Anti-osteoporotic effects of n-trans-hibiscusamide and its derivative alleviate ovariectomy-induced bone loss in mice by regulating RANKL-induced signaling

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dc.contributor.authorHyung Jin Lim-
dc.contributor.authorEun Jae Park-
dc.contributor.authorYeong-Seon Won-
dc.contributor.authorSeon Gyeong Bak-
dc.contributor.authorS H Cheong-
dc.contributor.authorSeung Woong Lee-
dc.contributor.authorSoyoung Lee-
dc.contributor.authorSeung Jae Lee-
dc.contributor.authorMun Chual Rho-
dc.date.accessioned2021-11-12T15:30:26Z-
dc.date.available2021-11-12T15:30:26Z-
dc.date.issued2021-
dc.identifier.issn1420-3049-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/24992-
dc.description.abstractOsteoporosis is characterized by the deterioration of bone structures and decreased bone mass, leading to an increased risk of fracture. Estrogen deficiency in postmenopausal women and aging are major factors of osteoporosis and are some of the reasons for reduced quality of life. In this study, we investigated the effects of n-trans-hibiscusamide (NHA) and its derivative 4-O-(E)-feruloyl-N-(E)-hibiscusamide (HAD) on receptor activator of nuclear factor kappa-B (NF- B) ligand (RANKL)-induced osteoclast differentiation and an ovariectomized osteoporosis mouse model. NHA and HAD significantly inhibited the differentiation of osteoclasts from bone marrow-derived macrophages (BMMs) and the expression of osteoclast differentiation-related genes. At the molecular level, NHA and HAD significantly downregulated the phosphorylation of mitogen-activated protein kinase (MAPK) signaling molecules. However, Akt and NF- B phosphorylation was inhibited only after NHA or HAD treatment. In the ovariectomy (OVX)-induced osteoporosis model, both NHA and HAD effectively improved trabecular bone structure. C-terminal telopeptide (CTX), a bone resorption marker, and RANKL, an osteoclast stimulation factor, were significantly reduced by NHA and HAD. The tartrate-resistant acid phosphatase (TRAP)-stained area, which indicates the osteoclast area, was also decreased by these compounds. These results show the potential of NHA and HAD as therapeutic agents for osteoporosis.-
dc.publisherMDPI-
dc.titleAnti-osteoporotic effects of n-trans-hibiscusamide and its derivative alleviate ovariectomy-induced bone loss in mice by regulating RANKL-induced signaling-
dc.title.alternativeAnti-osteoporotic effects of n-trans-hibiscusamide and its derivative alleviate ovariectomy-induced bone loss in mice by regulating RANKL-induced signaling-
dc.typeArticle-
dc.citation.titleMolecules-
dc.citation.number22-
dc.citation.endPage6820-
dc.citation.startPage6820-
dc.citation.volume26-
dc.contributor.affiliatedAuthorHyung Jin Lim-
dc.contributor.affiliatedAuthorEun Jae Park-
dc.contributor.affiliatedAuthorYeong-Seon Won-
dc.contributor.affiliatedAuthorSeon Gyeong Bak-
dc.contributor.affiliatedAuthorSeung Woong Lee-
dc.contributor.affiliatedAuthorSoyoung Lee-
dc.contributor.affiliatedAuthorSeung Jae Lee-
dc.contributor.affiliatedAuthorMun Chual Rho-
dc.contributor.alternativeName임형진-
dc.contributor.alternativeName박은재-
dc.contributor.alternativeName원영선-
dc.contributor.alternativeName박선경-
dc.contributor.alternativeName정선희-
dc.contributor.alternativeName이승웅-
dc.contributor.alternativeName이소영-
dc.contributor.alternativeName이승재-
dc.contributor.alternativeName노문철-
dc.identifier.bibliographicCitationMolecules, vol. 26, no. 22, pp. 6820-6820-
dc.identifier.doi10.3390/molecules26226820-
dc.subject.keywordn-trans-hibiscusamide-
dc.subject.keyword4-O-(E)-feruloyl-N-(E)-hibiscusamide-
dc.subject.keywordOsteoclastogenesis-
dc.subject.keywordOVX induced osteoporosis-
dc.subject.localn-trans-hibiscusamide-
dc.subject.local4-O-(E)-feruloyl-N-(E)-hibiscusamide-
dc.subject.localOsteoclastogenesis-
dc.subject.localosteoclastogenesis-
dc.subject.localOVX induced osteoporosis-
dc.description.journalClassY-
Appears in Collections:
Jeonbuk Branch Institute > Functional Biomaterial Research Center > 1. Journal Articles
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