CN106994157A - A kind of herb fermenting preparation, its preparation method and application for improving performance in layers - Google Patents
A kind of herb fermenting preparation, its preparation method and application for improving performance in layers Download PDFInfo
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Abstract
The invention discloses a kind of herb fermenting preparation, its preparation method and application for improving performance in layers, belong to herb fermenting preparation technique field.The parts by weight of its Chinese medicine each component are constituted:15~25 parts of Radix Codonopsis, 10~20 parts of psoralea corylifolia, 10~20 parts of motherwort, 5~15 parts of the bighead atractylodes rhizome, 5~10 parts of Poria cocos, 5~15 parts of sweet basil, 5~10 parts of honey-fried licorice root, 5~10 parts of the tuber of pinellia, 5~10 parts of dried orange peel.The inventive method choose traditional Chinese medicinal components are rational in infrastructure, ratio is appropriate, the advantages such as the active height of Lactobacillus plantarum, strong stress resistance, the adjustable gut flora of selection, in the presence of the Lactobacillus plantarum selected by the present invention, considerably improve the drug effect of original medicine, beneficial bacterium ratio in enteron aisle is improved, the production performance of laying hen can be improved using the herb fermenting preparation of the present invention.
Description
Technical field
The invention belongs to herb fermenting preparation technique field, and in particular to a kind of herb fermenting of raising performance in layers
Preparation, its preparation method and application.
Background technology
The traditional Chinese medical science says, kidney controlling essence storage, is congenital essence first, the formation of embryo, develops using kidney essense as material base, in
Jenny is then to promote egg development, with fecundity, when disease and evil invades kidney, can cause deficiency of kidney essence, essence is lost then
Infertile, laying hen shows as the phenomenons such as egg production, egg size decline and the thin, soft-shelled egg of eggshell, and breeder then can also go out in addition to above-mentioned phenomenon
Existing fertility rate of hatching egg declines;On the other hand, kidney also hides the essence of acquired essence, i.e. water paddy (nutrition), to maintain body vital movement,
Enhancing development.Kidney essence deficiency, then filoplume is matt, fluffy and disorderly, and premunition is poor, Body weight loss etc..
Chinese medicine not only has adjustment effect to the secretion of hormone, and some Chinese medicines are also containing similar to the structure of hormone
Bioactive substance, with some hormone-like effects, so as to adjust the growth performance of animal, reproductive capability and immunization machine
System.
Though traditional Chinese medicine compound preparation on sale can recover laying rate of laying hen in the market, to recover its production in a short time
Egg performance has certain difficulty.During the fermentation, can produce some has very powerful decomposition and inversion physical capacity to Chinese medicine
Microorganism, and a variety of secondary generations such as cellulase, lignoenzyme, amylase, protease can be produced during growth metabolism
Thank to product, the biochemical reaction of complexity is quickly completed at normal temperatures and pressures, than processing means typically physically or chemically more
Significantly strengthen and adjust the property of medicine, improve curative effect, reduce toxic side effect.
The content of the invention
For problems of the prior art, it is an object of the invention to provide a kind of natural safety, fast and effectively in
Medicine fermentation preparation and the method for preparing the fermentation preparation, while being improved there is provided a kind of having containing the herb fermenting preparation
The feed of performance in layers.
In order to solve the above-mentioned technical problem, the present invention is achieved using following technical scheme:
A kind of Chinese medicine composition for improving performance in layers, is prepared from by following components according to parts by weight:Radix Codonopsis
15~25 parts, 10~20 parts of psoralea corylifolia, 10~20 parts of motherwort, 5~15 parts of the bighead atractylodes rhizome, 5~10 parts of Poria cocos, 5~15 parts of sweet basil, process
5~10 parts of radix glycyrrhizae, 5~10 parts of the tuber of pinellia, 5~10 parts of dried orange peel.
On the basis of such scheme, described Chinese medicine composition is prepared from by following components according to parts by weight:Party
20 parts of ginseng, 15 parts of psoralea corylifolia, 15 parts of motherwort, 10 parts of the bighead atractylodes rhizome, 6 parts of Poria cocos, 10 parts of sweet basil, 6 parts of honey-fried licorice root, 6 parts of the tuber of pinellia, dried orange peel
6 parts.
A kind of herb fermenting preparation, it by traditional Chinese medicine ingredients mixed with Lactobacillus plantarum bacterium solution after through fermentation be made, it is described in
Medicine composition is by weight:15~25 parts of Radix Codonopsis, 10~20 parts of psoralea corylifolia, 10~20 parts of motherwort, the bighead atractylodes rhizome 5~15
Part, 5~10 parts of Poria cocos, 5~15 parts of sweet basil, 5~10 parts of honey-fried licorice root, 5~10 parts of the tuber of pinellia, 5~10 parts of dried orange peel.
On the basis of such scheme, the traditional Chinese medicine ingredients are by weight:20 parts of Radix Codonopsis, psoralea corylifolia 15
Part, 15 parts of motherwort, 10 parts of the bighead atractylodes rhizome, 6 parts of Poria cocos, 10 parts of sweet basil, 6 parts of honey-fried licorice root, 6 parts of the tuber of pinellia, 6 parts of dried orange peel.
