KR20130134730A - Composition for improving liver function containing fermented liquor of hovenia dulcis thunb extract as effective component - Google Patents

Abstract

The present invention relates to a composition for improving liver function containing fermented liquor of hovenia dulcis thunb extract as an effective component. According to the present invention, the fermented liquor of hovenia dulcis thunb extract is manufactured by adding and fermenting lactobacillus. The lactobacillus is lactobacillus brevis. [Reference numerals] (AA) LDH concentration (ng / mL);(BB) Acetaminophen (10mM);(CC) Hovenia dulcis thunb extract;(DD) Lactic acid fermented hovenia dulcis thunb extract;(EE) Samples (10 μg / mL)

Description

Composition for improving liver function containing fermented liquor of Hovenia dulcis Thunb extract as effective component

The present invention relates to a composition for improving liver function containing the fermented product of the barn extract as an active ingredient, and more particularly, a composition for improving liver function and a health food for improving liver function containing the fermented product of the barn extract as an active ingredient. It is about.

Recently, the mortality rate of liver cancer among Koreans was 23.4 per 100,000, ranking first in the world, and 28.8 in chronic liver disease. Recently, the National Statistical Office reported that 56.1 people per 100,000 population suffer from liver disease in their 40s, the highest cause of death. Alcoholic liver disease caused by excessive drinking, such as fatty liver, alcoholic hepatitis, alcoholic cirrhosis, etc., mental stress and smoking aggravate the liver damage, the body's defense and detoxification effect can cause the immune system and cause other diseases. As the damage caused by the liver-related diseases increases, the interest and demand of consumers for the liver functional improvement products are increasing not only in the liver-related therapeutic market but also in the health functional food market.

Hovenia dulis Thunb is a buckthorn (Rhamnaceae) used in folk medicine for hangovers. In the Ming Dynasty, the Sichuan River wrote, "In the fall, the fruit tree becomes a coral shape with the fruit larvae becoming larger, and it is used as a medicine and tastes sweet, so people eat it. It protects you. " According to a scientific study conducted by the Forestry Research Institute of the Korea Forest Service, the bark tree has the most active ingredient in the fruit stalk, including the fruit, among the fruits, leaves, and wood. As a result of analyzing the material extracted from the fruit bag, it was identified as a polysaccharide which has a hydrophilic property of the polymer, a molecular weight of about 114,500 which is strong against acid decomposition, and has a water-soluble structure. It is said that these substances include substances having anti-liver toxicity and hangover-relieving activity. It has also been reported that hawthorn has the effect of inhibiting glutamate-induced brain damage. Hazelnut tree has the effect of inhibiting carbon tetrachloride-induced liver damage (Hase K et al., Biol. Pharm. Bull. 20 (4): 381-385, 1997), and dihydroflavonone isolated from the fruit of Hazelnut tree. (dihydroflavonols), hovenitins I, II and III have been reported to have the effect of inhibiting alcohol-induced liver damage (Yoshikawa M et al., Yakugaku Zasshi 117 (2): 108-118, 1997). Barberry fruit has been reported to have an effect of promoting alcohol degradation upon acute alcohol administration (Ji Y. et al., Zhong Yao Cai 24 (2): 126-128, 2001).

Recently, researches are being conducted on fermenting herbal preparations such as herbal medicines to enhance useful ingredients and to increase the efficacy and absorption rate as functional food materials.

Therefore, the present inventors investigated whether the liver function was improved by treating the fermented product of the bark extract with hepatic cells damaged by acetaminophen using Lactobacillus brevis , a kind of Lactobacillus. Acetaminophen is a drug widely known as an analgesic or antipyretic. It is a drug that causes chronic hepatitis or liver failure when used in chronic alcohol patients or when overdose (Gyamlani GG, 2002 Crit. Care).

Korean Laid-open Patent No. 2012-0048801 discloses a buttercup fermentation broth for protecting and improving liver function, and a method for preparing the same, and Korean Patent No. 0808130 discloses an acetaminophen-induced liver disease comprising a protein isolated from red seaweed laver. Although a therapeutic composition is disclosed, it is not known as to the composition for improving liver function containing the fermented product of the barley extract as an active ingredient as in the present invention.

