JP2003508490A - Composition for extending postprandial satiety - Google Patents
Composition for extending postprandial satietyInfo
- Publication number
- JP2003508490A JP2003508490A JP2001521331A JP2001521331A JP2003508490A JP 2003508490 A JP2003508490 A JP 2003508490A JP 2001521331 A JP2001521331 A JP 2001521331A JP 2001521331 A JP2001521331 A JP 2001521331A JP 2003508490 A JP2003508490 A JP 2003508490A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- weight
- nutritional composition
- satiety
- nutritional
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 37
- 230000036186 satiety Effects 0.000 title claims abstract description 27
- 235000019627 satiety Nutrition 0.000 title claims abstract description 27
- 230000000291 postprandial effect Effects 0.000 title 1
- 235000016709 nutrition Nutrition 0.000 claims abstract description 29
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims abstract description 18
- 244000061456 Solanum tuberosum Species 0.000 claims abstract description 14
- 235000002595 Solanum tuberosum Nutrition 0.000 claims abstract description 14
- 235000012054 meals Nutrition 0.000 claims abstract description 13
- 239000000284 extract Substances 0.000 claims abstract description 7
- 235000019789 appetite Nutrition 0.000 claims abstract description 5
- 230000036528 appetite Effects 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000000843 powder Substances 0.000 claims abstract description 3
- 159000000007 calcium salts Chemical class 0.000 claims abstract 2
- 239000003086 colorant Substances 0.000 claims description 3
- 239000000796 flavoring agent Substances 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
- 239000005642 Oleic acid Substances 0.000 claims description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
- 235000019634 flavors Nutrition 0.000 claims description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- 244000144730 Amygdalus persica Species 0.000 claims 2
- 235000006040 Prunus persica var persica Nutrition 0.000 claims 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims 2
- 229930195729 fatty acid Natural products 0.000 claims 2
- 239000000194 fatty acid Substances 0.000 claims 2
- 150000004665 fatty acids Chemical class 0.000 claims 2
- 235000009434 Actinidia chinensis Nutrition 0.000 claims 1
- 244000298697 Actinidia deliciosa Species 0.000 claims 1
- 235000009436 Actinidia deliciosa Nutrition 0.000 claims 1
- 244000099147 Ananas comosus Species 0.000 claims 1
- 235000007119 Ananas comosus Nutrition 0.000 claims 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 claims 1
- 244000241235 Citrullus lanatus Species 0.000 claims 1
- 235000012828 Citrullus lanatus var citroides Nutrition 0.000 claims 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims 1
- 235000005979 Citrus limon Nutrition 0.000 claims 1
- 244000131522 Citrus pyriformis Species 0.000 claims 1
- 241000675108 Citrus tangerina Species 0.000 claims 1
- 235000015001 Cucumis melo var inodorus Nutrition 0.000 claims 1
- 240000002495 Cucumis melo var. inodorus Species 0.000 claims 1
- 241000220225 Malus Species 0.000 claims 1
- 235000011430 Malus pumila Nutrition 0.000 claims 1
- 235000015103 Malus silvestris Nutrition 0.000 claims 1
- 244000246386 Mentha pulegium Species 0.000 claims 1
- 235000016257 Mentha pulegium Nutrition 0.000 claims 1
- 235000004357 Mentha x piperita Nutrition 0.000 claims 1
- 240000008790 Musa x paradisiaca Species 0.000 claims 1
- 235000018290 Musa x paradisiaca Nutrition 0.000 claims 1
- 235000010401 Prunus avium Nutrition 0.000 claims 1
- 241001290151 Prunus avium subsp. avium Species 0.000 claims 1
- 240000008296 Prunus serotina Species 0.000 claims 1
- 235000014441 Prunus serotina Nutrition 0.000 claims 1
- 240000007651 Rubus glaucus Species 0.000 claims 1
- 235000011034 Rubus glaucus Nutrition 0.000 claims 1
- 235000009122 Rubus idaeus Nutrition 0.000 claims 1
- 240000006909 Tilia x europaea Species 0.000 claims 1
- 235000011941 Tilia x europaea Nutrition 0.000 claims 1
- 240000001717 Vaccinium macrocarpon Species 0.000 claims 1
- 235000012545 Vaccinium macrocarpon Nutrition 0.000 claims 1
- 235000002118 Vaccinium oxycoccus Nutrition 0.000 claims 1
- 235000009754 Vitis X bourquina Nutrition 0.000 claims 1
- 235000012333 Vitis X labruscana Nutrition 0.000 claims 1
- 240000006365 Vitis vinifera Species 0.000 claims 1
- 235000014787 Vitis vinifera Nutrition 0.000 claims 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 claims 1
- 235000019693 cherries Nutrition 0.000 claims 1
- 235000017803 cinnamon Nutrition 0.000 claims 1
- 235000004634 cranberry Nutrition 0.000 claims 1
- 239000000975 dye Substances 0.000 claims 1
- 235000012907 honey Nutrition 0.000 claims 1
- 235000001050 hortel pimenta Nutrition 0.000 claims 1
- 239000001034 iron oxide pigment Substances 0.000 claims 1
- 239000004571 lime Substances 0.000 claims 1
- 239000000049 pigment Substances 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 abstract description 10
- 108090000623 proteins and genes Proteins 0.000 abstract description 10
- 150000004668 long chain fatty acids Chemical class 0.000 abstract description 4
- 101800001982 Cholecystokinin Proteins 0.000 description 18
- 102100025841 Cholecystokinin Human genes 0.000 description 18
- 229940107137 cholecystokinin Drugs 0.000 description 18
- IZTQOLKUZKXIRV-YRVFCXMDSA-N sincalide Chemical compound C([C@@H](C(=O)N[C@@H](CCSC)C(=O)NCC(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)NC(=O)[C@@H](N)CC(O)=O)C1=CC=C(OS(O)(=O)=O)C=C1 IZTQOLKUZKXIRV-YRVFCXMDSA-N 0.000 description 18
- 235000018102 proteins Nutrition 0.000 description 9
- 235000003642 hunger Nutrition 0.000 description 7
- 235000005911 diet Nutrition 0.000 description 6
- 230000037213 diet Effects 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 239000000902 placebo Substances 0.000 description 6
- 229940068196 placebo Drugs 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- 229960005069 calcium Drugs 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052791 calcium Inorganic materials 0.000 description 5