On the basis of such scheme, Lactobacillus plantarum content >=10 in the bacterium solution8CFU/mL。
On the basis of such scheme, the preparation method of the herb fermenting preparation, step is as follows:
(1) by traditional Chinese medicinal components are measured, crush, cross 60 eye mesh screens, it is standby;
(2) each component after crushing is well mixed, adds the water of traditional Chinese medicine ingredients gross weight 80%, stir after
100 DEG C of steam sterilizing 30min, are cooled to 20-30 DEG C;
(3) bacterium solution is added into the medicine after cooling, bacterium solution consumption accounts for 10~15% of total amount after addition;It is placed in unidirectional row
In gas polybag, fermented 30 days under the conditions of 20 DEG C~30 DEG C.
Above-mentioned one-way exhaust polybag is Patent No.:200920100585.9 anaerobic fermentation feed, Chinese medicine and add
Plus the one-way exhaust bag of agent.
On the basis of such scheme, the bacterium solution is made by following methods:
Lactobacillus plantarum strain is inoculated in activation medium and carries out activation culture, cultivation temperature is 37 DEG C, time 24h;
The strain activated is inoculated in fermentation tank, 37 DEG C~43 DEG C of temperature, time 24h~36h is controlled.
On the basis of such scheme, the activation medium and the fermentation used medium are:MRS culture mediums, into
It is divided into (g/L):Peptone 10.0, meat extract 10.0, yeast extract 5.0, glucose 20.0, dipotassium hydrogen phosphate 2.0, hydrogen citrate two
Ammonium 2.0, sodium acetate 5.0, magnesium sulfate 0.58, manganese sulfate 0.28, cysteine 0.5, Tween 80 1.0, adjust pH6.2-6.4.
On the basis of such scheme, the herb fermenting formulation application is in the production performance for improving laying hen.
It is a kind of that there is the feed for improving performance in layers, it is herb fermenting system prepared by the above method of being added in feed
Agent, addition is 2kg/ tons.
The raising performance in layers Chinese medicine composition of the present invention, the property of medicine drug effect of each Chinese medicine is as follows:
Radix Codonopsis:Main component is alkaloid, saponin, protein, starch, vitamin B1, vitamin B2 etc., with bowl spares benefit
Gas, enrich blood, be depressured, eliminating phlegm and relieving cough the effects such as.
Psoralea corylifolia:For the ripe dry seed of pulse family annual herb plant psoralea corylifolia.Cultivation, also has wild.Containing Psoralen
Fat B prime, is natural chalcone;Contain a variety of Coumarins materials, predominantly psoralen and isopsoralene again.Have
It is warming spleen and stopping diarrha, tonifying kidney and strengthening yang, the effect of astringent sperm contracting urine.
Motherwort:For herb on the dry ground of labiate motherwort or great Hua motherworts.It is wild.Containing motherwort
Alkali first, leonurine second, separately containing compositions such as stachydrine, potassium chloride, laurate, oleic acid.The work(such as the stasis of blood are dissipated with promoting blood circulation for regulating menstruation, promoting circulation of blood
Effect.
The bighead atractylodes rhizome:For the dry rhizome of the composite family herbaceos perennial bighead atractylodes rhizome.Mostly cultivate, also there is wild.Main component is
Volatile oil, wherein predominantly atractylol, the material such as another ketone containing the bighead atractylodes rhizome, retinoid.With invigorating the spleen and benefiting qi, the work(such as eliminate dampness and have diuretic effect
Effect.
Poria cocos:To post the dry sclerotia of bacterium Polyporaceae Poria cocos.Wild survivor's multiparasitization is in the root of Japanese red pine or raw true masson pine
Portion, shiploads of merchandise is artificial cultivation.Mainly contain pachymose, pachymic acid, protein, fat, lecithin, histidine, choline, wheat
The composition such as angle sterol and sylvite, primary efficacy is clearing damp and promoting diuresis, beneficial spleen calming heart.
Sweet basil:For annual upright draft.For cultivated plant, also have wild, be born in hillside roadside, bushes more.Contain
Volatile oil 0.02~0.04%, main component be ocimenum, australene, 1, 8-Cineole, linalool, Geraniol, limonene,
Carene-3, estragole, Eugenol, methyleugenol, anisole, methyl cinnamate, hexene -8- alcohol -1, octanone -3
And furfural etc..The effects such as with analgesic, detumescence, the scattered stasis of blood, removing toxic substances.
Radix glycyrrhizae:Alias RADIX GLYCYRRHIZAE, is the dry root and root-like stock of leguminous perennial herb radix glycyrrhizae and glycyrrhiza glabra etc.
(reed head), it is mostly wild.Containing glycyrrhizin, liquiritigenin, glucose, mannitol, malic acid, asparagine etc. it is main into
Point, with invigorating the spleen and benefiting qi, it is clearing heat and detoxicating, the effects such as moisten the lung and relieve the cough.Honey-fried licorice root is the radix glycyrrhizae baked with honey, is commonly called as processing, is exactly
Honey is put middle honey is smelt in pot, used slow fire instead plus licorice piece is stirred uniformly, 3~5min takes the dish out of the pot, put 60 DEG C of barn or baking oven
Take out, cool when being dried to tack-free.
