Use este identificador para citar ou linkar para este item: http://www.repositorio.ufc.br/handle/riufc/22034
Título: Protective effects of simvastatin against alendronate-induced gastric mucosal injury in rats
Autor(es): Carvalho, Nathalia S.
Silva, Mônica M.
Silva, Renan O.
Nicolau, Lucas A. D.
Araújo, Thiago S. L.
Costa, Douglas S.
Sousa, Nayara A.
Souza, Luan K. M.
Soares, Pedro M. G.
Medeiros, Jand Venes R.
Palavras-chave: Simvastatina
Antioxidantes
Antioxidants
Data do documento: Fev-2016
Editor: Digestive Diseases and Sciences
Citação: CARVALHO, N. S. ; SILVA, M. M. ; SILVA, R. O. ; NICOLAU, L. A. D. ; ARAÚJO, T. S. L. ; COSTA, D. S. ; SOUSA, N. A. ; SOUZA, L. K. M. ; SOARES, P. M. G. ; MEDEIROS, J. V. R. (2016)
Abstract: Background It has been reported that simvastatin, a statin commonly prescribed for its anti-inflammatory and antioxidant effects, has gastroprotective effects in indo- methacin and ethanol-induced gastric ulcers. However, the effects of simvastatin on alendronate-induced gastric mucosal injury remain unexplored. Aim This study investigated the use of simvastatin for the treatment of alendronate-induced gastric ulcers in rats. Methods Female rats were pretreated with vehicle or simvastatin (20 and 60 mg/kg p.o.). After 1 h, the rats received alendronate (50 mg/kg p.o.). Simvastatin was administered once daily for 7 days, and from the fourth day of simvastatin treatment, alendronate was administered once daily for 4 days. On the final day of treatment, 4 h after alendronate administration, animals were euthanized, their stomachs were removed, and gastric damage was measured. Samples of the stomach were fixed in 10 % formalin immediately after their removal for subsequent histopathological assessment. Unfixed samples were weighed, frozen at - 80 ° C until assayed for glutathione (GSH), malondialdehyde (MDA), and cytokine levels and myeloperoxidase (MPO) activity. A third group was used to measure mucus and gastric secretion. Results Pretreatment with simvastatin prevented alen- dronate-induced macroscopic gastric damage and reduced the levels of MDA and GSH, TNF- a and IL-1 b , MPO activity, and mucus levels, in the stomach. Conclusions This study demonstrates the protective effects of simvastatin against alendronate-induced gastric ulceration. Maintenance of mucosal integrity, inhibition of neutrophil activity, and reduced oxidative stress associated with decreased gastric acidity may explain the gastropro- tective effects of simvastatin.
Descrição: CARVALHO, Nathalia S. et al. Protective effects of simvastatin against alendronate-Induced gastric mucosal injury in rats. Digestive Diseases and Sciences, New York, v. 61, n. 2, p. 400-409, fev. 2016.
URI: http://www.repositorio.ufc.br/handle/riufc/22034
ISSN: 0163-2116
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