Combined Effects of Soy Isoflavones and β-Carotene on Osteoblast Differentiation

Int J Environ Res Public Health. 2015 Oct 28;12(11):13750-61. doi: 10.3390/ijerph121113750.

Abstract

Soy isoflavones, genistein, daidzein and its metabolite equol, as well as β-carotene have been reported to be effective for maintaining bone health. However, it remains to be elucidated whether combining soy isoflavones with β-carotene is beneficial to bone formation. This study investigated the combined effect of soy isoflavones and β-carotene on the differentiation of MC3T3-E1 preosteoblastic cells. Daidzein and genistein alone did not affect cell growth but increased alkaline phosphatase (ALP) activity. Beta-carotene alone inhibited cell growth and markedly enhanced ALP activity. Soy isoflavones combined with β-carotene resulted in higher ALP activity than treatment with isoflavones or β-carotene alone. We observed significant main effects of β-carotene on the enhanced expression of Runx2, ALP, and ostepontin mRNA, whereas there was a significant main effect of soy isoflavones on the expression of osterix mRNA. To investigate how β-carotene affected osteoblast differentiation, MC3T3-E1 cells were treated with retinoic acid receptor (RAR) pan-antagonist combined with β-carotene. Osteopontin and ALP mRNA expression levels, which were increased following treatment with β-carotene, were significantly suppressed by the RAR pan-antagonist. This suggests treatment with β-carotene enhanced early osteoblastic differentiation, at least in part via RAR signaling. These results indicate that a combination of isoflavones and β-carotene may be useful for maintaining a positive balance of bone turnover by inducing osteoblast differentiation.

Keywords: bone; osteoblast differentiation; soy isoflavones; β-carotene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects*
  • Cell Line
  • Cell Proliferation / drug effects
  • Drug Synergism
  • Functional Food
  • Glycine max
  • Isoflavones / pharmacology*
  • Isoflavones / therapeutic use
  • Mice
  • Osteoblasts / drug effects*
  • Osteoporosis / prevention & control
  • Phytotherapy
  • RNA, Messenger / metabolism
  • Receptors, Retinoic Acid / antagonists & inhibitors
  • Signal Transduction
  • beta Carotene / pharmacology*
  • beta Carotene / therapeutic use

Substances

  • Isoflavones
  • RNA, Messenger
  • Receptors, Retinoic Acid
  • beta Carotene
  • daidzein