The tuber of pinellia:For the perennial herblet of Araeceae, the tuber of pinellia rubs the dry tuber for removing crust with the hands.Cultivation is wild.Contain
The composition such as B- sitosterol and its glycoside sitosterol, trace volatile oil, phytosterol, saponin, acidity material, biological alkali.
The effect of with anti-vomiting, removing dampness and eliminating phlegm, mass dissipating and swelling eliminating.
Dried orange peel:Mainly containing hesperidine, mysoinositol, volatile oil (main component is d-limonen) and vitamin B1 etc. into
Point.With stomach invigorating, wind dispelling, preventing or arresting vomiting, only oh, eliminating the phlegm the effects such as.
Wherein described Lactobacillus plantarum strain is Lactobacillus plantarum plant subspecies (Lactobacillus plantarum
Subsp.Plantarum), numbering AS1.557, from Institute of Microorganism, Academia Sinica.
The technical principle of the present invention:
In side Radix Codonopsis tonifying middle-Jiao and Qi and can blood-nourishing be monarch, psoralea corylifolia, motherwort, the yang-tonifying of bighead atractylodes rhizome principal drug assistance warm kidney, to train kidney
Sun this, promoting blood circulation, it is drying damp and strengthening spleen be minister, Poria cocos inducing diuresis with bland drug, sweet basil restore menstrual flow and invigorate blood circulation, dampness elimination helps digestion, make spleen be damp evil
It is stranded for adjutant, dried orange peel is added again to strengthen the effect of invigorating the spleen qi-regulating, plus tuber of pinellia regulating qi-flowing for harmonizing stomach, eliminating phlegm and lowering adverse QI is adjutant, honey-fried licorice root
Sweet temperature QI invigorating and can coordinating the drug actions of a prescription to make medicine.Full side has QI invigorating and stomach, and the work(of promoting the circulation of qi middle benefit gas, nature and flavor are gentle, all medicines share, mark
Originally it is simultaneous to control.
Herb fermenting preparation of the present invention has the characteristics that:(1) Chinese prescription fill blood, strengthening the spleen and stomach, liver and kidney benefiting, pass through
Quality of laying eggs etc. is improved to approach such as neuroendocrine regulations, performance in layers can be effectively improved.(2) present invention is selected
Lactobacillus plantarum can tens kinds of extracellular proteinase, cellulase, hemicellulase, pectase, amylase etc. in metabolic process
Ectoenzyme enters culture medium, and what these enzymes had can form new compound, what is had can decompose by drug ingedient decomposition and inversion
The compact texture such as cellulose, hemicellulose, pectic substance, lignin in plant cell wall, promotes active constituents of medicine to greatest extent
Release;(2) Lactobacillus plantarum and its metabolite that the present invention is selected effectively supplement or strengthened the function of original medicine;
(3) new active material is generated after Chinese medicine is converted through Lactobacillus plantarum, and brings new health care, prevent or controls treatment functions.
It is birds in vivo under hormone and trophic factor collective effect to lay eggs, and is regulated and controled by hypothalamic-pituitary-ovarian axis
Complex physiologic process.Effects of Bu Gu fat has an effect for promoting ovarian function, estrogen contained by Chinese medicine sweet basil can by acceptor and
Feedback mechanism promotes follicular development and the secretion of reproductive hormone in ovary, and to promote to ovulate and perfect luteal function, Chinese medicine benefit is female
Grass is enriched blood, excited uterus, ovulation rate.The secretion of testosterone can be significantly reduced using the herb fermenting preparation of the present invention, is improved
The secretion of progesterone and estradiol, so as to improve the laying rate of laying hen, reduce feedstuff-egg ratio and improve the quality of egg;This
Outside, the addition of herb fermenting preparation of the present invention can also reduce the content of yolk cholesterol.
The inventive method choose traditional Chinese medicinal components are rational in infrastructure, ratio appropriate, the Lactobacillus plantarum of selection it is active it is high,
The advantages such as strong stress resistance, adjustable gut flora, in the presence of the Lactobacillus plantarum selected by the present invention, are considerably improved
The drug effect of original medicine, improves beneficial bacterium ratio in enteron aisle, and laying hen can be improved using the herb fermenting preparation of the present invention
Production performance.
Embodiment
Below in conjunction with preferred embodiment, to according to the embodiment of the invention provided, details are as follows:
Embodiment 1
The preparation of bacterium solution:
The Lactobacillus plantarum strain of the present invention is inoculated in into activation medium to be cultivated, cultivation temperature is 37 DEG C, time
24h;The strain activated is inoculated in fermentation tank, 37 DEG C~43 DEG C of temperature is controlled, time 24h~36h prepares zymotic fluid.
Wherein described Lactobacillus plantarum strain is Lactobacillus plantarum plant subspecies (Lactobacillus plantarum
Subsp.Plantarum), numbering AS1.557, from Institute of Microorganism, Academia Sinica.
