CN109498660A - A kind of application for the lactobacillus plantarum CCFM8610 that can alleviate atopic dermatitis - Google Patents
A kind of application for the lactobacillus plantarum CCFM8610 that can alleviate atopic dermatitis Download PDFInfo
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- CN109498660A CN109498660A CN201811404822.0A CN201811404822A CN109498660A CN 109498660 A CN109498660 A CN 109498660A CN 201811404822 A CN201811404822 A CN 201811404822A CN 109498660 A CN109498660 A CN 109498660A
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- lactobacillus plantarum
- atopic dermatitis
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- plantarum ccfm8610
- ccfm8610
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Classifications
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- A—HUMAN NECESSITIES
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- A23L—FOODS, 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
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
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Abstract
The invention discloses the applications that one kind can alleviate the lactobacillus plantarum CCFM8610 of atopic dermatitis, belong to microorganisms technical field and pharmaceutical technology field.Present invention discover that lactobacillus plantarum CCFM8610 has the function of alleviating atopic dermatitis, it is embodied in: (1) significantly improves the ear swelling degree of atopic dermatitis mouse;(2) the dermatopathology symptom of atopic dermatitis mouse is significantly improved;(3) the SCORAD index of slight atopic dermatitis patients is significantly reduced;(4) the DLQI scoring of slight atopic dermatitis patients is significantly improved, therefore, lactobacillus plantarum CCFM8610 has huge application prospect in the product of preparation prevention and/or treatment atopic dermatitis.
Description
Technical field
The present invention relates to the applications that one kind can alleviate the lactobacillus plantarum CCFM8610 of atopic dermatitis, belong to microorganism
Technical field and pharmaceutical technology field.
Background technique
Atopic dermatitis (Atopic Dermatitis, AD) is a kind of chronic, recurrent, inflammatory skin disease, disease hair
When often with violent itch, while with the skin disease of other anaphylactias.Meanwhile AD is a kind of common non-infectious
Skin disease, global most countries influence up to 20% children and 2-8% adult (Wollenberg A etc.,
2018), clinical manifestations diversification, according to its occur, development and characteristic distributions, can be divided into infancy, childhood, blueness
Juvenile and adulthood three phases, wherein most of AD patients occur in infancy, and serious patient even may persist to adult
Phase is one of global public health problem since its repeatability seriously affects the quality of life of patient.
The factor relations such as the morbidity of AD and h and E are close, but really cause the pathogenesis of AD unclear.One
As be considered on the basis of inherent cause, patient contact anaphylactogen forms cutaneous immunisation abnormal response and inflammation, cause fash and
Itch.There are multiple abnormal immunes to react link during the occurrence and development of AD, and such as: Langerhans cell and skin dendron are thin
Born of the same parents to the offering of allergen, the abnormal immune reaction based on Th2, regulatory T cells dysfunction, IgE are excessively generated and acidophilus
Property granulocyte increase etc..
At this stage, there is no the therapeutic agents with clear curative effect for AD therefore presently mainly to pass through external application
Drug such as glucocorticoid medicine, Calcineurin inhibitors, external application anti-microbial agents, antihistamine and anti-inflammatory
Medium drug, immunosuppressor etc. alleviate the symptom of AD.
But there are biggish adverse reactions for said medicine, also, most of patients has misgivings to hormone medicine, this
Great difficulty all is brought to AD treatment a bit, meanwhile, also great puzzlement is brought to the life of patient.
Therefore, there is still a need for a kind of drug or therapeutic modality, will not both bring side effect, while also can be used in patient
Development to antianaphylactic breaking-out and scytitis, and can be applied to patient of all categories.
