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首页> 外文期刊>Inflammation research: Official journal of the European Histamine Research Society >Study of dexamethasone, baicalin and octreotide on brain injury of rats with severe acute pancreatitis
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Study of dexamethasone, baicalin and octreotide on brain injury of rats with severe acute pancreatitis

机译:地塞米松,黄ical苷和奥曲肽对重症急性胰腺炎大鼠脑损伤的研究

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Objective: To investigate the protecting effects of dexamethasone (DXM), baicalin and octreotide on brain injury of rats with severe acute pancreatitis (SAP) and explore their underlying mechanism. Methods: This experiment was divided into two different parts: (1) In the first part, 90 SAP rats were randomly divided into a model control group and a DXM treated group (n = 45, respectively). (2) In the second part, 135 SAP rats were randomly divided into a model control group, a baicalin treated group and an octreotide treated group (n = 45, respectively). In two different experiments, the same number of normal rats were considered as the sham-operated group (n = 45, respectively). At 3, 6 and 12 h after operation, the pathological changes in the brain were observed. The expression levels of nuclear factor-κB (NF-κB), Bax and Bcl-2 proteins were detected and apoptosis indexes were calculated, using brain tissue microarray section. Results: (1) First part: The expression levels of Bax and Bcl-2 were significantly higher in the DXM treated group than those in the model control group at different time points, while the content of NF-κB protein and pathological changes were significantly lower in the treated group than those in the model control group (P < 0.05, P < 0.01 or P < 0.001). But the apoptotic indexes of brain tissue were not significantly different at different time points (P > 0.05). (2) Second part: At all time points after operation, the expression levels of NF-κB in the brain of treated groups were, to varying degrees, significantly lower than those in the model control group while the expression levels of Bcl-2 protein in baicalin and octreotide group were significantly higher than those in model control group (P < 0.01, P < 0.01 and P < 0.05, respectively). At 12 h after operation, the expression level of Bax protein in baicalin treated group was significantly higher than those in model control group and octreotide treated group (P < 0.05 and P < 0.01, respectively). Conclusions: Dexamethasone, baicalin and octreotide can exert protective effects against brain injury in SAP rats mainly through inhibiting the expression of NF-κB protein.
机译:目的:探讨地塞米松(DXM),黄ical苷和奥曲肽对重症急性胰腺炎(SAP)大鼠脑损伤的保护作用,并探讨其潜在机制。方法:本实验分为两个不同的部分:(1)第一部分,将90只SAP大鼠随机分为模型对照组和DXM治疗组(分别为45只)。 (2)在第二部分中,将135只SAP大鼠随机分为模型对照组,黄ical苷治疗组和奥曲肽治疗组(分别为n = 45)。在两个不同的实验中,假手术组被认为是相同数量的正常大鼠(分别为n = 45)。术后3、6和12小时,观察到脑部的病理变化。用脑组织微阵列切片检测核因子-κB(NF-κB),Bax和Bcl-2蛋白的表达水平,并计算凋亡指数。结果:(1)第一部分:DXM治疗组在不同时间点的Bax和Bcl-2表达水平明显高于模型对照组,而NF-κB蛋白含量和病理变化明显。治疗组比模型对照组低(P <0.05,P <0.01或P <0.001)。但是在不同时间点脑组织的凋亡指数没有显着差异(P> 0.05)。 (2)第二部分:在手术后的所有时间点,治疗组脑中NF-κB的表达水平均显着低于模型对照组,而Bcl-2蛋白的表达水平明显低于模型对照组。黄ical苷和奥曲肽组的血脂显着高于模型对照组(分别为P <0.01,P <0.01和P <0.05)。术后12 h,黄ical苷治疗组Bax蛋白表达水平明显高于模型对照组和奥曲肽治疗组(分别为P <0.05和P <0.01)。结论:地塞米松,黄ical苷和奥曲肽可通过抑制NF-κB蛋白的表达对SAP大鼠脑损伤产生保护作用。

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