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Rice bran proteins and their hydrolysates modulate cholesterol metabolism in mice on hypercholesterolemic diets.

Food & function
January 1, 1970
Huijuan Zhang et al. (5 authors)
Journal ArticleAnimal Study
Extracted Claims (19)
InterventionDirectionEndpointPopulationDosageImpactClaim #
defatted rice bran protein (DRBP)
neutral
hypolipidemic properties
mice on high fat diets
-
hypolipidemic properties were determined
#1
fresh rice bran protein (FRBP)
neutral
hypolipidemic properties
mice on high fat diets
-
hypolipidemic properties were determined
#2
DRBP hydrolysates (DRBPH)
neutral
hypolipidemic properties
mice on high fat diets
-
hypolipidemic properties were determined
#3
FRBP hydrolysates (FRBPH)
neutral
hypolipidemic properties
mice on high fat diets
-
hypolipidemic properties were determined
#4
FRBPH diet
decrease
Very low-density lipoprotein cholesterol (VLDL-C) content
mice on high fat diets
-
reduced
#5
FRBPH diet
decrease
low-density lipoprotein cholesterol (LDL-C) content
mice on high fat diets
-
reduced
#6
FRBPH diet
decrease
hepatic total cholesterol content
mice on high fat diets
-
reduced
#7
FRBPH diet
increase
fecal total cholesterol content
mice on high fat diets
-
increased
#8
FRBPH diet
increase
total bile acid (TBA) content
mice on high fat diets
-
increased
#9
FRBPH diet
decrease
expression levels of hepatic genes for cholesterol biosynthesis HMG-CoAR
mice on high fat diets
-
lowest
#10
FRBPH diet
decrease
expression levels of hepatic genes for cholesterol biosynthesis SREBP-2
mice on high fat diets
-
lowest
#11
-
increase
mRNA level of HMG-CoAR
-
r = 0.82, P < 0.05
significantly positively correlated
#12
all test groups
increase
mRNA levels of genes related to bile acid biosynthesis and cholesterol efflux, CYP7A1
mice on high fat diets
-
up-regulated
#13
all test groups
increase
mRNA levels of genes related to bile acid biosynthesis and cholesterol efflux, ABCA1
mice on high fat diets
-
up-regulated
#14
all test groups
increase
mRNA levels of genes related to bile acid biosynthesis and cholesterol efflux, PPARγ
mice on high fat diets
-
up-regulated
#15
FRBPH
neutral
cholesterol metabolism
mice fed the high fat and cholesterol diet
-
regulates
#16
FRBPH
increase
fecal steroid excretion
mice fed the high fat and cholesterol diet
-
increasing
#17
FRBPH
increase
expression levels of genes related to bile acid synthesis and cholesterol efflux
mice fed the high fat and cholesterol diet
-
increasing
#18
FRBPH
decrease
expression levels of genes related to cholesterol biosynthesis
mice fed the high fat and cholesterol diet
-
down-regulation
#19
Abstract

The hypolipidemic properties of defatted rice bran protein (DRBP), fresh rice bran protein (FRBP), DRBP hydrolysates (DRBPH), and FRBP hydrolysates (FRBPH) were determined in mice on high fat diets for four weeks. Very low-density lipoprotein cholesterol (VLDL-C), low-density lipoprotein cholesterol (LDL-C) contents, and the hepatic total cholesterol content were reduced while fecal total cholesterol and total bile acid (TBA) contents were increased in the FRBPH diet group. The expression levels of hepatic genes for cholesterol biosynthesis HMG-CoAR and SREBP-2 were lowest in the FRBPH diet group. The mRNA level of HMG-CoAR was significantly positively correlated with the hepatic TG content (r = 0.82, P < 0.05). The mRNA levels of genes related to bile acid biosynthesis and cholesterol efflux, CYP7A1, ABCA1, and PPARγ were up-regulated in all test groups. The results suggest that FRBPH regulates cholesterol metabolism in mice fed the high fat and cholesterol diet by increasing fecal steroid excretion and expression levels of genes related to bile acid synthesis and cholesterol efflux, and the down-regulation of the expression levels of genes related to cholesterol biosynthesis.

Medical Subject Headings (MeSH)
ATP Binding Cassette Transporter 1AnimalsBile Acids and SaltsCholesterolCholesterol 7-alpha-HydroxylaseCholesterol, LDLCholesterol, VLDLDiet, High-FatFecesGene Expression RegulationLiverMaleMiceMice, Inbred ICROryzaPlant ProteinsProtein HydrolysatesRNA, MessengerSterol Regulatory Element Binding Protein 2Triglycerides
Study Links
PubMed ID27216972
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