The activation medium is:MRS culture mediums, composition is (g/L):Peptone 10.0, meat extract 10.0, yeast extract
5.0th, glucose 20.0, dipotassium hydrogen phosphate 2.0, diammonium hydrogen citrate 2.0, sodium acetate 5.0, magnesium sulfate 0.58, manganese sulfate 0.28,
Cysteine 0.5, Tween 80 1.0, adjust pH6.2-6.4.
Fermentation used medium be:MRS culture mediums, composition is ibid.
After the completion of fermentation, content >=10 of bacterium in bacterium solution8CFU/mL。
Embodiment 2
A kind of herb fermenting preparation for improving performance in layers, the parts by weight of its each component are:20 parts of Radix Codonopsis, Psoralen
15 parts of fat, 15 parts of motherwort, 10 parts of the bighead atractylodes rhizome, 6 parts of Poria cocos, 10 parts of sweet basil, 6 parts of honey-fried licorice root, 6 parts of the tuber of pinellia, 6 parts of dried orange peel.
Specific preparation method is as follows:
(1) by traditional Chinese medicinal components are measured, crush, cross 60 eye mesh screens, it is standby;
(2) each component after crushing is well mixed, adds the water of traditional Chinese medicine ingredients gross weight 80%, stir after
100 DEG C of steam sterilizing 30min, are cooled to 20-30 DEG C;
(3) bacterium solution is added into the medicine after cooling, bacterium solution consumption accounts for 10~15% of total amount after addition;It is placed in unidirectional row
In gas polybag, fermented 30 days under the conditions of 20 DEG C~30 DEG C.
Above-mentioned one-way exhaust polybag is Patent No.:200920100585.9 anaerobic fermentation feed, Chinese medicine and add
Plus the one-way exhaust bag of agent.
Embodiment 3
A kind of herb fermenting preparation for improving performance in layers, the parts by weight of its each component are:15 parts of Radix Codonopsis, Psoralen
10 parts of fat, 10 parts of motherwort, 5 parts of the bighead atractylodes rhizome, 5 parts of Poria cocos, 5 parts of sweet basil, 5 parts of honey-fried licorice root, 5 parts of the tuber of pinellia, 5 parts of dried orange peel.
Preparation method is same as Example 2.
Embodiment 4
A kind of herb fermenting preparation for improving performance in layers, the parts by weight of its each component are:25 parts of Radix Codonopsis, Psoralen
20 parts of fat, 20 parts of motherwort, 15 parts of the bighead atractylodes rhizome, 10 parts of Poria cocos, 15 parts of sweet basil, 10 parts of honey-fried licorice root, 10 parts of the tuber of pinellia, 10 parts of dried orange peel.
Preparation method is same as Example 2.
First, the test of pesticide effectiveness:
1.1 experiment prescriptions
1.1.1 the non-fermented Chinese medicine preparation group that prepared by traditional handicraft (is surpassed the medicine selected by the embodiment of the present invention 2
Crushing of Ultrafine, is crushed to 700 mesh, is well mixed)
1.1.2 2 groups of embodiment
1.1.3 3 groups of embodiment
1.1.4 4 groups of embodiment
1.1.5 blank control group
1.2 zooperies are designed
Experiment uses single-factor randomized complete-block design, and 48 weeks body weight health sea orchid close with laying rate brown is laid eggs
Chicken 600, is randomly divided into 5 processing, adds Ultramicro-powder, the herb fermenting preparation of embodiment 2, embodiment 3 respectively in feed
Herb fermenting preparation and embodiment 4 herb fermenting preparation, addition be 2kg/ tons, separately set one group of blank control group, other
Experimental condition is completely the same.Each 6 repetitions of processing, each repeat 20 chickens.It is each to handle search for food respectively a kind of feed, prerun
1 week phase, positive 30 days phases of examination.
1.3 experiment diets
Need to prepare Basic drawing with reference to NRC (1994) laying hen nutrition, diet composition and trophic level are shown in Table 1.
The Basic drawing of table 1 is constituted and trophic level (air bells dry basis)
Note:1) every kilogram of diet contains:VA 12000IU, VD33000IU, VE 20IU, VK 2m g, VB12
0.015mg, VB11.5mg, riboflavin riboflavin 4.5mg, VB63.0mg, biotin biotin 0.1mg, folic acid
Folic acid 0.5mg, nicotinic acid niacin 20mg, pantothenic acid pantothenic acid 10.0mg.
2) every kilogram of diet contains:Mn 60.0mg, Zn 50.0mg, Fe 25.0mg, Cu 5.0mg, I 0.5mg.
3) metabolic energy is calculated value, and remaining is measured value.
1.4 feeding management
Using the 3 layers of three-dimensional cage of semi open model hen house, connected 5 chicken coops (45cm × 30cm × 30cm) are often arranged as 1
Individual repetition, it is each to repeat to be evenly distributed on upper, middle and lower cage frame per 4 chickens of cage.
