Davallialactone from Mushroom Reduced Premature Senescence and Inflammation on Glucose Oxidative Stress in Human Diploid Fibroblast Cells

被引:24
作者
Yang, Tae-Ki [1 ]
Lee, Young-Hee [2 ]
Paudel, Usha [2 ]
Bhattarai, Govinda [2 ]
Yun, Bong-Sik [3 ]
Hwang, Pyoung-Han [1 ]
Yi, Ho-Keun [2 ]
机构
[1] Chonbuk Natl Univ, Sch Med, Dept Pediat, Jeonju 561712, South Korea
[2] Chonbuk Natl Univ, Sch Dent, Program BK21, Dept Oral Biochem,Inst Oral Biosci, Jeonju 561712, South Korea
[3] Chonbuk Natl Univ, Coll Environm & Biosource Sci, Devis Biotechnol, Jeonju 561712, South Korea
关键词
davallialactone; aging; diabetes mellitus; mushroom; glucose oxidative stress; inflammation; IN-VITRO; INONOTUS-XERANTICUS; METABOLIC-DISORDERS; INSULIN-RESISTANCE; HYDROGEN-PEROXIDE; VIVO; ANTIOXIDANTS; INHIBITION; PATHWAY; MODEL;
D O I
10.1021/jf401691y
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Mushrooms are both food and a source of natural compounds of biopharmaceutical interest. The purpose of this study was to clarify whether davallialactone from mushroom extract affected the pathogenesis of hyperglycemia oxidative stress and the aging process in human diploid fibroblast (HDF) cells. The high-glucose state with glucose oxidase resulted in glucose oxidative stress, induction of inflammatory molecules, dysfunction of antioxidant molecules, and activation of mitogen-activated protein kinase (MAPKs) and its downstream signaling in old HDF cells. The exposure of glucose oxidative stress in middle-stage cells led to stress-induced premature senescence (SIPS) via senescence-associated beta-galactosidase (SA beta-gal) activity and displayed replicative senescence phenomena. However, davallialactone reduces the pathogenesis of glucose oxidative stress and the aging process through down-regulation of SA beta-gal activity. These results strongly suggest that natural compounds, especially mushroom extract davallialactone, improve the pathogenesis of glucose oxidative stress and the aging process. Hence, davallialactone has potential in the treatment of diabetes mellitus or age-related disease complications.
引用
收藏
页码:7089 / 7095
页数:7
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