Huidobro-Toro J P, Zhu Y X
Eur J Pharmacol. 1984 Jul 13;102(2):237-50. doi: 10.1016/0014-2999(84)90255-3.
Neurotensin caused a complex muscular response of the longitudinal muscle-myenteric plexus preparation of guinea-pig ileum: picomoles of neurotensin produced inhibition while larger concentrations caused an inhibitory effect followed by a delayed dose-dependent contraction. The inhibitory phase of the neurotensin-induced muscular activity was not modified by tetrodotoxin but was potently antagonized in a non-competitive manner by apamin, a bee venom toxin. The contractile component was blocked by tetrodotoxin but not by apamin. These toxins were used to dissect the neurotensin muscular response into an inhibitory phase and an excitatory component. It was possible to further characterize the two neurotensin muscular components by their kinetics of desensitization. The inhibitory neurotensin response showed a fast rate of desensitization and presented a relatively low spare receptor capacity. In contrast, desensitization to the excitatory action of neurotensin was much slower, the excitatory receptors apparently having a larger spare receptor capacity. Desensitization to the action of neurotensin was selective for the neuropeptide not altering the contractile activity of substance P, angiotensin II, bradykinin, histamine or acetylcholine. These results strongly suggest the presence of two subsets of neurotensin receptors in the ileum: the inhibitory set probably localized at the postsynaptic effector level and excitatory neurotensin receptors probably of neuronal origin whose function is probably to modulate the release of neurotransmitters. The physiological implications of these two subtypes of neurotensin receptors in the control of gastrointestinal motility are discussed.
神经降压素可引起豚鼠回肠纵行肌-肌间神经丛标本复杂的肌肉反应:皮摩尔量的神经降压素产生抑制作用,而较高浓度则先产生抑制作用,随后出现延迟的剂量依赖性收缩。神经降压素诱导的肌肉活动的抑制阶段不受河豚毒素影响,但被蜂毒毒素蜂毒明肽以非竞争性方式强烈拮抗。收缩成分被河豚毒素阻断,但不受蜂毒明肽影响。这些毒素被用于将神经降压素的肌肉反应分解为抑制阶段和兴奋成分。通过脱敏动力学可以进一步表征神经降压素的两种肌肉成分。抑制性神经降压素反应显示出快速的脱敏速率,且备用受体容量相对较低。相比之下,对神经降压素兴奋作用的脱敏要慢得多,兴奋性受体显然具有更大的备用受体容量。对神经降压素作用的脱敏对该神经肽具有选择性,不改变P物质、血管紧张素II、缓激肽、组胺或乙酰胆碱的收缩活性。这些结果强烈提示回肠中存在两种神经降压素受体亚型:抑制性受体可能位于突触后效应器水平,兴奋性神经降压素受体可能起源于神经元,其功能可能是调节神经递质的释放。本文讨论了这两种神经降压素受体亚型在控制胃肠动力方面的生理意义。