PGE2/EP4 skeleton interoception activity reduces vertebral endplate porosity and spinal pain with low-dose celecoxib

查看全文 作　　者：Peng [1,2,3]Xue;Shenyu [1]Wang;Xiao [1]Lyu;Mei [1]Wan;Xialin [1]Li;Lei [4]Ma;Neil [5]CFord;Yukun [2]Li;Yun [5]Guan;Wenyuan [4]Ding;Xu [1]Cao

机构地区：[1]Department of Orthopaedic Surgery,The Johns Hopkins University School of Medicine,Baltimore,MD,USA;[2]Department of Endocrinology,The Third Hospital of Hebei Medical University,Shijiazhuang,Hebei,P.R.China;[3]Key Laboratory of Orthopaedic Biomechanics of Hebei Province,Shijiazhuang,Hebei,P.R.China;[4]Department of Spine Surgery,The Third Hospital of Hebei Medical University,Shijiazhuang,Hebei,P.R.China;[5]Department of Anesthesiology and Critical Care Medicine,The Johns Hopkins University School of Medicine,Baltimore,MD,USA

出　　处：《Bone Research》索引2021年第9卷第3期,共14页

基　　金：supported by National Institute on Aging of the National Institutes of Health under Award Number R01 AG068997 and P01 AG066603(to X.C.). 摘　　要：Skeletal interoception regulates bone homeostasis through the prostaglandin E2(PGE2)concentration in bone.Vertebral endplates undergo ossification and become highly porous during intervertebral disc degeneration and aging.We found that the PGE2 concentration was elevated in porous endplates to generate spinal pain.Importantly,treatment with a high-dose cyclooxygenase 2 inhibitor(celecoxib,80 mg·kg−1 per day)decreased the prostaglandin E2 concentration and attenuated spinal pain in mice with lumbar spine instability.However,this treatment impaired bone formation in porous endplates,and spinal pain recurred after discontinuing the treatment.Interestingly,low-dose celecoxib(20 mg·kg−1 per day,which is equivalent to one-quarter of the clinical maximum dosage)induced a latent inhibition of spinal pain at 3 weeks post-treatment,which persisted even after discontinuing treatment.Furthermore,when the prostaglandin E2 concentration was maintained at the physiological level with low-dose celecoxib,endplate porosity was reduced significantly,which was associated with decreased sensory nerve innervation and spinal pain.These findings suggest that low-dose celecoxib may help to maintain skeletal interoception and decrease vertebral endplate porosity,thereby reducing sensory innervation and spinal pain in mice. 关键词：pain DOSAGE IMPAIRED

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PGE2/EP4 skeleton interoception activity reduces vertebral endplate porosity and spinal pain with low-dose celecoxib

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