| Literature DB >> 34338322 |
Yixin Yang1,2, Jinsong Zhao1,3, Yunze Li1, Xiangyao Li4, Xiaowei Chen5, Zhiying Feng1.
Abstract
Studies have verified that Fragile X mental retardation protein (FMRP), an RNA-binding protein, plays a potential role in the pathogenesis of formalin- and (RS)-3,5-dihydroxyphenylglycine (DHPG)-induced abnormal pain sensations. However, the role of FMRP in inflammatory pain has not been reported. Here, we showed an increase in FMRP expression in the spinal dorsal horn (SDH) in a rat model of inflammatory pain induced by complete Freund's adjuvant (CFA). Double immunofluorescence staining revealed that FMRP was mainly expressed in spinal neurons and colocalized with proinflammatory cytokines [tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6)]. After consecutive intrathecal injection of fragile X mental retardation 1 (Fmr1) small interfering RNA (siRNA) for 3 days post-CFA injection, FMRP expression in the SDH was reduced, and CFA-induced hyperalgesia was decreased. In addition, the CFA-induced increase in spinal TNF-α and IL-6 production was significantly suppressed by intrathecal administration of Fmr1 siRNA. Together, these results suggest that FMRP regulates TNF-α and IL-6 levels in the SDH and plays an important role in inflammatory pain. This article is protected by copyright. All rights reserved.Entities:
Keywords: Fragile X mental retardation protein; inflammatory pain; interleukin-6; spinal dorsal horn; tumor necrosis factor-α
Year: 2021 PMID: 34338322 DOI: 10.1111/jnc.15485
Source DB: PubMed Journal: J Neurochem ISSN: 0022-3042 Impact factor: 5.372