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Current Pharmaceutical Biotechnology

Editor-in-Chief

ISSN (Print): 1389-2010
ISSN (Online): 1873-4316

Research Article

Icariin Accelerates Fracture Healing via Activation of the WNT1/β-catenin Osteogenic Signaling Pathway

Author(s): Xiao-Yun Zhang*, Yue-Ping Chen*, Chi Zhang, Xuan Zhang, Tian Xia, Jie Han, Nan Yang, Shi-Lei Song and Can-Hong Xu

Volume 21, Issue 15, 2020

Page: [1645 - 1653] Pages: 9

DOI: 10.2174/1389201021666200611121539

Price: $65

Abstract

Background: Icariin has been shown to enhance bone formation.

Objective: The present study aimed to investigate whether icariin also promotes bone fracture healing and its mechanisms.

Methods: First, we isolated and cultured rat bone marrow stromal cells (rBMSCs) with icariincontaining serum at various concentrations (0%, 2.5%, 5% and 10%) and then measured alkaline phosphatase (ALP) activity and the expression of Core-binding factor, alpha 1 (Cbfα1), bone morphogenetic protein-2 (BMP-2) and bone morphogenetic protein-4 (BMP-4) in the rBMSCs. Second, we established a model of fracture healing in rats and performed gavage treatment for 20 days. Then, we detected bone biochemical markers (ELISA kits) in the serum, fracture healing (digital radiography, DR), and osteocalcin expression (immunohistochemistry).

Results: Icariin treatment increased ALP activity and induced the expression of Cbfα1, BMP-2 and BMP-4 in rBMSCs in a dose-dependent manner. In addition, Icariin increased the serum levels of osteocalcin (OC), bone-specific alkaline phosphatase (BAP), N-terminal telopeptides of type I collagen (NTX-1), C-terminal telopeptide of type I collagen (CTX-1) and tartrate-resistant acid phosphatase 5b (TRACP-5b); promoted osteocalcin secretion at the fracture site; and accelerated fracture healing.

Conclusion: Icariin can promote the levels of bone-formation markers, accelerate fracture healing, and activate the WNT1/β-catenin osteogenic signaling pathway.

Keywords: Icariin, rat bone marrow stromal cells, fracture healing, WNT1/β-catenin, ELISA kits, osteocalcin expression.

Graphical Abstract

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