NEW USE OF LACTOBACILLUS PARACASEI SUBSP. PARACASEI K56 IN ALLEVIATION OF INTESTINAL INFLAMMATION

Abstract

The present invention provides novel use of Lactobacillus paracasei subsp. paracasei K56 in alleviation of intestinal inflammation. Lactobacillus paracasei subsp. paracasei K56 of the present invention has the deposit number CGMCC 15139 or DSM 27447. It was discovered in the present invention that the strain alone was highly efficacious at alleviating intestinal inflammation, reducing inflammatory factors IL-6 and/or TNF-α, promoting the anti-inflammatory factor IL-10, and reducing the tissue damage of colitis.

Claims

1. Use of Lactobacillus paracasei subsp. paracasei in the manufacture of a composition for alleviating intestinal inflammation, wherein the Lactobacillus paracasei subsp. paracasei has the deposit number CGMCC 15139 or DSM 27447.

2. The use according to claim 1, wherein the Lactobacillus paracasei subsp. paracasei is used in a form of solid or liquid bacterial preparation to manufacture the composition.

3. The use according to claim 1, wherein the composition comprises a food composition, a feed composition or a pharmaceutical composition.

4. The use according to claim 1, wherein the composition is for use in reducing inflammatory factors IL-6 and/or TNF-α.

5. The use according to claim 4, wherein the Lactobacillus paracasei subsp. paracasei is used in an amount of 1.0×10.sup.6 CFU to 1.0×10.sup.13 CFU/day, preferably 1.0×10.sup.9 CFU to 1.0×10.sup.11 CFU/day.

6. The use according to claim 1, wherein the composition is for use in promoting anti-inflammatory factor IL-10.

7. The use according to claim 6, wherein the Lactobacillus paracasei subsp. paracasei is used in an amount of 1.0×10.sup.6 CFU to 1.0×10.sup.13 CFU/day, preferably 1.0×10.sup.9 CFU to 1.0×10.sup.11 CFU/day.

8. The use according to claim 1, wherein the composition is for use in reducing tissue damage in colitis.

9. The use according to claim 8, wherein the Lactobacillus paracasei subsp. paracasei is used in an amount of 1.0×10.sup.6 CFU to 1.0×10.sup.13 CFU/day, preferably 1.0×10.sup.9 CFU to 1.0×10.sup.11 CFU/day.

10. The use according to any one of claims 4-9, wherein the composition is a food composition, preferably, the food is a fermented dairy product, cheese, a dairy-containing beverage, a solid beverage, or dairy powder.

Description

DESCRIPTION OF THE DRAWINGS

[0020] FIG. 1 shows the effect of Lactobacillus paracasei subsp. paracasei K56 on colonic IL-6 in mice.

[0021] FIG. 2 shows the effect of Lactobacillus paracasei subsp. paracasei K56 on colonic IL-10 in mice.

[0022] FIG. 3 shows the effect of Lactobacillus paracasei subsp. paracasei K56 on colonic TNF-α in mice.

[0023] FIG. 4 shows the results of pathological sections for the effect of Lactobacillus paracasei subsp. paracasei K56 on mice.

[0024] FIG. 5 shows the histology injury scores of mice under Lactobacillus paracasei subsp. paracasei K56.

DETAILED DESCRIPTION OF THE INVENTION

[0025] In order to provide a better understanding of the technical features, purpose and beneficial effects of the present invention, the following detailed description of the technical solutions of the present invention is provided in conjunction with specific examples, and it should be understood that these examples are used only to illustrate the invention and not to limit the scope of the invention.

[0026] In the examples, each original reagent and material are commercially available, and the experimental methods without specific conditions indicated are conventional methods under conventional conditions known in the art, or conducted under the conditions recommended by the manufacturer of instrument.

Example 1

[0027] Experiment on the efficacy of Lactobacillus paracasei subsp. paracasei K56 at alleviating intestinal inflammation

[0028] 1. Experimental Materials

[0029] Healthy BABL/c male mice, purchased from Beijing Huafukang Biotechnology Co. Ltd., were bred in the animal house of CDC maintained at room temperature (25±2° C.) and relative humidity of (55±2)%, under 12h/12h alternating day/night light, and allowed free access to food and water.