Using nature plus artificially feed, daily constant illumination 16h (automatic illuminating control system), intensity is 14LX.Feeding
Dry mash, free choice feeding, daily 08:00 and 14:30 each feedings 1 time, refining 4 times;Nipple-shaped drinker, free water.By just
Chang Chengxu prevents epidemic, and personal management picks up egg 2 times daily;Carry out disinfection and clear up weekly chicken manure 1 time, routine immunization.
1.5 testing indexs and method
1.5.1 egg-laying test
To be repeated as the daily egg number of unit record (including soft-shelled egg, check), day egg production, dead chicken number, weekly
Record the feed consumption rate of laying hen.Finally calculate laying rate, daily ingestion amount, average egg weight, feedstuff-egg ratio.
1.5.2 Egg Quality is determined
Eggshell strength, shell thickness, albumen height, yolk color and hangh unit are produced using ORKA companies of Israel
Serial egg quality analyzer is measured, and the egg shape index analyzer that egg shape index is produced using Japanese fuji level ground company is surveyed
It is fixed, every 2 weeks 1 time, totally 4 times.
1.5.3 enteric microorganism is analyzed
In before off-test early morning on same day feeding, often repeating to butcher 2 (totally 60) chickens, 5% bromogeramine solution leaching
Steep 5min, whole body sterilization;Under aseptic condition, caecum stage casing 10cm is cut, test in laboratory wherein chyme is taken back at ligation two ends
Bifidobacterium, Escherichia coli and Bacillus acidi lactici content.The quantity of flora is represented with lgCFU/g cecal contents.
1.5.4 reproductive hormone assay
It is each to repeat to randomly select after venous blood collection 3mL under 5 chickens, wing, standing respectively in the 15d and 30d of experiment
3000r/min centrifuges 10min, and to be placed on -20 DEG C of refrigerators standby for serum after separation.With automatic clinical chemistry analyzer (Hitachi
7600-020) determine testosterone (T), progesterone (P) and estradiol (E2) content in serum.
1.5.5 the measure of shell egg and cholesterol level of vitellus
Respectively in the 15d and 30d of experiment, every group is randomly selected 10 pieces of eggs, mark group, date, is placed in 4 DEG C of refrigerators
Preserve, for determining shell egg and cholesterol level of vitellus.Every piece of egg is weighed before measure, the reference of the yellow and white separation method
(research that Different Alfalfa grass meal level influences on laying hen cholesterol level of vitellus, Wang Chengzhang, Yang Yuxin, Hu Xi such as Wang Chengzhang
Peak etc., Acta Prataculture, 2005,14 (2):Method 76-83).To yolk correct amount, and calculate yolk relative weight.
Yolk relative weight (%)=(yolk weight/egg size) × 100%
Egg cholesterol amount is represented with 2 indexs of cholesterol level of vitellus and shell egg cholesterol level.Wherein, yolk
Cholesterol level refers to the content of cholesterol in every gram of yolk, and shell egg cholesterol level refers to containing for cholesterol in every piece of egg
Amount.Using GBT 22220-2008《The measure high performance liquid chromatography of Food Cholesterol》Prescriptive procedure is measured.
1.5.6 data analysis
All gathered datas carry out early stage processing using Excel softwares, then carry out statistical analysis, LSD with SPSS19.0
Multiple range test is carried out, is as a result represented using mean+SD.
2nd, result and analysis
Respectively influence of the experiment component to Layer Production Performance of 2.1 experimental periods, is shown in Table 2.
Respectively influence of the experiment component to performance in layers of the experimental period of table 2
Note:Same column shoulder marking-up parent phase is with the not notable (P of expression difference>0.05), the different lowercase letter indication differences of shoulder mark show
Write (P<0.05), the different capitalizations of shoulder mark represent difference extremely significantly (P<0.01).
Test chicken is managed during experiment everywhere in good condition, defecation is normal, no death.
As shown in Table 2, experimental period average egg weight and daily ingestion amount, there was no significant difference between each test group and control group (P
>0.05).Laying rate Ultramicro-powder group is higher than control group but there was no significant difference (P>0.05), 2.46% is improved than control group;It is real
Apply example 2,3 and 4 groups significantly improve 6.32%, 6.26% and 6.23% (P than control group respectively<0.05) Ultramicro-powder, is compared respectively
Group significantly improves 3.77%, 3.71% and 3.68% (P<0.05).Day egg production Ultramicro-powder group is improved than control group
1.86% (P>0.05);Embodiment 2,3 and 4 groups significantly improve 6.38%, 5.91% and 5.83% (P than control group respectively<
0.05);Respectively 4.44%, 3.98% and 3.90% (P is significantly improved than Ultramicro-powder group<0.05).Each test group of daily ingestion amount
There was no significant difference between control group (P>0.05).Feedstuff-egg ratio embodiment 2,4 groups significantly reduced respectively than control group pole
4.87% and 4.87% (P<0.01).
Respectively influence of the experiment component to Egg Production of Laying Hens quality of 2.2 experimental periods, is shown in Table 3.