- 235000001465 calcium Nutrition 0.000 description 5
- 230000004580 weight loss Effects 0.000 description 5
- 101000879758 Homo sapiens Sjoegren syndrome nuclear autoantigen 1 Proteins 0.000 description 4
- 102100037330 Sjoegren syndrome nuclear autoantigen 1 Human genes 0.000 description 4
- 229940019748 antifibrinolytic proteinase inhibitors Drugs 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000002496 gastric effect Effects 0.000 description 4
- 150000004667 medium chain fatty acids Chemical class 0.000 description 4
- 229920001592 potato starch Polymers 0.000 description 4
- 239000002753 trypsin inhibitor Substances 0.000 description 4
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 235000013361 beverage Nutrition 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 230000037406 food intake Effects 0.000 description 3
- 239000002858 neurotransmitter agent Substances 0.000 description 3
- 230000004936 stimulating effect Effects 0.000 description 3
- 101100298225 Caenorhabditis elegans pot-2 gene Proteins 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 229940122618 Trypsin inhibitor Drugs 0.000 description 2
- 101710162629 Trypsin inhibitor Proteins 0.000 description 2
- 108010046377 Whey Proteins Proteins 0.000 description 2
- 102000007544 Whey Proteins Human genes 0.000 description 2
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 2
- 239000001527 calcium lactate Substances 0.000 description 2
- 229960002401 calcium lactate Drugs 0.000 description 2
- 235000011086 calcium lactate Nutrition 0.000 description 2
- 235000015872 dietary supplement Nutrition 0.000 description 2
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 description 2
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 2
- 229940088598 enzyme Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 235000012631 food intake Nutrition 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 102220240796 rs553605556 Human genes 0.000 description 2
- 230000028327 secretion Effects 0.000 description 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 1
- 206010000060 Abdominal distension Diseases 0.000 description 1
- 208000019901 Anxiety disease Diseases 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229940122644 Chymotrypsin inhibitor Drugs 0.000 description 1
- 101710137926 Chymotrypsin inhibitor Proteins 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 206010022998 Irritability Diseases 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
- 230000036506 anxiety Effects 0.000 description 1
- 208000024330 bloating Diseases 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 239000003541 chymotrypsin inhibitor Substances 0.000 description 1
- 230000002844 continuous effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 235000018823 dietary intake Nutrition 0.000 description 1
- 229960003638 dopamine Drugs 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 239000003797 essential amino acid Substances 0.000 description 1
- 235000020776 essential amino acid Nutrition 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 231100000957 no side effect Toxicity 0.000 description 1
- 239000000820 nonprescription drug Substances 0.000 description 1
- 229960002748 norepinephrine Drugs 0.000 description 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 230000035922 thirst Effects 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 235000021119 whey protein Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/53—Lamiaceae or Labiatae (Mint family), e.g. thyme, rosemary or lavender
- A61K36/534—Mentha (mint)
-
- 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
- A23L33/40—Complete food formulations for specific consumer groups or specific purposes, e.g. infant formula
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/42—Cucurbitaceae (Cucumber family)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/45—Ericaceae or Vacciniaceae (Heath or Blueberry family), e.g. blueberry, cranberry or bilberry
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/73—Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/73—Rosaceae (Rose family), e.g. strawberry, chokeberry, blackberry, pear or firethorn
- A61K36/736—Prunus, e.g. plum, cherry, peach, apricot or almond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/75—Rutaceae (Rue family)
- A61K36/752—Citrus, e.g. lime, orange or lemon
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/81—Solanaceae (Potato family), e.g. tobacco, nightshade, tomato, belladonna, capsicum or jimsonweed
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/87—Vitaceae or Ampelidaceae (Vine or Grape family), e.g. wine grapes, muscadine or peppervine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/55—Protease inhibitors
- A61K38/56—Protease inhibitors from plants
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Botany (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Alternative & Traditional Medicine (AREA)
- Medical Informatics (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Food Science & Technology (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pediatric Medicine (AREA)
- Nutrition Science (AREA)
- Diabetes (AREA)
- Polymers & Plastics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Plant Substances (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
(57)【要約】 プロテイナーゼ阻害剤源を供給するジャガイモのエキスを含み、水と混合されて食前に摂取され、飽満を延長しそれによって食欲を減少させる乾燥粉末形態の栄養組成物。この栄養組成物は、約10〜約80重量%の蛋白質、約10〜約40重量%の中ないし長鎖脂肪酸、約2〜約5重量%のカルシウム塩、及びジャガイモのエキスによって供給される約1〜約5重量%のプロテイナーゼ阻害剤を含む。 (57) [Summary] A nutritional composition comprising a potato extract that provides a source of a proteinase inhibitor and taken in a meal before being mixed with water to prolong satiety and thereby reduce appetite in a dry powder form. The nutritional composition comprises about 10% to about 80% by weight of protein, about 10% to about 40% by weight of medium to long chain fatty acids, about 2% to about 5% by weight of a calcium salt, and about 5% by weight of a potato extract. 1 to about 5% by weight proteinase inhibitor.
