CN116870038A - Post-natal powder of lactobacillus plantarum J26 and application of post-natal powder in aspect of cholesterol reduction - Google Patents

Post-natal powder of lactobacillus plantarum J26 and application of post-natal powder in aspect of cholesterol reduction Download PDF

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CN116870038A
CN116870038A CN202310916587.XA CN202310916587A CN116870038A CN 116870038 A CN116870038 A CN 116870038A CN 202310916587 A CN202310916587 A CN 202310916587A CN 116870038 A CN116870038 A CN 116870038A
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lactobacillus plantarum
cholesterol
post
powder
metapowder
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姜毓君
王均豪
满朝新
张宇
郑淼
王晨晨
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Hubei Junyao Health Drink Co ltd
Northeast Agricultural University
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Northeast Agricultural University
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/66Microorganisms or materials therefrom
    • A61K35/74Bacteria
    • A61K35/741Probiotics
    • A61K35/744Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
    • A61K35/747Lactobacilli, e.g. L. acidophilus or L. brevis
    • 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
    • A23L33/135Bacteria or derivatives thereof, e.g. probiotics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • 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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Abstract

The invention discloses a post-generated powder of lactobacillus plantarum J26 and application thereof in cholesterol reduction, belonging to the technical field of microbial preparations, wherein the post-generated powder of lactobacillus plantarum J26 comprises 24.89 weight percent of lipid and lipid molecules, 18.10 weight percent of organic acid and derivative, 12.85 weight percent of organic oxygen compound and the balance of lactobacillus plantarum J26 inactivated thallus, and the concentration of the lactobacillus plantarum J26 inactivated thallus is 10 8 Cells of Lactobacillus plantarum J26/g. The metapowder has the effect of relieving hypercholesterolemia, and is specifically characterized in that: significantly alleviating weight gain and appetite loss in high-fat high-cholesterol diet mice; cholesterol lowering is lowering TC, TG, LDL-C levels in serum or liver, raising HDL-C levels; significantly improves the total cholesterol and total cholesterol in the feces of high-fat high-cholesterol diet miceBile acid levels.

Description

Post-natal powder of lactobacillus plantarum J26 and application of post-natal powder in aspect of cholesterol reduction
Technical Field
The invention relates to a metapowder of lactobacillus plantarum J26 and application thereof in cholesterol reduction, belonging to the technical field of microbial preparations.
Background
Hypercholesterolemia is an important risk factor for atherosclerosis, coronary heart disease, stroke and other diseases. There is evidence that every 1% increase in serum cholesterol levels increases the incidence of cardiovascular disease by 2-3%. World Health Organization (WHO) predicts that by 2030, mortality from cardiovascular related diseases will reach 40%, accounting for approximately 2360 ten thousand of deaths worldwide.
The etiology of hypercholesterolemia includes hereditary, eating, bad lifestyle, drugs, and other diseases. The main characteristics are that the concentration of Total Cholesterol (TC), low Density Lipoprotein (LDL) and Triglyceride (TG) in serum is high, and the concentration of High Density Lipoprotein (HDL) is low. With the increasing level of living, the need to treat hypercholesterolemia has become more urgent.
Currently the primary cholesterol lowering regimen involves exercise, diet control and the use of lipid-regulating drugs such as statins, inhibitors of intestinal cholesterol absorption, bile acid sequestrants and other drugs. However, the long-term administration of the medicine can cause gastrointestinal reactions such as nausea, vomiting, abdominal distension, constipation and the like, and increase the risk of diabetes. Therefore, there is a need to develop natural non-pharmaceutical cholesterol-lowering functional products.
Disclosure of Invention
The invention aims to provide a metapowder of lactobacillus plantarum J26 and application thereof in preparation of cholesterol-lowering drugs.
In order to solve the technical problems, the invention adopts the following technical scheme:
lactobacillus plantarumLactobacillus plantarum) The application of the metapowder of J26 in preparing cholesterol-lowering medicines.
The metapowder is obtained by drying and inactivating lactobacillus plantarum J26.
