COMPOSITION CONTAINING NICOTINAMIDE MONONUCLEOTIDE AND MOGROSIDE, AND APPLICATION THEREOF

Abstract

The present invention belongs to the medical and technical field and provides a medicine or health food composition of nicotinamide mononucleotide and mogroside. In addition, the present invention also provides the preparation method, formulation and application of the composition.

Claims

1. A pharmaceutical composition comprising nicotinamide mononucleotide and mogroside, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-10:0.1-100; mogroside is mogroside V or a Corsvenor Momordica Fruit extract containing mogroside V; and the method for extracting mogroside includes the following steps: (1) Corsvenor Momordica Fruit is extracted by heating with water and filtered; (2) the filtrate obtained in step (1) is purified with a D101 macroporous resin chromatography column, and the eluent eluted with 35-45% (V/V) ethanol is collected and concentrated; and (3) the concentrated solution obtained in step (2) is purified with an ADS-7 macroporous resin chromatography column, and the eluate eluted with 25-35% (V/V) ethanol is collected and concentrated to dryness.

2. The according to claim 1, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-5:1-30.

3. The according to claim 1, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-2:1-5.

4. The according to claim 1, wherein the content of mogroside V in the said extract is not less than 30% (w/w).

5. The according to claim 1, wherein the content of mogroside V in the said extract is not less than 60% (w/w).

6. A preparation method of the pharmaceutical composition according to claim 1, comprising the step of mixing nicotinamide mononucleotide and mogroside.

7. The method of claim 6, comprising an extraction method of mogroside, which comprises the following steps: (1) Corsvenor Momordica Fruit is extracted by heating with water and filtered; (2) the filtrate obtained in step (1) is purified with a D101 macroporous resin chromatography column, and the eluent eluted with 35-45% (V/V) ethanol is collected and concentrated; and (3) the concentrated solution obtained in step (2) is purified with an ADS-7 macroporous resin chromatography column, and the eluate eluted with 25-35% (V/V) ethanol is collected and concentrated to dryness.

8. A pharmaceutical preparation, comprising the pharmaceutical composition according to, and pharmaceutically acceptable excipients.

9. The pharmaceutical preparation of claim 8, wherein the preparation is a granule.

10. A use of the pharmaceutical composition according to claim 1 in preparation of pharmaceutical preparations for reducing blood glucose, promoting the growth and repair of pancreatic islet cells, preventing and treating hyperglycemia, and/or preventing and treating diabetes.

11. A use of the pharmaceutical composition according to claim 1 in preparation of pharmaceutical preparations for controlling fat accumulation and body weight, preventing and treating hyperlipidemia, and/or preventing and treating cardiovascular diseases.

12. A health food composition comprising nicotinamide mononucleotide and mogroside, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-10:0.1-100; mogroside is mogroside V or a Corsvenor Momordica Fruit extract containing mogroside V; and the method for extracting mogroside includes the following steps: (1) Corsvenor Momordica Fruit is extracted by heating with water and filtered; (2) the filtrate obtained in step (1) is purified with a D101 macroporous resin chromatography column, and the eluent eluted with 35-45% (V/V) ethanol is collected and concentrated; and (3) the concentrated solution obtained in step (2) is purified with an ADS-7 macroporous resin chromatography column, and the eluate eluted with 25-35% (V/V) ethanol is collected and concentrated to dryness.

13. The composition according to claim 12, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-5:1-30.

14. The composition according to claim 12, wherein the molar ratio of nicotinamide mononucleotide:mogroside is 1-2:1-5.

15. The composition according to claim 12, wherein the content of mogroside V in the said extract is not less than 30% (w/w).

16. The composition according to claim 12, wherein the content of mogroside V in the said extract is not less than 60% (w/w).

17. A preparation method of the health food composition according to claim 12, comprising the step of mixing nicotinamide mononucleotide and mogroside.

18. The method according to claim 17, further comprising an extraction method of mogroside, which comprises the following steps: (1) Corsvenor Momordica Fruit is extracted by heating with water and filtered; (2) the filtrate obtained in step (1) is purified with a D101 macroporous resin chromatography column, and the eluent eluted with 35-45% (V/V) ethanol is collected and concentrated; and (3) the concentrated solution obtained in step (2) is purified with an ADS-7 macroporous resin chromatography column, and the eluate eluted with 25-35% (V/V) ethanol is collected and concentrated to dryness.