The present invention is derived from the above requirements, the present invention, but the development of a functional material that can improve the liver function is desired, but these days, a lot of restrictions due to safety problems such as side effects, relatively high safety natural products The present invention was completed by developing a composition for improving liver function by fermenting the phosphorus barn extract with lactic acid bacteria.

In order to solve the above problems, the present invention provides a composition for improving liver function containing the fermented product of the bark extract as an active ingredient.

In addition, the present invention provides a health food for improving liver function containing a fermented product of the bark extract.

According to the present invention, the composition obtained by fermenting the bark extract with lactic acid bacteria is effective for improving liver function, and does not cause side effects because it uses a substance obtained from natural products, and can ensure safety, thereby improving the functional food industry for liver function. It would be a very useful invention.

Figure 1 shows the pH change according to the fermentation period of lactic acid extract of the barberry.
Figure 2 shows the change in acidity according to the fermentation period of lactic acid extract of the hut.
Figure 3 shows the hepatocyte vitality of mice according to the amount of acetaminophen.
Figure 4 is a result of the cell viability of the hepatic cells in rats for cytotoxicity induced by acetic acid-induced hepatic extract or fermentation of these extracts after fermentation with lactic acid bacteria of the liver protective effect (cell viability). Rat hepatocytes were treated with 10 μg / mL of fermented extract obtained after fermentation of these extracts or these extracts with lactic acid bacteria, and 10 mM acetaminophen for 24 hours. Cell viability was measured by MTT assay.
5 is a result of examining the protective effect of liver extract of fermented rat extract or fermentation obtained after fermenting these extracts with lactic acid bacteria against rat cytotoxicity induced by acetaminophen in LDH (lactate dehydrogenase) concentration. Rat hepatocytes were treated with 10 μg / mL of fermented extract obtained after fermentation of these extracts or these extracts with lactic acid bacteria, and 10 mM acetaminophen for 24 hours. Hepatoprotective effect was measured by LDH analysis.
FIG. 6 shows the hepatoprotective effect of acetic acid-induced cytotoxicity on rat hepatocytes, and the effect of liver protection on fermentation products obtained after fermenting these extracts with lactic acid bacteria at ALT (Alanine aminotransferase) concentration. Rat hepatocytes were treated with 10 μg / mL of fermented extract obtained after fermentation of these extracts or these extracts with lactic acid bacteria, and 10 mM acetaminophen for 24 hours. Hepatoprotective effect was measured by ALT analysis.

In order to achieve the object of the present invention, the present invention provides a composition for improving liver function containing the fermented product of the bark extract as an active ingredient.

In the composition according to an embodiment of the present invention, the fermentation product of the bardock extract may be prepared by fermentation after adding lactic acid bacteria to the bardock extract, and the lactic acid bacterium may be preferably a strain of the genus Lactobacillus, more preferably It may be Lactobacillus brevis , but is not limited thereto.

In the composition according to the embodiment of the present invention, the hut extract may be hut hot water extract, but is not limited thereto.

The term "extract" in the present invention refers to an active ingredient isolated from a natural product. The extract may be obtained by an extraction process using water, an organic solvent, or a mixed solvent thereof. Lt; RTI ID = 0.0 > formulated < / RTI > The extracted liquid can be used directly or by concentrating and / or drying. When extracted with an organic solvent, methanol, ethanol, isopropanol, butanol, ethylene, acetone, hexane, ether, chloroform, ethyl acetate, butyl acetate, dichloromethane, N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), 1,3-butylene glycol, propylene glycol, or a mixed solvent thereof may be used and extracted by room temperature or warming in a condition where the active ingredient of the waste is not destroyed or minimized. Depending on the organic solvent to be extracted, the degree of extraction and loss of the active ingredient of the medicine may be different, so select an appropriate organic solvent. The extraction method is not particularly limited, and examples thereof include hot water extraction, cold needle extraction, ultrasonic extraction, and reflux extraction.

The solvent extract may further comprise a step of filtering the extract to remove suspended solid particles. Particles may be filtered using cotton, nylon, or the like, or ultrafiltration, freezing, centrifugation, or the like may be used, but is not limited thereto.