Description
【0001】[0001]
発明の分野
本発明は、食事のあとの飽満を延ばすための栄養組成物に関する。さらに詳し
くは、その組成物は、蛋白質、中鎖及び/または長鎖脂肪酸及びコレシストキニ
ン胃腸ペプチドの分泌を刺激するためのカルシウム、及びコレシストキニンの分
解を防止するジャガイモから抽出されたプロテイナーゼ阻害剤の源、を包含する
。コレシストキニンの水準を増加し、維持することによって、本考案は飽満を引
き延ばす。 FIELD OF THE INVENTION The present invention relates to nutritional compositions for prolonging satiety after a meal. More particularly, the composition comprises a protein, medium and / or long chain fatty acids and calcium for stimulating the secretion of cholecystokinin gastrointestinal peptides, and a proteinase inhibitor extracted from potato that prevents the degradation of cholecystokinin. The source of the agent. By increasing and maintaining the level of cholecystokinin, the present invention prolongs satiety.
【0002】
先行技術の背景
過去40年にわたって、食事の摂取後の飽満を引き延ばすであろう機構につい
て広範囲な研究が行われてきている。そのような考案の恩恵は、体重の減量を行
う明らかな利用性を有する。体重減量研究は、三つの分野に焦点を置いている。
脳は食欲の制御において主要な役割を果たすので、研究者達は種々の神経伝達物
質、特にセロトニン(serotonine)、ドーパミン(dopamine
)及びノル−エピネフリン(nor−epinephrine)を調べてきてい
る。これらの神経伝達物質に影響を与える多数の処方薬及び一般薬製品が開発さ
れ、食欲を低減させている。薬理学的に食欲を低減させることは、ある時間の終
りまでに効果が失われること、を包含する多数の欠点を有する。神経伝達物質に
影響を与える薬剤は、中枢神経系統にも影響を与え、神経過敏及び不安を引起こ
しうる。さらには、これらの薬剤は、致命的であり得る心臓血管への影響を生じ
得る。Background of the Prior Art Over the last four decades, extensive research has been conducted on mechanisms that would prolong satiety after eating a meal. The benefit of such a device has the obvious utility of performing weight loss. Weight loss studies focus on three areas.
Since the brain plays a major role in the control of appetite, researchers are investigating various neurotransmitters, especially serotonin, dopamine.
) And nor-epinephrine have been investigated. Numerous prescription and over-the-counter products that affect these neurotransmitters have been developed to reduce appetite. Pharmacologically reducing appetite has a number of drawbacks, including loss of effect by the end of a period of time. Drugs that affect neurotransmitters can also affect the central nervous system, causing irritability and anxiety. Furthermore, these agents can cause cardiovascular effects that can be fatal.
【0003】
第2のアプローチは、胃腸が空になるのを遅延させ、それによって満腹感を生
じさせることに焦点が置かれてきている。このアプローチは、不溶性繊維を利用
し、繊維が胃腸管内の食物の移動を遅くする。繊維の使用に伴う欠点は、一定の
効果を生じさせるのに必要とされる量が、口当たりの良くない食物、ならびに鼓
脹、ガス及び下痢を含む多くの胃腸への影響、を生じさせる。The second approach has focused on delaying gastrointestinal emptying, thereby producing a feeling of satiety. This approach utilizes insoluble fiber, which slows the movement of food in the gastrointestinal tract. A drawback with the use of fiber is that the amount needed to produce a certain effect produces a poor mouthfeel and many gastrointestinal effects including bloating, gas and diarrhea.
【0004】
第3のアプローチは、身体の飽満機構を刺激することを研究する。食物が消費
されるときに、コレシストキニン放出蛋白質[Cholecystokinin
Releasing Protein(CCK−RP)]と称されるペプチドが
放出される。次いでコレシストキニン放出蛋白質が腸におけるコレシストキニン
の放出を刺激する。コレシストキニンは飽満を増大することが示されている。コ
レシストキニンが放出されるときに、それは、CCK−RPを不活性化させる酵
素の放出も刺激する。CCK−RPが不活性化されるときに、CCK水準が降下
し、飽満感は減少される。研究によって、コレシストキニンは食事摂取後の飽満
を引き延ばすのに極めて効果的であることが示されてきている。CCKは飽満を
延ばし、食物の採込みを低減させることが示されたが、主要な欠点は、それが静
脈注射で与えられなければならないことである。経口投与されるときには、CC
Kは胃腸酵素によって不活性化される。このことは、可能性のある体重減量剤と
してのその利用を著しく制限してきた。The third approach studies stimulating the satiety mechanism of the body. Cholecystokinin-releasing protein [Cholecystokinin] when food is consumed
The peptide called Releasing Protein (CCK-RP)] is released. The cholecystokinin-releasing protein then stimulates the release of cholecystokinin in the intestine. Cholecystokinin has been shown to increase satiety. When cholecystokinin is released, it also stimulates the release of an enzyme that inactivates CCK-RP. When CCK-RP is inactivated, CCK levels drop and satiety is reduced. Studies have shown that cholecystokinin is extremely effective in prolonging satiety after dietary intake. Although CCK has been shown to prolong satiety and reduce food intake, the major drawback is that it must be given intravenously. CC when orally administered
K is inactivated by gastrointestinal enzymes. This has severely limited its use as a potential weight loss agent.
【0005】
多数の栄養剤がコレシストキニンの放出を刺激することができる。研究者達は
蛋白質、脂肪(殊に、中鎖脂肪酸)、及びカルシウムがCCKの放出を刺激する
ことを明らかにしてきている。Many nutrients can stimulate the release of cholecystokinin. Researchers have shown that proteins, fats (particularly medium chain fatty acids), and calcium stimulate the release of CCK.
