KR101250198B1 - Composition of food components for appetite control comprising specific compounds as effective component - Google Patents
Composition of food components for appetite control comprising specific compounds as effective component Download PDFInfo
- Publication number
- KR101250198B1 KR101250198B1 KR1020100108541A KR20100108541A KR101250198B1 KR 101250198 B1 KR101250198 B1 KR 101250198B1 KR 1020100108541 A KR1020100108541 A KR 1020100108541A KR 20100108541 A KR20100108541 A KR 20100108541A KR 101250198 B1 KR101250198 B1 KR 101250198B1
- Authority
- KR
- South Korea
- Prior art keywords
- appetite
- ginsenoside
- ghrelin
- composition
- hesperetin
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 41
- 235000012041 food component Nutrition 0.000 title description 42
- 239000000306 component Substances 0.000 title description 11
- 235000021407 appetite control Nutrition 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 title description 3
- 239000005428 food component Substances 0.000 title description 3
- GNKDKYIHGQKHHM-RJKLHVOGSA-N ghrelin Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)CN)COC(=O)CCCCCCC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1N=CNC=1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C1=CC=CC=C1 GNKDKYIHGQKHHM-RJKLHVOGSA-N 0.000 claims abstract description 54
- 102000012004 Ghrelin Human genes 0.000 claims abstract description 53
- 101800001586 Ghrelin Proteins 0.000 claims abstract description 53
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 50
- 235000019789 appetite Nutrition 0.000 claims abstract description 31
- 230000036528 appetite Effects 0.000 claims abstract description 31
- YURJSTAIMNSZAE-HHNZYBFYSA-N ginsenoside Rg1 Chemical compound O([C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(C[C@@H]([C@H]4C(C)(C)[C@@H](O)CC[C@]4(C)[C@H]3C[C@H]2O)O[C@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)C)(C)CC1)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O YURJSTAIMNSZAE-HHNZYBFYSA-N 0.000 claims abstract description 28
- YURJSTAIMNSZAE-UHFFFAOYSA-N UNPD89172 Natural products C1CC(C2(CC(C3C(C)(C)C(O)CCC3(C)C2CC2O)OC3C(C(O)C(O)C(CO)O3)O)C)(C)C2C1C(C)(CCC=C(C)C)OC1OC(CO)C(O)C(O)C1O YURJSTAIMNSZAE-UHFFFAOYSA-N 0.000 claims abstract description 27
- 230000000694 effects Effects 0.000 claims abstract description 27
- CBEHEBUBNAGGKC-UHFFFAOYSA-N ginsenoside Rg1 Natural products CC(=CCCC(C)(OC1OC(CO)C(O)C(O)C1O)C2CCC3(C)C2C(O)CC4C5(C)CCC(O)C(C)(C)C5CC(OC6OC(CO)C(O)C(O)C6O)C34C)C CBEHEBUBNAGGKC-UHFFFAOYSA-N 0.000 claims abstract description 26
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 25
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 25
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 25
- 239000001100 (2S)-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chroman-4-one Substances 0.000 claims abstract description 24
- AIONOLUJZLIMTK-AWEZNQCLSA-N hesperetin Chemical compound C1=C(O)C(OC)=CC=C1[C@H]1OC2=CC(O)=CC(O)=C2C(=O)C1 AIONOLUJZLIMTK-AWEZNQCLSA-N 0.000 claims abstract description 24
- 229960001587 hesperetin Drugs 0.000 claims abstract description 24
- AIONOLUJZLIMTK-UHFFFAOYSA-N hesperetin Natural products C1=C(O)C(OC)=CC=C1C1OC2=CC(O)=CC(O)=C2C(=O)C1 AIONOLUJZLIMTK-UHFFFAOYSA-N 0.000 claims abstract description 24
- 235000010209 hesperetin Nutrition 0.000 claims abstract description 24
- FTODBIPDTXRIGS-UHFFFAOYSA-N homoeriodictyol Natural products C1=C(O)C(OC)=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2)=C1 FTODBIPDTXRIGS-UHFFFAOYSA-N 0.000 claims abstract description 24
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 21
- 239000002830 appetite depressant Substances 0.000 claims abstract description 9
- 235000013376 functional food Nutrition 0.000 claims abstract description 6
- 229940088597 hormone Drugs 0.000 claims abstract description 5
- 239000005556 hormone Substances 0.000 claims abstract description 5
- 239000004480 active ingredient Substances 0.000 claims description 12
- FYGDTMLNYKFZSV-WFYNLLPOSA-N (2s,3r,4s,5s,6r)-2-[(2r,4r,5r,6s)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(2r,3s,4r,5r,6s)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-WFYNLLPOSA-N 0.000 abstract description 25
- 229920002498 Beta-glucan Polymers 0.000 abstract description 25
- YJPIGAIKUZMOQA-UHFFFAOYSA-N Melatonin Natural products COC1=CC=C2N(C(C)=O)C=C(CCN)C2=C1 YJPIGAIKUZMOQA-UHFFFAOYSA-N 0.000 abstract description 21
- DRLFMBDRBRZALE-UHFFFAOYSA-N melatonin Chemical compound COC1=CC=C2NC=C(CCNC(C)=O)C2=C1 DRLFMBDRBRZALE-UHFFFAOYSA-N 0.000 abstract description 21
- 229960003987 melatonin Drugs 0.000 abstract description 21
- UFNDONGOJKNAES-UHFFFAOYSA-N Ginsenoside Rb1 Natural products CC(=CCCC(C)(OC1OC(COC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7OC8OC(CO)C(O)C(O)C8O)C(C)(C)C6CC(O)C45C)C UFNDONGOJKNAES-UHFFFAOYSA-N 0.000 abstract description 20
- GZYPWOGIYAIIPV-JBDTYSNRSA-N ginsenoside Rb1 Chemical compound C([C@H]1O[C@H]([C@@H]([C@@H](O)[C@@H]1O)O)O[C@@](C)(CCC=C(C)C)[C@@H]1[C@@H]2[C@@]([C@@]3(CC[C@H]4C(C)(C)[C@@H](O[C@H]5[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O5)O[C@H]5[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O5)O)CC[C@]4(C)[C@H]3C[C@H]2O)C)(C)CC1)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O GZYPWOGIYAIIPV-JBDTYSNRSA-N 0.000 abstract description 20
- TXEWRVNOAJOINC-UHFFFAOYSA-N ginsenoside Rb2 Natural products CC(=CCCC(OC1OC(COC2OCC(O)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7OC8OC(CO)C(O)C(O)C8O)C(C)(C)C6CCC45C)C TXEWRVNOAJOINC-UHFFFAOYSA-N 0.000 abstract description 20
- 239000005417 food ingredient Substances 0.000 description 39
- 206010061428 decreased appetite Diseases 0.000 description 21
- 230000003880 negative regulation of appetite Effects 0.000 description 21
- 210000004027 cell Anatomy 0.000 description 14
- 238000011282 treatment Methods 0.000 description 12
- 230000004663 cell proliferation Effects 0.000 description 11
- 235000013305 food Nutrition 0.000 description 11
- 208000008589 Obesity Diseases 0.000 description 10
- 235000020824 obesity Nutrition 0.000 description 10
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- AGBQKNBQESQNJD-UHFFFAOYSA-N lipoic acid Chemical compound OC(=O)CCCCC1CCSS1 AGBQKNBQESQNJD-UHFFFAOYSA-N 0.000 description 7
- 229960002663 thioctic acid Drugs 0.000 description 7
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 230000005764 inhibitory process Effects 0.000 description 6
- 239000000546 pharmaceutical excipient Substances 0.000 description 6
- UNAANXDKBXWMLN-UHFFFAOYSA-N sibutramine Chemical compound C=1C=C(Cl)C=CC=1C1(C(N(C)C)CC(C)C)CCC1 UNAANXDKBXWMLN-UHFFFAOYSA-N 0.000 description 6
- 230000004913 activation Effects 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- 210000002889 endothelial cell Anatomy 0.000 description 5
- 239000013641 positive control Substances 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 229940076279 serotonin Drugs 0.000 description 5
- 229960004425 sibutramine Drugs 0.000 description 5
- 210000003606 umbilical vein Anatomy 0.000 description 5
- FTVWIRXFELQLPI-ZDUSSCGKSA-N (S)-naringenin Chemical compound C1=CC(O)=CC=C1[C@H]1OC2=CC(O)=CC(O)=C2C(=O)C1 FTVWIRXFELQLPI-ZDUSSCGKSA-N 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 4
- 229930182494 ginsenoside Natural products 0.000 description 4
- 235000019136 lipoic acid Nutrition 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- -1 melaninin Chemical compound 0.000 description 4
- WGEYAGZBLYNDFV-UHFFFAOYSA-N naringenin Natural products C1(=O)C2=C(O)C=C(O)C=C2OC(C1)C1=CC=C(CC1)O WGEYAGZBLYNDFV-UHFFFAOYSA-N 0.000 description 4
- 235000007625 naringenin Nutrition 0.000 description 4
- 229940117954 naringenin Drugs 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 108010010803 Gelatin Proteins 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 3
- 229930006000 Sucrose Natural products 0.000 description 3
- 229940087168 alpha tocopherol Drugs 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 230000024245 cell differentiation Effects 0.000 description 3
- 239000013592 cell lysate Substances 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 235000005911 diet Nutrition 0.000 description 3
- 230000004069 differentiation Effects 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 235000003599 food sweetener Nutrition 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920000159 gelatin Polymers 0.000 description 3
- 239000008273 gelatin Substances 0.000 description 3
- 235000019322 gelatine Nutrition 0.000 description 3
- 235000011852 gelatine desserts Nutrition 0.000 description 3
- 229940089161 ginsenoside Drugs 0.000 description 3
- 230000036541 health Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000002062 proliferating effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- 239000000829 suppository Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000003765 sweetening agent Substances 0.000 description 3
