JP2905725B2 - Food composition derived from tomato - Google Patents
Food composition derived from tomatoInfo
- Publication number
- JP2905725B2 JP2905725B2 JP7198925A JP19892595A JP2905725B2 JP 2905725 B2 JP2905725 B2 JP 2905725B2 JP 7198925 A JP7198925 A JP 7198925A JP 19892595 A JP19892595 A JP 19892595A JP 2905725 B2 JP2905725 B2 JP 2905725B2
- Authority
- JP
- Japan
- Prior art keywords
- tomato
- serum
- blood pressure
- ace
- juice
- 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.)
- Expired - Lifetime
Links
- 235000013305 food Nutrition 0.000 title claims description 28
- 239000000203 mixture Substances 0.000 title claims description 21
- 235000007688 Lycopersicon esculentum Nutrition 0.000 title description 79
- 240000003768 Solanum lycopersicum Species 0.000 title description 79
- 210000002966 serum Anatomy 0.000 claims description 58
- 230000036772 blood pressure Effects 0.000 claims description 53
- 235000015193 tomato juice Nutrition 0.000 claims description 40
- 230000000694 effects Effects 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000012141 concentrate Substances 0.000 claims description 13
- 239000004480 active ingredient Substances 0.000 claims description 8
- 102100030988 Angiotensin-converting enzyme Human genes 0.000 description 29
- 230000002401 inhibitory effect Effects 0.000 description 19
- 239000005541 ACE inhibitor Substances 0.000 description 18
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 description 18
- 238000000034 method Methods 0.000 description 18
- 239000000796 flavoring agent Substances 0.000 description 13
- 108090000790 Enzymes Proteins 0.000 description 12
- 102000004190 Enzymes Human genes 0.000 description 12
- 235000019634 flavors Nutrition 0.000 description 12
- 230000009471 action Effects 0.000 description 11
- 206010020772 Hypertension Diseases 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 230000036541 health Effects 0.000 description 9
- 241001465754 Metazoa Species 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000009395 breeding Methods 0.000 description 7
- 230000001488 breeding effect Effects 0.000 description 7
- 230000005764 inhibitory process Effects 0.000 description 7
- 230000035488 systolic blood pressure Effects 0.000 description 7
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 6
- 241000700159 Rattus Species 0.000 description 6
- 235000013376 functional food Nutrition 0.000 description 6
- 238000005119 centrifugation Methods 0.000 description 5
- 235000013399 edible fruits Nutrition 0.000 description 5
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 5
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 230000001965 increasing effect Effects 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 235000013361 beverage Nutrition 0.000 description 4
- 102000005862 Angiotensin II Human genes 0.000 description 3
- 101800000734 Angiotensin-1 Proteins 0.000 description 3
- 102400000344 Angiotensin-1 Human genes 0.000 description 3
- 101800000733 Angiotensin-2 Proteins 0.000 description 3
- CZGUSIXMZVURDU-JZXHSEFVSA-N Ile(5)-angiotensin II Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C([O-])=O)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(N)=[NH2+])NC(=O)[C@@H]([NH3+])CC([O-])=O)C(C)C)C1=CC=C(O)C=C1 CZGUSIXMZVURDU-JZXHSEFVSA-N 0.000 description 3
- ORWYRWWVDCYOMK-HBZPZAIKSA-N angiotensin I Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC(C)C)C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C1=CC=C(O)C=C1 ORWYRWWVDCYOMK-HBZPZAIKSA-N 0.000 description 3
- 229950006323 angiotensin ii Drugs 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- OGNSCSPNOLGXSM-UHFFFAOYSA-N (+/-)-DABA Natural products NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 2
- 206010002091 Anaesthesia Diseases 0.000 description 2
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 102220547770 Inducible T-cell costimulator_A23L_mutation Human genes 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 230000037005 anaesthesia Effects 0.000 description 2
- 210000001367 artery Anatomy 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 230000017531 blood circulation Effects 0.000 description 2
- 210000004204 blood vessel Anatomy 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000000502 dialysis Methods 0.000 description 2
- 239000000385 dialysis solution Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 235000013402 health food Nutrition 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000011699 spontaneously hypertensive rat Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- UUUHXMGGBIUAPW-UHFFFAOYSA-N 1-[1-[2-[[5-amino-2-[[1-[5-(diaminomethylideneamino)-2-[[1-[3-(1h-indol-3-yl)-2-[(5-oxopyrrolidine-2-carbonyl)amino]propanoyl]pyrrolidine-2-carbonyl]amino]pentanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]-3-methylpentanoyl]pyrrolidine-2-carbon Chemical compound C1CCC(C(=O)N2C(CCC2)C(O)=O)N1C(=O)C(C(C)CC)NC(=O)C(CCC(N)=O)NC(=O)C1CCCN1C(=O)C(CCCN=C(N)N)NC(=O)C1CCCN1C(=O)C(CC=1C2=CC=CC=C2NC=1)NC(=O)C1CCC(=O)N1 UUUHXMGGBIUAPW-UHFFFAOYSA-N 0.000 description 1