【0006】
米国特許第4,491,578号は、コレシストキニンの放出を刺激すること
によって飽満を刺激するためにトリプシン阻害剤を経口投与することを開示して
いる。トリプシン阻害剤は、コレシストキニン分泌のための負のフィードバック
信号を抑制することによって作用すると仮定された。このようにして、トリプシ
ン阻害剤はコレシストキニンの水準を維持して、それによって飽満を引き延ばし
た。US Pat. No. 4,491,578 discloses the oral administration of trypsin inhibitors to stimulate satiety by stimulating the release of cholecystokinin. It was hypothesized that trypsin inhibitors act by suppressing the negative feedback signal for cholecystokinin secretion. In this way, the trypsin inhibitor maintained the level of cholecystokinin, thereby prolonging satiety.
【0007】
多くの研究が、ジャガイモから抽出されたプロテイナーゼ阻害剤がコレシスト
キニンの放出を刺激することを明らかにしている。
経口摂取でき、食事の開始前にコレシストキニンの水準を刺激し、そして食事
の消費の後の長時間にわたりコレシストキニンの水準及び飽満を維持する栄養干
渉組成物が当業において明確に必要とされている。この発明の重要な要素は、食
事の前の特定の間隔で摂取される製品の設計である。従って、飽満の水準は食事
の前に既に増大され、食事中に消費される食物の量を減少させる。A number of studies have revealed that proteinase inhibitors extracted from potato stimulate the release of cholecystokinin. There is a clear need in the art for a nutritional interfering composition that is orally ingestible, stimulates the levels of cholecystokinin before the start of a meal, and maintains the levels and satiety of cholecystokinin for long periods of time after the consumption of a meal. It is said that. A key element of this invention is the design of the product to be taken at specific intervals before meals. Thus, the level of satiety is already increased before meals, reducing the amount of food consumed during meals.
【0008】[0008]
本発明は、食事の摂取後に飽満を引き延ばすための乾燥粉末形態の栄養組成物
を提供する。The present invention provides a nutritional composition in dry powder form for prolonging satiety after eating a meal.
【0009】
その乾燥栄養組成物は、10%〜80%の範囲の蛋白質を含む。その蛋白質は
、大豆、ホエー、カゼイン、または必須アミノ酸含有特定アミノ酸混合物、ある
いはアミノ酸フェニルアラニンの特定アミノ酸混合物であり得る。The dry nutritional composition comprises protein in the range of 10% to 80%. The protein may be soybean, whey, casein, or a specific amino acid mixture containing essential amino acids, or a specific amino acid mixture of the amino acids phenylalanine.
【0010】
この乾燥栄養組成物は、2%〜6%の範囲のミネラルカルシウムも含む。その
カルシウムは、塩化カルシウム、炭酸カルシウム、乳酸カルシウム等を包含する
塩の形であり得る。The dry nutritional composition also contains mineral calcium in the range of 2% to 6%. The calcium may be in the form of salts including calcium chloride, calcium carbonate, calcium lactate and the like.
【0011】
この乾燥栄養組成物は、10%〜40%の範囲の中鎖及び/または長鎖脂肪酸
(C12−C22)も含む。
この乾燥栄養組成物は、ジャガイモから抽出されたプロテイナーゼ阻害剤の源
をも含み、そのプロテイナーゼ阻害剤は0.02%〜5%の範囲で存在する。The dry nutritional composition also includes medium and / or long chain fatty acids (C 12 -C 22 ) in the range of 10% to 40%. The dry nutritional composition also includes a source of proteinase inhibitor extracted from potato, the proteinase inhibitor being present in the range of 0.02% to 5%.
【0012】[0012]
飽満を引き延ばすための栄養干渉用栄養組成物は、栄養剤を含み、それら栄養
剤は蛋白質、中及び/または長鎖脂肪酸、カルシウム、プロテイナーゼ阻害剤を
含有するジャガイモのエキス、そして好ましい形態では、香味剤及び着色剤を含
む。プロテイナーゼ阻害剤は、ジャガイモ中及びジャガイモエキス中に存在する
熱安定性蛋白質であり、ほぼ21,000の分子量を有する。それはトリプシン
及びキモトリプシン両阻害剤であり、その重要な機能はコレシストキニンの放出
を刺激することである。所望の活性を有するプロテイナーゼ阻害剤は、ジャガイ
モ中に、そしてより濃厚な形で市販ジャガイモエキス、または粗いジャガイモ粉
及びジャガイモ繊維のようなジャガイモ画分中に、存在する。特に、ノンパリエ
ル(Nonpariel)社から入手できる粗ジャガイモ粉は1グラム当たり約
0.49mgのプロテイナーゼ阻害剤対を含み、またオランダのアヴェベ(Av
ebe)社から入手できるPaselli PPCジャガイモ粉は、1グラム当
たりやく1.35mgのジャガイモプロテアーゼ阻害剤対を含む。本発明の所望
の活性を持つ比較的純粋なプロテイナーゼ阻害剤の抽出方法は、Bryant,
J.,Green,T.R.Gurusaddalah,T.,及びRyan,
C.A.の(1976),Biochem.15,3418に記載されている。The nutritional composition for nutritional interference to prolong satiety comprises nutritional agents, which are protein, medium and / or long chain fatty acids, calcium, potato extract containing proteinase inhibitors, and in a preferred form, Includes flavoring and coloring agents. Proteinase inhibitors are thermostable proteins present in potatoes and potato extracts and have a molecular weight of approximately 21,000. It is both a trypsin and chymotrypsin inhibitor, an important function of which is to stimulate the release of cholecystokinin. Proteinase inhibitors with the desired activity are present in potatoes and in more concentrated form in commercial potato extracts or in potato fractions such as coarse potato flour and potato fibres. In particular, the crude potato flour available from Nonpariel contains about 0.49 mg of proteinase inhibitor pair per gram, and it also contains Aveve (Av.
