Silencing of spinal Trpv1 attenuates neuropathic pain in rats by inhibiting CAMKII expression and ERK2 phosphorylation

• Published in: Scientific reports Vol. 9; no. 1; p. 2769
• Main Authors: Guo, Shao-Hui, Lin, Jia-Piao, Huang, Ling-Er, Yang, Yan, Chen, Chao-Qin, Li, Na-Na, Su, Meng-Yun, Zhao, Xian, Zhu, Sheng-Mei, Yao, Yong-Xing
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 26.02.2019; Nature Publishing Group
• Subjects: 631/378/1689/2610; 692/617/375/1692; 82; 82/80; Ca2+/calmodulin-dependent protein kinase II; Calcium-binding protein; Calmodulin; Cancer; Capsaicin receptors; Extracellular signal-regulated kinase; Gene silencing; Humanities and Social Sciences; Inflammation; Kinases; multidisciplinary; Neuralgia; Pain; Pain perception; Phosphorylation; RNA-mediated interference; Sciatic nerve; Science; Science (multidisciplinary); siRNA; Spinal cord; Thermal stimuli; Transient receptor potential proteins; Western blotting
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-019-39184-4

Accumulating evidence suggests a potential role of transient receptor potential vanilloid 1 (TRPV1) channels in inflammatory and cancer-related pain. However, the role of TRPV1 in the maintenance of neuropathic pain remains elusive. The current study investigated the effects of transient Trpv1 gene silencing using a small interference RNA (siRNA) on neuropathic pain induced by chronic constriction injury (CCI) of the sciatic nerve in rats. Seven days after CCI, the TRPV1 siRNA was intrathecally administered (5 µg/15 µl, once daily for 2 days). TRPV1 and Ca 2+ /calmodulin-dependent protein kinase II (CAMKII) expression and extracellular signal-regulated kinase (ERK) phosphorylation in the spinal cord were detected using western blotting. The thresholds to mechanical and thermal stimuli were determined before and after intrathecal TRPV1 siRNA administration. TRPV1 and CAMKII expression and ERK2 phosphorylation in the spinal cord were upregulated after CCI. Intrathecal administration of the TRPV1 siRNA not only attenuated behavioural hyperalgesia but also reduced the expression of TRPV1 and CAMKII, as well as ERK2 phosphorylation. Based on these results, silencing of the TRPV1 gene in the spinal cord attenuates the maintenance of neuropathic pain by inhibiting CAMKII/ERK2 activation and suggests that TRPV1 represents a potential target in pain therapy.