Correlations of Molecular Weights of β-Glucans from Qingke (Tibetan Hulless Barley) to Their Multiple Bioactivities

Molecules. 2018 Jul 13;23(7):1710. doi: 10.3390/molecules23071710.

Abstract

β-glucans have been considered the major bioactive components in Qingke (Tibetan hulless barley). However, the structure⁻function relationships of β-glucans from Qingke have seldom been investigated. Whether the bioactivities of Qingke β-glucans are closely correlated to their molecular weights remains unknown. Therefore, in order to explore Qingke β-glucans as functional/healthy food ingredients for industrial applications, and to better understand their structure⁻function relationships, correlations of molecular weights of Qingke β-glucans to their in vitro binding properties, inhibitory activities on digestive enzymes (α-amylase and pancreatic lipase), anti-inflammatory activities, and anticancer activities were systematically investigated. Results showed that the in vitro binding properties and the inhibitory activities on α-amylase and pancreatic lipase of Qingke β-glucans were positively correlated to their molecular weights. However, the anti-inflammatory activities of Qingke β-glucans increased as their molecular weights decreased. Furthermore, Qingke β-glucans exhibited selectively anti-cancer activities in vitro. Positive and negative correlations of molecular weights to inhibitory effects against A549 cells and MDA-MB-231 cells were observed, respectively. However, the inhibitory effects of Qingke β-glucans against HCT116 cells were not associated with their molecular weights. Results suggested that the molecular weights of Qingke β-glucans significantly affected their bioactivities, which was beneficial for a better understanding of their structure⁻function relationships. Moreover, results showed that Qingke β-glucans could be further explored as functional/healthy food ingredients for industrial applications due to their multiple health benefits.

Keywords: Qingke; anti-cancer activity; anti-inflammatory activity; binding properties; inhibitory activities on digestive enzymes; molecular weight; β-glucans.

MeSH terms

  • A549 Cells
  • Enzyme Inhibitors / chemistry*
  • Hordeum / chemistry*
  • Humans
  • Lipase / antagonists & inhibitors*
  • Lipase / chemistry
  • Lipase / metabolism
  • Molecular Weight
  • alpha-Amylases / antagonists & inhibitors*
  • alpha-Amylases / chemistry
  • alpha-Amylases / metabolism
  • beta-Glucans / chemistry*

Substances

  • Enzyme Inhibitors
  • beta-Glucans
  • Lipase
  • alpha-Amylases