Holzer P
Department of Experimental and Clinical Pharmacology, University of Graz, Austria.
Am J Physiol. 1989 Mar;256(3 Pt 1):G540-5. doi: 10.1152/ajpgi.1989.256.3.G540.
Isolated segments of the guinea pig small intestine were used to examine the transmitter circuitry of the neural pathways subserving the ascending enteric reflex (AER) contraction of the circular muscle. Inflation of an intraluminal balloon provided the distension stimulus for the AER. The ascending contraction was reduced to 5% of its original amplitude by atropine and to 10% by hexamethonium, which indicates that cholinergic interneurons and cholinergic motor neurons constitute the main AER pathway. However, in the continued presence of atropine or hexamethonium for 60 min, the AER recovered to approximately 30% of its original amplitude. The atropine-resistant AER was blocked by hexamethonium and the tachykinin antagonist spantide [( D-Arg1,D-Trp7,9, Leu11]-substance P) suggesting that it involved cholinergic interneurons and tachykinin-utilizing motor neurons. The hexamethonium-resistant AER was abolished by atropine but left unaffected by spantide, suggesting the participation of as yet unidentified interneurons and cholinergic motor neurons. These findings demonstrate that the AER is mediated by multiple neural pathways with different transmitters and that adaptive interactions between these pathways take place after blockade of one of its neurotransmitters systems.
使用豚鼠小肠的离体节段来检查介导环行肌升结肠反射(AER)收缩的神经通路的递质回路。腔内气囊充气为AER提供扩张刺激。阿托品使升结肠收缩幅度降至其原始幅度的5%,六甲铵使其降至10%,这表明胆碱能中间神经元和胆碱能运动神经元构成了主要的AER通路。然而,在持续存在阿托品或六甲铵60分钟的情况下,AER恢复至其原始幅度的约30%。阿托品抵抗性AER被六甲铵和速激肽拮抗剂spantide [(D-Arg1,D-Trp7,9,Leu11)-P物质]阻断,表明其涉及胆碱能中间神经元和利用速激肽的运动神经元。六甲铵抵抗性AER被阿托品消除,但不受spantide影响,提示存在尚未明确的中间神经元和胆碱能运动神经元参与。这些发现表明,AER由具有不同递质的多条神经通路介导,并且在其一种神经递质系统被阻断后,这些通路之间会发生适应性相互作用。