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The Bioactive Phenolic Agents Diaryl Ether CVB2-61 and Diarylheptanoid CVB4-57 as Connexin Hemichannel Blockers. | LitMetric

AI Article Synopsis

  • Inflammation mediators activate connexin (Cx) hemichannels, particularly in epithelial and endothelial tissues, potentially leading to persistent inflammation through the release of injury signals.
  • Specific inhibition of Cx hemichannels could provide a strategy for preventing and treating chronic sterile inflammation.
  • The bioactive phenolic agents CVB2-61 and CVB4-57 were shown to inhibit Cx hemichannel activity in various cell types without disrupting gap junction communication or barrier function, suggesting their potential for safer therapeutic applications targeting Cx hemichannels.

Article Abstract

Inflammation mediators enhance the activity of connexin (Cx) hemichannels, especially in the epithelial and endothelial tissues. As potential release routes for injury signals, such as (oligo)nucleotides, Cx hemichannels may contribute to long-lasting inflammation. Specific inhibition of Cx hemichannels may therefore be a mode of prevention and treatment of long-lasting, chronic sterile inflammation. The activity of Cx hemichannels was analysed in N2A and HeLa cells transfected with human Cx26 and Cx46 as well as in Calu-3 cells, using dye uptake as functional assay. Moreover, the possible impacts of the bioactive phenolic agents CVB2-61 and CVB4-57 on the barrier function of epithelial cells was analysed using Calu-3 cells. Both agents inhibited the dye uptake in N2A cells expressing Cx26 (>5 µM) and Cx46 (>20 µM). In Calu-3 cells, CVB2-61 and CVB4-57 reversibly inhibited the dye uptake at concentrations as low as 5 µM, without affecting the gap junction communication and barrier function, even at concentrations of 20 µM. While CVB2-61 or CVB4-57 maintained a reduced dye uptake in Calu-3 cells, an enhancement of the dye uptake in response to the stimulation of adenosine signalling was still observed after removal of the agents. The report shows that CVB2-61 and CVB4-57 reversibly block Cx hemichannels. Deciphering the mechanisms of the interactions of these agents with Cx hemichannels could allow further development of phenolic compounds to target Cx hemichannels for better and safer treatment of pathologies that involve Cx hemichannels.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611528PMC
http://dx.doi.org/10.3390/ph15101173DOI Listing

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