Inhibition of GAP-43 by propentofylline in a rat model of neuropathic pain

International Journal of Clinical and Experimental Pathology

Yuming Sun¹  Jiaying Chen¹  Zhiqiang Liu¹  Xuerong Miao¹  Weifeng Yu¹  Feixiang Wu¹  Yong Tao¹ 

关键词: Astrocytes;    growth-associated protein-43;    interleukin 1β;    neuropathic pain;   

DOI  :  

学科分类：生理学与病理学

来源: e-Century Publishing Corporation

【 摘 要 】

Neural plasticity within the spinal nociceptive network may be fundamental to the chronic nature of neuropathic pain. The relation of growth-associated protein-43 (GAP-43), a protein involved in the nerve fiber growth and sprouting, to pain hypersensitivity has been investigated. Glial activation and inflammatory cytokines released by microglia and astrocytes are considered to be involved in the neural sprouting and plasticity. In the present study, the anti-nociception effect of propentofylline, a glial modulating agent, was investigated in a rat chronic constriction injury (CCI) model aiming to explore the role of GAP-43 expression. Our results demonstrated that propentofylline could attenuate the CCI-induced mechanical allodynia and thermal hyperalgesia and inhibit the astrocyte activation and production of IL-1β. GAP-43 expression was also down-regulated by intrathecal propentofylline. These findings suggest that astrocyte activation is involved in the regulation of GAP-43 expression and propentofylline might be used in the treatment of neuropathic pain.

【 授权许可】

Unknown