Peroxisome proliferator activated receptor ligand and process for producing the same
View Patent ↗The present invention easily and efficiently provides a peroxisome proliferator-activated receptor ligand, and a composition for amelioration of insulin resistance or for prevention and/or amelioration of the insulin resistance syndrome containing the same, as an active ingredient. The present invention relates to a peroxisome proliferator-activated receptor ligand which comprises a prenylflavonoid, a chalcone derivative exclusive of prenylflavonoids, a flavonol derivative exclusive of prenylflavonoids, and a salt, a glycoside and/or an esterified substance thereof acceptable as a pharmaceutical preparation or a food or a beverage; a composition containing the above ligand; a plant-derived extract containing the above ligand; and a process for producing the above extract.
1. A method for inhibiting or ameliorating an insulin resistance syndrome
which comprises administering a composition comprising, as an active ingredient, at least one prenylflavonoid selected from the group consisting of a 3-arylcoumarin compound, an isoflav-3-ene compound, an isoflavan compound, an isoflavanone compound, an isoflavone compound, a flavonol compound, a flavanone compound, a chalcone compound and a dibenzoylmethane compound to a subject,
wherein the prenylflavonoid has a peroxisome proliferator-activated receptor γ ligand activity.
2. The method according to claim 1 ,
wherein the prenylflavonoid comprises a 3-arylcoumarin compound represented by the general formula (1):
in the formula, at least one of R1 to R7 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
3. The method according to claim 2 ,
wherein the 3-arylcoumarin compound represented by the general formula (1) is glycycoumarin or glycyrin.
4. The method according to claim 1 ,
wherein the prenylflavonoid comprises an isoflav-3-ene compound represented by the general formula (2):
in the formula, at least one of R1 to R7 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
5. The method according to claim 4 ,
wherein the isoflav-3-ene compound represented by the general formula (2) is dehydroglyasperin D, dehydroglyasperin C or glabrene.
6. The method according to claim 1 ,
wherein the prenylflavonoid comprises an isoflavan compound represented by the general formula (3):
in the formula, at least one of R1 to R7 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
7. The method according to claim 6 ,
wherein the isoflavan compound represented by the general formula (3) is glyasperin D, glabridin, hispaglabridin B, 4′-O-methylglabridin or 3′-hydroxy-4′-O-methylglabridin.
8. The method according to claim 1 ,
wherein the prenylflavonoid comprises an isoflavanone compound represented by the general formula (4):
in the formula, at least one of R1 to R8 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
9. The method according to claim 8 ,
wherein the isoflavanone compound represented by the general formula (4) is glyasperin B or glycyrrhisoflavanone.
10. The method according to claim 1 ,
wherein the prenylflavonoid comprises an isoflavone compound represented by the general formula (5):
in the formula, at least one of R1 to R9 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
11. The method according to claim 1 ,
wherein the isoflavone compound represented by the general formula (5) is glyurallin B, lupiwighteone, semilicoisoflavone B or glycyrrhisoflavone.
12. The method according to claim 1 ,
wherein the prenylflavonoid comprises a flavonol compound represented by the general formula (6):
in the formula, R1 is OH or OCH 3 , at least one of R2 to R9 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
13. The method according to claim 12 ,
wherein the flavonol compound represented by the general formula (6) is isolicoflavonol, licoflavonol or topazolin.
14. The method according to claim 1 ,
wherein the prenylflavonoid comprises a flavanone compound represented by the general formula (7):
in the formula, at least one of R1 to R8 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
15. The method according to claim 14 ,
wherein the flavanone compound represented by the general formula (7) is glabrol.
16. The method according to claim 1 ,
wherein the prenylflavonoid comprises a chalcone compound represented by the general formula (8):
in the formula, at least one of R1 to R9 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
17. The method according to claim 16 ,
wherein the chalcone compound represented by the general formula (8) is licochalcone C.
18. The method according to claim 1 ,
wherein the prenylflavonoid comprises a dibenzoylmethane compound represented by the general formula (9):
in the formula, at least one of R1 to R7 represents a prenyl group or a structure wherein adjacent 2 R groups form a 6-membered ring comprising —CH═CHC(CH 3 ) 2 O—, and other R groups represent H, OH or OCH 3 .
19. The method according to claim 18 ,
wherein the dibenzoylmethane compound represented by the general formula (9) is glycyrdione A or glycyrdione C.
20. A method for inhibiting or ameliorating inflammations or cancers
which comprises administering a composition comprising, as an active ingredient, at least one prenylflavonoid selected from the group consisting of a 3-arylcoumarin compound, an isoflav-3-ene compound, an isoflavan compound, an isoflavanone compound, an isoflavone compound, a flavonol compound, a flavanone compound, a chalcone compound and a dibenzoylmethane compound to a subject,
wherein the prenylflavonoid has a peroxisome proliferator-activated receptor γ ligand activity.
21. The method according to claim 1 ,
wherein the insulin resistance syndrome is at least one symptom or disease selected from the group consisting of hyperinsulinemia, diabetes mellitus, dyslipidemia, obesity, hypertension and arteriosclerosis.
22. The method according to claim 21 ,
wherein the symptom or disease is diabetes mellitus.
23. The method according to claim 1 ,
wherein the composition comprises at least one member selected from the group consisting of glycycoumarin, glycyrin, glyurallin B, dehydroglyasperin D, isolicoflavonol, dehydroglyasperin C, glyasperin B, glycyrrhisoflavanone, lupiwighteone, glyasperin D, semilicoisoflavone B, licoflavonol, topazolin, glycyrrhisoflavone, glabridin, glabrene, hispaglabridin B, 4′-O-methylglabridin, 3′-hydroxy-4′-O-methylglabridin, glabrol, licochalcone C, glycyrdione A and glycyrdione C.
24. The method according to claim 1 ,
wherein the composition comprises at least one member selected from the group consisting of glabrene, glabridin, glabrol, 3′-hydroxy-4′-O-methylglabridin, 4′-O-methylglabridin and hispaglabridin B.