| Literature DB >> 27721901 |
Chenfei Gao1, Michael L King2, Zachary L Fitzpatrick2, Wenqian Wei3, Jason F King1, Mingming Wang1, Frank L Greenway4, John W Finley1, Jeffrey H Burton, William D Johnson4, Michael J Keenan5, Frederick M Enright6, Roy J Martin7, Jolene Zheng4.
Abstract
Prowashonupana barley (PWB) is high in β-glucan with moderate content of resistant starch. PWB reduced intestinal fat deposition (IFD) in wild type Caenorhabditis elegans (C. elegans, N2), and in sir-2.1 or daf-16 null mutants, and sustained a surrogate marker of lifespan, pharyngeal pumping rate (PPR), in N2, sir-2.1, daf-16, or daf-16/daf-2 mutants. Hyperglycaemia (2% glucose) reversed or reduced the PWB effect on IFD in N2 or daf-16/daf-2 mutants with a sustained PPR. mRNA expression of cpt-1, cpt-2, ckr-1, and gcy-8 were dose-dependently reduced in N2 or daf-16 mutants, elevated in daf-16/daf-2 mutants with reduction in cpt-1, and unchanged in sir-2.1 mutants. mRNA expressions were increased by hyperglycaemia in N2 or daf-16/daf-2 mutants, while reduced in sir-2.1 or daf-16 mutants. The effects of PWB in the C. elegans model appeared to be primarily mediated via sir-2.1, daf-16, and daf-16/daf-2. These data suggest that PWB and β-glucans may benefit hyperglycaemia-impaired lipid metabolism.Entities:
Keywords: aging; animal models; barley; insulin sensitivity; obesity
Year: 2015 PMID: 27721901 PMCID: PMC5052015 DOI: 10.1016/j.jff.2015.08.014
Source DB: PubMed Journal: J Funct Foods ISSN: 1756-4646 Impact factor: 4.451