Determination of Afzelin and Astragalin from Lespedeza cuneata on Aldose Reductase Inhibition

Author:

Lee Dong Gu1,Lee Ju Sung2,Quilantang Norman G2,Jacinto Sonia D3,Lee Sanghyun2ORCID

Affiliation:

1. BET Research Institute, Chung-Ang University, Seodongdaero, Daedukmyun, Anseong 17546, Republic of Korea

2. Department of Plant Science and Technology, Chung-Ang University, Seodongdaero, Daedukmyun, Anseong 17546, Republic of Korea

3. Institute of Biology, University of the Philippines, Regidor St., Diliman, Quezon City 1101, Philippines

Abstract

Abstract The bioactive chemicals in L. cuneata were investigated by repeated column chromatography and their effect on aldose reductase (AR), obtained from rat lenses, was examined. Results showed that the ethyl acetate and n-butanol fractions of L. cuneata exhibited potential inhibitory effect against AR with IC50 values of 0.57 and 0.49 μg/mL, respectively. Phytochemical analysis of these two fractions resulted in the isolation of five flavonoids namely, acacetin (1), afzelin (2), astragalin (3), kaempferol (4) and scutellarein 7-O-glucoside (5). The AR inhibitory effect of compounds 1-5 was explored; compounds 2, 3 and 5 showed potential AR-inhibitory effects with IC50 values of 2.20, 1.91 and 12.87 μM, respectively. Quantitative analysis of afzelin (2) and astragalin (3) in L. cuneata by high performance liquid chromatography with ultraviolet detection revealed its content to be 0.722–11.828 and 2.054–7.006 mg/g, respectively. Overall, this study showed that L. cuneata is rich in flavonoids with promising AR-inhibitory activities, which can be utilized for the development of natural therapies for treating and managing diabetic complications.

Funder

Chung-Ang University Research

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Analytical Chemistry

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