CN107114764A - A kind of new application of composition - Google Patents
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- CN107114764A CN107114764A CN201710223954.2A CN201710223954A CN107114764A CN 107114764 A CN107114764 A CN 107114764A CN 201710223954 A CN201710223954 A CN 201710223954A CN 107114764 A CN107114764 A CN 107114764A
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- kudzu vine
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- 230000008506 pathogenesis Effects 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229940126532 prescription medicine Drugs 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108700022737 rat Fat1 Proteins 0.000 description 1
- 108700028277 rat PRDM16 Proteins 0.000 description 1
- 238000003757 reverse transcription PCR Methods 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
- 230000007863 steatosis Effects 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
- A61K36/481—Astragalus (milkvetch)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
- A61K36/488—Pueraria (kudzu)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/60—Moraceae (Mulberry family), e.g. breadfruit or fig
- A61K36/605—Morus (mulberry)
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Alternative & Traditional Medicine (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicines Containing Plant Substances (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention discloses a kind of purposes of composition in food, medicine and the health products for preparing prevention or treatment obesity or hyperhomocysteinemiainjury, wherein, the composition includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=(1~2):(1~2):(0~2).Present invention firstly discovers that comprising the Radix Astragali, the root of kudzu vine and root bark of white mulberry composition can effective for obesity prevention and treatment, significant effect can be produced.It has also been found that this composition can effectively treat hyperhomocysteinemiainjury, the treatment for obesity and hyperhomocysteinemiainjury provides new selection.
Description
Technical field
The present invention relates to a kind of new application of the composition comprising the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, more particularly to said composition
Purposes in preventing or treating food, medicine and the health products of obesity or hyperhomocysteinemiainjury.
Background technology
The Radix Astragali, also known as continuous stilbene, its main active is Astragaloside IV, with suppression metabolic syndrome, delays cardiac muscle to lack
Blood Myocardial lesion and improve the effect such as heart function, modern medicine study shows, the Radix Astragali have enhancing body's immunity, liver protection,
Diuresis, anti-aging, resisting stress, decompression and wide antibacterial action.Jishengshenqiwan albuminuria can be eliminated, strengthens myocardial contraction
Power, adjusts blood-sugar content.The Radix Astragali can not only coronary artery dilator, improve myocardial blood supply, improve immunologic function, and can delay
The process of cell ageing.
The root of kudzu vine, is the dry root of legume pueraria lobata, practises and claims elegant jessamine.Chief active position is general flavone in the root of kudzu vine, wherein
Puerarin is one of its main active.Puerarin has hypoglycemic, lipid-loweringing, improves Insulin Resistance, and decompression, expansion
Open coronary artery, improve myocardial ischemia, anti anoxia reperfusion injury, protection endothelial function to improve Hemodynamics, suppress blood
Platelet aggregation etc. a variety of cardiovascular protective effects, therefore Puerarin be widely used in clinical treatment fro diabetic coronary heart disease and
A variety of angiocardiopathies.
The root bark of white mulberry is the dry root skin of moraceae plants mulberry.It contains flavones ingredient:Mulberrin, mulberrochromene, cyclomulberrin etc..
Separated in the root bark of white mulberry and confirm that blood sugar reducing component takes off dioxy imido grpup grape alcohol and MoranA sugar reducing substances, through overtesting,
Verified MoranA has dose-dependent hypoglycemic effect to the hyperglycaemia mouse of model induced by alloxan.
Obesity is a kind of common metabolic disease.It is reported that the whole world in 2008 have 200,000,000 adult males, 3 hundred million one-tenth
Year, women suffered from obesity.The year two thousand thirty is estimated, whole world obesity number will be up to 1,000,000,000.Obesity can make hypertension, glycosuria
The incidence of disease and the death rate of disease and cardiovascular and cerebrovascular disease etc. are dramatically increased, it has also become the major issue of harm global human health it
One, the focus as social extensive concern.Fat prevention and treatment have turned into the challenge that modern medicine faces.2008
Year, only the U.S. is used for just up to 147,000,000,000 dollars of fat medical expense.According to rich think of data statistics, global slimming drugs city in 2012
Field scale is 15.6 hundred million dollars, wherein 30.5 hundred million yuan of China's slimming drugs retail market scale, slimming drugs (prescription medicine) market scale
For 16.8 hundred million yuan.70,000,000,000 are up to by the following possible whole world of present market prediction, wherein nearly 10,000,000,000 yuan of China.
Homocysteine (High homocysteine, HHcy) mass formed by blood stasis is homocysteine
(homocysteine, Hcy) raises a kind of metabolic disease formed in blood, and HHcy mass formed by blood stasis is the danger of a variety of diseases
The dangerous factor, it is however generally that, homocysteine level rise can make angiocardiopathy mortality prediction increase by 4~6 times, there is research
It has been shown that, then increases by 60%, women then increases by 80% when the total Hcy levels of blood plasma often raise 5umol/L risk of coronary heart disease males,
And severe plasma homocysteine mostly occurs in the crowd with Other diseases, particularly diabetes, coronary artery are athero- hard
The diseases such as change, senile dementia, apoplexy, venous embolism, these patient's plasma homocysteine levels are apparently higher than normal person.
