METHOD FOR REDUCING BLOOD URIC ACID CONCENTRATION AND FOR DEGRADING PURINE

Abstract

A food composition and pharmaceutical composition with strains of lactic acid bacteria for reducing blood uric acid concentration are provided, comprising at least one or two isolated lactic acid bacteria strains selected from the following two: TSF331 (Lactobacillus fermentum) and TSR332 (Lactobacillus reuteri).

Claims

1. A method for reducing blood uric acid concentration, comprising administering a food composition with strains of lactic acid bacteria to a subject, wherein the food composition comprises: an isolated lactic acid bacteria strain, wherein the lactic acid bacteria strain comprises at least one of a TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and a TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528); and a physiologically-acceptable excipient or diluent.

2. The method according to claim 1, wherein the lactic acid bacteria strain is an active strain.

3. The method according to claim 1, wherein the excipient or diluent is a food.

4. The method according to claim 3, wherein the food is fermented milk, yoghurt, cheese, dairy food, powdered milk, tea, coffee, or a combination thereof.

5. A method for reducing blood uric acid concentration, comprising administering a pharmaceutical composition with strains of lactic acid bacteria to a patient, wherein the pharmaceutical composition comprises: an isolated lactic acid bacteria strain, wherein the lactic acid bacteria strain comprises at least one of a TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and a TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528); and a pharmaceutically-acceptable excipient or diluent.

6. The method according to claim 5, wherein the lactic acid bacteria strain is an active strain.

7. The method according to claim 5, which is in form of an oral dosage.

8. A method for degrading purine, comprising administering a composition with strains of lactic acid bacteria to a subject, wherein the composition comprises: an isolated lactic acid bacteria strain, wherein the lactic acid bacteria strain comprises at least one of a TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and a TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528); and a physiologically-acceptable or pharmaceutically-acceptable excipient or diluent.

9. The method according to claim 8, wherein the lactic acid bacteria strain is an active strain.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0017] FIG. 1 shows the appearance of colonies of Lactobacillus fermentum according to one embodiment of the present invention;

[0018] FIG. 2 shows the morphology of Lactobacillus fermentum according to one embodiment of the present invention;

[0019] FIG. 3 shows the appearance of colonies of Lactobacillus reuteri according to one embodiment of the present invention;

[0020] FIG. 4 shows the morphology of Lactobacillus reuteri according to one embodiment of the present invention; and

[0021] FIG. 5 shows the results of experiments using lactic acid bacteria strains to reduce blood uric acid according to one embodiment of the present invention.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] The present invention will be described in detail with embodiments and attached drawings below. However, these embodiments are only to exemplify the present invention but not to limit the scope of the present invention. In addition to the embodiments described in the specification, the present invention also applies to other embodiments. Further, any modification, variation, or substitution, which can be easily made by the persons skilled in that art according to the embodiment of the present invention, is to be also included within the scope of the present invention, which is based on the claims stated below. Although many special details are provided herein to make the readers more fully understand the present invention, the present invention can still be practiced under a condition that these special details are partially or completely omitted. Besides, the elements or steps, which are well known by the persons skilled in the art, are not described herein lest the present invention be limited unnecessarily. Similar or identical elements are denoted with similar or identical symbols in the drawings. It should be noted: the drawings are only to depict the present invention schematically but not to show the real dimensions or quantities of the present invention. Besides, matterless details are not necessarily depicted in the drawings to achieve conciseness of the drawings.

[0023] The freeze-dried cultures of the strains of lactic acid bacteria mentioned in the specification are deposited in China General Microbiological Culture Collection Center (CGMCC) of Chinese Academy of Sciences (NO. 1 West Beichen Road, Chaoyang District, Beijing 100101, China). The details thereof are listed in Table. 1.

TABLE-US-00001 TABLE 1 Data of Deposited Strains of Lactic Acid Bacteria Strain Specie Deposition No. Deposition Date TSF331 Lactobacillus CGMCC No. 15527 Mar. 29, 2018 fermentum TSR332 Lactobacillus CGMCC No. 15528 Mar. 29, 2018 reuteri

[0024] The two lactic acid bacteria strains listed in Table. 1, which are respectively the TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and the TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528), are able to decompose purine and decrease blood uric acid concentration. Therefore, they can prevent from/treat hyperuricemia and prevent from occurrence of gout.

