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1.
Ann Nutr Metab ; 62(1): 1-6, 2013.
Article in English | MEDLINE | ID: mdl-23171573

ABSTRACT

Bile acid-binding agents are known to lower blood cholesterol levels and have been clinically used for the treatment of hypercholesterolemia. We previously showed that tannin-rich fiber from young persimmon (Diospyros kaki) fruits had bile acid-binding properties. In this study, we performed a randomized, double-blind, placebo-controlled trial to investigate the hypocholesterolemic effects of tannin-rich fiber in humans. The subjects (n = 40, plasma total cholesterol levels 180-259 mg/dl) were divided into 3 groups and ingested cookie bars containing 0 g (placebo group, n = 14), 3 g (low-dose group, n = 13), or 5 g (high-dose group, n = 13) of tannin-rich fiber 3 times daily before meals for 12 weeks. Plasma total cholesterol levels decreased significantly in the low-dose (12 weeks, p < 0.005) and high-dose (6 weeks, p < 0.05; 12 weeks, p < 0.001) groups. In addition, plasma low-density lipoprotein cholesterol levels decreased significantly in the high-dose group (6 weeks, p < 0.05; 12 weeks, p < 0.001). These improvements were not accompanied by changes in plasma high-density lipoprotein cholesterol or plasma triglyceride levels. Our findings indicate that tannin-rich fiber from young persimmon fruits is a useful food material for treating hypercholesterolemia.


Subject(s)
Cholesterol, LDL/blood , Dietary Fiber/administration & dosage , Diospyros/chemistry , Plant Extracts/administration & dosage , Tannins/administration & dosage , Adult , Bile Acids and Salts/analysis , Blood Glucose/analysis , Cholesterol, HDL , Double-Blind Method , Female , Fruit/chemistry , Humans , Hypercholesterolemia/blood , Hypercholesterolemia/drug therapy , Male , Middle Aged , Triglycerides/blood
2.
Int J Mol Sci ; 12(4): 2088-99, 2011.
Article in English | MEDLINE | ID: mdl-21731428

ABSTRACT

Much attention has been focused recently on functional foods. Ume, the Japanese name for the apricot of Prunus mume Sieb. et Zucc., is an example of a Japanese traditional functional food. There are, however, few reports on the effects of fiber from this fruit on bowel function. With this objective, we prepared ume fiber to test the hypothesis that it can change gut function and intestinal flora in mice. Mice were fed an ume fiber (UF) or cellulose (CF) diet (control) for 40 days. The fecal weight, fecal lipids, plasma lipids and cecal composition of the microflora were analyzed. The amount of feces was significantly greater in the UF group than in the CF group (p < 0.01). The fecal lipids content (% DW) of the feces sampled on the final day of the experiment were significantly greater in the UF group than in the CF group (p < 0.01). Plasma non-esterified fatty acids (NEFA) concentrations tended to be lower in the UF compared to the CF group (p = 0.058). Occupation ratios of Bacteroides and Clostridium cluster IV were significantly greater in the cecal flora of the UF group. Our results suggest that ume fiber possesses the fecal lipid excretion effects and feces bulking effects.


Subject(s)
Gastrointestinal Tract/metabolism , Prunus/metabolism , Animals , Bacteroides/drug effects , Bacteroides/growth & development , Cecum/microbiology , Cellulose/pharmacology , Clostridium/drug effects , Clostridium/growth & development , Diet , Dietary Fiber/pharmacology , Fatty Acids, Unsaturated/blood , Feces/chemistry , Gastrointestinal Tract/drug effects , Gastrointestinal Tract/microbiology , Japan , Lipids/blood , Male , Mice , Mice, Inbred ICR , Plant Extracts/metabolism
3.
Phytother Res ; 25(4): 624-8, 2011 Apr.
Article in English | MEDLINE | ID: mdl-20922818

ABSTRACT

The bile acid-binding ability of a highly polymerized tannin (kaki-tannin) extracted from dried-young fruits of persimmon (Diospyros kaki) was examined. The kaki-tannin was composed mainly of epicatechin, epigallocatechin, epicatechin-3-O-gallate and epigallocatechin-3-O-gallate. Bile acid-binding ability of kaki-tannin was examined against cholic acid, glycocholic acid, taurocholic acid and deoxycholic acid in vitro, and its effect on fecal bile acid excretion in mice was also examined. Although the bile acid-binding ability of kaki-tannin was weaker than that of cholestyramine, kaki-tannin adsorbed all the bile acids tested and significantly promoted fecal bile acid excretion in mice when supplied at 1% (w/w) in the diet.


