Homoisoflavanones from Polygonatum odoratum Rhizomes Inhibit Advanced Glycation End Product Formation

被引:41
作者
Dong, Wei [1 ,2 ]
Shi, Hai Bo [1 ]
Ma, Heng [1 ]
Miao, Yan Bo [1 ]
Liu, Tong Jun [2 ]
Wang, Wei [1 ]
机构
[1] Jilin Acad Chinese Med Sci, Inst Phytochem, Changchun 130021, Peoples R China
[2] Jilin Univ, China Japan Union Hosp, Changchun 130021, Peoples R China
基金
中国国家自然科学基金;
关键词
Polygonatum odoratum; Homoisoflavanones; Advanced glycation end-products (AGEs); Diabetic complications; AMINOGUANIDINE; IDENTIFICATION; CONSTITUENTS; PROTEINS;
D O I
10.1007/s12272-010-0504-y
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Protein glycation inhibitors from Polygonatum odoratum rhizomes were investigated using a bioassay-guided procedure to characterize active compounds for preventing and treating diabetic complications. The EtOH extract and soluble fractions were evaluated using an in vivo model of renal advanced glycation end-product (AGE) accumulation in streptozotocin-induced diabetic rats and an in vitro bovine serum albumin-glucose assay. Three homoisoflavanones 3-(4'-hydroxybenzyl)-5,7-dihydroxy-6-methyl-8-methoxychroman-4-one (1), 3-(4'-hydroxybenzyl)-5,7-dihydroxy-6,8-dimethylchroman-4-one (2), and 3-(4'-methoxybenzyl)-5,7-dihydroxy-6-methyl-8-methoxychroman-4-one (3), isolated from the active CHCl3-soluble fraction of the EtOH extract, were subjected to in vitro bioassays to evaluate their inhibitory activities against AGE formation. All the isolates inhibited AGE formation more effectively than the positive control, aminoguanidine. These results indicate that pending further study these compounds could be used as novel natural product drug for mitigating diabetic complications.
引用
收藏
页码:669 / 674
页数:6
相关论文
共 20 条
[1]
Advanced glycation endproducts - role in pathology of diabetic complications [J].
Ahmed, N .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2005, 67 (01) :3-21
[2]
Randomized trial of an inhibitor of formation of advanced glycation end products in diabetic nephropathy [J].
Bolton, WK ;
Cattran, DC ;
Williams, ME ;
Adler, SG ;
Appel, GB ;
Cartwright, K ;
Foiles, PG ;
Freedman, BI ;
Raskin, P ;
Ratner, RE ;
Spinowitz, BS ;
Whittier, FC ;
Wuerth, JP .
AMERICAN JOURNAL OF NEPHROLOGY, 2004, 24 (01) :32-40
[3]
Biochemistry and molecular cell biology of diabetic complications [J].
Brownlee, M .
NATURE, 2001, 414 (6865) :813-820
[4]
DYER DG, 1991, J BIOL CHEM, V266, P11654
[5]
Huang PL, 1997, PHYTOCHEMISTRY, V44, P1369
[6]
N-epsilon-(carboxymethyl)lysine protein adduct is a major immunological epitope in proteins modified with advanced glycation end products of the Maillard reaction [J].
Ikeda, K ;
Higashi, T ;
Sano, H ;
Jinnouchi, Y ;
Yoshida, M ;
Araki, T ;
Ueda, S ;
Horiuchi, S .
BIOCHEMISTRY, 1996, 35 (24) :8075-8083
[7]
Constituents of the flowers of Erigeron annuus with inhibitory activity on the formation of advanced glycation end products (AGEs) and aldose reductase [J].
Jang, Dae Silk ;
Yoo, Nam Hee ;
Lee, Yun Mi ;
Yoo, Jeong Lim ;
Kim, Young Sook ;
Kim, Jin Sook .
ARCHIVES OF PHARMACAL RESEARCH, 2008, 31 (07) :900-904
[8]
Inhibitory effect of the compounds isolated from Rhus verniciflua on aldose reductase and advanced glycation endproducts [J].
Lee, Eun Ha ;
Song, Dae-Geun ;
Lee, Joo Young ;
Pan, Cheol-Ho ;
Um, Byung Hun ;
Jung, Sang Hoon .
BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2008, 31 (08) :1626-1630
[9]
Lin H. W., 1994, Yaoxue Xuebao, V29, P215
[10]
Structural requirements of flavonoids for inhibition of protein glycation and radical scavenging activities [J].
Matsuda, H ;
Wang, T ;
Managi, H ;
Yoshikawa, M .
BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (24) :5317-5323