[0025] In one embodiment, the present invention provides a food composition with strains of lactic acid bacteria for reducing blood uric acid concentration, which comprises an isolated lactic acid bacteria strain and a physiologically-acceptable excipient or diluent. The lactic acid bacteria strain comprises at least one of a TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and a TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528). Each of the lactic acid bacteria strains is an active one. The term “active strain” means the lactic acid bacteria strains of the present invention can proliferate. The physiologically-acceptable excipient/diluent is a food. The food may be but is not limited to be dairy food, tea, coffee, or a combination thereof. The dairy food may be fermented milk, yoghurt, cheese, or powdered milk. The number of the lactic acid bacteria strains may be over 10.sup.6 CFU (Colony-Forming Unit), preferably 10.sup.10 CFU.

[0026] In another embodiment, the present invention provides a pharmaceutical composition with strains of lactic acid bacteria for reducing blood uric acid concentration, which comprises an isolated lactic acid bacteria strain and a pharmaceutically-acceptable excipient or diluent. The lactic acid bacteria strain comprises at least one of a TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and a TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528). Each of the lactic acid bacteria strains is an active one. The pharmaceutic composition may be in form of an oral dosage, such as a tablet, a capsule, a solution, or a powder. The number of the lactic acid bacteria strains may be over 10.sup.6 CFU (Colony-Forming Unit), preferably 10.sup.10 CFU.

[0027] In fact, it is learned from the experimental results mentioned below: the tested lactic acid bacteria strains are not necessarily able to decrease blood uric acid concentration. Since the Otsuka pharmaceutical company proposed its patent, there have been some other researches about the effect of lactic acid bacteria on decreasing blood uric acid concentration. There are also researches about different mechanisms of decreasing uric acid. For example, some researches undertook in-vitro experiments to screen the strains able to inhibit purine nucleoside phosphorylase or xanthine oxidase. However, the characteristics of these strains need to be further examined with experiments. The strains do not necessarily all have the same characteristics and the same experimental results.

[0028] It should be particularly mentioned: the present invention does not extensively claim all lactic acid bacteria strains but only claims the two strains deposited in China General Microbiological Culture Collection Center (CGMCC), which are respectively the TSF331 strain of Lactobacillus fermentum (CGMCC No. 15527) and the TSR332 strain of Lactobacillus reuteri (CGMCC No. 15528).

[0029] Below, the taxonomic characteristics of the strains are identified with the 16S rDNA sequencing analysis and the API bacterial identification system. The morphologies and general properties of the strains are listed in Table. 2.

TABLE-US-00002 TABLE 2 Strain Morphology and Characteristics TSF331 1. While TSF331 is cultured in the MRS agar medium, strain of the colony thereof has a shape of a solid circle and a Lactobacillus color of white (as shown in FIG. 1), the bodies of the fermentum bacteria each have a shape of a short rod, and the ends of the body are circular-shaped. They often appear in single bodies (as shown in FIG. 2). 2. They are gram-positive bacilli, unlikely to generate spores, free of catalase, oxidase and motility, able to grow in aerobic and anaerobic environments, most suitable to grow at a temperature of 37 ± 1° C. They belong to a facultative heterofermentative strains and do not generate gas in glucose metabolism. TSR332 1. While TSR332 is cultured in the MRS agar medium, strain of the colonies thereof each have a shape of a solid circle Lactobacillus and a color of white (as shown in FIG. 3), the bodies of reuteri the bacteria each have a shape of a short rod, and the ends of the body are circular-shaped. They often appear in single bodies (as shown in FIG. 4). 2. They are gram-positive bacilli, unlikely to generate spores, free of catalase, oxidase and motility, able to grow in aerobic and anaerobic environments, most suitable to grow at a temperature of 37 ± 1° C. They belong to a facultative heterofermentative strains and do not generate gas in glucose metabolism.

[0030] Next, experiments are used to evaluate the purine decomposition ability of the lactic acid bacteria strains claimed by the present invention. In one embodiment of the present invention, in-vitro purine decomposition experiments of five kinds of lactic acid bacteria strains (listed in Table. 3) are undertaken.

