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Functional characterisation of tachykinin receptors in the circular muscle layer of the mouse ileum.

机译:小鼠回肠环形肌层中速激肽受体的功能表征。

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OBJECTIVES: Tachykinins are important mediators in neuromuscular signalling but have not been thoroughly characterised in the mouse gut. We investigated the participation of tachykinin receptors in contractility of circular muscle strips of the mouse ileum. RESULTS: Electrical field stimulation (EFS) of excitatory nonadrenergic noncholinergic (NANC) nerves induced frequency-dependent contractions which were mimicked by substance P (SP). Desensitisation of SP and NK(1), NK(2) or NK(3) receptors significantly reduced contractions to EFS. The NK(1) receptor blocker RP67580 significantly inhibited NANC contractions to EFS. The NK(2) and NK(3) receptor blockers nepadutant and SR142801 did not affect NANC contractions per se but increased the RP67580-induced inhibition of NANC contractions to EFS. Contractions to SP were significantly reduced by RP67580 but not affected by nepadutant or SR142801. The NK(1) and NK(2) receptor agonists, septide and [beta-ala(8)]-NKA 4-10 (beta-A-NKA), respectively, but not theNK(3) receptor agonist senktide-induced dose-dependent contractions. Atropine inhibited and l-NNA augmented contractions to septide. Contractions to beta-A-NKA were insensitive to atropine but augmented by l-NNA. CONCLUSIONS: Tachykinins mediate NANC contractions to EFS in the mouse small intestine. Endogenously released tachykinins activate mainly NK(1) receptors, located on cholinergic nerves and smooth muscle cells and, to a lesser degree, NK(2) and NK(3) receptors, most likely located presynaptically.
机译:目的:速激肽是神经肌肉信号传导的重要介体,但尚未在小鼠肠道中得到充分表征。我们调查了速激肽受体在小鼠回肠环形肌条收缩中的参与。结果:兴奋性非肾上腺能非胆碱能(NANC)神经的电场刺激(EFS)诱导了频率依赖性收缩,而收缩率则被P物质(SP)所模仿。 SP和NK(1),NK(2)或NK(3)受体的脱敏作用显着减少了对EFS的收缩。 NK(1)受体阻滞剂RP67580显着抑制NANC收缩至EFS。 NK(2)和NK(3)受体阻滞剂nepadutant和SR142801本身不影响NANC收缩,但增加了RP67580诱导的对EFS的NANC收缩的抑制作用。 RP67580显着降低了SP的收缩,但不受nepadutant或SR142801的影响。 NK(1)和NK(2)受体激动剂,肽和[β-ala(8)]-NKA 4-10(beta-A-NKA)分别,但不是NK(3)受体激动剂senktide诱导的剂量依赖性收缩。阿托品抑制和l-NNA收缩至肽段。 β-A-NKA的收缩对阿托品不敏感,但被l-NNA增强。结论:速激肽在小鼠小肠中介导NANC收缩至EFS。内源释放的速激肽主要激活位于胆碱能神经和平滑肌细胞上的NK(1)受体,以及在较小程度上最可能位于突触前的NK(2)和NK(3)受体。

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