- 229960000984 tocofersolan Drugs 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 235000004835 α-tocopherol Nutrition 0.000 description 3
- 239000002076 α-tocopherol Substances 0.000 description 3
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 239000004386 Erythritol Substances 0.000 description 2
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 101000942967 Homo sapiens Leukemia inhibitory factor Proteins 0.000 description 2
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
- 102100032352 Leukemia inhibitory factor Human genes 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 210000000577 adipose tissue Anatomy 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 230000003579 anti-obesity Effects 0.000 description 2
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
- 235000014121 butter Nutrition 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 230000037213 diet Effects 0.000 description 2
- 230000029087 digestion Effects 0.000 description 2
- 102000038379 digestive enzymes Human genes 0.000 description 2
- 108091007734 digestive enzymes Proteins 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 238000001647 drug administration Methods 0.000 description 2
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 2
- 235000019414 erythritol Nutrition 0.000 description 2
- 229940009714 erythritol Drugs 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000015203 fruit juice Nutrition 0.000 description 2
- 229960001031 glucose Drugs 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 239000008101 lactose Substances 0.000 description 2
- 230000004130 lipolysis Effects 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 235000010356 sorbitol Nutrition 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 229960002920 sorbitol Drugs 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000000811 xylitol Substances 0.000 description 2
- 235000010447 xylitol Nutrition 0.000 description 2
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 2
- 229960002675 xylitol Drugs 0.000 description 2
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- KIUMMUBSPKGMOY-UHFFFAOYSA-N 3,3'-Dithiobis(6-nitrobenzoic acid) Chemical compound C1=C([N+]([O-])=O)C(C(=O)O)=CC(SSC=2C=C(C(=CC=2)[N+]([O-])=O)C(O)=O)=C1 KIUMMUBSPKGMOY-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 108010011485 Aspartame Proteins 0.000 description 1
- 208000024172 Cardiovascular disease Diseases 0.000 description 1
- PTHCMJGKKRQCBF-UHFFFAOYSA-N Cellulose, microcrystalline Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC)C(CO)O1 PTHCMJGKKRQCBF-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 206010049119 Emotional distress Diseases 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 206010020772 Hypertension Diseases 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 244000131316 Panax pseudoginseng Species 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 229920002230 Pectic acid Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- 244000228451 Stevia rebaudiana Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 1
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 102000005789 Vascular Endothelial Growth Factors Human genes 0.000 description 1
- 108010019530 Vascular Endothelial Growth Factors Proteins 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 235000013334 alcoholic beverage Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000004596 appetite loss Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000605 aspartame Substances 0.000 description 1
- 235000010357 aspartame Nutrition 0.000 description 1
- IAOZJIPTCAWIRG-QWRGUYRKSA-N aspartame Chemical compound OC(=O)C[C@H](N)C(=O)N[C@H](C(=O)OC)CC1=CC=CC=C1 IAOZJIPTCAWIRG-QWRGUYRKSA-N 0.000 description 1
- 229960003438 aspartame Drugs 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229940093797 bioflavonoids Drugs 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 201000011529 cardiovascular cancer Diseases 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 1
- 229940093471 ethyl oleate Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 230000009246 food effect Effects 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000020510 functional beverage Nutrition 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 229960002897 heparin Drugs 0.000 description 1
- 229920000669 heparin Polymers 0.000 description 1
- 210000003630 histaminocyte Anatomy 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 238000000185 intracerebroventricular administration Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229960001375 lactose Drugs 0.000 description 1
- VMPHSYLJUKZBJJ-UHFFFAOYSA-N lauric acid triglyceride Natural products CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 1
- 230000037356 lipid metabolism Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 208000019017 loss of appetite Diseases 0.000 description 1
- 235000021266 loss of appetite Nutrition 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229960003511 macrogol Drugs 0.000 description 1
- 239000000845 maltitol Substances 0.000 description 1
- 235000010449 maltitol Nutrition 0.000 description 1
- VQHSOMBJVWLPSR-WUJBLJFYSA-N maltitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H]([C@H](O)CO)O[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O VQHSOMBJVWLPSR-WUJBLJFYSA-N 0.000 description 1
- 229940035436 maltitol Drugs 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960001855 mannitol Drugs 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 235000021096 natural sweeteners Nutrition 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000037081 physical activity Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 235000013550 pizza Nutrition 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 229960003415 propylparaben Drugs 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000001671 psychotherapy Methods 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- HELXLJCILKEWJH-NCGAPWICSA-N rebaudioside A Chemical compound O([C@H]1[C@H](O)[C@@H](CO)O[C@H]([C@@H]1O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)O[C@]12C(=C)C[C@@]3(C1)CC[C@@H]1[C@@](C)(CCC[C@]1([C@@H]3CC2)C)C(=O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HELXLJCILKEWJH-NCGAPWICSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 235000013580 sausages Nutrition 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 235000011888 snacks Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Images
Classifications
-
- 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
- A23L33/20—Reducing nutritive value; Dietetic products with reduced nutritive value
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2200/00—Function of food ingredients
- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/332—Promoters of weight control and weight loss
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Mycology (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
본 발명은 유효성분으로 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 함유하는 식욕억제 조성물에 관한 것으로, 더욱 상세하게는 식욕촉진 호르몬인 그렐린(ghrelin)의 활성을 억제함으로써 식욕억제 효과를 갖는 식욕억제 조성물 및 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제용 기능성 식품에 관한 것이다.The present invention is ascorbic acid (ascorbic acid), beta-D-glucan (β-D-glucan), hesperetin (hesperetin), melatonin (melatonin), ginsenoside-Rb1 (ginsenoside-Rb1) and gin The present invention relates to an appetite suppressant composition containing at least one component selected from the group consisting of ginsenoside-Rg1, and more particularly, has an appetite suppressing effect by inhibiting the activity of ghrelin, an appetite-stimulating hormone. Appetite suppressant compositions and ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin, melatonin, ginsenoside-Rb1 and ginsenosides -Rg1 (ginsenoside-Rg1) relates to a functional food for suppressing appetite containing at least one component selected from the group consisting of.
Description
본 발명은 유효성분으로 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드- Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 함유하는 식욕억제 조성물 및 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제용 기능성 식품에 관한 것이다.The present invention as an active ingredient (ascorbic acid), beta-D-glucan (β-D-glucan), hesperetin (hesperetin), melatonin (melatonin), ginsenoside-Rb1 (ginsenoside-Rb1) and gin Appetite suppressant composition and ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin containing at least one component selected from the group consisting of ginsenoside-Rg1. ), Melatonin, melatonin, ginsenoside-Rb1 (ginsenoside-Rb1) and ginsenoside-Rg1 (ginsenoside-Rg1) relates to a functional food for suppressing appetite containing an active ingredient containing at least one component will be.