- 108090001067 Angiotensinogen Proteins 0.000 description 1
- 102000004881 Angiotensinogen Human genes 0.000 description 1
- 101800004538 Bradykinin Proteins 0.000 description 1
- 102400000967 Bradykinin Human genes 0.000 description 1
- 108010016626 Dipeptides Proteins 0.000 description 1
- 239000004278 EU approved seasoning Substances 0.000 description 1
- 208000007530 Essential hypertension Diseases 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 102000008214 Glutamate decarboxylase Human genes 0.000 description 1
- 108091022930 Glutamate decarboxylase Proteins 0.000 description 1
- QXZGBUJJYSLZLT-UHFFFAOYSA-N H-Arg-Pro-Pro-Gly-Phe-Ser-Pro-Phe-Arg-OH Natural products NC(N)=NCCCC(N)C(=O)N1CCCC1C(=O)N1C(C(=O)NCC(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CO)C(=O)N2C(CCC2)C(=O)NC(CC=2C=CC=CC=2)C(=O)NC(CCCN=C(N)N)C(O)=O)CCC1 QXZGBUJJYSLZLT-UHFFFAOYSA-N 0.000 description 1
- 108090000882 Peptidyl-Dipeptidase A Proteins 0.000 description 1
- 102100028255 Renin Human genes 0.000 description 1
- 108090000783 Renin Proteins 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 235000013334 alcoholic beverage Nutrition 0.000 description 1
- 229940124277 aminobutyric acid Drugs 0.000 description 1
- 238000003975 animal breeding Methods 0.000 description 1
- 230000003276 anti-hypertensive effect Effects 0.000 description 1
- 239000002220 antihypertensive agent Substances 0.000 description 1
- 229940127088 antihypertensive drug Drugs 0.000 description 1
- 229940124572 antihypotensive agent Drugs 0.000 description 1
- 230000004872 arterial blood pressure Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000001164 bioregulatory effect Effects 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- QXZGBUJJYSLZLT-FDISYFBBSA-N bradykinin Chemical compound NC(=N)NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(=O)NCC(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CO)C(=O)N2[C@@H](CCC2)C(=O)N[C@@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)CCC1 QXZGBUJJYSLZLT-FDISYFBBSA-N 0.000 description 1
- 235000008429 bread Nutrition 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 210000004899 c-terminal region Anatomy 0.000 description 1
- 235000012970 cakes Nutrition 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 210000001715 carotid artery Anatomy 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014510 cooky Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000012495 crackers Nutrition 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 210000003191 femoral vein Anatomy 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001641 gel filtration chromatography Methods 0.000 description 1
- 238000002523 gelfiltration Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000009532 heart rate measurement Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 235000008960 ketchup Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000035485 pulse pressure Effects 0.000 description 1
- 230000036454 renin-angiotensin system Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000001223 reverse osmosis Methods 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000005526 vasoconstrictor agent Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Landscapes
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Jellies, Jams, And Syrups (AREA)
- Non-Alcoholic Beverages (AREA)
- Medicines Containing Plant Substances (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明はトマト由来の食品組
成物に関し、詳しくは血圧上昇抑制作用を有し、且つト
マトの良好な風味を保持したトマト由来の食品組成物に
関する。[0001] The present invention relates to a tomato-derived food composition, and more particularly, to a tomato-derived food composition having an action of suppressing an increase in blood pressure and maintaining good tomato flavor.
【0002】[0002]
【従来の技術】近年、遺伝子レベルで高血圧症とレニン
・アンジオテンシン系との関連を示唆する報告がでる
等、高血圧症の要因の一つとしてアンジオテンシン変換
酵素(以下、「ACE」と略す)作用の異常が挙げられ
るようになった。ACEは、主に2つの血圧調節系に関
与して昇圧作用を示す酵素であるが、この酵素が異常に
作用すると高血圧症を誘発するとされる。そこで、この
ようなACEの昇圧作用を阻害する物質を投与すること
により高血圧症を改善しようとする試みがなされ、現在
では、ACE阻害薬は既に、臨床的にも高血圧症の治療
に用いられており、目立った副作用もないことから全高
血圧治療薬に占める割合も増加している。2. Description of the Related Art In recent years, it has been reported that the relationship between hypertension and the renin-angiotensin system at the gene level has been reported. One of the causes of hypertension is the effect of angiotensin converting enzyme (hereinafter abbreviated as "ACE"). Anomalies came to be mentioned. ACE is an enzyme that is mainly involved in two blood pressure regulating systems and exhibits a blood pressure effect. It is said that abnormal action of this enzyme induces hypertension. Therefore, attempts have been made to improve hypertension by administering a substance that inhibits the pressor action of ACE. At present, ACE inhibitors have already been used clinically for the treatment of hypertension. As there are no noticeable side effects, the proportion of all antihypertensive drugs is increasing.
