Inhibition of phosphodiesterase‐4 in the spinal dorsal horn ameliorates neuropathic pain via cAMP‐cytokine‐Cx43 signaling in mice. (14th February 2022)

• Record Type: Journal Article
• Authors: Zhang, Fang‐fang; Wang, Hao; Zhou, Yan‐meng; Yu, Hai‐yang; Zhang, Melanie; Du, Xian; Wang, Dong; Zhang, Feng; Xu, Ying; Zhang, Ji‐guo; Zhang, Han‐Ting
• Is Part Of: CNS neuroscience & therapeutics. Volume 28:Number 5(2022)
• Page Start: 749
• Page End: 760
• Publication Date: 2022-02-14
• Subjects: connexin43 -- neuropathic pain -- phosphodiesterase‐4 -- roflumilast -- rolipram; Neuropharmacology -- Periodicals; Central nervous system -- Diseases -- Effect of drugs on -- Periodicals; 612.8
• DOI: 10.1111/cns.13807
• Languages: English
• ISSNs: 1755-5930

Abstract

Abstract: Background: The spinal phosphodiesterase‐4 (PDE4) plays an important role in chronic pain. Inhibition of PDE4, an enzyme catalyzing the hydrolysis of cyclic adenosine monophosphate AMP (cAMP), produces potent antinociceptive activity. However, the antinociceptive mechanism remains largely unknown. Connexin43 (Cx43), a gap junction protein, has been shown to be involved in controlling pain transduction at the spinal level; restoration of Cx43 expression in spinal astrocytes to the normal levels reduces nerve injury‐induced pain. Here, we evaluate the novel mechanisms involving spinal cAMP‐Cx43 signaling by which PDE4 inhibitors produce antinociceptive activity. Methods: First, we determined the effect of PDE4 inhibitors rolipram and roflumilast on partial sciatic nerve ligation (PSNL)‐induced mechanical hypersensitivity. Next, we observed the role of cAMP‐Cx43 signaling in the effect of PDE4 inhibitors on PSNL‐induced mechanical hypersensitivity. Results: Single or repeated, intraperitoneal or intrathecal administration of rolipram or roflumilast significantly reduced mechanical hypersensitivity in mice following PSNL. In addition, repeated intrathecal treatment with either of PDE4 inhibitors reduced PSNL‐induced downregulation of cAMP and Cx43, and upregulation of proinflammatory cytokines tumor necrosis factor‐α (TNF‐α) and interleukin‐1β. Furthermore, the antinociceptive effects of PDE4 inhibitors were attenuated by the protein kinase A (PKA) inhibitor H89, TNF‐α, or Cx43 antagonist carbenoxolone. Finally, PSNL‐induced upregulation of PDE4B and PDE4D, especially the PDE4B subtype, was reduced by treatment with either of the PDE4 inhibitors. Conclusions: The results suggest that the antinociceptive effect of PDE4 inhibitors is contributed by increasing Cx43 expression via cAMP‐PKA‐cytokine signaling in the spinal dorsal horn. Abstract : The present study provides not only solid demonstration for the analgesic effects of PDE4 inhibitors but also valued clues on the novel mechanism of cAMP‐PKA‐cytokine signaling whereby PDE4 inhibitors produce analgesic activity. The findings will aid in the development of novel antinociceptive agents.