Onori Luciano, Aggio Annalisa, Taddei Gennaro, Loreto Maria F, Ciccocioppo Rachele, Vicini Riccardo, Tonini Marcello
Dept. of Internal Medicine and Public Health, Univ. of L'Aquila, Italy.
Am J Physiol Gastrointest Liver Physiol. 2003 Aug;285(2):G325-31. doi: 10.1152/ajpgi.00411.2002. Epub 2003 Mar 26.
In the gastrointestinal tract, tachykinin NK1 receptors are widely distributed in a number of neuronal and nonneuronal cells involved in the control of gut motor activity. In particular, in the rabbit isolated distal colon, which is a suitable model system to investigate the contribution of tachykinins as noncholinergic excitatory transmitters, the influence of NK1 receptors in the regulation of peristalsis is not known. The selective NK1-receptor antagonists SR-140333 (0.3 and 1 nM) and MEN-10930 (0.3-10 nM) significantly enhanced the velocity of rabbit colonic propulsion to submaximal stimulation. The prokinetic effect of SR-140333 was prevented by N(omega)-nitro-L-arginine (L-NNA), a nitric oxide synthase inhibitor, indicating that NK1 receptors located on nitrergic innervation exert a functional inhibitory restraint on the circular muscle and probably on descending excitatory and inhibitory pathways during propulsion. Conversely, the selective NK1-receptor agonist septide (3-10 nM) significantly inhibited colonic propulsion. In the presence of L-NNA, the inhibitory effect of septide was reverted into a prokinetic effect, which is probably mediated by the activation of postjunctional excitatory NK1 receptors.
在胃肠道中,速激肽NK1受体广泛分布于许多参与肠道运动活动控制的神经元和非神经元细胞中。特别是在兔离体远端结肠中,这是一个研究速激肽作为非胆碱能兴奋性递质作用的合适模型系统,但NK1受体在蠕动调节中的影响尚不清楚。选择性NK1受体拮抗剂SR-140333(0.3和1 nM)和MEN-10930(0.3 - 10 nM)显著提高了兔结肠推进速度至次最大刺激水平。一氧化氮合酶抑制剂N(ω)-硝基-L-精氨酸(L-NNA)可阻止SR-140333的促动力作用,这表明位于氮能神经支配上的NK1受体在推进过程中对环行肌以及可能对下行的兴奋性和抑制性通路发挥功能性抑制作用。相反,选择性NK1受体激动剂septide(3 - 10 nM)显著抑制结肠推进。在L-NNA存在时.septide的抑制作用转变为促动力作用,这可能是由节后兴奋性NK1受体的激活介导的。