The Radix Astragali, the root of kudzu vine and the root bark of white mulberry are combined for treating diabetes, hyperlipoprotememia by certain ratio
Report, but by the Radix Astragali, the root of kudzu vine and the root bark of white mulberry be used for treat obesity and hyperhomocysteinemiainjury, at present also do not have appoint
What is studied and reported.
The content of the invention
On the one hand, it is an object of the invention to overcome above-mentioned the deficiencies in the prior art part there is provided comprising the Radix Astragali, Pueraria lobota
Purposes of the composition of root and the root bark of white mulberry in food, medicine and the health products for preparing prevention or treatment obesity.
The technical solution adopted by the present invention is:A kind of composition is in food, the medicine for preparing prevention or treatment obesity
Purposes in thing and health products, wherein, the composition includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the Radix Astragali, the root of kudzu vine and Sang Bai
The mass ratio of skin is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=(1~2):(1~2):(0~2).
Present inventor has found by numerous studies and experiment, the Radix Astragali of special ratios relation as described above, the root of kudzu vine and
The composition of root bark of white mulberry composition, has especially significant effect in terms of standby prevention or treatment obesity.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=2:1:1.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:2:1.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:1:2.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:1:1.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=2:1:0.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the composition prevents by reducing the accumulation of the white adipose in obesity or treats obesity
Disease.
As composition of the present invention in food, medicine and the health products for preparing prevention or treatment obesity
The preferred embodiment of purposes, the composition can reduce homocysteine caused by obesity and raise.
On the other hand, present invention also offers a kind of composition for preparing prevention or treatment homocysteine blood
Purposes in food, medicine and the health products of disease, wherein, the composition includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the Huang
The mass ratio of stilbene, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:The root bark of white mulberry=(1~2):(1~2):(0~2).
Present inventor has found by numerous studies and experiment, the Radix Astragali of special ratios relation as described above, the root of kudzu vine and
The composition of root bark of white mulberry composition, has especially significant effect in terms of standby prevention or treatment hyperhomocysteinemiainjury.
As composition of the present invention in food, the medicine for preparing prevention or treatment hyperhomocysteinemiainjury
With the preferred embodiment of the purposes in health products, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=2:1:1.
As composition of the present invention in food, the medicine for preparing prevention or treatment hyperhomocysteinemiainjury
With the preferred embodiment of the purposes in health products, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=1:2:1.
As composition of the present invention in food, the medicine for preparing prevention or treatment hyperhomocysteinemiainjury
With the preferred embodiment of the purposes in health products, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=1:1:2.
As composition of the present invention in food, the medicine for preparing prevention or treatment hyperhomocysteinemiainjury
With the preferred embodiment of the purposes in health products, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=1:1:1.
As composition of the present invention in food, the medicine for preparing prevention or treatment hyperhomocysteinemiainjury
With the preferred embodiment of the purposes in health products, the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=2:1:0.
Present invention firstly discovers that the composition comprising the Radix Astragali, the root of kudzu vine and the root bark of white mulberry can effective for obesity prevention and
Treatment, can produce significant effect.It has also been found that can effectively treat high same comprising the Radix Astragali, the root of kudzu vine and root bark of white mulberry composition
Type cysteinaemia, the treatment for obesity and hyperhomocysteinemiainjury provides new selection.
Brief description of the drawings
The model group rats (HFD groups) that Fig. 1 is obtained after being fed for the high lipid food through week for 7 weeks and normal rats (SD
Group) body weight and FPG, TC, TG, LDL-C level comparison diagram.
During Fig. 2 is preventive administration and therapeutic, the changes of weight comparison diagram of each group rat different times.
During Fig. 3 is preventive administration and therapeutic, the dietary amount comparison diagram of each group rat.
Fig. 4 is preventive administration after 7 weeks, each group rat FPG, TC, TG, LDL-C level change comparison diagram.
Fig. 5 is therapeutic after 9 weeks, each group rat FPG, TC, TG, LDL-C level change comparison diagram.
Fig. 6 is preventive administration after 12 weeks, each group rat FPG, TC, TG, LDL-C level change comparison diagram.
Fig. 7 is therapeutic after 14 weeks, each group rat FPG, TC, TG, LDL-C level change comparison diagram.
Fig. 8 preventive administrations 15 weeks and therapeutic are homogenized liver, each group rats'liver obtained after testing after 15 weeks
Dirty middle homocysteine level comparison diagram.
