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A comparatively study of menaquinone-7 isolated from Cheonggukjang with vitamin K and menaquinone-4 on osteoblastic cells differentiation and mineralization. | LitMetric

A comparatively study of menaquinone-7 isolated from Cheonggukjang with vitamin K and menaquinone-4 on osteoblastic cells differentiation and mineralization.

Food Chem Toxicol

Department of Oriental Medicine Resources, College of Environmental and Bioresource Sciences, Chonbuk National University, Iksan, 570-752, Republic of Korea. Electronic address:

Published: September 2019

The effect of menaquinone-7 isolated from cheonggukjang was comparatively investigated with vitamin K and menaquinone-4 on cell differentiation and mineralization of the osteoblastic cell line MC3T3-E1. Results indicated that all vitamin K species significantly increased MC3T3-E1 cell proliferation, cellular alkaline phosphatase activity, osteocalcin synthesis, and calcium deposition in a dose-dependent manner. Menaquinone-4 and menaquinone-7 had more potent effects on calcium deposition than vitamin K, and their effects were only partly reduced by warfarin (γ-carboxylation inhibitor) treatment, while warfarin abolished the induction activity of vitamin K on calcification. This suggests that vitamin K and K (menaquinone-4 & menaquinone-7) may have different mechanisms in stimulating osteoblast mineralization. In addition, the mRNA expression ratio of osteoprotegerin and the receptor activator of nuclear factor-kB ligand was also dramatically increased by treatment with vitamin K (62%), menaquinone-4 (247%), and menaquinone-7 (329%), suggesting that vitamin K may suppress the formation of osteoclast by up-regulating the ratio of osteoprotegerin/receptor activator of nuclear factor-kB ligand in osteoblasts. These results provide compelling evidence that vitamin K, menaquinone-4, and menaquinone-7 all can promote bone health, which might be associated with elevations in the osteoprotegerin/receptor activator of nuclear factor-kB ligand ratio.

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http://dx.doi.org/10.1016/j.fct.2019.05.048DOI Listing

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