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慢传输型便秘患者结肠环行肌中P物质介导的收缩性及速激肽NK1受体表达的环氧化酶依赖性改变

Cyclooxygenase-dependent alterations in substance P-mediated contractility and tachykinin NK1 receptor expression in the colonic circular muscle of patients with slow transit constipation.

作者信息

Liu Lu, Shang Fei, Morgan Matthew J, King Denis W, Lubowski David Z, Burcher Elizabeth

机构信息

Department of Pharmacology, School of Medical Sciences, University of New South Wales, Sydney 2052, Australia.

出版信息

J Pharmacol Exp Ther. 2009 Apr;329(1):282-9. doi: 10.1124/jpet.108.148148. Epub 2009 Jan 22.

Abstract

Tachykinins are important neurotransmitters regulating intestinal motility. Slow transit constipation (STC) represents an extreme colonic dysmotility with unknown etiology that predominantly affects women. We examined whether the tachykinin system is involved in the pathogenesis of STC. Isolated sigmoid colon circular muscle from female STC and control patients was studied using functional and quantitative reverse transcriptase-polymerase chain reaction methods. A possible alteration of neurotransmission was investigated by electrical field stimulation (EFS) and ganglionic stimulation by dimethylphenylpiperazinium (DMPP). Substance P (SP)-mediated contractions in circular muscle strips were significantly diminished in STC compared with age-matched control (P < 0.001). In contrast, contractile responses to neurokinin A, the selective tachykinin NK(2) receptor agonist, [Lys(5),MeLeu(9),Nle(10)]NKA(4-10), and acetylcholine were unaltered in STC. The reduced responses to SP in STC were fully restored by indomethacin, partially reversed by tetrodotoxin (TTX), but unaffected by atropine or hexamethonium. The restoration by indomethacin was blocked by the NK(1) receptor antagonist CP99994 [(2S,3S)-3-(2-methoxybenzylamino)-2-phenylpiperidine] and TTX. In STC colonic muscle, there was a significant increase of NK(1) receptor mRNA expression, but no difference in NK(2) mRNA level. DMPP generated biphasic responses, relaxation at lower and contraction at higher concentrations. Although the responses to DMPP were similar in STC and control, an altered contractile pattern in response to EFS was observed in STC circular muscle. In conclusion, we postulate that the diminished contractile response to SP in STC is due to an increased release of inhibitory prostaglandins through activation of up-regulated NK(1) receptors. Our results also indicate some malfunction of the enteric nervous system in STC.

摘要

速激肽是调节肠道运动的重要神经递质。慢传输型便秘(STC)是一种病因不明的极端结肠运动障碍,主要影响女性。我们研究了速激肽系统是否参与STC的发病机制。使用功能和定量逆转录聚合酶链反应方法,对来自女性STC患者和对照患者的离体乙状结肠环行肌进行了研究。通过电场刺激(EFS)和用二甲基苯基哌嗪(DMPP)进行神经节刺激,研究了神经传递的可能改变。与年龄匹配的对照组相比,STC患者结肠环行肌条中P物质(SP)介导的收缩明显减弱(P < 0.001)。相比之下,STC患者对神经激肽A、选择性速激肽NK(2)受体激动剂[Lys(5),MeLeu(9),Nle(10)]NKA(4-10)和乙酰胆碱的收缩反应未改变。吲哚美辛可使STC患者对SP的反应恢复正常,河豚毒素(TTX)可部分逆转该反应,但阿托品或六甲铵对此无影响。吲哚美辛的恢复作用被NK(1)受体拮抗剂CP99994 [(2S,3S)-3-(2-甲氧基苄基氨基)-2-苯基哌啶]和TTX阻断。在STC结肠肌中,NK(1)受体mRNA表达显著增加,但NK(2) mRNA水平无差异。DMPP产生双相反应,低浓度时舒张,高浓度时收缩。虽然STC患者和对照组对DMPP的反应相似,但在STC结肠环行肌中观察到对EFS的收缩模式改变。总之,我们推测STC患者对SP收缩反应减弱是由于上调的NK(1)受体激活导致抑制性前列腺素释放增加。我们的结果还表明STC患者存在肠神经系统的某些功能障碍。

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