Istanbul Medical Faculty, Department of General Surgery, Istanbul University, Istanbul, Turkey.
Dig Dis Sci. 2010 Mar;55(3):617-25. doi: 10.1007/s10620-009-0780-x. Epub 2009 Mar 18.
The aim of the present study was to investigate whether pentoxifylline (PTX) treatment could protect against induced acute radiation enteritis.
Rats received 100 mg/kg/day PTX for 7 days before irradiation and continued on treatment for 3 days after irradiation. The intestinal myeloperoxidase (MPO) activities and malondialdehyde (MDA), glutathione (GSH), prostaglandin E2, and thromboxane B2 levels were determined. Terminal ileum tissue was evaluated for morphological changes. Also, nuclear factor kappa (NF-kappa), tumor necrosis factor-alpha (TNF-alpha), and intercellular adhesion molecule 1 (ICAM-1) expressions were analyzed with immunohistochemisty methods.
PTX treatment was associated with increased GSH levels and decreased MPO activity and MDA, prostaglandin E2, and thromboxane B2 levels. Histopathologic examination showed that intestinal mucosal structure was preserved in the PTX-treated group while having significant decreases in NF-kappaB, TNF-a, and ICAM-1 expression.
PTX appears to have a protective effect against radiation damage. This protective effect is mediated in part by decreasing both inflammatory reactions and oxidative stress.
本研究旨在探讨己酮可可碱(PTX)治疗是否能预防诱导的急性放射性肠炎。
大鼠在照射前连续 7 天每天接受 100mg/kg 的 PTX 治疗,照射后继续治疗 3 天。测定肠道髓过氧化物酶(MPO)活性及丙二醛(MDA)、谷胱甘肽(GSH)、前列腺素 E2 和血栓素 B2 水平。用免疫组化法检测末端回肠组织的形态变化。还分析了核因子 kappa(NF-kappa)、肿瘤坏死因子-α(TNF-α)和细胞间黏附分子 1(ICAM-1)的表达。
PTX 治疗可增加 GSH 水平,降低 MPO 活性及 MDA、前列腺素 E2 和血栓素 B2 水平。组织病理学检查显示,PTX 治疗组肠黏膜结构得到保留,同时 NF-kappaB、TNF-a 和 ICAM-1 的表达明显降低。
PTX 对辐射损伤具有保护作用。这种保护作用部分是通过减少炎症反应和氧化应激来介导的。