In recent years, a large amount of studies have shown that enteric microorganism and immune-related allergic skin diseases relationship are very close, intestines
Road microorganism may play an important role in anaphylactic disease pathogenic process.For example, Shreiner etc. (2005) proposes that enteron aisle is micro-
Biology causes the hypothesis of anaphylactia, it is believed that and enteric microorganism plays a significant role reaching maturity for host immune system,
It is acted on especially in terms of maintaining mucosa-immune tolerance significant;In addition, transforming growth factor-β (the TGF- that enteric microorganism generates
Generation β), inhibit Th2 induction allergic inflammation and induction oral tolerance in terms of play an important role, can improve Th1 and
Balance between Th2, thus Reduce allergy disease;Also, studies have found that enteron aisle in adult atopic dermatitis patients excrement
Microbial status has correlation with coincident with severity degree of condition, and the diversity of Intestinal Mucosal Injury in Patients Undergoing microorganism reduces, Bifidobacterium
(Bifidobacterium) it is significantly dropped compared with the control group of health with the relative abundance of Bacillus acidi lactici (Lactobacillus)
Low (Watanabe S etc., 2003;B etc., 2010;B etc., 2001), to speculate that enteric microorganism can
It can be had an impact during the occurrence and development of atopic dermatitis.
Therefore, it perhaps can start with from enteric microorganism, attempt the novel drugs or new method that find treatment AD, it is existing to overcome
The defect of therapeutic agent and treatment method adverse reaction obviously etc..
Summary of the invention
Present invention discover that lactobacillus plantarum CCFM8610 has the function of alleviating atopic dermatitis, it is embodied in: (1) shows
Write the ear swelling degree for improving atopic dermatitis mouse;(2) the dermatopathology symptom of atopic dermatitis mouse is significantly improved;
(3) the SCORAD index of slight atopic dermatitis patients is significantly reduced;(4) DLQI of slight atopic dermatitis patients is significantly improved
Scoring, therefore, lactobacillus plantarum CCFM8610 have huge answer in the product of preparation prevention and/or treatment atopic dermatitis
Use prospect.
Technical scheme is as follows:
The present invention provides lactobacillus plantarum CCFM8610 in the product of preparation prevention and/or treatment atopic dermatitis
Using.
The lactobacillus plantarum CCFM8610 is recorded in the patent application text of Publication No. CN102827796A, in
On May 3rd, 2012 is in Yard 1, BeiChen xi Road, Chaoyang District, Beijing City 3 Institute of Microorganism, Academia Sinica China Microbiological bacterium
Kind preservation administration committee common micro-organisms center preservation, deposit number are CGMCC No.6077.
In one embodiment of the invention, in the product, the viable count of lactobacillus plantarum CCFM8610 is not low
In 1 × 106CFU/mL。
In one embodiment of the present invention, the product includes food, drug or health care product.
In one embodiment of the present invention, the drug contains lactobacillus plantarum CCFM8610, pharmaceutical carrier and/or medicine
Use auxiliary material.
In one embodiment of the present invention, the food includes to use the leavening containing lactobacillus plantarum CCFM8610
Produce obtained dairy products, bean product or fruit and vegetable product;Or the food includes the solid containing lactobacillus plantarum CCFM8610
Beverage.
The present invention provides a kind of for preventing and/or treating the product of atopic dermatitis, and the product contains plant cream
Bacillus CCFM8610.
In one embodiment of the present invention, in the product, the viable count of lactobacillus plantarum CCFM8610 is not less than 1
×106CFU/mL。
In one embodiment of the present invention, the product includes food, drug or health care product.
In one embodiment of the present invention, the drug contains lactobacillus plantarum CCFM8610, pharmaceutical carrier and/or medicine
Use auxiliary material.
In one embodiment of the present invention, the food includes to use the leavening containing lactobacillus plantarum CCFM8610
Produce obtained dairy products, bean product or fruit and vegetable product;Or the food includes the solid containing lactobacillus plantarum CCFM8610
Beverage.
