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The role of curcumin on intestinal oxidative stress, cell proliferation and apoptosis after ischemia/reperfusion injury in rats

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info:eu-repo/semantics/closedAccess

Date

2011

Author

Yücel, Ahmet Fikret
Kanter, Mehmet
Pergel, Ahmet
Erboğa, Mustafa
Güzel, Ahmet

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Citation

Yucel, A. F., Kanter, M., Pergel, A., Erboga, M., & Guzel, A. (2011). The role of curcumin on intestinal oxidative stress, cell proliferation and apoptosis after ischemia/reperfusion injury in rats. Journal of molecular histology, 42(6), 579–587. https://doi.org/10.1007/s10735-011-9364-0

Abstract

The aim of this study was to demonstrate the role of curcumin on oxidative stress, cell proliferation and apoptosis in the rat intestinal mucosa after ischemia/reperfusion (I/R). A total of 30 male Wistar albino rats were divided into three groups: sham, I/R and I/R+ curcumin; each group contain 10 animals. Sham group animals underwent laparotomy without I/R injury. After I/R groups animals underwent laparotomy, 1 h of superior mesenteric artery ligation were followed by 1 h of reperfusion. In the curcumin group, 3 days before I/R, curcumin (100 mg/kg) was administered by gastric gavage. All animals were sacrificed at the end of reperfusion and intestinal tissues samples were obtained for biochemical and histopathological investigation in all groups. Curcumin treatment significantly decreased the elevated tissue malondialdehyde levels and increased of reduced superoxide dismutase, and glutathione peroxidase enzyme activities in intestinal tissues samples. I/R caused severe histopathological injury including mucosal erosions and villous congestion and hemorrhage. Curcumin treatment significantly attenuated the severity of intestinal I/R injury, with inhibiting of I/R-induced apoptosis and cell proliferation. These results suggest that curcumin treatment has a protective effect against intestinal damage induced by intestinal I/R. This protective effect is possibly due to its ability to inhibit I/R-induced oxidative stress, apoptosis and cell proliferation. © 2011 Springer Science+Business Media B.V.

Source

Journal of Molecular Histology

Volume

42

Issue

6

URI

https://doi.org/10.1007/s10735-011-9364-0
https://hdl.handle.net/11436/3585

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  • PubMed İndeksli Yayınlar Koleksiyonu [2443]
  • Scopus İndeksli Yayınlar Koleksiyonu [6023]
  • TF, Cerrahi Tıp Bilimleri Bölümü Koleksiyonu [1224]



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