The method for high-density fermentation before the inactivation of the lactobacillus plantarum J26 comprises the following steps: inoculating lactobacillus plantarum J26 strain into 4L skim milk powder culture medium with an inoculum size of 5%, and performing high-density fermentation for 18h, wherein the liquid fermentation environment is as follows: the temperature is 37 ℃, the humidity is 70%, the pH is 5.5, the aeration rate is 1.5vvm, and the power of the stirrer is 1.5kwh/m 3 The method comprises the steps of carrying out a first treatment on the surface of the The glucose concentration in the feed medium is 750g/L, the glucose concentration in the culture medium fed to the skim milk powder in 10h, 12h and 14h is 30g/L, the glucose concentration in the culture medium fed to the skim milk powder in 16h and 18h is 40g/L, and the viable count of the obtained fermentation liquor reaches 3.23 multiplied by 10 11 cfu/mL。
And (3) carrying out spray drying on the obtained fermentation broth under the conditions of needle passing frequency of 8Hz, peristaltic speed of 5rmp and air inlet of 180 ℃ to obtain the metapowder of the lactobacillus plantarum J26.
The metapowder of the lactobacillus plantarum J26 comprises 24.89 weight percent of lipid and lipid molecules, 18.10 weight percent of organic acid and derivative, 12.85 weight percent of organic oxygen compound and the balance of lactobacillus plantarum J26 inactivated thallus, wherein the concentration of the lactobacillus plantarum J26 inactivated thallus is 10 8 Cells of Lactobacillus plantarum J26/g.
The lipid and lipid molecules include one or more of ursolic acid, acetylcarnitine, D-panthenol, glycerophosphorylcholine, phosphatidylethanolamine, linolenic acid, linoleic acid, solamargine and capsaicin.
The organic acids and derivatives include one or more of 4-hydroxyisoleucine, arginine, fucosyllactose-N-hexasaccharide, pantothenic acid and anserine.
The organic oxygen compound comprises one or more of 1, 4-d-xylobiose, 3.alpha. -galactobiose, 3.alpha. -mannobiose, 3' -sialyllactose, glucosamine sulfate, galacto-N-disaccharide, lactose, maltotetraose, melezitose and raffinose.
The dosage forms of the medicine comprise granules, capsules, tablets, pills or oral liquid.
The metapowder of the invention is applied to the preparation of medicines for reducing or assisting in reducing cholesterol.
The invention relates to an application of metapowder in preparing health care products for assisting in reducing cholesterol.
Cholesterol lowering is a lowering of TC, TG, LDL-C levels in serum or liver, increasing HDL-C levels.
Cholesterol is reduced in order to increase fecal total cholesterol and total bile acid levels.
Cholesterol lowering is the reduction of weight gain and appetite increase.
The invention has the following beneficial effects:
the invention provides a post-generated element powder of lactobacillus plantarum J26 and application thereof in cholesterol reduction, wherein the post-generated element powder has the effect of relieving hypercholesterolemia, and is specifically characterized in that:
(1) Significantly alleviating weight gain and appetite loss in high-fat high-cholesterol diet mice;
(2) Significantly reducing the serum TC, TG, LDL-C level of high-fat high-cholesterol diet mice and improving the HDL-C level;
(3) Significantly reducing the liver TC, TG, LDL-C, AST, ALT level of a high-fat high-cholesterol diet mouse and improving the HDL-C level;
(4) Significantly improving the fecal total cholesterol and total bile acid levels of high-fat high-cholesterol diet mice;
therefore, lactobacillus plantarum is [ ]Lactobacillus plantarum) The metapowder prepared by J26 has great application prospect in preparing products of diseases related to hypercholesteremia.
