<i>Lactiplantibacillus plantarum </i>strain for alleviating hyperuricemia and combination and use thereof

Abstract

The present disclosure provides a Lactiplantibacillus plantarum strain for alleviating hyperuricemia and a combination and use thereof, and belongs to the technical field of microorganisms. The Lactiplantibacillus plantarum strain was deposited in the China Center for Type Culture Collection (CCTCC), Wuhan, China on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596. The combination includes the Lactiplantibacillus plantarum strain BL-17, 0.01 wt % of a galacto-oligosaccharide, 0.01 wt % of an adenylic acid, and the balance of a sterilized skimmed milk solution. The combination according to the present disclosure can effectively alleviate the high serum uric acid levels in hyperuricemic rats, increase the urine uric acid levels in hyperuricemic rats, reduce the serum creatinine levels in hyperuricemic rats, reduce the serum urea nitrogen levels in hyperuricemic rats, and inhibit the activity of xanthine oxidase (XOD) in the serum and liver of hyperuricemic rats, and has an effect for alleviating hyperuricemia.

Claims

1. A method of preparing a combination for alleviating hyperuricemia, wherein the combination comprises a Lactiplantibacillus plantarum strain BL-17 at a viable bacterial cell concentration of higher than or equal to 110.sup.6 CFU/mL or higher than or equal to 110.sup.6 CFU/g, 0.01 wt % galacto-oligosaccharide, and 0.01 wt % adenylic acid in a 100 g/L sterilized skimmed milk aqueous solution, and the Lactiplantibacillus plantarum strain BL-17 is deposited in China Center for Type Culture Collection (CCTCC), Wuhan on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596; wherein the preparation method comprises the following steps: step 1, streaking the Lactiplantibacillus plantarum strain BL-17 on an MRS solid medium on a plate, picking a single colony for Gram staining, and after a single pure colony of the Lactiplantibacillus plantarum strain BL-17 is observed microscopically, subculturing the Lactiplantibacillus plantarum strain BL-17 twice in an MRS liquid medium to ensure the Lactiplantibacillus plantarum strain BL-17 is viable, to obtain an MRS liquid culture comprising the Lactiplantibacillus plantarum strain BL-17, and mixing 50% (v/v) glycerin aqueous solution and the MRS liquid culture in a volume ratio of 2:3 to obtain a resulting mixture, and storing the resulting mixture at 80 C. for later use; step 2, inoculating the cryopreserved Lactiplantibacillus plantarum strain BL-17 into 5 mL of the MRS liquid medium at an inoculum size of 4% to obtain a mixture, incubating the mixture at 37 C. for 20 hours, followed by subculturing the cryopreserved Lactiplantibacillus plantarum strain BL-17 for two passages to obtain an MRS liquid culture comprising a Lactiplantibacillus plantarum strain BL-17 at passage 2; and centrifuging the MRS liquid culture comprising the Lactiplantibacillus plantarum strain BL-17 at passage 2 at 4 C. and 6,000 r/min for 5 min to obtain a bacterial pellet, collecting the bacterial pellet, washing the bacterial pellet twice with sterile normal saline to obtain a washed bacterial pellet, and collecting the washed bacterial pellet for subsequent preparation of a bacterial suspension; and step 3, resuspending the washed bacterial pellet in the 100 g/L sterilized skimmed milk aqueous solution and performing colony counting by a serial dilution and spread plate method to prepare a bacterial suspension with a concentration of 4.010.sup.9 CFU/mL; and adding the galacto-oligosaccharide and the adenylic acid to the bacterial suspension contents such that the galacto-oligosaccharide and the adenylic acid are each at a concentration of 0.1 mg/mL; wherein the combination is capable of attenuating an intestinal absorption of an inosine and inosine-related purine compounds, and an adenosine and adenosine-related purine compounds.

2. A method for preventing and/or treating and alleviating hyperuricemia or preventing and/or treating gout, comprising administering to a subject a drug comprising a combination in an effective amount, wherein the combination comprises a Lactiplantibacillus plantarum strain BL-17 at a viable bacterial cell concentration of higher than or equal to 110.sup.6 CFU/mL or higher than or equal to 110.sup.6 CFU/g, 0.01 wt % galacto-oligosaccharide, and 0.01 wt % adenylic acid in a 100 g/L sterilized skimmed milk aqueous solution, and the Lactiplantibacillus plantarum strain BL-17 is deposited in China Center for Type Culture Collection (CCTCC), Wuhan on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596; and the combination is capable of attenuating an intestinal absorption of an inosine and inosine-related purine compounds, and an adenosine and adenosine-related purine compounds.

