Abstract

Abeliophyllum distichum Nakai is known as a monotypic genus endemic to South Korea. Currently, several pharmacological studies have revealed that A. distichum extract exhibits diverse biological functions, including anti-cancer, anti-diabetic, anti-hypertensive, and anti-inflammatory activities. In this study, we present the anti-osteoporotic activity of A. distichum extract by inhibiting osteoclast formation. First, we show that the methanolic extract of the leaves of A. distichum, but not extracts of the branches or fruits, significantly inhibits receptor activator of the NF-κB ligand (RANKL)-induced osteoclast differentiation. Second, our transcriptome analysis revealed that the leaf extract (LE) blocks sets of RANKL-mediated osteoclast-related genes. Third, the LE attenuates the phosphorylation of extracellular signal-related kinase. Finally, treatment with the LE effectively prevents postmenopausal bone loss in ovariectomized mice and glucocorticoid-induced osteoporosis in zebrafish. Our findings show that the extract of A. distichum efficiently suppressed osteoclastogenesis by regulating osteoclast-related genes, thus offering a novel therapeutic strategy for osteoporosis.

Highlights

  • Bone tissue is continuously maintained by osteoclasts and osteoblasts [1]

  • Considering the fact that osteoclast differentiation involves several distinct steps such as cell proliferation, we determined the effect of those extracts on Osteoclast precursor (OCP) cell proliferation

  • Prednisolone significantly attenuated bone mineralization in zebrafish larvae, which was counteracted by leaf extract (LE) treatment. These results strongly suggest that LE prevents both postmenopausal osteoporosis and by9,inhibiting osteoclast differentiation

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Summary

Introduction

Bone tissue is continuously maintained by osteoclasts and osteoblasts [1]. They are remodeled through life to regenerate damaged bones and maintain mechanical strength. An imbalance between bone resorption and bone formation can cause bone diseases, including osteoporosis and osteopetrosis [2]. Osteoporosis is a metabolic skeletal disorder caused by excessive bone resorption, which is characterized by low bone mass and the microstructural deterioration of bone tissue. These processes decrease the mechanical strength of the bone and increase the risk of fracture [3,4]. Osteoporosis has been classified into two main groups: primary and secondary

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