Protective effects of pentoxifylline in small intestine after ischemia-reperfusion

被引:5
|
作者
Egin, Seracettin [1 ]
Ilhan, Mehmet [2 ]
Bademler, Suleyman [2 ]
Gokcek, Berk [1 ]
Hot, Semih [1 ]
Ekmekci, Hakan [3 ]
Ekmekci, Ozlem Balci [3 ]
Tanriverdi, Gamze [4 ]
Dagistanli, Fatma Kaya [5 ]
Kamali, Gulcin [6 ]
Kamali, Sedat [1 ]
Guloglu, Recep [2 ]
机构
[1] Saglik Bilimleri Univ, Gen Surg, Okmeydani Educ & Res Hosp, Istanbul, Turkey
[2] Istanbul Univ, Istanbul Tip Fak, Gen Surg, Istanbul, Turkey
[3] Istanbul Univ, Cerrahpasa Tip Fak, Biochem, Istanbul, Turkey
[4] Istanbul Univ, Cerrahpasa Tip Fak, Histol & Embryol, Istanbul, Turkey
[5] Istanbul Univ, Cerrahpasa Tip Fak, Med Biol, Istanbul, Turkey
[6] Saglik Bilimleri Univ, Pathol, Okmeydani Educ & Res Hosp, Istanbul, Turkey
关键词
Pentoxifylline; small intestine; ischemia-reperfusion; Wistar rat; superior mesenteric artery; histopathology; NECROSIS-FACTOR-ALPHA; HYPERTONIC SALINE; RAT MODEL; INJURY; ISCHEMIA/REPERFUSION; INHIBITION; FLOW;
D O I
10.1177/0300060518786904
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective: This study was performed to determine the healing effects of pentoxifylline on molecular responses and protection against severe ischemic damage in the small intestine. Methods: Thirty-six Wistar albino rats were divided into six groups. The superior mesenteric artery was clamped for 120 minutes, and reperfusion was performed for 60 minutes. Saline (0.4 mL), pentoxifylline (1 mg/kg), and pentoxifylline (10 mg/kg) were intraperitoneally administered to the rats in the C-1, P-1, and P-3 groups, respectively, 60 minutes before ischemia and to the rats in the C-2, P-2, and P-4 groups, respectively, during reperfusion onset. Malondialdehyde, myeloperoxidase, tumor necrosis factor alpha, interleukin-1 beta, and interleukin-6 in serum and tissue were measured by enzyme-linked immunosorbent assay. Intestinal ischemic injury was histopathologically evaluated by the Chiu score and immunohistochemical staining. Results: All serum and tissue molecular responses were significantly blunted in the pentoxifylline-treated groups compared with the controls. Significant improvement in ischemic damage was demonstrated in the pentoxifylline-treated groups by histological grading and immunohistochemical scoring. Conclusions: The protective effects of pentoxifylline were confirmed by molecular responses and histopathological examination.
引用
收藏
页码:4140 / 4156
页数:17
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