Yeomans David C, Proudfit Herbert K
Department of Pharmacology, University of Illinois at Chicago, 835 S. Wolcott,Chicago, IL 60612USA.
Pain. 1996 Nov;68(1):141-150. doi: 10.1016/S0304-3959(96)03177-6.
Behavioral nociceptive responses evoked by relatively high rates of noxious radiant skin heating appear to be mediated by A delta nociceptor activation, whereas responses evoked by low rates of skin heating appear to be mediated by the activation of C-fiber nociceptors. This hypothesis was confirmed by the results of single unit recordings of A delta and C nociceptive afferent fibers isolated from the saphenous nerves of pentobarbital anesthetized rats. Heating the hind paw skin of the rat at a relatively high rate of 6.5 degrees C/sec activated A delta units within 2 sec after the onset of the stimulus. This response latency is similar to the 2.5 sec latency of the foot withdrawal response to a similar stimulus. In contrast, C-fibers were only slightly activated at a longer latency of 5-6 sec. Conversely, heating the hind paw skin at a relatively low rate of 0.9 degrees C/sec activated C-fibers, but evoked only a few action potentials in A delta nociceptors. C-fibers began firing at a rate less than 1 Hz between 8 and 10 sec after the onset of heating and fired at a mean rate of 1.5 Hz between 10 and 12 sec, which corresponds to the latency of the foot withdrawal response. Topical application of capsaicin to the hind paw skin decreased the latency of C-fiber responses from control values of 8-12 sec to approximately 4 sec after topical capsaicin treatment. The mean latency of the foot withdrawal response to skin heating at the low rate is also reduced from control values of 12-14 sec to 4-5 sec after capsaicin treatment. In contrast, capsaicin treatment did not significantly affect the responses of A delta nociceptors. These results support the conclusion that nociceptive foot withdrawal responses to a low rate of skin heating are mediated predominantly by the activation of C-fiber nociceptors. These results provide direct evidence that, under the conditions of these experiments, nociceptive foot withdrawal responses evoked by high rates of skin heating are primarily mediated by A delta nociceptors, and foot withdrawal responses evoked by low rates of skin heating are primarily mediated by C-fiber nociceptors.
相对较高速率的有害辐射皮肤加热所诱发的行为性伤害性反应似乎是由Aδ伤害感受器激活介导的,而低速皮肤加热所诱发的反应似乎是由C纤维伤害感受器的激活介导的。从戊巴比妥麻醉大鼠的隐神经分离出的Aδ和C伤害性传入纤维的单单位记录结果证实了这一假设。以6.5℃/秒的相对高速率加热大鼠后爪皮肤,在刺激开始后2秒内激活了Aδ单位。这种反应潜伏期与对类似刺激的足部退缩反应的2.5秒潜伏期相似。相比之下,C纤维仅在较长的5 - 6秒潜伏期时被轻微激活。相反,以0.9℃/秒的相对低速率加热后爪皮肤激活了C纤维,但在Aδ伤害感受器中仅诱发了少数动作电位。加热开始后8至10秒之间,C纤维开始以小于1赫兹的速率放电,10至12秒之间以平均1.5赫兹的速率放电,这与足部退缩反应的潜伏期相对应。将辣椒素局部应用于后爪皮肤,使C纤维反应的潜伏期从对照值8 - 12秒缩短至局部应用辣椒素处理后的约4秒。辣椒素处理后,对低速皮肤加热的足部退缩反应的平均潜伏期也从对照值12 - 14秒缩短至4 - 5秒。相比之下,辣椒素处理对Aδ伤害感受器的反应没有显著影响。这些结果支持这样的结论,即对低速皮肤加热的伤害性足部退缩反应主要由C纤维伤害感受器的激活介导。这些结果提供了直接证据,即在这些实验条件下,高速皮肤加热诱发的伤害性足部退缩反应主要由Aδ伤害感受器介导,而低速皮肤加热诱发的足部退缩反应主要由C纤维伤害感受器介导。