【0003】一方、食品の第三次機能としての生体調節
機能の解明が様々な食品についてなされ、その過程にお
いて食品やその酵素消化物中から多くの生理活性物質が
見出されてきているが、アッセイ法の簡便さも手伝って
か、上記のようなACE阻害物質を単離する報告も数多
くなされている。また、このような食品等から得られた
ACE阻害物質の中には、高血圧症のモデル動物への投
与で効果が確認されているものもあり、このような特徴
を利用した機能性食品の開発もなされている。[0003] On the other hand, elucidation of bioregulatory functions as a tertiary function of foods has been made for various foods, and in the process, many physiologically active substances have been found in foods and their enzyme digests. There have been many reports of isolating ACE inhibitors as described above, probably because of the simplicity of the assay method. In addition, among ACE inhibitors obtained from such foods and the like, some of them have been confirmed to be effective when administered to model animals of hypertension, and the development of functional foods utilizing such characteristics has been developed. Has also been made.
【0004】しかし、トマトがACE阻害作用を有する
物質を含有することは知られておらず、またトマトから
ACE阻害物質を含有する成分を取り出して、高血圧症
を改善する機能性食品として利用した報告もない。[0004] However, it is not known that tomato contains a substance having an ACE inhibitory action, and it has been reported that an ingredient containing an ACE inhibitory substance was extracted from tomato and used as a functional food for improving hypertension. Nor.
【0005】ところで、近年、トマト由来の機能性食品
もいくつか研究開発され、その機能として血圧上昇抑制
作用を有する食品も開発されている。例えば、特開平3
−224467号公報に記載されているトマト由来の機
能性食品等がこれである。しかし、上記発明は、完熟ト
マト処理物にグルタミン酸脱炭酸酵素を作用させて、完
熟トマトに含有するグルタミン酸の一部を血圧上昇抑制
作用を有するγ−アミノ酪酸にしたものであって、γ−
アミノ酪酸の含有量を増加させることにより血圧上昇を
抑制する作用を有するというものであり、トマト本来の
成分中に上記ACE阻害作用を有する物質が存在し、こ
れが血圧上昇抑制作用に関与する旨の記載はない。ま
た、この発明では、γ−アミノ酪酸の含有量を増加させ
る代わりにトマトの良好な風味を醸し出しているグルタ
ミン酸の含有量を減少させるので、得られた機能性食品
においてはトマトの良好な風味が十分でないという問題
があった。そこで、トマトの良好な風味を保持しなが
ら、血圧の上昇を抑制する作用を有するようなトマト由
来の食品組成物の開発が望まれていた。[0005] In recent years, some functional foods derived from tomato have been researched and developed, and foods having a function of suppressing an increase in blood pressure as a function thereof have been developed. For example, Japanese Unexamined Patent Publication
This is the functional food derived from tomato described in JP-A-224467. However, the above-mentioned invention is characterized in that glutamic acid decarboxylase is allowed to act on the processed ripe tomato to convert a part of the glutamic acid contained in the ripe tomato into γ-aminobutyric acid having a blood pressure increase inhibitory effect,
It has the effect of suppressing blood pressure increase by increasing the content of aminobutyric acid, and there is a substance having the ACE inhibitory effect in the tomato's original components, which indicates that it is involved in the blood pressure increase suppressing effect. There is no description. Also, in the present invention, instead of increasing the content of γ-aminobutyric acid, the content of glutamic acid that produces a good flavor of tomato is reduced, so that the resulting functional food has good tomato flavor. There was a problem that it was not enough. Therefore, development of a tomato-derived food composition having an action of suppressing an increase in blood pressure while maintaining good flavor of tomato has been desired.
【0006】[0006]
【発明が解決しようとする課題】本発明は、上記観点か
らなされたものであり、血圧上昇抑制作用を有し、且つ
トマトの良好な風味を保持したトマト由来の食品組成物
を提供することを課題とする。DISCLOSURE OF THE INVENTION The present invention has been made in view of the above, and an object of the present invention is to provide a food composition derived from tomato, which has an action of suppressing an increase in blood pressure and maintains a good flavor of tomato. Make it an issue.
