Flavonoids from the Leaves of Thuja orientalis Inhibit the Aldose Reductase and the Formation of Advanced Glycation Endproducts
- Authors
- Lee, Eun Ha; Song, Dae-Geun; Lee, Joo Young; Pan, Cheol-Ho; Um, Byung Hun; Jung, Sang Hoon
- Issue Date
- 2009-10
- Publisher
- KOREAN SOC APPLIED BIOLOGICAL CHEMISTRY
- Citation
- JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY, v.52, no.5, pp.448 - 455
- Abstract
- The purpose of this study is to evaluate the active properties of Thuja orientalis leaves for the treatment of diabetic complications. The ethyl acetate fraction showed a significantly higher inhibition both of recombinant human aldose reductase (rhALR2) inhibitory activity and advanced glycation endproducts (AGEs). The detected antioxidants (compounds 14) by online-HPLC-ABTS(+) method and other three compounds were isolated using preparative RP-HPLC and Sephadex LM-20 column chromatography. Among the seven compounds, compound 4 (quercitrin) which was isolated from ethyl acetate fraction, was found to show inhibition for both forms of rhALR2 and AGEs. This compound also inhibited oxidative stress which was measured by Photochem (R) apparatus. In conclusion, the ethyl acetate fraction from T orientalis demonstrated antioxidant activity as well as inhibitory effects on rhALR2 and AGEs. Quercitrin was shown to be the active compound and hence could be offered as an active material of standardization for the development of natural products for food or medicines.
- Keywords
- DIABETIC COMPLICATIONS; STRUCTURAL REQUIREMENTS; LIQUID-CHROMATOGRAPHY; ANTIOXIDANT ACTIVITY; PROTEIN GLYCATION; ONLINE; SORBINIL; DIABETIC COMPLICATIONS; STRUCTURAL REQUIREMENTS; LIQUID-CHROMATOGRAPHY; ANTIOXIDANT ACTIVITY; PROTEIN GLYCATION; ONLINE; SORBINIL; advanced glycation endproducts; aldose reductase; online-HPLC-ABTS(+) method; quercitrin; Thuja orientalis
- ISSN
- 1738-2203
- URI
- https://pubs.kist.re.kr/handle/201004/132084
- DOI
- 10.3839/jksabc.2009.078
- Appears in Collections:
- KIST Article > 2009
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