Respectively influence of the experiment component to Egg Production of Laying Hens quality of the experimental period of table 3
Note:Same column shoulder marking-up parent phase is with the not notable (P of expression difference>0.05), the different lowercase letter indication differences of shoulder mark show
Write (P<0.05), the different capitalizations of shoulder mark represent difference extremely significantly (P<0.01).
As shown in Table 3, there was no significant difference between experimental period shell thickness and each test group of eggshell strength and control group (P>
0.05).2 groups of egg shape index embodiment is significantly higher than control group (P<0.05), there was no significant difference with control group for other test groups
(P>0.05).Albumen height, embodiment 2,3 and 4 groups of poles are significantly higher than control group (P<0.01) it is, poor without conspicuousness with Ultramicro-powder group
Different (P>0.05), there was no significant difference between Ultramicro-powder group and control group (P>0.05).Each test group of Hough unit and control group
Between there was no significant difference (P>0.05).
Influence of the 2.3 each experiment components to laying hen cecum microorganisms, is shown in Table 4.
Respectively influence of the experiment component to laying hen cecum microorganisms of table 4
Note:Same column shoulder marking-up parent phase is with the not notable (P of expression difference>0.05), the different lowercase letter indication differences of shoulder mark show
Write (P<0.05), the different capitalizations of shoulder mark represent difference extremely significantly (P<0.01).
As shown in Table 4, Escherichia coli quantity embodiment 2,3 and 4 groups of poles are substantially less than control group (P<0.01);Ultramicro-powder group
With control group there was no significant difference (P>0.05).Bacillus acidi lactici quantity embodiment 2,3 and 4 groups be significantly higher than control group (P<
0.05), Ultramicro-powder group and control group there was no significant difference (P>0.05).Bifidobacteria embodiment 2,4 groups of poles are significantly higher than
Control group (P<0.01), 3 groups of Ultramicro-powder group and embodiment and control group there was no significant difference (P>0.05).
Influence of the 2.4 herb fermenting preparations to peak later stage Laying-hen Serum reproductive hormone content of laying eggs, is shown in Table 5.
Influence of the herb fermenting preparation of table 5 to peak later stage Laying-hen Serum reproductive hormone content of laying eggs
Note:Same column shoulder marking-up parent phase is with the not notable (P of expression difference>0.05), the different lowercase letter indication differences of shoulder mark show
Write (P<0.05), the different capitalizations of shoulder mark represent difference extremely significantly (P<0.01).
As shown in Table 5, test the 15th day, each test group of testosterone concentration is below control group, wherein embodiment 2,4 groups extremely show
Write and be less than control group (P<0.01), respectively than control group reduction by 9.36% and 8.36%;Compared with the 15th day, testosterone contains within the 30th day
Amount decreases, and embodiment 2,3 and 4 groups of other poles of ratio control component significantly reduce 29.46%, 12.45% and 29.04%.
Test the 15th day, pole significantly improves (P to each test group progesterone content compared with control group<0.01), Ultramicro-powder group, embodiment 2,
3 and 4 groups significantly improve 21.07%, 39.46%, 21.34% and 33.82% respectively;Test the 30th day, each test group progesterone
Content there was no significant difference (P>0.05).Test the 15th, 30 days, each test group estradiol content pole is significantly higher than control group (P
<0.01), the 15th day, Ultramicro-powder group, embodiment 2,3 and 4 groups respectively pole significantly improve 13.79%, 52.05%, 34.42%
With 35.83%;30th day, pole significantly improved 4.49%, 6.28%, 4.90% and 5.46% respectively.
Influence of the 2.5 herb fermenting preparations to shell egg and cholesterol level of vitellus, is shown in Table 6.
Influence of the herb fermenting preparation of table 6 to shell egg and cholesterol level of vitellus
Note:Shoulder marking-up parent phase go together with the not notable (P of expression difference>0.05), the different lowercase letter indication differences of shoulder mark show
Write (P<0.05), the different capitalizations of shoulder mark represent difference extremely significantly (P<0.01).
As shown in Table 6, experiment the 15th, 30 days, there was no significant difference between each test group of yolk relative weight and control group.
Test the 15th day, each test group cholesterol level of vitellus pole is substantially less than control group (P<0.01), Ultramicro-powder group, embodiment 2,
3 and 4 groups respectively than control group reduction by 8.44%, 14.66%, 13.18% and 13.35%;Test the 30th day, yolk cholesterol contains
Amount embodiment 2,3 and 4 groups significantly reduce 15.40%, 11.51% and 14.98% (P than control group pole respectively<0.01);Ultra micro
Powder group reduces 8.69% (P than control group>0.05).Test the 15th, 30 days, embodiment 2,3 and 4 groups of shell egg cholesterol levels point
Do not significantly reduce 15.24%, 10.41%, 11.31% and 14.74% than control group pole, 14.56%, 11.80% (P<
0.01);Ultramicro-powder group does not reduce 2.30% (P than control component>0.05) with 8.18% (P<0.01).
3rd, pharmacological toxicity is tested
3.1 acute toxicity test data
Detection reagent:Serum AST, ALT detection kits build up Bioengineering Research Institute purchased from Nanjing.
Detection device
Micro-200 semiautomatic biochemistry detectors, assay balance, disscting instrument, syringe, test tube etc..
