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动脉粥样硬化会加重肠道的缺血/再灌注损伤,以及肝脏和肺部的远处损伤。

Atherosclerosis aggravates ischemia/reperfusion injury in the gut and remote damage in the liver and the lung.

机构信息

Clinic of Cardiac Surgery, Ludwig-Maximilians-University of Munich-Grosshadern, Marchioninistr.15, 81377, Munich, Germany.

出版信息

Inflamm Res. 2011 Jun;60(6):555-67. doi: 10.1007/s00011-010-0304-3. Epub 2011 Jan 9.

Abstract

OBJECTIVE

We investigated whether mesenteric ischemia/reperfusion (I/R)-associated gut injury and remote liver and lung damage are affected by prevalent atherosclerosis.

METHODS

Mesenteric ischemia was induced in atherosclerotic ApoE-deficient (ApoE(-/-)) and control C57BL/6 mice by clamping the superior mesenteric artery for 30 min. Mesenteric microcirculatory dysfunction and leukocytic inflammation were studied in the terminal ileum by intravital fluorescence microscopy (IVM). Histological analyses included quantitative assessment of parenchymal injury in the terminal ileum, liver and lung.

RESULTS

In the gut, IVM of the terminal ileum revealed aggravated postischemic microcirculatory dysfunction and absence of reactive hyperemia-induced vasodilation in atherosclerotic mice compared to controls. In addition, leukocyte-endothelial cell adhesive interactions, i.e. rolling and firm adhesion, were significantly increased in atherosclerotic animals. This was associated with enhanced mucosal tissue damage in ApoE(-/-) mice. Moreover, mesenteric I/R-provoked remote parenchymal injury in the liver was found to be significantly aggravated in atherosclerotic mice. This was accompanied by enhanced neutrophilic lung inflammation in ApoE(-/-) mice.

CONCLUSION

Prevalent generalized atherosclerosis not only aggravates splanchnic microcirculatory dysfunction and leukocytic inflammation in response to mesenteric I/R, but also exacerbates mucosal tissue damage and remote injury in the liver and the lung.

摘要

目的

本研究旨在探讨普遍存在的动脉粥样硬化是否会影响肠系膜缺血/再灌注(I/R)相关的肠道损伤和远隔肝肺损伤。

方法

通过夹闭肠系膜上动脉 30 分钟的方法诱导动脉粥样硬化 ApoE 缺陷(ApoE(-/-))和对照 C57BL/6 小鼠发生肠系膜缺血。通过活体荧光显微镜(IVM)研究末端回肠的肠系膜微循环功能障碍和白细胞炎症。组织学分析包括末端回肠、肝和肺实质损伤的定量评估。

结果

在肠道中,与对照组相比,IVM 显示出严重的缺血后微循环功能障碍,并且在动脉粥样硬化小鼠中不存在反应性充血诱导的血管扩张。此外,在动脉粥样硬化动物中,白细胞-内皮细胞黏附相互作用,即滚动和牢固黏附,显著增加。这与 ApoE(-/-)小鼠的黏膜组织损伤增加有关。此外,发现肠系膜 I/R 引起的远隔实质损伤在动脉粥样硬化小鼠中明显加重。这伴随着 ApoE(-/-)小鼠中性粒细胞性肺炎症的增强。

结论

普遍存在的全身性动脉粥样硬化不仅加重了肠系膜 I/R 时的内脏微循环功能障碍和白细胞炎症,还加重了肝脏和肺部的黏膜组织损伤和远隔损伤。

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