Fig. 9 is preventive administration 15 weeks and therapeutic after 15 weeks, homogenate liver, each group rat obtained after testing
The horizontal comparison diagram of glutamyl transpeptidase in liver.
Figure 10 is preventive administration 15 weeks and therapeutic after 15 weeks, and homogenate liver, each group obtained after testing is big
Lipid (TC, TG) horizontal comparison diagram in mouse liver.
Figure 11 is preventive administration 15 weeks and therapeutic after 15 weeks, each group rat hepatocytes progress oil red O stain
Steatosis comparison diagram afterwards.
Figure 12 is preventive administration 15 weeks and therapeutic after 15 weeks, the brown fat and epididymal adipose tissues of each group rat
The ratio between comparison diagram.
Figure 13 is preventive administration 15 weeks and therapeutic after 15 weeks, the brown fat and perirenal fat of each group rat
The ratio between comparison diagram.
Figure 14 is therapeutic after 15 weeks, the bone weight coefficient ratio comparison diagram of each group rat.
Figure 15 is that the micro-CT scanning figures that body scan is obtained are carried out to live body rat using Latheta LCT200.
Figure 16 is preventive administration after 14 weeks, the white adipose content balance figure in each group rat live body;
Figure 17 is preventive administration after 14 weeks, the fat content comparison diagram in each group rat liver.
Figure 18 is preventive administration after 14 weeks, each group rat femur cortical bone density, cancellous bone density, the contrast of total bone density
Figure.
Figure 19 is therapeutic after 12 weeks, each group diabetes rat UCP-1 expression quantity comparison diagrams.
Figure 20 is therapeutic after 12 weeks, each group diabetes rat Cidea expression quantity comparison diagrams.
Figure 21 is therapeutic after 12 weeks, each group diabetes rat MCP-1 expression quantity comparison diagrams.
Figure 22 is therapeutic after 12 weeks, each group diabetes rat PRDM16 transcription factor mrna expression amount comparison diagrams.
Embodiment
To better illustrate the object, technical solutions and advantages of the present invention, below in conjunction with the drawings and specific embodiments pair
The present invention is described further.
Given in composition 1~composition of embodiment embodiment 5 available for preparation prevention or treatment obesity or high same
The example of the composition comprising the Radix Astragali, the root of kudzu vine and the root bark of white mulberry of the food of type cysteinaemia, medicine and health products.
Composition embodiment 1
A kind of composition, it includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is
The Radix Astragali:The root of kudzu vine:The root bark of white mulberry=2:1:1.
Composition embodiment 2
A kind of composition, it includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is
The Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:2:1.
Composition embodiment 3
A kind of composition, it includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is
The Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:1:2.
Composition embodiment 4
A kind of composition, it includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is
The Radix Astragali:The root of kudzu vine:The root bark of white mulberry=1:1:1.
Composition embodiment 5
A kind of composition, it includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is
The Radix Astragali:The root of kudzu vine:The root bark of white mulberry=2:1:0.
Illustrate that the composition comprising the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is preventing or treated fat below by way of specific embodiment
Purposes in disease or homocysteine.
Embodiment 1 includes application of the composition of the Radix Astragali, the root of kudzu vine, the root bark of white mulberry in prevention and treatment obesity
1. experiment packet
This experiment includes composition (HQS) prevention administration and therapeutic administratp two parts.Healthy answering property of male SD rat is raised
After one week, normal group (SD) and modeling group are randomly divided into, normal group is fed using basal feed, and modeling group is fed using high lipid food
Support, free water and feed, while it is model group (HFD) to choose 10 modeling group rats.Composition prevention administration:By modeling group
Rat is randomly divided into HQS-L-composition low dose group (1.2g/kg.d), HQS-H-composition high dose group (2.4g/
Kg.d), every group 8, while modeling is administered simultaneously.Composition treatment is administered:After the continuous high fat diet of modeling group rat 7 weeks,
Modeling group body weight is apparently higher than normal group (the SD rats of feeding basal feed), and modeling group FPG, TC, TG, LDL-C level is also bright
It is aobvious to be higher than normal group, show now model success, with significant difference, specifically as shown in Figure 1.Select more than normal rat
The rat of body weight 20% is obese rat model, is randomly divided into HQS-L-composition low dose group (1.2g/kg.d), HQS-H
- composition high dose group (2.4g/kg.d), Lipitor positive drug group (Lipitor, 2mg/kg), every group 8, high fat diet 7
Zhou Houzai starts administration.Normal group and model group rats give the physiological saline of equivalent respectively, and each administration group gives corresponding reagent,
Once a day.Wherein, the administration of composition high and low dose group is fat-reducing liver-protecting composition of the invention, the wherein Radix Astragali:The root of kudzu vine:
The mass ratio of the root bark of white mulberry is 1:2:1.
