2022
DOI: 10.1007/s11302-022-09861-7
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Analgesic effect of electroacupuncture on bone cancer pain in rat model: the role of peripheral P2X3 receptor

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Cited by 11 publications
(8 citation statements)
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“…[18] EA ameliorated MRMT-1-induced mechanical abnormal pain and thermal nociceptive hyperalgesia in a rat model of bone cancer pain (BCP), and exerted analgesic effects on BCP by reducing P2X3R overexpression and functional activity in the ipsilateral dorsal root ganglia of BCP rats. [19] The above experiments further support EA as a potential treatment option for clinical cancer pain. In addition, EA inhibited chemotherapy induced pains through activation of spinal 5-HT 1A receptors and suppression of p-CaMKII.…”
Section: Intervention Methodsmentioning
confidence: 62%
“…[18] EA ameliorated MRMT-1-induced mechanical abnormal pain and thermal nociceptive hyperalgesia in a rat model of bone cancer pain (BCP), and exerted analgesic effects on BCP by reducing P2X3R overexpression and functional activity in the ipsilateral dorsal root ganglia of BCP rats. [19] The above experiments further support EA as a potential treatment option for clinical cancer pain. In addition, EA inhibited chemotherapy induced pains through activation of spinal 5-HT 1A receptors and suppression of p-CaMKII.…”
Section: Intervention Methodsmentioning
confidence: 62%
“…As for immunology pathways, in a study of a rat model of prostate cancer bone metastases, electroacupuncture was found to inhibit pro-inflammatory cytokines, such as IL-1β, which attenuate nociceptive receptor sensitivity and inhibit pain transmission ( 40 ). Electroacupuncture can also directly downregulate the expression of nociceptive receptors in a rat model of cancer pain, such as P2X3 receptors in the dorsal root ganglion of rats ( 41 ). Electroacupuncture can modulate immune cells, such as macrophages ( 42 ), mast cells ( 43 ) and T cells ( 44 ), to reduce pain-causing substances produced by inflammation and tissue injury.…”
Section: Discussionmentioning
confidence: 99%
“…P2X3R was found to be distributed not only in the peripheral nervous system but also in the presynaptic portion of the spinal cord and in the periaqueductal gray matter (PAG) of the midbrain. Tian Shuxin et al showed that both peripheral and central P2X3Rs are involved in analgesia [ 46 ]. Moreover, Liu Min reported that the functional upregulation of P2X3R is involved in the pathogenesis of pain, as well as the fact that P2X3 receptors are involved in injurious transmission and modulation in the peripheral and central nervous system and that P2X3R blocks mechanically abnormal pain and nociceptive hyperalgesia, thus exerting a significant analgesic effect [ 47 ].…”
Section: Modulation Of Fd/mas Pain By Purinergic Receptors (P2xrs)mentioning
confidence: 99%
“…2018 Falk et al [49] Animal experiments on rats The P2X7R ion channel is expressed during OC (osteoclast) maturation, and it mediates inflammatory vesicle activation and IL-1β① release, which is needed for OC-mediated bone loss; it also mediates reduced mechanosensitivity of osteocytes P2X7R may be a potential pharmacological target for the treatment of MAS and could lead us to further investigate the role of this receptor in the progression of bone remodeling pain 2023 Sun et al [50] Overview P2X4 receptors mediate neuropathic pain in spinal cord injury and are significantly involved in mediating the pain hypersensitivity response to increased BDNF and p38-MAPK ② P2X4R and P2X7R may be trigger molecules in exercise-mediated changes in BDNF③ and provide a possible mechanism for MAS pain protection 2022 Yuan et al [47] Animal experiments on rats Pharmacological blockade of P2X3R has a significant analgesic effect on mechanical abnormal pain and thermal nociceptive sensitization It may serve as an important target for blocking pain during MAS 2023 Tian et al [46] Animal experiments on rats P2X3R is involved in analgesia, and P2X3R is distributed not only in the peripheral nervous system (such as primary afferent central terminals) but also in the presynaptic portion of the spinal cord and in the periaqueductal gray matter (PAG) of the midbrain conductors MAS pain process can be treated by blocking P2X3R as an important method of pain treatment Wang and Jiang Journal of Orthopaedic Surgery and Research (2024) 19:196 Table 4 Summary of studies on potential targeting mechanisms of brain-derived neurotrophic factor (BDNF) family receptors for bone pain ① GDNF/GFRα: GFRα is a high-affinity receptor for GDNF; ② NGF/TrkA: nerve growth factor (NGF)/promyosin receptor kinase A (TrKA) signaling axis; ③ Glial cell line-derived neurotrophic factor receptor α3…”
Section: Main Conclusionmentioning
confidence: 99%