Activation of mTOR in the spinal cord is required for pain hypersensitivity induced by chronic constriction injury in mice

• Published in: Pharmacology, biochemistry and behavior biochemistry and behavior, 2013-10, Vol.111, p.64-70
• Main Authors: Zhang, Wei, Sun, Xiao-Feng, Bo, Jin-Hua, Zhang, Juan, Liu, Xiao-Jie, Wu, Liu-Ping, Ma, Zheng-Liang, Gu, Xiao-Ping
• Format: Article
• Language: English
• Subjects: Animals; Behavior, Animal; Chronic Disease; Male; Mice; Mice, Inbred C57BL; mTOR; Neuropathic pain; Pain Threshold - physiology; Rapamycin; Sirolimus - pharmacology; Spinal Cord Compression - metabolism; Spinal Cord Compression - physiopathology; Spinal Cord Injuries - metabolism; Spinal Cord Injuries - physiopathology; TOR Serine-Threonine Kinases - physiology
• ISSN: 0091-3057; 1873-5177
• DOI: 10.1016/j.pbb.2013.07.017

The mammalian target of rapamycin (mTOR) is known to regulate cell growth, and it also participates in pain transmission as has been recently verified in inflammatory and neuropathic pain models. The targeting of mTOR represents a new strategy for the control of chronic pain. In the present study, we investigated the effect of mTOR in the expression of PSD95 and NR2B-PSD95 or GluA2-PSD95 interaction ratio in a chronic constriction injury (CCI) mice model. Paw mechanical withdrawal threshold (PMWT) and paw withdrawal thermal latency (PWTL) were respectively used to assess mechanical allodynia and thermal hyperalgesia after CCI operation and intrathecal injection of rapamycin. Western blot and co-immunoprecipitation were used to investigate the effects of rapamycin on the expression of PSD95 and interaction ratio of NR2B-PSD95 or GluA2-PSD95 in the spinal dorsal horn of mice. Our study demonstrated that the inhibition of spinal mTOR with intrathecal injections of rapamycin (1μg/5μL) for days 1–6 after CCI surgery led to an obvious decrease in CCI-induced neuropathic pain. Rapamycin significantly reduced the PMWT of CCI mice, whereas there was no significant effect on PWTL. The active form of the mTOR signaling pathway (p-mTOR, p-4EBP1 and p-p70S6k) at the spinal level remarkably increased in CCI mice, and rapamycin could inhibit this up-regulation. The increased expression of PSD95 and the interaction ratio of GluA2-PSD95 or NR2B-PSD95 could also be inhibited by intrathecal injection of rapamycin. These data suggest that the mTOR pathway is activated in the spinal dorsal horn in CCI-induced neuropathic pain, and the intrathecal injection of rapamycin can reduce mechanical allodynia. Our findings indicate that spinal mTOR is an important component of CCI-induced neuropathic pain, and mTOR may be a potential target for chronic pain therapy. •We investigated behavioral effect of rapamycin on CCI-induced neuropathic pain.•We examined changes of mTOR and interactions of GluA2/NR2B-PSD95 after CCI surgery.•The effect of rapamycin may partly due to the inhibition of GluA2/NR2B-PSD95.