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脊髓神经环氧化酶-2介导腰椎间盘突出症大鼠模型中的疼痛。

Spinal neural cyclooxygenase-2 mediates pain caused in a rat model of lumbar disk herniation.

作者信息

Ohtori Seiji, Takahashi Kazuhisa, Aoki Yasuchika, Doya Hideo, Ozawa T, Saito Tomoko, Moriya Hideshige

机构信息

Department of Orthopedic Surgery, Graduate School of Medicine, Chiba University School of Medicine, Chiba University, Chiba, Japan.

出版信息

J Pain. 2004 Sep;5(7):385-91. doi: 10.1016/j.jpain.2004.06.004.

Abstract

UNLABELLED

Application of nucleus pulposus to nerve root generates radicular pain. We demonstrated that these animals showed allodynia for 2 weeks, and cyclooxygenase-2 (COX-2) immunoreactivities were up-regulated in the spinal dorsal horn. COX-2 immunoreactivities were shown in neurons; however, they were not in astrocytes. Intrathecal administration of an antibody to COX-2 decreased allodynia. Our results suggest that COX-2 in spinal cord might be a target for treatment of patients with nerve root pain caused by lumbar disk herniation.

PERSPECTIVE

Neural COX-2 might mediate nerve root pain in the spinal cord caused by lumbar disk herniation in rats.

摘要

未标记

将髓核应用于神经根会产生神经根性疼痛。我们证明这些动物出现了2周的异常性疼痛,并且脊髓背角中环氧合酶-2(COX-2)免疫反应性上调。COX-2免疫反应性在神经元中显示,但在星形胶质细胞中未显示。鞘内注射COX-2抗体可减轻异常性疼痛。我们的结果表明,脊髓中的COX-2可能是治疗腰椎间盘突出症引起的神经根性疼痛患者的靶点。

观点

神经COX-2可能介导大鼠腰椎间盘突出症引起的脊髓神经根性疼痛。

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