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Ethanolic extract of Pyrrosia lingua (Thunb.) Farw. ameliorates OVX-induced bone loss and RANKL-induced osteoclastogenesis.

Authors :
Jang, Seon-A
Hwang, Youn-Hwan
Yang, Hyun
Ryuk, Jin Ah
Gu, Dong Ryun
Ha, Hyunil
Source :
Biomedicine & Pharmacotherapy. Mar2022, Vol. 147, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Pyrrosia lingua (Thunb.) Farw is a common plant that has been widely used as a traditional herbal medicine in China and Korea to treat patients suffering from pain, vaginal bleeding and urolithiasis. However, the pharmacological effects of P. lingua on bone remain unknown. We investigated the anti-osteoporotic effects of an ethanolic extract of P. lingua (EEPL). We found that EEPL suppressed osteoclast differentiation by directly acting on osteoclast precursor cells. EEPL suppressed the expression of receptor activator of nuclear factor-κB ligand (RANKL)-induced nuclear factor of activated T cells 1, a major transcription factor for osteoclastogenesis, by inhibiting RANKL-induced expression of aryl hydrocarbon receptor/c-Fos, and activation of nuclear factor-κB and mitogen-activated protein kinases. Moreover, administration of EEPL inhibited trabecular bone loss and weight gain in ovariectomized mice. Furthermore, we identified phytochemicals in EEPL that are known to exert anti-osteoclastogenic or anti-osteoporotic effects using ultra-high-performance liquid chromatography–tandem mass-spectrometry analysis. Overall, the results of this study suggest that EEPL is effective therapeutic candidate that can be used to prevent or treat postmenopausal osteoporosis. [Display omitted] • Ethanolic extract of Pyrrosia lingua (Thunb.) Farw. (EEPL) inhibits RANKL-induced osteoclastogenesis in vitro. • EEPL prevents OVX-induced bone loss in vivo. • EEPL could be explored as a potential therapeutic candidate for postmenopausal osteoporosis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
147
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
155208123
Full Text :
https://doi.org/10.1016/j.biopha.2022.112640