Baldwin Anne E, Cannon Timothy J
Neuroscience Program University of Scranton, Scranton, PA 18510-4596, USA Psychology Department, University of Scranton, Scranton, PA 18510-4596, USA.
Pain. 1996 Sep;67(1):163-172. doi: 10.1016/0304-3959(96)03084-9.
Although the tail-flick response to radiant heat is widely used in nociceptive research, there are indications that this benchmark test possesses some undesirable characteristics. Of present concern is the possibility that the supra-threshold stimuli associated with behavioral testing while under the influence of an effective hypoalgesic manipulation can alter subsequent tail-flick responses. To examine the effects of supra-threshold heating of the tail, we exposed anesthetized rats to either (1) manual restraint of the tail during a single tail-flick trial to a 5- or 7-sec cut-off, or (2) testing while under the analgesic effects of morphine (5 mg/kg/ml). A single prolonged trial produced hyperalgesia which lasted for 30 min. Following naltrexone injection, hyperalgesia was also found in animals that had been tested while under morphine analgesia. In contrast, animals that received morphine but were not tested under its influence did not exhibit hyperalgesia of similar magnitude. Analyses of tail temperature data in the second experiment indicate that these results are not dependent on shifts in tail temperature. These results suggest that, in anesthetized animals, exposure to prolonged tail-flick trials can produce hyperalgesia.
尽管对辐射热的甩尾反应在伤害性感受研究中被广泛应用,但有迹象表明,这个基准测试具有一些不良特性。目前令人担忧的是,在有效的镇痛操作影响下进行行为测试时,与超阈值刺激相关的因素可能会改变随后的甩尾反应。为了研究尾部超阈值加热的影响,我们将麻醉的大鼠暴露于以下两种情况之一:(1)在单次甩尾试验中手动固定尾部,截止时间为5秒或7秒;(2)在吗啡(5毫克/千克/毫升)的镇痛作用下进行测试。单次长时间试验产生了持续30分钟的痛觉过敏。注射纳曲酮后,在吗啡镇痛下接受测试的动物中也发现了痛觉过敏。相比之下,接受吗啡但未在其影响下进行测试的动物没有表现出类似程度的痛觉过敏。第二个实验中对尾部温度数据的分析表明,这些结果并不依赖于尾部温度的变化。这些结果表明,在麻醉动物中,长时间的甩尾试验会产生痛觉过敏。