Department of Traumatology and Reconstructive Surgery, University of Rostock, Rostock, Germany.
Anesth Analg. 2013 Jan;116(1):216-23. doi: 10.1213/ANE.0b013e31826e0fe0. Epub 2012 Dec 7.
Chronic constriction injury is a widely used model for neuropathic pain in rats. It presents with symptoms resembling human neuropathic pain, such as spontaneous pain, hyperalgesia, and allodynia. Recently, myocyte apoptosis was found in neuropathic rats as a possible promoter of pain and motor dysfunction. Our aim in this study was to demonstrate whether muscle cell apoptosis contributes to neuropathic pain in this animal model.
To clarify this issue, we examined pain, nutritive perfusion, and inflammation in muscle tissue as well as myocyte apoptosis in rats with neuropathic pain established by chronic constriction injury of the sciatic nerve. Animals received either the pan-caspase inhibitor zVAD (OMe)-fmk (n = 5) or equivalent volumes of vehicle (n = 6). Sham-operated rats served as controls (n = 6).
At day 4 after nerve ligation, there were no signs of perfusion failure or muscle tissue inflammation in all experimental groups. However, animals treated with the vehicle had marked myocyte apoptosis, which was found almost completely blocked in zVA-Dtreated animals. The zVA-Dtreated animals presented with a significant reduction of pain upon heat, cold, and mechanical stimulation comparable with values found in sham controls.
Myocyte apoptosis possibly contributes to thermal and mechanical allodynia in this experimental model for neuropathic pain. The development of neuropathic pain symptoms did not depend on disturbances in microcirculation or muscle tissue inflammation.
慢性缩窄性损伤是一种广泛应用于大鼠神经性疼痛的模型。它表现出与人类神经性疼痛相似的症状,如自发性疼痛、痛觉过敏和感觉异常。最近,研究发现神经性大鼠中存在肌细胞凋亡,这可能是疼痛和运动功能障碍的一个促进因素。我们在这项研究中的目的是证明这种动物模型中的肌细胞凋亡是否会导致神经性疼痛。
为了阐明这个问题,我们检查了神经性疼痛大鼠的疼痛、营养灌注和肌肉组织炎症以及肌细胞凋亡。动物接受了泛半胱天冬酶抑制剂 zVAD(OMe)-fmk(n = 5)或等效体积的载体(n = 6)治疗。假手术大鼠作为对照(n = 6)。
在神经结扎后第 4 天,所有实验组均未出现灌注衰竭或肌肉组织炎症的迹象。然而,接受载体治疗的动物有明显的肌细胞凋亡,而在 zVA-D 处理的动物中几乎完全阻断了这种凋亡。zVA-D 处理的动物在热、冷和机械刺激下的疼痛明显减轻,与假对照中发现的疼痛值相当。
肌细胞凋亡可能导致这种神经性疼痛实验模型中的热和机械性感觉异常。神经性疼痛症状的发展并不依赖于微循环紊乱或肌肉组织炎症。