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首页> 外文期刊>Neurogastroenterology and motility >Surgical intestinal manipulation increases gene expression of TrkA, CGRP, and PAR-2 IN dorsal root ganglia in the rat
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Surgical intestinal manipulation increases gene expression of TrkA, CGRP, and PAR-2 IN dorsal root ganglia in the rat

机译:肠内外科手术可增加大鼠背根神经节中TrkA,CGRP和PAR-2的基因表达

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摘要

Background Surgical handling of the bowel evokes degranulation of peritoneal mast cells (PMC). Nonetheless, role of PMCs in postoperative ileus (POI) is somewhat controversial. We aimed to investigate if intestinal manipulation elicits changes in afferent mediators related to MC activation and alteration of gastrointestinal (GI) motility. Methods Postoperative ileus was induced by intestinal manipulation in Sprague-Dawley rats. Additionally, compound 48/80 (C48/80) and ketotifen were used to modulate MC activity. Rat mast cell protease 6 (RMCP-6, ELISA) release was determined in peritoneal lavage 20 min after intestinal manipulation. At 24 h, GI transit was determined. Gene expression of calcitonin gene-related peptide (CGRP), protease-activated receptor-2 (PAR-2), nerve growth factor (NGF), and TrkA receptor was determined (PCR) in dorsal root ganglia (DRG). Ileal wall inflammation was assessed by myeloperoxidase (MPO) activity, interleukin-6 expression (IL-6). Key Results Intestinal manipulation and exposure to C48/80-induced degranulation of PMCs delayed GI transit and upregulated IL-6 and MPO activity. Intestinal manipulation, but not C48/80, up-regulated CGRP, PAR-2, and NGF/TrkA in DRGs. Ketotifen only improved gastric emptying and fecal output. Up-regulation of CGRP and TrkA expression in DRG was not prevented by ketotifen. Conclusions & Inferences Postoperative ileus is accompanied by activation of CGRP, NGFTrkA, and PAR-2 in DRGs. Our results suggest that these mediators could be a target in further POI studies in order to find new therapeutic targets for this medical condition.
机译:背景肠的外科手术会引起腹膜肥大细胞(PMC)脱粒。尽管如此,PMC在术后肠梗阻(POI)中的作用还是有争议的。我们旨在调查肠道操纵是否引起与MC激活和胃肠道(GI)运动改变有关的传入介体的变化。方法通过肠道操作在Sprague-Dawley大鼠中诱发肠梗阻。另外,化合物48/80(C48 / 80)和酮替芬用于调节MC活性。在肠操作20分钟后,在腹膜灌洗中测定大鼠肥大细胞蛋白酶6(RMCP-6,ELISA)的释放。在24小时,确定了胃肠道过境。在背根神经节(DRG)中测定降钙素基因相关肽(CGRP),蛋白酶激活受体2(PAR-2),神经生长因子(NGF)和TrkA受体的基因表达(PCR)。回肠壁炎症通过髓过氧化物酶(MPO)活性,白介素6表达(IL-6)进行评估。关键结果肠道操作和暴露于C48 / 80诱导的PMC脱粒会延迟GI转运并上调IL-6和MPO活性。肠道操纵(而非C48 / 80)在DRG中上调了CGRP,PAR-2和NGF / TrkA。酮替芬只能改善胃排空和排便量。酮替芬不能阻止DRG中CGRP和TrkA表达的上调。结论与结论术后肠梗阻伴有DRGs中CGRP,NGFTrkA和PAR-2的激活。我们的结果表明,这些介体可能是进一步POI研究的靶标,以便为这种医学状况找到新的治疗靶标。

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