19. A health food, comprising the health food composition according to claim 12, and food acceptable excipients.

20. The health food of claim 19 wherein the health food is a dairy product, a beverage or a biscuit.

Description

DESCRIPTION OF THE DRAWINGS

[0031] FIG. 1 shows the results of the establishment of the alloxan cell damage model, where ΔP<0.05 and ΔΔP<0.01, compared with the negative control group.

[0032] FIG. 2 shows the effect of GX999 on the survival rate of pancreatic islet cells damaged by alloxan, where, ΔP<0.05, ΔΔP<0.01 compared with the negative control group; *P<0.05, **P<0.01 compared with the alloxan damage group.

[0033] FIG. 3 shows the combination index CI value of GX999 with alloxan. 1: GX999 0.5 mM; 2: GX9991 mM; 3: GX999 5 mM; 4: GX999 10 mM.

[0034] FIG. 4 shows the effect of GX008A on the survival rate of alloxan-damaged islet cells, where ΔP<0.05 and ΔΔP<0.01, compared with the negative control group; *P<0.05, **P<0.01 compared with the alloxan damage group.

[0035] FIG. 5 shows the combination index CI value of GX008A with alloxan, wherein 1: GX008A 0.5 mM; 2: GX008A 1 mM; 3: GX008A 5 mM; 4: GX008A 10 mM.

[0036] FIG. 6 shows the effect of GX999 1 mM in combination with GX008A on the survival rate of alloxan-damaged islet cells, where ΔP<0.05 and ΔΔP<0.01, compared with the negative control group; *P<0.05, **P<0.01 compared with the alloxan damage group.

[0037] FIG. 7 shows the CI value of the combination index of GX008A/GX999 to alloxan, where 1: GX008A 0.5 mM+GX999 1 mM; 2: GX008A 1 mM+GX999 1 mM; 3: GX008A 5 mM+GX999 1 mM; 4: GX008A 10 mM+GX999

[0038] FIG. 8 shows the effect of GX999 on the survival rate of 3T3L1 cells, where *P<0.05 and **P<0.01, compared with the negative control group.

[0039] FIG. 9 shows the effect of GX008A on the survival rate of 3T3L1 cells, where *P<0.05 and **P<0.01, compared with the negative control group

[0040] FIG. 10 shows the effect of the combination of GX008A/GX999 on the survival rate of 3T3L1 cells, where *P<0.05, **P<0.01 compared with the negative control group; #P<0.05, ##P<0.01 compared with 10 mM GX999 group; ΔP<0.05 compared with GX008A alone group.

[0041] FIG. 11 shows the CI value of the GX008A/GX999 combination index, where 1: 5 mM GX008A+10 mM GX999, 2: 10 mM GX008A+10 mM GX999, 3: 30 mM GX008A+10 mM GX999, 4: 50 mM GX008A+10 mM GX999.

[0042] FIG. 12 shows the effect of GX999/GX008A on the differentiation of 3T3L1 cells.

[0043] FIG. 13 shows the effect of GX008A/GX999 on the differentiation of 3T3L1 cells, where *P<0.05, **P<0.01 compared with the differentiation group; ΔP<0.05 compared with the GX999/GX008A alone group.

DETAILED DESCRIPTION

[0044] The following embodiments further illustrate the content of the present invention. Unless otherwise specified, the technical means used in the embodiments are conventional means well-known to those skilled in the art and commercially available common instruments and reagents, and the manufacturer's instructions for the corresponding instruments and reagents can be referred to.

