Publication:
Cyperenoic acid suppresses osteoclast differentiation and delays bone loss in a senile osteoporosis mouse model by inhibiting non-canonical NF-κB pathway

dc.contributor.authorSupatta Chawalitpongen_US
dc.contributor.authorRatchanaporn Chokchaisirien_US
dc.contributor.authorApichart Suksamrarnen_US
dc.contributor.authorShigeru Katayamaen_US
dc.contributor.authorTakakazu Mitanien_US
dc.contributor.authorSoichiro Nakamuraen_US
dc.contributor.authorAhmad Ai Athamnehen_US
dc.contributor.authorPatcharee Ritprajaken_US
dc.contributor.authorAsada Leelahavanichkulen_US
dc.contributor.authorRatchaneevan Aeimlapaen_US
dc.contributor.authorNarattaphol Charoenphandhuen_US
dc.contributor.authorTanapat Palagaen_US
dc.contributor.otherUniversity of Phayaoen_US
dc.contributor.otherShinshu Universityen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherRamkhamhaeng Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2019-08-28T07:11:39Z
dc.date.available2019-08-28T07:11:39Z
dc.date.issued2018-12-01en_US
dc.description.abstract© 2018 The Author(s). Cyperenoic acid is a terpenoid isolated from the root of a medicinal plant Croton crassifolius with a wide range of biological activities. In this study, the effects of cyperenoic acid on osteoclast differentiation were investigated both in vitro and in vivo using receptor activator of nuclear factor-κB ligand (RANKL)-induced bone marrow-derived osteoclasts and senescence-accelerated mouse prone 6 (SAMP6). Cyperenoic acid significantly suppressed RANKL-induced osteoclast differentiation at the concentrations with no apparent cytotoxicity. The half maximum inhibitory concentration (IC50) for osteoclast differentiation was 36.69 μM ± 1.02. Cyperenoic acid treatment evidently reduced the expression of two key transcription factors in osteoclast differentiation, NFATc1 and c-Fos. Detailed signaling analysis revealed that cyperenoic acid did not affect MAPK pathways and canonical NF-κB pathway but impaired activation of p100/p52 in the non-canonical NF-κB pathway upon RANKL stimulation. Moreover, the expression of osteoclast-related genes, nfatc1, ctsk, irf8, acp5 and cfos were disrupted by cyperenoic acid treatment. The bone resorption activity by cyperenoic acid-treated osteoclasts were impaired. In a senile osteoporosis mouse model SAMP6, mice fed on diet supplemented with cyperenoic acid showed delay in bone loss, compared to the control. Taken together, plant-derived cyperenoic acid shows great potential as therapeutic agent for osteoporosis.en_US
dc.identifier.citationScientific Reports. Vol.8, No.1 (2018)en_US
dc.identifier.doi10.1038/s41598-018-23912-3en_US
dc.identifier.issn20452322en_US
dc.identifier.other2-s2.0-85044978366en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/47493
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044978366&origin=inwarden_US
dc.subjectMultidisciplinaryen_US
dc.titleCyperenoic acid suppresses osteoclast differentiation and delays bone loss in a senile osteoporosis mouse model by inhibiting non-canonical NF-κB pathwayen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044978366&origin=inwarden_US

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