Ho Kim Sun, Mo Chung Jin
Marine Biomedical Institute, University of Texas Medical Branch, Galveston, TX 77555, USA Department of Anatomy and Neurosciences University of Texas Medical Branch, Galveston, TX 77555, USA Department of Physiology and Biophysics, University of Texas Medical Branch, Galveston, TX 77555, USA.
Pain. 1992 Sep;50(3):355-363. doi: 10.1016/0304-3959(92)90041-9.
We attempted to develop an experimental animal model for peripheral neuropathic pain. Under sodium pentobarbital anesthesia, both the L5 and L6 spinal nerves (group 1) or the L5 spinal nerve alone (group 2) of one side of the rat were tightly ligated. For comparison, a parallel study was conducted with another group of rats (group 3) which received a partial tight sciatic nerve ligation, a paradigm developed previously as a neuropathy model. Withdrawal latencies to application of radiant heat to the foot were tested for the next 16 weeks in all 3 groups. Sensitivity of the hind paw to mechanical stimulation was tested with von Frey filaments. The general behavior of each rat was noted during the entire test period. Results suggested that the surgical procedure in all 3 groups produced a long-lasting hyperalgesia to noxious heat (at least 5 weeks) and mechanical allodynia (at least 10 weeks) of the affected foot. In addition, there were behavioral signs of the presence of spontaneous pain in the affected foot. Therefore, we believe we have developed an experimental animal model for peripheral neuropathy using tight ligations of spinal nerves. The model manifests the symptoms of human patients with causalgia and is compatible with a previously developed neuropathy model. The present model has two unique features. First, the surgical procedure is stereotyped. Second, the levels of injured and intact spinal segments are completely separated, allowing independent experimental manipulations of the injured and intact spinal segments in future experiments to answer questions regarding mechanisms underlying causalgia.
我们试图建立一种周围神经病理性疼痛的实验动物模型。在戊巴比妥钠麻醉下,将大鼠一侧的L5和L6脊神经(第1组)或仅L5脊神经(第2组)紧密结扎。为作比较,对另一组大鼠(第3组)进行了平行研究,该组大鼠接受了部分坐骨神经紧密结扎,这是先前开发的一种神经病变模型。在接下来的16周内,对所有3组大鼠测试了足部对辐射热刺激的缩足潜伏期。用von Frey细丝测试后爪对机械刺激的敏感性。在整个测试期间记录每只大鼠的一般行为。结果表明,所有3组的手术操作均使患足对有害热产生了长期的痛觉过敏(至少5周)和机械性异常性疼痛(至少10周)。此外,患足存在自发痛的行为迹象。因此,我们认为我们通过紧密结扎脊神经建立了一种周围神经病变的实验动物模型。该模型表现出灼性神经痛患者的症状,并且与先前开发的神经病变模型相符。本模型有两个独特之处。第一,手术操作是定型的。第二,损伤的和完整的脊髓节段水平完全分开,使得在未来的实验中能够对损伤的和完整的脊髓节段进行独立的实验操作,以回答有关灼性神经痛潜在机制的问题。