Serotonin derivatives, major safflower (Carthamus tinctorius L.) seed antioxidants, inhibit low-density lipoprotein (LDL) oxidation and atherosclerosis in apolipoprotein E-deficient mice

被引:102
作者
Koyama, N
Kuribayashi, K
Seki, T
Kobayashi, K
Furuhata, Y
Suzuki, K
Arisaka, H
Nakano, T
Amino, Y
Ishii, K
机构
[1] Ajinomoto Co Inc, Res Inst Hlth Fundamentals, Kawasaki Ku, Kawasaki, Kanagawa 2117609, Japan
[2] Ajinomoto Co Inc, Dept Appl Res, Kawasaki, Kanagawa 2117609, Japan
关键词
safflower; serotonin derivatives; antioxidants; LDL oxidation; apoE-deficient mice;
D O I
10.1021/jf060254p
中图分类号
S [农业科学];
学科分类号
09 [农学];
摘要
The effects of defatted safflower seed extract and its phenolic constituents, serotonin derivatives, on atherosclerosis were studied. Ethanol-ethyl acetate extract of safflower seeds (SSE) inhibited low-density lipoprotein (LDL) oxidation induced in vitro by an azo-containing free-radical initiator V70 or copper ions. Two serotonin derivatives [N-(p-coumaroyl) serotonin, CS; N-feruloylserotonin, FS] and their glucosides were identified as the major phenolic constituents of the extract. The study with chemically synthesized materials revealed that a majority of the antioxidative activity of SSE was attributable to the aglycones of these two serotonin derivatives. Orally administered CS and FS suppressed CuSO4-induced plasma oxidation ex vivo. Long-term (15 week) dietary supplementation of SSE (1.0 wt %/wt) and synthetic serotonin derivatives (0.2-0.4%) significantly reduced the atherosclerotic lesion area in the aortic sinus of apolipoprotein E-deficient mice (29.2-79.7% reduction). The plasma level of both lipid peroxides and anti-oxidized LDL autoantibody titers decreased concomitantly with the reduction of lesion formation. Serotonin derivatives were detected as both intact and conjugated metabolites in the plasma of C57BL/6J mice fed on 1.0% SSE diet. These findings demonstrate that serotonin derivatives of SSE are absorbed into circulation and attenuate atherosclerotic lesion development possibly because of the inhibition of oxidized LDL formation through their strong antioxidative activity.
引用
收藏
页码:4970 / 4976
页数:7
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