WO2019131759A1 - 腸管バリア機能改善用組成物 - Google Patents
腸管バリア機能改善用組成物 Download PDFInfo
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- WO2019131759A1 WO2019131759A1 PCT/JP2018/047840 JP2018047840W WO2019131759A1 WO 2019131759 A1 WO2019131759 A1 WO 2019131759A1 JP 2018047840 W JP2018047840 W JP 2018047840W WO 2019131759 A1 WO2019131759 A1 WO 2019131759A1
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- barrier function
- intestinal barrier
- composition
- gallic acid
- improving
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
- A61K31/05—Phenols
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7024—Esters of saccharides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7028—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages
- A61K31/7034—Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- the present invention relates to a composition for improving intestinal barrier function.
- the present invention also relates to an enhancer of the intestinal barrier function improving action of gallic acid.
- the invention also relates to methods of improving intestinal barrier function and the use of gallic acid to improve intestinal barrier function and the like.
- the functions of the intestine are mainly the absorption function of nutrients and the barrier function (intestinal barrier function) for preventing the penetration (permeation) of harmful substances.
- the intestinal barrier function is closely related to the chronic inflammatory diseases which increase with age.
- intestinal epithelial cells Under the intestinal epithelial cells, there are many cells of the immune system such as macrophages, dendritic cells, T cells and B cells.
- intestinal epithelial cells are firmly attached to each other by a structure called tight junction, and high molecular weight substances are strictly controlled not to permeate cell gaps.
- transporters for draining hydrophobic foreign substances from intestinal epithelial cells These tight junction structures, transporters and the like are responsible for the intestinal barrier function to prevent the entry of foreign matter.
- EGF Epidermal growth factor
- Non-Patent Document 1 describes that flavonoids such as quercetin promote the formation of tight junctions and the like to prevent chronic inflammation.
- Patent Document 1 describes an absorption inhibitor comprising, as an active ingredient, one or more selected from lindane, octagon, marnies, black tea, black tea, or their processed products.
- Patent Document 2 describes that a hexapeptide having a specific sequence and tryptophan have an absorption suppressing activity of an allergen.
- Patent Document 3 describes a supplement for enteral administration to maintain or restore the intestinal barrier of the intestine, which comprises a combination of glutamine, a substance having antioxidant activity and a short chain fatty acid.
- the present inventors have intensively studied to solve the above-mentioned problems, and are capable of disrupting intestinal barrier function in humans by adding inflammatory cytokines to an intestinal permeation model using human intestinal cell culture Caco-2
- gallic acid (3,4,5-trihydroxybenzoic acid) has an intestinal barrier function improving action.
- gallic acid and a phenolic compound other than gallic acid an excellent intestinal barrier function improving effect can be exhibited by these synergistic effects. It was a surprising finding that the combined use of gallic acid and the above-mentioned phenolic compound synergistically enhances the intestinal barrier function improving effect.
- the present inventors came to complete the present invention based on these findings.
- the present invention relates to the following composition for improving intestinal barrier function and the like.
- a composition for improving intestinal tract barrier function comprising gallic acid as an active ingredient.
- the composition for improving intestinal barrier function according to the above (1) which further comprises a phenolic compound.
- the composition for improving intestinal barrier function according to the above (2) wherein the phenolic compound is polyphenol and / or coumaric acid.
- the above-mentioned phenolic compounds are procyanidin B1, procyanidin B2, procyanidin B3, catechin, epicatechin, gallocatenin, epigallocatechin, epigallocatechin, catechin gallate, epicatechin gallate, epigallocatechin gallate, theaflavin, taxifolin, daidzein genistein, apigenin, Luteolin, Naringenin, Naringenin Chalcone, Kaempferol, Rutin, Quercetin-3-O-Glucopyranoside, Quercetin, Myricetin, Piceatannol, Petunizine, trans-Piceid, Corillagin, Stenophilinin A, Stenophilinin B, Kasallinin, Geraniin Terima, Glandin I, pedon clazine, precoxin A, eugeniflorin D2, 1,4,6-tri-O-galoyl- ⁇ -D-glu , 1,2,3,6-tetra
- composition for improving intestinal barrier function according to any one of the above (1) to (5) which is an oral composition.
- composition for improving intestinal barrier function according to the above (6) wherein the composition for oral use is a food or drink, a medicine or a quasi-drug.
- the composition for improving intestinal barrier function according to any one of the above (1) to (7) which is used for intestinal regulation.
- An enhancer for an intestinal barrier function improving action of gallic acid which comprises a phenol compound as an active ingredient.
- gallic acid for improving intestinal barrier function.
- a method for enhancing the intestinal barrier function improving action of gallic acid which is administered to a subject by combining gallic acid and a phenol compound.
- the intestinal barrier function can be improved by using the composition for improving the intestinal barrier function of the present invention.
- the enhancer of the intestinal barrier function improving action of the present invention when used, the intestinal barrier function improving action of gallic acid can be remarkably enhanced.
- the present invention can also contribute to the prevention or treatment of a condition or disease associated with an abnormality in intestinal barrier function, such as a chronic inflammatory disease or an allergic disease, by improving the intestinal barrier function.
- the composition for improving intestinal barrier function of the present invention contains gallic acid as an active ingredient.
- Gallic acid has an intestinal barrier function improving action.
- Gallic acid is a component contained in plants such as grapes and tea trees, and it is highly safe because it has few side effects even when taken over a long period of time.
- Gallic acid is not particularly limited depending on its origin or production method. For example, those derived from plants extracted from plants may be used, or those obtained by a synthetic method may be used.
- the composition for improving intestinal barrier function of the present invention preferably further contains a phenolic compound.
- a phenol compound refers to a compound having a phenolic hydroxyl group other than gallic acid or a glycoside thereof. Gallic acid is not included in the phenolic compound in the present invention.
- the glycoside refers to a compound formed by glycosidic linkage of a hydroxyl group of a sugar with a non-carbohydrate compound.
- the sugar in the glycoside may be a monosaccharide, or may be a disaccharide or a plurality of multiple saccharides, and is not particularly limited.
- the type of sugar is not particularly limited, and glucose, mannose, galactose, fucose, aldose such as rhamnose, arabinose, xylose, etc .; ketoses such as fructose; glucuronic acid, galacturonic acid, uronic acid such as mannuronic acid etc; apiose, rutinose etc Be
- the sugar in the glycoside may be D-form or L-form.
- the intestinal barrier function improving action of gallic acid can be enhanced. Therefore, when these are used in combination, an excellent intestinal barrier function improvement effect can be exhibited.
- the intestinal barrier function improvement effect obtained by the combination of gallic acid and a phenolic compound is a synergistic effect which is significantly superior to the additive effect predicted from the effect obtained by using each component alone.
- the composition for improving intestinal barrier function is preferably a composition for improving intestinal barrier function, which contains gallic acid and a phenol compound as active ingredients.
- polyphenol refers to a compound having two or more phenolic hydroxyl groups in the molecule or a glycoside thereof.
- coumaric acids include p-coumaric acid, 2-coumaric acid, 3-coumaric acid and glycosides thereof.
- flavan-3-ol polymers As the polyphenol, flavan-3-ol polymers, flavanols, flavonols, flavanones, flavones, isoflavones, anthocyanidins, flavanonols, stilbenoids, chalcones, hydrolyzable tannins and the like are preferable.
- the use of the above polyphenols can enhance the action of gallic acid on improving the intestinal barrier function.
- the flavan-3-ol polymer is a dimer or higher polymer in which the flavan-3-ol is a structural unit, and the flavan-3-ol is linked by condensation or polymerization at the 4-6 or 4-8 position. is there.
- Flavan-3-ol polymers are compounds which are also referred to as condensed tannins.
- the flavan-3-ol polymer may be a mixture of two or more polymers having different degrees of polymerization. In one aspect, the flavan-3-ol polymer may have a galloyl group.
- the degree of polymerization of the flavan-3-ol polymer is not particularly limited. For example, one having a degree of polymerization of 2 to 30 (a 2 to 30-mer) can be used.
- a dimer of flavan-3-ol is preferred.
- dimers of flavan-3-ol include procyanidin B1, procyanidin B2, procyanidin B3 and the like.
- flavanols examples include catechin, epicatechin, gallocatechin, epigallocatechin, catechin gallate, epicatechin gallate, gallocatechin gallate, flavan-3-ols such as epigallocatechin gallate, theaflavin and the like.
