Discovery Biology Research, Nagoya Laboratories, Pfizer Global Research and Development, Pfizer Inc., Taketoyo, Aichi, Japan.
J Pharm Pharmacol. 2012 May;64(5):747-55. doi: 10.1111/j.2042-7158.2012.01468.x. Epub 2012 Feb 21.
Post-operative pain is considered to involve inflammation caused by tissue injury. However, the mechanism and timing of the involvement of inflammation in the post-operative pain remain complicated because they can vary among different types of surgery. In this study a rat incision model was used to investigate how inflammation induced by cyclooxygenases (COXs) is involved in severe post-operative pain.
Longitudinal incision with a length of 1cm was made through skin and fascia on the right hind paw of rats, starting 0.5cm from the edge of the heel and extending towards the toes. Allodynia was evaluated using the von Frey hair test and its degree was recorded as the paw withdrawal threshold (PWT). Two non-steroidal anti-inflammatory drugs (NSAIDs), piroxicam and ketorolac, were given to rats after or before surgery, and the effects of the drugs on allodynia induced by the hind paw incision were examined.
The PWT reduction reached a sub-maximal level at 3h, a maximal level at one day after the surgery and lasted for more than 8 days, with the parallel development of inflammation (characterized by cell infiltration and oedema). Treatment with morphine (1mg/kg, s.c.) at one day after the surgery showed a significant anti-allodynic effect. Treatment with either piroxicam (10mg/kg, p.o.) or ketorolac (10mg/kg, p.o.) at one day after the surgery did not exhibit significant anti-allodynic effect, whereas pre-surgical treatment with each drug showed significant anti-allodynic effects at 3h after surgery.
These findings suggest the involvement of cyclooxygenases in evoking pain that occurs in the immediate post-operative period, and that an initial suppression of rapid inflammation by treatment with NSAIDs before major surgery plays an important role in the management of severe post-operative pain.
术后疼痛被认为涉及组织损伤引起的炎症。然而,由于不同类型的手术之间存在差异,炎症在术后疼痛中的作用机制和时间仍较为复杂。本研究采用大鼠切口模型,探讨环氧化酶(COXs)诱导的炎症如何参与严重术后疼痛。
在大鼠右后爪通过皮肤和筋膜做 1cm 长的纵向切口,从足跟边缘向外 0.5cm 处开始,向趾端延伸。使用 von Frey 毛发试验评估痛觉过敏,其程度记录为爪回缩阈值(PWT)。在手术后或之前给予大鼠两种非甾体抗炎药(NSAIDs),吡罗昔康和酮咯酸,并检查药物对后爪切口引起的痛觉过敏的影响。
PWT 降低在手术后 3 小时达到亚最大水平,在手术后第 1 天达到最大水平,并持续超过 8 天,与炎症(以细胞浸润和水肿为特征)平行发展。手术后第 1 天给予吗啡(1mg/kg,sc)表现出显著的抗痛觉过敏作用。手术后第 1 天给予吡罗昔康(10mg/kg,po)或酮咯酸(10mg/kg,po)治疗均未表现出显著的抗痛觉过敏作用,而术前给予每种药物治疗均在手术后 3 小时表现出显著的抗痛觉过敏作用。
这些发现表明环氧化酶在引发术后即刻发生的疼痛中起作用,并且在大手术前用 NSAIDs 抑制快速炎症的初始发作对严重术后疼痛的管理具有重要作用。