비만인구는 BMI(body mass index) 30 이상인 경우를 기준으로 미국이 전 인구의 32%로 가장 높으며, 멕시코가 30%, 영국 23%, 그리스, 호주, 뉴질랜드가 21%로 비만인구가 높은 국가들이 있다. 우리나라는 전 인구의 3.5%인 150~200만 명이 비만 인구이나, 식생활의 서구화, 다원화 등의 이유로 비만 인구가 매우 빠른 속도로 증가하고 있다.Obesity is the highest in the United States (32% of the population), with a body mass index (BMI) of 30 or higher, and Mexico, 30%, the UK, 23%, Greece, Australia, and New Zealand, 21%. have. In Korea, 1.5% to 2 million people, 3.5% of the total population, are obese, but the population of obesity is increasing very rapidly due to westernization and diversification of dietary life.
비만은 당뇨, 고혈압, 심혈관이상, 암, 정신적 고통 등 성인병 유발에서 사망원인의 일부에까지 이르게 되었으며 국가 생산성, 활동성 및 경쟁력에도 영향을 미친다. 특히 식생활과 교육환경의 변화를 많이 겪게 된 우리나라 소아, 청소년의 비만은 급격히 증가하고 있으며, 소아당뇨 등 발병된 후 치료회복이 쉽지않은 심각성을 야기하고 있다.Obesity has led to adult disease, including diabetes, hypertension, cardiovascular disease, cancer and mental distress, to some of the causes of death, and also affects national productivity, activity and competitiveness. In particular, the obesity of children and adolescents in Korea, which has undergone many changes in their diet and educational environment, is increasing rapidly, and the recovery of treatment after the onset of pediatric diabetes, etc., is not easy.
비만억제 관련 치료는 약물투여, 운동, 식이요법, 정신치료, 수술요법 등 다양한 시도가 있어왔으나 특정한 방법에 의하여 개선되기는 어려우며 복합적인 치료와 환자의 의지가 중요하다. 약물투여의 경우 지방분해나 소화효소저해에 의한 방법을 원리로 약제가 개발되었으나 부작용을 동반하고 있다.Obesity-related treatments have been tried in various ways such as drug administration, exercise, diet, psychotherapy, and surgery, but it is difficult to improve by specific methods, and complex treatments and patient will are important. In the case of drug administration, the drug was developed on the basis of lipolysis or digestive enzyme inhibition, but it has side effects.
비만의 해결방법으로 생성 및 축적된 비만세포를 분해하거나 소화효소를 저해하는 방법이 보편적으로 시도되었으나, 섭취하는 식품의 소화저해나 생성된 지방을 분해한다고 하더라도 비만환자의 폭식에 의하여 지속적으로 다량의 식품이 체내에 공급된다면 소화저해나 지방분해는 섭취하는 속도와 양에 비하여 역할이 제한적일 수밖에 없다.As a solution to obesity, a method of degrading and accumulating mast cells or inhibiting digestive enzymes has been generally attempted. If food is supplied to the body, digestion or lipolysis has a limited role compared to the rate and amount of ingestion.
따라서, 식품의 섭취를 근본적으로 조절하는 식욕조절(appetite control)은 근본적인 해결에 대한 접근방법이 될 수 있으며, 식품성분 조성물에 의한 식욕억제는 최초 시도로서 신규성, 독창성 및 진보성을 갖는 발명으로서 의의를 갖는다.Thus, appetite control (appetite control) to fundamentally regulate the intake of food can be an approach to the fundamental solution, the appetite suppression by the food ingredient composition as a first attempt is meaningful as an invention with novelty, originality and progressiveness Have
현재 식욕조절에 의한 비만억제는 약물로서 Reductil이 출시된 적이 있으나 식욕부진, 불면, 우울, 혈압 상승 등의 부작용을 동반하여 식품이나 천연물에 의한 접근이 요구된다. 따라서, 부작용을 최소화하면서 식욕억제 식품소재로서 새로운 가치를 창출하여 비만억제에 기여할 수 있는 식욕억제를 위한 조성물이 필요한 실정이다.Currently, reductil has been released as a drug to control obesity due to appetite control, but it is required to access food or natural products with side effects such as loss of appetite, insomnia, depression, and blood pressure. Therefore, there is a need for a composition for appetite suppression that can contribute to suppression of obesity by creating a new value as an appetite suppressing food material while minimizing side effects.
본 발명은 비만억제의 해결수단으로서 식품성분 조성물에 의한 식욕억제 방법을 최초로 개발하였으며, 식욕억제 효과를 증명하는 방법에 있어서도 식욕을 촉진하는 그렐린(Ghrelin)을 억제하는 시험계를 최초로 발굴하여 세포분화도에 따라 식품성분을 적용하고 식욕억제 효과를 과학적으로 검증하였다.The present invention first developed an appetite suppression method by a food ingredient composition as a means of preventing obesity, and in the method of proving appetite suppression effect, first discovered a test system that suppresses ghrelin that promotes appetite, and thus on the degree of cell differentiation. Therefore, food ingredients were applied and appetite suppression effects were scientifically verified.
한국공개특허 제2004-0097813호에는 식욕억제, 체지방 감소 및 배변 활성화 등 3가지 기능을 갖는 항비만 기능성 조성물이 개시되어 있으며, 한국공개특허 제2004-0036111호에는 인삼 및 폴리페놀계 물질 또는 바이오플라보노이드계 물질을 포함하는 식물의 분말 또는 추출물을 포함하는 지질대사 개선 및 항비만용 식품이 개시되어 있으나, 본 발명의 식욕억제 식품성분 조성물과는 상이하다.Korean Patent Publication No. 2004-0097813 discloses an anti-obesity functional composition having three functions such as appetite suppression, body fat reduction, and bowel activation. Korean Patent Publication No. 2004-0036111 discloses ginseng and polyphenol-based substances or bioflavonoids. Foods for improving lipid metabolism and anti-obesity including a powder or extract of a plant comprising a systemic substance have been disclosed, but differ from the appetite suppressing food ingredient composition of the present invention.
본 발명은 상기와 같은 요구에 의해 도출된 것으로서, 본 발명은 식욕을 억제시킬 수 있는 기능성 소재의 개발이 요망되고 있으나, 체지방분해, 소화저해 방법의 한계성 및 부작용 등 안전성의 문제 때문에 많은 제약을 받고 있는 요즘, 식품성분이면서 식욕을 억제할 수 있는 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드- Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제용 조성물을 개발함으로써 본 발명을 완성하였다.The present invention is derived from the above requirements, the present invention is desired to develop a functional material that can suppress the appetite, but many limitations due to safety problems such as limitations and side effects of body fat decomposition, digestion inhibition method Nowadays, ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin, melatonin, melaninin, ginsenoside-Rb1 (which is a food ingredient and can suppress appetite) The present invention was completed by developing a composition for suppressing appetite containing at least one component selected from the group consisting of ginsenoside-Rb1) and ginsenoside-Rg1 (ginsenoside-Rg1) as an active ingredient.
또한, 본 발명은 비만억제의 해결수단으로서 식품성분 조성물에 의한 식욕억제 방법을 최초로 개발하였으며, 식욕억제 효과를 증명하는 방법에 있어서도 식욕을 촉진하는 그렐린(ghrelin)을 억제하는 시험계를 최초로 발굴하여 세포분화도에 따라 식품성분을 적용하고 식욕억제효과를 과학적으로 검증하였다.In addition, the present invention first developed an appetite suppression method by a food ingredient composition as a solution to obesity suppression, and also in the method of demonstrating the appetite suppression effect, by first discovering a test system that suppresses ghrelin that promotes appetite, cells According to the degree of differentiation, food ingredients were applied and appetite suppression effect was scientifically verified.
상기 과제를 해결하기 위해, 본 발명은 유효성분으로 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 함유하는 식욕억제용 조성물을 제공한다. In order to solve the above problems, the present invention as an active ingredient ascorbic acid (ascorbic acid), beta-D-glucan (β-D-glucan), hesperetin (hesperetin), melatonin (melatonin), ginsenoside-Rb1 It provides a composition for suppressing appetite containing at least one component selected from the group consisting of (ginsenoside-Rb1) and ginsenoside-Rg1 (ginsenoside-Rg1).