- flavanols catechin, epicatechin, gallocatechin, epigallocatechin, catechin gallate, epicatechin gallate, epigallocatechin gallate from the viewpoint of strong action to enhance intestinal barrier function improving action when used in combination with gallic acid. , Theaflavin and the like are preferable.
- catechin gallate, epicatechin gallate, epigallocatechin gallate and the like are more preferable from the viewpoint of obtaining a better intestinal barrier function improvement effect when used in combination with gallic acid.
- the flavanols in the present invention do not include the above flavan-3-ol polymers.
- flavonol compounds examples include quercetin, myricetin, kaempferol, and their glycosides (quercetin-3-O-glucopyranoside, rutin, etc.) and the like.
- quercetin, kaempferol and glycosides thereof are preferable from the viewpoint of a strong action to enhance the intestinal barrier function improving action.
- flavanone compounds include naringenin, glycosides thereof and the like.
- apigenin, luteolin, their glycosides and the like can be mentioned.
- compounds of isoflavones, daidzein, genistein, their glycosides and the like can be mentioned.
- Examples of the anthocyanidin compounds include petunidin and glycosides thereof.
- Examples of compounds of flavanols include taxifolin, its glycoside and the like.
- Examples of stilbenoids, piceatannol, its glycoside (trans-piceide, cis-piceide etc.) and the like can be mentioned.
- Examples of chalcone compounds include naringenin chalcone (4,2 ′, 4 ′, 6′-tetrahydroxychalcone), glycosides thereof and the like.
- hydrolyzable tannins examples include gallotannins and ellagitannins.
- gallotannins for example, ⁇ -glucogalin, 1,4,6-tri-O-galloyl- ⁇ -D-glucose, 1,2,4,6-tetra-O-galloyl- ⁇ -D-glucose, 1,2 , 3,6-Tetra-O-galoyl- ⁇ -D-glucose, 2,3,4,6-Tetra-O-galoyl- ⁇ -D-glucose, 1,2,3,4,6-penta-O And galloyl- ⁇ -D-glucose.
- corilagin corilagin
- terrimaglandin I Teellimagrandin I
- pedounclazine Pedunculagin
- precoxin A Praecoxin A
- geraniin Geraniin
- stenophyllanin A Stenophyllinin A
- stenophilain B Stenophyllin B
- casuarinin Casuarinin
- Eugeniflorin D2 Eugeniflorin D2
- flavan-3-ol polymers flavanols and ellagitannins are preferable as the phenol compound from the viewpoint of obtaining higher intestinal barrier function improvement effects.
- flavan-3-ol polymers preferably, procyanidin B1, procyanidin B2, procyanidin B3, etc.
- catechin epicatechin, gallocatenin, epigallocatechin, catechin gallate, epicatechin gallate, epigallocatechin gallate , Theaflavin, taxofolin, daidzein, genistein, apigenin, luteolin, naringenin, naringenin chalcone, kaempferol, rutin, quercetin-3-O-glucopyranoside, quercetin, myricetin, piceatannol, petunidin, trans-piceid, corilagin, stenophilin A , Stenophilin B, casalinin,
- Plants containing hydrolyzable tannins can be used as a source of hydrolyzable tannins.
- plants containing hydrolyzable tannins include plants of the family Fagaceae (Fagaceae), Lythaceae (Lythraceae), Myrtaceae (Myrtaceae), and Rosaceae (Rosaceae). These plants are rich in hydrolyzable tannins.
- a plant such as a genus of Syzygium, a genus of Eucalyptus (Eucalyptus), a genus of Kunzea, and the like are preferable.
- Eucalyptus leaf extract contains a large amount of hydrolyzable tannins such as terimaglandin I and gallotannin.
- a commercial item can also be utilized for a phenol compound.
- the intestinal barrier function refers to a function to prevent the entry (permeation) of foreign substances (for example, toxins such as endotoxin, proinflammatory substances, undigested substances, etc.) from the outside (inside the intestinal tract) of intestinal epithelial cells.
- the intestinal tract includes the large and small intestines. A state in which the invasion of foreign substances from outside the intestinal epithelial cells into the body is promoted compared to the normal state is referred to as a state in which the permeability of the foreign substances in the intestinal epithelial cells is increased (increased).
- the improvement of intestinal barrier function means both suppressing the increase in the permeability of foreign substances in intestinal epithelial cells and reducing the permeability of foreign substances in intestinal epithelial cells.
- intestinal barrier function improvement is used in the meaning including suppressing the fall of the intestinal barrier function and enhancing the lowered intestinal barrier function.
- intestinal barrier function is improved by normalizing or enhancing tight junctions that adhere intestinal epithelial cells to each other.
- the composition for improving intestinal barrier function of the present invention can be used to improve intestinal barrier function by normalizing or enhancing tight junctions in intestinal epithelial cells.
- the intestinal barrier function improvement effect is shown, for example, by the increase in the electrical resistance (transepithelial electric resistance (TEER)) of intestinal epithelial cells, or by suppressing the decrease in TEER.
- the substance that elevates the TEER or suppresses its reduction has an effect of normalizing or enhancing tight junctions in intestinal epithelial cells.
- the intestinal barrier function improving effect is also shown by a decrease in the amount of substance that permeates from the intestinal side of intestinal epithelial cells to the inside of the body.
- a method of measuring TEER can be used by using an intestinal permeation model using human intestinal epithelial cells (Caco-2 cells). Specifically, inflammatory cytokines (TNF ⁇ , IL-1 ⁇ , IFN ⁇ , etc.) are added to Caco-2 monolayer culture cells to create a state in which human intestinal barrier function can be disrupted in humans, and the test substance is added to the cells. If the decrease in TEER is suppressed as compared to the case where no substance is added, it can be evaluated that the test substance has an effect of improving the intestinal barrier function.
- inflammatory cytokines TNF ⁇ , IL-1 ⁇ , IFN ⁇ , etc.
- gallic acid suppresses the decrease in TEER by the addition of inflammatory cytokines in an intestinal permeation model using Caco-2 cells, and has an intestinal barrier function.
- Gallic acid can normalize or enhance tight junctions in intestinal epithelial cells to improve intestinal barrier function.
- the combination of gallic acid and a phenol compound can exert a more excellent intestinal barrier function improving effect.
- composition for improving the intestinal barrier function of the present invention exhibits an effect of improving the intestinal barrier function by containing gallic acid as an active ingredient. Moreover, when the composition for intestinal barrier function improvement contains a phenol compound, the intestinal barrier function improvement effect is enhanced, and a more excellent intestinal barrier function improvement effect can be exhibited. Therefore, the composition for improving intestinal tract function according to the present invention is useful for the prevention or amelioration of a state or disease in which the improvement of the intestinal barrier function is effective, such as a state or disease associated with an abnormality in the intestinal barrier function.
- Abnormalities in intestinal barrier function include reduction in intestinal barrier function.
- a condition or disease associated with an abnormality in intestinal barrier function includes a condition or disease caused by an abnormality in intestinal barrier function, or a condition or disease with an abnormality in intestinal barrier function.
- condition or disease associated with such an abnormality in intestinal barrier function for example, inflammatory bowel disease, irritable bowel syndrome, systemic autoimmune disease (rheumatoid arthritis, erythematosus etc.), allergy (food allergy, hay fever etc.) And lifestyle-related diseases (eg, obesity, type 1 or 2 diabetes, hypertension, hyperlipidemia, nonalcoholic fatty liver disease (NAFLD), arteriosclerosis, etc.) and the like (eg, Camilleri et al., Am J Physiol Gastrointest Liver Physiol 303: G775-G785, 2012; Mu et al., Front. Immunol., Vol. 8, Article 598, 2017; Bischoff et al., BMC Gastroenterology 2014 14: 189).
- lifestyle-related diseases eg, obesity, type 1 or 2 diabetes, hypertension, hyperlipidemia, nonalcoholic fatty liver disease (NAFLD), arteriosclerosis, etc.
- Camilleri et al. Am J Physiol Ga
- compositions for improving intestinal barrier function of the present invention have an effect of improving the condition of the intestine by improving the intestinal barrier function. Therefore, the composition for improving the intestinal barrier function of the present invention can adjust the condition of the intestine by the improvement of the intestinal barrier function, and is useful for preventing or ameliorating the above-mentioned intestinal symptoms.
