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Effect of sodium rhein on electrically-evoked and agonist-induced contractions of the guinea-pig isolated ileal circular muscle

机译:大黄素钠对豚鼠离体回肠环形肌电诱发和激动剂诱导的收缩的影响

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摘要

class="enumerated" style="list-style-type:decimal">This study examined the effects of sodium rhein (0.03–30 μM) on the contractions of the isolated circular muscle of guinea-pig ileum induced by acetylcholine (100 nM), substance P (3 nM) and electrical stimulation (10 Hz for 0.3 s, 100 mA, 0.5 ms pulse duration). The effect of sodium rhein was also evaluated on the ascending excitatory reflex using a partitioned bath (oral and anal compartments). Ascending excitatory enteric nerve pathways were activated by electrical field stimulation (10 Hz for 2 s, 20 mA, 0.5 pulse duration) in the anal compartment and the resulting contraction of the guinea-pig intestinal circular muscle in the oral compartment was recorded.Sodium rhein (0.3, 3 and 30 μM) significantly potentiated (52±11% at 30 μM) acetylcholine-induced contractions. In the presence of tetrodotoxin (0.6 μM) or ω-conotoxin GVIA (10 nM) sodium rhein (3 and 30 μM) did not enhance, but significantly reduced (49±10% and 44±8%, respectively, at 30 μM) acetylcholine-induced contractions.Sodium rhein (0.3, 3 and 30 μM) significantly increased (65±11% at 30 μM) substance P-induced contractions. In the presence of tetrodotoxin (0.6 μM), ω-conotoxin GVIA (10 nM) or atropine (0.1 μM), sodium rhein (3 and 30 μM) significantly reduced (50±10%, 55±8% and 46±10%, respectively, at 30 μM) substance P-induced contractions.NG-nitro- class="small-caps">L-arginine methyl ester ( class="small-caps">L-NAME, 100 μ class="small-caps">M) abolished the potentiating effect of sodium rhein on acetylcholine and substance P-induced contractions. At the highest concentration (30 μ class="small-caps">M), sodium rhein, in presence of class="small-caps">L-NAME, reduced the acetylcholine (30±6%)- or substance P (36±6%)-induced contractions.Sodium rhein (30 μ class="small-caps">M) significantly potentiated (29±9%) the electrically-evoked contractions. class="small-caps">L-NAME (100 μ class="small-caps">M), but not phentolamine, enhanced the effect of sodium rhein. Sodium rhein (30 μ class="small-caps">M) significantly increased (32±9%) the ascending excitatory reflex when applied in the oral, but not in the anal compartment.These results indicate that sodium rhein (i) activates excitatory cholinergic nerves on circular smooth muscle presumably through a facilitation of Ca2+ entry through the N-type Ca2+ channel, (ii) has a direct inhibitory effect on circular smooth muscle and (iii) does not affect enteric ascending neuroneural transmission. Nitric oxide could have a modulatory excitatory role on sodium rhein-induced changes of agonist-induced contractions and an inhibitory modulator role on sodium rhein-induced changes of electrically-induced contractions.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 这项研究探讨了大黄酸钠(0.03–30 M)对乙酰胆碱(100 nM),P物质(3 nM)和电刺激(10 Hz持续0.3 s)诱导的豚鼠回肠离体环形肌收缩的影响。 ,100µmA,0.5µms脉冲持续时间)。还使用分隔水浴(口腔和肛门隔室)评估了大黄酸钠对上升兴奋性反射的作用。电场刺激(10 Hz 2 s,20 mA,0.5脉冲持续时间)激活肛门腔内的上升性兴奋性肠神经通路,并记录豚鼠肠内环形肌在口腔腔内的收缩情况。大黄酸钠(0.3、3和30μM)显着增强了乙酰胆碱引起的收缩(在30μM时为52±11%)。在存在河豚毒素(0.6μM)或ω-芋螺毒素GVIA(10 nM)的情况下,大黄素钠(3和30μM)没有增强,但显着降低(30μM时分别为49±10%和44±8%)。乙酰胆碱引起的收缩。 大黄素钠(0.3、3和30μm)显着增加(在30μμM时为65±11%)P物质引起的收缩。在存在河豚毒素(0.6μM),ω-芋螺毒素GVIA(10 nM)或阿托品(0.1μM)的情况下,大黄素钠(3和30μM)显着降低(50±10%,55±8%和46±10%) N G -硝基- class =“ small-caps”> L -精氨酸甲基酯( class =“ small-caps”> L -NAME,100μ class =“ small-caps”> M )取消了大黄素钠对乙酰胆碱和P物质的增强作用引起的收缩。在最高浓度(30μm class =“ small-caps”> M )下,大黄素钠在 class =“ small-caps”> L -NAME的存在下降低了乙酰胆碱(30±6%)-或P物质(36±6%)引起的收缩。 大黄酸钠(30μ class =“ small-caps”> M )明显增强(29±9%)电诱发的收缩。 class =“ small-caps”> L -NAME(100μ class =“ small-caps”> M )而非酚妥拉明可增强大黄酸钠的效果。口服时,大黄酸钠(30μm class =“ small-caps”> M )可显着提高(32±9%)上升兴奋性反射,但在肛门隔室则无作用。 这些结果表明,大黄素(i)可能通过促进Ca 2 + 通过N型Ca 2 + 通道,(ii)对圆形平滑肌具有直接抑制作用,并且(iii)不影响肠上行神经神经传递。一氧化氮可能对大黄素钠引起的激动剂收缩引起调节性兴奋作用,而对大黄素钠引起的电气收缩引起抑制作用。

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