Drawings
FIG. 1 shows the number of viable bacteria of the cells at different concentrations of glucose and culture times;
FIG. 2 is a comparison of weight gain, food intake and water intake of different groups of mice, wherein A is the weight gain of the different groups of mice after the end of the 14 th week experiment, B is the food intake of the different groups of mice during the 5 week treatment period, and C is the water intake of the different groups of mice during the 5 week treatment period; compared to HCD group, p <0.05, p <0.01, p <0.001, p <0.0001;
FIG. 3 shows comparison of serum biochemical indicators of different groups of mice; compared to HCD group, p <0.05, p <0.01, p <0.001, p <0.0001;
FIG. 4 is a comparison of liver biochemical indicators of different groups of mice; compared to HCD group, p <0.05, p <0.01, p <0.001, p <0.0001;
FIG. 5 is a comparison of total bile acid and total cholesterol levels in the feces of different groups of mice; compared to HCD groups, p <0.05, p <0.01, p <0.001, and p <0.0001.
Detailed Description
The invention will be further described with reference to the accompanying drawings.
In the invention, lactobacillus plantarum J26 is lactobacillus plantarum NDC75017, and the inventor purchases the lactobacillus plantarum through a strain collection center. The classification of Lactobacillus plantarum NDC75017 is named Lactobacillus plantarumLactobacillus plantarumThe strain is preserved in China general microbiological culture Collection center (CGMCC), beijing, and has a preservation date of 2011, 11 and 08, and a preservation number of CGMCC NO.5448; lactobacillus plantarum J26 is abbreviated asLactobacillus plantarumJ26、L. plantarum J26, LJ26 or J26.
Step one, lactobacillus plantarumLactobacillus plantarum) J26 preparation of metapowder
Preparing a skim milk powder culture medium: the components are prepared according to the weight percentage: 0.25% of maltose, 0.02% of sodium chloride, 0.8% of sodium acetate, 2-3% of peptone, 2-3% of beef extract, 2-3% of yeast extract, 8% of glucose, 0.35% of diammonium citrate, 0.15% of dipotassium hydrogen phosphate, 0.08% of magnesium sulfate, 0.03% of manganese sulfate, 0.03% of ferrous sulfate and the balance of skimmed milk powder. The above formulation was mixed with water (1:10, m/v) and autoclaved to prepare a skim milk powder medium.
The method for high-density fermentation comprises the following steps: plant milkThe bacillus J26 strain is inoculated in 4L skim milk powder culture medium with an inoculum size of 5 percent for high-density fermentation, and the liquid fermentation environment is as follows: the temperature is 37 ℃, the humidity is 70%, the pH is 5.5, the aeration rate is 1.5vvm, and the power of the stirrer is 1.5kwh/m 3 . The feed medium was 750g/L glucose. In connection with the results of FIG. 1, the feeding strategy was optimized to feed to a medium glucose concentration of 30g/L at 10h, 12h and 14h and 40g/L at 16h and 18 h. Under the optimized feeding strategy, the viable count of the obtained fermentation liquor reaches 3.23 multiplied by 10 11 cfu/mL, before optimization (lactobacillus plantarum J26 strain is inoculated in 4L of skim milk powder culture medium with an inoculum size of 5 percent, high-density fermentation is carried out, fermentation is carried out for 18 hours at 37 ℃, the liquid fermentation environment is the same as above, residual glucose in fermentation liquid at different time points is measured by using a glucose measuring kit, the feeding amount is determined, the feeding culture medium is 750g/L glucose, and the viable count of thallus is 3.15X10 when the glucose concentration of the culture medium is 40g/L after 10 hours, 12 hours, 14 hours, 16 hours and 18 hours 10 The cfu/mL thallus concentration is improved by 9.3 times.
Drying and inactivating method: and (3) spray drying the obtained fermentation broth under the conditions of needle passing frequency of 8Hz, peristaltic speed of 5rmp and air inlet of 180 ℃ to obtain the lactobacillus plantarum J26 metapowder (the inactivation rate is more than 99.99%).
The post-production powder of Lactobacillus plantarum J26 has a concentration of 10 8 Cells of Lactobacillus plantarum J26/g.