- the composition for improving intestinal barrier function of the present invention can be used for intestinal regulation (for example, for preventing or ameliorating diarrhea, constipation, abdominal discomfort and the like).
- the composition for improving intestinal barrier function of the present invention is useful for intestinal regulation by improving the intestinal barrier function.
- abnormalities in intestinal barrier function are also associated with lifestyle-related diseases and the like (for example, Bischoff et al., BMC Gastroenterology 2014 14: 189 described above). Improving the intestinal barrier function is also effective in preventing or ameliorating lifestyle-related diseases.
- Symptoms of lifestyle-related diseases include glucose metabolism disorder, lipid metabolism disorder, body fat increase, visceral fat increase, abdominal circumference fat increase, high blood pressure and the like. Therefore, the composition for improving intestinal barrier function according to the present invention improves glucose barrier function, improves lipid metabolism, and reduces or increases, suppresses, increases, and increases fat such as body fat, visceral fat and abdominal fat by improving intestinal barrier function. It can also contribute to the improvement of the blood pressure of
- prevention of a condition or disease refers to enhancing the subject's resistance to the condition or disease, delaying or preventing the onset of the condition or disease.
- aboration of a condition or disease recovering the subject from the condition or disease, alleviating the symptoms of the condition or disease, delaying or preventing the progression of the condition or disease Point to
- compositions of the invention can be applied for either therapeutic (medical) or non-therapeutic (non-medical) applications.
- the composition for improving intestinal barrier function of the present invention can be provided, for example, in the form of food and drink, medicine, quasi-drug, feed and the like, but is not limited thereto.
- the composition for improving intestinal barrier function of the present invention may itself be food and drink, medicine, quasi-drug, feed, etc., and may be a preparation such as an additive used for these, or a material.
- the composition for improving intestinal barrier function of the present invention can be provided, for example, in the form of an agent, but is not limited to this form.
- the agent can be provided as it is as a composition or as a composition containing the agent.
- the composition for improving intestinal barrier function of the present invention is preferably an oral composition. According to the present invention, it is possible to provide an oral composition having an excellent intestinal barrier function improving action.
- the composition for oral use includes food and drink, medicine, quasi-drug, and preferably food and drink.
- composition for improving intestinal barrier function of the present invention contains the above-described gallic acid and one or more components (other components) other than the optionally compounded phenolic compound as long as the effects of the present invention are not impaired. It may be In one embodiment, for example, lactic acid bacteria, bifidobacteria, dietary fiber, polysaccharides and the like may be contained as other components.
- the lactic acid bacteria and bifidobacteria are preferably bacteria which can be taken orally.
- the dietary fiber may be any of water-insoluble dietary fiber and water-soluble dietary fiber.
- water-insoluble dietary fibers include cellulose, lignin, hemicellulose, wheat bran, apple fiber, sweet potato fiber, chitin and the like.
- Water-soluble dietary fibers are roughly classified into high-viscosity substances and low-viscosity substances, and examples of high-viscosity substances include pectin, konjac mannan, alginic acid, sodium alginate, guar gum, agar and the like.
- the low-viscosity, water-soluble dietary fiber contains at least 50% by weight of dietary fiber and is a low-viscosity solution dissolved in normal temperature water, approximately 5% by weight It refers to a dietary fiber material that becomes a solution exhibiting a viscosity of 20 mPa ⁇ s or less in an aqueous solution.
- low-viscosity substances of water-soluble dietary fiber those of resistant digestive dextrin, polydextrose, guar gum degradation products, Lytes (polydextrose) and the like can be mentioned.
- any low-viscosity, water-soluble dietary fiber material is included.
- the dietary fiber may be used alone or in combination of two or more.
- polysaccharide examples include oligosaccharides such as galactooligosaccharides, xylooligosaccharides, mannooligosaccharides, agarooligosaccharides, fructooligosaccharides, isomaltooligosaccharides, raffinose and the like. These may be used alone or in combination of two or more.
- the composition for improving intestinal barrier function of the present invention may contain any additive and any component other than the above.
- additives and components can be selected according to the form etc. of the composition for improving intestinal barrier function, and in general, those usable for food and drink, medicine, quasi-drug, feed and the like can be used.
- various additives which are orally or orally pharmaceutically acceptable, such as excipients, lubricants, stabilizers, dispersants, binders, diluents, flavors, sweeteners, flavors , Coloring agents and the like can be exemplified.
- compositions for improving intestinal barrier function of the present invention when used as a composition for oral use, vitamins, vitamin-like substances, proteins, amino acids, fats and oils, organic acids other than the above, as long as the effects of the present invention are not impaired.
- Ingredients that can be orally ingested such as carbohydrates, plant-derived materials, animal-derived materials, microorganisms, additives for foods and beverages, additives for pharmaceuticals, etc. can be appropriately contained.
- components such as materials used for food and drink, medicines, quasi-drugs, feeds and the like can be appropriately blended according to the use.
- composition for improving intestinal barrier function of the present invention is not particularly limited as long as it has the effect of the present invention, and for example, tablets, pills, granules, fine granules, lozenges, capsules (soft capsules Agents, including hard capsules), solutions, chewable agents, beverages and the like. Other food forms may be used. These dosage forms can be prepared using conventional methods commonly known in the art.
- composition for improving intestinal barrier function of the present invention when used as a food or drink, it is possible to use gallic acid and optionally compounded phenol compounds as ingredients usable for food and drink (for example, food and drink materials, if necessary Additives and the like that are used) can be blended to make various food and drink (food and drink composition).
- Food-drinks are not specifically limited, For example, general food-drinks, health food, functional indication food, food for specific health, food for sick people, food additive, these raw materials etc. are mentioned.
- the forms of food and drink are not particularly limited, and solid preparations for oral use such as tablets, coated tablets, fine granules, granules, powders, pills, capsules (including soft capsules and hard capsules), dry syrups, chewables, etc. It may be in the form of various preparations of liquid preparations for oral use such as internal liquid solutions and syrups.
- the food and drink may contain one or more of the above-mentioned lactic acid bacteria, bifidobacteria, dietary fiber, and polysaccharides.
- compositions for improving intestinal barrier function of the present invention When the composition for improving intestinal barrier function of the present invention is used as a drug or quasi-drug, additives such as pharmaceutically acceptable excipients are added to gallic acid and an optionally formulated phenolic compound. And pharmaceuticals (pharmaceutical compositions) or quasi-drugs (quasi-drug compositions) of various dosage forms.
- the dosage form of the pharmaceutical or quasi-drug is preferably orally administered.
- the pharmaceutical or quasi-drug dosage form may be a dosage form suitable for the administration form.
- a dosage form for oral pharmaceuticals or quasi-drugs for example, tablets, coated tablets, fine granules, granules, powders, pills, capsules (including soft capsules and hard capsules), dry syrups, chewables, etc.
- conventional coated forms may be used, for example, sugar-coated tablets, gelatin capsules, enteric-coated agents, film-coating agents, etc.
- the tablets can also be multi-layered tablets such as double tablets.
- composition for improving intestinal barrier function of the present invention When the composition for improving intestinal barrier function of the present invention is used as food, drink, medicine, quasi-drug, feed, etc., its production method is not particularly limited, and it is possible to use gallic acid and an optionally compounded phenolic compound. , Can be manufactured by a general method.
- the present invention also encompasses the use of gallic acid for producing a composition for improving intestinal barrier function.
- the present invention also encompasses the use of gallic acid and phenolic compounds other than gallic acid for producing a composition for improving intestinal barrier function.
- a composition for improving intestinal barrier function can also be prepared using a plant extract containing gallic acid and a phenolic compound. Plant extracts containing gallic acid and phenolic compounds are not particularly limited. For example, grape seed extract, green tea extract, oolong tea extract, black tea extract, eucalyptus extract, guava extract, mulberry tea extract, rosehip extract A thing etc. can be used.
- the composition for improving intestinal barrier function of the present invention has one or more of applications such as packaging, containers or instructions, types of active ingredients, effects described above, methods of use (eg, intake method, administration method), etc. You may display it.
- the composition for improving intestinal barrier function of the present invention may be labeled as having an effect based on the intestinal barrier function improving action or the intestinal barrier function improving action. As such a display, for example, it may be displayed that it has an intestinal adjustment effect.
