Mulberry (Morus alba L.) leaves and their major flavonol quercetin 3-(6-malonylglucoside) attenuate atherosclerotic lesion development in LDL receptor-deficient mice

被引:161
作者
Enkhmaa, B
Shiwaku, K [1 ]
Katsube, T
Kitajima, K
Anuurad, E
Yamasaki, M
Yamane, Y
机构
[1] Shimane Univ, Sch Med, Dept Environm & Prevent Med, Izumo, Shimane 6938501, Japan
[2] Shimane Inst Ind Technol, Matsue, Shimane 6900816, Japan
关键词
mulberry; quercetin 3-(6-malonylglucoside); LDL oxidation; atherosclerosis; LDLR-/-; mice;
D O I
10.1093/jn/135.4.729
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The effects of dietary consumption of mulberry (Morus alba L.) leaves and their major flavonol glycoside, quercetin 3-(6-malonylglucoside) (Q3MG), on the development of atherosclerotic lesions, in relation to the susceptibility of plasma LDL to oxidative modification, was studied in LDL receptor-deficient (LDLR-/-) mice. Male mice aged 8 wk were randomly assigned to 4 groups (control, quercetin, Q3MG, and mulberry). The control group was fed an atherogenic-diet containing 3 g cholesterol and 15 g cocoa butter/100 g. The other experimental groups were fed the same atherogenic diet supplemented with 0.05 g quercetin/100 g for the quercetin group, 0.05 g Q3MG/100 g for the Q3MG group, and 3 g dried mulberry-leaf powder/100 g for the mulberry group. The mice were fed their respective diets for 8 wk. The susceptibility of LDL to oxidative modification was significantly decreased in the Q3MG- and mulberry-treated mice, as evidenced by the 44.3 and 42.2% prolongation of the lag phase for conjugated diene formation compared with that of the control mice. The atherosclerotic lesion area in both the Q3MG- and mulberry-treated mice was significantly reduced by 52% compared with that of the controls. However, in the quercetin group, no protective effects were observed against LDL oxidation or atherosclerotic lesion formation. In conclusion, mulberry leaves attenuated the atherosclerotic lesion development in LDLR-/- mice through enhancement of LDL resistance to oxidative modification, and these antioxidative and antiatherogenic protective effects were attributed mainly to Q3MG, the quantitatively major flavonol glycoside in mulberry leaves.
引用
收藏
页码:729 / 734
页数:6
相关论文
共 49 条
[1]   Methods for monitoring oxidative stress, lipid peroxidation and oxidation resistance of lipoproteins [J].
Abuja, PM ;
Albertini, R .
CLINICA CHIMICA ACTA, 2001, 306 (1-2) :1-17
[2]   CHELATING AND FREE-RADICAL SCAVENGING MECHANISMS OF INHIBITORY-ACTION OF RUTIN AND QUERCETIN IN LIPID-PEROXIDATION [J].
AFANASEV, IB ;
DOROZHKO, AI ;
BRODSKII, AV ;
KOSTYUK, VA ;
POTAPOVITCH, AI .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (11) :1763-1769
[3]   Flavonoids in vegetable foods commonly consumed in brazil and estimated ingestion by the Brazilian population [J].
Arabbi, PR ;
Genovese, MI ;
Lajolo, FM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (05) :1124-1131
[4]   N-ALKYLATED NITROGEN-IN-THE-RING SUGARS - CONFORMATIONAL BASIS OF INHIBITION OF GLYCOSIDASES AND HIV-1 REPLICATION [J].
ASANO, N ;
KIZU, H ;
OSEKI, K ;
TOMIOKA, E ;
MATSUI, K ;
OKAMOTO, M ;
BABA, M .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (13) :2349-2356
[5]  
Bown D., 1995, ENCY HERBS THEIR USE, P313
[6]   LIPOPROTEIN METABOLISM IN THE MACROPHAGE - IMPLICATIONS FOR CHOLESTEROL DEPOSITION IN ATHEROSCLEROSIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1983, 52 :223-261
[7]  
Carr AC, 2000, CIRC RES, V87, P349, DOI 10.1161/01.RES.87.5.349
[8]   HYPOGLYCEMIC ACTIVITY AND MECHANISMS OF EXTRACTS FROM MULBERRY LEAVES (FOLIUM-MORI) AND CORTEX-MORI-RADICIS IN STREPTOZOTOCIN-INDUCED DIABETIC MICE [J].
CHEN, FJ ;
NAKASHIMA, N ;
KIMURA, I ;
KIMURA, M .
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 1995, 115 (06) :476-482
[9]   Dietary flavonoid and isoflavone glycosides are hydrolysed by the lactase site of lactase phlorizin hydrolase [J].
Day, AJ ;
Cañada, FJ ;
Díaz, JC ;
Kroon, PA ;
Mclauchlan, R ;
Faulds, CB ;
Plumb, GW ;
Morgan, MRA ;
Williamson, G .
FEBS LETTERS, 2000, 468 (2-3) :166-170
[10]   Deglycosylation of flavonoid and isoflavonoid glycosides by human small intestine and liver β-glucosidase activity [J].
Day, AJ ;
DuPont, MS ;
Ridley, S ;
Rhodes, M ;
Rhodes, MJC ;
Morgan, MRA ;
Williamson, G .
FEBS LETTERS, 1998, 436 (01) :71-75