Effects of statins in an indomethacin-induced gastric injury model in rats
Statins have additional pleiotropic effects beyond their lipid-lowering effects. In this study, the effects of statins were evaluated in an indomethacin-induced gastric injury model in rats. Animals were divided into eight groups. Distilled water (control group), omeprazole (30 mg/kg), atorvastatin...
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Veröffentlicht in: | The Turkish journal of gastroenterology 2012-10, Vol.23 (5), p.456-462 |
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Sprache: | eng |
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Zusammenfassung: | Statins have additional pleiotropic effects beyond their lipid-lowering effects. In this study, the effects of statins were evaluated in an indomethacin-induced gastric injury model in rats.
Animals were divided into eight groups. Distilled water (control group), omeprazole (30 mg/kg), atorvastatin (20 and 40 mg/kg), simvastatin (20 and 40 mg/kg), and rosuvastatin (20 and 40 mg/kg) were given orally (gavage). Thirty minutes later, indomethacin (25 mg/kg) was administered orally to all groups. Six hours later, the animals were sacrificed by decapitation. The mean ulcer indexes for each group were calculated, and the stomachs were evaluated histopathologically.
The ulcer indexes were as follows: control 1.72 ± 0.16, omeprazole 0 ± 0.00, and atorvastatin, simvastatin and rosuvastatin (at 20 and 40 mg/kg doses, respectively) 4.28 ± 0.39, 4.99 ± 0.96, 1.72 ± 0.73, 1.90 ± 0.48, 1.85 ± 0.26, and 1.67 ± 0.18. Atorvastatin significantly increased the indomethacin-induced ulcer index at both doses and the erosion score at 40 mg/kg dose. Although the 20 mg/kg dose of simvastatin inhibited mononuclear leukocyte infiltration, the 40 mg/kg dose induced hyperemia. Rosuvastatin did not decrease mononuclear leukocyte or neutrophil infiltrations at 20 mg/kg dose, and only neutrophil infiltration at the 40 mg/kg dose.
In patients with gastric discomfort, statins must be used carefully. If statin therapy is needed, we recommend to avoid using atorvastatin and to use the other statins only in the minimum effective dose. |
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ISSN: | 1300-4948 2148-5607 |
DOI: | 10.4318/tjg.2012.0393 |