Wang X M, Zhang K M, Long L O, Mokha S S
Department of Anatomy and Physiology, Meharry Medical College, Nashville, TN 37208, USA.
Neuroscience. 1999;93(2):703-12. doi: 10.1016/s0306-4522(99)00188-8.
The present investigation details the modulation of medullary dorsal horn neuron responses to excitatory amino acids and peripheral cutaneous stimuli by orphanin FQ (nociceptin), an endogenous ligand for the opioid receptor-like, receptor. Effects of orphanin FQ, administered microiontophoretically or given intracerebroventricularly, were tested on the responses of nociceptive-specific, wide dynamic range and low threshold neurons recorded in the superficial and deeper dorsal horn of the medulla (trigeminal nucleus caudalis) in anesthetized (urethane or pentobarbital) male rats. Microiontophoretic application of orphanin FQ reduced the N-methyl-D-aspartate-evoked responses in 86% (71/82) of neurons, and the (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-evoked responses in 86% (30/35) of neurons. However, orphanin FQ produced a longer lasting inhibitory effect on the N-methyl-D-aspartate-evoked responses relative to the (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-evoked responses. The inhibitory effect of orphanin FQ was not modality-specific, responses evoked by noxious as well as non-noxious stimuli were reduced in 22/23 neurons. However, the inhibitory effect was more pronounced on noxious stimulus-evoked responses. Naloxone applied at currents that antagonized the inhibitory effects of selective agonists at mu and kappa opioid receptors failed to inhibit the effects of orphanin FQ. Microiontophoretic co-application of substance P with N-methyl-D-aspartate facilitated the N-methyl-D-aspartate-evoked responses in 52% (26/50) of nociceptive neurons. Orphanin FQ blocked or reduced the substance P-induced facilitation by 86+/-24.4% (n = 14). In order to compare electrophysiological data with previous behavioral observations, effects of orphanin FQ administered intracerebroventricularly were tested on the excitatory amino acid-evoked responses. Orphanin FQ reduced the N-methyl-D-aspartate-evoked responses in 85% (11/13) of neurons whereas the (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid-evoked responses were facilitated in 69% (9/13) of neurons. We suggest that orphanin FQ produces a predominantly inhibitory effect on, (i) noxious stimuli evoked responses, (ii) excitatory amino acid receptor-mediated transmission and, (iii) the substance P-induced facilitation of the N-methyl-D-aspartate-evoked responses. We conclude that orphanin FQ primarily produced an antinociceptive action at the level of the dorsal horn of the medulla.
本研究详细阐述了孤啡肽FQ(痛敏肽)对延髓背角神经元对兴奋性氨基酸和外周皮肤刺激反应的调节作用,孤啡肽FQ是阿片样受体样受体的内源性配体。通过微量离子导入法或脑室内注射给予孤啡肽FQ,检测其对麻醉(乌拉坦或戊巴比妥)雄性大鼠延髓(三叉神经尾核)浅部和深部背角记录的伤害性特异性、广动力范围和低阈值神经元反应的影响。微量离子导入法应用孤啡肽FQ可使86%(71/82)的神经元中N-甲基-D-天冬氨酸诱发的反应降低,86%(30/35)的神经元中(±)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸诱发的反应降低。然而,相对于(±)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸诱发的反应,孤啡肽FQ对N-甲基-D-天冬氨酸诱发的反应产生的抑制作用持续时间更长。孤啡肽FQ的抑制作用并非模式特异性,在22/23个神经元中,有害和无害刺激诱发的反应均降低。然而,对有害刺激诱发的反应,抑制作用更为明显。在能拮抗μ和κ阿片受体选择性激动剂抑制作用的电流下应用纳洛酮,未能抑制孤啡肽FQ的作用。微量离子导入法将P物质与N-甲基-D-天冬氨酸共同应用,可使52%(26/50)的伤害性神经元中N-甲基-D-天冬氨酸诱发的反应增强。孤啡肽FQ可阻断或降低P物质诱导的增强作用,降低幅度为86±24.4%(n = 14)。为了将电生理数据与先前的行为观察结果进行比较,检测了脑室内注射孤啡肽FQ对兴奋性氨基酸诱发反应的影响。孤啡肽FQ可使85%(11/13)的神经元中N-甲基-D-天冬氨酸诱发的反应降低,而69%(9/13)的神经元中(±)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸诱发的反应增强。我们认为,孤啡肽FQ对(i)有害刺激诱发的反应、(ii)兴奋性氨基酸受体介导的传递以及(iii)P物质诱导的N-甲基-D-天冬氨酸诱发反应的增强作用主要产生抑制效应。我们得出结论,孤啡肽FQ主要在延髓背角水平产生抗伤害感受作用。