Preparation Embodiment. Preparation of Mogroside Extract (60% MGV)

[0045] 15 kg of fresh Corsvenor Momordica Fruit (MGV content was about 1.2%) was treated with high temperature steam, crushed with a pulverizer, and 80L of water was added, heated to boil, filtered, and the filtrate was kept for later use. After adding 60L of water to the filter residue, it was heated to boil, filtered, and 2 filtrates were combined; the combined filtrate was loaded on a D101 macroporous resin chromatography column equilibrated with deionized water, and first eluted with deionized water and 20% (V/V) ethanol until colorless, and then eluted with 6 times the column volume of 40% (V/V) ethanol, and the eluate was concentrated under reduced pressure until there was no alcohol; then the concentrated solution was loaded on an ADS-7 macroporous resin chromatography column equilibrated with deionized water, and eluted with 8 times the column volume of deionized water, and then eluted with 5 times the column volume of 30% (V/V) ethanol, the ethanol eluate was collected, and concentrated and dried to obtain the mogroside extract of the present invention (abbreviated as 60% MGV). The above preparation process was repeated in multiple batches, the MGV content was between 60.2 and 62.5%, and the composition was stable, all greater than 60%.

[0046] Embodiment 1. The protective effect of MG (GX008A) and NMN (GX999) on alloxan-induced (3 cell damage and the combination effect of the two compounds

[0047] In the experiment of this embodiment, GX999 or GX008A alone and GX999 and GX008A in combination were used to evaluate the protective effects of GX999 and GX008A on alloxan-induced (3 cell damage. The experimental results showed that GX999 and GX008A alone had a protective effect on damaged cells within a certain concentration range. When 1 mM GX999 was combined with different concentrations of GX008A, it had a significant protective effect on damaged cells, and the combination had a synergistic protective effect.

1. Purpose of Experiment

[0048] In vitro experiments were used to study the protective effects of GX008A and GX999 on the islet β-cell damage caused by alloxan, and to explore the combination effect of the two.

2. Materials and Methods

2.1 Materials

2.1.1 Test Article

[0049] Name: Mogroside V, number GX008A, MW: 1287.44; Nicotinamide mononucleotide, number: GX999, MW: 334.22.

[0050] Source: GX008A was provided by Beijing Huibaoyuan Biotechnology Co., Ltd.; GX999 was purchased from Bontac Bio-engineering (Shenzhen) Co., Ltd.

[0051] Storage conditions: dry, protected from light, and stored at 4° C.

2.1.2 Cell Line

[0052] Rat insulinoma cells (RINm5f): purchased from the Basic Medical Cell Center, Institute of Basic Medicine, Chinese Academy of Medical Sciences.

2.1.3 Experimental Reagents

[0053] Fetal bovine serum (FBS) and RPMI1640 basal medium were purchased from GBICO, USA; Methyl thiazolyl tetrazolium (MTT), dimethyl sulfoxide (DMSO), and alloxan were purchased from Beijing Solarbio Science & Technology Co., Ltd.

2.2 Test Method

2.2.1 Cell Culture

[0054] RINm5f cells were inoculated in RPMI1640 culture medium containing penicillin, streptomycin, and 10% inactivated fetal bovine serum.

[0055] Culture was carried out at 37° C., 5% CO2, and saturated humidity, and cell growth was observed under an inverted microscope. After the cells grew to 80%-90% of the wall of the bottle, passage was performed.

2.2.2 Grouping and Treatment

[0056] RINm5F cells were cultured to the logarithmic growth phase, inoculated in 96-well culture plates at a cell density of 5×104/ml, cultured for 24 hours, and then drugs were added. The experiment was divided into a negative control group, an alloxan damage group (AXN group) and a protection group. Both the AXN group and the protection group were added with alloxan at a final concentration of 15 mM, and the protection group was added with different concentrations of GX999 and GX008A, pretreated for 1h. The experiment set up 4 duplicate wells and the experiment was repeated three times.

[0057] GX008A and GX999 were dissolved in the culture medium and freshly prepared. The final concentration was 200 mM and 500 mM.

2.2.3 Experimental Procedure

[0058] Cell Viability Assay-MTT Method:

[0059] RINm5F cells were cultured to the logarithmic growth phase, inoculated in 96-well culture plates at a cell density of 5×104/ml, cultured for 24 hours, and then drugs were added. The experiment was divided into a negative control group, an alloxan damage group (AXN group) and a protection group. Both the AXN group and the protection group were added with alloxan at a final concentration of 15 mM, and the protection group was added with different concentrations of GX999 and GX008A, pretreated for 1h. The experiment set up 4 duplicate wells and they were placed in a carbon dioxide incubator for regular culture for 24 hours. MTT 20 ul (5 mg/mL) was added to each well and incubated for 4 hours. Then the culture medium was discarded, 150 ul DMSO was added to each well and shaken for 10 minutes, and the OD value of the optical density was detected at 490 nm with a microplate reader.

