Author:
Zhang Chi,Huang Qian,Ford Neil C.,Limjunyawong Nathachit,Lin Qing,Yang Fei,Cui Xiang,Uniyal Ankit,Liu Jing,Mahabole Megha,He Hua,Wang Xue-Wei,Duff Irina,Wang Yiru,Wan Jieru,Zhu Guangwu,Raja Srinivasa N,Jia Hongpeng,Yang Dazhi,Dong Xinzhong,Cao Xu,Tseng Scheffer C.,He Shao-Qiu,Guan Yun
Abstract
AbstractPain 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.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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