Neuropeptide y modulates c-fos protein expression in the cuneate nucleus and contributes to mechanical hypersensitivity following rat median nerve injury

Yi Ju Tsai, Chi Te Lin, Chun Ta Huang, Hsin Ying Wang, Lu Tai Tien, Seu Hwa Chen, June Horng Lue

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26 引文 斯高帕斯(Scopus)

摘要

This study sought to investigate the effects of injury-induced neuropeptide Y (NPY) on c-Fos expression in the cuneate neurons and neuropathic pain after median nerve injury. Four weeks after median nerve transection (MNT), the injured nerves stimulated at low intensity (0.1mA) expressed significantly less NPY-like immunoreactive (NPY-LI) fibers in the cuneate nucleus (CN) than those stimulated at high intensities (1.0mA and 10mA). Conversely, a significantly higher number of c-Fos-LI cells were observed in the CN in rats stimulated with 0.1mA compared to those stimulated with 1.0mA or 10mA. These results suggest that more NPY was released following low-intensity stimulation, and consequently fewer NPY-LI fibers and more c-Fos-LI cells were identified in the CN. Furthermore, the number of c-Fos-LI cells as well as the percentage of c-Fos-LI cuneothalamic projection neurons (CTNs) in the CN was markedly decreased after injection of NPY receptor antagonist along with retrograde tract-tracing method, indicating that NPY regulated c-Fos expression. In rats with median nerve chronic constriction injury (CCI), intracerebroventricular injection of NPY aggravated mechanical allodynia and low-intensity stimulus-evoked c-Fos expression, both of which were reversed by injection of NPY receptor antagonist. However, thermal hyperalgesia was not affected by injection of these two reagents. Taken together, these findings suggest that more NPY release, following low-intensity electrical stimulation of the injured nerve, significantly induces c-Fos expression in the CTNs, which possibly provide the ascending thalamic transmission of neuropathic pain signals.

原文英語
頁(從 - 到)1609-1621
頁數13
期刊Journal of Neurotrauma
26
發行號9
DOIs
出版狀態已發佈 - 九月 1 2009

ASJC Scopus subject areas

  • 神經病學(臨床)

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