[0060] CI Analysis of Drug Combination Index:

[0061] According to the inhibition rates of different concentrations of drugs alone and in combination, the Calcusyn software was used to analyze and process data such as the inhibition rates of GX999 and GX008A alone at different concentrations and the inhibition rates in combination at corresponding concentrations to obtain the combination index (CI) value. According to the definition of combination index, the synergistic effect of drugs was judged, and the synergistic effect is indicated by less than 1.0, and the antagonistic effect is indicated by greater than 1.0.

2.2.4 Statistical Methods

[0062] All experimental data were from at least 3 independent experiments and were expressed as mean±standard deviation. Statistical analysis was performed using SPSS16.0 software. Two-independent-sample t-test was used for data comparison between the two groups. One-way analysis of variance was used for data comparison between multiple groups. P<0.05 was considered statistically significant.

3. Experimental Results

[0063] Establishment of Alloxan Cell Damage Model

[0064] The experiment set up a negative control group and a damage group with different concentrations of alloxan (concentrations of 4 mM, 7 mM, 10 mM, 15 mM, 20 mM), after 24 hours of exposure, then 4 duplicate wells were set up, and the MTT method was used to detect the cell survival rate. The results are shown in FIG. 1. As the concentration of the drug increased, the rate of cell damage increased, which inhibited cell proliferation in a concentration-dependent manner. Compared with the blank control group, the P value was less than 0.01, and the difference was statistically significant.

[0065] Protective Effect of GX999 Alone on Alloxan-Damaged RINm5f Cells

[0066] The MTT method was used to detect the effect of GX999 on the cell survival rate of alloxan-damaged pancreatic β-cells. According to the above experimental results, the concentration of alloxan was selected as 15 mM, and the experiment was divided into negative control group, alloxan damage group (AXN group) and GX999 (0.5, 1, 5, 10 mM) protection group. The results are shown in FIG. 2. Compared with the negative control group, the cell survival rate of the AXN group was significantly reduced, and the difference was statistically significant (P<0.01); after adding GX999 treatment, the cell survival rate could be significantly improved, and with the increase of the concentration of the protection group, the cell survival rate gradually increased. Compared with the AXN group, when the concentration of GX999 was 5 mM (P<0.05), 10 mM (P<0.01), the difference was statistically significant.

[0067] Analysis of the Effect of GX999 on Alloxan

[0068] Calcusyn software was used for calculation, and the results are shown in FIG. 3. The CI value of GX999 with alloxan was all greater than 1.0, indicating that GX999 has an antagonistic effect on alloxan, that is, GX999 antagonizes alloxan-induced damage and plays a cytoprotective effect.

[0069] Protective Effect of GX008A Alone on Alloxan-Damaged RINm5f Cells

[0070] The MTT method was used to detect the effect of GX008A on the cell survival rate of alloxan-damaged pancreatic β-cells. The experiment was divided into negative control group, alloxan damage group (AXN group) and GX008A (0.5, 1, 5, 10 mM) protection group. The results are shown in FIG. 4. Compared with the negative control group, the cell survival rate of the AXN group was significantly reduced, and the difference was statistically significant (P<0.01); after adding GX008A treatment, the cell survival rate could be significantly improved, and with the increase of the concentration of the protection group, the cell survival rate gradually increased. Compared with the AXN group, when the concentration of GX008A was 5 mM (P<0.05), 10 mM (P<0.01), the difference was statistically significant.

[0071] Analysis of the Effect of GX008A on Alloxan

[0072] Calcusyn software was used for calculation, and the results are shown in FIG. 5. The CI value of GX008A with alloxan was all greater than 1.0, indicating that GX008A has an antagonistic effect on alloxan, that is, GX008A antagonizes alloxan-induced damage and plays a cytoprotective effect.