Subject(s)
Bile Acids and Salts/metabolism , Diospyros/chemistry , Tannins/metabolism , Animals , In Vitro Techniques , Male , Mass Spectrometry , Mice , Mice, Inbred C57BL , Spectroscopy, Fourier Transform Infrared
4.
Phytother Res ; 24(2): 205-10, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19585467

ABSTRACT

The hypolipidemic effects and bile acid-binding properties of young persimmon (Diospyros kaki) fruit were examined. In an animal experiment, male C57BL/6.Cr mice (n = 5) were fed an AIN-76-modified high fat diet supplemented with 2% or 5% (w/w) dried young persimmon fruit (YP) for 10 weeks. The intake of YP significantly enhanced fecal bile acid excretion and lowered the concentration of hepatic lipids and plasma cholesterol. Analysis of gene expression in liver tissue showed that 2% or 5% YP up-regulated the expression of the sterol regulatory element-binding protein-2 gene. In the 5% group, there were increased expressions of the genes for cholesterol 7alpha-hydroxylase and the low-density lipoprotein receptor. Next, the bile acid-binding ability of YP was analysed in vitro using cholic acid (CA). In 100-2000 microM CA solutions, 1% (w/v) YP adsorbed approximately 60% of CA, while dried mature persimmon fruit adsorbed approximately 20% of CA. The positive control, cholestyramine, adsorbed approximately 80% of CA in the 100-2000 microM CA solutions. A crude tannin extract from YP, which contained 54.7% condensed tannins, adsorbed approximately 78% of CA in the 2000 microM CA solutions. These results suggest that the ability of YP to bind bile acid contributes to its hypolipidemic effect in mice.


Subject(s)
Bile Acids and Salts/metabolism , Diospyros/chemistry , Hyperlipidemias/prevention & control , Hypolipidemic Agents/pharmacology , Adsorption , Animals , Cholesterol/analysis , Cholic Acid/metabolism , Dietary Fats/adverse effects , Fruit/chemistry , Hyperlipidemias/drug therapy , Liver/metabolism , Male , Mice , Mice, Inbred C57BL , Proanthocyanidins/pharmacology , Triglycerides/analysis
5.
Biosci Biotechnol Biochem ; 72(10): 2651-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18838807

ABSTRACT

We investigated the hypolipidemic effects of young persimmon fruit (YP) on apolipoprotein E-deficient C57BL/6.KOR-ApoEshl mice. These mice exhibited higher plasma cholesterols, except for high-density lipoprotein (HDL), and lower plasma HDL cholesterol than C57BL/6.Cr mice that had the same genetic background as the C57BL/6.KOR-ApoEshl mice. Male C57BL/6.KOR-ApoEshl mice (n=5) were fed a diet supplemented with dry YP, Hachiya-kaki, at a concentration of 5% (w/w) for 10 weeks. YP treatment significantly lowered plasma chylomicron, very low-density lipoprotein (VLDL) and low-density lipoprotein (LDL) cholesterols, and triglyceride, and this response was accompanied by an elevation of fecal bile acid excretion. In the liver, sterol regulatory element binding protein-2 gene expression was significantly higher in mice fed YP, while the mRNA and protein levels of the LDL receptor did not change. These results indicate that acceleration of fecal bile acid excretion is a major mechanism of the hypolipidemic effect induced by YP in C57BL/6.KOR-ApoEshl mice.


Subject(s)
Apolipoproteins E/metabolism , Diospyros/chemistry , Diospyros/growth & development , Fruit/chemistry , Fruit/growth & development , Hypolipidemic Agents/pharmacology , Animals , Apolipoproteins E/genetics , Bile Acids and Salts/metabolism , Blood Glucose/metabolism , Body Weight/drug effects , Feces , Gene Expression , Liver/drug effects , Liver/metabolism , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic
6.
Life Sci ; 72(6): 659-67, 2002 Dec 27.
Article in English | MEDLINE | ID: mdl-12467906

ABSTRACT

Bainiku-ekisu, the fruit-juice concentrate of the Oriental plum (Prunus mume) has recently been shown to improve human blood fluidity. We have shown that angiotensin II (AngII) stimulates growth of vascular smooth muscle cells (VSMCs) through epidermal growth factor (EGF) receptor transactivation that involves reactive oxygen species (ROS) production. To better understanding the possible cardiovascular protective effect of Bainiku-ekisu, we have studied whether Bainiku-ekisu inhibits AngII-induced growth promoting signals in VSMCs. Bainiku-ekisu markedly inhibited AngII-induced EGF receptor transactivation. H(2)O(2)-induced EGF receptor transactivation was also inhibited by Bainiku-ekisu. Thus, Bainiku-ekisu markedly inhibited AngII-induced extracellular signal-regulated kinase (ERK) activation. However, EGF-induced ERK activation was not affected by Bainiku-ekisu. AngII stimulated leucine uptake in VSMCs that was significantly inhibited by Bainiku-ekisu. Also, Bainiku-ekisu possesses a potent antioxidant activity. Since the activation of EGF receptor, ERK and the production of ROS play central roles in mediating AngII-induced vascular remodeling, these data suggest that Bainiku-ekisu could exert a powerful cardiovascular protective effect with regard to cardiovascular diseases.


Subject(s)
Angiotensin II/pharmacology , Citric Acid/analogs & derivatives , Citric Acid/pharmacology , Furans/pharmacology , Muscle, Smooth, Vascular/drug effects , Prunus , Signal Transduction , Animals , Calcium/metabolism , Cells, Cultured , Citric Acid/isolation & purification , Dose-Response Relationship, Drug , ErbB Receptors/antagonists & inhibitors , ErbB Receptors/metabolism , Furans/isolation & purification , Lipid Peroxidation , Microsomes, Liver/drug effects , Microsomes, Liver/metabolism , Mitogen-Activated Protein Kinases/metabolism , Muscle, Smooth, Vascular/cytology , Muscle, Smooth, Vascular/metabolism , Plant Extracts/isolation & purification , Plant Extracts/pharmacology , Protein Biosynthesis , Rats , Rats, Sprague-Dawley , Rats, Wistar , Transcriptional Activation
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