3. A fermented food, comprising a combination, wherein the combination comprises a Lactiplantibacillus plantarum strain BL-17 at a viable bacterial cell concentration of higher than or equal to 110.sup.6 CFU/mL or higher than or equal to 110.sup.6 CFU/g, 0.01 wt % galacto-oligosaccharide, and 0.01 wt % adenylic acid in a 100 g/L sterilized skimmed milk aqueous solution, and the Lactiplantibacillus plantarum strain BL-17 is deposited in China Center for Type Culture Collection (CCTCC), Wuhan on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596; and the combination is capable of attenuating an intestinal absorption of an inosine and inosine-related purine compounds, and an adenosine and adenosine-related purine compounds.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the effect of the combination of the present disclosure on the serum uric acid levels in hyperuricemic rats.

(2) FIG. 2 shows the effect of the combination of the present disclosure on the serum creatinine levels in hyperuricemic rats.

(3) FIG. 3 shows the effect of the combination of the present disclosure on the serum urea nitrogen levels in hyperuricemic rats.

(4) FIG. 4 shows the effect of the combination of the present disclosure on the urine uric acid levels in hyperuricemic rats.

(5) FIG. 5A and FIG. 5B show the effect of the combination of the present disclosure on the activity of XOD in the serum and liver of hyperuricemic rats.

(6) FIG. 6 shows the effect of the combination of the present disclosure on the intestinal absorption of IMP in rats.

(7) FIG. 7 shows the effect of the combination of the present disclosure on the intestinal absorption of inosine in rats.

(8) FIG. 8 shows the effect of the combination of the present disclosure on the intestinal absorption of hypoxanthine in rats.

DETAILED DESCRIPTION OF THE EMBODIMENTS

(9) The present disclosure is further described below with reference to the accompanying drawings.

(10) In the present disclosure, the Lactiplantibacillus plantarum strain BL-17 was deposited in the China Center for Type Culture Collection (CCTCC), Wuhan, China on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596. The Lactiplantibacillus plantarum strain BL-17 can be purchased by the public from the China Center for Type Culture Collection (CCTCC).

Example 1

(11) The Lactiplantibacillus plantarum strain BL-17 was isolated from a naturally-fermented yak yogurt prepared by herders in Gansu Province, China.

(12) The Lactiplantibacillus plantarum strain BL-17 for alleviating hyperuricemia was provided, and the Lactiplantibacillus plantarum strain BL-17 was deposited in the China Center for Type Culture Collection (CCTCC), Wuhan, China on Oct. 19, 2022, with an accession number of CCTCC NO: M20221596.

(13) A combination including the Lactiplantibacillus plantarum strain BL-17 for alleviating hyperuricemia was provided, where the combination included the Lactiplantibacillus plantarum strain BL-17 at a viable bacterial cell concentration of higher than or equal to 110.sup.6 CFU/mL or higher than or equal to 110.sup.6 CFU/g, 0.01 wt % of a galacto-oligosaccharide, 0.01 wt % of an adenylic acid, and the balance of a sterilized skimmed milk solution.

(14) A preparation method of the combination was provided, including the following steps.

(15) Step 1: activation of the Lactiplantibacillus plantarum strain BL-17: The Lactiplantibacillus plantarum strain BL-17 was streaked on an MRS solid medium (formula: peptone: 5.0 g, tryptone: 10.0 g, sodium acetate: 5.0 g, a yeast extract: 5.0 g, glucose: 20.0 g, Tween-80:1.0 g, manganese sulfate: 0.25 g, diammonium hydrogen citrate: 2.0 g, magnesium sulfate: 0.58 g, dipotassium phosphate: 2.0 g, a beef extract: 5.0 g, and an agar: 16.0 g, which were mixed and made up to 1 L with distilled water, then adjusted to a pH of 5.8, and sterilized at 121 C. for 15 min) on a plate. A single colony was picked for Gram staining, and after a single pure colony of the Lactiplantibacillus plantarum strain BL-17 was observed microscopically, the Lactiplantibacillus plantarum strain BL-17 was passaged twice in an MRS liquid medium (formula: peptone: 5.0 g, tryptone: 10.0 g, sodium acetate: 5.0 g, a yeast extract: 5.0 g, glucose: 20.0 g, Tween-80:1.0 g, manganese sulfate: 0.25 g, diammonium hydrogen citrate: 2.0 g, magnesium sulfate: 0.58 g, dipotassium phosphate: 2.0 g, and a beef extract: 5.0 g, which were mixed and made up to 1 L with distilled water, then adjusted to a pH of 5.8, and sterilized at 121 C. for 15 min) until the bacterial viability of the Lactiplantibacillus plantarum strain BL-17 was restored to obtain an MRS liquid culture including the Lactiplantibacillus plantarum strain BL-17. Finally, 50% glycerin and the MRS liquid culture were mixed in a volume ratio of 2:3 to obtain a resulting mixture, and the resulting mixture was stored at 80 C. for later use.

