CN107997174A - A kind of health composition and health food for having effects that to improve sleep and/or antidepression - Google Patents

A kind of health composition and health food for having effects that to improve sleep and/or antidepression Download PDF

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Publication number
CN107997174A
CN107997174A CN201711336886.7A CN201711336886A CN107997174A CN 107997174 A CN107997174 A CN 107997174A CN 201711336886 A CN201711336886 A CN 201711336886A CN 107997174 A CN107997174 A CN 107997174A
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parts
health
gaba
extracts
theanine
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CN107997174B (en
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汪玉芳
贺瑞坤
张旭光
韦经强
肖健
彭辉
林芸
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BY Health Co Ltd
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BY Health Co Ltd
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Priority to PCT/CN2018/111880 priority patent/WO2019114428A1/en
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/17Amino acids, peptides or proteins
    • A23L33/175Amino acids
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

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  • Mycology (AREA)
  • Health & Medical Sciences (AREA)
  • Nutrition Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
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  • Proteomics, Peptides & Aminoacids (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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Abstract

The present invention relates to technical field of health care food, more particularly to a kind of health composition and health food for having effects that to improve sleep and/or antidepression.In parts by weight, which is made of 1~20 part of GABA aminobutyric acid, 1~30 part of theanine, 1~50 part of Rhizoma Gastrodiae extract and 1~80 part of Radix Morindae Officinalis extract.The technique effect that the present invention has is:After GABA aminobutyric acids, theanine, Rhizoma Gastrodiae extract and Radix Morindae Officinalis extract are used cooperatively by health composition of the present invention, there is significant synergistic function in terms of sleep and/or antidepression effect is improved.

Description

It is a kind of to have effects that to improve sleep and/or health composition and the health care of antidepression Food
Technical field
It is more particularly to a kind of that there is to improve sleep and/or antidepression the present invention relates to technical field of health care food Health composition and health food.
Background technology
Depression is also known as depressive disorder, low for main clinical characteristics with notable and lasting mental state, is mood disorder Main Types.Clinical visible mental state is low unbecoming with its situation, and the downhearted of mood can be from depressed to extremely grieved, certainly Inferior depression, in addition it is pessimistic and worldweary, can there are conamen or behavior;Even occur numb;Some cases have obvious anxiety and fortune Dynamic property is intense;Severe patient may occur in which the psychotic symptoms such as illusion, vain hope.Somatization mainly has sleep-disorder, weak, appetite Decline, weight loss, constipation, the pain at any position of body, sexual hypoesthesia, impotence, amenorrhoea etc..Sleep-disorder is mainly shown as Early awakening, when generally early awakening 2~3 is small than usual, cannot fall asleep, this has characteristic meaning to paralepsy again after waking up.
Drug therapy is the primary treatment measure of moderate above paralepsy.Clinically the antidepressants of a line are main at present Including selective serotonin reuptake inhibitor (SSRI, represent agents fluoxetine, Paxil, Sertraline, Fluvoxamine, Citalopram and escitalopram), (SNRI, represents medicine text and draws for serotonin and norepinephrine reuptake inhibitors Method is pungent and Duloxetine), norepinephrine and specific serotonin energy antidepressants (NaSSA, represents medicine Mirtazapine) Deng.Traditional tricyclic antidepressants, tetracyclic antidepressants and monoamine oxidase inhibitors is since adverse reaction is larger, using substantially subtracting It is few.
GABA aminobutyric acids (γ-aminobutyric acid) are a kind of naturally occurring nonprotein functional aminos, Yi Zhongtian Right active ingredient, is the main inhibitory neurotransmitter of central nervous system, mediates nervous system rapid inhibitory effect, γ-ammonia Base butyric acid is to study a kind of more deep important inhibitory neurotransmitter, it participates in a variety of metabolic activities, is had very high Physiological activity., can also be anti-spiritual uneasy available for hepatic coma and dysbolism of brain, it is to anti-depression anxiety, improves mood, alleviation Pressure, promote sleep, improve cerebration, a kind of pure natural substance that removing toxic substances is sobered up.
