Wang L, Stanisz A M, Wershil B K, Galli S J, Perdue M H
Intestinal Disease Research Programme, McMaster University, Hamilton, Ontario, Canada.
Am J Physiol. 1995 Jul;269(1 Pt 1):G85-92. doi: 10.1152/ajpgi.1995.269.1.G85.
We used genetically mast cell-deficient WBB6F1 W/Wv (W/Wv) mice and congenic WBB6F1 +/+ normal (+/+) mice to examine the role of mast cells in substance P-induced intestinal ion secretion. Isolated sheets prepared from segments of the midportion of the small intestine were studied in Ussing chambers. Substance P caused a dose-dependent increase in short-circuit current (Isc) that was approximately 50% less in intestine from W/Wv than from +/+ mice. Similar results were obtained for substance P-(4-11) (the COOH terminus) and substance P methyl ester [a selective neurokinin (NK)-1 agonist]. Histamine H1 or H2 antagonists reduced the Isc responses to substance P in intestine from +/+ mice but had no effect in intestine from W/Wv mice. In addition, reconstitution of intestinal mast cells in W/Wv mice by intravenous injection of +/+ bone marrow cells normalized the tissues' secretory responses to substance P or substance P methyl ester. However, in W/Wv and +/+ mice, the selective NK1 antagonist CP-96345 virtually abolished intestinal responses to substance P, and the responses were also markedly inhibited by neural blockade with tetrodotoxin. In contrast, in tetrodotoxin-pretreated intestine, histamine antagonism caused a further reduction in the responses to substance P only in +/+ mouse tissues. Taken together, our results suggest that the effects of substance P on intestinal Isc KN1 receptors but that the neuropeptide acts via effects on enteric nerves and mast cells. The data thus support the concept that mast cells and enteric nerves participate in the regulation of substance P-induced intestinal ion secretion.
我们使用基因工程构建的肥大细胞缺陷型WBB6F1 W/Wv(W/Wv)小鼠和同基因的WBB6F1 +/+正常(+/+)小鼠,来研究肥大细胞在P物质诱导的肠道离子分泌中的作用。从小肠中部切取的肠段制备成离体肠片,置于Ussing chamber中进行研究。P物质可引起短路电流(Isc)呈剂量依赖性增加,W/Wv小鼠小肠中的增加幅度比+/+小鼠约低50%。P物质(4 - 11)(羧基末端)和P物质甲酯[一种选择性神经激肽(NK)-1激动剂]也得到了类似结果。组胺H1或H2拮抗剂可降低+/+小鼠小肠对P物质的Isc反应,但对W/Wv小鼠小肠无影响。此外,通过静脉注射+/+骨髓细胞对W/Wv小鼠的肠道肥大细胞进行重建,可使组织对P物质或P物质甲酯的分泌反应恢复正常。然而,在W/Wv和+/+小鼠中,选择性NK1拮抗剂CP - 96345几乎完全消除了肠道对P物质的反应,河豚毒素进行神经阻滞也可显著抑制该反应。相反,在经河豚毒素预处理的小肠中,组胺拮抗作用仅在+/+小鼠组织中进一步降低了对P物质的反应。综上所述,我们的结果表明,P物质对肠道Isc的作用是通过NK1受体介导的,但该神经肽是通过作用于肠神经和肥大细胞发挥作用的。这些数据支持肥大细胞和肠神经参与调节P物质诱导的肠道离子分泌这一概念。