- the intestinal regulation action is not particularly limited as long as it is an intestinal regulation action based on the improvement of the intestinal barrier function.
- the content of gallic acid in the composition for improving intestinal barrier function of the present invention can be appropriately set according to the form of the composition and the like.
- the content of gallic acid is at least 0.0001% by weight in the composition.
- 0.001% by weight or more is more preferable, 10% by weight or less is preferable, and 1% by weight or less is more preferable.
- the content of gallic acid in the composition for improving intestinal barrier function is preferably 0.0001 to 10% by weight, and more preferably 0.001 to 1% by weight.
- the content of gallic acid can be measured according to a known method, and for example, an HPLC method or the like can be used.
- the content ratio of gallic acid and phenolic compound is preferably 0.1 to 10 in molar ratio, more preferably Is 0.3-5.
- Use of gallic acid and a phenol compound in the above ratio can further improve the intestinal barrier function improving effect.
- the composition for improving intestinal barrier function of the present invention can be taken or administered by an appropriate method according to the form.
- the composition for improving intestinal barrier function of the present invention is preferably orally administered or orally ingested.
- the intake amount (which can also be referred to as a dose) of the composition for improving intestinal barrier function of the present invention is not particularly limited, as long as it is an amount such that the effect of improving intestinal barrier function can be obtained. It may be set appropriately according to the situation.
- the intake amount of the composition for improving intestinal barrier function is preferably 0.01 to 500 mg per day as the intake of gallic acid 0.1 to 300 mg is more preferable, and 1 to 100 mg is more preferable.
- the above-mentioned amount is orally administered or taken, for example, once a day or divided into two or three times.
- the composition for improving intestinal barrier function is taken for the purpose of obtaining the effect of improving intestinal barrier function in humans (adults)
- the composition for improving intestinal barrier function so that the intake of gallic acid is in the above range.
- the substance is orally taken or administered to the subject.
- the composition for improving intestinal barrier function according to the present invention contains an effective amount of gallic acid such that the desired effect of the present invention can be obtained in consideration of its administration form, administration method and the like. Is preferred.
- the composition for improving intestinal barrier function is an oral composition
- the daily intake of the composition per adult the content of gallic acid is 0.01 to 500 mg.
- 0.1 to 300 mg is more preferable, and 1 to 100 mg is more preferable.
- the composition for improving intestinal barrier function contains a phenolic compound in addition to the above amount of gallic acid.
- the subject (hereinafter, also simply referred to as a subject to be administered) to which the composition for improving intestinal barrier function of the present invention is administered or ingested is preferably a human or non-human animal, more preferably a mammal (human or non-human mammal) Humans are further preferred.
- a subject to be administered in the present invention a subject requiring or desired improvement in intestinal barrier function is preferable.
- a subject having a reduced intestinal barrier function, a subject that desires to prevent or ameliorate a condition or disease associated with the aforementioned intestinal barrier function abnormality, and the like can be mentioned as suitable subjects.
- the present invention also includes the following intestinal barrier function improvement methods and the like.
- a method for improving intestinal barrier function wherein gallic acid is administered to a subject.
- a phenol compound By combining administration of gallic acid and a phenol compound, an excellent intestinal barrier function improving effect can be obtained.
- Preferred embodiments of the phenolic compound are the same as those of the composition for improving intestinal barrier function.
- gallic acid and a phenolic compound When gallic acid and a phenolic compound are administered, they may be administered separately or simultaneously. Preferably, gallic acid and the phenolic compound are administered simultaneously.
- the gallic acid and the optionally used phenolic compound may be administered as they are, or may be administered a composition containing gallic acid and the like.
- the composition for improving intestinal barrier function of the present invention described above can be administered.
- the invention also encompasses the following uses: Use of gallic acid to improve intestinal barrier function.
- gallic acid and phenol compounds In the above use, it is preferred to use gallic acid and phenol compounds.
- gallic acid, an optionally used phenolic compound, a subject (administered subject), an administration method, a dose and a preferable embodiment thereof are the compositions for intestinal barrier function improving described above.
- the dose of gallic acid is not particularly limited as long as it is an amount capable of obtaining an intestinal barrier function improvement effect, that is, an effective amount.
- the amount of gallic acid described above can be administered.
- the ratio of gallic acid to the phenolic compound is preferably 0.1 to 10, more preferably 0.3 to 5 in molar ratio.
- the intestinal barrier function improving effect can be further improved.
- the combined use of gallic acid and a phenol compound can enhance the intestinal barrier function improving action of gallic acid.
- the above phenolic compounds can be used to enhance the intestinal barrier function improving action of gallic acid.
- Another aspect of the present invention is an enhancer of the intestinal barrier function improving action of gallic acid, which comprises a phenolic compound as an active ingredient; use of the phenolic compound for enhancing the intestinal barrier function improving action of gallic acid.
- the present invention also encompasses a method of enhancing the intestinal barrier function improving action of gallic acid, wherein gallic acid and a phenolic compound are administered in combination to a subject.
- the phenol compound and its preferable embodiment are the same as those of the composition for intestinal barrier function improvement described above.
- the preferred ratio of the amount used of gallic acid and phenolic compound is also the same as in the case of the composition for improving intestinal barrier function described above, and the molar ratio of gallic acid and phenolic compound (gallic acid / phenolic compound) is preferably 0.1. 10 to 10, more preferably 0.3 to 5.
- the intestinal barrier function improving action can be further enhanced.
- the above methods and uses may be therapeutic methods and uses, and may be non-therapeutic methods and uses.
- “Non-therapeutic” is a concept that does not include medical practice, i.e. surgery, treatment or diagnosis.
- the intestinal barrier function improving action of a test compound (hereinafter referred to as a sample) was evaluated using Caco-2 cells by the following method. Evaluation of components for improving intestinal barrier function using Caco-2 cells Caco-2 cells were cultured at 37 ° C. for 3 weeks in Transwell (Millicell) using DMEM (Dulbecco's modified Eagle's medium). Media was removed from the plates of cultured Caco-2 cells, the wells were washed three times each with serum free DMEM and the wells were filled with the media.
- DMEM Dulbecco's modified Eagle's medium
- TEER transepithelial electrical resistance
- inflammatory cytokines TNF ⁇ , IL-1 ⁇ and IFN ⁇
- a sample was set as normal.
- inflammatory cytokines were added, and a well to which no sample was added was provided as a control.
- TEER was again measured to evaluate whether the sample suppressed the reduction (reduction) of TEER due to inflammatory cytokines.
- TEER reduction inhibition rate (%) 100 ⁇ ((TEER of the well to which the sample was added)-(TEER of control) / ((TEER of normal)-(TEER of control))
- TEER reduction inhibition rate (%) 100 ⁇ ((TEER of the well to which the sample was added)-(TEER of control) / ((TEER of normal)-(TEER of control))
- Example 1 Using gallic acid as a sample, the intestinal barrier function improving action in Caco-2 cells was evaluated by the above evaluation method.
- Gallic acid Nacalai Tesque, Inc.
- 100 ⁇ M of quercetin (Funakoshi Co., Ltd.) was added to the test solution instead of gallic acid, and the intestinal barrier function improving action was similarly evaluated.
- quercetin the tight junction barrier function improvement effect is reported (nonpatent literature 1).
- the TEER reduction inhibition rate was 86.5% for gallic acid and 75.0% for quercetin. It was confirmed that gallic acid has a TEER reduction inhibitory rate that is about 1.15 times higher than that of quercetin at the same concentration at 100 ⁇ M.
- Example 2 In evaluations 1 to 4, gallic acid and the following phenol compounds were used as samples. Evaluation 1: Catechin (CA) (Wako Pure Chemical Industries, Ltd.) Evaluation 2: Epicatechin (EC) (Wako Pure Chemical Industries, Ltd.) Evaluation 3: Gallocatechin (GC) (Wako Pure Chemical Industries, Ltd.) Evaluation 4: Epigallocatechin (EGC) (Wako Pure Chemical Industries, Ltd.) The phenol compounds used in Example 2 are flavanols.
- the relative values shown in Table 1 are the values of (i) to (iii) when the TEER reduction inhibition rate (%) of the phenol compound (i) used in each of the evaluation systems in evaluations 1 to 4 is 1.0. It is a relative value of the TEER reduction suppression rate (%).