When the extract is concentrated, methods such as reduced pressure concentration, reverse osmosis concentration and the like can be used. The post-concentration drying step includes, but is not limited to, freeze drying, vacuum drying, hot air drying, spray drying, vacuum drying, foam drying, high frequency drying, infrared drying and the like.

In the composition according to an embodiment of the present invention, the fermentation of the barb extract is preferably

(a) adding glucose and skim milk powder to the barley hydrothermal extract to sterilize at 120-122 ° C. for 13-17 minutes; And (b) after cooling the sterilized additive of step (a), Lactobacillus brevis ( Lactobacillus) brevis ) can be prepared by inoculating the strain and fermentation at 35 ~ 39 ℃ 12-16 days,

More preferably,

(a) adding 0.8 to 1.2% of glucose and 0.8 to 1.2% of skim milk powder to the barley hydrothermal extract to sterilize at 120 to 122 ° C. for 13 to 17 minutes; And (b) after cooling the sterilized additive of step (a), Lactobacillus brevis ( Lactobacillus) brevis ) can be prepared by inoculating the strain and fermentation at 35 ~ 39 ℃ 12-16 days,

Most preferably,

(a) adding 1% glucose and 1% skim milk powder to the barley hydrothermal extract to sterilize at 121 ° C. for 15 minutes; And (b) after cooling the sterilized additive of step (a), Lactobacillus brevis ( Lactobacillus) brevis ) can be prepared by inoculating a strain for 14 days at 37 ℃, but is not limited thereto.

In addition, the present invention provides a functional food for improving liver function containing fermented product by lactic acid bacteria fermentation of the bark extract.

When the fermented product by the lactic acid bacteria fermentation of the barn extract of the present invention is used as a food additive, the fermented products by the lactic acid bacterium fermentation of the barn extract may be added as it is, or may be used together with other food or food ingredients, in a conventional method Can be used accordingly. The amount of the active ingredient to be mixed can be suitably determined according to its intended use (prevention, health or therapeutic treatment). Generally, in the preparation of food or beverages, the fermented products of the present invention are added in an amount of up to 15 parts by weight, preferably up to 10 parts by weight relative to the raw materials. However, in the case of long-term consumption intended for health and hygiene purposes or for health control purposes, the amount may be less than the above range, and since there is no problem in terms of safety, the active ingredient may be used in an amount exceeding the above range .

There is no particular limitation on the kind of the food. As a specific example, the fermented product may be used to produce processed foods that improve the shelf life while simultaneously modifying the characteristics of agricultural products, livestock products or aquatic products. Such processed foods include, for example, confectionery, drinks, liquor, fermented foods, canned foods, milk processed foods, meat processed foods, noodles and the like. The sweets include biscuits, pies, breads, candies, jellies, gums, cereals (including dinner utensils such as cereal flakes). Beverages include carbonated drinks, functional hot drinks, juices (eg, apples, pears, grapes, aloes, citrus fruits, peaches, carrots, tomato juices, etc.), Sikhye, and the like. Alcoholic beverages include sake, whiskey, shochu, beer, liquor and fruit wine. Fermented foods include soy sauce, miso, and kochujang. Canned food includes canned seafood (eg, tuna, mackerel, canned meat, canned seashells, etc.), canned animal products (eg beef, pork, chicken, turkey canned, etc.), canned produce (corn, peaches, canned pineapples, etc.). Milk processed foods include cheese, butter, yogurt and the like. Meat processed foods include pork cutlet, beef cutlet, chicken cutlet, sausage, sweet and sour pork, nuggets, nubucki, and the like. And noodles such as sealed packaging raw noodles. In addition, the composition may be used in retort food, soup and the like.

In addition, the fermented product may be used to produce a functional food, health food or health supplement food. Functional food, health food or dietary supplement means a food that provides a bioregulatory function, including a physiologically active ingredient in addition to the nutritional function, the fermented product of the present invention has a variety of specific natural Since the extract is included as an active ingredient, it can be used in the manufacture of functional foods, health foods or health supplements.

Hereinafter, the present invention will be described in detail by way of examples. However, the following examples are illustrative of the present invention, and the present invention is not limited to the following examples.

Materials and methods

1) Raw materials

The hut was purchased from PNK Co., Ltd. and Dongbu Herbal Cooperative.