Theanine (L-Theanine) is distinctive free amino acid in tealeaves, and theanine is glutamic acid gamma-buserelin, It is pleasantly sweet.Theanine is similar to intracerebral active material glutamine, glutamic acid on chemical constitution, is the master promoted the production of body fluid in tealeaves and moisten sweet tea Want composition.Theanine can solution disappear fatigue, reduce blood pressure and improve ability of learning and memory.
Rhizoma Gastrodiae (scientific name:Gastrodia elata Bl.), also known as rhizoma gastrodiae, solely shake sesame, from it is female, close and superintended and directed from grass, god's grass, ghost Postal, Mokpo, RHIZONA GASTRODIAE, wind grass, Bai Longpi etc., are orchid family Gastrodia herbaceos perennials.Its rhizome is used as medicine to treat Have a dizzy spell, the disease such as extremity numbness, child convulsion, be rare Chinese medicine, treatment headache and insomnia is shared with Qiongzhen Ganoderma Lucidum.
Morinda officinalis (scientific name:Morinda officinalis How), it is dicotyledon Rubiaceae, main product is in Guangdong, wide The ground such as west.Medicinal plant, cures mainly impotence and seminal emission, uterus cold infertile, irregular menstruation, few abdomen crymodynia, arthralgia pain due to rheumatism, muscles and bones impotence.
It yet there are no the report for being used cooperatively GABA- aminobutyric acids, theanine, Rhizoma Gastrodiae extract and Radix Morindae Officinalis extract Road.
The content of the invention
In view of this, the present invention provides a kind of health composition and guarantor for having effects that to improve sleep and/or antidepression Health food.After GABA- aminobutyric acids, theanine, Rhizoma Gastrodiae extract and Radix Morindae Officinalis extract are used cooperatively by the health composition, There is significant synergistic function in terms of sleep and/or antidepression effect is improved.
In order to realize foregoing invention purpose, the present invention provides following technical scheme:
The present invention provides a kind of health composition, and in parts by weight, the health composition is by 1~20 part of GABA- amino Butyric acid, 1~30 part of theanine, 1~50 part of Rhizoma Gastrodiae extract and 1~80 part of Radix Morindae Officinalis extract are made.
Preferably, in parts by weight, the health composition by 5~10 parts of GABA- aminobutyric acids, 5~25 parts of theanine, 10~35 parts of Rhizoma Gastrodiae extracts and 30~60 parts of Radix Morindae Officinalis extracts are made.
In a specific embodiment provided by the invention, in parts by weight, the health composition is by 5 parts of GABA- amino fourths Acid, 25 parts of theanine, 30 parts of Rhizoma Gastrodiae extracts and 40 parts of Radix Morindae Officinalis extracts are made.
In another specific embodiment provided by the invention, in parts by weight, the health composition is by 10 parts of GABA- amino Butyric acid, 25 parts of theanine, 35 parts of Rhizoma Gastrodiae extracts and 30 parts of Radix Morindae Officinalis extracts are made.
In another specific embodiment provided by the invention, in parts by weight, the health composition is by 10 parts of GABA- amino Butyric acid, 20 parts of theanine, 10 parts of Rhizoma Gastrodiae extracts and 60 parts of Radix Morindae Officinalis extracts are made.
In another specific embodiment provided by the invention, in parts by weight, the health composition is by 5 parts of GABA- amino Butyric acid, 5 parts of theanine, 30 parts of Rhizoma Gastrodiae extracts and 60 parts of Radix Morindae Officinalis extracts are made.
Present invention also offers the health composition to prepare the application in improving sleep and/or antidepression health food.
Present invention also offers a kind of health food, including health composition provided by the invention.
Preferably, the formulation of the health food is capsule, tablet, pulvis or granule.
