(1), 32-40; doi: 10.5099/aj140100032 |
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. Download the full article (PDF)
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