[0073] Protective Effect of GX008A/GX999 Combination Application on Alloxan-Damaged RINm5f Cells

[0074] MTT method was used to detect the effect of GX008A/GX999 combination application on the cell survival rate of alloxan-damaged pancreatic β-cells. The experiment was divided into negative control group, alloxan damage group (AXN group) and GX999 (1 mM) combined with GX008A (0.5, 1, 5, 10 mM) protection group. The results are shown in FIG. 6. Compared with the negative control group, the cell survival rate of the AXN group was significantly reduced, and the difference was statistically significant (P<0.01); the combination protection group could increase the survival rate of the cells and with the increase of the concentration, the cell survival rate gradually increased. Compared with the AXN group, the differences with GX999 (1 mM) combined with GX008A 1 mM (P<0.05), 5 mM and 10 mM (P<0.01) were statistically significant.

[0075] Analysis of the Combination Effect of GX008A/GX999

[0076] The combination application efficiency was calculated using Calcusyn software. The results are shown in FIG. 7. When the combination protection group was compared with the single-drug protection group, drug combination index CI of GX999 (1 mM) combined with GX008A 1 mM, 5 mM<1.0, suggesting that GX999 and GX008A have a synergistic protective effect on alloxan-induced damage.

4. Experimental Conclusion

[0077] The experimental results showed that GX999 and GX008A alone had a protective effect on damaged cells within a certain concentration range. When 1 mM GX999 was combined with different concentrations of GX008A, it had a significant protective effect on damaged cells, and the combination had a synergistic protective effect.

[0078] Embodiment 2. The effect of mogroside (MG, GX008A) and nicotinamide mononucleotide (NMN, GX999) on the differentiation of 3T3-L1 preadipocytes and the combination effect of the two compounds

[0079] The experiment of this embodiment used GX999 or GX008A alone, and GX999 and GX008A in combination to evaluate the effects of GX999 and GX008A on the proliferation of preadipocytes. The experimental results showed that GX999 and GX008A can inhibit the proliferation of 3T3L1 adipocytes with a concentration-dependent effect. The combination application of the two drugs can synergistically inhibit cell proliferation; GX999 and GX008A can significantly inhibit the adipogenesis of adipocytes, and the combination application can synergistically inhibit adipogenesis to a certain extent, that is, the combination application has a synergistic inhibitory effect on the differentiation of 3T3L1 preadipocytes.

1. Purpose of Experiment

[0080] To study the effects of GX008A and GX999 on the proliferation and differentiation of 3T3-L1 preadipocytes, and observe the combination effect of the two compounds.

2. Materials and Methods

2.1 Materials

2.1.1 Test Article

[0081] Same as embodiment 1.

2.1.2 Cell Line

[0082] 3T3-L1 cell line: purchased from the Basic Medical Cell Center, Institute of Basic Medicine, Chinese Academy of Medical Sciences.

2.1.3 Experimental Reagents

[0083] Calf calf serum (CS), fetal bovine serum (FBS), and DMEM basal medium were purchased from GBICO, USA; IBMX, dexamethasone, and insulin were purchased from SIGMA, USA; oil red O powder, tetramethylazazole blue (MTT) was purchased from Beijing Solarbio Science & Technology Co., Ltd.

2.2 Test Method

2.2.1 Cell Culture

[0084] 3T3L1 cells were placed in DMEM high-glucose medium containing 10% calf serum and cultured at 37° C. and 5% CO2. When the cells reached 90% confluence, they were digested with 0.25% trypsin, passaged, and inoculated in a 96-well cell culture plate.

2.2.2 Grouping and Treatment

[0085] GX008A and GX999 were dissolved in the culture medium and freshly prepared. The final concentration was 200 mM and 500 mM.

2.2.3 Experimental Procedure

[0086] Cell Viability Assay-MTT Method:

[0087] The logarithmic growth phase cells were taken and inoculated in a 96-well plate at a density of 5×103 cells/mL, with 4 replicate wells in each group. After the cells grew to about 40%-50% confluence, the fresh drug-containing medium was replaced with and they were divided into a GX999 alone group, a GX008A group, and a GX999+GX008A combination group. After culturing for 48h, MTT 20 ul (5 mg/mL) was added to each well and incubated for 4h. Then the culture medium was discarded, 150 ul DMSO was added to each well and shaken for 10 minutes, and the OD value of the optical density was detected at 490 nm with a microplate reader, and the cell survival rate was calculated according to the formula. [0113] Analysis of drug synergy:

[0088] Combination method: 10 mM GX999 in combination with GX008A (0, 5, 10, 30, 50 mM) group. According to the inhibition rates of different concentrations of drugs alone and in combination, the Calcusyn software was used to analyze and process data such as the inhibition rates of GX999 and GX008A alone at different concentrations and the inhibition rates in combination at corresponding concentrations to obtain the combination index (CI) value. According to the definition of combination index, the synergistic effect of drugs was judged, and the synergistic effect is indicated by less than 1.0, and the antagonistic effect is indicated by greater than 1.0.

