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

Author:

Baek Jong Gwon12,Park Do Hwi3,Vu Ngoc Khanh1,Muvva Charuvaka1,Hwang Hoseong1,Song Sungmin1,Lee Hyeon-Seong1,Kim Tack-Joong2ORCID,Kwon Hak Cheol12ORCID,Park Keunwan1ORCID,Kang Ki Sung3,Kwon Jaeyoung14ORCID

Affiliation:

1. KIST Gangneung Institute of Natural Products, Korea Institute of Science and Technology, Gangneung 25451, Republic of Korea

2. Department of YM-KIST Bio-Health Convergence, Yonsei University, Wonju 26593, Republic of Korea

3. College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea

4. Division of Bio-Medical Science and Technology, KIST School, University of Science and Technology (UST), Gangneung 25451, Republic of Korea

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-β-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 γ (PPARγ). Gingerglycolipid A docked computationally into the active site of IRS-1, AMPK1, AMPK2, and PPARγ (−5.8, −6.9, −6.8, and −6.8 kcal/mol).

Funder

Korea Institute of Science and Technology research program

Publisher

MDPI AG

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