CN114028434A - A composition for treating diabetes - Google Patents

A composition for treating diabetes Download PDF

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CN114028434A
CN114028434A CN202110012077.0A CN202110012077A CN114028434A CN 114028434 A CN114028434 A CN 114028434A CN 202110012077 A CN202110012077 A CN 202110012077A CN 114028434 A CN114028434 A CN 114028434A
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composition
diabetes
selenium
chromium
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周游
于慧敏
高艳杰
周广刚
张常胜
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Heilongjiang Ruzhong Medical Technology Co ltd
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Abstract

The invention provides a composition for treating diabetes, and belongs to the technical field of medicines. The invention comprises the following components in percentage by mass: 5 to 60 percent of beta-nicotinamide mononucleotide, 5 to 60 percent of chromium-enriched yeast, 5 to 60 percent of selenium-enriched yeast, 5 to 60 percent of agaricus blazei polysaccharide and 5 to 60 percent of coenzyme Q10. The preparation method comprises the following steps: mixing the above materials, and making into capsule or tablet. The composition for treating diabetes provided by the invention can activate insulin activity, treat and prevent various types of diabetes, prevent and assist in treating various tumors, inhibit viruses, improve the immunity of organisms, strengthen heart and liver, regulate blood pressure, keep young and shape, and delay aging.

Description

A composition for treating diabetes
Technical Field
The invention relates to a composition for treating diabetes, and belongs to the technical field of medicines.
Background
Diabetes is a group of metabolic diseases characterized by hyperglycemia. Hyperglycemia is caused by a defect in insulin secretion or an impaired biological action, or both. The chronic hyperglycemia results in chronic damage and dysfunction of various tissues, particularly eyes, kidneys, heart, blood vessels and nerves.
Diabetes is prevalent worldwide and the number of patients is increasing dramatically. The prevalence rate of diabetes in China is increased from 0.67% in early 1980 to 9.7% in 2008, and the prevalence rate is increased by 13 times in nearly 30 years. According to the diabetes map published by International Diabetes Federation (IDF) in 2017, nearly 4.25 million people worldwide have diabetes in 2017, of which 80% are in mid-low income countries and one third are elderly people over 65 years old; if no positive action is taken, the number of diabetic patients in 2045 years will reach 6.29 billion. Wherein southeast Asia and western Tai district are serious areas of diabetes, and 1.21 hundred million diabetics exist in China. In adults over 18 years of age in our country, there are 1 diabetic patient per 10 and 1 pre-diabetic patient per 3. On one hand, the incidence of diabetes in China tends to be younger, and the diabetes in rural people is rapidly increased. On the other hand, the absolute number of diabetic patients continues to increase with the aging population and the life span of diabetic patients. Epidemiological survey results at home and abroad show that about one fourth of people over 60 years old suffer from diabetes; by age 80, the probability of diabetes can be as high as one-half. In addition, more huge people in the early stage of diabetes mellitus are provided, more than half of the middle-aged and the elderly in China have abnormal sugar metabolism, and the people are the people in diabetes mellitus or the people in the early stage of diabetes mellitus.
Diabetic complications are what cause disability and death and serious economic burden to diabetic patients. Very few of those with diabetes will actually die of severe hyperglycemia, and approximately two-thirds to three-quarters of those with diabetes will die of cardiovascular and cerebrovascular complications. Diabetes is the first cause of blindness in developed countries and is about the second cause in our country. One-third to forty percent of patients undergoing hemodialysis are due to diabetic nephropathy. According to our investigation, after removing malignant tumor in non-invasive amputation in large hospitals in China, about one half of the amputation is caused by diabetes. Diabetic neuropathy can cause multiple organ and tissue lesions, seriously reducing the quality of life of patients, and serious painful neuropathy can make patients feel undried. I have seen cases of diabetes suicided for severe painful neuropathy. Recent published investigations of large samples have shown that diabetics in our country die on average 7 years earlier than those without diabetes.
At present, no safe and definite diabetes product which can be adjusted from a whole body system to a healthy state to recover the functions of the pancreatic islets and finally replace injected insulin and oral hypoglycemic drugs exists all over the world.
