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神经调节蛋白 1 异构体在神经病理性疼痛模型大鼠中的表达变化。

Expression changes of the neuregulin 1 isoforms in neuropathic pain model rats.

机构信息

Department of Anesthesiology & Resuscitology, Okayama, Japan.

出版信息

Neurosci Lett. 2012 Feb 6;508(2):78-83. doi: 10.1016/j.neulet.2011.12.023. Epub 2011 Dec 28.

Abstract

The neuregulin1 (Nrg1) gene that is expressed in the dorsal root ganglion (DRG) contains an EGF-like domain, which is known to be a direct ligand for ErbB3 and ErbB4. Multiple splice variants of the Nrg1 gene are broadly classified into 3 groups by structural features (type I, type II and type III) and their functions differ in various tissues. The Nrg1 gene has emerged as a key mediator of axon-Schwann cell interactions and as a regulator of Schwann cell development. The Nrg1 gene is indicated as a promising growth factor for neuronal development. However, the function of the Nrg1 in pain has not been clarified. We therefore, examined the expression profiles of each type of the Nrg1 transcript in the bilateral L4/L5 DRGs using L5 spinal nerve ligation (SNL) model rats and complete Freund's adjuvant (CFA) model rats. Behavior tests have shown typical mechanical hyperalgesia in both the L5SNL model and the CFA model. In the L5SNL model, expression of the Nrg1 type I and type II were significantly increased in the L5 DRG. On the other hand, the expression of the Nrg1 type III was decreased in the L5 DRG. We demonstrated that the expression changes of the Nrg1 isoforms in the ipsilateral DRGs were preferentially related to the response to nerve injury. Our findings suggest that the aberrant expression may play an important role in nerve injury, regeneration and subsequent neuropathic pain on the L5SNL.

摘要

神经调节蛋白 1(Nrg1)基因在背根神经节(DRG)中表达,含有一个表皮生长因子样结构域,已知其是 ErbB3 和 ErbB4 的直接配体。Nrg1 基因的多个剪接变体根据结构特征(I 型、II 型和 III 型)广泛分为 3 组,其在不同组织中的功能也不同。Nrg1 基因已成为轴突-施万细胞相互作用的关键介质,也是施万细胞发育的调节剂。Nrg1 基因被认为是神经元发育的有前途的生长因子。然而,Nrg1 在疼痛中的作用尚未阐明。因此,我们使用 L5 脊神经结扎(SNL)模型大鼠和完全弗氏佐剂(CFA)模型大鼠,检查了双侧 L4/L5 DRG 中每种 Nrg1 转录本的表达谱。行为测试表明,L5SNL 模型和 CFA 模型均出现典型的机械性痛觉过敏。在 L5SNL 模型中,L5 DRG 中 Nrg1 型 I 和型 II 的表达显著增加。另一方面,L5 DRG 中 Nrg1 型 III 的表达减少。我们证明了同侧 DRG 中 Nrg1 同工型的表达变化与对神经损伤的反应优先相关。我们的发现表明,异常表达可能在 L5SNL 中的神经损伤、再生和随后的神经性疼痛中发挥重要作用。

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