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首页> 外文期刊>Journal of the American College of Nutrition >Effect of Pomegranate Juice on Intestinal Recovery Following Methotrexate-Induced Intestinal Damage in a Rat Model
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Effect of Pomegranate Juice on Intestinal Recovery Following Methotrexate-Induced Intestinal Damage in a Rat Model

机译:石榴汁对大鼠甲氨蝶呤诱导肠损伤后肠道恢复的影响

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摘要

Background/Aims: Several studies have demonstrated the antimicrobial, antihelminthic, and antioxidant potential of the active ingredients of pomegranate (PMG) extracts, suggesting their preventive and curative role in several gastrointestinal disorders. In the present study, the authors evaluated the effects of oral PMG supplementation on intestinal structural changes, enterocyte proliferation, and apoptosis during methotrexate (MTX)-induced intestinal damage in a rat.Methods: Male rats were divided into 4 experimental groups: control rats; CONTR-PMG rats were treated with oral PMG given by gavage once a day 72hours before and 72hours following vehicle injection; MTX rats were treated with single dose of methotrexate; and MTX-PMG rats were treated with oral PMG following injection of MTX. Intestinal mucosal damage, mucosal structural changes, enterocyte proliferation, and enterocyte apoptosis were determined 72hours following MTX injection. Western blotting was used to determine phosphorylated extracellular signal-regulated kinase (p-ERK) and caspase 3 protein levels.Results: MTX-PMG rats demonstrated greater jejunal and ileal bowel and mucosal weights, greater jejunal and ileal mucosal DNA and protein levels, greater villus height in jejunum and ileum and crypt depth in ileum, compared with MTX animals. A significant decrease in enterocyte apoptosis in ileum of MTX-PMG rats (vs MTX) was associated with a decrease in caspase 3 protein expression as well as increased cell proliferation, which was correlated with elevated p-ERK protein levels.Conclusions: Treatment with oral PMG prevents mucosal injury and improves intestinal recovery following MTX injury in the rat.
机译:背景/目的:几项研究已经证明了石榴(PMG)提取物的活性成分的抗微生物,抗骨型和抗氧化剂潜力,表明其在几种胃肠道病症中的预防和治愈性作用。在本研究中,作者评估了口服PMG补充对甲氨蝶呤(MTX)诱导的肠道结构变化,肠细胞增殖和细胞凋亡的影响 - 甲醛尿素损伤。方法:将雄性大鼠分为4个实验组:对照大鼠;通过饲喂饲养前72小时的饲养饲养,每天饲喂饲养场72小时,并在载体注射后进行对方的大鼠。 MTX大鼠用单剂量的甲氨蝶呤治疗;在注射MTX后,用口服PMG处理MTX-PMG大鼠。肠粘膜损伤,粘膜结构变化,肠溶细胞增殖和肠细胞凋亡72小时后测定MTX注射。蛋白质印迹用于确定磷酸化的细胞外信号调节激酶(P-ERK)和Caspase 3蛋白水平。结果:MTX-PMG大鼠展示了更大的Jejunal和Ileal肠和粘膜重量,更大的Jejunal和ILEAL粘膜DNA和蛋白质水平与MTX动物相比,Jejunum和Hileum和Hyptpt Depress的别墅身高。在MTX-PMG大鼠(VS MTX)的Ileum中肠细胞凋亡的显着降低与Caspase 3蛋白表达的降低以及增加的细胞增殖,其与升高的P-ERK蛋白水平相关。结论:用口服处理PMG可防止粘膜损伤并改善大鼠MTX损伤后的肠道回收。

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