Preferably, the formulation of health food is capsule, its raw material includes:1~10 part of GABA~aminobutyric acid, 5~ 20 parts of theanine, 10~30 parts of Rhizoma Gastrodiae extracts, 10~30 parts of Radix Morindae Officinalis extracts, 10~30 parts of pregelatinized starch, 5~10 parts Ac-Di-Sol, 1~5 part of magnesium stearate.
Preferably, the formulation of health food is tablet, its raw material includes:1~10 part of GABA~aminobutyric acid, 5~20 Part theanine, 10~30 parts of Rhizoma Gastrodiae extracts, 10~30 parts of Radix Morindae Officinalis extracts, 10~15 parts of microcrystalline celluloses, 5~10 parts of nothings Water and milk sugar, 1~5 part of Ac-Di-Sol, 1~5 part of silica, 1~2 part of magnesium stearate, 0.5~1 part of brown are thin Film coating powder.
The present invention provides a kind of health composition and health food for having effects that to improve sleep and/or antidepression.With Parts by weight meter, the health composition by 1~20 part of GABA- aminobutyric acid, 1~30 part of theanine, 1~50 part of Rhizoma Gastrodiae extract and 1~80 part of Radix Morindae Officinalis extract is made.The technique effect that the present invention has is:Health composition of the present invention is by GABA- amino fourths After acid, theanine, Rhizoma Gastrodiae extract and Radix Morindae Officinalis extract are used cooperatively, have in terms of sleep and/or antidepression effect is improved There is significant synergistic function.
Embodiment
The invention discloses a kind of health composition and health food for having effects that to improve sleep and/or antidepression, sheet Field technology personnel can use for reference present disclosure, be suitably modified technological parameter realization.In particular, it is all similar Replace and change apparent to those skilled in the art, they are considered as being included in the present invention.The present invention's Method and application are described by preferred embodiment, and related personnel can substantially not depart from present invention, spirit Method described herein and application are modified or suitably changed with combining with scope, to realize and using skill of the present invention Art.
Original used in the health composition and health food provided by the invention for having effects that to improve sleep and/or antidepression Material or auxiliary material can be bought by market.Rhizoma Gastrodiae extract and Radix Morindae Officinalis extract are water extract, its extracting method is ability Extracting method known to field technique personnel.
With reference to embodiment, the present invention is further explained:
Test example 1
(1) depressed animal experiment is improved
1.1 experimental animal
SPF grades of male SD rats, 180 ± 10g of weight are selected, animal is purchased from Guangdong Medical Lab Animal Center, tests Animal uses credit number:SYXK (Guangdong) 2013-0002.
1.2 experiment packet
SD strains male rat 110, weight 200g or so.Animal training adapts to syrup before experiment, according to syrup preference Degree is layered so that the degree distribution of every group of rat preference syrup is averaged.Experiment is divided into 11 groups, is respectively:Normal group, Model group, positive controls Citalopram group, the first control group, the second control group, the 3rd control group, the 4th control group, first Test group, the second test group, the 3rd test group, the 4th test group, every group 10.
Table 1 tests each group administration component
2 control group of table and test group administration composition proportion
1.3 test method
The raising of each group equal single cage, rats in normal control group are placed in other room, 5/cage, in identical room temperature, illumination Under the conditions of normally feed, except syrup preference experiment and forced swim test before fasting, prohibit water in addition to, do not receive stimulation.Except normal right Outer according to group, remaining each group prepares depression model using chronic unpredictable gentle stimulation (CUMS)+lonely foster mode.CUMS has Body method is as follows:24h/ times fasting for solids and liquids, 4 degree of water are swum 5min/ times, bedding and padding humidity 8h/ times, and constraint cage fetters 2h/ times, hemostasis Clamp tail 1min/ times, 36V electro photoluminescence 1min interval 30s totally 30 circulation/time, being given once daily 3 kinds according to table of random number stress. Since 8 week old of rat, continued stimulus gives given the test agent intervention after 4 weeks, is continued for whole experiment terminating.