2. medication
2.1 preventive administrations (prevention group is administered when high lipid food is fed);
2.1.1 dosage is set
The dosage of composition low dosage (HQS-L) and composition high dose (HQS-H) is set to be tried according to the multiple drug effect of early stage
Test set effective dose, dosage be respectively 1.2g/kg.d and
2.4g/kg.d。
2.1.2 medication
Once a day, successive administration 15 weeks.
2.2 therapeutics (treatment group is that high fat diet starts administration again after 7 weeks).
2.2.1 dosage is set
The dosage of composition low dosage (HQS-L) and composition high dose (HQS-H) is set to be tried according to the multiple drug effect of early stage
Test set effective dose, dosage be respectively 1.2g/kg.d and
2.4g/kg.d.Lipitor dosage is that dosage is 2g/kg.d according to set by people's clinical equivalent dosage.
2.2.2 medication
Once a day, successive administration 15 weeks.
3. experimental working technique
3.1 body weight
In experimentation situations such as observation each group rat body weight change daily, feed, fur, activity, body weight is recorded weekly
Change.
3.2 glycolipid biochemical indicators
Prevention administration:In 7 weekends and 12 weekends of administration are administered, Rat Fast can't help water 12h, etherization, eyeground vein
Clump takes blood, and anticoagulant heparin, 4 DEG C of centrifugations (3000r/min, 15min) point take blood plasma, determine fasting blood-glucose (FPG), cholesterol
(TC), triglycerides (TG), low-density lipoprotein (LDL-C);
Therapeutic administratp:In 9 weekends and 14 weekends of administration are administered, Rat Fast can't help water 12h, etherization, eyeground vein
Clump takes blood, and anticoagulant heparin, 4 DEG C of centrifugations (3000r/min, 15min) point take blood plasma, determine FPG, TC, TG, LDL-C.
3.3 experiment materials and organ coefficient
At the end of experiment, each group rat weight, and (0.35ml/100g body weight) is injected intraperitoneally with 10% chloraldurate, will
Lie on the back and be fixed on dissection plate after rat anesthesia, rat anesthesia, carry out abdominal aortic blood execution, obtain blood specimen a part of quiet
Put after 2h 3000r/min and centrifuge 30min and obtain serum, a part is whole blood, and dispense that to be placed in -20 DEG C of refrigerators standby.It is rapid to take out
The organs and tissues such as the heart, liver, spleen, lung, kidney, epididymal adipose, perirenal adipose tissue, brown adipose tissue, femur, weigh, point
Dress, places -80 DEG C of freezen protectives of cryopreservation tube.Calculate each organ coefficient, organ coefficient=Organ weight/body weight × 100% simultaneously.
A part of liver organization is taken to be dyed for HE simultaneously, a part of liver organization is used for oil red O stain.
3.4 liver lipids levels are determined
A pipe liver organization is taken in -80 DEG C of cold storage refrigerators.Tissue about 100mg is taken during detection, isopropanol, volume is added
1ml/50mg.Stood overnight after homogenate.Supernatant is taken after centrifugation in second day, wherein TC and TG contents are determined, the result conversion measured
As a result lipid content to contain in every kilogram of internal organs is converted into g/kg in terms of g.Molecular weight:Triglycerides 639g/mol;Total courage
Sterol 386.65g/mol.
3.5 liver homocysteines, determination of glutamyl-transpeptidase
A pipe liver organization is taken in -80 DEG C of cold storage refrigerators.Tissue about 100mg is taken during detection, blood stains are washed away with PBS.Cut
It is put into fritter in tissue grinder, adds 1ml PBS, homogenate is made, is subsequently placed in -20 DEG C overnight.By multigelation 2 times
After processing destruction cell membrane, tissue is homogenized and takes supernatant within 5 minutes in 4 DEG C of 5000g centrifugations, takes appropriate supernatant to test immediately.Survey
Method is determined according to ELISA method, is operated according to kit specification.
3.6 rat live body micro-CT are tested
One week before dissection of prevention administration group rat, carries out live body micro-CT experiments.Utilize Latheta LCT200
Toy CT, a micro-CT systems that multi-functional 3D scannings are carried out for animals such as rat, mouse and rabbits.Before experiment,
Each group rat first with 10% chloraldurate intraperitoneal injection of anesthesia 1-2h, is put into row abdomen simple scan in groove, to rat bone parameter, subcutaneously
The parameters such as fat, interior fat, fatty liver CT values are measured.The experiment is real in The Third Affiliated Hospital of Southern Medical University's medical science
Test research center progress.
4. result of the test
4.1 body weight curvilinear motions are compared
During prevention administration and therapeutic administratp, the changes of weight such as table 1~2 of each group rat different times and Fig. 2 institutes
Show.
