Barthó L, Sebök B, Szolcsányi J
Eur J Pharmacol. 1982 Feb 5;77(4):273-9. doi: 10.1016/0014-2999(82)90129-7.
There is good evidence indicating that hyoscine-resistant contractions of the guinea-pig ileum evoked by stimulation of the intramural nerves are mediated by substance P (SP). In the present experiments, non-cholinergic neurogenic ileum contractions to field stimulation (100 imp., 5-50 Hz) were inhibited by the opiate agonists morphine and [D-Met2,Pro5]enkephalinamide (10(-6) M) in a naloxone-reversible manner. Neither morphine nor naloxone influenced the musculodirect contracting effect of histamine. Capsaicin, a drug that has been shown to deplete SP from primary afferent neurones, exerted no long-lasting effect on non-cholinergic contractions to field stimulation. Repeated administration of long trains of stimuli (900 impulses) resulted in a progressive decrease of the contractions evoked. Addition of naloxone (3 X 10(-7) M) restored the original height of the responses. The above inhibitory action of opiate agonists and of repeated long-train stimulation was 3-6 times greater at 5 Hz than at 50 Hz. It is concluded that opiate agonists inhibit the release of SP from intramural neurones of the guinea-pit ileum. The decrease in responses to repeated long-train stimulations is mediated, at least in part, by the release of endogenous opioid substance(s).
有充分证据表明,刺激豚鼠回肠壁内神经所诱发的对东莨菪碱耐药的收缩是由P物质(SP)介导的。在本实验中,阿片类激动剂吗啡和[D-蛋氨酸2,脯氨酸5]脑啡肽酰胺(10⁻⁶ M)以纳洛酮可逆的方式抑制了对场刺激(100次脉冲,5 - 50赫兹)的非胆碱能神经源性回肠收缩。吗啡和纳洛酮均未影响组胺的直接肌肉收缩作用。辣椒素是一种已被证明能使初级传入神经元中的P物质耗竭的药物,对场刺激引起的非胆碱能收缩没有持久影响。重复给予长时间的刺激序列(900次脉冲)导致诱发的收缩逐渐减少。加入纳洛酮(3×10⁻⁷ M)可恢复反应的原始高度。阿片类激动剂和重复长时间刺激的上述抑制作用在5赫兹时比在50赫兹时大3 - 6倍。结论是阿片类激动剂抑制豚鼠回肠壁内神经元释放P物质。对重复长时间刺激反应的降低至少部分是由内源性阿片类物质的释放介导的。