Paselli PPC potato flour available from ebe) contains as little as 1.35 mg potato protease inhibitor pair per gram. The method for extracting a relatively pure proteinase inhibitor having the desired activity of the present invention is described by Bryant,
J. , Green, T .; R. Gurusaddalah, T .; , And Ryan,
C. A. (1976), Biochem . 15, 3418.
【0013】[0013]
実験1
この研究は、平均BMI=31.2kg/m2(範囲27.0〜35.8)及
び平均年齢=30.9歳(範囲22〜45歳)の21人の被験者で行われた。二
つの群からなるクロスオーバー計画であった。第1の相では、被験者は、その等
カロリー組成が栄養ドリンク組成物に等しいプラシーボ、または栄養ドリンク組
成物を与えられた。両方の処理剤は食事の前15分に8オンスの水で服用された
。食事は、460カロリーであった。被験者は食事を15分内に食い尽くすこと
が要求された。食事を摂った後に被験者は、3.5時間にわたって15分毎に6
つの視覚アナログスケールで、空腹及び飽満感を評定するように依頼された。Experiment 1 This study was performed on 21 subjects with a mean BMI = 31.2 kg / m 2 (range 27.0-35.8) and a mean age = 30.9 years (range 22-45 years). It was a crossover plan consisting of two groups. In the first phase, the subject was given a placebo, or nutritional drink composition, whose isocaloric composition was equal to that of the nutritional drink composition. Both treatments were taken 15 minutes before meals with 8 ounces of water. The diet was 460 calories. Subjects were required to eat up within 15 minutes. Subjects ate 6 every 15 minutes after eating for 3.5 hours.
He was asked to rate hunger and satiety on two visual analog scales.
【0014】 その栄養ドリンク組成物は、下に示されている。[0014] The nutritional drink composition is shown below.
【0015】[0015]
【表1】 栄養ドリンク組成物 成分 グラム数 % ホエー蛋白質 13.00 71.5 50%のオレイン酸含有の 非乳クリーマー 4.00 22.0 乳酸カルシウム 0.635 3.5 フレーバー 0.19 1.0 色素 0.05 0.3 POT 2I 0.30 1.7 IPOT 2は約10重量%のプロテイナーゼ阻害剤を含む。Table 1 Nutritional drink composition ingredients Grams% Whey protein 13.00 71.5 Non-dairy creamer containing 50% oleic acid 4.00 22.0 Calcium lactate 0.635 3.5 Flavor 0.19 1. 0 dye 0.05 0.3 POT 2 I 0.30 1.7 I POT 2 contains about 10% by weight proteinase inhibitor.
【0016】
栄養ドリンク組成物の摂取後の空腹評定は、食後測定期間全体にわたって著し
く低減し、食後3時間までに30%の低減に達した(p=0.033)。この知
見と一致して、飽満評定は食後3時間から顕著に大きくなった(37%増大、p
=0.043)。空腹関連事項、または渇きの主観的評定における差異は、両条
件の間で観察されなかった。The post-ingestion hunger rating of the nutritional drink composition was significantly reduced over the post-meal measurement period, reaching a 30% reduction by 3 hours post-meal (p = 0.033). Consistent with this finding, satiety ratings increased significantly from 3 hours after meal (37% increase, p
= 0.043). No differences in hunger-related matters or subjective assessment of thirst were observed between both conditions.
【0017】
従って、本発明の一利点は、本発明が食事の終了後飽満を引伸ばしそして空腹
を低減するための栄養干渉組成物を提供することである。
実験2
この研究は、平均BMI=31.2kg/m2(範囲27.0〜35.8)及
び平均年齢=30.9歳(範囲22〜45歳)の21人の被験者で行われた。規
定食餌期中に被験者は、昼食及び夕食の前15分に毎日2回実験1の栄養ドリン
ク組成物8オンス(80kcal)を飲んだ。飽満に対するその栄養ドリンク組
成物の効果を規定食餌期の前及び4週間の規定食餌期に研究室で測定した。間隔
を置いた日に、350カロリーの食事の前15分に、被験者は本栄養ドリンク組
成物飲料、またはプラシーボ飲料(容積及びエネルギーについて釣合わせた)を
摂取した。被験者は、3.5時間にわたり15分毎に視覚アナログスケールで飽
満及び空腹を評定した。Accordingly, one advantage of the present invention is that it provides a nutritional interference composition for prolonging satiety and reducing hunger after the end of a meal. Experiment 2 This study was performed on 21 subjects with a mean BMI = 31.2 kg / m 2 (range 27.0-35.8) and a mean age = 30.9 years (range 22-45 years). During the diet, subjects drank 8 ounces (80 kcal) of the nutritional drink composition of Experiment 1 twice daily 15 minutes before lunch and dinner. The effect of the nutritional drink composition on satiety was measured in the laboratory before the regular diet period and at the regular diet period of 4 weeks. On spaced days, 15 minutes prior to a 350 calorie diet, subjects took the present nutritional drink composition beverage, or a placebo beverage (balanced for volume and energy). Subjects rated satiety and hunger on a visual analog scale every 15 minutes for 3.5 hours.
【0018】
研究の結果は、規定食餌での4週間後、昼食後の満腹評価は、プラシーボ飲料
よりも本栄養ドリンク組成物の摂取後の方が高かった(全ての時間間隔について
の平均±SD=71.0±17.3に対し65.5±16.7、p<0.05)
。空腹評価はプラシーボ飲料よりも本プロテアーゼ阻害剤の後が32%低かった
(10.5±12.0に対して15.4±13.3、p<0.01)。本栄養ド
リンク組成物に対しての副作用はなく、被験者は本栄養ドリンク組成物が彼等の
食物取込みを低減する助けとなったと報告した。体重減少は顕著であった(4週
間で2.0±1.1kg、p<0.05)。The results of the study showed that satiety evaluation after 4 weeks on the diet and after lunch was higher after ingestion of the present nutritional drink composition than placebo drink (mean ± SD for all time intervals). = 61.0 ± 17.3 vs. 71.0 ± 17.3, p <0.05)
. Hunger evaluation was 32% lower after the protease inhibitor than placebo beverage (15.4 ± 13.3 vs. 10.5 ± 12.0, p <0.01). There were no side effects on the present nutritional drink composition and subjects reported that the present nutritional drink composition helped reduce their food intake. Weight loss was significant (2.0 ± 1.1 kg at 4 weeks, p <0.05).
