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Cited 19 time in webofscience Cited 22 time in scopus
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Isoflavones extracted from Sophorae fructus upregulate IGF-I and TGF-beta and inhibit osteociastogenesis in rat born marrow cells

Authors
Joo, SSWon, TJKang, HCLee, DI
Issue Date
Jan-2004
Publisher
PHARMACEUTICAL SOCIETY KOREA
Keywords
isoflavone; Sophorae fructus; osteoclastogenesis; growth factors; nitric oxide
Citation
ARCHIVES OF PHARMACAL RESEARCH, v.27, no.1, pp 99 - 105
Pages
7
Journal Title
ARCHIVES OF PHARMACAL RESEARCH
Volume
27
Number
1
Start Page
99
End Page
105
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24896
DOI
10.1007/BF02980054
ISSN
0253-6269
1976-3786
Abstract
Isoflavones have been a central subject in research on the natural phytoestrogens found in Leguminosee. Their effects on bone formation and remodeling are important in that they can act like estrogen by binding on estrogen receptors on the target cell surface. We, therefore, believed that isoflavones may help in the treatment of patients with estrogen deficiency disease such as estrogen replacement therapy (ERT) for osteoporosis. As commonly known, osteoporosis is one of the hormonal deficiency diseases, especially in menopausal women. When estrogen is no longer produced in the body a remarkable bone remodeling process occurs, and the associated events are regulated by growth factors in the osteoblast lineage. In the present study, we investigated whether isoflavones (Isocal) extracted from Sophorae fructus affect the growth factors IGF-I and TGF-beta that have been known to be related with bone formation. In the study, we found that the active control (PIII) effectively enhanced the level of nitric oxide (NO) and growth factors, and thereby inhibited osteoclastogenesis. The most efficient concentration was 10(-8)% within five days, whereas the comparative control (soybean isoflavone) was not as effective even at a lower concentration. In conclusion, the products which contain enriched glucosidic isoflavone and nutrient supplements such as shark cartilage and calcium can be used for osteoporosis therapy by enhancing the production of IGF-I and TGF-beta. Furthermore, the NO produced through endothelial constitutive NO synthase (ecNOS) may play a role in inhibiting bone reabsorption.
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