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豚鼠回肠运动反射过程中神经元NK1和NK3受体在突触传递中的作用。

Roles of neuronal NK1 and NK3 receptors in synaptic transmission during motility reflexes in the guinea-pig ileum.

作者信息

Johnson P J, Bornstein J C, Burcher E

机构信息

Department of Physiology, University of Melbourne, Parkville, Victoria, Australia.

出版信息

Br J Pharmacol. 1998 Aug;124(7):1375-84. doi: 10.1038/sj.bjp.0701967.

Abstract
  1. The role of NK1 and NK3 receptors in synaptic transmission between myenteric neurons during motility reflexes in the guinea-pig ileum was investigated by recording intracellularly the reflex responses of the circular muscle to distension or compression of the mucosal villi. Experiments were performed in a three-chambered organ bath that enabled drugs to be selectively applied to different sites along the reflex pathways. 2. When applied in the recording chamber, an NK1 receptor antagonist, SR140333 (100 nM), reduced by 40-50% the amplitudes of inhibitory junction potentials (i.j.ps) evoked in the circular muscle by activation of descending reflex pathways. This effect was abolished when synaptic transmission in the stimulus region was blocked with physiological saline containing 0.1 mM Ca2+ plus 10 mM Mg2+, leaving only the component of the descending reflex pathway conducted via long anally directed collaterals of intrinsic sensory neurons. 3. SR140333 (100 nM) had no effect on descending reflex i.j.ps when applied to the stimulus region. Ascending reflexes were also unaffected by SR140333 in the stimulus region or between the stimulus and recording sites. 4. Septide (10 nM), an NK1 receptor agonist, enhanced descending reflexes by 30-60% when in the recording chamber. [Sar9,Met(O2)11]substance P had no effect at 10 nM, but potentiated distension-evoked reflexes at 100 nM. 5. A selective NK3 receptor antagonist, SR142801 (100 nM), when applied to the stimulus region, reduced the amplitude of descending reflex responses to compression by 40%, but had no effect on responses to distension. SR142801 (100 nM) had no effect when applied to other regions of the descending reflex pathways. 6. SR142801 (100 nM) only inhibited ascending reflexes when applied at the recording site. However, after nicotinic transmission in the stimulus region was blocked, SR142801 (100 nM) at this site reduced responses to compression. 7. Contractions of the circular muscle of isolated rings of ileum evoked by low concentrations of septide, but not [Sar9,Met(O2)11]substance P, were potentiated by tetrodotoxin (300 nM). 8. Contractile responses evoked by an NK3 receptor agonist, senktide, were non-competitively inhibited by SR142801. After excitatory neuromuscular transmission was blocked, senktide produced inhibitory responses that were also antagonised by SR142801, but to a lesser extent and in an apparently competitive manner. 9. These results indicate that tachykinins acting via NK1 receptors partly mediate transmission to inhibitory motor neurons. NK3 receptors play a role in transmission from intrinsic sensory neurons and from ascending interneurons to excitatory motor neurons during motility reflexes.
摘要
  1. 通过细胞内记录豚鼠回肠运动反射期间环形肌对黏膜绒毛扩张或压迫的反射反应,研究了NK1和NK3受体在豚鼠回肠肌间神经元突触传递中的作用。实验在三室器官浴槽中进行,该浴槽能使药物选择性地作用于反射通路的不同部位。2. 当在记录室中应用NK1受体拮抗剂SR140333(100 nM)时,激活下行反射通路在环形肌中诱发的抑制性接头电位(i.j.ps)幅度降低了40 - 50%。当用含0.1 mM Ca2+加10 mM Mg2+的生理盐水阻断刺激区域的突触传递时,这种效应消失,仅留下通过内在感觉神经元向肛门方向的长侧支传导的下行反射通路成分。3. 当将SR140333(100 nM)应用于刺激区域时,对下行反射i.j.ps无影响。刺激区域或刺激与记录部位之间的上行反射也不受SR140333影响。4. NK1受体激动剂Septide(10 nM)在记录室中时,可使下行反射增强30 - 60%。[Sar9,Met(O2)11]P物质在10 nM时无作用,但在100 nM时增强扩张诱发的反射。5. 选择性NK3受体拮抗剂SR142801(100 nM)应用于刺激区域时,可使对压迫的下行反射反应幅度降低40%,但对扩张反应无影响。SR142801(100 nM)应用于下行反射通路的其他区域时无作用。6. SR142801(100 nM)仅在应用于记录部位时抑制上行反射。然而,在刺激区域的烟碱样传递被阻断后,该部位的SR142801(100 nM)可降低对压迫的反应。7. 低浓度的Septide而非[Sar9,Met(O2)11]P物质诱发的离体回肠环行肌收缩,被河豚毒素(300 nM)增强。8. NK3受体激动剂senktide诱发的收缩反应被SR142801非竞争性抑制。在兴奋性神经肌肉传递被阻断后,senktide产生的抑制性反应也被SR142801拮抗,但程度较轻且呈明显的竞争性。9. 这些结果表明,通过NK1受体起作用的速激肽部分介导向抑制性运动神经元的传递。NK3受体在运动反射期间从内在感觉神经元以及从上行中间神经元向兴奋性运动神经元的传递中起作用。

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