[0030] 2. Experimental Methods

[0031] 2.1 Animal Grouping and Handling

[0032] 112 healthy BABL/c male mice, aged 6-8 weeks and weighing 20-22 g, were randomly divided based on body weight into 8 groups, with 14 mice per group. Each group was bred in two cages with 7 animals per cage, numbered with picric acid, and adapted for 5 days with normal feed. The details of the groups and sample volumes are shown in Table 1. The mice were subjected to intervention by gavage with a volume of 0.4 ml/20 g. The intervention period was 14 days.

TABLE-US-00001 TABLE 1 Experimental grouping Test Number of Gavage volume for mice Grouping drug animals (cfu/20 g) Control group PBS 14 — Model group PBS 14 — K56 low-dose group K56 14 1 × 10.sup.7 K56 medium-dose group K56 14 1 × 10.sup.8 K56 high-dose group K56 14 1 × 10.sup.9

[0033] Among the eight groups of mice, except for the control group, 7 groups required DSS induction for establishment of an experimental colitis model. On day 8 of the experiment, a 5.0% aqueous solution of DSS was prepared to replace drinking water and the mice consumed it freely for 7 days, while the normal group consumed distilled water. The mice were observed every day for changes in physical signs.

[0034] 2.2 Colon Length and Weight Measurement

[0035] After the intervention, the mice were anesthetized by intraperitoneal injection of sodium pentobarbital, blood was taken from the abdominal aorta, and serum was separated by centrifugation. The colon of each mouse was isolated, rinsed several times with PBS, and measured for length, and ⅔ of the colon was cut and stored in a centrifuge tube at −80° C. The other ⅓ was stored in a 10% formalin solution for fixation.

[0036] 2.3 Observation and Scoring of Histopathology of the Colon

[0037] After the colon was fixed in the formalin solution, it was sequentially dehydrated, waxed, embedded, sectioned, bathed and baked, dewaxed and rehydrated, HE stained, and finally microscopically observed for histomorphology.

[0038] Histological scoring was performed using the Fedorak histological scoring criteria. The histology injury scoring criteria are shown in Table 2.

TABLE-US-00002 TABLE 2 Histology injury scoring criteria Lesion Extent of Score Inflammation depth Recess damage lesion 0 none none none / 1 Mild Submucosa Basal ⅓ recess, 1%-25% damaged 2 Medium Muscular Basal ⅔ recess, 26%-50%  layer damaged 3 / Serosa layer Intact surface 51%-75%  epithelium only 4 / / All recess and 76%-100% epithelium damaged

[0039] 2.4 Measurement of Cytokines in Serum

[0040] The levels of cytokines IL-6, IL-10, and TNF-α in the colons of mice were measured according to the ELISA kit instructions.

[0041] 2.5 Statistical Analysis Methods

[0042] Experimental data were expressed as Mean±S.E.M. Data were processed using PRISM version 5.0 (GraphPad, San Diego, Calif., USA). Differences between groups were evaluated using one-way ANOVA following Tukery's multiple comparison test. P<0.05 indicates a statistically significant difference.

[0043] 3. Experimental Results and Analysis

[0044] 3.1 Changes in Body Weight of Mice

[0045] The body weights of mice at 0, 7, and 14 days were measured and the results are shown in Table 3.

TABLE-US-00003 TABLE 3 Changes in body weight of mice Grouping Day 0 Day 7 Day 14 Control group 20.92 ± 0.56 22.25 ± 0.88 22.68 ± 1.02  Model group 21.36 ± 0.99 23.18 ± 1.21 19.19 ± 2.28* Low-dose group 21.36 ± 0.69 22.98 ± 1.19 20.22 ± 1.73* Medium-dose group 21.10 ± 0.82 23.12 ± 0.84 19.54 ± 2.61* High-dose group 20.87 ± 0.64 22.08 ± 0.70 18.87 ± 1.75* Note: *The difference is significant as compared with the control group.