【0019】
従って、本発明の一利点は、30日の期間にわたり継続的な効果を与え、そし
て飽満を引延ばすことによって、顕著な体重減少をもたらすことである。
プロテアーゼ阻害剤の源は本発明の飽満引延ばし製品のための個々の応用に応
じて変わり得る。例えば、粗ジャガイモ粉は著量のプロテアーゼ阻害剤を含むが
、それは水に分散させるのが困難である。当業者は、上記に示された本発明の教
示に従って、プロテアーゼ阻害剤の適切な源、ならびに食感、味等の特性を改善
するために組成物に添加することができるその他の成分の決定を容易に行うこと
ができる。上記の説明は多くの特定事項を含むが、これらは本発明の範囲を限定
するものとして解釈されるべきでなく、本発明の現在の好ましい具体例をのいく
つかの例示を与えるに過ぎない。Therefore, one advantage of the present invention is that it provides a significant effect on weight loss by providing a continuous effect over a period of 30 days and prolonging satiety. The source of the protease inhibitor may vary depending on the particular application for the satiety prolonging product of the present invention. For example, crude potato flour contains significant amounts of protease inhibitors, which are difficult to disperse in water. One of ordinary skill in the art, in accordance with the teachings of the present invention provided above, will determine the appropriate source of protease inhibitors, as well as other ingredients that may be added to the composition to improve properties such as texture, taste and the like. It can be done easily. While the above description contains many specifics, these should not be construed as limiting the scope of the invention, but only as providing some of the presently preferred embodiments of the invention.
【図1】 図1は、食事後の3.5時間にわたる15分間隔での飽満感に関
しての被験者の応答のグラフ表示であり、プラシーボを投与された被験者、及び
本発明による栄養サプリメントを投与された被験者の両方を示している。FIG. 1 is a graphical representation of a subject's response to satiety at 15-minute intervals over a 3.5 hour post-meal period, with subjects receiving placebo and a nutritional supplement according to the invention. Both of the tested subjects are shown.
【図2】 図2は、食事後の3.5時間にわたる15分間隔での空腹感に関
しての被験者の応答のグラフ表示であり、プラシーボを投与された被験者、及び
本発明による栄養サプリメントを投与された被験者の両方を示している。FIG. 2 is a graphical representation of a subject's response to hunger at 15-minute intervals over a 3.5 hour post-meal period, subjects receiving placebo and a nutritional supplement according to the present invention. Both subjects are shown.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) A61K 35/78 A61K 35/78 W 4C206 A61P 3/04 A61P 3/04 A61K 37/02 (81)指定国 EP(AT,BE,CH,CY, DE,DK,ES,FI,FR,GB,GR,IE,I T,LU,MC,NL,PT,SE),OA(BF,BJ ,CF,CG,CI,CM,GA,GN,GW,ML, MR,NE,SN,TD,TG),AP(GH,GM,K E,LS,MW,MZ,SD,SL,SZ,TZ,UG ,ZW),EA(AM,AZ,BY,KG,KZ,MD, RU,TJ,TM),AL,AM,AT,AU,AZ, BA,BB,BG,BR,BY,CA,CH,CN,C U,CZ,DE,DK,EE,ES,FI,GB,GE ,GH,GM,HR,HU,ID,IL,IN,IS, JP,KE,KG,KP,KR,KZ,LC,LK,L R,LS,LT,LU,LV,MD,MG,MK,MN ,MW,MX,NO,NZ,PL,PT,RO,RU, SD,SE,SG,SI,SK,SL,TJ,TM,T R,TT,UA,UG,UZ,VN,YU,ZW Fターム(参考) 4B018 LE03 MD04 MD10 MD20 MD53 ME01 4C076 AA29 BB01 CC21 FF36 GG09 GG47 4C084 AA02 BA44 CA62 MA02 MA43 MA52 NA14 ZA661 ZC211 4C086 AA01 AA02 HA04 MA03 MA43 NA14 ZA66 ZC21 4C088 AB12 AB48 AB51 AB62 BA08 MA02 MA07 MA43 MA52 NA14 ZA66 ZC21 4C206 AA01 AA02 DA04 MA03 MA63 MA72 NA14 ZA66 ZC21 ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 7 Identification code FI theme code (reference) A61K 35/78 A61K 35/78 W 4C206 A61P 3/04 A61P 3/04 A61K 37/02 (81) Designated country EP (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE), OA (BF, BJ, CF, CG, CI, CM, GA, GN, GW, ML, MR, NE, SN, TD, TG), AP (GH, GM, KE, LS, MW, MZ, SD, SL, SZ, TZ, UG, ZW) , EA (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM), AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, A, CH, CN, CU, CZ, DE, DK, EE, ES, FI, GB, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR , KZ, LC, LK, LR, LS, LT, LU, LV, MD, MG, MK, MN, MW, MX, NO, NZ, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, UA, UG, UZ, VN, YU, ZW F terms (reference) 4B018 LE03 MD04 MD10 MD20 MD53 ME01 4C076 AA29 BB01 CC21 FF36 GG09 GG47 4C084 AA02 BA44 CA62 MA02 MA43 MA52 NA14 ZA661 ZC211 4C086 AA01 AA02 HA04 MA03 MA43 NA14 ZA66 ZC21 4C088 AB12 AB48 AB51 AB62 BA08 MA02 MA07 MA43 MA52 NA14 ZA66 ZC21 4C206 AA01 AA02 DA04 MA03 MA63 MA72 NA14 ZA66 ZC21
Claims (5)
を減少させる乾燥粉末形態の栄養組成物であって: (a)その乾燥組成物の約10〜約80重量%をなす蛋白質; (b)その乾燥組成物の約10〜約40重量%をなす1種またはそれ以上の脂肪
酸; (c)その乾燥組成物の約2〜約5重量%をなすカルシウム塩;及び (d)その乾燥組成物の約0.02〜約5重量%をなす、プロテイナーゼ阻害剤
源を供給するジャガイモのエキス; を含む上記栄養組成物。1. A nutritional composition in the form of a dry powder that is mixed with water and taken before meals to prolong satiety and thereby reduce appetite: (a) from about 10 to about 80 of the dry composition. (B) one or more fatty acids that make up about 10 to about 40% by weight of the dry composition; (c) calcium salts that make up about 2 to about 5% by weight of the dry composition. And (d) about 0.02 to about 5% by weight of the dry composition, an extract of potato supplying a source of a proteinase inhibitor.