1.4 Testing index
1) syrup preference experiment (before intervention, intervening 15d, intervene 30d):
After 24h fasting for solids and liquids, weigh in, while give the sucrose water 100mL and 1 bottle of 100mL of every 1 bottle 2% of animal Pure water, observes animal in 1h and drinks sucrose solution amount, calculate syrup preference, compare each group syrup preference and whether there is Difference:
Preference=(syrup consumption/total liquid-consumed) * 100%.
2) forced swimming test (before intervention, intervening 15d, intervene 30d)
Transparent cylindrical swim cylinder, high 45cm, diameter 20cm, 25 degrees Celsius of water temperature, detection rat since swimming into Enter the time needed for motionless state.It whether there is difference the time required to comparing each group.
1.5 data statistical approach
Data useRepresent, statistical analysis is carried out using SPSS21.0 softwares.If measurement data data variance Variance is neat after neat or converted, then using one-way analysis of variance, comparison among groups LSD methods, if heterogeneity of variance, data are converted Variance is still uneven afterwards, and statistical analysis is carried out using rank sum test.Insolation level α=0.05.
1.6 results and analysis
1.6.1 Chronic Moderate imprevision stress be to the influence of rat syrup consumption:
Compared with blank group, model group rats syrup consumption significantly reduces, and has significant difference (P<0.01) mould, is illustrated The modeling of type group success, compared with model group, positive group and control 1 group, control 2 groups of rat syrup consumptions also significantly increase, have There is significant difference (P<0.01 or P<0.05) rats in test groups syrup consumption showed increased, has significant difference (P< 0.01).Illustrate that test group has the function that to increase syrup consumption.
3 Chronic Moderate imprevision of table stress be to the influence of rat syrup consumption
Group Number of animals Syrup consumption (%)
Blank group 10 75.50±9.35
Model group 10 27.63±5.71▲▲
Positive group 10 47.50±9.35**
Compare 1 group 10 30.10±3.87
Compare 2 groups 10 28.27±4.56
Compare 3 groups 10 26.79±4.93
Compare 4 groups 10 30.12±5.78
Test 1 group 10 35.00±7.29*
Test 2 groups 10 38.13±6.64*
Test 3 groups 10 42.68±5.89**
Test 4 groups 10 45.32±3.76**
Note:Compared with blank control group,P<0.05,▲▲P<0.01;Compared with model group, * P<0.05, * * P<0.01.
1.6.2 Chronic Moderate imprevision stress be to the influence of forced swimming test dead time
Compared with blank group, the model group rats forced swimming dead time is obviously prolonged, and has significant difference (P< 0.05) modeling success, is illustrated.Compared with model group, the positive group rat forced swimming dead time is obviously shortened, and has statistics Difference (P<0.05);Compare 1 group, 2 groups of rat forced swimmings of control have the trend of shortening, but no difference of science of statistics (P > 0.05), The rats in test groups forced swimming dead time is obviously shortened, and has significant difference (P<0.05), illustrate that test group can improve greatly Mouse as Chronic Moderate imprevision stress caused by the forced swimming test dead time.
4 Chronic Moderate imprevision of table stress be to the influence of forced swimming test dead time
Group Number of animals Dead time (second)
Blank group 10 85.13±12.79
Model group 10 123.50±18.54▲▲
Positive controls 10 98.63±11.49*
Compare 1 group 10 109.13±11.95
Compare 2 groups 10 108.25±10.82
Compare 3 groups 10 114.13±15.44
Compare 4 groups 10 112.88±13.30
Test 1 group 10 102.75±17.29*
Test 2 groups 10 104.00±16.59*
Test 3 groups 10 102.75±12.50*
Test 4 groups 10 100.75±12.17*
Note:Compared with blank control group,P<0.05,▲▲P<0.01;Compared with model group, * P<0.05, * * P<0.01.