2) Lactic Acid Bacteria

Lactobacillus brevis was used for lactic acid bacteria fermentation.

3) Sample preparation method

The manufacturing method for the bark extract and lactic acid bacteria fermentation is as follows. That is, 4L of purified water was added to 1 kg of the sample, and extracted at 100 ° C. for 3 hours, and the resultant was concentrated to 57 brix. The concentration of the extract was adjusted to distilled water to a final volume of 1L to include 1%, 3%, 5%, respectively, and then sterilized at 121 ° C. for 15 minutes by adding 1% glucose and 1% skim milk powder. 10 ml of lactic acid bacterium culture solution was inoculated into the sterilized extract cooled at room temperature and then fermented at 37 ° C. for 14 days. The control group was used as sterilized extract without performing the lactic acid bacteria fermentation treatment.

4) General ingredient analysis

General ingredients were analyzed according to the Association of Official Analytical Chemists (AOAC) method. In other words, 5g of each sample is placed in a weighing bottle and dried in a 105 ℃ dry oven until it is weighed. The weight is measured and the content is calculated. Inquiry content is pre-incubated at 250 ° C after about 2g of sample. In the direct ingestion method, the crude protein content was calculated by multiplying the nitrogen content measured by the Kjeldahl method by the nitrogen coefficient of 6.25, and the crude fat content was measured by Soxhlet extraction method after drying the sample. In addition, crude fiber was analyzed by the Hennerberg Stohmann improved AOAC method, and the content of soluble nitrogen was calculated by subtracting moisture, crude ash, crude protein, crude fat, crude fiber content from the total amount.

5) Free Sugar Analysis

The free sugar component was analyzed according to the method of Wilson et al. That is, distilled water was added to 20 g of the sample, ground with a homogenizer, stirred, leached to a constant volume of 100 mL, centrifuged (3,000 rpm, 30 minutes), and the supernatant was collected and filtered (Whatman No. 2). The filtered filtrate was purified by Sep-pak C ₁₈ and then filtered through a 0.45㎛ membrane filter (Millipore Co., USA) was used as an analytical sample for HPLC, the content is calculated by the external standard method and HPLC conditions are shown in Table 1.

6) Organic Acid Analysis

Organic acid analysis was performed in the same manner as the pretreatment of free sugar analysis, and the filtrate extracted was analyzed under the conditions of Table 2 using HPLC.

7) Amino Acid Analysis

A) Amino Acid Analysis

1 g of the sample was placed in a test tube, 10 mL of 6N-HCl solution was added, and the filtrate obtained by hydrolysis at 110 ° C. for 24 hours was centrifuged. The supernatant was concentrated at 50 ° C. to completely evaporate hydrochloric acid and water, followed by 20 mM HCl (pH 2.2). ) Was filtered to 0.4 mL membrane filter, and the filtrate was derivatized with AccQ-Tag reagent and used as analytical sample for HPLC. Analysis conditions are shown in Table 3, and the amino acid content was calculated by an external standard method by an integrator.

B) free amino acid analysis

Free amino acid analysis of the sample was analyzed by Ohara and Ariyosh's method for filtrate obtained by pretreatment in the same way as free sugar quantification. 25 mg of sulfosalicylic acid was added to 10 ml of the filtrate, which was allowed to stand at 4 ° C. for 4 hours, followed by centrifugation (50000 rpm, 30 minutes) to remove proteins, and the supernatant was filtered through a 0.45 μm membrane filter. The obtained filtrate was derivatized with AccQ-Tag reagent and analyzed by HPLC. The analysis conditions are shown in Table 3.

8) pH measurement

The pH change during the fermentation period of the sample was measured using a pH meter (Orion 940. USA) taking 20 mL of the sample.

9) pH measurement

The total acid content during the fermentation period of the sample was centrifuged to give 10 mL of the supernatant, and 1% phenolphthalein was used as an indicator. After titration with 01 N NaOH solution, the total acid content was multiplied by lactic acid coefficient 0.009 to convert lactic acid.

