Antiallodynic effects of the selective NaV1.7 inhibitor Pn3a in a mouse model of acute postsurgical pain: evidence for analgesic synergy with opioids and baclofen. Issue 8 (August 2019)

• Record Type: Journal Article
• Authors: Mueller, Alexander; Starobova, Hana; Morgan, Michael; Dekan, Zoltan; Cheneval, Olivier; Schroeder, Christina I.; Alewood, Paul F.; Deuis, Jennifer R.; Vetter, Irina
• Is Part Of: Pain. Volume 160:Issue 8(2019)
• Publication Date: 2019-08
• Subjects: Postoperative pain -- Voltage-gated sodium channel -- NaV1.7 inhibition -- Analgesia -- Oxycodone -- Baclofen -- Transcriptome; Pain -- Periodicals; Douleur -- Périodiques; Anesthésie -- Périodiques; Pain; Electronic journals; Periodicals; Electronic journals; 616.0472
• DOI: 10.1097/j.pain.0000000000001567
• Languages: English
• ISSNs: 0304-3959

Abstract

Abstract : Abstract: Pain is the leading cause of disability in the developed world but remains a poorly treated condition. Specifically, postsurgical pain continues to be a frequent and undermanaged condition. Here, we investigate the analgesic potential of pharmacological NaV 1.7 inhibition in a mouse model of acute postsurgical pain, based on incision of the plantar skin and underlying muscle of the hind paw. We demonstrate that local and systemic treatment with the selective NaV 1.7 inhibitor μ-theraphotoxin-Pn3a is effectively antiallodynic in this model and completely reverses mechanical hypersensitivity in the absence of motor adverse effects. In addition, the selective NaV 1.7 inhibitors ProTx-II and PF-04856264 as well as the clinical candidate CNV1014802 also reduced mechanical allodynia. Interestingly, co-administration of the opioid receptor antagonist naloxone completely reversed analgesic effects of Pn3a, indicating an involvement of endogenous opioids in the analgesic activity of Pn3a. In addition, we found superadditive antinociceptive effects of subtherapeutic Pn3a doses not only with the opioid oxycodone but also with the GABAB receptor agonist baclofen. Transcriptomic analysis of gene expression changes in dorsal root ganglia of mice after surgery did not reveal any changes in mRNA expression of endogenous opioids or opioid receptors; however, several genes involved in pain, including Runx1 (Runt related transcription factor 1), Cacna1a (CaV 2.1), and Cacna1b (CaV 2.2), were downregulated. In summary, these findings suggest that pain after surgery can be successfully treated with NaV 1.7 inhibitors alone or in combination with baclofen or opioids, which may present a novel and safe treatment strategy for this frequent and poorly managed condition. Abstract : Supplemental Digital Content is Available in the Text.The selective NaV 1.7 inhibitor Pn3a provides superadditive analgesia in combination with the Gαi/o -coupled G protein-coupled receptor agonists oxycodone and baclofen.