4.7 Article

N-Butanol Extract of Modified You-Gui-Yin Attenuates Osteoclastogenesis and Ameliorates Osteoporosis by Inhibiting RANKL-Mediated NF-κB Signaling

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2022.925848

Keywords

N-butanol extraction; Modified You-Gui-Yin; postmenopausal osteoporosis; osteoclast formation; NF-kappa B pathway

Funding

  1. Natural Science Foundation of China [81904223]
  2. Hangzhou Medical and health science and Technology Project [B20200552]

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This study found that the N-butanol extract of modified You-Gui-Yin (MYGY-Nb) was more effective in suppressing bone loss in ovariectomized (OVX)-induced osteoporosis mice than the original formula. Liquid chromatography and mass spectrometry analysis identified 16 critical compounds in MYGY-Nb, some of which affect osteoclast functions. In vivo and in vitro experiments further demonstrated that MYGY-Nb attenuated osteoclastogenesis by down-regulating NF-kappa B signaling.
Postmenopausal Osteoporosis (PMOP) is the most prevalent primary osteoporosis, attributable to an imbalance in osteoblast and osteoclast activity. Modified You-Gui-Yin (MYGY), a traditional Chinese herbal formula, is able to effectively treat PMOP, while the critical components and pharmacological mechanisms of MYGY are still unclear. In this study, we aimed to investigate the therapeutic effects and underlying mechanisms of N-butanol extract of MYGY (MYGY-Nb) in ovariectomized (OVX)-induced osteoporosis mice. Histological staining and micro-computed tomography (mu CT) analysis showed that MYGY-Nb was more effective in the suppression of OVX-induced bone loss than MYGY original formula. Subsequently, liquid chromatography and mass spectrometry analysis identified 16 critical compounds of MYGY-Nb and some of them are reported to affect osteoclast functions. Furthermore, in vivo and in vitro experiments demonstrated that MYGY-Nb significantly attenuated osteoclastogenesis by down-regulating RANKL-mediated NF-kappa B signaling. In conclusion, our study indicated that MYGY-Nb suppresses NF-kappa B signaling and osteoclast formation to mitigate bone loss in PMOP, implying that MYGY-Nb and its compounds are potential candidates for development of anti-PMOP drugs.

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