10) Liver protection and liver function improvement experiment

Collagenase perfusion

Sprague-Dawley (SD) rat hepatocytes were isolated by Berry and Friend's modified two-stage collagenase perfusion method. To obtain hepatocytes, SD rats were anesthetized with ether, sterilized the abdomen with 70% ethanol, and then opened to open the right atrium to remove the blood and to remove the Hank's balanced salt with a 21 gauge syringe in the left ventricle. solution; HBSS) 150 ml was injected into the blood vessel. After removing the blood, 100 ml of Korean herbal equilibrium saline containing collagenase (100 U / ml) was recycled to release the hepatocytes. Remove liver tissue and add 60 ml of oriental equilibrium saline solution in 100 mm culture dish. One blade was obtained by cutting with 11 blades. To remove collagenase in this cell suspension, three times Weymouth MB 752/1 medium (5% fetal bovine serum, 2.0 mg / ml bovine serum albumin, 10) ^-6 M dexamethasone, 10 ^-7 M insulin, 5.32 x 10 ^-2 M L-serine, 4.09 x 10 ^-2 M L-alanine, 2.67 x 10 ^-2 M NaHCO ₃ , 100 IU / ml penicillin Rinse with 100 IU / ml streptomycin, 50 / ml gentamicin sulfate. Thus obtained hepatocytes were diluted to 5 x 10 ⁵ cell / ml and attached to a 96-well plate (96-well plate) coated with collagen (collagen) for 4 hours, and then treated with each sample.

B) Cytotoxicity analysis

The primary liver cells of the rats were treated with samples by incubating in 96 well plates at a concentration of 5 x 10 ⁵ cells / ml. After 24 hours of treatment, formazan was formed for 4 hours by adding 0.5 μg / ml tetrazolium-based colorimetric (MTT). After the reaction, the medium was removed, and formazan was dissolved in dimethyl sulfoxide (DMSO), and the absorbance was measured at 540 nm using a microplate reader. Cell viability of each sample was calculated by the untreated group with 100% control.

C) liver function test

Enzymes were quantitatively measured using a rat alanine transaminase (ALT) and rat lactate dehydrogenase (LDH) ELISA kit purchased from BlueGene Co. (Shanghai, China) for liver function tests. .

Example  1. Analysis of common components, free sugars, organic acids and amino acids

1) General ingredient content

The hut used in the present invention General ingredient contents are shown in Table 4. The moisture content was 13.23% and the ash content was 4.22%. Crude protein content was high as 5.62%. Crude fat content was 2.67% and crude fiber content was 7.11%.

2) free sugar content

Of hut extract used in the present invention Free sugar content is shown in Table 5. The main sugars were glucose and fructose. Glucose and fructose contents were 18.81% and 16.41%, respectively.

Maltose was found to be 1.40% in the dry sample, but was not detected in the sample using the extract.

The free sugar content of the lactic acid fermentation solution prepared by varying the content of the barley extract was lower than the total free sugar content, including the total free sugar content, before the lactic acid bacteria fermentation.

3) organic acid content

The organic acid content of the sample used in the present invention is shown in Table 6. The main organic acids detected were malic acid, lactic acid and acetic acid. The total organic acid content according to the extract content was increased in proportion to the amount of extracts added in the test groups not inoculated with lactic acid bacteria. Lactic acid bacteria fermentation product as a final product was confirmed that the total organic acid content increases as the content of the bark extract increases.

4) amino acid content

A) Amino Acid Content

Amino acid analysis results of the samples used in the present invention are shown in Table 7. A total of 16 amino acids were detected in the constituent amino acids of the sample, and the total content was 3,735.65 mg% of barley and 1,753.29 mg% of barley extract. It was found in propolis, valine extract, and proline, valine, glutamic acid, and arginine.

B) free amino acid content

Free amino acid analysis results of the samples used in the present invention are shown in Table 8. Like the constituent amino acids, a total of 16 amino acids were detected in the sample, and the total free amino acid content was 1,045.89 mg% of barley and 308.54 mg% of barley extract. The main free amino acids of the barley and barley extracts were arginine, threonine, and aspartic acid, and threonine and glycine were not detected in the extracts.