- the TEER reduction inhibitory rate (measured value of (iii) relative value ((iii) calculated from the TEER reduction suppressing rate (measured value: MV) obtained in the actual evaluation) ) / (I) TEER decrease inhibition rate of the phenol compound) is shown as a relative value of the measured value (phenol compound + gallic acid (measured value)).
- a relative value is a relative value of the TEER fall suppression rate when the TEER fall suppression rate of (i) catechin (CA) is 1.0.
- the relative value of the TEER reduction inhibitory rate of gallic acid (GA) was 0.4.
- the relative value ((CA + GA) (theoretical value)) of the theoretical value of the TEER reduction inhibition rate in the case of combined use of catechin and gallic acid (CA + GA) was 1.4.
- the relative value of this theoretical value is the sum of (i) TEER reduction inhibition rate of CA and (ii) TEER reduction inhibition rate of GA ((i) + (ii)), and (i) TEER reduction inhibition rate of CA It asked for.
- the relative value ((CA + GA) (measured value)) of the measured value calculated from the TEER reduction inhibition rate of (iii) (CA + GA) obtained in the actual evaluation was 2.8.
- the synergetic effect was determined by dividing the relative value (2.8) of the above measured value by the relative value (1.4) of the theoretical value.
- intestinal barrier function improvement effect obtained by combined use of gallic acid and the above-mentioned phenol compound is (ii) intestinal barrier function improvement effect when gallic acid alone (i) the phenol Compared with the calculation effect (theoretical value) which added the intestinal barrier function improvement effect in the case of a compound alone, it was found to be high.
- Example 3 Gallic acid and the phenolic compounds shown in Tables 2 to 3 were used as samples in the above evaluation method using Caco-2 cells to evaluate the improvement effect on intestinal barrier function (Evaluation 5 to 43).
- the TEER reduction inhibition rate (measured value: MV) obtained by the above evaluation is shown in Table 2 and Table 3 as "+ gallic acid (measured value)".
- the sum of (i) the TEER reduction inhibition rate of the phenol compound and (ii) the TEER reduction inhibition rate of gallic acid (TEER reduction inhibition rate of (i) + TEI decrease suppression of (ii)) Rate) was taken as the “theoretical value” of the TEER reduction inhibition rate in the case of using the phenol compound and gallic acid in combination (theoretical value of the TEER reduction inhibition rate in the case of using the phenol compound and gallic acid in combination).
- Tables 2 and 3 show the results.
- "phenol compound” is a phenol compound used in each evaluation system.
- Table 2 shows the results when the concentration of the phenolic compound and gallic acid in the test solutions is 10 ⁇ M.
- Table 3 shows the results of the concentrations of the phenolic compound and gallic acid in the test solutions each being 1 ⁇ M.
- gallic acid was used alone ((ii) above), gallic acid inhibited the decrease in TEER due to inflammatory cytokines in Caco-2 cells at any concentration of 1 ⁇ M and 10 ⁇ M.
- the intestinal barrier function improvement effect (measured value) obtained by combined use with gallic acid of (iii) is (ii) the intestinal barrier function improvement effect in the case of only gallic acid.
- (i) was higher than the calculated effect (theoretical value) obtained by adding the intestinal barrier function improvement effect in the case of the phenol compound alone.
- Petunidine Chloride Cayman Chemical Company Catechin gallate, epicatechin gallate, epigallocatechin gallate: Wako Pure Chemical Industries, Ltd. Theaflavin: Cosmo Bio Co., Ltd. Piceatannol: Tokyo Chemical Industry Co., Ltd. Naringenin Chalcone (4,2 ′, 4 ′, 6′-Tetrahydroxychalcone): Carbosynth Limited
- hydrolyzable tannins listed in Table 3 Kollagigin used was manufactured by SIGMA, and ⁇ -glucogalin used was manufactured by Carbocins (CAB). About hydrolysable tannins other than these, what was refine
- hydrolyzable tannins Purification of hydrolyzable tannins from plants is carried out according to the method described in the literature (Naoki Kajishima, "Studies on the constituents of Kunzea ambigua and Eucalyptus cypellocarpa", published on September 2005, Ph.D. thesis, Okayama University, pp. 76-95). went.