Step two, metabolites in J26 metameal
Taking 20mg of the lactobacillus plantarum J26 metapowder obtained in the step one, adding 0.5mL of precooled methanol/acetonitrile/water solution (2:2:1, v/v) at 4 ℃, mixing by vortex, carrying out low-temperature ultrasonic treatment at 4 ℃ for 30min, standing at-20 ℃ for 10min, centrifuging at 14000g at 4 ℃ for 20min, taking supernatant, drying in vacuum, adding 100 mu L of acetonitrile water solution (acetonitrile: water=1:1, v/v) for redissolution during mass spectrometry, carrying out vortex, centrifuging at 14000g at 4 ℃ for 15min, and taking supernatant for sample injection analysis. After the sample is separated by an Agilent 1290 information LC ultra-high performance liquid chromatography (UHPLC), a Triple TOF 6600 mass spectrometer (AB SCIEX) is used for mass spectrometry, and electrospray ionization (ESI) positive ion mode and negative ion mode are respectively used for detection. And firstly carrying out metabolite structure identification and data pretreatment on the extracted data, then carrying out experimental data quality evaluation, and finally carrying out data analysis. The ratio of lipid and lipid molecules in the lactobacillus plantarum J26 metameal is 24.89 percent, the ratio of organic acid and derivative is 18.10 percent, and the ratio of organic oxygen compound is 12.85 percent. The ratio of lipid and lipid molecules in lactobacillus plantarum J26 viable bacteria (prepared by a high-density fermentation process before optimization) is 21.16%, the ratio of organic acid and derivative is 13.25%, and the ratio of organic oxygen compound is 12.35%.
Effect of Lactobacillus plantarum J26 metaplasia powder on cholesterol reduction in high-fat high-cholesterol diet mice
The C57BL/6J mice referred to in the examples below were purchased from Beijing Vietnam Liwa.
1. Mouse modeling and grouping
80 male C57BL/6J mice (6 weeks old, weight 20-22 g) were placed at room temperature (22.+ -. 2 ℃) for 12h light/12 h dark period. After one week of adaptation, mice were randomly assigned to two groups: normal diet (ND group, n=10) and high fat high cholesterol diet (HCD, n=70) for 8 weeks. Mice fed HCD were then randomized into seven groups (n=10): (1) HCD group; (2) group L-J26P, lavage 200mg/kg body weight of mice; (3) group M-J26P, gavage 400mg/kg mouse body weight; (4) H-J26P group, gavage 800mg/kg mouse body weight; (5) Group J26, gavage 0.2mL Lactobacillus plantarum J26 (1X 10) 8 cfu/mL); (6) group of Atorvastatin, lavage 10mg/kg body weight of mice; (7) BB536 group, lavage 0.2mL commercial cholesterol lowering probiotic preparation bifidobacterium longum BB536 (1X 10) 8 cfu/mL). Mice in ND and HCD groups were orally given 0.2mL of sterile Phosphate Buffered Saline (PBS).
The experiment was performed for 14 weeks: after mice were acclimatized for one week, the blank group was fed with maintenance feed (energy ratio: 23.07% protein, 11.85% fat, 65.08% carbohydrate), the remaining group was fed with high fat high cholesterol feed (maintenance feed +15% lard +20% sucrose +1.2% cholesterol +0.2% sodium cholate), the mice serum biochemical index was measured every week, modeling was successful at the end of week 9, and from week 10, each of the metagroups was perfused with the corresponding metapowder, lactobacillus plantarum J26 lyophilized powder, drug atorvastatin, and commercial cholesterol lowering probiotic formulation bifidobacterium BB536 (dissolved in normal saline at the corresponding dose) at an amount of 0.2 mL/day, and the blank group and model group were perfused with the same amount of PBS solution as the control until the end of the experiment. All groups were free drinking and ingestion. The experimental animals were grouped as shown in table 1 below.
Table 1 experimental animal groups
2. Data monitoring
Mice morphology was observed. The body weight, food intake, water intake of the mice were recorded.
And (5) collecting blood and tissues of the mice. Blood was taken after the end of the experiment and mice were sacrificed. The liver was dissected and rapidly removed and rinsed in ice-cold physiological saline. The blood samples were centrifuged at 3000g for 10min at 4℃and serum was collected and stored at-80 ℃.
And (5) measuring blood lipid indexes. TG (triglyceride), TC (total cholesterol), HDL-C (high density lipoprotein cholesterol) and LDL-C (low density lipoprotein cholesterol) in blood lipid were measured by using the kit.