In one embodiment of the invention, the preparation method of the leavening is to press lactobacillus plantarum CCFM8610
It is inoculated into culture medium according to the inoculum concentration for accounting for culture medium gross mass 2~4%, cultivates 18h at 37 DEG C, obtain culture solution;It will training
Nutrient solution centrifugation, obtains thallus;It is resuspended after thallus is cleaned 2~4 times with the phosphate buffer that pH is 7.2 with protective agent dense to bacterium
Degree is not less than 1 × 1010CFU/ml obtains bacteria suspension;Suspension is placed after 60min carries out preculture at 37 DEG C and uses freeze-drying
Method freeze-drying, obtains leavening.
In one embodiment of the invention, the culture medium includes the water for accounting for culture medium gross mass 87.7%, 10%
Enzyme hydrolysis skimmed milk, 0.5% glucose, 1.5% tryptone and 0.3% yeast extract dissolution.
In one embodiment of the invention, the pH of the culture medium is 6.8.
In one embodiment of the invention, the protective agent include the skimmed milk power of 100g/L, 30mL/L glycerol,
The L-sodium of the maltodextrin of 100g/L, the trehalose of 150g/L and 10g/L.
The utility model has the advantages that
Present invention discover that lactobacillus plantarum CCFM8610 has the function of alleviating atopic dermatitis, it is embodied in: (1) shows
Write the ear swelling degree for improving atopic dermatitis mouse;(2) the dermatopathology symptom of atopic dermatitis mouse is significantly improved;
(3) the SCORAD index of slight atopic dermatitis patients is significantly reduced;(4) DLQI of slight atopic dermatitis patients is significantly improved
Scoring, therefore, lactobacillus plantarum CCFM8610 are special in preparation prevention and/or treatment atopic dermatitis or even prevention and/or treatment
In the product of answering property dermatitis, there is huge application prospect.
Detailed description of the invention
Fig. 1: different groups reduce the Contrast on effect of atopic dermatitis mouse ear thickness;
Fig. 2: different groups alleviate the Contrast on effect of atopic dermatitis mouse skin inflammation;
Fig. 3: the SCORAD index clinical test process of atopic dermatitis patients;
Fig. 4: different groups reduce the Contrast on effect of slight atopic dermatitis patients SCORAD index;
Fig. 5: different groups reduce the Contrast on effect of slight atopic dermatitis patients DLQI scoring.
Specific embodiment
The present invention will be further elaborated combined with specific embodiments below.
Enzyme hydrolysis skimmed milk, glucose, tryptone and yeast extract involved in following embodiments are purchased from Shanghai medicine
Group Plc.
Detection method involved in following embodiments is as follows:
The detection method of viable count: national standard " GB 4789.35-2016 national food safety standard Food Microbiology is used
Detect lactic acid bacteria detection ".
Embodiment 1: influence of the lactobacillus plantarum CCFM8610 to atopic dermatitis mouse ear thickness
Weight is taken in the Healthy female C57BL/6 mouse 50 of 18-20g, is randomly divided into 5 groups, every group 10,5 groups of difference
Are as follows: blank group (Control), the model group that 2,4-dinitrofluorobenzene (2,4-dinitrofluorobenzene, DNFB) is administered
(Model), the CCFM8610 group that lactobacillus plantarum CCFM8610 is administered, is given at the Bb-12 group that animal bifidobacteria Bb-12 is administered
The LGG group of cascara buckthorn sugar Lactobacillus rhamnosus GG, wherein CCFM8610 group, Bb-12 group, LGG group are treatment group.
Model group is put in the DNFB solution painting that experiment the totally two weeks: 1st day is 0.5% with 50 μ L concentration on the skin and treatment group mouse is right
Skin lesion sensitization and excitation are carried out at ear, are applied with the DNFB solution that 20 μ L concentration are 0.2% within the 5th day, the 8th day, the 11st day, the 14th day
Putting model group on the skin, (naive mice auris dextra only applies equivalent and puts acetone/olive oil matrix solution conduct pair on the skin at treatment group's mouse right ear
According to);Wherein, treatment group started in the 7th day respectively with lactobacillus plantarum CCFM8610, Bb-12 and LGG (viable count is 1 ×
109CFU/mL stomach-filling) is carried out with 0.2mL bacterium solution// time dosage, (blank group and model group are not until modeling in the 14th day terminates
Bacterium solution intervention is carried out, only stomach-filling same amount of normal saline is as control);All groupings are free water and ingest.
