TY - JOUR
T1 - Regulation of osteoclastogenesis by Simon extracts composed of caffeic acid and related compounds
T2 - Successful suppression of bone destruction accompanied with adjuvant-induced arthritis in rats
AU - Quan, Yong Tang
AU - Kukita, Toshio
AU - Ushijima, Yuki
AU - Kukita, Akiko
AU - Nagata, Kengo
AU - Sandra, Ferry
AU - Watanabe, Toshiyuki
AU - Toh, Kazuko
AU - Okuma, Yutaka
AU - Kawasaki, Sadamichi
AU - Rasubala, Linda
AU - Teramachi, Junpei
AU - Miyamoto, Ichiko
AU - Wu, Zhou
AU - Iijima, Tadahiko
N1 - Funding Information:
Acknowledgements We thank Dr. Go Hirata of Department of Orthopedic Surgery, Faculty of Medical Science, Kyushu University for kind suggestions. This work was supported in part by a Grant for Scientific Research from the Japanese Ministry of Education, Science, and Culture (project 14571738). The authors have no conflicting financial interests.
PY - 2006/3
Y1 - 2006/3
N2 - Simon extracts are vitamin K1-rich food materials extracted from the leaves of the Simon sweet potato. Although vitamin K is known to stimulate bone formation, we postulated that Simon extracts also contain unknown biological compounds having the ability to regulate bone resorption. Here we prepared the vitamin K-free fraction from the Simon extracts and investigated the ability of this fraction on the differentiation of osteoclasts. A remarkable inhibitory effect of osteoclastogenesis was observed when osteoclast precursors were treated with this fraction in rat bone marrow culture systems as well as in a pure differentiation system using murine osteoclast precursor cell line. The vitamin K-free Simon extracts markedly suppressed severe bone destruction mediated by abundant osteoclasts associated with adjuvant-induced arthritis in rats. High performance liquid chromatography (HPLC) analysis revealed that the vitamin K-free Simon extracts contained three types of low molecular weight inhibitors for osteoclastogenesis; caffeic acid, chlorogenic acids and isochlorogenic acids. Among these substances, caffeic acid showed the most powerful inhibitory effects on osteoclastogenesis. Caffeic acid significantly suppressed expression of NFATc1, a key transcription factor for the induction of osteoclastogenesis. Our current study enlightened a high utility of the Simon extracts and their chemical components as effective regulators for bone resorption accompanied with inflammation and metabolic bone diseases.
AB - Simon extracts are vitamin K1-rich food materials extracted from the leaves of the Simon sweet potato. Although vitamin K is known to stimulate bone formation, we postulated that Simon extracts also contain unknown biological compounds having the ability to regulate bone resorption. Here we prepared the vitamin K-free fraction from the Simon extracts and investigated the ability of this fraction on the differentiation of osteoclasts. A remarkable inhibitory effect of osteoclastogenesis was observed when osteoclast precursors were treated with this fraction in rat bone marrow culture systems as well as in a pure differentiation system using murine osteoclast precursor cell line. The vitamin K-free Simon extracts markedly suppressed severe bone destruction mediated by abundant osteoclasts associated with adjuvant-induced arthritis in rats. High performance liquid chromatography (HPLC) analysis revealed that the vitamin K-free Simon extracts contained three types of low molecular weight inhibitors for osteoclastogenesis; caffeic acid, chlorogenic acids and isochlorogenic acids. Among these substances, caffeic acid showed the most powerful inhibitory effects on osteoclastogenesis. Caffeic acid significantly suppressed expression of NFATc1, a key transcription factor for the induction of osteoclastogenesis. Our current study enlightened a high utility of the Simon extracts and their chemical components as effective regulators for bone resorption accompanied with inflammation and metabolic bone diseases.
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U2 - 10.1007/s00418-005-0062-4
DO - 10.1007/s00418-005-0062-4
M3 - Article
C2 - 16205940
AN - SCOPUS:32444432178
SN - 0948-6143
VL - 125
SP - 215
EP - 225
JO - Histochemistry and Cell Biology
JF - Histochemistry and Cell Biology
IS - 3
ER -