During the prevention administration of table 1, the changes of weight results of each group rat different times (N=8)
During the therapeutic administratp of table 2, the changes of weight results of each group rat different times (N=8)
Interpretation of result:As shown in table 1~2 and accompanying drawing 2, normal group (SD groups) is compared with model group (HFD groups) rat body weight
Understand:The continued weight increase of model group, and with significant difference, show obesity rat model success.From composition prevention
The body weight interpretation of result of rat is understood after administration and therapeutic administratp:Composition high dose group (HQS-H groups), composition low dose group
(HQS-L groups) has preferable prevention effect to obesity, and administration group body weight is significantly lower than model group, close to normal group body
Weight, and Lipitor group (Lipitor groups) is substantially better than, Lipitor group body weight is dramatically increased, close to model group.Prevention group rat
MicroCT experiments are done within one week before administration, hence it is evident that feel that rat body weight increasess slowly, especially composition administration group rat body weight
Decline.
As shown in Figure 3, by counting each group rat averagely diet situation of every daily, it is known that feed each of high lipid food
Indifference between group rat diet situation.Show that the change of each group rat body weight is unrelated with dietary amount.
4.2 glycolipid biochemical indicators compare
4.2.1 prevention administration 7 weeks and therapeutic administratp after 9 weeks glycolipid biochemical indicator compare
Prevention administration 7 weeks and therapeutic administratp are after 9 weeks, each group rat FPG, TC, TG, LDL-C level change such as Fig. 4~5
It is shown.
From the point of view of the prevention administration 7 weeks and 9 weeks glycolipid results of therapeutic administratp shown in accompanying drawing 4~5, model group (HFD groups) and
Normal group (SD groups) is compared, and FPG, TC, TG, LDL-C level are significantly raised, and with significant difference.With model group phase
Than, composition high dose group (HQS-H groups), composition low dose group (HQS-L groups) have preferable hypoglycemic, effect for reducing fat, and
There is certain dose dependent.
4.2.2 prevention administration 12 weeks and therapeutic administratp after 14 weeks glycolipid biochemical indicator compare
Preventive administration 12 weeks and therapeutic administratp are after 14 weeks, and the change of each group rat FPG, TC, TG, LDL-C level is such as attached
Shown in Fig. 6~7.
From the point of view of the prevention administration 12 weeks and 14 weeks glycolipid results of therapeutic administratp shown in Fig. 6~7, model group (HFD groups) and
Normal group (SD groups) is compared, and FPG, TC, TG, LDL-C level are significantly raised, and with significant difference.With model group phase
Than, energy preferably hypoglycemic, the lipid-loweringing of composition high dose group (HQS-H groups), composition low dose group (HQS-L groups), and have
Doses dependence.And in terms of hypoglycemic, composition is better than Lipitor group.
4.3 homocysteines, glutamyl transpeptidase compare
Preventive administration 15 weeks and therapeutic are after 15 weeks, homocysteine level and paddy in each group rat liver
Aminoacyl transpeptidase level is as shown in Fig. 8~9.
Homocysteine (Hcy) is a kind of sulfur-containing amino acid in human body, is methionine and cysteine metabolic process
In important intermediate.Hcy too high is cardiovascular and cerebrovascular disease, osteoporosis, the hazards of the nervous system disease.Such as accompanying drawing
Shown in 8, by detecting Hcy levels in each group rat liver, model group (HFD groups) level of discovery is significantly raised, and composition it is high,
Low dose group (HQS-H groups, HQS-L groups) is significantly reduced, and showing the Rats adiposis hepatica of administration group is substantially improved.
Glutamyl transpeptidase (GTT1) has been one of liver function test project.As shown in accompanying drawing 9, by detecting liver
Middle GTT1 levels, it is known that model group level is significantly raised, and composition high and low dose group (HQS-H groups, HQS-L groups), Lipitor
Group (Lipitor groups) can be significantly reduced.
4.4 liver lipids compare
Preventive administration 15 weeks and therapeutic are after 15 weeks, and lipid (TC, TG) level is as schemed in each group rat liver
Shown in 10.
Lipid dystopy deposition refers to that body lipid is deposited in non-fat tissue, mostly occurs in liver, muscle and pancreas, most easily
The position of generation is liver.As shown in Figure 10, by detecting lipid in liver (TC, TG), model group (HFD groups) liver is found
Lipid is significantly raised, and administration group can significantly improve liver lipids deposition, and prevention group is more notable compared with treatment group.
4.5 liver oil red O stains compare
Preventive administration 15 weeks and therapeutic are after 15 weeks, and each group rat hepatocytes carry out the fat after oil red O stain
Fat denaturation contrast is as shown in figure 11.
As shown in Figure 11, nearly no fat drips in normal group liver cell.The fat drips of a large amount of bulla samples after model group dyeing,
Mutually fusion, and the high fat diet time is more long, fat drips are more obvious.Composition prevention high and low dose group (prevention HQS-H groups, prevention
HQS-L groups) hepatic cell fattydegeneration substantially mitigate, better than the high low dose group of composition treatment (treatment HQS-H groups, treatment
HQS-L groups), become apparent from high dose group degree of alleviation.The hepatic cell fattydegeneration and mould of composition height therapeutic dose group
Type group is compared, and is also substantially improved, and better than Lipitor group;Wherein, A represents normal group, and I representative model groups, K represents Li Pu
Appropriate group.