(i.e. the 0th day) measures the ear thickness of 5 groups of mouse using digital display spiral micrometer before modeling starts, after modeling
(i.e. the 15th day) takes blood and puts to death mouse, then measures mouse ear thickness, testing result such as Fig. 1 at once.
As shown in Figure 1, lactobacillus plantarum CCFM8610 and bifidobacterium bifidum Bb-12 treatment group significantly reduces after the test
The thickness (P < 0.05) of model group mouse ear, also, compared with Bb-12 group and LGG group, lactobacillus plantarum CCFM8610
It is bigger to the reduction degree of mouse ear thickness, it is stronger to the relief capabilities of mouse ear swelling degree.
By experimental result it is found that significantly alleviating mouse after lactobacillus plantarum CCFM8610 stomach-filling of the present invention treatment
The swelling degree and histopathology inflammation of ear, and it is more preferable than the remission effect of Bb-12 and LGG.
Embodiment 2: influence of the lactobacillus plantarum CCFM8610 to atopic dermatitis mouse skin inflammation
Weight is taken in the Healthy female C57BL/6 mouse 50 of 18-20g, is randomly divided into 5 groups, every group 10,5 groups of difference
Are as follows: blank group (Control), the model group that 2,4-dinitrofluorobenzene (2,4-dinitrofluorobenzene, DNFB) is administered
(Model), the CCFM8610 group that lactobacillus plantarum CCFM8610 is administered, is given at the Bb-12 group that animal bifidobacteria Bb-12 is administered
The LGG group of cascara buckthorn sugar Lactobacillus rhamnosus GG, wherein CCFM8610 group, Bb-12 group, LGG group are treatment group.
Experiment the totally two weeks: 1st day carries out depilation processing to 5 groups of back of mice skins, area be about 2.5cm ×
2.5cm, and model group is put in the DNFB solution painting for being 0.5% with 50 μ L concentration on the skin and treatment group's back of mice hair removal section carries out skin lesion cause
Quick and excitation is put model group on the skin with 20 μ L concentration for 0.2% DNFB solution painting and is treated for the 5th day, the 8th day, the 11st day, the 14th day
Group back of mice hair removal section (naive mice auris dextra only applies equivalent and puts acetone/olive oil matrix solution on the skin as control);Wherein, it controls
Treatment group started respectively that (viable count is 1 × 10 with lactobacillus plantarum CCFM8610, Bb-12 and LGG in the 7th day9CFU/mL) with
0.2mL bacterium solution// time dosage carries out stomach-filling, until modeling in the 14th day terminates, (blank group and model group are dry without bacterium solution
In advance, only stomach-filling same amount of normal saline is used as control);All groupings are free water and ingest.
(i.e. the 15th day) takes blood and puts to death mouse after modeling, and back of mice hair removal section skin is taken to carry out histopathology
Analysis carries out hematoxylin eosin staining by being sliced to back of mice histopathology of skin, then passes through vocational technology personnel
It carries out histopathology scoring (result such as Fig. 2).
As shown in Figure 2, naive mice skin of back epidermal cell structure is normal, and each layer of epidermis has no inflammatory reaction;It makes
Mould group back of mice skin lesion pathology are sexually revised in obvious inflammation hyperplasia, lymphocyte and plasmocyte infiltrating, while skin of back
Erosion, there are proliferations of fibrous tissue;There is fiber in lactobacillus plantarum CCFM8610 and the back of mice skin of Bb-12 treatment group
Hyperblastosis, epidermal hyperkeratosis and a small amount of inflammation;And the proliferation of fibrous tissue of LGG treatment group is obvious, epidermis is imperfect,
Speculate that skin has ulceration, incrustation, there are serious inflammatory reactions.
