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石榴汁对甲氨蝶呤诱导的大鼠肠损伤后肠道恢复的影响。

Effect of Pomegranate Juice on Intestinal Recovery Following Methotrexate-Induced Intestinal Damage in a Rat Model.

机构信息

a Laboratory of Intestinal Adaptation and Recovery, The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology , Haifa , Israel.

b Pediatric Gastroenterology and Nutrition Institute, Ruth Children's Hospital of Haifa, Rambam Medical Center , Haifa , Israel.

出版信息

J Am Coll Nutr. 2018 Jul;37(5):406-414. doi: 10.1080/07315724.2017.1413961. Epub 2018 Mar 13.

Abstract

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 72 hours before and 72 hours 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 72 hours 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.

摘要

背景/目的:多项研究表明,石榴(PMG)提取物的活性成分具有抗菌、抗蠕虫和抗氧化作用,这表明它们在几种胃肠道疾病中有预防和治疗作用。在本研究中,作者评估了口服 PMG 补充剂对 MTX 诱导的大鼠肠道损伤期间肠道结构变化、肠细胞增殖和细胞凋亡的影响。

方法

雄性大鼠分为 4 个实验组:对照组;CONTR-PMG 组在给予 vehicle 注射前 72 小时和后 72 小时通过灌胃给予口服 PMG 治疗;MTX 组给予单次 MTX 治疗;MTX-PMG 组在给予 MTX 后给予口服 PMG 治疗。在给予 MTX 后 72 小时测定肠道黏膜损伤、黏膜结构变化、肠细胞增殖和肠细胞凋亡。Western 印迹法测定磷酸化细胞外信号调节激酶(p-ERK)和 caspase 3 蛋白水平。

结果

与 MTX 组相比,MTX-PMG 组的空肠和回肠肠和黏膜重量更大,空肠和回肠黏膜 DNA 和蛋白质水平更高,空肠和回肠的绒毛高度更高,回肠的隐窝深度更深。MTX-PMG 组回肠肠细胞凋亡减少(与 MTX 相比)与 caspase 3 蛋白表达降低以及细胞增殖增加相关,这与 p-ERK 蛋白水平升高相关。

结论

口服 PMG 治疗可预防 MTX 损伤后大鼠的黏膜损伤并改善肠道恢复。

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