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EW-7197,一种转化生长因子-β 型 I 受体激酶抑制剂,可改善小鼠尾巴模型中的获得性淋巴水肿。

EW-7197, a Transforming Growth Factor-Beta Type I Receptor Kinase Inhibitor, Ameliorates Acquired Lymphedema in a Mouse Tail Model.

机构信息

Department of Biomedical Engineering Research Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.

出版信息

Lymphat Res Biol. 2020 Oct;18(5):433-438. doi: 10.1089/lrb.2018.0070. Epub 2020 Feb 27.

Abstract

Acquired lymphedema is a common consequence of cancer surgery. Fibrosis is one of the main causes of chronic lymphedema since it hinders lymphatic regeneration and this causes a significant decrease in lymphatic flow and accumulation of excessive protein-rich fluid. The transforming growth factor-β1 (TGF-β1) signaling pathway is known in a process of wound repair and fibrosis. In our study, the purpose was to evaluate the efficacy of EW-7197, a peroral TGF-β type I receptor kinase inhibitor, in treating acquired lymphedema. For lymphedema mouse tail model, we used 10- to 12-week-old female C57BL/6 mice. The skin was circumferentially excised, making a circular band followed by cauterization of lymphatic collecting vessels. Two groups were made in this study: control and treatment. The treatment group ( = 12) received a solution consisting of 0.1 mL of artificial gastric juice and 20 mg/kg EW-7197 by gavage once daily. For evaluation, tail diameter measurement, fluorescence lymphography, and immunofluorescence images were used. EW-7197 treatment ameliorates acquired lymphedema in a mouse tail model by increasing lymphangiogenesis and interstitial flow of the lymphatics by inhibition of the fibrosis. The differences in maximal tail thicknesses between the control and treatment groups were statistically significant from 2 to 4 weeks after surgery. The treatment group showed a greater number of lymphatic vessels at the surgery site than the control group. The treatment group also showed more FITC coverage area at the surgery site. EW-7197 treatment ameliorates acquired lymphedema in a mouse tail model by increasing lymphangiogenesis and interstitial flow.

摘要

获得性淋巴水肿是癌症手术后的常见后果。纤维化是慢性淋巴水肿的主要原因之一,因为它阻碍了淋巴管的再生,这导致了淋巴流量的显著减少和过多富含蛋白质的液体的积累。转化生长因子-β1(TGF-β1)信号通路在伤口修复和纤维化过程中是已知的。在我们的研究中,目的是评估 EW-7197(一种口服 TGF-β 型 I 受体激酶抑制剂)在治疗获得性淋巴水肿中的疗效。对于淋巴水肿鼠尾模型,我们使用 10 至 12 周龄的雌性 C57BL/6 小鼠。皮肤被环形切除,形成一个圆形带,然后对淋巴管收集血管进行烧灼。在这项研究中,我们分为两组:对照组和治疗组。治疗组(n=12)每天通过灌胃接受由 0.1ml 人工胃液和 20mg/kg EW-7197 组成的溶液。用于评估的方法有尾直径测量、荧光淋巴造影和免疫荧光图像。EW-7197 通过抑制纤维化来增加淋巴管生成和淋巴管的间质流动,从而改善鼠尾模型中的获得性淋巴水肿。手术后 2 至 4 周,对照组和治疗组之间的最大尾厚差异具有统计学意义。与对照组相比,治疗组在手术部位的淋巴管数量更多。治疗组在手术部位也显示出更多的 FITC 覆盖面积。EW-7197 通过增加淋巴管生成和间质流动来改善鼠尾模型中的获得性淋巴水肿。

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