Barbara Giovanni, Wang Bingxian, Stanghellini Vincenzo, de Giorgio Roberto, Cremon Cesare, Di Nardo Giovanni, Trevisani Marcello, Campi Barbara, Geppetti Pierangelo, Tonini Marcello, Bunnett Nigel W, Grundy David, Corinaldesi Roberto
Department of Internal Medicine and Gastroenterology, and CRBA, University of Bologna, St. Orsola Hospital, Via Massarenti 9, I-40138 Bologna, Italy.
Gastroenterology. 2007 Jan;132(1):26-37. doi: 10.1053/j.gastro.2006.11.039.
BACKGROUND & AIMS: Intestinal mast cell infiltration may participate to abdominal pain in irritable bowel syndrome (IBS) patients. However, the underlying mechanisms remain unknown. We assessed the effect of mast cell mediators released from the colonic mucosa of IBS patients on the activation of rat sensory neurons in vitro. METHODS: Colonic mast cell infiltration and mediator release were assessed with quantitative immunofluorescence and immunoenzymatic assays. The effect of mucosal mediators was tested on mesenteric sensory nerve firing and Ca(2+) mobilization in dorsal root ganglia in rats. RESULTS: Mediators from IBS patients, but not controls, markedly enhanced the firing of mesenteric nerves (14.7 +/- 3.2 imp/sec vs 2.8 +/- 1.5 imp/sec; P < .05) and stimulated mobilization of Ca(2+) in dorsal root ganglia neurons (29% +/- 4% vs 11% +/- 4%; P < .05). On average, 64% of dorsal root ganglia responsive to mediators were capsaicin-sensitive, known to mediate nociception. Histamine and tryptase were mainly localized to mucosal mast cells. IBS-dependent nerve firing and Ca(2+) mobilization were correlated with the area of the colonic lamina propria occupied by mast cells (r = 0.74; P < .01, and r = 0.78; P < .01, respectively). IBS-dependent excitation of dorsal root ganglia was inhibited by histamine H(1) receptor blockade and serine protease inactivation (inhibition of 51.7%; P < .05 and 74.5%; P < .05; respectively). CONCLUSIONS: Mucosal mast cell mediators from IBS patients excite rat nociceptive visceral sensory nerves. These results provide new insights into the mechanism underlying visceral hypersensitivity in IBS.
背景与目的:肠道肥大细胞浸润可能参与肠易激综合征(IBS)患者的腹痛。然而,其潜在机制仍不清楚。我们在体外评估了IBS患者结肠黏膜释放的肥大细胞介质对大鼠感觉神经元激活的影响。 方法:采用定量免疫荧光和免疫酶测定法评估结肠肥大细胞浸润和介质释放。测试黏膜介质对大鼠肠系膜感觉神经放电和背根神经节中Ca(2+)动员的影响。 结果:IBS患者而非对照组的介质显著增强了肠系膜神经的放电(14.7±3.2次/秒对2.8±1.5次/秒;P<.05),并刺激了背根神经节神经元中Ca(2+)的动员(29%±4%对11%±4%;P<.05)。平均而言,对介质有反应的背根神经节中64%对辣椒素敏感,已知辣椒素可介导伤害感受。组胺和类胰蛋白酶主要定位于黏膜肥大细胞。IBS相关的神经放电和Ca(2+)动员与肥大细胞占据的结肠固有层面积相关(r=0.74;P<.01和r=0.78;P<.01)。组胺H(1)受体阻断和丝氨酸蛋白酶失活可抑制IBS相关的背根神经节兴奋(分别抑制51.7%;P<.05和74.5%;P<.05)。 结论:IBS患者的黏膜肥大细胞介质可兴奋大鼠伤害性内脏感觉神经。这些结果为IBS内脏高敏感性的潜在机制提供了新的见解。
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