首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >The role of protease-activated receptor-2 (PAR2) in the modulation of beating of the mouse isolated ureter: lack of involvement of mast cells or sensory nerves
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The role of protease-activated receptor-2 (PAR2) in the modulation of beating of the mouse isolated ureter: lack of involvement of mast cells or sensory nerves

机译:蛋白酶激活受体2(PAR2)在调节小鼠离体输尿管搏动中的作用:肥大细胞或感觉神经缺乏参与

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class="enumerated" style="list-style-type:decimal">The localization of protease-activated receptor-2 (PAR2) and the effects of PAR2 activators were investigated in the mouse isolated ureter in order to test the hypothesis that PAR2 activation may initiate neuropeptide release from sensory nerve fibres and hence contribute to inflammation.PAR2 was localized by fluorescence immunohistochemistry to both the smooth muscle and epithelium of the ureter. Macrophage-like cells in the adventitia of the ureter were also PAR2-immunoreactive. PAR2-immunoreactivity was not observed in mast cells or nerve fibres.In circular muscle preparations of the ureter in which continuous rhythmic beating was induced by KCl (20 mM) and the thromboxane A2 mimetic U46619 (0.3 μM), trypsin (0.3 U ml−1) reduced beat frequency to 84.6±2.0% of control rates. The PAR2-selective peptide agonist SLIGRL-NH2 concentration-dependently (0.1–3.0 μM) slowed beat frequency to a maximum of 72.7±2.0%.Histamine (1–300 μM) was more efficacious than SLIGRL-NH2 in inhibiting ureter beat frequency in a concentration-dependent manner to a maximum (at 300 μM) of 7.9±2.5% of the control rate.Pretreatment of preparations with capsaicin (10 μM for 30 min) markedly attenuated the inhibitory effect of histamine, but not that of SLIGRL-NH2, indicating a role for sensory nerves in the inhibitory effect of histamine only.The inhibitory effect of SLIGRL-NH2 on ureter beat frequency was unaffected by the nitric oxide (NO) synthase inhibitor, L-NOARG (100 μM) or the cyclo-oxygenase inhibitor, indomethacin (3 μM).In conclusion, PAR2 activation causes inhibition of beating in the mouse ureter that is not mediated by axon reflex release of inhibitory neuropeptides. This inhibitory effect of PAR2 appears to be mediated directly on smooth muscle cells, although the contribution of non-NO, non-prostanoid epithelium-derived factors cannot be ruled out.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在小鼠离体输尿管中研究了蛋白酶激活受体2(PAR2)的定位和PAR2激活剂的作用,以检验PAR2激活可能启动感觉神经纤维释放神经肽从而导致炎症的假设。通过荧光免疫组织化学将li 2 PAR2定位于输尿管的平滑肌和上皮。输尿管外膜中的巨噬细胞样细胞也具有PAR2免疫反应性。在肥大细胞或神经纤维中未观察到PAR2免疫反应。 在输尿管的环形肌肉制剂中,KCl(20 mM)和血栓烷A2模仿U46619(0.3μM)引起连续节律性跳动。 ,胰蛋白酶(0.3 U ml -1 )将搏动频率降低至控制率的84.6±2.0%。 PAR2选择性肽激动剂SLIGRL-NH2浓度依赖性地(0.1–3.0μM)将搏动频率减慢至最大72.7±2.0%。 组胺(1–300μM)比SLIGRL-更有效NH2以浓度依赖的方式抑制输尿管搏动的频率,最大达到控制速率的7.9±2.5%(在300μM时)。 用辣椒素预处理制剂(10μM持续30 min)减弱了组胺的抑制作用,但没有减弱SLIGRL-NH2的抑制作用,表明感觉神经仅在抑制组胺中起作用。 SLIGRL-NH2对输尿管搏动频率的抑制作用不受一氧化氮(NO)合酶抑制剂L-NOARG(100μm)或环加氧酶抑制剂吲哚美辛(3μμM)。 总而言之,PAR2激活会抑制小鼠输尿管的跳动,即不是由抑制性神经肽的轴突反射释放介导的。尽管不能排除非NO,非前列腺素上皮衍生因子的作用,但PAR2的这种抑制作用似乎直接在平滑肌细胞上介导。

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