CN104095868A - Medicine composition improving sugar tolerance and pharmacy use of medicine composition - Google Patents

Medicine composition improving sugar tolerance and pharmacy use of medicine composition Download PDF

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Publication number
CN104095868A
CN104095868A CN201410355498.3A CN201410355498A CN104095868A CN 104095868 A CN104095868 A CN 104095868A CN 201410355498 A CN201410355498 A CN 201410355498A CN 104095868 A CN104095868 A CN 104095868A
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glucose
chrysoeriol
medicine composition
glucose glycosides
tolerance
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CN104095868B (en
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刘学键
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Nantong Fayink High Tech Material Technology Co ltd
Qidong Binhua Water Supply Co ltd
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Abstract

The invention discloses a medicine composition improving sugar tolerance and pharmacy use of the medicine composition. The composition is prepared by an active ingredient and an auxiliary material; the active ingredient comprises thermopsoside. The medicine can not only reduce body mass, but also improve sugar tolerance, and is suitable for preventing and curing an obesity type diabetes patient and a sugar tolerance reducing patient that has not developed into diabetes yet.

Description

A kind of pharmaceutical composition and pharmaceutical applications thereof that improves carbohydrate tolerance
Technical field
The invention belongs to medical technical field, in particular to a kind of pharmaceutical composition and pharmaceutical applications thereof that improves carbohydrate tolerance.
Background technology
Impaired glucose tolerance is an interstage in type Ⅱdiabetes mellitus evolution, and after the several years, these crowd's great majority may develop into diabetes patient, and the incidence rate of impaired glucose tolerance crowd macroangiopathy is also high than general population.Therefore, preventing that impaired glucose tolerance from developing into diabetes, even make it to return to NGT, is important measures that prevent and treat diabetes, is also an important indicator evaluating diabetes control medicine.
The therapeutic intervention of impaired glucose tolerance has non-medication and Drug two aspects.Non-medication comprises diet intervention, and as total amount of heat and fat constituent that dietary restriction is taken in, sugar is drunk, eaten less in restriction, encourages polyphagia containing coarse grain and the fresh vegetables of the trace element such as chromium, magnesium, high fiber food.In addition, among the pharmaceutical intervention treatment multinational positive execution in the Zheng world.Conventional medicine has metformin, thiazolidinediones medicine, alpha-glucosidase inhibitor, sulfonylureas drugs for diabetes etc.If these drug mains are respectively by improving insulin resistant, the glucose that increases patients with impaired glucose tolerance shifts out rate and insulin sensitivity index, and reduces on an empty stomach and insulin level after the meal.By slow down disaccharidase and starch based polysaccharide, change glucose into, thereby the stimulation that reduces postprandial hyperglycemia, alleviates β cell reduces hyperinsulinemia.Yet, existing as the medicines such as metformin be chemicals, be mainly used in diabetics, for the patients with impaired glucose tolerance that not yet develops into diabetes, take these medicines after side effect larger.
Chrysoeriol-7-O-β-D-Glucose glycosides (thermopsoside) is present in several kinds of Chinese medicinal materials, as Saussurea medusa Maxim., Herba Vernoniae Cinereae, etc.CN101474196A discloses separation a kind of herb from ironweed plant Herba Vernoniae Cinereae or root and has obtained a flavonoid active site, and method for making method: utilize chromatographic separation technology separated preparation one class active site from the herb of Herba Vernoniae Cinereae, this active site comprises 7 flavone compounds, respectively: apiolin, chrysoeriol, luteolin, chrysoeriol-7-O-β-D-Glucose glycosides, luteolin-7-O-β-D-Glucose glycosides, Quercetin, apiolin-4 '-O-β-D-Glucose glycosides, this active site is in the news and has the effect of anti-senile dementia.By retrieval domestic and foreign literature, still do not find that chrysoeriol-7-O-β-D-Glucose glycosides has the bioactive bibliographical information of blood sugar lowering or raising carbohydrate tolerance at present.
Summary of the invention
The object of the invention is to by natural drug is studied, a kind of medicine of plant-derived raising carbohydrate tolerance is provided.It is active component that this medicine be take chrysoeriol-7-O-β-D-Glucose glycosides, can be used for not yet developing into the treatment of the patients with impaired glucose tolerance of diabetes.
The object of the present invention is achieved like this:
Improve a pharmaceutical composition for carbohydrate tolerance, by active component and adjuvant, be prepared from, described active component comprises chrysoeriol-7-O-β-D-Glucose glycosides.
Preferably, improve as mentioned above the pharmaceutical composition of carbohydrate tolerance, wherein said active component is comprised of as unique component chrysoeriol-7-O-β-D-Glucose glycosides.
