Suppr超能文献

肥大细胞在急性肠缺血期间驱动肠系膜传入信号。

Mast cells drive mesenteric afferent signalling during acute intestinal ischaemia.

机构信息

Department of Biomedical Science, Florey Building, Firth Court, University of Sheffield, Sheffield S10 2TN, UK.

出版信息

J Physiol. 2011 Aug 1;589(Pt 15):3867-82. doi: 10.1113/jphysiol.2011.209478. Epub 2011 Jun 13.

Abstract

Acute intestinal ischaemia stimulates visceral afferent nerves but the mechanisms responsible for this excitation are not fully understood. Mast cells may participate in this process as they are known to signal to mesenteric afferents during intestinal anaphylaxis and contribute to early inflammation and neuronal damage in response to cerebral ischaemia. We therefore hypothesised that mast cells are early responders to acute intestinal ischaemia and their activation initiates rapid signalling to the CNS via the excitation of mesenteric afferents. Primary afferent firing was recorded from a mesenteric nerve bundle supplying a segment of jejunum in anaesthetized adult rats. Acute focal ischaemia was produced by clamping theme senteric vessels for 8 min, and reperfusion followed removal of the vessel clip. Two episodes of ischaemia–reperfusion (I–R) separated by a 30 min interval were performed. Drugs or their vehicles were administered 10 min before the 2nd I–R episode. Ischaemia caused a reproducible, intense and biphasic afferent firing that was temporally dissociated from the concomitantly triggered complex pattern of intestinal motor activity. The L-type calcium channel blocker, nifedipine, significantly attenuated this afferent firing by a mechanism independent of its action on intestinal tone. Ischaemia-induced afferent firing was also abrogated by the mast cell stabilizer, doxantrazole, and the H1 histamine receptor antagonist, pyrilamine. In contrast, the nicotinic receptor antagonist, hexamethonium, and the N-type calcium channel toxin, ω-conotoxin GVIA, each reduced the ischaemia-evoked motor inhibition but not the concurrent afferent discharge. Similarly, the cyclooxygenase inhibitor, naproxen, had no effect on the ischaemic afferent response but reduced the intestinal tone shortly from the onset of ischaemia to the early period of reperfusion. These data support a critical role for mast cell-derived histamine in the direct chemoexcitation of mesenteric afferents during acute intestinal ischaemia, whereas enteric reflex mechanisms and cyclooxygenase products contribute primarily to ischaemia-induced changes in intestinal motility. Therefore, targeting mast cells may provide benefits in patients with abdominal pain resulting from an ischaemic insult to the gastrointestinal tract.

摘要

急性肠道缺血会刺激内脏传入神经,但负责这种兴奋的机制尚未完全理解。肥大细胞可能参与这个过程,因为它们在肠道过敏反应期间向肠系膜传入神经发出信号,并在大脑缺血时导致早期炎症和神经元损伤。因此,我们假设肥大细胞是急性肠道缺血的早期反应者,它们的激活通过兴奋肠系膜传入神经,迅速向中枢神经系统发出信号。在麻醉成年大鼠的一段空肠供应的肠系膜神经束上记录初级传入放电。通过夹住肠系膜血管 8 分钟来产生急性局灶性缺血,并在移除血管夹后进行再灌注。进行两次缺血-再灌注(I-R),间隔 30 分钟。在第二次 I-R 发作前 10 分钟给予药物或其载体。缺血引起可重现的、强烈的双相传入放电,与同时触发的复杂肠道运动模式在时间上分离。L 型钙通道阻滞剂硝苯地平通过独立于其对肠道张力作用的机制显著减弱这种传入放电。肥大细胞稳定剂 doxantrazole 和 H1 组胺受体拮抗剂 pyrilamine 也消除了缺血诱导的传入放电。相比之下,烟碱受体拮抗剂 hexamethonium 和 N 型钙通道毒素 ω-conotoxin GVIA 都减少了缺血引起的运动抑制,但没有同时减少传入放电。同样,环氧化酶抑制剂萘普生对缺血传入反应没有影响,但在缺血开始后不久就减少了肠道张力,并持续到再灌注早期。这些数据支持肥大细胞衍生的组胺在急性肠道缺血期间直接刺激肠系膜传入神经的关键作用,而肠反射机制和环氧化酶产物主要导致缺血引起的肠道运动变化。因此,靶向肥大细胞可能对因胃肠道缺血损伤而导致腹痛的患者有益。

相似文献

本文引用的文献

2
Neuroimmune mechanisms in postoperative ileus.术后肠梗阻的神经免疫机制
Gut. 2009 Sep;58(9):1300-11. doi: 10.1136/gut.2008.169250.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验