(16) Step 2: the cryopreserved Lactiplantibacillus plantarum strain BL-17 was inoculated in 5 mL of an MRS liquid medium at an inoculum size of 4%, incubated at 37 C. for 20 hours, and activated for two generations to obtain an MRS liquid culture including an activated second-generation Lactiplantibacillus plantarum strain BL-17. The MRS liquid culture including the activated second-generation Lactiplantibacillus plantarum strain BL-17 was centrifuged at 4 C. and 6,000 r/min for 5 min to obtain a bacterial pellet. The bacterial pellet was collected and washed twice with sterile normal saline to obtain a washed bacterial pellet, and the washed bacterial pellet was collected for subsequent preparation of a bacterial suspension.

(17) Step 3: the washed bacterial pellet was resuspended in a 100 g/L sterilized skimmed milk solution, and subjected to colony counting by a serial dilution and spread plate method, to prepare a bacterial suspension with a concentration of 4.010.sup.9 CFU/mL. The galacto-oligosaccharide and the adenylic acid were added to the bacterial suspension to allow the contents of the galacto-oligosaccharide and the adenylic acid each to be a concentration of 0.1 mg/mL.

(18) A use of the combination in the preparation of a drug for preventing and/or treating and alleviating hyperuricemia was provided.

(19) A use of the combination in the preparation of a drug for preventing and/or treating gout was provided.

(20) A use of the Lactiplantibacillus plantarum strain BL-17 for alleviating hyperuricemia in the preparation of a fermented food was provided.

(21) 1. Experimental Animals and Group Design

(22) The animal experiment was divided into three stages: a rat acclimating and grouping stage (one week), a hyperuricemia modeling stage (one week), and a group treatment stage (two weeks). The specific experimental protocol of each stage was as follows.

(23) First Stage (Rat Acclimating and Experimental Grouping):

(24) 48 healthy specific pathogen-free (SPF) male Wistar rats (7 weeks, body weight: (20020) g) were selected. In order to acclimate to a new environment, the 48 male rats were maintained in the animal house with the temperature of 22 C., the humidity of 10% to 60%, and 12 h/12 h light/dark cycle, and fed with standard diet and water ad libitum for 1 week. After the 1 week of acclimating, all experimental rats were randomly assigned to the following 6 groups with 8 rats per group: a control group (group A), a model group (group B), a Lactiplantibacillus plantarum strain BL-17 treated group (group C), a galacto-oligosaccharide-adenylic acid treated group (group D), a combination treated group (group E), and an allopurinol intervention treated group (positive control) (group F).

(25) Second Stage (Hyperuricemia Modeling):

(26) Starting from day 8, rats in the control group were intraperitoneally injected with a 0.5% sodium carboxymethyl cellulose (CMC-Na) solution and then subcutaneously injected with a 0.5% CMC-Na solution (the injection volume of the 0.5% CMC-Na solution was the same as the intraperitoneal injection volume of 300.00 mg/kg xanthine/CMC-Na solution and the subcutaneous injection volume of 300.00 mg/kg potassium oxonate/CMC-Na solution), and rats in the 5 groups other than the control group were intraperitoneally injected with the 300.00 mg/kg xanthine/CMC-Na solution (which was prepared by dissolving xanthine in a 0.5% CMC-Na aqueous solution) and then subcutaneously injected with the 300.00 mg/kg potassium oxonate/CMC-Na solution (which was prepared by dissolving potassium oxonate in a 0.5% CMC-Na aqueous solution) to establish the hyperuricemia model.