The above experiment shows that LGG group can not alleviate mouse skin pathological state, and lactobacillus plantarum CCFM8610 with
Bb-12 group is suitable to mouse skin pathological symptom remission effect, can significantly alleviate the ear swelling of atopic dermatitis model mouse
Degree improves the pathological characters of back of mice skin, to effectively alleviate the atopic dermatitis symptom of mouse.
Embodiment 3: influence of the lactobacillus plantarum CCFM8610 to atopic dermatitis patients SCORAD index
85 atopic dermatitis patients are recruited in this clinical test altogether, and all patients are randomly divided into 3 groups, and three groups are respectively
A group: the placebo (26 people) of maltodextrin, the oligosaccharide group (12 people) for taking prebiotic oligosaccharide are taken, takes plant cream
Treatment group's CCFM8610 group (47 people) of bacillus CCFM8610, wherein the product that placebo is taken is low not comprising prebiotics
Chitosan component is also free of the maltodextrin of probiotic ingredient;The product ingredient containing prebiotic oligosaccharides that oligosaccharide group is taken, but
Without probiotic ingredient;What CCFM8610 group was taken is containing lactobacillus plantarum CCFM8610 (viable count 1 × 109Cfu/ item),
The probiotics bacterial powder of appropriate oligosaccharide (1/3 inulin, 1/3 oligofructose, 1/3 galactooligosaccharide).
During the whole test process, lactobacillus plantarum CCFM8610's is probiotics bacterial powder to bacterium mode, can directly be taken
With or warm water (be no more than 37 DEG C) take after mixing it with water and take, dosage is 1/day.
Test probationary period 2 weeks the clinical test phase 8 weeks, amounts to 10 weeks.
Probationary period refers to the period of preparation before clinical test, contacts within 2 weeks patient in advance before the test, counts patient
Number informs that it tests property and content, signs informed consent form, while coordinating hospital and the time of doctor, and prepares examination
Test required material;The clinical test phase refer to made a definite diagnosis by doctor and voluntary participation test patient, taken after physical examination
Placebo, oligosaccharide or the time of probiotics continue 8 weeks.
After testing probationary period, the clinical test phase starts preceding first visit, answers after clinical test the 8th week all patients
It examines, the observation index such as record skin lesion area, the skin being grievously injured degree, itch degree and score value inquire compliance, record bad anti-
It answers, specific experiment process such as Fig. 3, experimental result such as Fig. 4, wherein T0 represents the time that clinical test starts, and T8 represents 8 weeks benefits
The time that raw bacterium Intervention trial is completed.
This clinical test uses the standardization severity index-SCORING Atopic Dermatitis index of AD
(SCORAD index) assesses the diagnosis to mild AD.
As shown in figure 4, final 8 patients are left out, totally 77 complete clinical research, and patient takes 8 weeks respectively
Probiotics bacterial powder, after placebo or oligosaccharide, lactobacillus plantarum CCFM8610 group patient its SCORAD index after assessment
It is remarkably decreased (P < 0.05) compared to before taking probiotics, apparent improve occurs in patient symptom.
Points for attention:
1, all patients are apprised of before the test and not eat during test the fermentation containing viable microbial and produce
Product.
2, it is arranged in period of pregnancy or nursing period with the patient of active anaphylaxis (respiratory tract or skin) disease or infectious disease
In addition in this research.
3, probiotics, antibiotic or immunomodulator treatment have been received within 3 months before recruitment time
Patient, or the patient for having received oral steroid therapy for one month before recruitment are also excluded from and study it at this
Outside.
4, all patients are both needed to signature informed consent form in registration.
