Vierck C J, Yezierski R P, Light A R
Department of Neuroscience, University of Florida College of Medicine, Gainesville, FL 32610-0244, USA.
Neuroscience. 2008 May 2;153(2):501-6. doi: 10.1016/j.neuroscience.2008.02.027. Epub 2008 Feb 29.
Subcutaneous formalin injection has been used extensively to evaluate acute effects (over several hours) of chemical nociceptive stimulation on nociceptive reflexes. Also, a persistent hyperreflexia for mechanical and thermal stimulation, lasting 3 weeks after formalin injection, has been revealed and related to microglial activation in the spinal dorsal horn. The present study demonstrates more prolonged effects of formalin injection, lasting 6 weeks, on operant escape from nociceptive thermal stimulation. Operant escape requires cerebral processing of nociceptive input and can detect effects that are not limited to spinal or spinal-brain stem-spinal reflex circuits. Compared with rats injected with saline, escape responding to 44.5 degrees C and 47 degrees C stimulation was increased after bilateral s.c. injection of 5% formalin into the dorsal hind paws. The hyperalgesia outlasted visible signs of trauma (e.g. paw edema). Responses to 36 degrees C were not altered after formalin injection, providing a control for effects of the peripheral injury on activity levels or exploratory tendencies. Skin temperature recordings from the forepaws and contralateral hind paw during 44.5 degrees C stimulation of the left hind paw provided an indirect measure of cutaneous blood flow in formalin- and saline-injected animals. Normal reductions in skin temperature during thermal stimulation were attenuated (nearly eliminated) at 1 and 2 weeks after formalin injection and partially recovered by 10 weeks. Thus, formalin-induced tissue injury produced a long-term secondary hyperalgesia, accompanied by a reduced sympathetic responsivity. The similar time-course for these phenomena suggests that there are mechanistic linkages between focal injury, autonomic dysregulation and enhanced pain sensitivity.
皮下注射福尔马林已被广泛用于评估化学性伤害性刺激在数小时内对伤害性反射的急性影响。此外,还发现福尔马林注射后持续3周的对机械和热刺激的持续性反射亢进,这与脊髓背角的小胶质细胞激活有关。本研究表明,福尔马林注射对操作性逃避伤害性热刺激具有更持久的影响,持续6周。操作性逃避需要对伤害性输入进行大脑处理,并且可以检测不限于脊髓或脊髓-脑干-脊髓反射回路的影响。与注射生理盐水的大鼠相比,双侧后足背皮下注射5%福尔马林后,对44.5℃和47℃刺激的逃避反应增加。痛觉过敏持续时间超过了可见的创伤迹象(如爪水肿)。福尔马林注射后对36℃的反应没有改变,这为外周损伤对活动水平或探索倾向的影响提供了对照。在对左后爪进行44.5℃刺激期间,对前爪和对侧后爪的皮肤温度记录提供了福尔马林和生理盐水注射动物皮肤血流量的间接测量。在福尔马林注射后1周和2周,热刺激期间皮肤温度的正常降低减弱(几乎消除),并在10周时部分恢复。因此,福尔马林诱导的组织损伤产生了长期的继发性痛觉过敏,并伴有交感反应性降低。这些现象的相似时间进程表明,局部损伤、自主神经调节异常和疼痛敏感性增强之间存在机制联系。