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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Effect of a synthetic analog of prostaglandin E1 on the intestinal mucosa of methotrexate-treated rats.
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Effect of a synthetic analog of prostaglandin E1 on the intestinal mucosa of methotrexate-treated rats.

机译:前列腺素E1的合成类似物对甲氨蝶呤治疗的大鼠肠粘膜的影响。

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摘要

Administration of methotrexate to rats sometimes induces small intestinal damage. A synthetic analog of prostaglandin E1, OP-1206 [17S,20-dimethyl-trans-delta2-prostaglandin E1] may possibly provide therapeutic benefits to help recovery from such small intestinal damage. The purpose of this study was to evaluate the effect of OP-1206 on methotrexate-induced small intestinal damage in rats. Methotrexate (15 mg/kg body weight) was orally administered to rats once daily for 5 days. OP-1206 (0.5 microg/kg body weight) was orally administered to rats twice a day for 5 days and on the 6th day the small intestine of the rats were examined histologically and biochemically. The methotrexate treatment of rats caused a severe histological change in the small intestinal mucosa, whereas the treatment combined of OP-1206 with methotrexate showed similar histological features of the small intestinal mucosa as that of the control rats. On the other hand, an acute intestinal inflammation was evaluated by determining myeloperoxidase activity. The myeloperoxidase activity in the small intestinal mucosa of the methotrexate-treated rats increased remarkably, whereas that of the methotrexate and OP-1206-treated rats was significantly lower than that of the methotrexate-treated rats. Thus, it was shown histologically and biochemically that OP-1206 was effective in protecting the small intestine from methotrexate-induced damage.
机译:给大鼠服用甲氨蝶呤有时会引起小肠损伤。前列腺素E1的合成类似物OP-1206 [17S,20-二甲基-反式-δ2-前列腺素E1]可能会提供治疗益处,以帮助从如此小的肠损伤中恢复过来。这项研究的目的是评估OP-1206对甲氨蝶呤致大鼠小肠损伤的作用。每天一次对大鼠口服甲氨蝶呤(15 mg / kg体重),持续5天。每天两次对大鼠口服OP-1206(0.5微克/千克体重),持续5天,并在第6天通过组织学和生化检查大鼠的小肠。大鼠的甲氨蝶呤治疗引起小肠粘膜的严重组织学改变,而OP-1206与甲氨蝶呤的联合治疗显示小肠粘膜的组织学特征与对照大鼠相似。另一方面,通过确定髓过氧化物酶活性来评估急性肠道炎症。甲氨蝶呤治疗组大鼠小肠黏膜中的髓过氧化物酶活性显着增加,而甲氨蝶呤和OP-1206治疗组大鼠的肠粘膜中的髓过氧化物酶活性明显低于甲氨蝶呤治疗组大鼠。因此,从组织学和生化方面显示,OP-1206可有效保护小肠免受甲氨蝶呤引起的损害。

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