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脱氢二异丁香酚对小鼠模型肠炎及并发的运动功能障碍的缓解作用

Mitigative effects of dehydrodiisoeugenol on enteritis and co-occurring dysmotility in murine model.

作者信息

Xu Jiaheng, Li Xinlei, Yuan Zimin, Li Feng, Xu Zhili

机构信息

Naval Medical University, Shanghai, PR China.

College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Liaoning, PR China.

出版信息

Pak J Pharm Sci. 2022 Sep;35(5):1347-1355.

Abstract

The actions and mechanisms of dehydrodiisoeugenol (DEH) on releasing clinical symptoms such as diarrhea caused by inflammatory bowel diseases or colorectal cancer is still unclear. The main purpose is to reveal the mechanism and describe the impacts of DEH on enteritis and accompanying intestinal dysmotility in murine model. The animal model of diarrhea was established through being given acetic acid by intracolonic instillation and restraint stress and the weight of the diarrhea mouse, diarrhea index (the product of stool rate and stool grade) evaluation and then, myeloperoxidase (MPO) activity were determined after administrated with DEH. Meanwhile, the expression of myosin light chain kinase (MLCK) was research by WB method. Moreover, the isolated jejunal segment (IJS) of rats was separated from the intact jejunum and the contractility was measured through BL-420F physiological recording system. DEH could significantly inhibit the intestinal transit in normal mice or diarrhea-predominated mice and reduce the diarrhea index and the level of MPO in mice. DEH concentration-dependently inhibited motility of IJS in different states. DEH significantly markedly ameliorated the histopathology condition and reduce the MLCK expression in acetic acid induced diarrhea mice. DEH simultaneously improved enteritis and co-occurring dysmotility in diarrhea mice characterized by reducing the contractility and MLCK contents in acetic acid induced diarrhea mice.

摘要

脱氢二异丁香酚(DEH)对缓解由炎症性肠病或结直肠癌引起的腹泻等临床症状的作用及机制仍不清楚。主要目的是揭示DEH对小鼠模型肠炎及伴随的肠道运动障碍的作用机制并描述其影响。通过结肠内滴注乙酸和束缚应激建立腹泻动物模型,给予DEH后测定腹泻小鼠的体重、腹泻指数(粪便率与粪便等级的乘积),并检测髓过氧化物酶(MPO)活性。同时,采用蛋白质免疫印迹法研究肌球蛋白轻链激酶(MLCK)的表达。此外,从完整空肠分离大鼠离体空肠段(IJS),通过BL-420F生理记录系统测定其收缩性。DEH可显著抑制正常小鼠或腹泻为主型小鼠的肠道转运,降低小鼠腹泻指数和MPO水平。DEH浓度依赖性地抑制不同状态下IJS的运动。DEH显著改善乙酸诱导腹泻小鼠的组织病理学状况并降低MLCK表达。DEH通过降低乙酸诱导腹泻小鼠的收缩性和MLCK含量,同时改善腹泻小鼠的肠炎及并发的运动障碍。

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