- the structures of hydrolyzable tannins listed in Table 3 are shown in Tables 4 and 5.
- composition and the like for improving intestinal barrier function of the present invention is useful in the field of food and drink, in the field of medicine, and the like.
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Abstract
Description
(1)没食子酸を有効成分として含む腸管バリア機能改善用組成物。
(2)さらに、フェノール化合物を含む上記(1)に記載の腸管バリア機能改善用組成物。
(3)上記フェノール化合物が、ポリフェノール及び/又はクマル酸類である上記(2)に記載の腸管バリア機能改善用組成物。
(4)上記ポリフェノールが、フラバン-3-オール重合体、フラバノール類、フラボノール類、フラバノン類、フラボン類、イソフラボン類、アントシアニジン類、フラバノノール類、スチルベノイド類、カルコン類及び加水分解性タンニンからなる群より選択される1以上の化合物である、上記(3)に記載の腸管バリア機能改善用組成物。
(5)上記フェノール化合物が、プロシアニジンB1、プロシアニジンB2、プロシアニジンB3、カテキン、エピカテキン、ガロカテキン、エピガロカテキン、カテキンガレート、エピカテキンガレート、エピガロカテキンガレート、テアフラビン、タキシフォリン、ダイゼイン、ゲニステイン、アピゲニン、ルテオリン、ナリンゲニン、ナリンゲニンカルコン、ケンフェロール、ルチン、ケルセチン-3-O-グルコピラノシド、ケルセチン、ミリセチン、ピセアタンノール、ペチュニジン、trans-ピセイド、コリラギン、ステノフィラニンA、ステノフィラニンB、カスアリニン、ゲラニイン、テリマグランジンI、ペドゥンクラジン、プレコキシンA、ユーゲニフロリンD2、1,4,6-トリ-O-ガロイル-β-D-グルコース、1,2,3,6-テトラ-O-ガロイル-β-D-グルコース、2,3,4,6-テトラ-O-ガロイル-β-D-グルコース、1,2,4,6-テトラ-O-ガロイル-β-D-グルコース、1,2,3,4,6-ペンタ-O-ガロイル-β-D-グルコース、β-グルコガリン、2-クマル酸及び3-クマル酸からなる群より選択される1以上の化合物である上記(2)~(4)のいずれかに記載の腸管バリア機能改善用組成物。
(6)経口用組成物である、上記(1)~(5)のいずれかに記載の腸管バリア機能改善用組成物。
(7)上記経口用組成物が、飲食品、医薬品又は医薬部外品である上記(6)に記載の腸管バリア機能改善用組成物。
(8)整腸のために使用される上記(1)~(7)のいずれかに記載の腸管バリア機能改善用組成物。
(9)整腸作用を有する旨の表示を付した、上記(1)~(8)のいずれかに記載の腸管バリア機能改善用組成物。
(10)フェノール化合物を有効成分として含む、没食子酸の腸管バリア機能改善作用の増強剤。
(11)没食子酸を対象に投与する、腸管バリア機能改善方法。
(12)没食子酸の、腸管バリア機能改善のための使用。
(13)没食子酸及びフェノール化合物を組み合わせて対象に投与する、没食子酸の腸管バリア機能改善作用を増強する方法。
(14)没食子酸の腸管バリア機能改善作用を増強するための、フェノール化合物の使用。
没食子酸は、腸管バリア機能改善作用を有する。没食子酸は、ブドウ、チャノキ等の植物に含まれる成分であり、長期間摂取しても副作用が少なく安全性が高いものである。
没食子酸は、その由来や製造方法によって特に限定されるものではない。例えば、植物から抽出した植物由来のものを用いてもよく、合成法によって得られたものを用いてもよい。
本発明において、フェノール化合物は、没食子酸以外のフェノール性水酸基を有する化合物又はその配糖体を指す。没食子酸は、本発明におけるフェノール化合物には含まれない。
配糖体とは、糖の水酸基が非糖質化合物とグリコシド結合してできる化合物をいう。配糖体における糖は、単糖であってもよく、二糖又はそれ以上の複数の糖であってもよく、特に限定されない。糖の種類も特に限定されず、グルコース、マンノース、ガラクトース、フコース、ラムノース、アラビノース、キシロース等のアルドース;フルクトース等のケトース;グルクロン酸、ガラクツロン酸、マンヌロン酸等のウロン酸;アピオース、ルチノース等が挙げられる。また、配糖体における糖はD体であってもよいし、L体であってもよい。
本発明の一態様において、腸管バリア機能改善用組成物は、没食子酸及びフェノール化合物を有効成分として含む腸管バリア機能改善用組成物であることが好ましい。
なお本発明におけるフラバノール類には、上記のフラバン-3-オール重合体は含まれない。
フラバノン類の化合物として、ナリンゲニン、その配糖体等が挙げられる。
フラボン類の化合物として、アピゲニン、ルテオリン、これらの配糖体等が挙げられる。
イソフラボン類の化合物として、ダイゼイン、ゲニステイン、これらの配糖体等が挙げられる。
フラバノノール類の化合物として、タキシフォリン、その配糖体等が挙げられる。
スチルベノイド類の化合物として、ピセアタンノール、その配糖体(trans-ピセイド、cis-ピセイド等)等が挙げられる。
カルコン類の化合物として、ナリンゲニンカルコン(4,2’,4’,6’-テトラヒドロキシカルコン)、その配糖体等が挙げられる。
フェノール化合物は、市販品を利用することもできる。
例えば、腸管上皮細胞を互いに接着するタイトジャンクションを正常化又は強化することによって、腸管バリア機能が改善される。一態様において、本発明の腸管バリア機能改善用組成物は、腸管上皮細胞におけるタイトジャンクションを正常化又は強化することによって腸管バリア機能を改善するために使用され得る。
実施例に示されるように、没食子酸は、Caco-2細胞を用いた腸管透過モデルにおいて、炎症性サイトカインの添加によるTEERの低下を抑制し、腸管バリア機能作用を有する。没食子酸は、腸管上皮細胞におけるタイトジャンクションを正常化又は強化して、腸管バリア機能を改善することができる。また、実施例に示されるように、没食子酸及びフェノール化合物の組み合わせは、より優れた腸管バリア機能改善効果を発揮し得る。
このため本発明の腸管機能改善用組成物は、腸管バリア機能の改善が有効な状態又は疾患、例えば腸管バリア機能の異常が関連する状態又は疾患の予防又は改善に有用である。腸管バリア機能の異常には、腸管バリア機能の低下が含まれる。腸管バリア機能の異常が関連する状態又は疾患としては、腸管バリア機能の異常に起因する状態若しくは疾患、又は、腸管バリア機能の異常を伴う状態若しくは疾患が挙げられる。このような腸管バリア機能の異常が関連する状態又は疾患として、例えば、炎症性腸疾患、過敏性腸症候群、全身性自己免疫疾患(関節リウマチ、エリテマトーデス等)、アレルギー(食物アレルギー、花粉症等)、生活習慣病(肥満、1型又は2型糖尿病、高血圧、高脂血症、非アルコール性脂肪性肝疾患(NAFLD)、動脈硬化等)等が挙げられる(例えば、Camilleri et al., Am J Physiol Gastrointest Liver Physiol 303: G775-G785, 2012; Mu et al., Front. Immunol., Vol.8, Article 598, 2017; Bischoff et al., BMC Gastroenterology 2014 14:189)。
本発明の腸管バリア機能改善用組成物は、例えば、飲食品、医薬品、医薬部外品、飼料等の形態で提供することができるが、これらに限定されるものではない。本発明の腸管バリア機能改善用組成物は、それ自体が飲食品、医薬品、医薬部外品、飼料等であってもよく、これらに使用される添加剤等の製剤、素材であってもよい。本発明の腸管バリア機能改善用組成物は、一例として、剤の形態で提供することができるが、本形態に限定されるものではない。当該剤をそのまま組成物として、又は、当該剤を含む組成物として提供することもできる。
一態様において、本発明の腸管バリア機能改善用組成物は、好ましくは経口用組成物である。本発明によれば、優れた腸管バリア機能改善作用を有する経口用組成物を提供することができる。経口用組成物として、飲食品、医薬品、医薬部外品が挙げられ、好ましくは飲食品である。
一態様において、他の成分として、例えば、乳酸菌、ビフィズス菌、食物繊維、多糖類等を含有していてもよい。
乳酸菌及びビフィズス菌は、経口的に摂取することができる菌であることが好ましい。
上記以外にも、その用途に応じて、飲食品、医薬品、医薬部外品、飼料等に使用される素材等の成分を適宜配合することができる。
本発明においては、没食子酸及びフェノール化合物を含む植物抽出物を用いて腸管バリア機能改善用組成物を調製することもできる。没食子酸及びフェノール化合物を含む植物抽出物は特に限定されず、例えば、ブドウ種子抽出物、緑茶抽出物、ウーロン茶抽出物、紅茶抽出物、ユーカリ抽出物、グアバ抽出物、甜茶抽出物、ローズヒップ抽出物等を用いることができる。
整腸作用は、腸管バリア機能の改善に基づく整腸作用であればよく、特に限定されない。上記整腸作用を有する旨の表示の一例として、「便秘又は下痢気味な方に」、「おなかの調子が気になる方に」、「おなかの不快感を感じやすい方に」、「便通を改善」、「便の状態を改善」、「排便回数を改善」、「排便量を改善」、「おなかすっきり」、「おなかの調子を整える」、「腸の調子を整える」、「おなかの不快感を改善」、「ガスの発生を和らげる」、「おなかの張りを和らげる」、「おなかのごろごろ感を和らげる」等が挙げられる。本発明の腸管バリア機能改善用組成物には、このような表示の1又は2以上が付されていてもよい。
没食子酸の含有量は、公知の方法に従って測定することができ、例えば、HPLC法等を用いることができる。