Research and development of safe, healthy and effective revolutionary products for diabetes mellitus are the leading directions of research of new drugs and are urgent demands of the sick population all over the world.
Disclosure of Invention
The present invention has been made to solve the above-mentioned problems occurring in the prior art, and an object of the present invention is to provide a composition for treating diabetes.
The purpose of the invention is realized by the following technical scheme:
the composition for treating diabetes comprises the following components in percentage by mass: 5 to 60 percent of NMN (beta-nicotinamide mononucleotide), 5 to 60 percent of chromium-enriched yeast, 5 to 60 percent of selenium-enriched yeast, 5 to 60 percent of agaricus blazei polysaccharide and 5 to 60 percent of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 5 to 50 percent of NMN (beta-nicotinamide mononucleotide), 5 to 50 percent of chromium-enriched yeast, 5 to 50 percent of selenium-enriched yeast, 5 to 50 percent of agaricus blazei polysaccharide and 5 to 50 percent of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 5 to 45 percent of NMN (beta-nicotinamide mononucleotide), 5 to 45 percent of chromium-enriched yeast, 5 to 45 percent of selenium-enriched yeast, 5 to 45 percent of agaricus blazei polysaccharide and 5 to 45 percent of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 15% of NMN (beta-nicotinamide mononucleotide), 25% of chromium-rich yeast, 25% of selenium-rich yeast, 25% of agaricus blazei polysaccharide and 10% of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 20% of NMN (beta-nicotinamide mononucleotide), 20% of chromium-rich yeast, 20% of selenium-rich yeast, 20% of agaricus blazei polysaccharide and 20% of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 15% of NMN (beta-nicotinamide mononucleotide), 35% of chromium-rich yeast, 15% of selenium-rich yeast, 25% of agaricus blazei polysaccharide and 10% of coenzyme Q10.
Preferably, the composition comprises the following components in percentage by mass: 10% of NMN (beta-nicotinamide mononucleotide), 35% of chromium-rich yeast, 15% of selenium-rich yeast, 25% of agaricus blazei polysaccharide and 15% of coenzyme Q10.
The invention also provides a preparation method of the diabetes treatment product, which comprises the following steps: mixing the above materials, and making into capsule or tablet.
Preferably, the weight of the capsule is 0.45-0.55 g.
The invention has the beneficial effects that:
the invention provides a composition for treating diabetes and a preparation method thereof, wherein the composition comprises the following components in percentage by mass: 5 to 60 percent of NMN (beta-nicotinamide mononucleotide), 5 to 60 percent of chromium-rich yeast, 5 to 60 percent of selenium-rich yeast, 5 to 60 percent of agaricus blazei polysaccharide and 105 to 60 percent of coenzyme Q.
The composition I is as follows: NMN (beta-nicotinamide mononucleotide)
NMN is an abbreviation for β -nicotinamide mononucleotide, occurs naturally in living cells, and is a precursor of coenzyme 1NAD + (nicotinamide adenine dinucleotide). The life can be properly prolonged. What really plays an anti-aging role is an important energy metabolite called nicotinamide adenine dinucleotide (NAD +).
With age, a decrease in NAD + levels leads to a decrease in DNA repair capacity, accumulation of DNA damage, driving the aging process. NAD + participates in cellular respiration and promotes energy metabolism (e.g., oxidation of glucose, fats, amino acids). NAD + is not only a coenzyme for hundreds of redox reactions in living cells, but it is also involved as a substrate in regulating various physiological functions such as cell survival, apoptosis, DNA repair, immune response, circadian rhythm, and the like.
NMN is a nutrient that is converted to NAD + in cells, is classified as a novel vitamin B3, and surpasses the efficacy of common vitamins, and is considered as a supplement for preventing aging and restoring youth. Since their discovery in 1906, NAD + has received scientific attention due to its abundance in the human body and its key role in the molecular pathways that maintain human functioning. In animal studies, increasing the level of NAD + in vivo has shown encouraging results in the areas of research such as metabolism and age-related diseases, and even certain anti-aging properties. Age-related diseases such as diabetes, cardiovascular disease, neurodegeneration and a general decline of the immune system.