(2) sleeping animal experiment is improved
1.1 experimental animal
SPF grades of thorn property ICR mouse, 20 ± 2g of weight are selected, animal is purchased from Guangdong Medical Lab Animal Center, and experiment is dynamic Thing uses credit number:SYXK (Guangdong) 2013-0002.
1.2 experiment packet
Reference《Health food is examined and assessment technique specification》Method in (2003 editions).By Healthy female ICR mouse, weight 18g~22g, 120, divides 3 batches to be used to test, when the 1st batch of animal is slept for direct sleep experiments and extension yellow Jackets Between test, the 2nd batch of animal is tested for the hypnosis of yellow Jackets sub-threshold dose, and the 3rd batch of animal be used for barbital sodium sleep latency Phase tests.
Experiment is divided into 9 groups, and every group of 20 animals, are respectively:Blank group, 1 group of control, 2 groups of control, 3 groups of control, control 4 Group, 1 group of experiment, 2 groups of experiment, 3 groups of experiment, 4 groups of experiment, by the oral gavages of 0.2mL/10gBW, negative control group gives equivalent Solvent, daily gavage 1 time.
Table 5 tests each group administration component
6 control group of table and test group administration composition proportion
1.3 test method
According to the Ministry of Public Health《Health food is examined and assessment technique specification》(version in 2003) method carries out.Experiment sets 3 portions Point:Extend the experiment of the yellow Jackets length of one's sleep, yellow Jackets sub-threshold dose hypnosis experiment and barbital sodium Sleep latency Experiment.
1.3.1 direct sleep experiments:Observe after tested group of animal give given the test agent, it is molten that negative control group gives same volume After agent, if sleep phenomenon occur.Sleep is using righting reflex loss as index.Such as more than 30s~60s cannot the person of righting, both recognized For righting reflex loss, into sleep.Righting reflex recovers to be to awaken, and righting reflex loss is animal to this period is recovered The length of one's sleep.Record control group and test sample group sleep number of animals and the length of one's sleep.
1.3.2 the experiment of the yellow Jackets length of one's sleep is extended::Carry out on the basis of direct sleep experiments, such as directly sleep Experiment sleep for feminine gender, then carries out extending the experiment of the yellow Jackets length of one's sleep.Preliminary experiment is first carried out before doing formal experiment, determines to make Animal 100% falls asleep, but does not make the length of one's sleep long yellow Jackets dosage, and formal experiment (this experiment is done with this dosage Dosage is:47mg/kg·BW).After animal last gives solvent and various concentrations given the test agent, occur peak effect before 10min~ 15min, yellow Jackets are injected intraperitoneally to each group animal, and using righting reflex loss as index, can observation given the test agent extend The yellow Jackets length of one's sleep.
1.3.3 the hypnosis of yellow Jackets sub-threshold dose is tested:Preliminary experiment is first carried out before doing formal experiment, determines amobarbital The yellow Jackets maximum sub-threshold dose that sodium subthreshold hypnotic dosage, i.e. 80%~90% mouse righting reflex do not disappear.Animal end It is secondary give solvent and various concentrations given the test agent after, occur peak effect before 10min~15min, to each group animal intraperitoneal injection penta (this test dose is barbital sodium maximum subthreshold hypnotic dosage:29mg/kgBW), sleep number of animals in 30min is recorded (to right Areflexia reaches more than 1min persons).
1.3.4 yellow Jackets Sleep latency is tested:Preliminary experiment is first carried out before doing formal experiment, determines to make animal 100% falls asleep, but does not make the dosage of the length of one's sleep long barbital sodium, is formally tested with this dosage.Animal last is given After solvent and various concentrations given the test agent 10min~20min, to each group animal intraperitoneal injection barbital sodium, (this test dose is: 240mg/kgBW), using righting reflex loss as index, influence of the observation given the test agent to barbital sodium Sleep latency.
