Loescher A R, Boissonade F M, Robinson P P
Department of Oral and Maxillofacial Surgery, School of Clinical Dentistry, Sheffield, UK.
Neurosci Lett. 2001 Mar 9;300(2):71-4. doi: 10.1016/s0304-3940(01)01536-1.
Previous studies in our laboratory have shown that the neuropeptide, calcitonin gene-related peptide (CGRP) accumulates at a site of inferior alveolar nerve injury at the time when high levels of spontaneous activity and mechanical sensitivity are recorded electrophysiologically. The present study was undertaken to determine whether or not the CGRP could be playing a role in initiating or modulating the neuronal activity. In 18 anaesthetised adult ferrets the left inferior alveolar nerve was sectioned and ligated and recovery permitted for 3 days. Under a second anaesthetic recordings were made from a fine nerve filament, containing up to four active or silent units, dissected from the nerve proximal to the injury. After recording activity for a 30 min control period, CGRP and then the CGRP antagonist (CGRP 8-37) were applied either by close-arterial injection or topically (10(-4) M, 0.2 ml). After each application activity was recorded for a 30 min period. Recordings were made from 52 units, of which 26 (50%) were spontaneously active and 30 (58%) were mechanically sensitive. The spontaneous activity in five units was increased by the application of CGRP, and the CGRP antagonist subsequently reduced the activity in two of these units. Activity was induced by CGRP in three previously silent units. Overall, activity was affected in 19% of the units studied. We conclude that CGRP present within a neuroma may initiate or modulate the level of ectopic discharge from some damaged nerve fibres and therefore may contribute to the sensory disturbances which follow nerve injury.
我们实验室之前的研究表明,神经肽降钙素基因相关肽(CGRP)在电生理记录到高水平自发活动和机械敏感性时,会在牙槽下神经损伤部位积聚。本研究旨在确定CGRP是否在启动或调节神经元活动中发挥作用。在18只麻醉的成年雪貂中,切断并结扎左侧牙槽下神经,使其恢复3天。在第二次麻醉下,从损伤近端的神经中分离出一根细神经纤维进行记录,该纤维包含多达四个活跃或静息单位。在记录30分钟的对照期活动后,通过动脉内近距离注射或局部应用(10⁻⁴M,0.2ml)施加CGRP,然后施加CGRP拮抗剂(CGRP 8-37)。每次施加后记录30分钟的活动。共记录了52个单位,其中26个(50%)自发活跃,30个(58%)对机械敏感。应用CGRP后,五个单位的自发活动增加,随后CGRP拮抗剂降低了其中两个单位的活动。CGRP在三个先前静息的单位中诱导了活动。总体而言,在所研究的单位中有19%的活动受到影响。我们得出结论,神经瘤内存在的CGRP可能启动或调节一些受损神经纤维的异位放电水平,因此可能导致神经损伤后的感觉障碍。