And (2) component two: chromium-rich yeast
The natural blood sugar regulator has the functions of activating insulin activity, regulating blood sugar and inhibiting the conversion of sugar into fat.
The main function of chromium-rich yeast
Enhance insulin activity and control blood sugar. Can regulate fat storage amount and help reduce weight. Reducing blood cholesterol and triglyceride content, and preventing cardiovascular diseases. It has the main functions as follows:
1. reducing blood sugar of diabetic patients, improving hypoglycemia reaction, regulating blood sugar, controlling diabetes effectively, and eliminating abnormal phenomena of glucose tolerance.
2. Can obviously reduce serum cholesterol level of the calluses and relieve arteriosclerosis symptoms.
3. Can be used for correcting abnormal sugar tolerance of children with chromium deficiency and patients with long-term parenteral nutrition.
4. Can effectively increase human muscle and reduce fat.
5. The addition of chromium to the growing/finishing pig ration can significantly improve carcass lean meat percentage, improve feed conversion rate, reduce back fat thickness, and improve breeding performance of sows and survival rate of piglets.
6. Can increase laying rate of laying hens, reduce egg cholesterol, increase growth speed of broiler chickens, and reduce fat content of breast muscle.
7. Can improve animal endocrine and enhance anti-stress capability.
The chromium-rich yeast has the advantages that:
1. toxicity tests prove that the yeast chromium is safe to eat and has no toxicity.
2. The yeast chromium contains bioactive chromium with high human body absorptivity, wherein the absorptivity is 311% of methylpyridine chromium and 672% of chromium chloride.
3. The yeast chromium is rich in protein, sugar and B vitamins, and can be used as a chromium source and also provide other beneficial nutrients.
4. The yeast chromium can be industrially produced in a large scale, has low production and taking cost and is easy to popularize.
The composition III: selenium-enriched yeast
Selenium-enriched yeast is added with selenium element in the process of culturing yeast, and the selenium is absorbed and utilized during the growth of the yeast, so that the selenium is organically combined with protein and polysaccharide in the yeast body and converted into biological selenium, thereby eliminating the toxic and side reaction and the gastrointestinal stimulation of chemical selenium (such as sodium selenite) to a human body, and enabling the selenium to be absorbed and utilized by the human body more efficiently and more safely. The selenium-enriched yeast is the most efficient, safest and balanced nutritional selenium supplement preparation at home so far. Selenium is a trace element necessary for human bodies, has important physiological functions and is closely related to the health of human beings. Selenium can prevent and inhibit tumor, resist aging, maintain normal function of cardiovascular system, and prevent arteriosclerosis and coronary heart disease. Selenium deficiency can cause keshan disease and large bone disease, and can also induce cataract, liver disease, pancreatic disease, etc. Selenium stimulates the production of immunoglobulins and enables various immune functions of the human body such as: cellular immunity, humoral immunity, non-specificity, etc. are improved. The blood selenium of the diabetics is obviously lower than that of normal people. Selenium supplement can lower blood glucose level and increase GPX activity. Selenium has insulin-like action and can stimulate transport of glucan carrier in fat cell membrane. The glutathione peroxidase activity in the body of a diabetic is at an extremely low level, the activity is lower as the disease time is longer, and the selenium-rich yeast is taken regularly, so that the effects of protecting and recovering pancreas functions can be achieved, the metabolic regulation of the diabetes mellitus can be improved, and the level of the glucosylated hemoglobin in urine can be reduced. Therefore, the selenium-enriched yeast is a very ideal functional food base material, and has a very wide development prospect, just as the authoritative doctor fieldry of trace elements in the world: "selenium is like an atomic bomb, the quantity is very small, the action and power are very large, once recognized, it will have profound effect on health".
