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Antioxidant-Based Therapy Reduces Early-Stage Intestinal Ischemia-Reperfusion Injury in Rats

机译:基于抗氧化的疗法减少了大鼠早期肠缺血再灌注损伤

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摘要

Intestinal ischemia-reperfusion injury (i-IRI) is a rare disorder with a high mortality rate, resulting from the loss of blood flow to an intestinal segment. Most of the damage is triggered by the restoration of flow and the arrival of cytokines and reactive oxygen species (ROS), among others. Inactivation of these molecules before tissue reperfusion could reduce intestinal damage. The aim of this work was to analyze the preventive effect of allopurinol and nitroindazole on intestinal mucosal damage after i-IRI. Wag/RijHsd rats were subjected to i-IRI by clamping the superior mesenteric artery (for 1 or 2 h) followed by a 30 min period of reperfusion. Histopathological intestinal damage (HID) was assessed by microscopic examination of histological sections obtained from injured intestine. HID was increased by almost 20% by doubling the ischemia time (from 1 to 2 h). Nitroindazole reduced HID in both the 1 and 2 h period of ischemia by approximately 30% and 60%, respectively (p < 0.001). Our preliminary results demonstrate that nitroindazole has a preventive/protective effect against tissue damage in the early stages of i-IRI. However, to better understand the molecular mechanisms underlying this phenomenon, further studies are needed.
机译:肠缺血再灌注损伤(I-IRI)是一种罕见的死亡率,因血流丧失到肠部而导致。大部分损害是通过恢复流动和细胞因子和反应性氧(ROS)的到达而引发的损伤。在组织再灌注之前,这些分子的失活可能降低肠道损伤。这项工作的目的是分析Allopurinol和Nitininzole对I-Iri后肠粘膜损伤的预防效果。通过夹紧高级肠系膜动脉(1或2小时),然后再灌注30分钟的再灌注时,对I-IRI进行I-IRI进行摇头/ rijhsd大鼠。通过对受伤肠道获得的组织学部分进行评估组织病理肠损伤(HID)。通过将缺血时间加倍(从1到2小时增加),HID增加了近20%。 Nitroindazole分别将1和2小时的缺血周期减少约30%和60%(P <0.001)。我们的初步结果表明,Nitroindazole对I-Iri的早期阶段的组织损伤具有预防/保护作用。然而,为了更好地了解这种现象的分子机制,需要进一步研究。

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