1.4 result judgement:
Extend the yellow Jackets length of one's sleep experiment, the hypnosis of yellow Jackets (or barbital sodium) sub-threshold dose experiment, bar Being tested than appropriate sodium Sleep latency has two positives in three experiments, and is acted on without obvious directly sleep, can determine that the tested material Sample has improvement sleep function effect.
1.5 statistical method
Data carry out statistical analysis using SPSS 17.0.The length of one's sleep is measurement data, and data are carried out using variance analysis The data of abnormal or heterogeneity of variance are carried out appropriate variable and changed by statistics, after normal state is met or variance requires together, with turning Data after changing are counted;If being still not up to normal state or the neat purpose of variance after variable conversion, use rank sum test instead and unite Meter.Sleep number of animals is enumeration data, using chi-square criterion.
1.6 results and analysis
1.6.1 direct sleep experiments
Each test group gives given the test agent, after negative control group gives same volume solvent, it is observed that 30min, righting reflex In the presence of not occurring sleep phenomenon.
Influence of 7 sample of table to direct sleep laboratory
Group Number of animals Sleeping animal number Sleep rate (%)
Blank group 20 0 0
Compare 1 group 20 0 0
Compare 2 groups 20 0 0
Compare 3 groups 20 0 0
Compare 4 groups 20 0 0
Test 1 group 20 0 0
Test 2 groups 20 0 0
Test 3 groups 20 0 0
Test 4 groups 20 0 0
Note:Blank control group compares,P<0.05,▲▲P<0.01。
1.6.2 the experiment of the yellow Jackets length of one's sleep is extended
Compared with blank control group, the average length of one's sleep of 1,2 group of control and test group mouse slightly extends, wherein testing The length of one's sleep of group mouse dramatically increases (P ﹤ 0.05) compared with the control group, and has statistical significance, i.e., test group is to penta There is extension effect in mouse length of one's sleep that is averaged of calmine induction.
Influence of 8 sample of table to the extension yellow Jackets length of one's sleep
Note:Blank control group compares,P<0.05,▲▲P<0.01。
1.6.3 the hypnosis of yellow Jackets sub-threshold dose is tested
Compared with blank group, control group 1, control group 2, the sleep incidence of test group mouse are without substantially changeing, no statistics Meaning (P ﹥ 0.05) is learned, therefore the mice sleep incidence that this product induces sub-threshold dose carbrital is without obvious effect.
Influence of 9 sample of table to yellow Jackets sub-threshold dose hypnosis test
Note:Blank control group compares,P<0.05,▲▲P<0.01。
1.6.4 yellow Jackets Sleep latency is tested
Compared with blank group, the average length of one's sleep of 1,2 group of control and test group mouse slightly extends, and wherein test group is small Be averaged sleep latency and control group of mouse has and significantly shortens (P ﹤ 0.05), and has statistical significance.
Influence of the table 10 to the yellow Jackets Sleep latency time
Note:Blank control group compares,P<0.05,▲▲P<0.01。
1 capsule product formula of embodiment and technique
First, it is formulated (by weight):
2nd, production technology:
1. weigh, stock:Weigh the GABA- aminobutyric acids of recipe quantity, theanine, Rhizoma Gastrodiae extract, Radix Morindae Officinalis extract, Pregelatinized starch, Ac-Di-Sol and magnesium stearate, it is spare.
It is 2. total mixed:The above-mentioned material got ready is added in mixer, mixing 30 minutes to discharging after mixing.
3. filling:Uniformly mixed material is added in capsule filling machine, is filled with 0# Capsuleses, 400mg/, dress Within ± 4.5%, disintegration time is less than 60 minutes for amount control.
4. bottling:Equipment is adjusted on request, capsule is loaded in 150ml browns, 60/bottle, drier 1 wraps.
3rd, amount and eating method:2 times a day, every time 2 bags, 150ml warm water is taken after mixing it with water.