The component IV is as follows: agaricus blazei Murill polysaccharide
The Agaricus blazei Murill polysaccharide is effective active ingredient extracted from high-quality Agaricus blazei Murill fruiting body, has fragrant smell, remarkable effect, and effects of enhancing energy, inhibiting growth of tumor cells, resisting tumor, and absorbing and eliminating carcinogenic substances. It also has effects in lowering blood sugar, improving diabetes, reducing cholesterol, and improving arteriosclerosis. The pharmacological actions thereof have been confirmed mainly as follows: anti-tumor effect, immunoregulation effect, cell repairing effect, and acid-base balance regulation. The agaricus blazei polysaccharide has wide food therapy and clinical symptom improvement range. Not only has obvious effects on enhancing immunity, preventing cancer and resisting cancer, but also has obvious effects on hypertension, thrombus, arteriosclerosis and the like of a circulatory system; for gastritis, gastric ulcer, hepatomegaly, enteritis, renal insufficiency, etc. of digestive system; diabetes, allergy, high cholesterol, etc. to the endocrine system; has certain dietotherapy effect and symptom improving effect on bought bronchitis, asthma and the like of a respiratory system, gynecological diseases of a reproductive system, climacteric syndrome and the like. Agaricus blazei polysaccharide has been used in Japan for treating 4 cases of cancer, 2 cases of diabetes, 3 cases of hemorrhoid, 1 case of neuralgia, 3 cases of tinea pedis, and 1 case of liver disease, and enhancing many cases of physical quality. The clinical observation of China proves that the Chinese medicinal composition has certain curative effect on diabetes, digestive tract tumor and chronic hepatitis.
The fifth component: coenzyme Q10
Coenzyme Q10 is a fat-soluble antioxidant, coenzyme Q10 is one of essential important elements for human life, can activate the nutrition of human cells and cell energy, has the functions of improving human immunity, enhancing antioxidation, delaying senility, enhancing human vitality and the like, and is widely used for cardiovascular system diseases in medicine. The main functions are as follows:
1. coenzyme Q10 is used as a strong antioxidant alone or in combination with vitamin B6 (pyridoxine), and can inhibit the modification of free radicals on microtubule system of immune cell receptor related to cell differentiation and activity, enhance immune system, and delay aging.
2. Coenzyme Q10 helps to provide sufficient oxygen to the heart muscle and prevent sudden heart disease, and coenzyme Q10 plays a key role especially during myocardial hypoxia.
3. The coenzyme Q10 can accelerate fat metabolism, and make energy supply of limbs and brain abundant and energy invigorating.
4. Can be used as skin care product for improving skin elasticity.
The scientific combination of the components improves the functions of human organs, enhances the immunity of the organism, emphasizes on recovering the function of pancreatic islets, accurately treats various types of diabetes, considers the treatment and maintenance of complications and the treatment of tumors, strengthens the heart, nourishes the liver, regulates the blood pressure, beautifies and builds up the body, and delays aging from the whole and the root of the organism.
The invention realizes the all-around improvement of the disease resistance of each organ through scientific proportioning and makes up for the defect of single component. Not only improves the aging speed of human cells from the perspective of gene, but also weakens the degradation of system function from the perspective of supplementing necessary micro-amount for human body, and simultaneously stimulates the vitality and the anti-cancer variable ability of human body from the perspective of immunity. Through the scientific compatibility, the functions of all the components are brought into full play, and simultaneously, more beneficial comprehensive effects are generated.
Secondly, through the synergistic compatibility, the fundamental problem of diabetes is accurately, efficiently and safely solved, the origin is really activated, and both principal and secondary aspects of diseases are treated. Because the project focuses on restoring the system at first and then restoring the islet function at first, the diabetes mellitus is treated by the project not only by the surface phenomenon of blood sugar data, but also by the project which stands for a long time, the islet function is completely restored, the mechanism of relevant visceral organs entering virtuous cycle is promoted, the defects of blood sugar rebound, drug dependence and the like are effectively avoided, and a safer and healthier blood sugar reducing product is created.
Detailed Description
The invention will be described in further detail below with reference to the accompanying drawings: the present embodiment is implemented on the premise of the technical solution of the present invention, and a detailed embodiment is given, but the scope of the present invention is not limited to the following embodiments.