The pharmaceutical composition of raising carbohydrate tolerance of the present invention, wherein chrysoeriol-7-O-β-D-Glucose glycosides has carried out relevant animal experiment as active component in gavage mode, result medicine absorbs significantly through gastrointestinal, and therefore described pharmaceutical composition can be oral formulations.Wherein said oral formulations comprises tablet, capsule, granule.
It should be noted that, according to the common process of formulation art, those skilled in the art is easy to adjuvant available on chrysoeriol-7-O-β-D-Glucose glycosides and pharmaceutics to be prepared into conventional solid orally ingestible, as granule, tablet, capsule.Wherein, on pharmaceutics, available adjuvant comprises filler, disintegrating agent, binding agent, correctives, lubricant etc.
The present invention has studied the impact of chrysoeriol-7-O-β-D-Glucose glycosides on normal mouse blood sugar and exogenous glucose tolerance and body weight by animal experiment.Result of study shows, 10d gavage gives chrysoeriol-7-O-β-D-Glucose glycosides continuously, and the fasting glucose of normal mouse is not made significant difference, effect that may non-stimulated normal insulin secretion.And when a certain amount of exogenous glucose of normal mouse gavage, blood glucose raises rapidly, but the mice that gives in advance chrysoeriol-7-O-β-D-Glucose glycosides can significantly suppress blood sugar increasing, the dosis tolerata that strengthens exogenous glucose, this is significant for prevent diabetes and macroangiopathy.It is likely by reducing body, to absorb speed or the quantity of glucose that chrysoeriol-7-O-β-D-Glucose glycosides improves glucose tolerance in mice, thereby regulates blood glucose.Research also finds that chrysoeriol-7-O-β-D-Glucose glycosides administration group Mice Body quality obviously alleviates than blank group, shows that control has potential effect to chrysoeriol-7-O-β-D-Glucose glycosides to weight.As can be seen here, chrysoeriol-7-O-β-D-Glucose glycosides on the one hand on normal mouse fasting glucose without impact, another aspect can ameliorate body quality can improve carbohydrate tolerance again, this means that chrysoeriol-7-O-β-D-Glucose glycosides can further be developed to medicine or the slimming health food into control obese diabetic.
Based on above result of study, the present invention also provides a kind of pharmaceutical applications, that is: the purposes of chrysoeriol-7-O-β-D-Glucose glycosides in the medicine of preparation raising carbohydrate tolerance; Or: chrysoeriol-7-O-β-D-Glucose glycosides is in the medicine of preparation control obese diabetic or the purposes in health product.
Compared with prior art, the pharmaceutical composition that contains chrysoeriol-7-O-β-D-Glucose glycosides the present invention relates to has following outstanding advantage: (1) can ameliorate body quality can improve carbohydrate tolerance again, the patients with impaired glucose tolerance that is applicable to preventing and treating obese diabetic patient and not yet develops into diabetes; (2) to orthoglycemic crowd without effect, avoided hypoglycemic generation.
The specific embodiment
The present invention has studied the impact of chrysoeriol-7-O-β-D-Glucose glycosides on normal mouse blood sugar and exogenous glucose tolerance and body weight by animal experiment.Result of study shows, 10d gavage gives chrysoeriol-7-O-β-D-Glucose glycosides continuously, and the fasting glucose of normal mouse is not made significant difference, effect that may non-stimulated normal insulin secretion.And when a certain amount of exogenous glucose of normal mouse gavage, blood glucose raises rapidly, but the mice that gives in advance chrysoeriol-7-O-β-D-Glucose glycosides can significantly suppress blood sugar increasing, strengthens the dosis tolerata of exogenous glucose.The present invention also finds that chrysoeriol-7-O-β-D-Glucose glycosides administration group Mice Body quality obviously alleviates than blank group, shows that control has potential effect to chrysoeriol-7-O-β-D-Glucose glycosides to weight.Following examples are concrete processs of the test:
The affect experimental study of embodiment 1 chrysoeriol-7-O-β-D-Glucose glycosides on normal mouse blood sugar
Kunming mouse, clean level, male and female half and half, weight (20 ± 2g), be divided at random blank group, positive controls (glibenclamide 400mg/kg), test high and low (chrysoeriol-7-O-β-D-Glucose glycosides 260,130mg/kg) dosage group, 12 every group.Each administration group gavage every day 1 time, blank group gives equal-volume distilled water (20m1/kg), continuously 10d.Before last administration, water 12h is can't help in mice fasting, and 1 h after last administration, gets blood from eye socket rear vein beard, and separation of serum is measured blood glucose value by the explanation of glucose oxidase method test kit.
Result of the test by table 1 can find out, after normal mouse administration 10d, positive drug glibenclamide can significantly reduce mouse blood sugar ( p< 0.05), and chrysoeriol-7-O-β-D-Glucose glycosides high and low dose does not have a significant effect to mouse blood sugar.
Table 1 is respectively organized mouse blood sugar value comparison (mmol/L)
With the comparison of blank group, * p< 0.05.
 