또한, 본 발명은 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제용 기능성 식품을 제공한다. 식욕억제 효과를 증명하는 방법에서도 식욕을 촉진하는 그렐린(ghrelin)을 억제하는 시험계를 최초로 발굴하여 세포분화도에 따라 식품성분을 적용하고 식품성분의 식욕억제효과를 과학적으로 검증하였다.In addition, the present invention is ascorbic acid (ascorbic acid), beta-D-glucan (β-D-glucan), hesperetin (hesperetin), melatonin (melatonin), ginsenoside-Rb1 (ginsenoside-Rb1) and ginsenosides It provides a functional food for suppressing appetite containing at least one component selected from the group consisting of side-Rg1 (ginsenoside-Rg1) as an active ingredient. In the method of proving appetite suppression effect, a test system that suppresses ghrelin that promotes appetite was first discovered, and food ingredients were applied according to the degree of cell differentiation, and the appetite suppression effect of food ingredients was scientifically verified.
본 발명에 따르면, 본 발명의 식욕억제 조성물은 식욕억제에 효과적이며, 식품성분을 이용하기 때문에 장기간 복용하여도 부작용이 나타나지 않고, 안전성을 확보할 수 있어, 식욕억제를 위한 기능성 식품산업상 매우 유용한 발명이 될 것이다.According to the present invention, the appetite suppressant composition of the present invention is effective for suppressing appetite, and because it uses food ingredients, no side effects appear even after taking for a long time, and it is possible to secure safety, very useful in functional food industry for appetite suppression It will be an invention.
또한 식욕억제 효과를 증명하는 방법에서도 식욕을 촉진하는 그렐린(ghrelin) 시험계를 최초로 발굴하여 세포분화도에 따라 식품성분을 적용함으로써 식욕억제효과를 과학적으로 검증하는 모델을 최초로 제공하였다.In addition, the method to prove the appetite suppression effect was the first to discover the ghrelin test system that promotes appetite, and to provide the first model to scientifically verify the appetite suppression effect by applying food ingredients according to the degree of cell differentiation.
도 1은 HUVEC(human umbilical vein endothelial cell) 세포에 각각의 식품성분을 1 또는 10 ㎍/㎖씩 첨가하였을 때 대조구와 비교하여 그렐린(ghrelin)의 농도를 다핵(multinucleate) 분화 억제 활성으로 측정한 것이다.
1: 시부트라민(sibutramine, positive control), 2: 아스코르브산(ascorbic acid), 3: 베타-D-글루칸(β-D-glucan), 4: 헤스페레틴(hesperetin), 5: 알파-리포산(α-lipoic acid), 6: 세로토닌(serotonin), 7: 멜라토닌(melatonin), 8: 알파-토코페롤(α-tocopherol), 9: 진세노사이드-Rb1(ginsenoside-Rb1), 10: 진세노사이드-Rg1(ginsenoside-Rg1), 11: 나린제닌(naringenin)
도 2는 각각의 식품성분을 60℃, 80℃ 및 100℃에서 5분간 처리한 후, HUVEC(human umbilical vein endothelial cell) 세포에 식품성분을 각각 첨가하여, 세포증식능과 그렐린(ghrelin)의 양을 측정한 것이다.
1: 시부트라민(sibutramine, positive control), 2: 아스코르브산(ascorbic acid), 3: 베타-D-글루칸(β-D-glucan), 4: 헤스페레틴(hesperetin), 5: 알파-리포산(α-lipoic acid), 6: 세로토닌(serotonin), 7: 멜라토닌(melatonin), 8: 알파-토코페롤(α-tocopherol), 9: 진세노사이드-Rb1(ginsenoside-Rb1), 10: 진세노사이드-Rg1(ginsenoside-Rg1), 11: 나린제닌(naringenin)
도 3은 각각의 식품성분을 pH 2, 5 및 7에서 5분 이내로 처리한 후, HUVEC(human umbilical vein endothelial cell) 세포에 식품성분을 각각 첨가하여, 세포증식능과 그렐린(ghrelin)의 양을 측정한 것이다.
1: 시부트라민(sibutramine, positive control), 2: 아스코르브산(ascorbic acid), 3: 베타-D-글루칸(β-D-glucan), 4: 헤스페레틴(hesperetin), 5: 알파-리포산(α-lipoic acid), 6: 세로토닌(serotonin), 7: 멜라토닌(melatonin), 8: 알파-토코페롤(α-tocopherol), 9: 진세노사이드-Rb1(ginsenoside-Rb1), 10: 진세노사이드-Rg1(ginsenoside-Rg1), 11: 나린제닌(naringenin)1 shows the concentration of ghrelin as a multinucleate differentiation inhibitory activity when 1 or 10 ㎍ / ml of each food ingredient is added to human umbilical vein endothelial cells (HUVEC) cells. .
1: sibutramine (positive control), 2: ascorbic acid, 3: beta-D-glucan, 4: hesperetin, 5: alpha-lipoic acid (α) -lipoic acid), 6: serotonin, 7: melatonin, 8: alpha-tocopherol, 9: ginsenoside-Rb1, 10: ginsenoside-Rg1 (ginsenoside-Rg1), 11: naringenin
FIG. 2 shows that each food ingredient is treated at 60 ° C., 80 ° C., and 100 ° C. for 5 minutes, and then food ingredients are added to human umbilical vein endothelial cells (HUVECs), respectively, to determine cell proliferation and ghrelin levels. It is measured.
1: sibutramine (positive control), 2: ascorbic acid, 3: beta-D-glucan, 4: hesperetin, 5: alpha-lipoic acid (α) -lipoic acid), 6: serotonin, 7: melatonin, 8: alpha-tocopherol, 9: ginsenoside-Rb1, 10: ginsenoside-Rg1 (ginsenoside-Rg1), 11: naringenin
FIG. 3 shows that each food ingredient is treated within 5 minutes at
1: sibutramine (positive control), 2: ascorbic acid, 3: beta-D-glucan, 4: hesperetin, 5: alpha-lipoic acid (α) -lipoic acid), 6: serotonin, 7: melatonin, 8: alpha-tocopherol, 9: ginsenoside-Rb1, 10: ginsenoside-Rg1 (ginsenoside-Rg1), 11: naringenin
본 발명의 목적을 달성하기 위해, 본 발명은 유효성분으로 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 함유하는 식욕억제용 조성물을 제공한다.In order to achieve the object of the present invention, the present invention is ascorbic acid (ascorbic acid), beta-D-glucan (β-D-glucan), hesperetin (hesperetin), melatonin (melatonin), ginsenoside Provided is a composition for suppressing appetite containing at least one component selected from the group consisting of -gin (R) (ginsenoside-Rbl) and ginsenoside (Rg1).
본 발명의 조성물에서, 상기 식욕억제는 식욕촉진 호르몬인 그렐린(ghrelin)의 활성을 억제하는 효과일 수 있다.In the composition of the present invention, the appetite suppression may be an effect of inhibiting the activity of ghrelin (ghrelin), an appetite-stimulating hormone.
본 발명의 조성물에 포함된 유효성분은 60~100℃의 온도에서 5분간 처리 후에도 그렐린 억제 활성이 유지될 수 있다. 이로부터 식품성분을 가열하는 경우에도 그렐린(ghrelin) 억제 활성이 유지되므로 가공 중 식품성분의 식욕억제 활성유지 가능성을 간접적으로 확인할 수 있었다.The active ingredient included in the composition of the present invention may maintain ghrelin inhibitory activity even after 5 minutes treatment at a temperature of 60 ~ 100 ℃. From this, the ghrelin inhibitory activity is maintained even when the food ingredient is heated, thereby indirectly confirming the possibility of maintaining appetite suppressing activity of the food ingredient during processing.