4.6 browns, white adipose coefficients comparison
4.6.1 white adipose coefficients comparison
Mammal mainly contains two kinds of white adipose (WAT) brown adipose tissue (BAT).And white adipose is generally wrapped
Include subcutaneous white adipose and internal organ white adipose.It is now recognized that subcutaneous white adipose and brown fat participate in maintaining human body energy
Stable state and the balance of metabolism, and internal organ white adipose then participates in the generation of metabolic disease.Subcutaneous white adipose mainly includes abdomen
Butt crack, oxter, thyroid gland side fat;Internal organ white adipose mainly includes epididymal adipose tissues, perirenal fat, mesenteric fat.Human body
Correlative study think, the correlation ratio of the risk factors of cardiovascular diseases such as internal organ white adipose and insulin resistance, diabetes
Subcutaneous white adipose is higher.Animal different parts adipose tissue form and function difference are inquired into, can preferably be Metabolic syndrome
The pathogenesis levied provides foundation.
Research finds, white adipose tissue by some physiological stimulations (cold expoure), hormonal stimulation (such as Irisin) with
And body receives after drug therapy (such as PPAR gamma agonists or beta-adrenergic are stimulated), may occur in which that brown fat phenotype is special
Levy, as fat drips diminish, it is excessive that line grain crosses number.Because white adipose milkproduct shows that energy balance switchs to energy by energy storage
Amount expenditure, thus as the novel targets of the metabolic diseases such as treatment obesity.
Preventive administration 15 weeks and therapeutic are after 15 weeks, and the epididymal adipose tissues and perirenal fat coefficient of each group rat are such as
Shown in table 3~4.
3 preventive administration of table 15 weeks and therapeutic are after 15 weeks, the epididymal adipose tissues of each group rat and perirenal fat system
Number
4 therapeutic of table 15 weeks and therapeutic are after 15 weeks, the epididymal adipose tissues of each group rat and perirenal fat system
Number
Interpretation of result:As shown in table 3~4, epididymal adipose tissues and perirenal fat are used as white adipose, composition high and low dose
Group (HQS-H groups, HQS-L groups) significantly reduces white adipose coefficient, and better than Lipitor group.
4.6.2 brown/white adipose coefficients comparison
Preventive administration 15 weeks and therapeutic be after 15 weeks, the brown fat of each group rat and white adipose such as
Shown in Figure 12~13.
As shown in accompanying drawing 12~13, by by the ratio between brown fat and white adipose it is also seen that come composition is high and low
Dosage group (HQS-H groups, HQS-L groups) can improve brown white ratio, better than Lipitor (Lipitor groups).
To sum up, epididymal adipose tissues coefficient, the perirenal fat coefficient for the obese rat model set up using pure high fat diet modeling
All apparently higher than normal rats.From administration, composition administration group can substantially reduce the epididymal adipose tissues system of animal pattern
Number, perirenal fat coefficient (reduction white adipose, the white ratio of raising palm fibre), and reduction is substantially, and to the base of white adipose milkproduct
Because influence is obvious;Substantial amounts of aliphatic acid, which is consumed, while reducing white adipose, improving brown fat serves reducing blood lipid
Act on (one of mechanism of reducing blood lipid).
4.7 bone weight coefficient ratios compare
As shown in Figure 14, by femur and the ratio of body weight, nothing between normal group (SD groups) and model group (HFD groups) is found
Difference, and composition high and low dose group (HQS-H groups, HQS-L groups), compared with model group, bone weight coefficient is significantly raised,
And with significant difference, show that composition has the effect for improving bone mass, and better than Lipitor (Lipitor groups).
4.8 living imagings observe the influence of medicine
Show medicine to skeleton, liver, fatty influence as shown in figures 15 to 18 by living imaging.Utilize Latheta
LCT200 carries out body scan, by calculating fat percentage, it has been found that compared with normal group, model group rats fat to live body rat
Fat rate and liver fat percentage are significantly raised, and with significant difference.Compared with model group, the fat percentage of the high low dose group of composition
Substantially reduced with liver fat rate, and with dose dependent.Total bone density to femur has also been lifted simultaneously.
As shown in Figure 16, can be with from figure which show the white adipose content of each group rat after prevention administration 14 weeks
Finding out the fat percentage of the high low dose group of fat-reducing liver-protecting composition substantially reduces.
As shown in Figure 17, after which show preventive administration 14 weeks, the fat content contrast in each group rat liver, from
The liver fat rate of the high low dose group of it can be seen from the figure that fat-reducing liver-protecting composition is substantially reduced.
