Beleslin D B, Terzić B
Acta Physiol Hung. 1987;69(1):105-14.
Leucine (leu)-enkephalin depresses or inhibits the peristaltic reflex of the isolated guinea-pig ileum. Opiate antagonists (naloxone and nalorphine), choline esters (acetylcholine, methacholine and carbachol), cholinomimetics (muscarine and arecoline) and polypeptides which stimulate peristalsis (eledoisin and angiotensin) antagonize the peristaltic block caused by leu-enkephalin. On the other hand, nicotinic ganglionic stimulants (nicotine and dimethylphenylpiperazine) as well as muscarinic ganglionic stimulants (McN-A-343 and AHR-602) do not restore the peristaltic reflex abolished by leu-enkephalin. Thus the inhibitory effect of leu-enkephalin is due mainly to an action on myenteric ganglia as well as on axon terminals of the myenteric plexus subserving the peristaltic reflex. The inhibitory action of leu-enkephalin may be ascribed to the opiate as well as to the cholinoceptive sites in the nervous elements in the myenteric plexus. The blocking action of leu-enkephalin is not associated with ganglionic muscarinic M-1 receptors as well as with ganglionic nicotinic receptors in the myenteric plexus of the guinea-pig isolated ileum.
亮氨酸脑啡肽可抑制或减弱离体豚鼠回肠的蠕动反射。阿片拮抗剂(纳洛酮和烯丙吗啡)、胆碱酯类(乙酰胆碱、醋甲胆碱和卡巴胆碱)、拟胆碱药(毒蕈碱和槟榔碱)以及刺激蠕动的多肽(依地多辛和血管紧张素)可拮抗亮氨酸脑啡肽引起的蠕动阻断。另一方面,烟碱型神经节兴奋剂(尼古丁和二甲基苯基哌嗪)以及毒蕈碱型神经节兴奋剂(McN-A-343和AHR-602)不能恢复被亮氨酸脑啡肽消除的蠕动反射。因此,亮氨酸脑啡肽的抑制作用主要是由于其作用于肌间神经节以及支配蠕动反射的肌间神经丛的轴突终末。亮氨酸脑啡肽的抑制作用可能归因于肌间神经丛神经元件中的阿片样物质以及胆碱能感受位点。亮氨酸脑啡肽的阻断作用与豚鼠离体回肠肌间神经丛中的神经节毒蕈碱M-1受体以及神经节烟碱受体无关。