Measurement of relevant indicators in the liver. Part of liver tissue is mixed with 0.1mmol/L phosphate buffer solution according to the mass ratio of 1:10, homogenizing with a homogenizer, centrifuging for 10min at 10000g, collecting supernatant, and determining the contents of TG (triglyceride), TC (total cholesterol), HDL-C (high density lipoprotein cholesterol), LDL-C (low density lipoprotein cholesterol), ALT (glutamic pyruvic transaminase) and AST (glutamic oxaloacetic transaminase) according to the procedures of the kit.
Measurement of total bile acid and total cholesterol in feces. The assay was performed using an enzyme-linked immunosorbent assay (ELISA).
3. Experimental results
3.1 Mouse morphology
As shown in fig. 2, compared with the model group HCD, the medium and high dose metapowder groups, the viable bacteria control group, the drug control group and the commercial product control group all significantly inhibited the weight gain of the high-fat high-cholesterol diet mice after five weeks of administration, and the effect of the high dose lactobacillus plantarum J26 metapowder administration was most obvious, and was inferior to that of the atorvastatin drug treatment group. The intermediate and high dose Lactobacillus plantarum J26 metameal groups remarkably relieve the appetite reduction of mice caused by high-fat and high-cholesterol diet.
3.2 Mouse blood fat index
Serum TC, TG, LDL-C, HDL-C levels are critical for health monitoring of hypercholesterolemic patients. As can be seen from fig. 3, the biochemical index related to lipid metabolism was improved in the serum of mice after 5 weeks in the other treatment group compared with the HCD group. Serum TC levels in the H-J26P group were reduced by 28.82% and were next to atorvastatin drug treatment (32.29%). Serum TG levels were also significantly reduced in all treatment groups, 38.33% after H-J26P treatment. In vivo, when there is an excess of low density lipoproteins, the cholesterol carried by them accumulates on the arterial wall, causing atherosclerosis over time. Serum LDL-C levels were significantly reduced five weeks after gavage M-J26P, H-J26P, J, atorvastatin, and b.longum BB536 compared to the HCD group. The in vivo high density lipoproteins are mainly responsible for transport of cholesterol from extrahepatic tissues to the liver where it is converted to bile acids or directly excreted from the gut via bile, thus preventing deposition of free cholesterol on extrahepatic tissue cells and serum HDL-C levels are markedly elevated in high fat high cholesterol diet mice following treatment with H-J26P, J and atorvastatin.
3.3 Biochemical index of mouse liver.
As shown in fig. 4, the liver is a major site of lipid metabolism and is easily affected by eating habits. Damaged hepatocytes release liver-specific enzymes, such as ALT and AST, resulting in elevated levels of both enzymes in the liver, consistent with the results of the HCD group in this study. After treatment, gavage J26P decreased TC, TG, LDL-C, AST and ALT levels in the liver of hypercholesterolemic mice and increased HDL-C levels consistent with previous serum biochemical results. The J26P can relieve liver lipid metabolism abnormality and restore liver function.
3.4 Total bile acid and total cholesterol content in mouse feces.
As shown in fig. 5, bile acids in feces are the main products of cholesterol metabolism. Thus, increased bile acid excretion in the feces may reduce serum cholesterol levels. This study showed that J26P intervention increased total cholesterol and total bile acid content in the feces of mice in the HCD group, suggesting that J26P may be directly eliminated by inducing cholesterol to convert to bile acid and then be partially excreted with the feces. This partly explains the reduction of liver fat deposition and the improvement of serum lipid status.
In summary, the effect of Lactobacillus plantarum J26 metameal on hypercholesterolemia mice was studied in this experiment. The result shows that the lactobacillus plantarum J26 metaplasia powder has good effect of improving the blood lipid and liver lipid metabolism disorder of a high cholesterol mouse, can improve liver injury and lipid accumulation, provides a certain pharmacological basis for the adjuvant therapy of hypercholesterolemia and related diseases, and provides a thinking for developing new products of the lactobacillus plantarum J26 metaplasia powder.
