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Title 

Genistein-derivatives from Tetracera scandens stimulate glucose-uptake in L6 myotubes

Authors 

Myung Sun LeeChung-Hee KimD M HoangBo Yeon KimC B SohnM R KimJong Seog Ahn

Publisher 

Pharmaceutical Society of Japan

Issue Date 

2009

Citation 

Biological & Pharmaceutical Bulletin, vol. 32, no. 3, pp. 504-508

Keywords 

diabetesglucose-uptakeisoflavoneL6 myotubetetracera scandens3',5' diprenylgenistein6,8 diprenylgenisteingenisteinglucose transporter 1glucose transporter 4

Abstract 

An EtOAc-soluble partition of the MeOH extract of a branch of Tetracera scandens (Dilleniaceae family) was subjected to a glucose-uptake assay, which led to the isolation and identification of five isoflavones of previously known structure namely, genistein (1), its derivatives 3′,5′- diprenylgenistein (2), 6,8-diprenylgenistein (3), derrone (4) and alpinumisoflavone (5). of these, compounds 2-5 exhibited significant glucose-uptake activity in basal and insulin-stimulated L6 myotubes. The findings from adenosine monophosphate-activated kinase (AMPK) activation and glucose transport protein4 (GLUT4) and GLUT1 over-expression revealed certain characteristics of compounds 2-5. These compounds inhibited protein tyrosine phosphatase 1B (PTP1B) activities with IC50 values ranging from 20.63±0.17 to 37.52±0.31 μM. No muscle cell toxicity was reported with compounds 3-5, while compounds 1 and 2 reduced muscle cell viability with IC50 values of 34.27±0.35 and 18.69±0.19 μM, respectively. It was concluded that T. scandens and its constituents exerted highly desirable activities on type 2 diabetes mellitus treatment since they significantly stimulated the uptake of glucose, AMPK phosphorylation, GLUT4 and GLUT1 mRNA expressions and PTP1B inhibition in L6 myotubes.

ISSN 

0918-6158

Link 

http://dx.doi.org/10.1248/bpb.32.504

Appears in Collections

1. Journal Articles > Journal Articles

Registered Date

2019-05-02


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