또한, 본 발명의 조성물에 포함된 유효성분은 pH 2~10에서 5분간 처리 후에도 그렐린 억제 활성이 유지될 수 있다. 이로부터 식품성분의 체내섭취시에도 그렐린(ghrelin) 활성 억제로 식욕 억제 효과는 전반적으로 유지됨을 간접적으로 판단할 수 있었다.In addition, the active ingredient included in the composition of the present invention can maintain the ghrelin inhibitory activity even after 5 minutes treatment at
본 발명의 식욕억제용 조성물은 약학적 조성물의 제조에 통상적으로 사용하는 적절한 담체, 부형제 및 희석제를 포함할 수 있다.Appetite suppressing compositions of the present invention may include suitable carriers, excipients and diluents commonly used in the manufacture of pharmaceutical compositions.
본 발명의 식욕억제용 조성물의 약학적 투여 형태는 이들의 약학적 허용 가능한 염의 형태로도 사용될 수 있고, 또한 단독으로 또는 타 약학적 활성 화합물과 결합뿐만 아니라 적당한 집합으로 사용될 수 있다.Pharmaceutical dosage forms of the appetite suppressant composition of the present invention may be used in the form of their pharmaceutically acceptable salts, and may be used alone or in combination with other pharmaceutically active compounds, as well as in a suitable collection.
본 발명에 따른 식욕억제용 조성물은, 각각 통상의 방법에 따라 산제, 과립제, 정제, 캡슐제, 현탁액, 에멀젼, 시럽, 에어로졸 등의 경구형 제형, 외용제, 좌제 및 멸균 주사용액의 형태로 제형화하여 사용될 수 있다. 식욕억제용 조성물에 포함될 수 있는 담체, 부형제 및 희석제로는 락토즈, 덱스트로즈, 수크로스, 솔비톨, 만니톨, 자일리톨, 에리스리톨, 말티톨, 전분, 아카시아 고무, 알지네이트, 젤라틴, 칼슘 포스페이트, 칼슘 실리케이트, 셀룰로즈, 메틸 셀룰로즈, 미정질 셀룰로스, 폴리비닐 피롤리돈, 물, 메틸히드록시벤조에이트, 프로필히드록시벤조에이트, 탈크, 마그네슘 스테아레이트 및 광물유 등을 포함한 다양한 화합물 혹은 혼합물을 들 수 있다. 제제화할 경우에는 보통 사용하는 충진제, 증량제, 결합제, 습윤제, 붕해제, 계면활성제 등의 희석제 또는 부형제를 사용하여 조제된다. 경구투여를 위한 고형제제에는 정제, 환제, 산제, 과립제, 캡슐제 등이 포함되며, 이러한 고형제제는 상기 성분에 적어도 하나 이상의 부형제 예를 들면, 전분, 칼슘카보네이트(calcium carbonate), 수크로스(sucrose) 또는 락토오스(lactose), 젤라틴 등을 섞어 조제된다. 또한 단순한 부형제 이외에 마그네슘 스테아레이트, 탈크 같은 윤활제들도 사용된다. 경구를 위한 액상 제제로는 현탁제, 내용액제, 유제, 시럽제 등이 해당되는데 흔히 사용되는 단순 희석제인 물, 리퀴드 파라핀 이외에 여러 가지 부형제, 예를 들면 습윤제, 감미제, 방향제, 보존제 등이 포함될 수 있다. 비경구 투여를 위한 제제에는 멸균된 수용액, 비수성용제, 현탁제, 유제, 동결건조 제제, 좌제가 포함된다. 비수성용제, 현탁제로는 프로필렌글리콜(propylene glycol), 폴리에틸렌 글리콜, 올리브 오일과 같은 식물성 기름, 에틸올레이트와 같은 주사 가능한 에스테르 등이 사용될 수 있다. 좌제의 기제로는 위텝솔(witepsol), 마크로골, 트윈 (tween) 61, 카카오지, 라우린지, 글리세로제라틴 등이 사용될 수 있다.The appetite suppressing composition according to the present invention is formulated in the form of powders, granules, tablets, capsules, suspensions, emulsions, syrups, aerosols and the like, external preparations, suppositories, and sterile injectable solutions, respectively, according to a conventional method. Can be used. Carriers, excipients and diluents that may be included in the appetite suppressant composition include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, Various compounds or mixtures, including cellulose, methyl cellulose, microcrystalline cellulose, polyvinyl pyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate, mineral oil and the like. In the case of formulation, a diluent or excipient such as a filler, an extender, a binder, a wetting agent, a disintegrant, or a surfactant is usually used. Solid formulations for oral administration include tablets, pills, powders, granules, capsules and the like, which may contain at least one excipient such as starch, calcium carbonate, sucrose ), Lactose, gelatin and the like. In addition to simple excipients, lubricants such as magnesium stearate and talc are also used. Oral liquid preparations include suspensions, solvents, emulsions, and syrups, and may include various excipients, such as wetting agents, sweeteners, fragrances, and preservatives, in addition to commonly used simple diluents such as water and liquid paraffin. . Formulations for parenteral administration include sterilized aqueous solutions, non-aqueous solutions, suspensions, emulsions, freeze-dried preparations, and suppositories. Examples of the suspending agent include propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate, and the like. As the base of the suppository, witepsol, macrogol, tween 61, cacao butter, laurin butter, glycerogelatin and the like can be used.
본 발명의 식욕억제용 조성물의 바람직한 투여량은 환자의 상태 및 체중, 질병의 정도, 약물형태, 투여경로 및 기간에 따라 다르지만, 당업자에 의해 적절하게 선택될 수 있다. 그러나, 바람직한 효과를 위해서, 본 발명의 식욕억제용 조성물은 1일 0.0001 내지 100 mg/kg으로, 바람직하게는 0.001 내지 100 mg/kg으로 투여하는 것이 좋다. 투여는 하루에 한번 투여할 수도 있고, 수회 나누어 투여할 수도 있다. 상기 투여량은 어떠한 면으로든 본 발명의 범위를 한정하는 것은 아니다.Preferred dosages of the appetite suppressant composition of the present invention vary depending on the condition and weight of the patient, the extent of the disease, the form of the drug, the route of administration and the duration, and may be appropriately selected by those skilled in the art. However, for the desired effect, the appetite suppressing composition of the present invention is preferably administered at 0.0001 to 100 mg / kg, preferably 0.001 to 100 mg / kg per day. The administration may be carried out once a day or divided into several times. The dose is not intended to limit the scope of the invention in any way.
본 발명의 식욕억제용 조성물은 쥐, 생쥐, 가축, 인간 등의 포유동물에 다양한 경로로 투여될 수 있다. 투여의 모든 방식은 예상될 수 있는데, 예를 들면, 경구, 직장 또는 정맥, 근육, 피하, 자궁 내 경막 또는 뇌혈관내 (intracerebroventricular) 주사에 의해 투여될 수 있다.The appetite suppressant composition of the present invention can be administered to various mammals such as mice, mice, livestock, humans. All modes of administration can be expected, for example by oral, rectal or intravenous, intramuscular, subcutaneous, intrauterine dural or intracerebroventricular injection.
본 발명은 또한, 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1)으로 이루어진 군으로부터 선택되는 하나 이상의 성분을 유효성분으로 함유하는 식욕억제용 기능성 식품을 제공한다.The present invention also provides ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin, melatonin, ginsenoside-Rb1 and ginsenoside. It provides a functional food for suppressing appetite containing at least one component selected from the group consisting of side-Rg1 (ginsenoside-Rg1) as an active ingredient.
본 발명의 상기 식욕억제용 조성물을 식품첨가물로 사용하는 경우, 상기 식욕억제용 조성물을 그대로 첨가하거나 다른 식품 또는 식품 성분과 함께 사용될 수 있고, 통상적인 방법에 따라 적절하게 사용될 수 있다. 유효 성분의 혼합양은 그의 사용 목적(예방, 건강 또는 치료적 처치)에 따라 적합하게 결정될 수 있다. 일반적으로, 식품 또는 음료의 제조시에 본 발명의 성분은 원료에 대하여 15 중량부 이하, 바람직하게는 10 중량부 이하의 양으로 첨가된다. 그러나, 건강 및 위생을 목적으로 하거나 또는 건강 조절을 목적으로 하는 장기간의 섭취의 경우에는 상기 양은 상기 범위 이하일 수 있으며, 안전성 면에서 아무런 문제가 없기 때문에 유효성분은 상기 범위 이상의 양으로도 사용될 수 있다.When the appetite suppressing composition of the present invention is used as a food additive, the appetite suppressing composition may be added as it is or used with other foods or food ingredients, and may be appropriately used according to a conventional method. The amount of the active ingredient to be mixed can be suitably determined according to its intended use (prevention, health or therapeutic treatment). Generally, in the manufacture of food or beverages the components of the invention are added in an amount of up to 15 parts by weight, preferably up to 10 parts by weight relative to the raw materials. However, in the case of long-term consumption intended for health and hygiene purposes or for health control purposes, the amount may be less than the above range, and since there is no problem in terms of safety, the active ingredient may be used in an amount exceeding the above range .