(27) Third Stage (Group Treatment):

(28) Starting from day 15, rats in drug groups were orally gavaged with corresponding drugs once daily, respectively. Specifically, rats in the control group and the model group were orally gavaged with 10.00 mL/kg normal saline. Rats in the Lactiplantibacillus plantarum strain BL-17 treated group were administered with a suspension of Lactiplantibacillus plantarum strain BL-17 at 110.sup.9 CFU/rat. Rats in the galacto-oligosaccharide-adenylic acid treated group were administered with the galacto-oligosaccharide at 10 mg/kg and the adenylic acid at 10 mg/kg, where the galacto-oligosaccharide and the adenylic acid were prepared with a 100 g/L sterilized skimmed milk solution (commercially available) into a solution in which concentrations of the galacto-oligosaccharide and the adenylic acid each were 0.1 mg/mL, and then the rats were orally gavaged with the solution at 10.00 mL/kg. Rats in the combination treated group were orally gavaged with the combination of the Lactiplantibacillus plantarum strain BL-17 (110.sup.9 CFU/rat) with the galacto-oligosaccharide and the adenylic acid (10 mg/kg), that is, orally gavaged with 10.00 mL/kg the combination. Rats in the allopurinol intervention treated group were orally gavaged with 5 mg/kg allopurinol/CMC-Na solution (which was prepared by dissolving allopurinol in a 0.5% CMC-Na aqueous solution). The group treatment was performed for 14 days.

(29) At the late stage of the experiment, fresh feces of the rats were collected and frozen in a 80 C. refrigerator. At the end of the experiment, the rats were fasted without water deprivation for 12 h and then intraperitoneally injected with a pentobarbital sodium solution at 0.1 mL/10 g for anaesthetization, blood was collected from retro-orbital venous plexuses of rats in each group, then the rats were sacrificed through cervical dislocation, and liver tissues of the rats were collected on ice. The blood sample was centrifuged at 3,500 r/min for 15 min to obtain the supernatant, and the supernatant was collected and frozen at 80 C. for blood indicator analysis. After being collected, the liver tissue was immediately rinsed with pre-cooled normal saline to remove blood, rapidly frozen in liquid nitrogen and then frozen at 80 C., and subsequently homogenized into liver homogenate, and then relevant indicators were determined.

(30) 2. Experiments of the Combination to Reduce Serum Uric Acid, Creatinine, and Urea Nitrogen Levels in Hyperuricemic Rats

(31) The supernatant of blood sample was taken and added to a 1.5 mL centrifuge tube to obtain a serum sample, and contents of uric acid, creatinine, and urea nitrogen in the serum sample were determined according to determination methods provided by respective assay kits.

(32) The effect of the combination on serum uric acid levels in rats is shown in FIG. 1. The serum uric acid concentration in the model group (the group B) is (424.336.03) mol/L, which is significantly higher than the serum uric acid concentration in the control group (the group A) (P<0.01), indicating that the combination of potassium oxonate and xanthine has a prominent effect for inducing a hyperuricemia model. Compared with the serum uric acid concentration in rats of the model group (the group B), serum uric acid concentrations in rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C), the galacto-oligosaccharide-adenylic acid treated group (the group D), the combination treated group (the group E), and the allopurinol intervention treated group (the group F) all decrease. There is a limited effect in the galacto-oligosaccharide-adenylic acid treated group (the group D). There is a significant difference between the Lactiplantibacillus plantarum strain BL-17 treated group (the group C) and the model group (the group B), and serum uric acid levels in rats of the Lactiplantibacillus plantarum strain BL-17 treated group can be adjusted to some extent. The serum uric acid levels in rats of the combination treated group (the group E) are significantly lower than the serum uric acid levels in rats of the model group (the group B) and the Lactiplantibacillus plantarum strain BL-17 treated group (the group C), and are close to serum uric acid levels in rats of the allopurinol intervention treated group (the group F) in a practical sense. Compared with serum uric acid levels in rats of the hyperuricemia model group (the group B), serum uric acid levels in hyperuricemic rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C) are reduced by 40.85%, and serum uric acid levels in hyperuricemic rats of the combination treated group (the group E) are reduced by 62.13%. The uric acid-lowering effect of the combination is similar to the uric acid-lowering effect of the drug allopurinol, which can prevent and reduce the occurrence of hyperuricemia and gout.

(33) The serum creatinine level is used to evaluate a glomerular filtration rate. Serum uric acid and creatinine levels are higher than normal levels when a renal function is impaired. The effect of the combination on serum creatinine levels in rats is shown in FIG. 2. Compared with serum creatinine levels in rats of the hyperuricemia model group, serum creatinine levels in rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C), the galacto-oligosaccharide-adenylic acid treated group (the group D), the combination treated group (the group E), and the allopurinol intervention treated group (the group F) all decrease, and serum creatinine levels in hyperuricemic rats of the combination treated group (the group E) decrease by 34.31%. The creatinine-lowering effect of the combination is similar to the creatinine-lowering effect of the drug allopurinol, which can prevent and reduce the occurrence of hyperuricemia and gout.