2 tablet formula of embodiment and technique
First, it is formulated (by weight):
2nd, production technology:
1. weigh, stock:Weigh the GABA- aminobutyric acids of recipe quantity, theanine, Rhizoma Gastrodiae extract, Radix Morindae Officinalis extract, Microcrystalline cellulose, Lactis Anhydrous, Ac-Di-Sol, silica, magnesium stearate and brown film coating powder are (water-soluble Property), it is spare.
It is 2. total mixed:The above-mentioned material got ready is added in mixer (except magnesium stearate and brown film coating powder), mixing The magnesium stearate that formula ratio is added after 25 minutes mixes 5 minutes, uniformly discharges afterwards to mixture.
3. tabletting:Use elongated mould tabletting, 800mg/ pieces, hardness 22-27kg/cm2, it is ensured that tablet weight variation ± Within 4.5%, disintegration time limited is less than 30 minutes, and checks slice, thin piece appearance at any time.
4. coating:It is coated using brown film coating powder (water solubility), weightening 3.63%, solid content 16%.
5. bottling:Equipment is adjusted on request, coating tablet is loaded in 150ml browns, 60 pieces/bottle, drier 1 wraps.
3rd, amount and eating method:2 times a day, 2 tablets once, swallows.
The above is only the preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art For member, various improvements and modifications may be made without departing from the principle of the present invention, these improvements and modifications also should It is considered as protection scope of the present invention.

Claims (10)

1. a kind of health composition, it is characterised in that in parts by weight, by 1~20 part of GABA- aminobutyric acid, 1~30 part of tea ammonia Acid, 1~50 part of Rhizoma Gastrodiae extract and 1~80 part of Radix Morindae Officinalis extract are made.
2. health composition according to claim 1, it is characterised in that in parts by weight, by 5~10 parts of GABA- amino Butyric acid, 5~25 parts of theanine, 10~35 parts of Rhizoma Gastrodiae extracts and 30~60 parts of Radix Morindae Officinalis extracts are made.
3. health composition according to claim 1 or 2, it is characterised in that in parts by weight, by 5 parts of GABA- amino fourths Acid, 25 parts of theanine, 30 parts of Rhizoma Gastrodiae extracts and 40 parts of Radix Morindae Officinalis extracts are made.
4. health composition according to claim 1 or 2, it is characterised in that in parts by weight, by 10 parts of GABA- amino Butyric acid, 25 parts of theanine, 35 parts of Rhizoma Gastrodiae extracts and 30 parts of Radix Morindae Officinalis extracts are made.
5. health composition according to claim 1 or 2, it is characterised in that in parts by weight, by 10 parts of GABA- amino Butyric acid, 20 parts of theanine, 10 parts of Rhizoma Gastrodiae extracts and 60 parts of Radix Morindae Officinalis extracts are made.
6. any one of claim 1 to 5 health composition answering in improvement sleep and/or antidepression health food is prepared With.
7. a kind of health food, it is characterised in that including any one of claim 1 to 5 health composition.
8. health food according to claim 7, it is characterised in that the formulation of the health food for capsule, tablet, Pulvis or granule.
9. health food according to claim 8, it is characterised in that the formulation of the health food is capsule, it is former Material includes:1~10 part of GABA~aminobutyric acid, 5~20 parts of theanine, 10~30 parts of Rhizoma Gastrodiae extracts, 10~30 parts of Morinda officinalis Extract, 10~30 parts of pregelatinized starch, 5~10 parts of Ac-Di-Sols, 1~5 part of magnesium stearate.
10. health food according to claim 8, it is characterised in that the formulation of the health food is tablet, its raw material Including:1~10 part of GABA~aminobutyric acid, 5~20 parts of theanine, 10~30 parts of Rhizoma Gastrodiae extracts, 10~30 parts of Morinda officinalis carry Take thing, 10~15 parts of microcrystalline celluloses, 5~10 parts of Lactis Anhydrouses, 1~5 part of Ac-Di-Sol, 1~5 part of titanium dioxide Silicon, 1~2 part of magnesium stearate, 0.5~1 part of brown film coating powder.
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