상기 식품의 종류에는 특별한 제한은 없다. 상기 물질을 첨가할 수 있는 식품의 예로는 육류, 소세지, 빵, 쵸코렛, 캔디류, 스넥류, 과자류, 피자, 라면, 기타 면류, 껌류, 아이스크림류를 포함한 낙농제품, 각종 스프, 음료수, 차, 드링크제, 알콜 음료 및 비타민 복합제 등이 있으며, 통상적인 의미에서의 식품을 모두 포함한다.There is no particular limitation on the kind of the food. Examples of the food to which the substance can be added include dairy products including meat, sausage, bread, chocolate, candy, snacks, confectionery, pizza, ramen, other noodles, gums, ice cream, various soups, drinks, tea, drinks, Alcoholic beverages and vitamin complexes, and the like and include all foods in a conventional sense.
본 발명의 식육억제용 조성물이 함유된 기능성 음료 조성물은 통상의 음료와 같이 여러 가지 향미제 또는 천연 탄수화물 등을 추가 성분으로서 함유할 수 있다. 상술한 천연 탄수화물은 포도당, 과당과 같은 모노사카라이드, 말토스, 슈크로스와 같은 디사카라이드, 및 덱스트린, 사이클로덱스트린과 같은 폴리사카라이드, 자일리톨, 소르비톨, 에리트리톨 등의 당알콜이다. 감미제로서는 타우마틴, 스테비아 추출물과 같은 천연 감미제나, 사카린, 아스파르탐과 같은 합성 감미제 등을 사용할 수 있다. 상기 천연 탄수화물의 비율은 본 발명의 조성물 100 ㎖당 일반적으로 약 0.01~0.04 g, 바람직하게는 약 0.02~0.03 g 이다.The functional beverage composition containing the meat suppressing composition of the present invention may contain various flavors or natural carbohydrates as additional components, as in general beverages. Such natural carbohydrates are monosaccharides such as glucose and fructose, disaccharides such as maltose and sucrose, and polysaccharides such as dextrin and cyclodextrin, and sugar alcohols such as xylitol, sorbitol and erythritol. Examples of sweeteners include natural sweeteners such as tau martin and stevia extract, synthetic sweeteners such as saccharin and aspartame, and the like. The ratio of the natural carbohydrate is generally about 0.01 to 0.04 g, preferably about 0.02 to 0.03 g per 100 ml of the composition of the present invention.
상기 외에 본 발명의 식욕억제용 조성물은 여러가지 영양제, 비타민, 전해질, 풍미제, 착색제, 펙트산 및 그의 염, 알긴산 및 그의 염, 유기산, 보호성 콜로이드 증점제, pH 조절제, 안정화제, 방부제, 글리세린, 알콜, 탄산음료에 사용되는 탄산화제 등을 함유할 수 있다. 그 밖에 본 발명의 식욕억제용 조성물은 천연 과일쥬스, 과일쥬스 음료 및 야채 음료의 제조를 위한 과육을 함유할 수 있다. 이러한 성분은 독립적으로 또는 혼합하여 사용할 수 있다. 이러한 첨가제의 비율은 크게 중요하진 않지만 본 발명의 조성물 100 중량부당 0.01 ~ 0.1 중량부의 범위에서 선택되는 것이 일반적이다.
In addition to the above, the appetite suppressing composition of the present invention includes various nutrients, vitamins, electrolytes, flavoring agents, coloring agents, pectic acid and salts thereof, alginic acid and salts thereof, organic acids, protective colloid thickeners, pH adjusting agents, stabilizers, preservatives, glycerin, Alcohols, carbonating agents used in carbonated drinks, and the like. In addition, the appetite suppressing composition of the present invention may contain a flesh for preparing natural fruit juice, fruit juice beverage and vegetable beverage. These components may be used independently or in combination. The proportion of such additives is not critical, but is generally selected in the range of 0.01 to 0.1 parts by weight per 100 parts by weight of the composition of the present invention.
이하 본 발명을 실시예를 통하여 보다 상세하게 설명한다. 그러나, 이들 실시예는 본 발명을 예시적으로 설명하기 위한 것으로 본 발명의 범위가 이들 실시예에 한정되는 것은 아니다.
Hereinafter, the present invention will be described in more detail with reference to examples. However, these examples are for illustrative purposes only, and the scope of the present invention is not limited to these examples.
1. 시료의 확보1. Securing Sample
(1) 식욕 억제 소재의 선발(1) Selection of appetite suppression material
식욕억제 시험계 적용을 위한 식품성분은 단일성분의 확보가 가능한 성분으로 하였으며 항비만 가능성이 있는 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 리포산(lipoic acid), 세로토닌(serotonin), 멜라토닌(melatonin), 토코페롤(tocopherol), 진세노사이드-Rb1(ginsenoside-Rb1), 진세노사이드-Rg1(ginsenoside-Rg1), 나린제닌(naringenin), 시부트라민(sibutramin, positive control)을 확보하였다.
The food ingredient for appetite suppression test system was to be a single ingredient, and ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin, Lipoic acid, serotonin, serotonin, melatonin, tocopherol, ginsenoside-Rb1, ginsenoside-Rg1, ginsenoside-Rg1, naringenin, sibutramine (sibutramin, positive control) was secured.
(2) 세포시험용 검액 제조(2) Preparation of Cell Test Sample Solution
대상 식품성분은 DMSO 또는 증류수(distilled water)에 용해한 후 희석하여 농도별로 사용하였고, DMSO의 최종농도는 0.1% 이하로 하여 세포시험용 검액을 제조하였다.
The target food ingredients were dissolved in DMSO or distilled water, diluted and used for each concentration. The final concentration of DMSO was 0.1% or less to prepare a cell test sample.
2. 식욕 촉진 호르몬 2. Appetite Promoting Hormones 그렐린(ghrelin)의Ghrelin 활성 시험 Active test
(1) HUVEC 세포 배양(1) HUVEC cell culture
HUVEC(human umbilical vein endothelial cell)은 영사이언스에서 분양받아 사용하였다. 2% 젤라틴(gelatin) 코팅한 100 mm 디쉬(dish)에 EGM-2 배지(FBS, Hydrocortisone, hFGF, VEGF. R3-IGF-1, Ascorbic acid, hEGF, GA-1000, Heparin)를 이용하여 37℃, 5% CO2가 유지되는 배양기에서 배양하였다. 세포가 컨플루언트(confluent)되면 trypsin-EDTA로 처리하여 계대 배양하였으며 배지는 2~3일에 한 번씩 교환하였다.
HUVEC (human umbilical vein endothelial cell) was used by Young Science. 37 ° C using EGM-2 medium (FBS, Hydrocortisone, hFGF, VEGF.R3-IGF-1, Ascorbic acid, hEGF, GA-1000, Heparin) in a 100 mm dish coated with 2% gelatin , And incubated in an incubator maintained at 5% CO 2 . When the cells were confluent, the cells were passaged by treatment with trypsin-EDTA, and the medium was exchanged every 2 to 3 days.
(2) 그렐린 분석(ghrelin assay)(2) ghrelin assay
그렐린(ghrelin) 분석을 위한 시료는 상등액과 cell lysate로 분리하여 사용하였다. 실험 종료 후 회수한 배양액은 원심분리(3,000 rpm, 20분, 4℃)하여 상층액만을 회수하였고, cell lysate는 Trypsin-EDTA로 세포를 분리한 후 10000 rpm에서 10분간 원심분리하였다. 상등액을 제거하고 얻어진 세포에 1%의 Triton X-100을 함유하는 용액을 이용하여 cell lysate를 제조한 후 HUMAN unacylated ghrelin kit(SPI-Bio)를 이용하여 그렐린(ghrelin) 함량을 측정하였다. 즉, 그렐린(ghrelin)의 측정법은 standard diluent buffer와 샘플 100 ul를 웰(well)에 넣고, Anti-unacylated ghrelin-AChE tracer 100 ul를 첨가하였다. 실온에서 3시간 배양 후 배양액을 완전히 제거하고 diluted wash solution으로 5회 이상 세척하였다. 그리고 플레이트를 건조한 후, Ellman's reagent 200 ul 첨가 후 405 nm에서 흡광도를 측정하였다.
