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首页> 外文期刊>Molecular medicine reports >Mesenchymal stem cells improve intestinal integrity during severe acute pancreatitis.
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Mesenchymal stem cells improve intestinal integrity during severe acute pancreatitis.

机译:间充质干细胞可改善严重急性胰腺炎期间的肠道完整性。

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Severe acute pancreatitis (SAP) is an acute inflammatory disease of the pancreas that involves various distant tissues and organs. This study aimed to investigate post-tissue injury repair by mesenchymal stem cells (MSCs) in a rat model of SAP. A total of 54 pathogen-free adult male SD rats were randomly assigned to the groups SAP, SAP + MSCs and sham-operated (SO). SAP was induced by 4% sodium taurocholate, and MSCs were injected via the dorsal penile vein 1 h later. The amylase activity, and tumor necrosis factor (TNF)-α and diamine oxidase (DAO) levels were measured with an enzyme-linked immunosorbent assay (ELISA), while the expression of aquaporin (AQP)-1 was evaluated by immunohistochemical staining. The pathological score of intestinal tissues was also compared among groups. Marked improvement in intestinal necrosis, villi shedding and infiltration of inflammatory cells was observed in the SAP + MSCs group compared to the SAP and SO groups. Amylase, TNF-α, and DAO levels were significantly increased in the SAP + MSCs group. The intestinal expression of AQP-1 was increased at 12 and 24 h post-MSC transplantation compared to the SO group. Rats of the SAP + MSCs group displayed higher pathological scores compared to the SAP group at all time points. Overall, these data showed that MSCs can inhibit systemic inflammation and reduce TNF-α release in a rat model of SAP-induced intestinal injury, suggesting that MSCs exert protective effects on the intestinal barrier during SAP.
机译:严重急性胰腺炎(SAP)是一种胰腺炎性疾病,涉及各种远处的组织和器官。这项研究旨在研究在大鼠的SAP模型中由间充质干细胞(MSCs)修复组织损伤。将总共​​54只无病原体的成年雄性SD大鼠随机分为SAP,SAP + MSC和假手术(SO)组。 4%的牛磺胆酸钠诱导SAP,1小时后经阴茎背静脉注射MSC。通过酶联免疫吸附试验(ELISA)测定淀粉酶活性,肿瘤坏死因子(TNF)-α和二胺氧化酶(DAO)的水平,同时通过免疫组织化学染色评价水通道蛋白(AQP)-1的表达。还比较了各组肠道组织的病理评分。与SAP和SO组相比,SAP + MSCs组的肠道坏死,绒毛脱落和炎性细胞浸润明显改善。 SAP + MSCs组中的淀粉酶,TNF-α和DAO水平显着增加。与SO组相比,MSC移植后12和24 h AQP-1的肠道表达增加。在所有时间点上,SAP + MSCs组的大鼠均显示出比SAP组更高的病理评分。总体而言,这些数据表明,在大鼠诱发的SAP肠损伤模型中,MSC可以抑制全身性炎症并减少TNF-α的释放,表明MSC在SAP期间对肠屏障起保护作用。

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