Benzothiazole derivatives augment glucose uptake in skeletal muscle cells and stimulate insulin secretion from pancreatic β-cells via AMPK activation

2014 ◽  
Vol 50 (76) ◽  
pp. 11222-11225 ◽  
Author(s):  
L. Pasternak ◽  
E. Meltzer-Mats ◽  
G. Babai-Shani ◽  
G. Cohen ◽  
O. Viskind ◽  
...  

Development of the unique bi-functional AMPK activators (glucose uptake and insulin secretion enhancers) for potential antidiabetic treatment.

2008 ◽  
Vol 46 (1-2) ◽  
pp. 96-104 ◽  
Author(s):  
Ali Benhaddou-Andaloussi ◽  
Louis C. Martineau ◽  
Danielle Spoor ◽  
Tri Vuong ◽  
Charles Leduc ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3129
Author(s):  
Jyotsana Pandey ◽  
Kapil Dev ◽  
Sourav Chattopadhyay ◽  
Sleman Kadan ◽  
Tanuj Sharma ◽  
...  

Estrogenic molecules have been reported to regulate glucose homeostasis and may be beneficial for diabetes management. Here, we investigated the estrogenic effect of β-sitosterol-3-O-D-glucopyranoside (BSD), isolated from the fruits of Cupressus sempervirens and monitored its ability to regulate glucose utilization in skeletal muscle cells. BSD stimulated ERE-mediated luciferase activity in both ERα and ERβ-ERE luc expression system with greater response through ERβ in HEK-293T cells, and induced the expression of estrogen-regulated genes in estrogen responsive MCF-7 cells. In silico docking and molecular interaction studies revealed the affinity and interaction of BSD with ERβ through hydrophobic interaction and hydrogen bond pairing. Furthermore, prolonged exposure of L6-GLUT4myc myotubes to BSD raised the glucose uptake under basal conditions without affecting the insulin-stimulated glucose uptake, the effect associated with enhanced translocation of GLUT4 to the cell periphery. The BSD-mediated biological response to increase GLUT4 translocation was obliterated by PI-3-K inhibitor wortmannin, and BSD significantly increased the phosphorylation of AKT (Ser-473). Moreover, BSD-induced GLUT4 translocation was prevented in the presence of fulvestrant. Our findings reveal the estrogenic activity of BSD to stimulate glucose utilization in skeletal muscle cells via PI-3K/AKT-dependent mechanism.


Nitric Oxide ◽  
2009 ◽  
Vol 21 (2) ◽  
pp. 126-131 ◽  
Author(s):  
Darren C. Henstridge ◽  
Brian G. Drew ◽  
Melissa F. Formosa ◽  
Alaina K. Natoli ◽  
David Cameron-Smith ◽  
...  

2014 ◽  
Vol 92 (2) ◽  
pp. 380-388 ◽  
Author(s):  
Ragadeepthi Tunduguru ◽  
Tim T. Chiu ◽  
Latha Ramalingam ◽  
Jeffrey S. Elmendorf ◽  
Amira Klip ◽  
...  

2015 ◽  
Vol 29 (6) ◽  
pp. 873-881 ◽  
Author(s):  
Hye Jeong Lee ◽  
Jung Ok Lee ◽  
Nami Kim ◽  
Joong Kwan Kim ◽  
Hyung Ip Kim ◽  
...  

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