AI Article Synopsis

  • * Research has shown that a product called Clarix Flo (FLO), derived from human amniotic membranes, can effectively reduce post-surgical pain in mice without the negative effects associated with opioids, by directly acting on pain-signaling neurons.
  • * The study identified a purified component from human amniotic membrane, HC-HA/PTX3, which not only mimics the pain-relief effects of FLO but also works by altering neuron behavior to reduce pain, signaling the potential of biologics from birth tissues as a safer alternative for pain management.

Article Abstract

Pain after surgery causes significant suffering. Opioid analgesics cause severe side effects and accidental death. Therefore, there is an urgent need to develop non-opioid therapies for managing post-surgical pain. Local application of Clarix Flo (FLO), a human amniotic membrane (AM) product, attenuated established post-surgical pain hypersensitivity without exhibiting known side effects of opioid use in mice. This effect was achieved through direct inhibition of nociceptive dorsal root ganglion (DRG) neurons via CD44-dependent pathways. We further purified the major matrix component, the heavy chain-hyaluronic acid/pentraxin 3 (HC-HA/PTX3) from human AM that has greater purity and water solubility than FLO. HC-HA/PTX3 replicated FLO-induced neuronal and pain inhibition. Mechanistically, HC-HA/PTX3 induced cytoskeleton rearrangements to inhibit sodium current and high-voltage activated calcium current on nociceptive neurons, suggesting it is a key bioactive component mediating pain relief. Collectively, our findings highlight the potential of naturally derived biologics from human birth tissues as an effective non-opioid treatment for post-surgical pain. Moreover, we unravel the underlying mechanisms of pain inhibition induced by FLO and HC-HA/PTX3.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11142121PMC
http://dx.doi.org/10.1101/2024.05.19.594874DOI Listing

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