The foregoing is only a preferred embodiment of the invention, it being noted that: it will be apparent to those skilled in the art that various modifications and adaptations can be made without departing from the principles of the present invention, and such modifications and adaptations are intended to be comprehended within the scope of the invention.

Claims (9)

1. Lactobacillus plantarumLactobacillus plantarum) The application of the metapowder of J26 in preparing cholesterol-lowering medicines.
2. Use according to claim 1, characterized in that the metapowder is obtained by dry inactivation of lactobacillus plantarum J26.
3. Use according to claim 2, characterized in that the method of high-density fermentation before inactivation of lactobacillus plantarum J26 is: inoculating lactobacillus plantarum J26 strain into 4L skim milk powder culture medium with an inoculum size of 5%, and performing high-density fermentation for 18h, wherein the liquid fermentation environment is as follows: the temperature is 37 ℃, the humidity is 70%, the pH is 5.5, the aeration rate is 1.5vvm, the power of the stirrer is 1.5kwh +.m 3 The method comprises the steps of carrying out a first treatment on the surface of the The glucose concentration in the feed medium is 750g/L, the glucose concentration in the culture medium fed to the skim milk powder in 10h, 12h and 14h is 30g/L, the glucose concentration in the culture medium fed to the skim milk powder in 16h and 18h is 40g/L, and the viable count of the obtained fermentation liquor reaches 3.23 multiplied by 10 11 cfu/mL。
4. Use according to claim 3, characterized in that the fermentation broth obtained is subjected to spray drying under conditions of a needle passing frequency of 8Hz, a peristaltic speed of 5rmp, an air intake of 180 ℃, obtaining the metapowder of lactobacillus plantarum J26.
5. The post-production powder of Lactobacillus plantarum J26 obtained by the method according to claim 4, wherein the post-production powder comprises 24.89wt% of lipid and lipid molecules, 18.10wt% of organic acid and derivative, 12.85wt% of organic oxygen compound and the balance of Lactobacillus plantarum J26 inactivated thallus, wherein the concentration of the Lactobacillus plantarum J26 inactivated thallus is 10 8 Cells of Lactobacillus plantarum J26/g.
6. The post-cursor powder of lactobacillus plantarum J26 of claim 5, wherein the lipid and lipid molecules comprise one or more of ursolic acid, acetylcarnitine, D-panthenol, glycerophosphorylcholine, phosphatidylethanolamine, linolenic acid, linoleic acid, solamargine and capsaicin.
7. The metapowder of lactobacillus plantarum J26 according to claim 5, wherein the organic acid and derivative comprises one or more of 4-hydroxyisoleucine, arginine, fucosyllactose-N-hexasaccharide, pantothenic acid and anserine.
8. The metapowder of lactobacillus plantarum J26 according to claim 5, wherein the organic oxygen compound comprises one or more of 1, 4-d-xylobiose, 3.alpha.—galactobiose, 3.alpha.—mannobiose, 3' -sialyllactose, glucosamine sulfate, galactose-N-disaccharide, lactose, maltotetraose, melezitose and raffinose.
9. The use according to any one of claims 1 to 4, wherein the pharmaceutical dosage form comprises a granule, a capsule, a tablet, a pill or an oral liquid.
CN202310916587.XA 2023-07-25 2023-07-25 Post-natal powder of lactobacillus plantarum J26 and application of post-natal powder in aspect of cholesterol reduction Pending CN116870038A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117547029A (en) * 2024-01-11 2024-02-13 东北农业大学 Lactobacillus plantarum J26 metazoan freeze-dried powder with weight-losing and lipid-lowering effects, and preparation method and application thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117547029A (en) * 2024-01-11 2024-02-13 东北农业大学 Lactobacillus plantarum J26 metazoan freeze-dried powder with weight-losing and lipid-lowering effects, and preparation method and application thereof
CN117547029B (en) * 2024-01-11 2024-04-05 东北农业大学 Lactobacillus plantarum J26 metazoan freeze-dried powder with weight-losing and lipid-lowering effects, and preparation method and application thereof

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