Embodiment 4: the influence that lactobacillus plantarum CCFM8610 scores to atopic dermatitis patients DLQI
85 atopic dermatitis patients are recruited in this clinical test altogether, and all patients are randomly divided into 3 groups, and three groups are respectively
A group: the placebo (26 people) of maltodextrin, the oligosaccharide group (12 people) for taking prebiotic oligosaccharide are taken, takes plant cream
Treatment group's CCFM8610 group (47 people) of bacillus CCFM8610, wherein the product that placebo is taken is low not comprising prebiotics
Chitosan component is also free of the maltodextrin of probiotic ingredient;The product ingredient containing prebiotic oligosaccharides that oligosaccharide group is taken, but
Without probiotic ingredient;What CCFM8610 group was taken is containing lactobacillus plantarum CCFM8610 (viable count 1 × 109Cfu/ item),
The probiotics bacterial powder of appropriate oligosaccharide (1/3 inulin, 1/3 oligofructose, 1/3 galactooligosaccharide).
During the whole test process, lactobacillus plantarum CCFM8610's is probiotics bacterial powder to bacterium mode, can directly be taken
With or warm water (be no more than 37 DEG C) take after mixing it with water and take, dosage is 1/day.
Test probationary period 2 weeks the clinical test phase 8 weeks, amounts to 10 weeks.
Probationary period refers to the period of preparation before clinical test, contacts within 2 weeks patient in advance before the test, counts patient
Number informs that it tests property and content, signs informed consent form, while coordinating hospital and the time of doctor, and prepares examination
Test required material;The clinical test phase refer to made a definite diagnosis by doctor and voluntary participation test patient, taken after physical examination
Placebo, oligosaccharide or the time of probiotics continue 8 weeks.
All patients after testing probationary period, the clinical test phase start before, fill in after clinical test the 8th week
DLQI grade form influences size caused by patient's various aspects for assessing 7 days atopic dermatitis in the past.
This clinical test uses most common dermatology quality of life index (dermatology life
Quality index, DLQI) scale, patient's complete independently scale fills in, and it is right at the past 7 days that investigation content is related to skin disease
It is influenced caused by patient, including physiology, psychology, social activities, human communication, family, treatment etc., each topic uses 4 grades
Point-score, total score 30 are divided, and the score value the high, prompt skin disease bigger to patient effect, evaluation AD life in patients variation.
As shown in figure 5, patient is after placebo or oligosaccharide intervention in 8 weeks, DLQI's DLQI appraisal result scores
Without downward trend, on the various aspects of minimal invasive treatment almost without influence;And the patient by 8 weeks probiotics bacterial dried bean noodles after pre-,
Downward trend, with placebo compared with oligosaccharide group, lactobacillus plantarum CCFM8610 of the present invention is presented in its quality of life index
Group, there is significantly more decline in DLQI scoring, although not occurring the difference of conspicuousness in data statistics meaning, this
It may be intervention time deficiency, the influence to the physiology of patient, psychology, social activities, human communication and family etc. is not yet
Enough influences are generated, but have changed the quality of life of AD patient, so that the quality of life of patient is towards positive side
To development.
Embodiment 5: the preparation of the fermentation beverage made of fruits or vegetables containing lactobacillus plantarum CCFM8610
Specific step is as follows:
First by fresh vegetables, fruit clean after squeeze the juice, then by the juice squeezed at 140 DEG C of temperature high temperature thermal sterilization
About 37 DEG C of temperature are cooled to after 2 seconds immediately, then is inoculated with and plants according to the inoculum concentration of percent by volume 5% in juice after sterilization
Object lactobacillus CCFM8610, finally by the juice after inoculation in the 16h that ferments at 30 DEG C to get containing lactobacillus plantarum
The fermentation beverage made of fruits or vegetables of CCFM8610 viable bacteria.
