Increased glucose metabolism and alpha-glucosidase inhibition in Cordyceps militaris water extract-treated HepG2 cells

被引:18
作者
Kim, Dae Jung [1 ]
Kang, Yun Hwan [2 ]
Kim, Kyoung Kon [3 ]
Kim, Tae Woo [1 ]
Park, Jae Bong [4 ]
Choe, Myeon [1 ,3 ]
机构
[1] Kangwon Natl Univ, Wellbeing Bioprod RIC, Chunchon 25209, Gangwon, South Korea
[2] Natl Dev Inst Korean Med, Gyeongbuk 38540, South Korea
[3] Kangwon Natl Univ, Dept Biohlth Technol, 1 Gangwondaehak Gil, Chunchon 24341, Gangwon, South Korea
[4] Hallym Univ, Coll Med, Dept Biochem, Gangwon 24252, South Korea
关键词
Cordyceps militaris; antidiabetics; glucose transporter; glucokinase; glycogen; ACTIVATED PROTEIN-KINASE; INSULIN SIGNALING BLOCKADE; GLUT2; GENE-EXPRESSION; PANCREATIC BETA-CELLS; HIGH-FAT; EPIGALLOCATECHIN GALLATE; AMPK; GLUCOKINASE; AKT; ACID;
D O I
10.4162/nrp.2017.11.3.180
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
BACKGROUND/OBJECTIVES: Recent living condition improvements, changes in dietary habits, and reductions in physical activity are contributing to an increase in metabolic syndrome symptoms including diabetes and obesity. Through such societal developments, humankind is continuously exposed to metabolic diseases such as diabetes, and the number of the victims is increasing. This study investigated Cordyceps militaris water extract (CMW)-induced glucose uptake in HepG2 cells and the effect of CMW treatment on glucose metabolism. MATERIALS/METHODS: Colorimetric assay kits were used to determine the glucokinase (GK) and pyruvate dehydrogenase (PDH) activities, glucose uptake, and glycogen content. Either RT-PCR or western blot analysis was performed for quantitation of glucose transporter 2 (GLUT2), hepatocyte nuclear factor 1 alpha (HNF-1 alpha), phosphatidylinositol 3-kinase (P13k), protein kinase B (Akt), phosphorylated AMP-activated protein kinase (pAMPK), phosphoenolpyruvate carboxykinase, GK, PDH, and glycogen synthase kinase 3 beta (GSK-3 beta) expression levels. The alpha-glucosidase inhibitory activities of acarbose and CMW were evaluated by absorbance measurement. RESULTS: CMW induced glucose uptake in HepG2 cells by increasing GLUT2 through HNF-1 alpha expression stimulation. Glucose in the cells increased the CMW-induced phosphorylation of AMPK. In turn, glycolysis was stimulated, and glyconeogenesis was inhibited. Furthermore, by studying the mechanism of action of P13k, Akt, and GSK-3 beta, and measuring glycogen content, the study confirmed that the glucose was stored in the liver as glycogen. Finally, CMW resulted in a higher level of alpha-glucosidase inhibitory activity than that from acarbose. CONCLUSION: CMW induced the uptake of glucose into HepG2 cells, as well, it induced metabolism of the absorbed glucose. It is concluded that CMW is a candidate or potential use in diabetes prevention and treatment.
引用
收藏
页码:180 / 189
页数:10
相关论文
共 58 条
  • [1] Ahn H. C., 2015, KOREAN J FOOD SCI TE, V47, P164
  • [2] Structure of the pyruvate dehydrogenase multienzyme complex E1 component from Escherichia coli at 1.85 Å resolution
    Arjunan, P
    Nemeria, N
    Brunskill, A
    Chandrasekhar, K
    Sax, M
    Yan, Y
    Jordan, F
    Guest, JR
    Furey, W
    [J]. BIOCHEMISTRY, 2002, 41 (16) : 5213 - 5221
  • [3] Berg JM, 2002, BIOCHEMISTRY-US, P668
  • [4] Ten years of protein kinase B signalling: a hard Akt to follow
    Brazil, DP
    Hemmings, BA
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (11) : 657 - 664
  • [5] Transcription-dependent and -independent control of neuronal survival by the PI3K-Akt signaling pathway
    Brunet, A
    Datta, SR
    Greenberg, ME
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (03) : 297 - 305
  • [6] The AMP-activated protein kinase cascade - a unifying system for energy control
    Carling, D
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2004, 29 (01) : 18 - 24
  • [7] Cerf ME, 2007, MED SCI MONITOR, V13, pRA12
  • [8] Identification of transacting factors responsible for the tissue-specific expression of human glucose transporter type 2 isoform gene -: Cooperative role of hepatocyte nuclear factors 1α and 3β
    Cha, JY
    Kim, H
    Kim, KS
    Hur, MW
    Ahn, YH
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) : 18358 - 18365
  • [9] Chang Xiu-ting, 2013, Chinese Pharmacological Bulletin, V29, P234, DOI 10.3969/j.issn.1001-1978.2013.02.20
  • [10] Cherrington AD, 1997, DIABETES, V1999, P1198