As shown in Figure 18, after which show preventive administration 14 weeks, each group rat cortex bone density, cancellous bone density,
Total bone density (cortical bone density, cancellous bone density, total bone density that are followed successively by each group in Figure 18 from left to right).Can be with from figure
Find out that the high low dose group of fat-reducing liver-protecting composition has also been lifted to total bone density of femur.
The fat gene of composition for improved of the embodiment 2 comprising the Radix Astragali, the root of kudzu vine and the root bark of white mulberry
1st, experiment packet
This experiment is divided into 8 groups, and every group of difference is as follows:
A --- SD groups, N=8
B --- SD+GC groups, N=10
C --- HFD groups, N=8
D --- HFD+GC groups, N=12
The composition group of I --- HFD+GC+ embodiments 2, N=10
The composition group of J --- SD+GC+ embodiments 2, N=10
2. test method
SPF rank SD rats divide rat after regular grade Animal House adaptability is raised two weeks (about 200-220g) at random
For normal group, glucocorticoid group, high lipid food group, high fat sugaring cortin group, high fat sugaring cortin+composition
Group, glucocorticoid add composition group.Normal group, glucocorticoid group and glucocorticoid add composition group to feed with basis feeding
Material, other each groups are fed with high lipid food.In addition to normal group and high lipid food group give normal saline, remaining each group starts to fill
Stomach prednisone acetate 3.5mg/kg, once a day, while starting gastric infusion composition (2.96g/kg) after 1 hour, wherein yellow
Stilbene:The root of kudzu vine:The mass ratio of the root bark of white mulberry is 1:2:1, continuous 12 weeks.Thereafter, test operation is carried out in accordance with the following methods:
(1) extraction of total serum IgE
1. the white adipose and brown fat of animal are collected, preserving liquid with RNA preserves.Deposit in -80 DEG C of refrigerators.
2. thaw tissue, first takes out sample with tweezers, is put on filter paper and blots preservation liquid, weighs, after be transferred to it is another dry
In net 1.5ml Ep pipes, 1mltrizol is added, is shredded with small scissors in trizol liquid, anvil is broken in glass homogenizer
Be invisible to the naked eye bulky grain.5min is centrifuged in 10000rpm, carefully discards upper strata oily hyaline layer (fat deposit).
3. often pipe chlorination imitates 0.2ml, and acutely shaking mixes 15s, puts room temperature 5min and is allowed to be layered, 4 DEG C of 10000 × g centrifugations
5min, carefully moves to upper strata aqueous phase in another 1.5ml centrifuge tubes.
4. often pipe adds 0.5ml isopropanols, and room temperature places 10min, and 4 DEG C of 10000 × g centrifuge 10min.Carefully by upper strata
Clear liquid is discarded, and precipitation is washed with 70% ethanol 1ml, and 4 DEG C of 5000 × g centrifuge 5min, abandon supernatant, room temperature, which is placed, makes ethanol complete
Volatilization, ttom of pipe visible white dot is RNA.
5. 30 μ l are added without RNase water in precipitating, 58 DEG C of water-bath 10min make precipitation fully dissolve.
(2) detection of RNA concentration, purity
With DU800 nucleic acid/protein analyzer at wavelength 260nm and 280nm respectively determine RNA samples OD-A260 and
A280 (the A260/ A280 ratios of the high sample of RNA purity>1.7), and RNA concentration is measured.Take and determined on a small quantity with nucleic acid-protein
Instrument determines A260, calculates rna content.And it is 1.8~2.0 to determine A260/A280, it was demonstrated that RNA purity.Remaining puts -80 DEG C of jellies
Deposit standby.
(3) RT synthesizes cDNA
The RNA sample extracted using upper step, RT reactions are carried out with reference to RT reagents specification.RT reaction systems such as following table institute
Show.
* according to added by being calculated RNA concentration the μ g of total serum IgE amount 3.0 RNA volumes, then adjust RNas-free ultrapure water consumption, make
Reaction cumulative volume is 20 μ l.
Following thermocycling program is set to be reacted (following table) in RT-PCR thermal cyclers:
After reaction terminates, gained cDNA products put -20 DEG C of preservations.
(4)Real time PCR
1. PCR primer design and synthesis
Primer is designed according to real time PCR primers design principle.NCBI GenBank databases are retrieved, it is designed
Primer is directed to different extrons, the calibrating cdna compareed using β-actin as internal reference respectively.Using Primer
Premier5.0 softwares separately design MCP-1, UCP-1, PRDM16, Cidea and β-actin PCR primer, different primers
Sequence is shown in Table 15, and all PCR primers are synthesized by Shanghai Sangon Biological Engineering Technology And Service Co., Ltd.