The present embodiment relates to a composition for treating diabetes, comprising:
the invention provides a composition for treating diabetes and a preparation method thereof, wherein the composition comprises the following components in percentage by mass: 5 to 60 percent of NMN (beta-nicotinamide mononucleotide), 5 to 60 percent of chromium-rich yeast, 5 to 60 percent of selenium-rich yeast, 5 to 60 percent of agaricus blazei polysaccharide and 105 to 60 percent of coenzyme Q.
In the present invention, the diabetes treatment product includes 5% to 60% by mass of NMN (β -nicotinamide mononucleotide), more preferably 5% to 45%, and still more preferably 10%.
In the present invention, the diabetes treatment product includes 5 to 60 mass% of chromium-rich yeast, more preferably 35 mass%, and still more preferably 10 mass%.
In the invention, the diabetes treatment product comprises 5-60% of selenium-enriched yeast by mass, more preferably 5-45%, and even more preferably 15%.
In the present invention, the diabetes treatment product includes 5 to 60 mass% of agaricus blazei murrill polysaccharide, more preferably 5 to 45 mass%, and still more preferably 25 mass%.
In the present invention, the diabetes treatment product includes 5% to 60% by mass of coenzyme Q10, more preferably 5% to 45%, and still more preferably 15%.
The diabetes treatment product provided by the invention is taken orally, and only needs to be taken once every day, 2 granules each time. One month is a treatment course.
The invention also provides a preparation method of the diabetes treatment product, which comprises the following steps: mixing the above materials, and making into capsule or tablet.
Example 1
A composition for treating diabetes comprises the following components in parts by mass:
150g of NMN (beta-nicotinamide mononucleotide), 250g of chromium-enriched yeast, 250g of selenium-enriched yeast, 250g of agaricus blazei murrill polysaccharide and 100g of coenzyme Q10. The raw materials are purchased from domestic production enterprises meeting the standards and specifications of the product industry. 1000g of the product is prepared, and 2000 grains of the product are prepared.
The preparation method comprises the following steps: mixing the above materials, and making into capsule or tablet.
Example 2
A composition for treating diabetes comprises the following components in parts by mass:
200g of NMN (beta-nicotinamide mononucleotide), 200g of chromium-enriched yeast, 200g of selenium-enriched yeast, 200g of agaricus blazei murill polysaccharide and 200g of coenzyme Q10. The raw materials are purchased from domestic production enterprises meeting the standards and specifications of the product industry. 1000g of the product is prepared, and 2000 grains of the product are prepared.
The source of the raw materials and the preparation method are the same as those of example 1.
Example 3
A composition for treating diabetes comprises the following components in parts by mass:
150g of NMN (beta-nicotinamide mononucleotide), 350g of chromium-enriched yeast, 150g of selenium-enriched yeast, 250g of agaricus blazei murrill polysaccharide and 100g of coenzyme Q10. The raw materials are purchased from domestic production enterprises meeting the standards and specifications of the product industry. 1000g of the product is prepared, and 2000 grains of the product are prepared.
The source of the raw materials and the preparation method are the same as those of example 1.
Example 4
A composition for treating diabetes comprises the following components in parts by mass:
100g of NMN (beta-nicotinamide mononucleotide), 350g of chromium-enriched yeast, 150g of selenium-enriched yeast, 250g of agaricus blazei murill polysaccharide and coenzyme Q10150 g. The raw materials are purchased from domestic production enterprises which meet the standards and specifications of the product industry. 1000g of the product is prepared, and 2000 grains of the product are prepared.
The source of the raw materials and the preparation method are the same as those of example 1.