3.2 test method
The ICR mouse 100 that body weight is 18~22g are chosen, after being raised through 3 days adaptability, 5 groups are divided at random, and (male and female are each
Half), Ultramicro-powder group, 2 groups of embodiment, 3 groups of embodiment, 4 groups of embodiment and blank control group, every group each 20;Blank control group
Gavage physiological saline, the Chinese medicine composition that Ultramicro-powder used in Ultramicro-powder group is selected in the embodiment of the present invention 2 carries out ultramicro grinding and obtained
The Ultramicro-powder arrived;Ultramicro-powder group is gavaged Ultramicro-powder is soluble in water, and 2 groups of embodiment, 3 groups of embodiment, 4 groups of embodiment respectively will be each
The fermentation preparation of embodiment preparation is soluble in water to be gavaged, Ultramicro-powder group, 2 groups of embodiment, 3 groups of embodiment, the medicine of 4 groups of embodiment
Addition is 0.1g/mL, 0.4mL/ times, three times a day, continuous 7 days.
3.3 testing indexs and method
(1) clinicing symptom observation:The state of mind, the diet situation of daily viewing test mouse, dead feelings of being fallen ill per day entry
Condition.
(2) pathological observation:Cut open inspection observation internal organ change is carried out for dead mouse.
(3) growth indexes are observed:Routine weighing is carried out to experiment mouse;Off-test, slaughter mouse weigh in, internal organs weight,
Organ index is determined:Cut open inspection rat, core dirty, spleen, liver, kidney, testis, ovary, is weighed, and internal organs are calculated according to the following formula and are referred to
Number:Organ index=internal organs weight/body weight × 100.
(4) change in liver function is observed:After off-test, mouse is slaughtered, takes blood to separate serum, AST, ALT is determined.
3.4 data process&analysis
All gathered datas carry out early stage processing using Excel softwares, then carry out statistical analysis, LSD with SPSS19.0
Multiple range test is carried out, is as a result represented using mean+SD.
3.5 clinicing symptom observation
Control group and test group mouse, the state of mind and diet desire, to external world respond have no obvious exception.Each group mouse
Morbidity and death condition such as table 7 below.
The mouse of table 7 falls ill and death condition
Packet | Sum | Dead (only) | The death rate (%) |
Ultramicro-powder | 20 | 0 | 0 |
2 groups of embodiment | 20 | 0 | 0 |
3 groups of embodiment | 20 | 0 | 0 |
4 groups of embodiment | 20 | 0 | 0 |
Control group | 20 | 0 | 0 |
Pathological observation:Control group and test group, progress cut open inspection, which is observed, after mouse is slaughtered has no the obvious pathology of internal organs
Change.
Growth indexes are observed:Off-test, slaughters that mouse weighs in, internal organs weight analysis are shown in Table 8.
The mouse internal organs weight analysis of table 8
Packet | Liver index | Cardiac index | Renal index | Lungs index | Index and spleen index |
Ultramicro-powder | 54.05±1.30a | 4.36±0.12a | 13.44±0.22a | 6.69±0.43a | 4.61±0.55a |
2 groups of embodiment | 54.21±1.14a | 4.71±0.20a | 13.49±0.18a | 6.81±0.35a | 4.96±0.45a |
3 groups of embodiment | 54.18±1.32a | 4.66±0.25a | 13.50±0.23a | 6.74±0.38a | 5.01±0.40a |
4 groups of embodiment | 54.09±1.24a | 4.72±0.19a | 13.47±0.22a | 6.75±0.33a | 4.92±0.42a |
Control group | 53.92±1.43a | 4.30±0.18a | 13.36±0.19a | 6.61±0.36a | 4.52±0.51a |
Note:Same column shoulder marking-up parent phase represents difference not significantly (P with or without letter>0.05), the female different small letters of shoulder marking-up
Matrix shows significant difference (P<0.05).
As shown in Table 8, each organ index analysis, there was no significant difference between each test group and control group (P>0.05).
Change in liver function is observed
After off-test, mouse is slaughtered, takes blood to separate serum, AST (glutamic-oxalacetic transaminease), ALT (third turn of ammonia of paddy is determined
Enzyme) it is shown in Table 9.As a result show that each group of data difference compared with blank control group is not notable, all in normal range (NR).
Table 9 AST, ALT measurement result
Packet | Sum | ALT | AST |
Ultramicro-powder | 20 | 39.04±2.55a | 105.46±4.62a |
2 groups of embodiment | 20 | 39.22±2.07a | 105.74±4.19a |
3 groups of embodiment | 20 | 39.18±1.99a | 105.57±3.36a |
4 groups of embodiment | 20 | 39.23±2.11a | 105.69±4.03a |
Control group | 20 | 39.08±2.25a | 105.41±5.05a |
Note:Same column shoulder marking-up parent phase represents difference not significantly (P with or without letter>0.05), the female different small letters of shoulder marking-up
Matrix shows significant difference (P<0.05).