2. Real time PCR reaction products are verified
Reaction system (following table) is formulated as follows by the operational manual of SYBR qPCR Mix kits
Real time PCR are carried out with ABI7500 type real time PCR instruments, amplification condition is as shown in the table:
3. the expression of Real time PCR testing goals gene and internal reference β-actin genes in each group adipose tissue
In 50 μ l reaction systems, contain template cDNA200ng, remaining reacted constituent, amplification condition and melt curve analysis
Setting with product confirmatory experiment.MCP-1, UCP-1, PRDM16, Cidea and β-actin DNA fragmentation are expanded respectively.Adopt
Data analysis is carried out to real time PCR results with 2- △ △ CT methods, the numerical value of wherein Normal group is 1.
3. result of the test
UCP-1 gene expressions in 3.1 brown adipose tissues
UCP-1 genes expressed in abundance in brown adipose tissue, is seldom expressed in white adipose tissue, is brown fat
Cell-specific genes.As shown in Figure 19, in addition to high lipid food group, remaining each group in UCP-1 gene expressions all substantially under
Drop, wherein the UCP-1 gene expressions of I groups (the composition group of HFD+GC+ embodiments 2) are apparently higher than D groups (HFD+GC groups), explanation
Composition can promote brown fat cell-specific genes UCP-1 expression, illustrate that composition has product in resistance obesity
Pole meaning.
Cidea gene expressions in 3.2 brown adipose tissues
As shown in Figure 20, I groups (the composition group of HFD+GC+ embodiments 2) substantially rise in Cidea gene expressions, high
In other each groups, illustrate that composition has positive effect in resistance obesity.
MCP-1 gene expressions in 3.3 white adipose tissues
As shown in Figure 21, compared with normal group, remaining each group all substantially rises in MCP-1 gene expressions.Compared with D groups
(high lipid food sugaring cortin group), composition administration group (I, J group) is decreased obviously in MCP-1 gene expressions.
PRDM16 gene expressions in 3.4 brown adipose tissues
Accompanying drawing 22 shows that PRDM16 transcription factors play an important role in regulation and control brown fat and sarcoblast conversion, are
Keep necessary to brown fat phenotype, can also promote brown fat formation, energy expenditure.
In summary, composition is obvious to the effect gene of white adipose milkproduct.
Finally, it should be noted that the above embodiments are merely illustrative of the technical solutions of the present invention rather than the present invention is protected
The limitation of scope is protected, although being explained in detail with reference to preferred embodiment to the present invention, one of ordinary skill in the art should
Understand, technical scheme can be modified or equivalent substitution, without departing from the essence of technical solution of the present invention
And scope.
Claims (14)
1. a kind of purposes of composition in food, medicine and the health products for preparing prevention or treatment obesity, wherein, institute
State composition and include the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:The root of kudzu vine:Sang Bai
Skin=(1~2):(1~2):(0~2).
2. purposes as claimed in claim 1, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:Pueraria lobota
Root:The root bark of white mulberry=2:1:1.
3. purposes as claimed in claim 1, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:Pueraria lobota
Root:The root bark of white mulberry=1:2:1.
4. purposes as claimed in claim 1, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:Pueraria lobota
Root:The root bark of white mulberry=1:1:2.
5. purposes as claimed in claim 1, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:Pueraria lobota
Root:The root bark of white mulberry=1:1:1.
6. purposes as claimed in claim 1, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:Pueraria lobota
Root:The root bark of white mulberry=2:1:0.
7. purposes as claimed in claim 1, it is characterised in that the composition is accumulated by reducing the white adipose in obesity
Tire out to prevent or treat obesity.
8. purposes as claimed in claim 1, it is characterised in that the composition can reduce the Guang of homotype half caused by obesity
Propylhomoserin is raised.
9. a kind of composition is in food, medicine and the health products for preparing prevention or treatment hyperhomocysteinemiainjury
Purposes, wherein, the composition includes the Radix Astragali, the root of kudzu vine and the root bark of white mulberry, and the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is Huang
Stilbene:The root of kudzu vine:The root bark of white mulberry=(1~2):(1~2):(0~2).
10. purposes as claimed in claim 9, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:
The root of kudzu vine:The root bark of white mulberry=2:1:1.
11. purposes as claimed in claim 9, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:
The root of kudzu vine:The root bark of white mulberry=1:2:1.
12. purposes as claimed in claim 9, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:
The root of kudzu vine:The root bark of white mulberry=1:1:2.
13. purposes as claimed in claim 9, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:
The root of kudzu vine:The root bark of white mulberry=1:1:1.
14. purposes as claimed in claim 9, it is characterised in that the mass ratio of the Radix Astragali, the root of kudzu vine and the root bark of white mulberry is the Radix Astragali:
The root of kudzu vine:The root bark of white mulberry=2:1:0.
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CN107854522B (en) * | 2017-09-13 | 2020-10-30 | 北京宜生堂医药科技研究有限公司 | Composition and preparation method and application thereof |
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