Examples of the experiments
The pharmacodynamic test result of the invention is as follows:
in the experiment, 60 healthy rats are randomly divided into 6 groups which are respectively blank control groups, a small, medium and large dose (0.17, 0.5 and 1.5g/kg) group of a composition for treating diabetes mellitus, a 0.5g/kg group of ginseng and astragalus blood-glucose-reducing capsules and a 0.075g/kg group of a composition for treating diabetes mellitus are filled into the stomach according to the volume of 1ml/100g of body weight, the blank group is filled with distilled water with the same volume once a day and continuously for 15d, the fasting is not forbidden for 12h before the last administration, the fasting is not forbidden for 15h after the last administration, the ip adrenaline is 0.5mg/kg in each group, the glucose solution is filled into the stomach at the dose of 1g/kg, the model is accelerated, and the fasting blood glucose changes of 1h, 2h and 3h after the model is respectively measured. The blood is collected by cutting the tail, and the blood sugar content of the serum is measured by a glucose oxidase method.
Table 1 effect of a composition for treating diabetes on adrenergic hyperglycemic rat levels (n-10)
Figure BDA0002885549350000091
)
Figure BDA0002885549350000092
Note that t-tests were performed between groups, P < 005 and P < 001 compared to the blank control group.
Table 2 effect of a composition capsule for treating diabetes on blood sugar, blood lipid, SOD, MAD, insulin levels in alloxan type diabetic rats (n-8)
Figure BDA0002885549350000093
)
Figure BDA0002885549350000094
Figure BDA0002885549350000101
Note that the t test between groups compares the delta P with the model control group to be less than 005 and the delta P with the model control group to be less than 001; model control group compared with blank control group # # P < 001.
Table 3 effect of a composition capsule for treating diabetes on normal mouse blood glucose (n-10)
Figure BDA0002885549350000102
)
Figure BDA0002885549350000103
TABLE 4 glucose tolerance of a composition capsule for the treatment of diabetesInfluence (n ═ 10)
Figure BDA0002885549350000104
)
Figure BDA0002885549350000105
The pharmacodynamic test result of the project shows that: (see tables 1-4)
1. The invention can reduce the blood sugar level of the rat with the adrenergic hyperglycemia.
2. After the rat model building of the diabetes mellitus by the alloxan, the blood sugar is increased, the serum insulin level is reduced, the generation of in vivo free radicals is increased, the MDA content is increased, the SOD content is reduced, and the triglyceride and cholesterol content is increased. A composition for treating diabetes can obviously inhibit the change, protect insulin secretion, reduce MDA content and improve SOD activity, has obvious statistical significance compared with a model group, and has the effects of resisting oxidation, reducing blood sugar and increasing insulin secretion which are stronger than the blood fat reducing effect.
3. The invention has no obvious influence on the blood sugar of normal mice.
4. The glucose tolerance of the invention has no obvious influence.
The clinical observation statistical table of the invention is as follows:
TABLE 5 comparison of the therapeutic effects of the treated groups with those of the control group
Figure BDA0002885549350000111
Group of n Display efficiency High efficiency Inefficiency of Total effective rate
Treatment group 180 44.0 43.3 14.7 87.3
Control group 180 24.5 19.6 45.9 44.1
P < 005 compared to control.
The evaluation standard of curative effect is as follows: the effect is shown: three more and one less and other symptoms disappear, the body has no discomfort, the FBG is within 6.1mmol/L, and the blood sugar (PBG) after 2 hours of meal is within 7.2 mmol/L; the method has the following advantages: three more or one less and other symptoms are obviously relieved, the blood sugar of 2 hours after the meal and the fasting blood sugar are obviously reduced than the original blood sugar or the fasting blood sugar is reduced to 8 mmol/L-10 mmol/L, and the blood sugar of 2 hours after the meal is reduced to 10 mmol/L-13 mmol/L; and (4) invalidation: "three more and one less" and other symptoms are not improved, and the blood sugar is not obviously reduced or changed.
