New screenings of the improving factors for lipid metabolism derived from foods and their functional evaluation
食物源性脂质代谢改善因子的新筛选及其功能评价
基本信息
- 批准号:10660120
- 负责人:
- 金额:$ 2.11万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 1999
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1. (1) In the study about anti-atherogenic factors, effects of polyphenol on apolipoprotein A-I (ApoA-I) gene expression were studied. The results demonstrated that soy genistein increases ApoA-I secretion and its mRNA levels in HepG2 cells. (2) Genistein or hesperetin feeding increses serum ApoA-I and liver ApoA-I mRNA levels in rats.2. In the study about suppressive factors of cholesterol absorption, improving effects for cholesterol metabolism concerning to our soy peptides with bound phospholipids (pepsin peptides or sumizyme peptides) were compared with soy peptides or chitosan which approved by the ministry of health as Food for specified health use. (1) Chitosan feeding decreases body weight gains in rats. Serum and liver cholesterol levels were significantly decreased in soy peptides with bound phospholipids, soy peptides, chitosan-feeding compared with casein feeding. The degree of the cholesterol lowering activity of soy peptides with bound phospholipids was strongest among experimental groups. (2) Cholesterol uptake in Caco-2 cells was decreased by soy peptides with bound phospholipids compared with casein tryptic hydrolysate. Thus, improving effects for cholesterol metabolism of soy peptides with bound phospholipids is superior to those of soy peptides and chitosan which approved by the Ministry of Health and Welfare as Food for specified health use.
1. (1)在抗动脉粥样硬化因子的研究中,研究了多酚对载脂蛋白A-I(ApoA-I)基因表达的影响。结果表明,大豆金雀异黄素可增加 HepG2 细胞中 ApoA-I 的分泌及其 mRNA 水平。 (2)金雀异黄素或橙皮素喂养可增加大鼠血清ApoA-I和肝脏ApoA-I mRNA水平。2.在胆固醇吸收抑制因素的研究中,将本公司的结合磷脂的大豆肽(胃蛋白酶肽或泥酶肽)改善胆固醇代谢的效果与卫生部批准的特定保健用途食品的大豆肽或壳聚糖进行了比较。 (1) 喂食壳聚糖可降低大鼠的体重增加。与酪蛋白喂养相比,结合磷脂的大豆肽、大豆肽、壳聚糖喂养的血清和肝脏胆固醇水平显着降低。结合磷脂的大豆肽降低胆固醇的活性程度在实验组中最强。 (2) 与酪蛋白胰蛋白酶水解产物相比,结合磷脂的大豆肽降低了 Caco-2 细胞中的胆固醇摄取。因此,结合磷脂的大豆肽改善胆固醇代谢的效果优于经厚生省批准为特定保健食品的大豆肽和壳聚糖。
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Nagaoka, S., Miwa, K., Eto, M., Kuzuya, Y., Hori, G. & Yamamoto, K.: "Soyprotein peptic hydrolyzate with bound phospholipids decrease micellar solubility and cholesterol absorption in rats and Caco-2 cells."Journal of Nutrition. 129(9). 1725-1730 (1999)
长冈,S.,美轮,K.,江藤,M.,葛也,Y.,堀,G.
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Nagaoka,S.: "Soyprotein peptic hydrolyzate with bound phospholipids decrease micellar solubility and cholesterol absorption in rats and Caco-2 cells"Journal of Nutrition. 129. 1725-1730 (1999)
Nagaoka,S.:“具有结合磷脂的大豆蛋白消化水解产物降低了大鼠和 Caco-2 细胞中的胶束溶解度和胆固醇吸收”营养学杂志。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Nagaoka S.: "Soyprotein peptic hydrolyzate with bound phospholipids decrease micellar solubility and cholesterol absorption in rats and Caco-2 cells."Journal of Nutrition. 129・9. 1725-1730 (1999)
Nagaoka S.:“结合磷脂的大豆蛋白消化液降低了大鼠和 Caco-2 细胞中的胶束溶解度和胆固醇吸收。”营养学杂志 129・9(1999)。
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- 影响因子:0
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NAGAOKA Satoshi其他文献
NAGAOKA Satoshi的其他文献
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{{ truncateString('NAGAOKA Satoshi', 18)}}的其他基金
Identification, exhaustive analysis, clarification of action mechanism and efficient modification of novel hypolipidemic peptides
新型降血脂肽的鉴定、详尽分析、作用机制阐明及高效修饰
- 批准号:
23380075 - 财政年份:2011
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
The clarification and application of mechanism of hypocholesterolemic peptides by peptide array
肽芯片阐明降胆固醇肽的作用机制及应用
- 批准号:
20380075 - 财政年份:2008
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Mechanism of action of new hypocholesterolemic pentapeptidei
新型降胆固醇五肽的作用机制
- 批准号:
14560095 - 财政年份:2002
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
The analysis of the mechanism of the anti-atherogenic action of polyphenol utilizing new evaluation technology
利用新评价技术分析多酚抗动脉粥样硬化作用机制
- 批准号:
12660114 - 财政年份:2000
- 资助金额:
$ 2.11万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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8819561 - 财政年份:2012
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Impact of self-association on structure and function of apolipoprotein A-I
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8460476 - 财政年份:2012
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Impact of self-association on structure and function of apolipoprotein A-I
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- 批准号:
8644314 - 财政年份:2012
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Impact of self-association on structure and function of apolipoprotein A-I
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- 批准号:
9024607 - 财政年份:2012
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载脂蛋白 A-I 脂质结合的启动机制
- 批准号:
10189632 - 财政年份:2010
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载脂蛋白 A-I 脂质结合的启动机制
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10436238 - 财政年份:2010
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