MFGE8和HMGB1表达水平对钝性腹部损伤大鼠肠黏膜屏障功能和炎症反应的潜在影响

Li-Ping Tao, Hongbo Xu, Qianggui He
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引用次数: 1

摘要

摘要目的:探讨乳脂球- egf因子8蛋白(MFGE8)通过RhoA/ROCK信号通路对SD大鼠钝性腹部损伤的影响。方法:建立SD大鼠钝性腹部损伤模型。将44只大鼠随机分为三组。采用简易损伤量表(AIS)评定大鼠钝性腹部损伤。处死大鼠,观察腹腔和肠道形态。采用苏木精和伊红染色观察大鼠肠道的病理变化。免疫组化染色检测大鼠肠道中MFGE8和高迁移率组1 (HMGB1)的阳性表达。Western blot检测蛋白水平。采用酶联免疫吸附法(ELISA)检测血清肿瘤坏死因子α (TNF-α)、IL-1β、IL-6和丙二醛(MDA)水平。结果:钝性腹部损伤引起大鼠肠道组织炎症反应,血清TNF-α、IL-1β、IL-6、MDA水平升高,HMGB1、RhoA、ROCK2水平上调,MFGE8水平下调,而rhMFGE8干预可显著缓解上述症状。结论:MFGE8通过下调HMGB1对钝性腹部损伤大鼠肠黏膜屏障功能的保护作用。通过下调RhoA和ROCK,减轻大鼠钝性腹部损伤引起的炎症反应和氧化应激。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential influences of expression levels of MFGE8 and HMGB1 on the intestinal mucosal barrier function and inflammatory response after blunt abdominal injury in rats
ABSTRACT Purpose: To explore the influence of milk fat globule-EGF factor 8 protein (MFGE8) on blunt abdominal injury in Sprague Dawley (SD) rats through the RhoA/ROCK signaling pathway. Methods: The blunt abdominal injury model was generated in SD rats. A total of 44 rats was randomly assigned into three groups. Rat blunt abdominal injury was assessed by the abbreviated injury scale (AIS). The rats were sacrificed for observing the morphology of the abdominal cavity and intestines. Hematoxylin and eosin staining was performed to visualize the pathological changes of rat intestines. Positive expressions of MFGE8 and high mobility group box 1 (HMGB1) in rat intestines were examined by immunohistochemical staining. Protein levels were determined by Western blot. Serum levels of tumor necrosis factor α (TNF-α), IL-1β, IL-6 and malondialdehyde (MDA) were measured by enzyme linked immunosorbent assay (ELISA). Results: Blunt abdominal injury resulted in inflammatory response of intestinal tissues, increased serum levels of TNF-α, IL-1β, IL-6 and MDA, upregulation of HMGB1, RhoA and ROCK2, and downregulation of MFGE8 in rats, which were significantly alleviated by intervention of rhMFGE8. Conclusions: MFGE8 protects the intestinal mucosal barrier function after blunt abdominal injury in rats by downregulating HMGB1. Moreover, it alleviates inflammatory response and oxidative stress caused by blunt abdominal injury in rats through downregulating RhoA and ROCK.
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