4.7 Article

Structural characterization and osteoprotective effects of a novel oligo-glucomannan obtained from the rhizome of Cibotium barometz by alkali extraction

期刊

INDUSTRIAL CROPS AND PRODUCTS
卷 113, 期 -, 页码 202-209

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.indcrop.2018.01.034

关键词

Ciborium barometz; Oligosaccharide; Structural characterization; Anti-osteoporosis; Osteoblasts

资金

  1. National Natural Science Foundation of China [81673557, U1703110]
  2. Science and Technology Program of Guangdong Province [2014A050503067, 2015A020211032]

向作者/读者索取更多资源

Cibotium barometz is mainly distributed in eastern, southern, and southwest China as an important industrial export crop of great economical and medicinal value. The rhizome of C. barometz is widely used in Traditional Chinese Medicine clinics to treat conditions such as lumbago, limb-ache, rheumatism, and sciatica. In this study, the results of in vivo pharmacological experiments conclusively demonstrated that crude saccharides from C. barometz (CBB) exhibited osteoprotective effects in ovariectomized rats, which significantly increased bone mineral content (BMC) and bone mineral density (BMD), and prevented damage of the trabecular bone, consequently improving its biomechanical properties. To investigate the biological active ingredient(s), a novel oligo-glucomannan (denoted CBBP-1) was isolated and purified from CBB via anion-exchange and size-exclusion chromatography. Structural analysis indicated that CBBP-1 consisted of (1 -> 4)-linked a-D-glucose, (1 -> 6) linked beta-D-glucose with (1 -> 3, 6)-linked a-D-mannose, and a terminal alpha-D-glucose. Morphological analysis revealed that CBBP-1 had an irregular sheet structure. Furthermore, osteoblastic MC3T3-E1 cells treated with CBBP-1 had significantly increased mRNA expression of runt-related transcription factor 2, osterix, osteopontin, osteocalcin, and bone sialoprotein, indicating that CBBP-1 may stimulate osteoblastic differentiation. In conclusion, this study provides evidence that CBBP-1 may have potential as an anti-osteoporosis agent in the pharmaceutical industry.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据