Example  2. Hut  Of Lactic Acid Bacteria Fermentation pH  Changes and Lactic Acid Bacteria Fermentation water  PH change

1) pH change by lactic acid bacteria fermentation

The pH change according to the fermentation period of the samples to which the extract was added as shown in FIG. The pH of the barley extract was the lowest between 1 and 3 days, after which the constant pH was maintained without significant change. The initial acidity was higher in the 1% barley extract than in the other addition ratios, and the final acidity was lower in the 1% barberry extract. The 1% barley extract was the lowest between 1 and 3 days of fermentation and thereafter maintained a constant pH. The 3% and 5% extracts were slowly lowered to 7 days and then maintained constant pH.

2) Change in Acidity of Lactic Acid Bacteria Fermentation

The change in acidity according to the fermentation period of the samples to which the extract was added to bark is shown in FIG. 2. There was no significant change in the concentrations of the barley extracts, and the acidity increased up to 11 days of fermentation and then decreased on the 13th day after 3% and 5% of the barley extracts were added. . Lactic acid bacteria fermented with 1% of barley extract decreased from 9 to 11 days of fermentation and then increased again.

Example  3. Hut  Lactic Acid Bacteria in Extracts Fermented  Liver protection and liver function improvement effect

A) Effect of Lactic Acid Bacteria Fermentation of Arachnid Extract on Cytotoxicity of Acetaminophen

Rat primary hepatocytes were treated with acetaminophen at concentrations of 0, 0.5, 2.5, 10, 50 mM and then incubated for 24 hours. As a result of MTT experiment in each well after the reaction, cell viability decreased depending on the concentration. When 10 mM acetaminophen was treated to induce hepatotoxicity, hepatocyte cytotoxicity was induced, and hepatotoxicity was induced with 10 mM acetaminophen, and hepatocellular protective effect and liver function improvement effect experiment were performed (FIG. 3).

In order to confirm the hepatocellular protective effect of the bark extract and the fermented bark extract fermented with lactic acid bacteria, 10 mM acetaminophen and 10 ㎍ / mL of each sample was treated to confirm the hepatocyte protective effect due to liver toxicity (Fig. 4). As a result, the cell viability of the extract was measured to be 98.6%, and the extract of the barn fermented with lactic acid bacteria was measured to be 134.6%. It was confirmed that the extracts protected the hepatocytes, but the bark extract fermented with lactic acid bacteria increased the hepatocyte protection effect by 36.0%. According to these results, it was judged that the fermentation with lactic acid bacteria rather than the extract enhanced the hepatocellular protective effect.

B) Liver function improvement effect test (LDH)

When 10 mM acetaminophen was toxic to hepatocytes, the secretion of lactate dehydrogenase (LDH) secreted was confirmed to be increased compared to the control (FIG. 5). The barley extracts were measured at 52.5 ng / mL, but the barley extract fermented with lactic acid bacteria was measured at 33.4 ng / mL, and when fermented with lactic acid bacteria, the secretion of lactate dehydrogenase was lowered by 19.1 ng / mL. The fermented extract was confirmed to improve the liver function.

C) Liver function improvement effect test (ALT)

ALT of primary rat hepatocytes induced by hepatic toxicity with 10 mM acetaminophen increased (FIG. 6). When the fermented barley extracts were fermented with lactic acid bacteria, the secretion of ALT was reduced by 4.9 ng / mL, and these results confirmed that the extracts fermented with lactic acid bacteria were superior to liver function improvement.

Claims (6)

A composition for improving liver function containing the fermented product of the bark extract as an active ingredient. The composition of claim 1, wherein the fermented product of the bardock extract is prepared by fermentation after adding lactic acid bacteria to the bardock extract. The composition of claim 2, wherein the lactic acid bacteria is Lactobacillus brevis . The composition of claim 1, wherein the hut extract is a hut hydrothermal extract. The method of claim 1, wherein the fermentation of the hut extract
(a) adding glucose and skim milk powder to the barley hydrothermal extract to sterilize at 120-122 ° C. for 13-17 minutes; And
(b) After cooling the sterilized additive of step (a), Lactobacillus brevis ( Lactobacillus brevis ) inoculated with the strain, the composition characterized in that it is prepared by fermentation at 35 ~ 39 ℃ for 12 to 16 days. Health foods for improving liver function, containing fermented products of barley extract.

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