Physiological effects of extraction juices from apple, grape, and red beet pomaces in rats

被引:58
作者
Sembries, Sabine
Dongowski, Gerhard [1 ]
Mehrlaender, Katri
Will, Frank
Dietrich, Helmut
机构
[1] German Inst Human Nutr, Dept Food Chem & Prevent Nutr, D-14558 Nuthetal, Germany
[2] State Res Inst, Dept Wine Anal & Beverage Res, D-65366 Geisenheim, Germany
关键词
extraction juices; apples; grapes; red beets; physiological effects; rats;
D O I
10.1021/jf0618168
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
In comparison to classical fruit juice processing, polyphenols and dietary fiber can be extracted from pomace by means of pectinases and cellulases. In the present study, rats were fed with such produced extraction juices from apples, grapes, and red beets as drinking fluids instead of water for 4 weeks to evaluate their physiological effects. In all test groups, the intake of extraction juices was greater as compared to control (water intake), resulting in a higher urine excretion. In the apple and grape group, pH values in feces was lower than control. Administration of extraction juices from apples increased fecal counts of Lactobacillus and Bifidobacterium. More acetate and total short-chain fatty acids appeared in intestinal contents of the apple and red beet group. Furthermore, the intestinal contents of test groups contained higher concentrations of primary bile acids, cholesterol, and cholesterol metabolites but lower concentrations of secondary bile acids. The total amount of steroids excreted by these groups was also greater than control. Quercetin and isorhamnetin appeared in urine of rats fed extraction juices from apples and grapes; in urine of the former group, phloretin was found also. Administration of the extraction juices, enriched in secondary plant metabolites and dietary fiber, resulted in beneficial nutritional effects in rats.
引用
收藏
页码:10269 / 10280
页数:12
相关论文
共 77 条
[11]   The degree of methylation influences the degradation of pectin in the intestinal tract of rats and in vitro [J].
Dongowski, G ;
Lorenz, A ;
Proll, A .
JOURNAL OF NUTRITION, 2002, 132 (07) :1935-1944
[12]   Intestinal steroids in rats are influenced by the structural parameters of pectin [J].
Dongowski, G ;
Lorenz, A .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2004, 15 (04) :196-205
[13]   Steroids in the intestinal tract of rats are affected by dietary-fibre-rich barley-based diets [J].
Dongowski, G ;
Huth, M ;
Gebhardt, E .
BRITISH JOURNAL OF NUTRITION, 2003, 90 (05) :895-906
[14]   Effects of commercial pectolytic and cellulolytic enzyme preparations on the apple cell wall [J].
Dongowski, G ;
Sembries, S .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (09) :4236-4242
[15]   Polyphenols from alcoholic apple cider are absorbed, metabolized and excreted by humans [J].
DuPont, MS ;
Bennett, RN ;
Mellon, FA ;
Williamson, G .
JOURNAL OF NUTRITION, 2002, 132 (02) :172-175
[16]   THE ROLE OF LIPID-PEROXIDATION AND ANTIOXIDANTS IN OXIDATIVE MODIFICATION OF LDL [J].
ESTERBAUER, H ;
GEBICKI, J ;
PUHL, H ;
JURGENS, G .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 13 (04) :341-390
[17]   Grape seed extract suppresses lipid peroxidation and reduces hypoxic ischemic brain injury in neonatal rats [J].
Feng, YZ ;
Liu, YM ;
Fratkins, JD ;
LeBlanc, MH .
BRAIN RESEARCH BULLETIN, 2005, 66 (02) :120-127
[18]   Urinary pharmacokinetics of betalains following consumption of red beet juice in healthy humans [J].
Frank, T ;
Stintzing, FC ;
Carle, R ;
Bitsch, I ;
Quaas, D ;
Strass, G ;
Bitsch, R ;
Netzel, M .
PHARMACOLOGICAL RESEARCH, 2005, 52 (04) :290-297
[19]   Microbial aromatic acid metabolites formed in the gut account for a major fraction of the polyphenols excreted in urine of rats fed red wine polyphenols [J].
Gonthier, MP ;
Cheynier, V ;
Donovan, JL ;
Manach, C ;
Morand, C ;
Mila, I ;
Lapierre, C ;
Rémésy, C ;
Scalbert, A .
JOURNAL OF NUTRITION, 2003, 133 (02) :461-467
[20]   Pharmacokinetics and bioavailability of quercetin glycosides in humans [J].
Graefe, EU ;
Wittig, J ;
Mueller, S ;
Riethling, AK ;
Uehleke, B ;
Drewelow, B ;
Pforte, H ;
Jacobasch, G ;
Derendorf, H ;
Veit, M .
JOURNAL OF CLINICAL PHARMACOLOGY, 2001, 41 (05) :492-499