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Adenoviral transfer of human interleukin-10 gene in lethal pancreatitis

机译:人白细胞介素10基因在致命性胰腺炎中的腺病毒转移

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摘要

AIM: To evaluate the therapeutic effect of adenoviral-vector-delivered human interleukin-10 (hIL-10) gene on severe acute pancreatitis (SAP) rats.METHODS: Healthy Sprague-Dawley (SD) rats were intraperitoneally injected with adenoviral IL-10 gene (AdvhIL-10), empty vector (Adv0) or PBS solution. Blood, liver, pancreas and lung were harvested on the second day to examine hIL-10 level by ELISA and serum amylase by enzymatic assay. A SAP model was induced by retrograde injection of sodium taurocholate through pancreatic duct. SAP rats were then administered with AdvhIL-10, Adv0 and PBS solution by a single intraperitoneal injection 20 min after SAP induction. In addition to serum amylase assay, levels of hIL-10 and tumor necrosis factor-α (TNF-α ) were detected by RT-PCR, ELISA and histological study. The mortality rate was studied and analyzed by Kaplan–Meier and log rank analysis.RESULTS: The levels of hIL-10 in the pancreas, liver and lung of healthy rats increased significantly after AdvhIL-10 injection (1.42 ng/g in liver, 0.91 ng/g in pancreas); while there was no significant change of hIL-10 in the other two control groups. The concentration of hIL-10 was increased significantly in the SAP rats after AdvhIL-10 injection (1.68 ng/g in liver, 1.12 ng/g in pancreas) compared to the other two SAP groups with blank vector or PBS treatment (P < 0.05). The serum amylase levels remained normal in the AdvhIL-10 transfected healthy rats. However, the serum amylase level was significantly elevated in the other two control SAP rats. In contrast, serum amylase was down-regulated in the AdvhIL-10 treated SAP groups. The TNF-α expression in the AdvhIL-10 treated SAP rats was significantly lower compared to the other two control SAP groups. The pathohistological changes in the AdvhIL-10 treated group were better than those in the other two control groups. Furthermore, the mortality of the AdvhIL-10 treated group was significantly reduced compared to the other two control groups (P < 0.05).CONCLUSION: Adenoviral hIL-10 gene can significantly attenuate the severity of SAP rats, and can be used in the treatment of acute inflammation process.
机译:目的:评价腺病毒载体介导的人白介素10(hIL-10)基因对重症急性胰腺炎(SAP)大鼠的治疗作用。方法:对健康的Sprague-Dawley(SD)大鼠腹腔注射腺病毒IL-10。基因(AdvhIL-10),空载体(Adv0)或PBS溶液。第二天收集血液,肝,胰腺和肺,通过ELISA检测hIL-10水平,通过酶法检测血清淀粉酶。通过胰管逆行注射牛磺胆酸钠可诱发SAP模型。然后在诱导SAP后20分钟通过一次腹膜内注射向SAP大鼠施用AdvhIL-10,Adv0和PBS溶液。除血清淀粉酶检测外,还通过RT-PCR,ELISA和组织学研究检测hIL-10和肿瘤坏死因子-α(TNF-α)的水平。结果通过Kaplan–Meier和log rank分析研究并分析了死亡率。结果:AdvhIL-10注射后,健康大鼠的胰腺,肝和肺中的hIL-10水平显着增加(肝脏中1.42 ng / g,0.91) ng / g胰腺);而其他两个对照组的hIL-10则无明显变化。与其他两个空白载体或PBS处理的SAP组相比,注射AdvhIL-10后SAP大鼠中的hIL-10浓度显着增加(肝脏为1.68 ng / g,胰腺为1.12 ng / g)(P <0.05 )。在AdvhIL-10转染的健康大鼠中,血清淀粉酶水平保持正常。然而,在另两只对照SAP大鼠中,血清淀粉酶水平显着升高。相反,在AdvhIL-10处理的SAP组中血清淀粉酶被下调。与其他两个对照组SAP组相比,用AdvhIL-10治疗的SAP大鼠中的TNF-α表达明显较低。 AdvhIL-10治疗组的病理组织学变化优于其他两个对照组。此外,与其他两个对照组相比,AdvhIL-10治疗组的死亡率显着降低(P <0.05)。结论:腺病毒hIL-10基因可以显着减轻SAP大鼠的病情,可用于治疗急性炎症过程。

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