本発明の腸管バリア機能改善用組成物の摂取量(投与量ということもできる)は特に限定されず、腸管バリア機能改善効果が得られるような量であればよく、投与形態、投与方法等に応じて適宜設定すればよい。一態様として、ヒト(成人)を対象に経口で投与する又は摂取させる場合、腸管バリア機能改善用組成物の摂取量は、没食子酸の摂取量として、1日あたり、0.01~500mgが好ましく、0.1~300mgがより好ましく、1~100mgがさらに好ましい。上記量を、例えば1日1回で又は2~3回に分けて経口投与又は摂取させることが好ましい。ヒト(成人)を対象に腸管バリア機能改善効果を得ることを目的として腸管バリア機能改善用組成物を摂取させる場合は、没食子酸の摂取量が上記範囲となるように、腸管バリア機能改善用組成物を対象に経口で摂取させる又は投与することが好ましい。
没食子酸を対象に投与する、腸管バリア機能改善方法。
上記腸管バリア機能改善方法においては、さらにフェノール化合物を投与することが好ましい。没食子酸及びフェノール化合物を組み合わせて投与することにより、優れた腸管バリア機能改善効果が得られる。フェノール化合物の好ましい態様は、腸管バリア機能改善用組成物の場合と同じである。
没食子酸の、腸管バリア機能改善のための使用。
上記使用においては、没食子酸及びフェノール化合物を使用することが好ましい。
上記腸管バリア機能改善方法及び使用において、没食子酸、任意で使用されるフェノール化合物、対象(投与対象)、投与方法、投与量及びそれらの好ましい態様等は、上述した腸管バリア機能改善用組成物の場合と同じである。
例えば、没食子酸の投与量は、腸管バリア機能改善効果が得られる量、すなわち有効量であればよく、特に限定されない。例えば上述した量の没食子酸を投与することができる。フェノール化合物を使用する場合、没食子酸とフェノール化合物の比率(没食子酸/フェノール化合物)は、モル比で好ましくは0.1~10、より好ましくは0.3~5である。没食子酸及びフェノール化合物の比率が上記範囲であると、腸管バリア機能改善効果をより向上し得る。
本発明の別の態様は、フェノール化合物を有効成分として含む、没食子酸の腸管バリア機能改善作用の増強剤;没食子酸の腸管バリア機能改善作用を増強するための、フェノール化合物の使用、である。
腸管バリア機能改善作用の増強剤及び腸管バリア機能改善作用を増強する方法等において、フェノール化合物及びその好ましい態様等は、上述した腸管バリア機能改善用組成物の場合と同じである。没食子酸及びフェノール化合物の使用量の好ましい比率も、上述した腸管バリア機能改善用組成物の場合と同じであり、没食子酸及びフェノール化合物のモル比(没食子酸/フェノール化合物)が好ましくは0.1~10、より好ましくは0.3~5である。没食子酸及びフェノール化合物の比率が上記範囲であると、腸管バリア機能改善作用をより増強し得る。
上記方法及び使用は、治療的な方法及び使用であってもよく、非治療的な方法及び使用であってもよい。「非治療的」とは、医療行為、すなわち手術、治療又は診断を含まない概念である。
実施例において、被験化合物(以下、サンプルという)の腸管バリア機能改善作用は、Caco-2細胞を用いて以下の方法で評価した。
Caco-2細胞を用いた腸管バリア機能を改善する成分の評価
DMEM(ダルベッコ改変イーグル培地)を用いて、トランズウェル(Millicell社製)でCaco-2細胞を37℃で3週間培養した。培養したCaco-2細胞のプレートから培地を除去し、血清不含DMEMでウェルをそれぞれ3回洗浄し、その培地でウェルを満たした。その後、Millicell-ERS(ミリポア社製)によりCaco-2単層細胞の経上皮電気抵抗(TEER)を測定し、充分なタイトジャンクションが形成されていると判断される細胞(TEER≧1000Ω・cm2)を選抜して、次のスクリーニングに用いた。次いで、粘膜側、基底膜側両方の試験液(培地)にサンプルとTNFα(40ng/mL)、IL-1β(20ng/mL)及びIFNγ(10ng/mL)とを添加し、48時間培養した。なお、サンプルは、ジメチルスルホキシド(DMSO)に溶解後、試験液に添加した。この際に、炎症性サイトカイン(TNFα、IL-1β及びIFNγ)及びサンプルを添加しないウェルをノーマルとして設けた。また、炎症性サイトカインを添加し、サンプルを添加しないウェルをコントロールとして設けた。培養後、再びTEERを測定し、炎症性サイトカインによるTEERの低下(減少)をサンプルが抑制するかを評価した。
(TEER低下抑制率の計算式)
TEER低下抑制率(%)=100×((サンプルを添加したウェルのTEER)-(コントロールのTEER))/((ノーマルのTEER)-(コントロールのTEER))
この評価系では、TEER低下抑制率(%)が高いほど、腸管バリア改善作用が高い。
サンプルとして没食子酸を使用して、上記の評価方法でCaco-2細胞における腸管バリア機能改善作用を評価した。没食子酸(ナカライテスク(株))は、試験液中の濃度が100μM(μmol/L)となるように添加した。
参考として、没食子酸の代わりにケルセチン(フナコシ(株))を試験液中に100μM添加して、同様に腸管バリア機能改善作用を評価した。ケルセチンについては、タイトジャンクションバリア機能改善作用が報告されている(非特許文献1)。
その結果、TEER低下抑制率は、没食子酸が86.5%であり、ケルセチンが75.0%であった。没食子酸は、100μMにおいて同濃度のケルセチンと比較して1.15倍程度TEER低下抑制率が高いことが確認された。
評価1~4において、サンプルとして没食子酸及び以下のフェノール化合物を使用した。
評価1:カテキン(CA)(和光純薬工業(株))
評価2:エピカテキン(EC)(和光純薬工業(株))
評価3:ガロカテキン(GC)(和光純薬工業(株))
評価4:エピガロカテキン(EGC)(和光純薬工業(株))
実施例2で用いたフェノール化合物は、フラバノール類である。
(i)フェノール化合物(CA、EC、GC又はEGC)(1μM)
(ii)没食子酸(GA)(1μM)
(iii)フェノール化合物(1μM)及び没食子酸(1μM)の併用(フェノール化合物+GA)
サンプルは、試験液中の濃度が上記濃度となるように、試験液に添加した。評価結果を表1に示す。
(iii)フェノール化合物及び没食子酸の併用については、実際の評価で得られたTEER低下抑制率(実測値:M.V.)から計算した相対値((iii)のTEER低下抑制率(実測値)/(i)フェノール化合物のTEER低下抑制率)を、実測値(フェノール化合物+没食子酸(実測値))の相対値として示した。また、(i)フェノール化合物のTEER低下抑制率と、(ii)没食子酸のTEER低下抑制率との和((i)のTEER低下抑制率+(ii)のTEER低下抑制率)を、フェノール化合物及び没食子酸併用の場合のTEER低下抑制率の「理論値」(T.V.)とした。このTEER低下抑制率の理論値を、(i)フェノール化合物のTEER低下抑制率で除した値を、理論値の相対値(フェノール化合物+没食子酸(理論値))として表1に示した。
表1中の相乗効果は、(iii)の実測値の相対値及び理論値の相対値から、以下の計算式で算出した。
相乗効果=(実測値の相対値)/(理論値の相対値)
相対値は、(i)カテキン(CA)のTEER低下抑制率を1.0としたときの、TEER低下抑制率の相対値である。(ii)没食子酸(GA)のTEER低下抑制率の相対値は、0.4であった。カテキン及び没食子酸の併用(CA+GA)の場合のTEER低下抑制率の理論値の相対値((CA+GA)(理論値))は、1.4であった。この理論値の相対値は、(i)CAのTEER低下抑制率及び(ii)GAのTEER低下抑制率の和((i)+(ii))を、(i)CAのTEER低下抑制率で除して求めた。実際の評価で得られた(iii)(CA+GA)のTEER低下抑制率から計算した実測値の相対値((CA+GA)(実測値))は、2.8であった。相乗効果は、上記実測値の相対値(2.8)を、理論値の相対値(1.4)で除して求めた。
上記のCaco-2細胞を使用する評価方法で、没食子酸並びに表2~表3に示すフェノール化合物をサンプルとして用いて、腸管バリア機能改善効果を評価した(評価5~43)。
(i)フェノール化合物(表2に示す化合物は、10μM;表3に示す化合物は、1μM)
(ii)没食子酸(表2に示す化合物の評価系においては、10μM;表3に示す化合物の評価系においては1μM)
(iii)フェノール化合物及び没食子酸の併用(表2に示す化合物の評価系においては、それぞれ10μM;表3に示す化合物の評価系においては、それぞれ1μM)
サンプルは、試験液中の濃度が上記濃度となるように、試験液に添加した。
また実施例2と同様に、(i)フェノール化合物のTEER低下抑制率と、(ii)没食子酸のTEER低下抑制率との和((i)のTEER低下抑制率+(ii)のTEER低下抑制率)を、フェノール化合物及び没食子酸併用の場合のTEER低下抑制率の「理論値」(フェノール化合物及び没食子酸併用の場合のTEER低下抑制率の理論値)とした。このTEER低下抑制率の理論値を、表2及び表3に「+没食子酸(理論値)」として示した。
表2及び表3に示す相乗効果は、「+没食子酸(実測値)」(M.V.)及び、「+没食子酸(理論値)」(T.V.)から、以下の式で算出した。
相乗効果=(+没食子酸(実測値)(M.V.))/(+没食子酸(理論値)(T.V.))
表2は、フェノール化合物及び没食子酸の試験液中の濃度がそれぞれ10μMの結果である。表3は、フェノール化合物及び没食子酸の試験液中の濃度がそれぞれ1μMの結果である。なお、没食子酸を単独で使用した場合(上記の(ii))、没食子酸は、1μM及び10μMのいずれの濃度でも、Caco-2細胞において炎症性サイトカインによるTEERの低下を抑制した。
プロシアニジンB1:AdooQ BioScience社
プロシアニジンB2:Toronto Research Chemicals Inc.