Through detecting, the pH of this fermentation beverage made of fruits or vegetables for containing lactobacillus plantarum CCFM8610 viable bacteria is 3.6, and viable count is reachable
1.3×109cfu/mL。
By this contain lactobacillus plantarum CCFM8610 viable bacteria fermentation beverage made of fruits or vegetables continuous one week to atopic dermatitis patients
It takes, the affected part swelling of patient's dermatitis can be effectively relieved, also can effectively reduce patient SCORAD index and DLQI scoring, make patient's disease
There is apparent improve in shape and quality of life.
Embodiment 6: the preparation of the acidified milk containing lactobacillus plantarum CCFM8610
Specific step is as follows:
At first by raw milk (defatted milk, fresh milk, recovery milk etc.) through 95 DEG C, 20min or 140 DEG C, 2 seconds high-strength hots
It is cooled to 37 DEG C after reason, lactobacillus plantarum CCFM8610 is then inoculated into sterilizing according to the inoculum concentration of percent by volume 3~5%
Raw milk afterwards, then according to the inoculum concentration of percent by volume 3~5% in the raw milk for being vaccinated with lactobacillus plantarum CCFM8610
Inoculation can symbiosis the commercial fermentation agent lactobacillus bulgaricus for preparing Yoghourt or streptococcus thermophilus, finally by the raw material after inoculation
Cream in 37 DEG C of mixed fungus fermentations to titratable acidity be 0.6%~0.7% (in terms of lactic acid) to get to contain lactobacillus plantarum of the present invention
The acidified milk of CCFM8610 viable bacteria.
Through detecting, this titratable acidity for containing lactobacillus plantarum CCFM8610 viable bacteria fermentation cream has reached 75 ° of T, viable count
Reach 1.23 × 109CFU/mL。
Acidified milk continuous one week that this is contained lactobacillus plantarum CCFM8610 viable bacteria is taken to atopic dermatitis patients, can
The affected part swelling of patient's dermatitis is effectively relieved, also can effectively reduce patient SCORAD index and DLQI scoring, make patient symptom and life
There is apparent improve in bioplasm amount.
Although the present invention has been described by way of example and in terms of the preferred embodiments, it is not intended to limit the invention, any to be familiar with this skill
The people of art can do various change and modification, therefore protection model of the invention without departing from the spirit and scope of the present invention
Enclosing subject to the definition of the claims.
Claims (10)
1. application of the lactobacillus plantarum CCFM8610 in the product of preparation prevention and/or treatment atopic dermatitis.
2. lactobacillus plantarum CCFM8610 as described in claim 1 is in preparation prevention and/or the product for the treatment of atopic dermatitis
In application, which is characterized in that in the product, the viable count of lactobacillus plantarum CCFM8610 is not less than 1 × 106CFU/
mL。
3. lactobacillus plantarum CCFM8610 as claimed in claim 1 or 2 is in preparation prevention and/or the production for the treatment of atopic dermatitis
Application in product, which is characterized in that the product includes food, drug or health care product.
4. lactobacillus plantarum CCFM8610 as claimed in claim 3 is in preparation prevention and/or the product for the treatment of atopic dermatitis
In application, which is characterized in that the drug contains lactobacillus plantarum CCFM8610, pharmaceutical carrier and/or pharmaceutic adjuvant.
5. lactobacillus plantarum CCFM8610 as claimed in claim 3 is in preparation prevention and/or the product for the treatment of atopic dermatitis
In application, which is characterized in that the food includes to be produced using leavening containing lactobacillus plantarum CCFM8610
Dairy products, bean product or fruit and vegetable product;Or the food includes the solid beverage containing lactobacillus plantarum CCFM8610.
6. a kind of for preventing and/or treating the product of atopic dermatitis, which is characterized in that the product contains lactobacillus plantarum
CCFM8610。
7. as claimed in claim 6 a kind of for preventing and/or treating the product of atopic dermatitis, which is characterized in that described
In product, the viable count of lactobacillus plantarum CCFM8610 is not less than 1 × 106CFU/mL。
8. as claimed in claims 6 or 7 a kind of for preventing and/or treating the product of atopic dermatitis, which is characterized in that institute
Stating product includes food, drug or health care product.