[0046] On day 0, there was no significant difference (p<0.05) in body weight between the mice groups, indicating that the mice were in the same condition at the beginning of the experiment, and the experimental deviation caused by a difference in body weight of the mice can be excluded. After 7 days of sample administration, the body weight of mice increased in all groups, with no significant difference (p<0.05) in body weight between the mice groups, indicating that the short-time sample intervention had no effect on the body weight gain of mice. After 7 days under 5% DSS instead of drinking water, the body weight of all mice in the model group decreased significantly (p<0.05), while there was no significant change in the body weight of the control group (p>0.05). Meanwhile, the mouse status observation results indicated successful modeling in the model group. After modeling, the body weight of mice in both the model group and the intervention groups significantly decreased, indicating that despite the sample intervention, the body weight of mice still decreased due to the intestinal damage caused by DSS. After modeling, the body weight of mice in each intervention group was significantly lower than that in the control group (p<0.05), but showed no significant difference from that in the model group (p>0.05), indicating that the samples had a limited intervention effect on the body weight of mice molded by DSS.

[0047] 3.2 Characterization of DSS-Induced Colonic Inflammation in Mice

[0048] From day 0 to day 7, mice in each group showed smooth fur, an active spirit, a quick response, normal feeding activity, and spherical or striped stools without diarrhea or bloody stools. After 7 days of modeling, mice in both the model group and the intervention groups were induced with 5.0% DSS to build an experimental colitis model. The changes in the physical signs of the mice in each experimental group during the modeling period were observed separately, and the relevant results are shown in Table 4.

TABLE-US-00004 TABLE 4 Observation of physical signs of mice Time of Time of diarrhea bloody stools Number of Number (n days after (n days after mice with Number Grouping of mice modeling) modeling) bloody stools of deaths Control group 14 — — 0 0 Model group 14 3 3 14 0 Low-dose group 14 3 4 6 0 Medium-dose group 14 3 4 7 0 High-dose group 14 3 4 6 1

[0049] The observation of intestinal inflammation symptoms in mice showed that the intervention effect of each sample on DSS-modeled mice was manifested in two aspects: (1) the number of mice with bloody stools decreased at the end of the experiment; (2) the time of appearance of bloody stools in mice was delayed by 1-2 days compared with the model group. Because this modeling was done with 5% DSS instead of drinking water, and probably because the mice had different uptake and tolerance of DSS, the number of death did not change with the dose.

[0050] 3.3 Spleen Weight of Mice in the Groups

[0051] The spleen weights of mice in each group are shown in Table 5. As compared with the control group, the splenic indices of mice in the model group were all significantly higher than those in the control group (p<0.05), indicating that 5% DSS can stimulate proliferation of lymphocytes and macrophages in the spleen of mice and stimulate the body to exert cellular and humoral immunological functions. The K56-medium-dose group showed a decreasing tendency in splenic index, suggesting that the K56-medium-dose group may have a function of reducing inflammatory responses of the organism.

TABLE-US-00005 TABLE 5 The spleen weight and splenic index of mice Grouping Spleen weight (g) Splenic index Control group 0.081 ± 0.011 0.36 ± 0.05  Model group 0.085 ± 0.021 0.44 ± 0.09* Low-dose group 0.090 ± 0.021 0.45 ± 0.11* Medium-dose group 0.074 ± 0.019 0.38 ± 0.09  High-dose group 0.093 ± 0.025 0.49 ± 0.11* Note: *The difference is significant as compared with the control group.

[0052] 3.4 Test Indicators

[0053] 3.4.1 Measurement of Mouse Colon Length

[0054] The results of mouse colon length are shown in Table 6. After modelling, the colon length of mice in the model group was significantly lower than that of the control group (p<0.05). After the sample intervention, there was no significant difference in colon length between each mice group and the model group (p>0.05), indicating that the main effect on the colon length of mice in this experiment was from the 5% DSS, and the short-term sample intervention showed no significant effect on the colon length of mice.

TABLE-US-00006 TABLE 6 Results of colon length measurement in mice Grouping Colon length (cm) Control group 12.51 ± 0.92  Model group 7.78 ± 1.53* Low-dose group 8.66 ± 0.92* Medium-dose group 8.43 ± 1.10* High-dose group 8.53 ± 0.59* Note: *The difference is significant as compared with the control group.

[0055] 3.4.2 Colonic IL-6 Assay Results

[0056] The results of changes in colonic IL-6 are shown in FIG. 1. As compared with the control group, colonic IL-6 was significantly higher in the model group mice (p<0.05), indicating that DSS intervention in mice can cause an increase in intestinal inflammatory responses in mice, as evidenced by an increase in the inflammatory factor IL-6. As compared with the model group, the colonic IL-6 of mice in the K56-medium-dose group was significantly lower than that in the model group (p<0.05); indicating that the probiotic intervention reduced intestinal inflammatory responses of mice at medium and high doses of K56.