TABLE-US-00003 TABLE 3 Example 1 TSF331 (of Lactobacillus fermentum) claimed by the present invention Example 2 TSR332 (of Lactobacillus reuteri) claimed by the present invention Comparison 1 Lactobacillus brevis (BCRC 14045) Comparison 2 L. gasseri (BCRC 17616) Comparison 3 L. plantarum (Lp323) Comparison 4 L. acidophilus (La322)

[0031] Lactobacillus brevis and L. gasseri are purchased from Bioresource Collection and Research Center. L. plantarum is purchased from American Type Culture Collection.

[0032] The abovementioned lactic acid bacteria strains are preserved in a solution containing 20% glycerol at a temperature of −80° C. Before experiments, the strains are activated two times at a temperature of 37° C. for 24 hours with an MRS broth (DIFCO) containing 0.05% cysteine. The in-vitro purine decomposition experiment includes the following steps:

1. Activate the lactic acid bacteria strains, which are preserved in glycerol at a temperature of −80° C., with the MRS broth (DIFCO); inoculate 2% (v/v) of each lactic acid bacteria strain to a fresh MRS broth; anaerobically culture the MRS brothes containing lactic acid bacteria strains at a temperature of 37° C. overnight; centrifugalize the cultured MRS brothes at a speed of 3000 rpm for 10 minutes (at a temperature of 4° C.) to collect the bacteria bodies.
2. Use the bacteria bodies and a 0.1M phosphate buffer solution to prepare suspension liquids containing bacteria at a concentration of 1×10.sup.9 CFU/ml.
3. Add two types of purines, which are respectively inosine and guanosine (purchased from Sigma), to the abovementioned suspension liquids to make the final concentrations of them be 1.26 mM; place the suspension liquids in an incubator rotating at a horizontal rotation speed of 140 rpm at a temperature of 37° C. for 30 minutes to 2 hours for reaction.
4. Use 0.1M HClO4 to terminate the reactions; suck 200 μl of product liquid from each group; centrifugalize the bottom bacteria bodies; use a 0.22 μm filter membrane to filter the supernatant liquids; take 50 μl of filtered liquid for high performance liquid chromatography (HPLC) analysis with analysis conditions: column: RP-18(MERCK); radius: 5 μm; size: 4.6×250 mm; flowrate: 1 ml/min; mobile phase: A: 0.1% acetic acid, B: methanol; gradient A/B (min): 2% (0 min), 20% (10 min), 20% (13 min), 2% (15 min).
5. Use a photodiode array (HITACHI L-2455) to detect a light with a wavelength of 254 nm.

[0033] The formula for calculating the purine residual rate is expressed as

Purine residual rate (%)=[(1−A (mM))/1.26 (mM)]×100%

wherein A=the post-reaction purine concentration.

[0034] The experimental results of the abilities of the abovementioned lactic acid bacteria strains in decomposing inosine and guanosine are shown in Table. 4.

TABLE-US-00004 TABLE 4 Purine residual rate (%) inosine guanosine 0 hour 1 hour 0 hour 1 hour reaction reaction reaction reaction Control 100 100 100 100 group Example 1 100 44 100 15 Example 2 100 0 100 0 Comparison 1 100 50 100 15 Comparison 2 100 51 100 13 Comparison 3 100 32 100 44 Comparison 4 100 38 100 12

[0035] The experimental results show that Example 1, Example 2, Comparison 3 and Comparison 4 have better ability in degrading inosine and guanosine. Especially, the concentrations of inosine and guanosine are both reduced from 100% to 0% within one hour in Example 2. The purine degrading speed of Example 2 is 2 times that of the other groups. Therefore, Example 2 obviously has better purine degrading ability. The experimental results show that the lactic acid bacteria strains claimed by the present invention have better purine degrading ability than that of a portion of Comparisons.

[0036] HPLC is used to analyze the metabolite produced in a one-hour purine degradation of each group, and the results are shown in Table. 5.

TABLE-US-00005 TABLE 5 Metabolite of purine degradation (%) Hypoxanthine Guanine Uric acid Example 1 76 83 0 Example 2 86 77 0 Comparison 1 73 61 0 Comparison 3 95 73 0 Comparison 4 82 70 0

[0037] Different groups of lactic acid bacteria strains respectively have different concentrations of the metabolites of purine degradations. The metabolites of purine degradation are mainly guanine and hypoxanthine, and no uric acid exists therein.

