首页> 外文期刊>The Journal of Comparative Neurology >Anatomical evidence that the uninjured adjacent L4 nerve plays a significant role in the development of peripheral neuropathic pain after L5 spinal nerve ligation in rats
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Anatomical evidence that the uninjured adjacent L4 nerve plays a significant role in the development of peripheral neuropathic pain after L5 spinal nerve ligation in rats

机译:解剖证据表明,未受伤的邻近L4神经在大鼠结扎L5脊神经后在周围神经性疼痛的发展中起重要作用

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Rats develop hyperalgesia and allodynia in the hind paw after L5 spinal nerve ligation. Phosphorylated extracellular regulated kinase (pERK) was used as a pain marker to investigate the potential role of adjacent uninjured L4 nerve in the development of heat hyperalgesia after L5 nerve injury. Left L5 nerve was ligated and sectioned in rats. Three days later, rats were randomly assigned to five groups; each had both hind paws immersed in water at different temperatures (no heat, 37, 42, 47, and 52 degrees C) under sevoflurane anesthesia for 2 minutes. Five minutes after stimulation the rats were sacrificed and sections of L3-L6 spinal segments were stained immunocytochemically with pERK antibody. pERK immunoreactivity, which is not detectable in the normal spinal cord, was discernible in neurons (not glia) of the superficial dorsal horn after noxious heat stimuli. pERK-positive neurons clearly overlapped in laminae I-II with normal unmyelinated and thin myelinated afferents labeled with calcitonin gene-related peptide and isolectin B4, and injured unmyelinated afferents labeled with vasoactive intestinal polypeptide. There was a linear increase in pERK immunoreactivity on both sides with an increase in temperature. Importantly, the number of positive pERK neurons was significantly higher in the ipsilateral side of L4 spinal segment, which receives innervation from uninjured L4 nerve, compared with the contralateral control side, which receives both uninjured L4 and L5 spinal nerves. The data demonstrate that the uninjured L4 nerve plays an important role in the development of heat hyperalgesia at the spinal cord level after L5 nerve injury. J. Comp. Neurol. 523:1731-1747, 2015. (c) 2015 Wiley Periodicals, Inc.
机译:L5脊髓神经结扎后,大鼠后爪出现痛觉过敏和异常性疼痛。磷酸化的细胞外调节激酶(pERK)被用作疼痛标记,以研究邻近的未损伤L4神经在L5神经损伤后热痛觉过敏发展中的潜在作用。结扎大鼠左L5神经并切片。三天后,将大鼠随机分为五组。两只后爪均在七氟醚麻醉下于不同温度(无热,37、42、47和52摄氏度)下浸入水中2分钟。刺激后五分钟,处死大鼠,并用pERK抗体对L3-L6脊髓节段进行免疫细胞化学染色。在有害的热刺激后,在浅表背角的神经元(不是神经胶质细胞)中可以辨别出在正常脊髓中无法检测到的pERK免疫反应性。 pERK阳性神经元在I-II层中明显重叠,降钙素基因相关肽和isolectin B4标记的正常未髓鞘和稀有髓鞘的传入神经,而血管活性肠多肽标记的受伤的未髓鞘的传入神经。随着温度的升高,两侧的pERK免疫反应性呈线性增加。重要的是,与接受未损伤的L4和L5脊髓神经的对侧对照侧相比,接受未损伤的L4神经支配的L4脊柱节段同侧的pERK神经元的阳性数目明显增加。数据表明,未损伤的L4神经在L5神经损伤后脊髓水平的热痛觉过敏的发展中起重要作用。 J.比较神经元。 523:1731-1747,2015.(c)2015威利期刊公司

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