[0057] 3.4.3 Colonic IL-10 Assay Results

[0058] The results of changes in colonic IL-10 are shown in FIG. 2. As compared with the control group, colonic IL-10 in the model group increased but the difference was not significant (p>0.05), indicating that the modeling has a tendency of causing increased secretion of the intestinal anti-inflammatory factor IL-10. As compared with the model group, IL-10 increased in all groups, with a significant increase (p<0.05) in colonic IL-10 in the K56-high-dose group (2.5×10.sup.9 cfu/mL) of mice, indicating that K56 intervention has an effect of promoting production of the anti-inflammatory factor IL-10 by intestinal anti-inflammatory cells.

[0059] 3.4.4 Colonic TNF-α Assay Results The results of changes in colonic TNF-α are shown in FIG. 3. As compared with the model group, the low-, medium-, and high-dose groups of probiotic K56 according to the present invention all showed a decreasing trend for colonic TNF-α, indicating that K56 can reduce intestinal inflammatory responses and reduce secretion of the colonic inflammatory factor TNF-α.

[0060] 3.4.5 Pathology Results

[0061] 3.4.5.1 Pathological Sections

[0062] The results of pathological sections are shown in FIG. 4. Histological observation of mice in the control group showed intact colonic epithelial cells and clear recess structures and goblet cells. Histological observation of colitis mice in the model group induced by DSS showed that intact colonic epithelial cells could not be seen, and also showed incomplete recess and damaged goblet cells, with the damaged area being more than 50%, and in some mice the recesses disappeared completely and the goblet cells were destroyed completely. Inflammatory cell infiltration, such as neutrophils and lymphocytes, can also be observed in the mice.

[0063] Mice modeled by DSS after K56 intervention showed inflammatory cell infiltration, disappearance of a few recesses, and destruction of goblet cells, with a more severe inflammatory response in the low-dose group, with lesions ranging from 50 to 75%, and more limited lesions in the middle and high-dose groups, mostly within 25%.

[0064] 3.4.5.2 Analysis of Histology Injury Scores in Mice

[0065] The histology injury scores are shown in FIG. 5. As compared with the model group, the histological injury scores of all groups showed a decreasing trend, among which the histology injury scores of the K56 low- and high-dose groups were significantly lower than that of the model group (p<0.05), indicating that K56 had an effect of reducing the symptoms of colonic inflammation in mice.

[0066] DSS-induced colitis is the most common method for establishing experimental animal colitis models, which are usually formed by allowing mice to drink freely for about 7 days. In this test, 5% DSS was used as the modeling concentration, and the model group had no death, and the mice started to have bloody stools on the third day, with the blood in stools and the number of mice having bloody stools increasing with time, indicating that the model was established with good stability. The mice in each K56 dose group showed bloody stools later than the model group, had the number of mice having bloody stools less than that of the model group and showed milder symptoms, which directly indicates the anti-inflammatory effect of the probiotic.

[0067] IL-6 is a multifunctional crucial cytokine that regulates expression of other cytokines. In the course of DSS-induced experimental colitis, the level of expression of IL-6, a pro-inflammatory factor, was closely related to the degree of inflammation in colitis, and mice lacking IL-10 exhibited severe intestinal inflammation, and IL-10 showed good therapeutic effects in animal models of colitis. TNF-α is a cytokine involved in systemic inflammation. In this study, a medium dose of Lactobacillus paracasei subsp. paracasei K56 lowered the level of colonic inflammatory factor IL-6, the level of serum TNF-α and the colonic tissue injury score; and a high dose increased the level of the colonic tissue anti-inflammatory factor IL-10 and lowered the colonic tissue injury score.

[0068] The above results confirmed that Lactobacillus paracasei subsp. paracasei K56 significantly inhibits inflammatory factors IL-6 and TNF-α, elevates the level of anti-inflammatory factor IL-10, recovers the loss of colonic tissue, and is useful in food products such as fermented milk, cheese, milk-containing beverages, milk powder or any other kind of food containing the strain or derivatives thereof.