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首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Dexamethasone pretreatment alleviates intestinal ischemiaereperfusion injury
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Dexamethasone pretreatment alleviates intestinal ischemiaereperfusion injury

机译:地塞米松预处理可减轻肠缺血再灌注损伤

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Background: Activated mast cells are involved in the pathogenesis of intestinal ischemiae reperfusion (I/R)-related injury. Dexamethasone has been widely used to protect organs from I/R injury. This study was conducted to investigate the impact of treatment with dexamethasone at different stages of the II/R process on mast cell infiltration and activity and intestinal injury. Methods: Kunming mice were randomized and subjected to a sham surgery or the II/R induction by clamping the superior mesenteric artery for 30 min and then reperfusion. During the II/R induction, the mice were treated intravenously with dexamethasone (10 mg/kg) for 30 min before ischemia (pretreatment group), at 5 min after clamping the superior mesenteric artery (isc-treatment group), or at the beginning of perfusion (reptreatment group), respectively. The levels of intestinal injury, mast cell infiltration and activity, tumor necrosis factor α (TNFα) and myeloperoxidase (MPO) activity in the intestines, and mouse survival rates were measured. Results: The death rates, levels of intestinal injury, mast cell infiltration and activity, and tumor necrosis factor a and myeloperoxidase activity in the intestinal tissues from the II/R group were similar to those from the isc-treatment and rep-treatment groups of mice and were significantly higher than those from the sham group. In contrast, pretreatment with dexamethasone significantly mitigated the II/R-induced mast cell infiltration and activity, inflammation, and intestinal injury and reduced the death rates in mice. Conclusions: Pretreatment with dexamethasone inhibits II/R injury by reducing mast celle related inflammation in mice.
机译:背景:活化的肥大细胞参与肠缺血再灌注(I / R)相关损伤的发病机制。地塞米松已被广泛用于保护器官免受I / R损伤。进行该研究以研究在II / R过程的不同阶段用地塞米松治疗对肥大细胞浸润,活性和肠损伤的影响。方法:将昆明小鼠随机分为假手术或II / R诱导,方法是夹住肠系膜上动脉30分钟,然后再灌注。在II / R诱导过程中,在缺血前(预处理组),在夹闭肠系膜上动脉后5分钟(缺血治疗组)或开始时,对小鼠进行地塞米松(10 mg / kg)静脉内治疗30分钟。灌注(再治疗组)。测量肠的损伤水平,肥大细胞浸润和活性,肠中的肿瘤坏死因子α(TNFα)和髓过氧化物酶(MPO)活性以及小鼠存活率。结果:II / R组肠道组织的死亡率,肠损伤水平,肥大细胞浸润和活性以及肿瘤坏死因子α和髓过氧化物酶活性与Isc治疗组和rep治疗组相似。小鼠,明显高于假手术组。相反,地塞米松预处理可显着减轻II / R诱导的肥大细胞浸润和活性,炎症和肠道损伤,并降低小鼠的死亡率。结论:地塞米松预处理可减轻小鼠肥大细胞相关的炎症,从而抑制II / R损伤。

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