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An Integrative Study on the Inhibition of Bone Loss Via Osteo-F Based on Network Pharmacology, Experimental Verification, and Clinical Trials in Postmenopausal Women

Overview
Journal Cells
Publisher MDPI
Date 2023 Aug 11
PMID 37566071
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Abstract

The inhibition of bone loss remains a challenge for postmenopausal women, considering the fact that only three anabolic treatments for osteoporosis have been approved by the FDA. This study aimed to investigate the osteogenic capacities of Osteo-F, a newly developed herbal formula, upon integrating network analysis and pre-clinical studies into clinical trials. The network pharmacology analysis showed that a potential mechanism of Osteo-F is closely related to osteoblast differentiation. Consistent with the predicted mechanism, Osteo-F treatment significantly enhanced bone matrix formation and mineralization with collagen expression in osteoblasts. Simultaneously, secreted bone-forming molecules were upregulated by Osteo-F. After the administration of Osteo-F to osteoporotic mice, the femoral BMD and osteocalcin in the serum and bone tissues were significantly improved. Subsequently, a randomized, double-blinded, placebo-controlled clinical trial showed that 253 mg of Osteo-F supplementation for 24 weeks resulted in significant improvements in the Z-score and serum osteocalcin levels of postmenopausal women compared to the placebo, thus indicating bone anabolic efficacy. In the current study, the bone anabolic effect of Osteo-F was determined by activating the differentiation and mineralization of osteoblasts through integrating experiments based on network analysis into clinical trials, with synchronized, reliable evidence, demonstrating that Osteo-F is a novel bone anabolic treatment in postmenopausal women.

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References
1.
Siddiqui J, Partridge N . Physiological Bone Remodeling: Systemic Regulation and Growth Factor Involvement. Physiology (Bethesda). 2016; 31(3):233-45. PMC: 6734079. DOI: 10.1152/physiol.00061.2014. View

2.
Tu K, Lie J, Wan C, Cameron M, Austel A, Nguyen J . Osteoporosis: A Review of Treatment Options. P T. 2018; 43(2):92-104. PMC: 5768298. View

3.
Steinmetz K, Spack E . The basics of preclinical drug development for neurodegenerative disease indications. BMC Neurol. 2009; 9 Suppl 1:S2. PMC: 2697630. DOI: 10.1186/1471-2377-9-S1-S2. View

4.
Licata A . Diagnosing primary osteoporosis: it's more than a T score. Cleve Clin J Med. 2006; 73(5):473-6. DOI: 10.3949/ccjm.73.5.473. View

5.
Chen D, Harris M, Rossini G, Dunstan C, Dallas S, Feng J . Bone morphogenetic protein 2 (BMP-2) enhances BMP-3, BMP-4, and bone cell differentiation marker gene expression during the induction of mineralized bone matrix formation in cultures of fetal rat calvarial osteoblasts. Calcif Tissue Int. 1997; 60(3):283-90. DOI: 10.1007/s002239900230. View