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首页> 外文期刊>American Journal of Physiology >Cellular pathways of mast cell- and capsaicin-sensitive nerve-evoked ileal submucosal arteriolar dilations.
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Cellular pathways of mast cell- and capsaicin-sensitive nerve-evoked ileal submucosal arteriolar dilations.

机译:肥大细胞和辣椒素敏感的神经诱发的回肠粘膜下小动脉扩张的细胞途径。

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摘要

This study characterized mast cell- and capsaicin-sensitive sensory nerve vasodilator mechanisms regulating submucosal arterioles in the guinea pig ileum. The outside diameter of arterioles in in vitro submucosal preparations from milk-sensitized guinea pigs was monitored using videomicroscopy. Superfusion of the cow's milk protein, beta-lactoglobulin (beta-Lg; 5 microM), evoked large dilations, which became completely desensitized. beta-Lg-evoked dilations were blocked by pyrilamine or NG-monomethyl-L-arginine plus indomethacin but not by TTX. Electron microscopic studies revealed that mast cells, in preparations receiving beta-Lg, demonstrated significant reductions of the dispersed and intact granule areas compared with preparations not exposed to beta-Lg. Paired experiments were conducted to determine if capsaicin-sensitive, nerve-evoked responses involved mast cell degranulation. One preparation received capsaicin (200 nM) followed by beta-Lg (5 microM); the other preparation received the drugs in reverse order. Prior treatment with capsaicin or beta-Lg had no effect on subsequent dilations evoked by the alternate treatment. Electron microscopy showed that nerve-arteriole associations were 10 times closer than nerve-mast cell associations. Mast cell numbers were not increased by milk sensitization. These findings suggest that mast cell- and capsaicin-sensitive nerve-evoked vasodilator mechanisms act independently in a model in which mast cell numbers are not increased.
机译:这项研究的特点是调节豚鼠回肠粘膜下小动脉的肥大细胞和辣椒素敏感的感觉神经血管舒张机制。使用视频显微镜对牛奶致敏的豚鼠的体外粘膜下制剂中小动脉的外径进行监控。牛奶蛋白β-乳球蛋白(β-Lg; 5 microM)的过度融合引起了较大的扩张,从而使它们完全脱敏。 β-Lg诱发的扩张被吡拉明或NG-单甲基-L-精氨酸加消炎痛阻断,但未被TTX阻断。电子显微镜研究表明,与未暴露于β-Lg的制剂相比,接受β-Lg的制剂中的肥大细胞显示出分散和完整颗粒区域的显着减少。进行配对实验以确定辣椒素敏感的,神经诱发的反应是否涉及肥大细胞脱粒。一种制剂接受辣椒素(200 nM),然后接受β-Lg(5 microM);另一种制剂则以相反的顺序收到药物。辣椒素或β-Lg先前治疗对替代治疗引起的后续扩张没有影响。电子显微镜显示,神经-小动脉关联比神经-肥大细胞关联近十倍。乳汁致敏并未增加肥大细胞数目。这些发现表明,肥大细胞和辣椒素敏感的神经诱发的血管舒张机制在肥大细胞数量不增加的模型中独立起作用。

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