Gilchrist Hart D, Allard Brandon L, Simone Donald A
Department of Psychiatry, Division of Neuroscience Research,Minneapolis, MN 55455, USA Graduate Program in Neuroscience, University of Minnesota, 420 Delaware St. S.E., Box 392, Minneapolis, MN 55455, USA.
Pain. 1996 Sep;67(1):179-188. doi: 10.1016/0304-3959(96)03104-1.
Withdrawal responses to heat and mechanical stimuli applied to the plantar surface of the rat hindpaw were measured before and after an intraplantar injection of capsaicin. In separate groups of rats, capsaicin doses of 1, 10 and 30 micrograms, and the vehicle were given into the center of the plantar surface in a volume of 10 microliters. Withdrawal latency evoked by radiant heat and the frequency of withdrawal evoked by mechanical stimuli (von Frey monofilaments) were obtained from both hindpaws before and after injection. Hyperalgesia to heat was defined as a decrease in withdrawal latency and mechanical hyperalgesia was indicated by an increase in withdrawal response frequency. Intraplantar injection of capsaicin evoked nocifensive behavior characterized by lifting and guarding the injected paw which typically lasted up to 3 min following injection. Capsaicin produced a decrease in withdrawal latency to heat and increased the frequency of withdrawal to mechanical stimuli in a dose-dependent manner. These effects were observed on the injected paw only. The duration of hyperalgesia produced by capsaicin was also dose-dependent. Withdrawal latencies to heat were decreased up to 45 min following capsaicin while withdrawal responses to mechanical stimuli remained elevated up to 4 h. The area of mechanical hyperalgesia included most of the plantar surface and extended approximately 9 mm proximal and distal to the injection. Injection of the vehicle did not significantly alter withdrawal responses to heat or mechanical stimuli. These studies demonstrate that intraplantar injection of capsaicin in rats produces hyperalgesia to heat and mechanical stimuli. This model should be useful for correlative behavioral, physiological and pharmacological studies of underlying mechanisms of capsaicin-evoked hyperalgesia.
在大鼠后爪足底注射辣椒素前后,测量其对施加于足底表面的热刺激和机械刺激的退缩反应。在不同组的大鼠中,将1、10和30微克的辣椒素剂量以及赋形剂以10微升的体积注入足底表面中心。在注射前后,从双侧后爪获取由辐射热诱发的退缩潜伏期以及由机械刺激(von Frey细丝)诱发的退缩频率。热痛觉过敏定义为退缩潜伏期缩短,机械性痛觉过敏表现为退缩反应频率增加。足底注射辣椒素诱发防御性 nocifensive行为,其特征为抬起并护住注射的爪子,注射后通常持续长达3分钟。辣椒素以剂量依赖性方式使热刺激的退缩潜伏期缩短,并增加对机械刺激的退缩频率。这些效应仅在注射侧爪子上观察到。辣椒素产生的痛觉过敏持续时间也呈剂量依赖性。辣椒素注射后,热刺激的退缩潜伏期缩短长达45分钟,而对机械刺激的退缩反应在长达4小时内仍保持升高。机械性痛觉过敏区域包括大部分足底表面,在注射部位近端和远端约9毫米范围内延伸。注射赋形剂并未显著改变对热刺激或机械刺激的退缩反应。这些研究表明,大鼠足底注射辣椒素会产生对热刺激和机械刺激的痛觉过敏。该模型对于辣椒素诱发痛觉过敏潜在机制的相关行为、生理和药理学研究应是有用 的。