ドウ、ハニーデュウ、ハチミツ、キウイ、レモン、ライム、オレンジ、モモ、ペ
パーミント、パイナップル、ラズベリー、タンジェリン、スイカ、及びワイルド
チェリーの天然エキス及び人造エキス成分を包含する群より選択された水溶性香
味料をさらに含む請求項1に記載の栄養組成物。3. Natural and artificial extracts of apple, banana, cherry, cinnamon, cranberry, grape, honeydew, honey, kiwi, lemon, lime, orange, peach, peppermint, pineapple, raspberry, tangerine, watermelon and wild cherry. The nutritional composition of claim 1, further comprising a water soluble flavor selected from the group including ingredients.
人工染料を包含する群より選択された着色料をさらに含む請求項1に記載の栄養
組成物。4. The nutritional composition of claim 1, further comprising a colorant selected from the group comprising water-soluble natural or artificial dyes of blue, green, orange, red, violet and yellow.
包含する群より選択された着色料をさらに含む請求項1に記載の栄養組成物。5. The nutritional composition of claim 1 further comprising a colorant selected from the group including iron oxide pigments, blue, peach, red and violet ultramarine pigments.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14589299P | 1999-07-27 | 1999-07-27 | |
US60/145,892 | 1999-07-27 | ||
PCT/US2000/020157 WO2001017541A1 (en) | 1999-07-27 | 2000-07-25 | Composition for extending post meal satiety |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2005235268A Division JP2005336208A (en) | 1999-07-27 | 2005-08-15 | Composition for extending post meal satiety |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2003508490A true JP2003508490A (en) | 2003-03-04 |
Family
ID=22515008
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001521331A Pending JP2003508490A (en) | 1999-07-27 | 2000-07-25 | Composition for extending postprandial satiety |
JP2005235268A Pending JP2005336208A (en) | 1999-07-27 | 2005-08-15 | Composition for extending post meal satiety |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2005235268A Pending JP2005336208A (en) | 1999-07-27 | 2005-08-15 | Composition for extending post meal satiety |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1115409A4 (en) |
JP (2) | JP2003508490A (en) |
KR (1) | KR20010075394A (en) |
AU (1) | AU779377C (en) |
BR (1) | BR0006959A (en) |
CA (1) | CA2348067A1 (en) |
MX (1) | MXPA01003054A (en) |
WO (1) | WO2001017541A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008535919A (en) * | 2005-04-11 | 2008-09-04 | ユニバーシティ オブ テネシー リサーチ ファウンデーション | Stable milk ingredients that are effective in reducing fat |
JP2010094085A (en) * | 2008-10-17 | 2010-04-30 | Pola Chem Ind Inc | Food composition for dieting use |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6686456B2 (en) | 2001-07-06 | 2004-02-03 | Kemin Foods, L.C. | Method for the elimination of Kunitz and Bowman-Birk trypsin inhibitors and carboxypeptidase inhibitor from potato proteins |
JP2005015358A (en) * | 2003-06-25 | 2005-01-20 | Pharma Design Inc | Medicinal composition used for treating eating disorder |
JP5691105B2 (en) * | 2009-01-30 | 2015-04-01 | 株式会社東洋新薬 | Taste improvement method of food containing potato extract |
EP2227966B1 (en) * | 2009-02-25 | 2016-07-27 | Coöperatie Avebe U.A. | Condiment |
JP5672588B2 (en) * | 2009-05-26 | 2015-02-18 | 株式会社東洋新薬 | Diet composition |
JP5721232B2 (en) * | 2009-12-04 | 2015-05-20 | 株式会社東洋新薬 | Glucagon-like peptide-1 secretion promoter |
CN107334875A (en) * | 2017-08-30 | 2017-11-10 | 南宁学院 | A kind of medicinal liquor for treating diarrhoea and preparation method thereof |
CN111493254A (en) * | 2020-04-10 | 2020-08-07 | 苏州绿叶日用品有限公司 | A solid beverage containing rhizoma Solani Tuber osi extract and its preparation method |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4491578A (en) * | 1982-06-14 | 1985-01-01 | Peikin Steven R | Method of stimulating satiety in mammals |
US4833128A (en) * | 1984-12-28 | 1989-05-23 | Neil Solomon | Dietary supplement |
JPH0699321B2 (en) * | 1990-01-22 | 1994-12-07 | 不二製油株式会社 | Appetite suppressant and food containing the same |
US5468727A (en) * | 1990-12-13 | 1995-11-21 | Board Of Regents, The University Of Texas System | Methods of normalizing metabolic parameters in diabetics |
US5221668A (en) * | 1992-02-26 | 1993-06-22 | Abbott Laboratories | Nutritional product for trauma and surgery patients |
NZ260933A (en) * | 1993-07-16 | 1996-07-26 | Hercules Inc | Cation-complexed polysaccharides; use in foods and pharmaceuticals |
US5340603A (en) * | 1993-08-30 | 1994-08-23 | Abbott Laboratories | Nutritional product for human infants having chronic lung disease |
WO1996004933A2 (en) * | 1994-08-05 | 1996-02-22 | Wisconsin Alumni Research Foundation | Cck antibodies used to improve feed efficiency |
US5595772A (en) * | 1995-06-07 | 1997-01-21 | Massachusetts Institute Of Technology | Composition and methods for losing weight |