プロシアニジンB3、ケルセチン、ケルセチン-3-O-グルコピラノシド、ナリンゲニン:フナコシ(株)
2-クマル酸、3-クマル酸:ChromaDex社
ゲニステイン:SIGMA社
アピゲニン、ルテオリン、ケンフェロール、ミリセチン、タキシフォリン:EXTRASYNTHESE社
ルチン、trans-ピセイド:ナカライテスク(株)
ダイゼイン、塩化ペチュニジン:Cayman Chemical Company
カテキンガレート、エピカテキンガレート、エピガロカテキンガレート:和光純薬工業(株)
テアフラビン:コスモ・バイオ(株)
ピセアタンノール:東京化成工業(株)
ナリンゲニンカルコン(4,2’,4’,6’-テトラヒドロキシカルコン):Carbosynth Limited
Claims (14)
- 没食子酸を有効成分として含む腸管バリア機能改善用組成物。
- さらに、フェノール化合物を含む請求項1に記載の腸管バリア機能改善用組成物。
- 前記フェノール化合物が、ポリフェノール及び/又はクマル酸類である請求項2に記載の腸管バリア機能改善用組成物。
- 前記ポリフェノールが、フラバン-3-オール重合体、フラバノール類、フラボノール類、フラバノン類、フラボン類、イソフラボン類、アントシアニジン類、フラバノノール類、スチルベノイド類、カルコン類及び加水分解性タンニンからなる群より選択される1以上の化合物である、請求項3に記載の腸管バリア機能改善用組成物。
- 前記フェノール化合物が、プロシアニジンB1、プロシアニジンB2、プロシアニジンB3、カテキン、エピカテキン、ガロカテキン、エピガロカテキン、カテキンガレート、エピカテキンガレート、エピガロカテキンガレート、テアフラビン、タキシフォリン、ダイゼイン、ゲニステイン、アピゲニン、ルテオリン、ナリンゲニン、ナリンゲニンカルコン、ケンフェロール、ルチン、ケルセチン-3-O-グルコピラノシド、ケルセチン、ミリセチン、ピセアタンノール、ペチュニジン、trans-ピセイド、コリラギン、ステノフィラニンA、ステノフィラニンB、カスアリニン、ゲラニイン、テリマグランジンI、ペドゥンクラジン、プレコキシンA、ユーゲニフロリンD2、1,4,6-トリ-O-ガロイル-β-D-グルコース、1,2,3,6-テトラ-O-ガロイル-β-D-グルコース、2,3,4,6-テトラ-O-ガロイル-β-D-グルコース、1,2,4,6-テトラ-O-ガロイル-β-D-グルコース、1,2,3,4,6-ペンタ-O-ガロイル-β-D-グルコース、β-グルコガリン、2-クマル酸及び3-クマル酸からなる群より選択される1以上の化合物である請求項2~4のいずれか一項に記載の腸管バリア機能改善用組成物。
- 経口用組成物である、請求項1~5のいずれか一項に記載の腸管バリア機能改善用組成物。
- 前記経口用組成物が、飲食品、医薬品又は医薬部外品である請求項6に記載の腸管バリア機能改善用組成物。
- 整腸のために使用される請求項1~7のいずれか一項に記載の腸管バリア機能改善用組成物。
- 整腸作用を有する旨の表示を付した、請求項1~8のいずれか一項に記載の腸管バリア機能改善用組成物。
- フェノール化合物を有効成分として含む、没食子酸の腸管バリア機能改善作用の増強剤。
- 没食子酸を対象に投与する、腸管バリア機能改善方法。
- 没食子酸の、腸管バリア機能改善のための使用。
- 没食子酸及びフェノール化合物を組み合わせて対象に投与する、没食子酸の腸管バリア機能改善作用を増強する方法。
- 没食子酸の腸管バリア機能改善作用を増強するための、フェノール化合物の使用。
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002009734A1 (fr) * | 2000-08-01 | 2002-02-07 | Oryza Oil & Fat Chemical Co.,Ltd. | Inhibiteurs d'absorption de sucre et leur procede de production |
JP2004262905A (ja) * | 2003-03-04 | 2004-09-24 | Inabata Koryo Kk | 抗アレルギー剤及び該抗アレルギー剤を含有する食品組成物 |
JP2010503609A (ja) * | 2006-05-05 | 2010-02-04 | オムニカ ゲーエムベーハー | キーウィ抽出物 |
JP2011084543A (ja) * | 2009-09-18 | 2011-04-28 | Masumi Takemoto | 生活習慣病予防及び改善剤 |
JP2011514347A (ja) * | 2008-03-06 | 2011-05-06 | ノバ ラボラトリーズ エスディーエヌ ビーエイチディー | フェノール酸を含むアブラヤシ葉からの抽出物 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002193819A (ja) * | 2000-12-26 | 2002-07-10 | Kirin Brewery Co Ltd | 吸収抑制剤及びそれを含む飲食品・医薬品 |
JP5865524B2 (ja) | 2015-01-09 | 2016-02-17 | Fontec R&D株式会社 | ゲンノショウコ組成物の製造方法 |
-
2018
- 2018-12-26 CA CA3086827A patent/CA3086827A1/en active Pending
- 2018-12-26 JP JP2019562106A patent/JP7252904B2/ja active Active
- 2018-12-26 CN CN201880084290.9A patent/CN111526735A/zh active Pending
- 2018-12-26 SG SG11202005327YA patent/SG11202005327YA/en unknown
- 2018-12-26 US US16/957,577 patent/US20200315998A1/en not_active Abandoned
- 2018-12-26 WO PCT/JP2018/047840 patent/WO2019131759A1/ja active Application Filing
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002009734A1 (fr) * | 2000-08-01 | 2002-02-07 | Oryza Oil & Fat Chemical Co.,Ltd. | Inhibiteurs d'absorption de sucre et leur procede de production |
JP2004262905A (ja) * | 2003-03-04 | 2004-09-24 | Inabata Koryo Kk | 抗アレルギー剤及び該抗アレルギー剤を含有する食品組成物 |
JP2010503609A (ja) * | 2006-05-05 | 2010-02-04 | オムニカ ゲーエムベーハー | キーウィ抽出物 |
JP2011514347A (ja) * | 2008-03-06 | 2011-05-06 | ノバ ラボラトリーズ エスディーエヌ ビーエイチディー | フェノール酸を含むアブラヤシ葉からの抽出物 |
JP2011084543A (ja) * | 2009-09-18 | 2011-04-28 | Masumi Takemoto | 生活習慣病予防及び改善剤 |
Non-Patent Citations (5)
Title |
---|
ABIODUN, O. O. ET AL.: "Antiinflammatory and immunomodulatory activity of an ethanolic extract from the stem bark of Terminalia catappa L. (Combretaceae) : In vitro and in vivo evidences", JOURNAL OF ETHNOPHARMACOLOGY, vol. 192, 21 July 2016 (2016-07-21), pages 309 - 319, XP029763365 * |
CREMONINI, E. ET AL.: "Anthocyanins inhibit tumor necrosis alpha-induced loss of Caco-2 cell barrier integrity", FOOD & FUNCTION, vol. 8, no. 8, 18 July 2017 (2017-07-18) - 1 August 2017 (2017-08-01), pages 2915 - 2923, XP055623342 * |
PARK, H. Y. ET AL.: "Theaflavins enhance intestinal barrier of Caco-2 Cell monolayers through the expression of AMP-activated protein kinase-mediated Occludin, claudin-1, and ZO-1", BIOSCIENCE, BIOTECHNOLOGY, AND BIOCHEMISTRY, vol. 79, no. 1, 30 August 2014 (2014-08-30) - 2015, pages 130 - 137, XP055623330 * |
ROGOLL, D. ET AL.: "Influence of apple polyphenols on the intestinal barrier in a colonic cell model", JOURNAL OF APPLIED BOTANY AND FOOD QUALITY, vol. 83, no. 2, 2010 - 5 December 2012 (2012-12-05), pages 110 - 117, XP055623335 * |
XUAN, Y. ET AL.: "Pomegranate leaf attenuates lipid absorption in the small intestine in hyperlipidemic mice by inhibiting lipase activity", CHINESE JOURNAL OF NATURAL MEDICINES, vol. 15, no. 10, 2017, pages 732 - 739, XP085279163 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112791091A (zh) * | 2021-01-15 | 2021-05-14 | 江南大学 | 王不留行黄酮苷在改善肠道屏障功能中的应用 |
CN112791091B (zh) * | 2021-01-15 | 2022-04-29 | 江南大学 | 王不留行黄酮苷在改善肠道屏障功能中的应用 |
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TW201936065A (zh) | 2019-09-16 |
TWI778202B (zh) | 2022-09-21 |
SG11202005327YA (en) | 2020-07-29 |
CN111526735A (zh) | 2020-08-11 |
CA3086827A1 (en) | 2019-07-04 |
US20200315998A1 (en) | 2020-10-08 |
JPWO2019131759A1 (ja) | 2020-12-24 |
JP7252904B2 (ja) | 2023-04-05 |
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