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研究猪降结肠环形平滑肌中神经源性兴奋和抑制性运动反应及其 5-HT(4)受体的控制作用。

Investigation of neurogenic excitatory and inhibitory motor responses and their control by 5-HT(4) receptors in circular smooth muscle of pig descending colon.

机构信息

Heymans Institute of Pharmacology, Ghent University, Ghent, Belgium.

出版信息

Eur J Pharmacol. 2011 Sep 30;667(1-3):365-74. doi: 10.1016/j.ejphar.2011.06.021. Epub 2011 Jun 26.

Abstract

The aim of this study was to investigate whether the pig colon descendens might be a good model for the responses mediated via the different locations of human colonic 5-HT(4) receptors. The intrinsic excitatory and inhibitory motor neurotransmission in pig colon descendens was therefore first characterized. In circular smooth muscle strips, electrical field stimulation (EFS) at basal tone induced only in the combined presence of the NO synthase inhibitor N(ω)-nitro-L-arginine methyl ester hydrochloride (L-NAME) and the SK channel blocker apamin voltage-dependent on-contractions. These on-contractions were largely reduced by the neuronal conductance blocker tetrodotoxin (TTX) and by the muscarinic receptor antagonist atropine, illustrating activation of cholinergic neurons. The 5-HT(4) receptor agonist prucalopride facilitated submaximal EFS-evoked cholinergic contractions and this effect was prevented by the 5-HT(4) receptor antagonist GR113808, supporting the presence of facilitating 5-HT(4) receptors on the cholinergic nerve endings innervating circular muscle in pig colon descendens. Relaxations were induced by EFS in strips pre-contracted with substance P in the presence of atropine. The responses at lower stimulation voltages were abolished by TTX. L-NAME or apamin alone did not influence or only moderately reduced the relaxations, but L-NAME plus apamin abolished the relaxations at lower stimulation voltages, suggesting that NO and ATP act as inhibitory neurotransmitters in a redundant way. Prucalopride did not influence the EFS-induced relaxations at lower stimulation voltage, nor did it per se relax contracted circular muscle strips. No evidence for relaxing 5-HT(4) receptors, either on inhibitory neurons or on the muscle cells was thus obtained in pig colon descendens circular muscle.

摘要

本研究旨在探讨猪降结肠是否可以成为人类结肠 5-HT(4)受体不同部位介导反应的良好模型。因此,首先对猪降结肠的内在兴奋性和抑制性运动神经传递进行了特征描述。在环形平滑肌条带中,基础张力下的电刺激(EFS)仅在一氧化氮合酶抑制剂 N(ω)-硝基-L-精氨酸甲酯盐酸盐(L-NAME)和 SK 通道阻滞剂蜂毒肽的共同存在下才会引起电压依赖性的收缩。这些收缩主要被神经元电导率阻滞剂河豚毒素(TTX)和毒蕈碱受体拮抗剂阿托品所减少,这表明胆碱能神经元被激活。5-HT(4)受体激动剂普卡必利促进了次最大 EFS 诱发的胆碱能收缩,而这种作用被 5-HT(4)受体拮抗剂 GR113808 所阻止,这支持了促进 5-HT(4)受体存在于支配猪降结肠环形肌的胆碱能神经末梢上。在有阿托品存在的情况下,在预先用 P 物质收缩的条带中进行 EFS 诱导松弛。较低刺激电压的反应被 TTX 消除。L-NAME 或蜂毒肽单独使用不会影响或仅适度减少松弛,但 L-NAME 加蜂毒肽会消除较低刺激电压下的松弛,这表明 NO 和 ATP 以冗余方式作为抑制性神经递质发挥作用。普卡必利对较低刺激电压下的 EFS 诱导松弛没有影响,也不能使收缩的环形肌条带本身松弛。因此,在猪降结肠环形肌中,没有证据表明 5-HT(4)受体具有松弛作用,无论是在抑制性神经元上还是在肌肉细胞上。

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