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Cited 94 time in webofscience Cited 116 time in scopus
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Saffron (Crocus sativus L.) increases glucose uptake and in muscle cells via multipathway mechanisms

Authors
Kang, ChangkeunLee, HyunkyoungJung, Eun-SunSeyedian, RaminJo, MiNaKim, JeheinKim, Jong-ShuKim, Euikyung
Issue Date
15-Dec-2012
Publisher
ELSEVIER SCI LTD
Keywords
Saffron; Glucose uptake; Skeletal muscle cells; AMPK; Insulin sensitivity
Citation
FOOD CHEMISTRY, v.135, no.4, pp 2350 - 2358
Pages
9
Indexed
SCI
SCIE
SCOPUS
Journal Title
FOOD CHEMISTRY
Volume
135
Number
4
Start Page
2350
End Page
2358
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/21851
DOI
10.1016/j.foodchem.2012.06.092
ISSN
0308-8146
1873-7072
Abstract
Saffron (Crocus sativus Linn.) has been an important subject of research in the past two decades because of its various biological properties, including anti-cancer, anti-inflammatory, and anti-atherosclerotic activities. On the other hand, the molecular bases of its actions have been scarcely understood. Here, we elucidated the mechanism of the hypoglycemic actions of saffron through investigating its signaling pathways associated with glucose metabolism in C2C12 skeletal muscle cells. Saffron strongly enhanced glucose uptake and the phosphorylation of AMPK (AMP-activated protein kinase)/ACC (acetyl-CoA carboxylase) and MAPKs (mitogen-activated protein kinases), but not PI 3-kinase (Phosphatidylinositol 3-kinase)/Akt. Interestingly, the co-treatment of saffron and insulin further improved the insulin sensitivity via both insulin-independent (AMPK/ACC and MAPKs) and insulin-dependent (PI 3-kinase/Akt and mTOR) pathways. It also suggested that there is a crosstalk between the two signaling pathways of glucose metabolism in skeletal muscle cells. These results could be confirmed from the findings of GLUT4 translocation. Taken together, AMPK plays a major role in the effects of saffron on glucose uptake and insulin sensitivity in skeletal muscle cells. Our study provides important insights for the possible mechanism of action of saffron and its potential as a therapeutic agent in diabetic patients. (C) 2012 Elsevier Ltd. All rights reserved.
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