Samples for ghrelin analysis were separated into supernatant and cell lysate. After the end of the experiment, the recovered culture was centrifuged (3,000 rpm, 20 minutes, 4 ℃) to recover only the supernatant, cell lysate was centrifuged for 10 minutes at 10000 rpm after separating the cells with Trypsin-EDTA. After removing the supernatant and preparing a cell lysate using a solution containing 1% of Triton X-100 in the obtained cells, the content of ghrelin was measured using a HUMAN unacylated ghrelin kit (SPI-Bio). That is, in the measurement of ghrelin, 100 ul of standard diluent buffer and 100 ul of sample were put in a well, and 100 ul of anti-unacylated ghrelin-AChE tracer was added. After 3 hours of incubation at room temperature, the culture solution was completely removed and washed 5 times with diluted wash solution. After drying the plate, absorbance was measured at 405 nm after adding 200 ul of Ellman's reagent.
3. 온도와 3. Temperature and pHpH 에 따른 식품성분의 Of food ingredients 세포증식능과Cell proliferation 그렐린Ghrelin (( ghrelinghrelin ) 억제 활성) Inhibitory activity
(1) 온도에 따른 식품성분의 세포증식능과 그렐린(ghrelin) 억제 활성화 변화(1) Changes in Cell Proliferation and Ghrelin Inhibition Activation of Food Ingredients with Temperature
식품성분의 가공 중 안정성을 조사하기 위하여 그렐린(ghrelin)에 대한 억제 활성이 높았던 식품성분 농도를 대상으로 가열온도에 따른 식욕촉진 호르몬인 그렐린(ghrelin)의 억제 활성도를 조사하였다. 일정량의 식품성분을 60℃, 80℃ 및 100℃에서 각각 5분간 처리하고 그렐린(ghrelin)에 대한 억제 활성이 높았던 농도로 제조한 후 세포증식능과 그렐린(ghrelin)의 양을 측정하였다.
In order to investigate the stability during processing of food ingredients, the inhibitory activity of ghrelin, an appetite-stimulating hormone according to heating temperature, was investigated for food ingredient concentrations that had high inhibitory activity against ghrelin. After a certain amount of food ingredients were treated at 60 ° C., 80 ° C. and 100 ° C. for 5 minutes, and prepared at concentrations having high inhibitory activity against ghrelin, the cell proliferation ability and the amount of ghrelin were measured.
(2) pH에 따른 식품성분의 세포증식능과 그렐린(ghrelin) 억제 활성화 변화(2) Changes in Cell Proliferation and Ghrelin Inhibition Activation of Food Ingredients According to pH
식품성분의 식욕 억제의 체내 활성을 간접 시험하고자 산성, 중성, 염기성의 조건에서 식품성분의 pH 변화에 따른 그렐린(ghrelin) 억제 활성을 조사하였다. 각 pH 용액에 10%의 농도로 각각의 식품성분을 5분 이내로 담근 다음 동결 건조하여 그렐린(ghrelin)에 대한 억제 활성이 높았던 농도로 제조한 후 세포증식능과 그렐린(ghrelin)의 양을 측정하였다.
To indirectly test the body's activity of appetite suppression of food ingredients, the ghrelin inhibitory activity was investigated according to the pH change of food ingredients under acidic, neutral and basic conditions. Each food solution was dipped in each pH solution at a concentration of 10% within 5 minutes, and then lyophilized to prepare a concentration having high inhibitory activity against ghrelin, and then the cell proliferation ability and the amount of ghrelin were measured.
실시예Example 1: 식품성분 첨가 시 1: When adding food ingredients 그렐린(ghrelin)의Ghrelin 농도변화 Concentration change
HUVEC(human umbilical vein endothelial cell) 세포에 식품성분을 1 또는 10 ㎍/㎖로 각각 첨가하였을 때 대조구와 비교하여 그렐린(ghrelin)의 농도를 다핵(multinucleate) 분화 억제 활성으로 측정하였다(도 1). 다핵(multinucleate) 상태는 증식률의 급격히 상승하는 시점을 계대 배양 30시간으로 정하여 시료를 처리하였다. When food ingredients were added to human umbilical vein endothelial cells (HUVEC) cells at 1 or 10 μg / ml, respectively, the concentration of ghrelin was measured as multinucleate differentiation inhibitory activity compared to the control (FIG. 1). In the multinucleate state, the samples were treated by setting the time of rapid increase in the proliferation rate to 30 hours of passage culture.
그 결과, 양성대조구인 시부트라민(sibutramine)의 경우 1 ug/ml의 농도에서 75%(억제율 25%)의 함량을 나타냈고, 10 ug/ml에서 68%(억제율 32%)로 높은 그렐린(ghrelin) 억제활성을 나타냈고, 아스코르브산(ascorbic acid)은 1 ug/ml과 10 ug/ml의 농도에서 각각 93%와 94%의 분비율을 나타냈다. 글루칸(glucan)의 경우 농도 의존적으로 시료농도가 증가하면서 그렐린(ghrelin)의 함량이 감소하여 10 ug/ml의 농도에서 85%로 가장 낮은 함량을 보였고, 헤스페레틴(hesperetin)의 경우 1 ug/ml의 농도에서는 79%의 함량으로 가장 높은 억제활성을 보였으며, 10 ug/ml에서도 85%의 낮은 값을 나타냈다. 멜라토닌(melatonin)의 경우 10 ug/ml에서 87%로 낮은 그렐린(ghrelin) 함량을 보였으며, 진세노사이드-Rb1(ginsenoside-Rb1)은 농도가 증가하면서 점차적으로 감소하여 10 ug/ml에서 76%의 낮은 함량을 보였으며, 진세노사이드-Rg1 (ginsenoside-Rg1) 역시 농도 의존적으로 그렐린(ghrelin)의 함량이 감소하는 경향을 보이며 10 ug/ml에서 84%의 낮은 함량을 나타내었다.As a result, sibutramine, a positive control, had a content of 75% (25% inhibition) at a concentration of 1 ug / ml, and high ghrelin (68% (32% inhibition) at 10 ug / ml). Inhibitory activity was ascorbic acid (ascorbic acid) showed a secretion rate of 93% and 94% at concentrations of 1 ug / ml and 10 ug / ml, respectively. In the case of glucan, the concentration of ghrelin decreased as the concentration of sample increased in concentration-dependent manner, showing the lowest content of 85% at the concentration of 10 ug / ml, and 1 ug / for hesperetin. At the concentration of ml, the highest inhibitory activity was shown to be 79%, and low value of 85% even at 10 ug / ml. Melatonin had a low ghrelin content of 87% at 10 ug / ml, and ginsenoside-Rb1 gradually decreased with increasing concentrations to 76% at 10 ug / ml. Ginsenoside-Rg1 (ginsenoside-Rg1) also showed a tendency to decrease the content of ghrelin in a concentration-dependent manner, showing a low content of 84% at 10 ug / ml.
따라서, 아스코르브산(ascorbic acid), 베타-D-글루칸(β-D-glucan), 헤스페레틴(hesperetin), 멜라토닌(melatonin), 진세노사이드-Rb1(ginsenoside-Rb1) 및 진세노사이드-Rg1(ginsenoside-Rg1) 처리구에서 대조구와 비교했을 때 그렐린(ghrelin)의 함량이 감소하여 식욕 억제의 효과가 있음을 확인할 수 있었다.
Thus, ascorbic acid, beta-D-glucan, β-D-glucan, hesperetin, melatonin, ginsenoside-Rb1 and ginsenoside-Rg1 Compared to the control in the (ginsenoside-Rg1) treatment, the content of ghrelin was decreased, and it was confirmed that the appetite suppression effect was observed.
