Jeanjean A P, Maloteaux J M, Laduron P M
Laboratoire de Neurochimie, Université Catholique de Louvain, Bruxelles, Belgium.
Neurosci Lett. 1994 Aug 15;177(1-2):75-8. doi: 10.1016/0304-3940(94)90048-5.
Chronic pain and inflammation increase substance P in sensory fibres of peripheral nerves in which opiate receptors are known to undergo axonal transport. The aim of the present study was to evaluate a possible modulation of axonal transport of opiate receptors in peripheral nerves during inflammation. After intraplantar injection of Freund's adjuvant to rats, the accumulation of mu and kappa opiate receptors increased on both sides of ligature in sciatic nerves of the injected paw. The contralateral side was unaffected and may serve as control. When IL-1 beta was injected into rat paws, the axonal transport of opiate receptors was increased in a similar way. This suggests that IL-1 beta represents a major mediator to sensitize nociceptors during inflammation through a process requiring retrograde signals.
慢性疼痛和炎症会增加外周神经感觉纤维中的P物质,已知阿片受体在这些纤维中会进行轴突运输。本研究的目的是评估炎症期间外周神经中阿片受体轴突运输的可能调节情况。给大鼠足底注射弗氏佐剂后,注射侧爪坐骨神经结扎两侧的μ和κ阿片受体积累增加。对侧未受影响,可作为对照。当将白细胞介素-1β注入大鼠爪时,阿片受体的轴突运输也以类似方式增加。这表明白细胞介素-1β是炎症期间通过需要逆行信号的过程使伤害感受器敏感化的主要介质。