9. as claimed in claim 8 a kind of for preventing and/or treating the product of atopic dermatitis, which is characterized in that described
Drug contains lactobacillus plantarum CCFM8610, pharmaceutical carrier and/or pharmaceutic adjuvant.
10. a kind of product for atopic dermatitis as claimed in claim 8, which is characterized in that the food includes to use
Dairy products, bean product or the fruit and vegetable product that leavening containing lactobacillus plantarum CCFM8610 produces;Or the food packet
Containing the solid beverage containing lactobacillus plantarum CCFM8610.
Priority Applications (1)
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110616167A (en) * | 2019-08-22 | 2019-12-27 | 江南大学 | Bifidobacterium capable of relieving atopic dermatitis and application thereof |
CN111955740A (en) * | 2020-08-12 | 2020-11-20 | 量子高科(中国)生物股份有限公司 | Composition for relieving and treating atopic dermatitis and application thereof |
WO2021138599A1 (en) * | 2020-01-03 | 2021-07-08 | Forte Subsidiary, Inc. | Cosmetic compositions |
CN116042426A (en) * | 2021-10-28 | 2023-05-02 | 南京盛德生物科技研究院有限公司 | Lactobacillus plantarum WSH048, screening method thereof and preparation method of fermentation product thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102827796A (en) * | 2012-09-03 | 2012-12-19 | 江南大学 | Lactobacillus plantarum with cadmium removing function and usage thereof |
CN106573023A (en) * | 2014-08-13 | 2017-04-19 | 雀巢产品技术援助有限公司 | Lactobacillus plantarum CNCM I-4026 preparations and skin health |
CN107308190A (en) * | 2017-07-04 | 2017-11-03 | 宇萃达生物科技(苏州)有限公司 | Adjust the probiotic composition and its culture, preparation, purposes of human body microecological balance |
WO2018143678A1 (en) * | 2017-01-31 | 2018-08-09 | 경희대학교 산학협력단 | Novel lactic acid bacteria and use thereof |
-
2018
- 2018-11-23 CN CN201811404822.0A patent/CN109498660A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102827796A (en) * | 2012-09-03 | 2012-12-19 | 江南大学 | Lactobacillus plantarum with cadmium removing function and usage thereof |
CN106573023A (en) * | 2014-08-13 | 2017-04-19 | 雀巢产品技术援助有限公司 | Lactobacillus plantarum CNCM I-4026 preparations and skin health |
WO2018143678A1 (en) * | 2017-01-31 | 2018-08-09 | 경희대학교 산학협력단 | Novel lactic acid bacteria and use thereof |
CN107308190A (en) * | 2017-07-04 | 2017-11-03 | 宇萃达生物科技(苏州)有限公司 | Adjust the probiotic composition and its culture, preparation, purposes of human body microecological balance |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110616167A (en) * | 2019-08-22 | 2019-12-27 | 江南大学 | Bifidobacterium capable of relieving atopic dermatitis and application thereof |
CN110616167B (en) * | 2019-08-22 | 2022-02-01 | 江南大学 | Bifidobacterium capable of relieving atopic dermatitis and application thereof |
WO2021138599A1 (en) * | 2020-01-03 | 2021-07-08 | Forte Subsidiary, Inc. | Cosmetic compositions |
CN111955740A (en) * | 2020-08-12 | 2020-11-20 | 量子高科(中国)生物股份有限公司 | Composition for relieving and treating atopic dermatitis and application thereof |
CN116042426A (en) * | 2021-10-28 | 2023-05-02 | 南京盛德生物科技研究院有限公司 | Lactobacillus plantarum WSH048, screening method thereof and preparation method of fermentation product thereof |
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