The affect experimental study of embodiment 2 chrysoeriols-7-O-β-D-Glucose glycosides on normal glucose tolerance in mice and weight
Kunming mouse, clean level, male and female half and half, weight (20 ± 2g), be divided at random blank group, model control group, positive controls (metformin group 750mg/kg), test high and low (chrysoeriol-7-O-β-D-Glucose glycosides 260,130mg/kg) dosage group, 12 every group.Each administration group gavage every day 1 time, blank group and model control group give equal-volume distilled water (20m1/kg), continuously 10d.Before last administration, water 12h is can't help in mice fasting, each is organized mice and claims weight, after last administration 1 h, except blank group gavage distilled water, all the other respectively organize equal gavage glucose solution (2.5g/kg), respectively at before filling sugar (being 0h blood glucose), fill with sugar rear 30min, lh and 2h, from mouse orbit rear vein beard, get blood, separation of serum, measures blood glucose value by the explanation of glucose oxidase method test kit.
Result of the test by table 2 can find out, each organize mouse stomach and give glucose after blood glucose start to raise, to 0.5h, reach summit.With model control group contrast, positive drug metformin and chrysoeriol-7-O-β-D-Glucose glycosides high and low dose to glucose cause hyperglycemia and have the inhibitory action of highly significant ( p< 0.05 or p< 0.01).After lh, the blood sugar reducing function highly significant of metformin and chrysoeriol-7-O-β-D-Glucose glycosides high dose ( p< 0.01), low dosage have obvious blood sugar reducing function ( p< 0.05).After 2h, chrysoeriol-7-O-β-D-Glucose glycosides high dose still have highly significant blood sugar reducing function ( p< 0.01), be better than metformin.
Table 2 is respectively organized glucose tolerance in mice comparison (mmol/L)
With model control group comparison, p< 0.05, ★ ★ p< 0.01.
Result of the test by table 3 can find out, after normal mouse administration 10d, positive drug metformin and chrysoeriol-7-O-β-D-Glucose glycosides can significantly reduce Mice Body quality ( p< 0.05 or p< 0.01), especially the chrysoeriol of high dose-7-O-β-D-Glucose glycosides effect is more obvious.
Table 3 is respectively organized Mice Body mass ratio (g)
With model control group comparison, p< 0.05, ★ ★ p< 0.01.

Claims (6)

1. improve a pharmaceutical composition for carbohydrate tolerance, by active component and adjuvant, be prepared from, it is characterized in that: described active component comprises chrysoeriol-7-O-β-D-Glucose glycosides.
2. improve according to claim 1 the pharmaceutical composition of carbohydrate tolerance, it is characterized in that: described active component is comprised of as unique component chrysoeriol-7-O-β-D-Glucose glycosides.
3. according to the pharmaceutical composition that improves carbohydrate tolerance described in claim 1 or 2, it is characterized in that: described pharmaceutical composition is oral formulations.
4. improve according to claim 3 the pharmaceutical composition of carbohydrate tolerance, it is characterized in that: described oral formulations is tablet, capsule or granule.
5. chrysoeriol-7-O-β-D-Glucose glycosides improves the purposes in the medicine of carbohydrate tolerance in preparation.
6. chrysoeriol-7-O-β-D-Glucose glycosides is in the medicine of preparation control obese diabetic or the purposes in health product.
CN201410355498.3A 2014-07-25 2014-07-25 A kind of pharmaceutical composition and pharmaceutical applications thereof improving sugar tolerance Active CN104095868B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105816473A (en) * 2015-07-06 2016-08-03 武汉华纳联合药业有限公司 Flavonoid glycoside composition, preparation and production method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101474196A (en) * 2009-02-17 2009-07-08 南京中医药大学 Flavone active site of Vernonia cinerea as well as preparation method and use thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101474196A (en) * 2009-02-17 2009-07-08 南京中医药大学 Flavone active site of Vernonia cinerea as well as preparation method and use thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105816473A (en) * 2015-07-06 2016-08-03 武汉华纳联合药业有限公司 Flavonoid glycoside composition, preparation and production method thereof

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