Antrodia cinnamomea prevents ovariectomized‐promoted bone loss by inhibiting osteoclast formation

Author:

Po‐Chun Chang1,Su Hui‐Kan2,Liu Shan‐Chi3,Thuong Le Huynh Hoai4,Wu Yang‐Chang456,Chen Hsien‐Te78,Wu Tung‐Ying9,Tang Chih‐Hsin410111213ORCID

Affiliation:

1. Department of Orthopedic An Nan Hospital, China Medical University Tainan Taiwan

2. Department of Pathology Laboratory Pingtung Veterans General Hospital Pingtung County Taiwan

3. Institute of Biomedical Sciences, Mackay Medical College New Taipei City Taiwan

4. Graduate Institute of Biomedical Science, China Medical University Taichung Taiwan

5. Chinese Medicine Research and Development Center, China Medical University Hospital Taichung Taiwan

6. Graduate Institute of Integrated Medicine, China Medical University Taichung Taiwan

7. Department of Sports Medicine College of Health Care, China Medical University Taichung Taiwan

8. Department of Orthopedic Surgery China Medical University Hospital Taichung Taiwan

9. Department of Food Science and Nutrition Meiho University Pingtung Taiwan

10. Department of Pharmacology School of Medicine, China Medical University Taichung Taiwan

11. Department of Medical Laboratory Science and Biotechnology Asia University Taichung Taiwan

12. Chinese Medicine Research Center, China Medical University Taichung Taiwan

13. Department of Medical Research China Medical University Hsinchu Hospital Hsinchu Taiwan

Abstract

AbstractOsteoporosis is a common bone disease in aging populations, particularly in postmenopausal women. Anti‐resorptive and anabolic drugs have been applied to prevent and cure osteoporosis and are linked with a variety of adverse effects. Antrodia cinnamomea extracts (ACE) are highly renowned for their anticancer, antioxidative, and anti‐inflammatory properties. However, whether ACE‐enriched anti‐osteoporosis functions are largely unknown. In a preclinical animal model, we found that ovariectomy significantly decreased bone volume in the ovariectomized (OVX) rats. Administration of ACE antagonized OVX‐induced bone loss. In addition, ACE reversed OVX‐reduced biomechanical properties. The serum osteoclast marker also showed improvement in the ACE‐treated group. In the cellular model, it was indicated that ACE inhibits RANKL‐induced osteoclast formation. Taken together, ACE seems to be a hopeful candidate for the development of novel anti‐osteoporosis treatment.

Funder

Ministry of Science and Technology of Taiwan

TMANH

China Medical University Hospital

Publisher

Wiley

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