[0038] According to the abovementioned experimental results, the strains able to degrade purine are selected to feed rats suffering hyperuricemia to verify the ability of these strains in decreasing blood uric acid. The Inventors referred to the method established by Li, et al. (PLoS One. 2014 Sep. 3; 9(9):e105577. doi: 10.1371/journal.pone.0105577) for the experiment of verifying the ability of decreasing blood uric acid. The experiment of verifying the ability of decreasing blood uric acid includes the following steps:

1. Provide SPF-grade 30-day-old male Wistar rats; feed the rats with AIN-93G forage and sterile water for a week; collect blood from the eye sockets in a non-fast state; set the blood still for 30 minutes at an ambient temperature, and centrifugalize the blood at a speed of 3500 rpm for 10 minutes to obtain serum; store the serum at a temperature of −80° C. to make ready for detecting uric acid concentration.
2. Divide the rats into the groups listed in Table. 6,

TABLE-US-00006 TABLE 6 Tube-feeding lactic Abdomen- acid bacteria liquid injecting 1 ml/day Oxonate (10.sup.9 CFU/ml in (0.35 mg/ Group Forage 0.85% NaCl) 100 g BW) Blank experiment AIN-93G — — group forage Induced Comparison High — + group group purine forage Example 1 High TSF331 strain of + purine Lactobacillus forage fermentum Example 2 High TSR332 strain of + purine Lactobacillus forage reuteri Comparison High L. plantarum (Lp323) + + 5 purine L. acidophilus (La322) forage
wherein each 100 g the high purine forage contain 87 g Yeast Extract (Sigma) and 1.5 g RNA (Torula Yeast) (R6625 Sigma). In this embodiment, Comparison 5 is a combination of Comparison 4 (L. plantarum (Lp323)) and Comparison 3 (L. acidophilus (La322)).
3. Raise the rats for 7 days; collect 1 ml of blood from the eye sockets in the eighth day; set the blood still for 30 minutes at an ambient temperature, and centrifugalize the blood at a speed of 3500 rpm for 10 minutes to obtain serum; store the serum at a temperature of −80° C. to make ready for detecting uric acid concentration.

[0039] The experimental results are shown in FIG. 5. In comparison with the blank experiment group, the comparison group, which no lactic acid bacteria strain is suppled to, has greatly increased blood uric acid concentration while they have been raised to the eighth day. In the groups, which the lactic acid bacteria strains are supplied to, the blood uric acid concentrations of Example 1 where the rats are fed with the TSF331 strain (of Lactobacillus fermentum) claimed by the present invention and Example 2 where the rats are fed with the TSR332 strain (of Lactobacillus reuteri) claimed by the present invention are significantly decreased, in comparison with that of the comparison group. The blood uric acid concentration of Comparison 5, which L. plantarum (Lp323) and L. acidophilus (La322) are simultaneously supplied to, does not change obviously while they have been raised to the eighth day, in comparison with that of the comparison group. In other words, the effect of L. plantarum (Lp323)+L. acidophilus (La322) is insignificant in decreasing blood uric acid concentration.

[0040] As shown in Table. 4, it is a special phenomenon: although L. plantarum (Lp323) in Comparison 3 and L. acidophilus (La322) in Comparison 4 are both able to degrade purine, the effect of L. plantarum (Lp323)+L. acidophilus (La322) in Comparison 5 is insignificant in decreasing blood uric acid concentration. Therefore, the lactic acid bacteria strains able to degrade purine are not necessarily able to decrease blood uric acid concentration. The TSF331 strain (of Lactobacillus fermentum) and the TSR332 strain (of Lactobacillus reuteri), which are claimed by the present invention, can exactly degrade purine and decrease blood uric acid concentration simultaneously.

[0041] In conclusion, the food composition and pharmaceutical composition with strains of lactic acid bacteria of the present invention can effectively degrade purine, generating neither degradation metabolites nor uric acid, and decreasing blood uric acid concentration significantly. Therefore, the present invention can apply to prevent from or treat hyperuricemia. In comparison with the conventional uric acid synthesis inhibitors and the conventional uric acid excretion promoters (such as Allopurino and Benzbromarone), the food composition and pharmaceutical composition with strains of lactic acid bacteria of the present invention generates less side effects and decreases blood uric acid more significantly, having high potential in controlling blood uric acid concentration and preventing from gout.

Bioresource Deposition

CGMCC No. 15527, Institute of Microbiology, Chinese Academy of Sciences, Mar. 29, 2018

CGMCC No. 15528, Institute of Microbiology, Chinese Academy of Sciences, Mar. 29, 2018