ES2206821T3 (en) * | 1997-06-23 | 2004-05-16 | Societe Des Produits Nestle S.A. | USE OF A NUTRITIVE COMPOSITION FOR THE PREPARATION OF A LIQUID COMPOSITION FOR DIABETICS. |
US6475539B1 (en) * | 1998-05-07 | 2002-11-05 | Abbott Laboratories | Nutritionally complete low pH enteral formula |
US6051236A (en) * | 1998-11-12 | 2000-04-18 | Pacifichealth Laboratories, Inc. | Composition for optimizing muscle performance during exercise |
US6025363A (en) * | 1998-11-17 | 2000-02-15 | Giles, Jr.; James A. | Composition for suppressing appetite |
-
2000
- 2000-07-25 WO PCT/US2000/020157 patent/WO2001017541A1/en not_active Application Discontinuation
- 2000-07-25 AU AU63704/00A patent/AU779377C/en not_active Ceased
- 2000-07-25 MX MXPA01003054A patent/MXPA01003054A/en active IP Right Grant
- 2000-07-25 CA CA002348067A patent/CA2348067A1/en not_active Abandoned
- 2000-07-25 JP JP2001521331A patent/JP2003508490A/en active Pending
- 2000-07-25 BR BR0006959-0A patent/BR0006959A/en not_active IP Right Cessation
- 2000-07-25 KR KR1020017003896A patent/KR20010075394A/en not_active Application Discontinuation
- 2000-07-25 EP EP00950624A patent/EP1115409A4/en not_active Withdrawn
-
2005
- 2005-08-15 JP JP2005235268A patent/JP2005336208A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008535919A (en) * | 2005-04-11 | 2008-09-04 | ユニバーシティ オブ テネシー リサーチ ファウンデーション | Stable milk ingredients that are effective in reducing fat |
JP2010094085A (en) * | 2008-10-17 | 2010-04-30 | Pola Chem Ind Inc | Food composition for dieting use |
Also Published As
Publication number | Publication date |
---|---|
WO2001017541A1 (en) | 2001-03-15 |
EP1115409A1 (en) | 2001-07-18 |
MXPA01003054A (en) | 2003-07-14 |
AU779377C (en) | 2005-06-30 |
JP2005336208A (en) | 2005-12-08 |
AU6370400A (en) | 2001-04-10 |
BR0006959A (en) | 2001-06-26 |
KR20010075394A (en) | 2001-08-09 |
AU779377B2 (en) | 2005-01-20 |
EP1115409A4 (en) | 2005-04-13 |
CA2348067A1 (en) | 2001-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2005336208A (en) | Composition for extending post meal satiety | |
US5290571A (en) | Biologically active whey protein concentrate | |
US6019976A (en) | Formulations for treating male pattern baldness containing Serenoa repens, Vitamin B6, Vitamin B3, zinc and L-Arginine | |
US20020119915A1 (en) | Nutritional intervention composition containing a source of proteinase inhibitor extending post meal satiety | |
Trevisanato et al. | Tea and health | |
EP0374390B1 (en) | Whey protein composition, a method for producing it and application of the whey protein composition | |
JP2002538802A (en) | Food supplement and method for cosmetic treatment based on grape extract rich in polyphenols | |
JP3018053B2 (en) | Food and drink | |
JP2003517018A (en) | Nutritional compositions, methods of making the compositions, and methods of using the compositions | |
CA2627314C (en) | Composition for treating obesity comprising extract from white kidney beans, red kidney beans, and green tea leaves | |
KR20000035798A (en) | Nutritional formula for phenylketonuria patients | |
TW200533333A (en) | Human beta-defensin production accelerator | |
US9308161B2 (en) | Substance for restoring normal co-expression and interaction between the LOX and NRAGE proteins | |
WO2005122798A1 (en) | Functional beverage composition for improving ability of learning, concentration and memory | |
JP4459540B2 (en) | Functional health food | |
JP2002526413A (en) | Reduction of oxidative stress factors | |
JPH11137212A (en) | Beauty culture composition | |
JP2001518484A (en) | Composition for suppressing withdrawal symptoms and craving for alcohol in alcoholics and for preventing abuse of alcohol in healthy people | |
TW201111479A (en) | Antioxidant composition | |
TW201026317A (en) | Use of cycloartane compounds for treating arthritis | |
US20040077530A1 (en) | Composition for reducing caloric intake | |
JP3241609B2 (en) | Pharmaceuticals containing bean tea extract as an active ingredient, and foods and cosmetics containing the same | |
JP2003327540A (en) | Hyaluronidase-inhibiting, antiallergically-activating, and immune-potentiating substance | |
US20060135444A1 (en) | Combination of flavonoid and procyanidin for the reduction of the mammalian appetite | |
JPH0667831B2 (en) | Amino acid composition for improving hepatic substance synthesis dysfunction |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20050215 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20050513 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20050520 |
|
A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20050815 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20060214 |