Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus

<i>Melia toosendan</i> fructus, traditionally employed in traditional Chinese and Korean herbal medicine, exhibits diverse biological properties encompassing anti-tumor, anti-inflammatory, and anti-viral effects. However, its influence on bone metabolism remains largely unexplored. In th...

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Main Authors: Seong Cheol Kim, Dong Ryun Gu, Hyun Yang, Sung-Ju Lee, Jin Ah Ryuk, Hyunil Ha
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/15/10/2454
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author Seong Cheol Kim
Dong Ryun Gu
Hyun Yang
Sung-Ju Lee
Jin Ah Ryuk
Hyunil Ha
author_facet Seong Cheol Kim
Dong Ryun Gu
Hyun Yang
Sung-Ju Lee
Jin Ah Ryuk
Hyunil Ha
author_sort Seong Cheol Kim
collection DOAJ
description <i>Melia toosendan</i> fructus, traditionally employed in traditional Chinese and Korean herbal medicine, exhibits diverse biological properties encompassing anti-tumor, anti-inflammatory, and anti-viral effects. However, its influence on bone metabolism remains largely unexplored. In this study, we investigated the impact of an ethanolic extract of <i>Melia toosendan</i> fructus (MTE) on osteoclast differentiation and characterized its principal active constituent in osteoclast differentiation and function, as well as its effects on bone protection. Our findings demonstrate that MTE effectively inhibits the differentiation of osteoclast precursors induced by receptor activator of nuclear factor κB ligand (RANKL). Utilizing a bioassay-guided fractionation approach coupled with UHPLC-MS/MS analysis, we isolated and identified the triterpenoid compound toosendanin (TSN) as the active constituent responsible for MTE’s anti-osteoclastogenic activity. TSN treatment downregulated the expression of nuclear factor of activated T cells c1, a pivotal osteoclastogenic transcription factor, along with molecules implicated in osteoclast-mediated bone resorption, including tumor necrosis factor receptor-associated factor 6, carbonic anhydrase II, integrin beta-3, and cathepsin K. Furthermore, treatment of mature osteoclasts with TSN impaired actin ring formation, acidification, and resorptive function. Consistent with our in vitro findings, TSN administration mitigated trabecular bone loss and reduced serum levels of the bone resorption marker, C-terminal cross-linked telopeptides of type I collagen, in a mouse bone loss model induced by intraperitoneal injections of RANKL. These results suggest that TSN, as the principal active constituent of MTE with inhibitory effects on osteoclastogenesis, exhibits bone-protective properties by suppressing both osteoclast differentiation and function. These findings imply the potential utility of TSN in the treatment of diseases characterized by excessive bone resorption.
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spelling doaj.art-d12b610cc0e04e42be6a8e5ffd0fbdb82023-11-19T17:44:44ZengMDPI AGPharmaceutics1999-49232023-10-011510245410.3390/pharmaceutics15102454Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> FructusSeong Cheol Kim0Dong Ryun Gu1Hyun Yang2Sung-Ju Lee3Jin Ah Ryuk4Hyunil Ha5KM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of KoreaKM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of KoreaKM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of KoreaKM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of KoreaKM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of KoreaKM Convergence Research Division, Korea Institute of Oriental Medicine (KIOM), Yuseong-daero 1672, Yuseong-gu, Daejeon 34054, Republic of Korea<i>Melia toosendan</i> fructus, traditionally employed in traditional Chinese and Korean herbal medicine, exhibits diverse biological properties encompassing anti-tumor, anti-inflammatory, and anti-viral effects. However, its influence on bone metabolism remains largely unexplored. In this study, we investigated the impact of an ethanolic extract of <i>Melia toosendan</i> fructus (MTE) on osteoclast differentiation and characterized its principal active constituent in osteoclast differentiation and function, as well as its effects on bone protection. Our findings demonstrate that MTE effectively inhibits the differentiation of osteoclast precursors induced by receptor activator of nuclear factor κB ligand (RANKL). Utilizing a bioassay-guided fractionation approach coupled with UHPLC-MS/MS analysis, we isolated and identified the triterpenoid compound toosendanin (TSN) as the active constituent responsible for MTE’s anti-osteoclastogenic activity. TSN treatment downregulated the expression of nuclear factor of activated T cells c1, a pivotal osteoclastogenic transcription factor, along with molecules implicated in osteoclast-mediated bone resorption, including tumor necrosis factor receptor-associated factor 6, carbonic anhydrase II, integrin beta-3, and cathepsin K. Furthermore, treatment of mature osteoclasts with TSN impaired actin ring formation, acidification, and resorptive function. Consistent with our in vitro findings, TSN administration mitigated trabecular bone loss and reduced serum levels of the bone resorption marker, C-terminal cross-linked telopeptides of type I collagen, in a mouse bone loss model induced by intraperitoneal injections of RANKL. These results suggest that TSN, as the principal active constituent of MTE with inhibitory effects on osteoclastogenesis, exhibits bone-protective properties by suppressing both osteoclast differentiation and function. These findings imply the potential utility of TSN in the treatment of diseases characterized by excessive bone resorption.https://www.mdpi.com/1999-4923/15/10/2454<i>Melia toosendan</i>toosendaninbone resorptionosteoporosisRANKL
spellingShingle Seong Cheol Kim
Dong Ryun Gu
Hyun Yang
Sung-Ju Lee
Jin Ah Ryuk
Hyunil Ha
Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
Pharmaceutics
<i>Melia toosendan</i>
toosendanin
bone resorption
osteoporosis
RANKL
title Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
title_full Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
title_fullStr Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
title_full_unstemmed Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
title_short Isolation and Characterization of an Anti-Osteoporotic Compound from <i>Melia toosendan</i> Fructus
title_sort isolation and characterization of an anti osteoporotic compound from i melia toosendan i fructus
topic <i>Melia toosendan</i>
toosendanin
bone resorption
osteoporosis
RANKL
url https://www.mdpi.com/1999-4923/15/10/2454
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