실시예Example 2: 온도에 따른 식품성분의 2: of food ingredients according to temperature 세포증식능과Cell proliferation 그렐린Ghrelin (( ghrelinghrelin ) 억제 활성화 변화Inhibitory activation changes
식품성분의 가열 온도에 따른 세포(HUVEC)의 증식능과 그렐린(ghrelin)의 함량을 도 2에 나타내었다. 온도에 따른 세포의 증식능은 온도를 60~100℃로 증가시킨 경우에도 세포 증식능은 전반적으로 유지됨을 알 수 있었다. 또한, 온도 변화에 따른 그렐린(ghrelin)의 함량은 안정적으로 유지됨을 알 수 있었다. 그렐린(ghrelin)은 60~100℃ 온도 대에서 대부분 80~90% 함량으로 억제효과가 20~10% 정도 유지되는 것으로 판단되었다. 이로부터 식품성분을 가열하는 경우에도 세포 증식과 그렐린(ghrelin) 억제활성이 유지되므로 가공 중 식품성분의 식욕억제 활성유지 가능성을 간접적으로 확인할 수 있었다.
The proliferative capacity of the cells (HUVEC) and the content of ghrelin according to the heating temperature of the food ingredient are shown in FIG. 2. The cell proliferative capacity according to temperature was found to be maintained overall even when the temperature was increased to 60 ~ 100 ℃. In addition, it was found that the content of ghrelin according to the temperature change is maintained stably. Ghrelin (ghrelin) is mostly 80 ~ 90% content in the temperature range of 60 ~ 100 ℃ it was judged that the inhibitory effect is maintained about 20 to 10%. From this, even when the food ingredients are heated, cell proliferation and ghrelin inhibitory activity is maintained, thereby indirectly confirming the possibility of maintaining appetite suppressing activity of the food ingredients during processing.
실시예Example 3: 3: pHpH 에 따른 식품성분의 Of food ingredients 세포증식능과Cell proliferation 그렐린Ghrelin (( ghrelinghrelin ) 억제 활성화 변화Inhibitory activation changes
식품성분의 체내 활성을 간접 판단하고자 산성, 중성, 염기성 조건에서 식품성분의 pH 변화에 따른 세포의 증식능과 그렐린(ghrelin)의 함량을 조사하였다(도 3). 시료에 pH 변화 처리를 한 경우 HUVEC 세포의 증식능은 pH 7에서 가장 안정적이었다. HUVEC 세포는 시료의 pH 2, pH 10 처리구에서 60 ~ 92%의 다소 약한 분화를 보였으나 pH 7에서는 모든 시료처리구에서 90% 전후의 분화도를 유지하였다.In order to indirectly determine the in vivo activity of the food ingredients, the cell proliferation ability and the content of ghrelin according to the pH change of the food ingredients under acidic, neutral, and basic conditions were investigated (FIG. 3). When the sample was treated with pH change, the proliferative capacity of HUVEC cells was the most stable at
그렐린(ghrelin) 잔존량은 식품성분에 pH 2, 7 및 10 변화처리시에도 대체적으로 모든 처리구에서 그렐린(ghrelin) 잔존량이 대조구보다 낮아 억제 효과를 나타내어 온도처리의 경우와 유사하였다. 이로부터 식품성분의 체내섭취시에도 그렐린(ghrelin) 활성 억제로 식욕 억제 효과는 전반적으로 유지됨을 간접적으로 판단할 수 있었다.The residual amount of ghrelin was similar to that of the temperature treatment because the residual amount of ghrelin was lower than that of the control in all the treatments even when
Claims (5)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020100108541A KR101250198B1 (en) | 2010-11-03 | 2010-11-03 | Composition of food components for appetite control comprising specific compounds as effective component |
PCT/KR2010/008111 WO2012036344A1 (en) | 2010-09-17 | 2010-11-16 | Appetite suppressant food composition comprising a specific compound as an active ingredient |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020100108541A KR101250198B1 (en) | 2010-11-03 | 2010-11-03 | Composition of food components for appetite control comprising specific compounds as effective component |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20120046967A KR20120046967A (en) | 2012-05-11 |
KR101250198B1 true KR101250198B1 (en) | 2013-04-03 |
Family
ID=46265874
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020100108541A KR101250198B1 (en) | 2010-09-17 | 2010-11-03 | Composition of food components for appetite control comprising specific compounds as effective component |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR101250198B1 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101358197B1 (en) * | 2011-07-18 | 2014-02-06 | 한국식품연구원 | Composition for promoting leptin secretion comprising specific compounds as effective component |
-
2010
- 2010-11-03 KR KR1020100108541A patent/KR101250198B1/en active IP Right Grant
Non-Patent Citations (3)
Title |
---|
Etou, H. et al., Nihon Yakurigaku Zasshi (1988) vol.91, no.1, pp.9-15 * |
Mustonen, A-.M. et al., Endocrine (2001) vol.16, no.1, pp.43-46 * |
Wang, Z. et al., Asian-Australasian Journal of Animal Science (2008) vol.21, no.5, pp.707-714 * |
Also Published As
Publication number | Publication date |
---|---|
KR20120046967A (en) | 2012-05-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6086953B2 (en) | AMPK activator | |
US10925918B2 (en) | Composition for food and fat absorption inhibitor | |
KR20060121998A (en) | Composition containing eupatilin for inhibiting breast cancer | |
KR101358197B1 (en) | Composition for promoting leptin secretion comprising specific compounds as effective component | |
KR101250198B1 (en) | Composition of food components for appetite control comprising specific compounds as effective component | |
KR20200023576A (en) | Composition for improving hepatic function comprising extract of fermented Protaetia brevitarsis larva as effective component | |
KR101793256B1 (en) | Food composition and pharmaceutical composition for improving and preventing diabetes mellitus with a new variety of red pepper (KCTC18413P) | |
KR102178199B1 (en) | a composition comprising an extract of Rhus verniciflua and Eucommia ulmoides, as an active ingredient for preventing or treating obesity | |
KR20110098500A (en) | Composition comprising nardostachys jatamansi extract for preventing and treating insulin dependent diabetes mellitus, food comprising thereof | |
WO2012036344A1 (en) | Appetite suppressant food composition comprising a specific compound as an active ingredient | |
KR102395338B1 (en) | Oral composition for improving systemic symptoms including sensitivity to cold | |
WO2019083264A1 (en) | Composition for preventing, alleviating or treating liver diseases, containing fermented product of aged sprout ginseng extract as active ingredient | |
KR101155426B1 (en) | Composition of food components for appetite control | |
KR20130094553A (en) | Food composition, pharmaceutical composition and animal medicine against cancer containing gingerenone a | |
KR20130082249A (en) | Composition for preventing or improving the metabolic syndrome containing parthenocissus tricuspidata extract | |
KR20050107362A (en) | Health improving food containing an extract of the root bark of ulmus davidiana var | |
KR101159442B1 (en) | Composition comprising isolated sulfuretin from Rhus verniciflura for preventing and treating insulin dependent diabetes mellitus, food comprising thereof | |
KR101271478B1 (en) | Composition for promoting leptin secretion comprising 3-hydroxyflavone, hesperidin, quercetin, catechin and caffeine as effective component | |
KR20170087794A (en) | Composition comprising the compounds for preventing or treating obesity or hyperlipidermia | |
KR100552425B1 (en) | Composition for inhibiting liver cancer containing hirsutenone | |
KR20120029985A (en) | Functional beverage composition for appetite control | |
KR100700358B1 (en) | Composition containing tetramethoxyhydroxyflavone for inhibiting breast cancer | |
KR101732968B1 (en) | Pharmaceutical compositions for preventing or treating osteoporosis comprising an extract of Allium hookeri | |
KR20220028260A (en) | A composition for improving, preventing and treating of obesity comprising Ulva pertusa Kjellman extracts | |
KR20070041467A (en) | Food composition containing eupatilin for inhibiting breast cancer matastasis |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E902 | Notification of reason for refusal | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20170102 Year of fee payment: 5 |
|
FPAY | Annual fee payment |
Payment date: 20190408 Year of fee payment: 7 |
|
FPAY | Annual fee payment |
Payment date: 20200102 Year of fee payment: 8 |