[0089] Induction of Differentiation Experiment of Adipocytes:

[0090] 2 days after the 3T3-L1 preadipocytes grew to complete confluence, the induction of differentiation began. That is, the DMEM complete medium was discarded, and replaced with DMEM complete medium containing 5 ug/ml insulin, 0.5 mM IBMX, 1 uM dexamethasone, and after 2 days, it was replaced with DMEM complete culture medium containing 5 ug/ml insulin and cultured for 2 days. Then DMEM complete culture medium was used to continue culturing for 2 days. From the first day of differentiation, the experimental group was given a culture medium containing 10 mM GX999 or 10 mM GX008A to intervene in the whole process of cell differentiation, and the control group was added with conventional inducers.

[0091] Oil Red O Staining:

[0092] After 8 days of induced differentiation, the cells were fixed with 4% paraformaldehyde for 30 minutes, washed 3 times with balanced salt solution (PBS), incubated with oil red O staining solution for 60 minutes, the pipetted liquid was rinsed 3 times with PBS, and observed for the formation of lipid droplets under an inverted microscope and a video was taken. Isopropanol (200 ul per well) was added, and the absorbance at A490 nm was measured with a microplate reader after 5 minutes.

2.2.4 Statistical Methods

[0093] All experimental data were from at least 3 independent experiments and were expressed as mean±standard deviation. Statistical analysis was performed using SPSS16.0 software. Two-independent-sample t-test was used for data comparison between the two groups. One-way analysis of variance was used for data comparison between multiple groups. P<0.05 was considered statistically significant.

3. Experimental Results

[0094] The Effect of GX999 on the Proliferation of 3T3L1 Preadipocytes

[0095] The MTT method was used to detect the cell survival rate. The results are shown in FIG. 8. When GX999 (0, 10, 20, 40, 60 mM) was used alone to treat 3T3L1 cells for 48 hours, as the drug concentration increased, the survival rate of 3T3L1 cells decreased, and it inhibited cell proliferation in a concentration-dependent manner. Compared with the blank control group, the P values were all less than 0.01, and the differences were statistically significant. According to the above inhibition rate, the IC50 of GX999 was 51.7±1.5 mM.

[0096] The Effect of GX008A on the Proliferation of 3T3L1 Preadipocytes

[0097] The results are shown in FIG. 9. When GX008A (0, 5, 10, 30, 50, 100, 200 mM) was used alone to treat 3T3L1 cells for 48 hours, as the drug concentration increased, the survival rate of 3T3L1 cells decreased, and it inhibited cell proliferation in a concentration-dependent manner. Compared with the blank control group, the P values were all less than 0.01, and the differences were statistically significant.

[0098] The Effect of GX008A Combined with GX999 on the Proliferation of 3T3L1 Preadipocytes

[0099] When GX008A and GX999 acted alone, with the increase of the concentration of administration, the growth inhibitory effect on 3T3L1 preadipocytes also gradually increased, showing an obvious dose-dependent effect relationship. When 10 mM GX999 was used in combination with different concentrations of GX008A (0, 5, 10, 30, 50 mM), the results are shown in FIG. 10 (only part of data in the GX008A alone group shown in FIG. 9 is listed for visual comparison). With the increase of the concentration of GX008A, the combination inhibitory effect of the two showed an increasing trend; compared with the single-agent group, the inhibitory effect of GX999 combined with GX008A 10, 30, and 50 mM was significantly greater than that of the 10 mM GX999 group (P<0.01) and GX008A alone group (P<0.05).

[0100] Synergy Analysis of 10 mM GX999 Combined with GX008A:

[0101] Using Calcusyn software for calculation, the results are shown in FIG. 11. The CI values of 10 mM GX999 combined with GX008A were all less than 1.0, suggesting that the combination of the two drugs has a synergistic effect. GX008A can have a synergy with GX999 to inhibit the growth of 3T3L1 preadipocytes to a certain extent.