(34) The effect of the combination on a serum urea nitrogen level in rats is shown in FIG. 3, and is similar to the effect of the combination on a serum creatinine level. Compared with serum urea nitrogen levels in rats of the hyperuricemia model group, serum urea nitrogen levels in hyperuricemic rats of the combination treated group (the group E) decrease by 44.88%, indicating that the combination treated group (the group E) has a strong scavenging effect for serum urea nitrogen.

(35) 3. An Experiment of the Combination to Adjust an Amount of Uric Acid Excreted by Hyperuricemic Rats

(36) The collected urine was diluted with distilled water at 10-fold volume of the collected urine, heated at 50 C. to allow precipitates to be dissolved, and centrifuged at 2,000 r/min for 10 min to obtain a supernatant, and the supernatant was collected and assayed for urinary uric acid level according to a determination method of a uric acid assay kit.

(37) The effect of the combination on a urinary uric acid level in rats is shown in FIG. 4. Compared with urinary uric acid contents in rats of the control group (the group A), urinary uric acid contents in hyperuricemic rats of groups other than the allopurinol intervention treated group (the group F) significantly increase (P<0.01). Compared with urinary uric acid levels in rats of the model group (the group B), urinary uric acid levels in rats of the allopurinol intervention treated group (the group F) decrease to urinary uric acid levels in rats of the control group (the group A) and reach urinary uric acid levels in disease-free rats. Urinary uric acid levels in rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C) and the galacto-oligosaccharide-adenylic acid treated group (the group D) decrease to some extent, and urinary uric acid levels in rats of the combination treated group (the group E) significantly decrease and are close to urinary uric acid levels in rats of the allopurinol intervention treated group (the group F).

(38) 4. Experiments of the Combination to Reduce the Activity of XOD in Serum and Liver Tissues of Hyperuricemic Rats

(39) Liver tissue was added to 0.9% normal saline according to a weight (mg)/volume (L) ratio of 1:9 and mechanically homogenized in an ice water bath to obtain a 10% homogenate, the homogenate was centrifuged at 3,000 r/min for 10 min to obtain a supernatant, and the supernatant was collected and assayed for XOD content by enzymatic colorimetry according to instructions of an XOD assay kit. The activity of XOD in serum was also determined by a kit.

(40) XOD is the key enzyme in purine metabolism to synthesize uric acid. The mechanism by which most existing uric acid-lowering substances exert the uric acid-lowering effect is to effectively inhibit the activity of XOD to reduce the synthesis of uric acid, thereby exerting the uric acid-lowering effect. As shown in FIG. 5A and FIG. 5B, compared with activities of XOD in serum and liver of hyperuricemic rats of the model group, activities of XOD in serum and liver of hyperuricemic rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C), the galacto-oligosaccharide-adenylic acid treated group (the group D), the combination treated group (the group E), and the allopurinol intervention treated group (the group F) decrease to varying degrees. In particular, activities of XOD in serum and liver of hyperuricemic rats of the Lactiplantibacillus plantarum strain BL-17 treated group (the group C) and the combination treated group (the group E) decrease by 49.10% and 76.28%, respectively, such that activities of XOD in the serum and liver of the hyperuricemic rats are close to normal levels, and the synthesis of uric acid in the rats is reduced, which is conducive to the prevention and treatment of hyperuricemia and gout.

(41) As a major regulator organ of uric acid excretion, kidney plays an important role in the uric acid excretion, including glomerular filtration, tubular reabsorption, and secretion. It is reported that about 90% of hyperuricemia cases is mainly caused by insufficient renal uric acid excretion. The combination treated group (the group E) can significantly reduce the serum uric acid, creatinine, and urea nitrogen levels, reduce the urinary uric acid excretion, and inhibit the activity of XOD in the serum and liver in hyperuricemic rats, indicating that the present disclosure has prominent uric acid-lowering and liver and kidney-protecting effects for potassium oxonate and xanthine-induced hyperuricemic rats.

