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Glycolipids Derived from the Korean Endemic Plant Aruncus aethusifolius Inducing Glucose Uptake in Mouse Skeletal Muscle C2C12 Cellsopen access

Authors
Baek, Jong GwonPark, Do HwiVu, Ngoc KhanhMuvva, CharuvakaHwang, HoseongSong, SungminLee, Hyeon-SeongKim, Tack-JoongKwon, Hak CheolPark, KeunwanKang, Ki SungKwon, Jaeyoung
Issue Date
Mar-2024
Publisher
MDPI
Keywords
Aruncus aethusifolius; glycolipid; glucose uptake; Korean endemic plant; molecular docking
Citation
PLANTS-BASEL, v.13, no.5
Journal Title
PLANTS-BASEL
Volume
13
Number
5
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/91061
DOI
10.3390/plants13050608
ISSN
2223-7747
2223-7747
Abstract
Aruncus spp. has been used as a traditional folk medicine worldwide for its anti-inflammatory, hemostatic, and detoxifying properties. The well-known species A. dioicus var. kamtschaticus has long been used for multifunctional purposes in Eastern Asia. Recently, it was reported that its extract has antioxidant and anti-diabetic effects. In this respect, it is likely that other Aruncus spp. possess various biological activities; however, little research has been conducted thus far. The present study aims to biologically identify active compounds against diabetes in the Korean endemic plant A. aethusifolius and evaluate the underlying mechanisms. A. aethusifolius extract enhanced glucose uptake without toxicity to C2C12 cells. A bioassay-guided isolation of A. aethusifolius yielded two pure compounds, and their structures were characterized as glycolipid derivatives, gingerglycolipid A, and (2S)-3-linolenoylglycerol-O-beta-d-galactopyranoside by an interpretation of nuclear magnetic resonance and high-resolution mass spectrometric data. Both compounds showed glucose uptake activity, and both compounds increased the phosphorylation levels of insulin receptor substrate 1 (IRS-1) and 5 ' -AMP-activated protein kinase (AMPK) and protein expression of peroxisome proliferator-activated receptor gamma (PPAR gamma). Gingerglycolipid A docked computationally into the active site of IRS-1, AMPK1, AMPK2, and PPAR gamma (-5.8, -6.9, -6.8, and -6.8 kcal/mol).
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Kang, Ki Sung
College of Korean Medicine (Premedical course of Oriental Medicine)
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