TABLE 6 two sets of FBG, PBG and HbAlC changes
Figure BDA0002885549350000112
Figure BDA0002885549350000113
Compared with the group before treatment, # P < 0.05; p <0.05 after treatment compared to control group
TABLE 7 blood lipid changes in two groups
Figure BDA0002885549350000121
Figure BDA0002885549350000122
Compared with the group before treatment, # P < 0.05; p <0.05 after treatment compared to control group
Clinical trials of this project showed that: (see tables 5-7)
Clinical study the clinical efficacy of the composition for treating type 2 diabetes was verified by observing the changes in clinical symptoms, blood glucose, glycated hemoglobin, blood lipids, etc., before and after treatment of 360 patients with diabetes by using one composition for treating diabetes. 360 patients with type 2 diabetes mellitus of last five years at home and abroad, 192 men and 168 women, and the age of 35-80 years; the disease course of diabetes is 2 to 28 years; 168 cases of combined macroangiopathy (144 cases of hypertension, 18 cases of cerebral infarction and 12 cases of diabetic heart disease) and 180 cases of microangiopathy (36 cases of diabetic retinopathy, 33 cases of diabetic nephropathy and 117 cases of peripheral neuropathy).
The research finds that the total effective rate of the composition for treating diabetes mellitus is 86.3 percent and is superior to that of a control group. The blood sugar and the glycosylated hemoglobin of the treatment group are obviously improved before and after treatment; the triacylglycerol, cholesterol and low-density lipoprotein cholesterol were significantly reduced and the high-density lipoprotein cholesterol was increased before and after treatment in the two groups, and the treatment group and the control group had statistical significance.
The above description is only a preferred embodiment of the present invention, and these embodiments are based on different implementations of the present invention, and the scope of the present invention is not limited thereto, and any changes or substitutions that can be easily conceived by those skilled in the art within the technical scope of the present invention are included in the scope of the present invention. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.

Claims (8)

1. The composition for treating diabetes is characterized by comprising the following components in percentage by mass: 5 to 60 percent of beta-nicotinamide mononucleotide, 5 to 60 percent of chromium-enriched yeast, 5 to 60 percent of selenium-enriched yeast, 5 to 60 percent of agaricus blazei polysaccharide and 5 to 60 percent of coenzyme Q10.
2. The composition for treating diabetes according to claim 1, which comprises the following components in percentage by mass: 5 to 50 percent of beta-nicotinamide mononucleotide, 5 to 50 percent of chromium-enriched yeast, 5 to 50 percent of selenium-enriched yeast, 5 to 50 percent of agaricus blazei polysaccharide and 5 to 50 percent of coenzyme Q10.
3. The composition for treating diabetes according to claim 1, which comprises the following components in percentage by mass: 5 to 45 percent of beta-nicotinamide mononucleotide, 5 to 45 percent of chromium-enriched yeast, 5 to 45 percent of selenium-enriched yeast, 5 to 45 percent of agaricus blazei polysaccharide and 5 to 45 percent of coenzyme Q10.
4. The composition for treating diabetes according to claim 1, which comprises the following components in percentage by mass: 15% of beta-nicotinamide mononucleotide, 25% of chromium-enriched yeast, 25% of selenium-enriched yeast, 25% of agaricus blazei polysaccharide and 10% of coenzyme Q10.
5. The composition for treating diabetes according to claim 1, which comprises the following components in percentage by mass: 20% of beta-nicotinamide mononucleotide, 20% of chromium-enriched yeast, 20% of selenium-enriched yeast, 20% of agaricus blazei polysaccharide and 20% of coenzyme Q10.
6. The composition for treating diabetes according to claim 1, which comprises the following components in percentage by mass: 15% of beta-nicotinamide mononucleotide, 35% of chromium-enriched yeast, 15% of selenium-enriched yeast, 25% of agaricus blazei polysaccharide and 10% of coenzyme Q10.
7. The method for preparing a composition for treating diabetes according to any one of claims 1 to 6, comprising the steps of: mixing the above materials, and making into capsule or tablet.
8. The method of claim 7, wherein the capsule has a weight of 0.45 to 0.55 g.
CN202110012077.0A 2021-01-06 2021-01-06 A composition for treating diabetes Pending CN114028434A (en)

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US20080268066A1 (en) * 2005-03-30 2008-10-30 Pficker Pharmaceuticals Ltd. Synergistic Formulation for Preventing and/or Treating Diabetes
CN101658537A (en) * 2008-08-27 2010-03-03 安琪酵母股份有限公司 Hypoglycemic ferment compound
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