(42) 5. Research on a Mechanism of the Combination of the Present Disclosure to Alleviate Hyperuricemia

(43) 5.1. Animal Experiment Design

(44) Male Wistar rats (8 weeks, body weight: 190 g to 210 g) were selected and maintained in an animal laboratory under controlled environmental conditions: the temperature: 20 C. to 26 C., the relative humidity: 40% to 70%, and a light/dark cycle: 12 h/12 h. All rats were given with a normal diet and tap water for one week. According to body weights, the rats were randomly assigned to a control group (8 rats), a purine treated group (8 rats), and a purine-combination treated group (8 rats). The rats were fasted for 16 h. Rats in the control group each were orally gavaged with 2 mL of normal saline, rats in the purine treated group each were orally gavaged with 10 mL of .sup.14C-inosinic acid, .sup.14C-inosine, or .sup.14C-hypoxanthine at a concentration of 0.5 wt %, and rats in the purine-combination treated group each were orally administered with 10 mL of .sup.14C-inosinic acid, .sup.14C-inosine, or .sup.14C-hypoxanthine at a concentration of 0.5 wt % and 2 mL of the combination. At 0 min, 15 min, 30 min, 45 min, 60 min, 90 min, 120 min, and 180 min, blood (60 L) was collected from a tail vein of each rat and mixed with an equal volume of 2 mg/mL Na.sub.2-EDTA. The sample was added to a scintillation solution, and the radioactivity was measured in a liquid scintillation counter.

(45) 5.2. An Experiment of the Combination to Reduce the Intestinal Absorption of Purines in Rats

(46) Rats were administered with labeled purines (.sup.14C-inosinic acid (i.e. .sup.14C-IMP), .sup.14C-inosine, or .sup.14C-hypoxanthine) and the combination, and then at different time points, radioactive purine contents in blood of rats were determined. Results are shown in FIG. 6, FIG. 7, and FIG. 8. At 45 min, 60 min, and 180 min after administration, the radioactivities in blood of rats administered with .sup.14C-IMP and the combination are significantly lower than radioactivities in blood of rats administered with .sup.14C-IMP alone. Similarly, at 30 min, 45 min, 60 min, 90 min, and 180 min after administration, radioactivities in blood of rats administered with .sup.14C-inosine and the combination are significantly lower than radioactivities in blood of rats administered with .sup.14C-inosine alone, and at 15 min, 30 min, 45 min, 60 min, and 90 min, radioactivities in blood of rats administered with .sup.14C-hypoxanthine and the combination are significantly lower than radioactivities in blood of rats administered with .sup.14C-hypoxanthine alone.

(47) The combination contains a small amount of inosine, and the Lactiplantibacillus plantarum strain BL-17 can reduce the absorption of inosinic acid in rats through the direct uptake of inosine in the combination. The results observed with regard to inosine may be due to the fact that inosine is bound by the Lactiplantibacillus plantarum strain BL-17 and subsequently degraded to hypoxanthine which is less absorbed than inosine. The results observed with regard to hypoxanthine may be due to the fact that hypoxanthine is absorbed by the Lactiplantibacillus plantarum strain BL-17, and is absorbed at low levels in the intestinal tract. Due to the degradation of nucleosides and the absorption of purines by the Lactiplantibacillus plantarum strain BL-17, the intestinal absorption of purines is reduced. In addition, the effectiveness of nucleotides and nucleosides may be reduced because nucleotides and nucleosides are easily absorbed in the intestinal tract. As a functional oligosaccharide, the galacto-oligosaccharide can serve as a rich nutrient source for the Lactiplantibacillus plantarum strain BL-17 to promote the activity of the Lactiplantibacillus plantarum strain BL-17, enhancing the competitiveness of the Lactiplantibacillus plantarum strain BL-17 in an organism. The adenylic acid in the combination can promote the growth of the Lactiplantibacillus plantarum strain BL-17, thereby promoting the absorption of exogenous adenylic acid, adenosine, and adenine by the Lactiplantibacillus plantarum strain BL-17 and reducing the intestinal absorption of these purines in rats. The combination of the Lactiplantibacillus plantarum strain BL-17 with the galacto-oligosaccharide and the adenylic acid can attenuate the intestinal absorption of inosine and inosine-related purine compounds, and adenosine and adenosine-related purine compounds. The reduction of intestinal absorption of food-derived purines is important for maintaining a normal serum uric acid level. The combination of the Lactiplantibacillus plantarum strain BL-17 with the galacto-oligosaccharide and the adenylic acid may contribute to the health of patients with a high blood uric acid level and hyperuricemia.

(48) The above are merely preferred embodiments of the present disclosure. It should be noted that a person of ordinary skill in the art may further make several improvements and modifications without departing from the principle of the present disclosure, but such improvements and modifications should be deemed as falling into the protection scope of the present disclosure.