[0102] Effect of GX999/GX008A on the Differentiation of Preadipocytes

[0103] Based on the results of the above-mentioned combination application experiment, the drug concentration and combination concentration were selected. During the induction of differentiation, 10 mM GX999, 10 mM GX008A, 10 mM GX999+10 mM GX008A were added and treated for 8 days, stained with Oil Red 0, observed and photographed under a microscope, and Oil Red 0 was extracted with isopropanol, the OD value was read. FIG. 12 shows exemplary photos of each group. FIG. 13 shows the quantitative lipid droplet content, indicating that GX999 and GX008A alone or in combination can inhibit adipogenesis. Compared with the differentiation group, the lipid droplet content in cells was significantly reduced (P<0.01); the lipid droplet content of the GX008A/GX999 combination group was significantly lower than that of the single-agent group (P<0.05).

4. Experimental Conclusion

[0104] The experimental results indicated that: GX999 and GX008A can inhibit the proliferation of 3T3L1 adipocytes with a concentration-dependent effect. The combination application of the two drugs can synergistically inhibit cell proliferation; GX999 and GX008A can significantly inhibit the adipogenesis of adipocytes, and the combination application can synergistically inhibit adipogenesis to a certain extent, that is, the combination application has a synergistic inhibitory effect on the differentiation of 3T3L1 preadipocytes.

[0105] Embodiment 3. Hypoglycemic effect of mogroside (60% MGV) and nicotinamide

[0106] mononucleotide (NMN, GX999)

[0107] 1. Preparation of Test Samples

[0108] (1) Preparation of NMNMG200 [0109] 20 g of NMN (purity 98%) and 0.5 g of 60% MGV (prepared in the foregoing preparation embodiment) were dissolved into 100 ml of an aqueous solution containing 10% glycerol to prepare NMNMG200.

[0110] (2) Preparation of NMN200 [0111] 20 grams of NMN (98% purity) was dissolved into 100 ml of 10% glycerin-containing aqueous solution to prepare NMN200.

[0112] (3) Preparation of MG5 [0113] 0.5 g of 60% MGV (prepared in the foregoing preparation embodiment) was dissolved into 100 ml of 10% glycerin-containing aqueous solution to prepare MG5.

[0114] 2. Blood Glucose Effect Test Before Lunch

[0115] Volunteers with pre-meal blood glucose>6.0 in the morning were tested for fasting blood glucose (Om) every morning, and then they took 1 ml of NMNMG200, NMN200 or MG5 prepared in embodiment 1; method of administration: 1 ml of the solution was added into 100 ml of drinking water and was drunk by them and then the blood glucose levels for 30 minutes (30 min) and 60 minutes (60 min) were measured respectively. The results are shown in Table 1:

TABLE-US-00001 TABLE 1 Tests of blood glucose levels of volunteers taking different samples Number within Admin- Admin- Admin- the istration istration istration Sample name group Gender Age at 0 min at 30 min at 60 min NMNMG200 001 60 6.6 6.3 6.3 002 61 6.5 6.1 6.0 003 60 6.3 5.9 5.9 NMN200 001 60 6.3 6.3 6.5 002 63 6.6 6.5 6.5 003 60 7.2 7.1 7.1 004 50 5.9 6.3 6.6 MG5 001 60 6.2 6.2 6.2 002 63 6.5 6.5 6.5 003 63 6.7 6.7 6.7

[0116] As described in the above experimental procedure, the volunteers with the usual blood glucose before meals in the morning>6.0 were chosen to test the pre-meal fasting blood glucose in the morning. The time of taking NMNMG200 was about 1 hour before going to bed every night, and the blood glucose level was tested after taking it. The results are shown in Table 2: [0148] Table 2 Test results of blood glucose levels of volunteers before and after taking NMNMG200

TABLE-US-00002 Volunteer Before After Number Gender administration administration 001 Male 6.3 4.8 002 Male 6.5 5.4 003 Male 6.7 5.6 004 Male 6.6 5.2

[0117] The results show that the combined use of mogroside and nicotinamide mononucleotide has the effect of lowering blood glucose.