Department of Gastroenterology, National Center of Neurology and Psychiatry, Tokyo, Japan.
Department of Psychosomatic Research, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan.
Neurogastroenterol Motil. 2020 Oct;32(10):e13842. doi: 10.1111/nmo.13842. Epub 2020 Mar 20.
Urocortin 1 (Ucn1), a stress-related peptide, is a member of the corticotropin-releasing factor (CRF) family and acts as a CRF1 receptor agonist. Ucn1 and CRF1 receptor immunoreactivity are present in the enteric nervous system (ENS), and Ucn1 elicits contraction of colonic muscle strips. Considering these findings, we have hypothesized that Ucn1 acts as an excitatory neurotransmitter in the ENS. The present study was conducted to determine whether exogenously applied Ucn1 causes contractions, whether it participates in neurally mediated contraction, and whether it is released from the ENS of the rat colon.
Isometric tension of the rat colonic muscle strips (middle to distal colon) in a longitudinal direction was measured. The effects of Ucn1 on phasic contractions were examined in the absence and presence of antalarmin (CRF1 receptor antagonist), tetrodotoxin (TTX), and atropine. The effects of antalarmin on electrical field stimulation (EFS)-induced contractions were examined in the absence and presence of atropine. Ucn1 peptide in the bath solution was measured after EFS using an EIA kit.
Ucn1 caused a significant and dose-dependent increase in phasic contractions. These effects were completely inhibited by antalarmin, TTX, and atropine. EFS-induced contractions were inhibited by antalarmin. Atropine markedly reduced EFS-induced contractions, and antalarmin did not decrease these contractions further. EFS elicited a significant increase in the concentration of Ucn1 in the bath solution, and this increase was completely inhibited by TTX.
These results suggest that Ucn1 acts as an excitatory neurotransmitter in the ENS enhancing the cholinergic neurotransmission.
加压素原 1(Ucn1)是一种与应激相关的肽,是促肾上腺皮质激素释放因子(CRF)家族的成员,作为 CRF1 受体激动剂发挥作用。Ucn1 和 CRF1 受体免疫反应性存在于肠神经系统(ENS)中,Ucn1 引起结肠肌条收缩。鉴于这些发现,我们假设 Ucn1 在 ENS 中作为兴奋性神经递质发挥作用。本研究旨在确定外源性应用 Ucn1 是否引起收缩,是否参与神经介导的收缩,以及是否从大鼠结肠 ENS 释放。
测量大鼠结肠肌条(中至远端结肠)的纵向等长张力。在无和存在 antalarmin(CRF1 受体拮抗剂)、TTX 和阿托品的情况下,检查 Ucn1 对相位收缩的影响。在无和存在阿托品的情况下,检查 antalarmin 对电刺激(EFS)诱导收缩的影响。使用 EIA 试剂盒测量 EFS 后浴液中的 Ucn1 肽。
Ucn1 引起明显的、剂量依赖性的相位收缩增加。这些作用完全被 antalarmin、TTX 和阿托品抑制。EFS 诱导的收缩被 antalarmin 抑制。阿托品显著降低 EFS 诱导的收缩,antalarmin 进一步降低这些收缩。EFS 引起浴液中 Ucn1 浓度显著增加,该增加被 TTX 完全抑制。
这些结果表明,Ucn1 在 ENS 中作为兴奋性神经递质发挥作用,增强胆碱能神经传递。