3.6 long term toxicity test data
The fermentation preparation of the present invention prepared according to embodiment 2,20g/kg, 100g/kg give to 1 monthly age ICR mouse continuous gavage
Medicine 1 month, the fur of animal, the colour of skin, ingest, activity, urine, feces etc. it is without exception;The blood such as blood routine, the Liver and kidney function of animal
Liquid biochemical indicator and the main organs index of animal are in normal range (NR), and normal kinetic indifference;Histopathologic examination's table
Bright, the important organ such as the heart, liver, spleen, lung, kidney, adrenal gland, tracheae, testis, ovary is without pathological change.Checked after being discontinued two weeks with
Upper indices react without overt toxicity, show no cumulative toxicity.
The above described is only a preferred embodiment of the present invention, being not the limitation for making other forms to the present invention, appoint
What those skilled in the art changed or be modified as possibly also with the technology contents of the disclosure above equivalent variations etc.
Imitate embodiment.But it is every without departing from technical solution of the present invention content, the technical spirit according to the present invention is to above example institute
Any simple modification, equivalent variations and the remodeling made, still fall within the protection domain of technical solution of the present invention.
Claims (10)
1. a kind of Chinese medicine composition for improving performance in layers, it is characterised in that:Prepared by following components according to parts by weight
Form:15~25 parts of Radix Codonopsis, 10~20 parts of psoralea corylifolia, 10~20 parts of motherwort, 5~15 parts of the bighead atractylodes rhizome, 5~10 parts of Poria cocos, sweet basil 5
~15 parts, 5~10 parts of honey-fried licorice root, 5~10 parts of the tuber of pinellia, 5~10 parts of dried orange peel.
2. Chinese medicine composition according to claim 1, it is characterised in that:By following components according to parts by weight preparation
Into:20 parts of Radix Codonopsis, 15 parts of psoralea corylifolia, 15 parts of motherwort, 10 parts of the bighead atractylodes rhizome, 6 parts of Poria cocos, 10 parts of sweet basil, 6 parts of honey-fried licorice root, the tuber of pinellia 6
Part, 6 parts of dried orange peel.
3. a kind of herb fermenting preparation, it is characterised in that:It by traditional Chinese medicine ingredients mixed with Lactobacillus plantarum bacterium solution after through fermentation make
Into the traditional Chinese medicine ingredients are by weight:15~25 parts of Radix Codonopsis, 10~20 parts of psoralea corylifolia, 10~20 parts of motherwort,
5~15 parts of the bighead atractylodes rhizome, 5~10 parts of Poria cocos, 5~15 parts of sweet basil, 5~10 parts of honey-fried licorice root, 5~10 parts of the tuber of pinellia, 5~10 parts of dried orange peel.
4. herb fermenting preparation according to claim 3, it is characterised in that:The traditional Chinese medicine ingredients are by weight
For:20 parts of Radix Codonopsis, 15 parts of psoralea corylifolia, 15 parts of motherwort, 10 parts of the bighead atractylodes rhizome, 6 parts of Poria cocos, 10 parts of sweet basil, 6 parts of honey-fried licorice root, the tuber of pinellia 6
Part, 6 parts of dried orange peel.
5. the herb fermenting preparation according to claim 3 or 4, it is characterised in that:Lactobacillus plantarum content in the bacterium solution
≥108CFU/mL。
6. according to the preparation method of any one of the claim 3-5 herb fermenting preparations, it is characterised in that:Step is as follows:
(1) by traditional Chinese medicinal components are measured, crush, cross 60 eye mesh screens, it is standby;
(2) each component after crushing is well mixed, adds the water of traditional Chinese medicine ingredients gross weight 80%, stir after 100 DEG C
Steam sterilizing 30min, is cooled to 20-30 DEG C;
(3) bacterium solution is added into the medicine after cooling, bacterium solution consumption accounts for 10~15% of total amount after addition;It is placed in one-way exhaust modeling
In pocket, fermented 30 days under the conditions of 20 DEG C~30 DEG C.
7. the preparation method of Chinese medicine preparation according to claim 6, it is characterised in that:The bacterium solution is made by following methods:
Lactobacillus plantarum strain is inoculated in activation medium and carries out activation culture, cultivation temperature is 37 DEG C, time 24h;Will be living
The strain changed is inoculated in fermentation tank, controls 37 DEG C~43 DEG C of temperature, time 24h~36h.
8. the preparation method of herb fermenting preparation according to claim 7, it is characterised in that:The activation medium and described
Fermentation used medium be:MRS culture mediums, composition is (g/L):Peptone 10.0, meat extract 10.0, yeast extract 5.0, glucose
20.0th, dipotassium hydrogen phosphate 2.0, diammonium hydrogen citrate 2.0, sodium acetate 5.0, magnesium sulfate 0.58, manganese sulfate 0.28, cysteine
0.5th, Tween 80 1.0, adjust pH 6.2-6.4.
9. according to the application of any one of the claim 3-8 herb fermenting preparations, it is characterised in that:Life for improving laying hen
Produce performance.
10. a kind of have the feed for improving performance in layers, it is characterised in that:Addition such as claim 6 method in feed
The herb fermenting preparation of preparation, addition is 2kg/ tons.
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