【0007】[0007]
【課題を解決するための手段】本発明者は、上記課題を
解決するために鋭意研究を行った結果、トマト果実中に
ACE阻害作用を有する物質が存在することを見出し、
トマト搾汁液の漿液及び/又はその濃縮物がトマトの良
好な風味を保持した状態で得られ、これらが実際に血圧
上昇を抑制する作用を有すること、更に、トマト搾汁液
の漿液から得られる分子量4000以下の水溶性化合物
がACE阻害物質をより高濃度に含有すし、血圧上昇抑
制作用に優れることを見出し、本発明を完成するに至っ
た。Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above problems, and as a result, have found that a substance having an ACE inhibitory action is present in tomato fruits.
Serum of tomato juice and / or a concentrate thereof are obtained while maintaining a good flavor of tomato, and these have an effect of actually suppressing an increase in blood pressure. Furthermore, molecular weight obtained from serum of tomato juice The present inventors have found that a water-soluble compound of 4000 or less contains an ACE inhibitor in a higher concentration and is excellent in an effect of suppressing an increase in blood pressure, thereby completing the present invention.
【0008】すなわち本発明は、トマト搾汁液の漿液及
び/又はその濃縮物を有効成分として含有する血圧上昇
抑制作用を有する食品組成物及びトマト搾汁液の漿液に
含まれる分子量4000以下の水溶性化合物を有効成分
として含有する血圧上昇抑制作用を有する食品組成物で
ある。[0008] That is, the present invention relates to a food composition having a blood pressure increase-inhibiting action containing a serum of tomato juice and / or a concentrate thereof as an active ingredient, and a water-soluble compound having a molecular weight of 4000 or less contained in the serum of tomato juice. Is a food composition having an effect of suppressing an increase in blood pressure, which comprises the following as an active ingredient:
【0009】以下、本発明を詳細に説明する。本発明の
血圧上昇抑制作用を有する食品組成物は、トマト搾汁液
の漿液及び/又はその濃縮物を有効成分として含有す
る。あるいは、トマト搾汁液の漿液に含まれる分子量4
000以下の水溶性化合物を有効成分として含有する。
トマトの果実中には、ACE阻害作用を有する物質が存
在しており、これを例えば高血圧症の人に投与すれば、
その体内でこの物質がACEの昇圧作用を阻害し高血圧
が改善されるものと推定される。従って、完熟した生の
トマトそのもの、あるいはこれを細かく粉砕したもの、
トマト搾汁液等もACE阻害物質による血圧上昇抑制作
用を有するが、血圧上昇抑制作用を効果的に引き出すに
は、トマト搾汁液から遠心分離等により前記ACE阻害
物質を高濃度に含有する漿液を取り出し、更に必要に応
じてこれを濃縮して本発明の食品組成物の有効成分とし
て用いることが好ましい。また、上記トマト搾汁液の漿
液からACE阻害物質をより高濃度に含有する成分とし
て分子量4000以下の水溶性化合物を取り出して、本
発明の血圧上昇抑制作用を有する食品組成物の有効成分
として用いることも可能である。Hereinafter, the present invention will be described in detail. The food composition having an effect of suppressing blood pressure elevation according to the present invention contains a serum of tomato juice and / or a concentrate thereof as an active ingredient. Alternatively, the molecular weight 4 contained in the serum of tomato juice
Contains no more than 000 water-soluble compounds as active ingredients.
In tomato fruit, there is a substance having an ACE inhibitory action, and if this is administered to a person with hypertension, for example,
It is presumed that this substance inhibits the ACE pressor action in the body and improves hypertension. Therefore, ripe raw tomato itself, or a finely ground one,
Tomato juice and the like also have a blood pressure increase inhibitory action by the ACE inhibitor, but in order to effectively bring out the blood pressure increase inhibitory action, a serum containing the ACE inhibitor at a high concentration is removed from the tomato juice by centrifugation or the like. It is preferable that the concentrate is further concentrated, if necessary, and used as an active ingredient of the food composition of the present invention. In addition, a water-soluble compound having a molecular weight of 4000 or less is extracted from the serum of the tomato juice as a component containing a higher concentration of an ACE inhibitor, and used as an active ingredient of the food composition having a blood pressure increase inhibitory effect of the present invention. Is also possible.
【0010】ここで、トマト果実から前記ACE阻害物
質含有のトマト搾汁液漿液を得る方法であるが、まず、
通常の方法に従いトマト果実からトマト搾汁液を得る。
搾汁液を得る具体的な方法としては、洗浄及び選別した
生トマトをクラッシャー等を用いて破砕し、チューブヒ
ータ等で加熱して殺菌および酵素失活を行った後、エク
ストラクター等を用いて搾汁する、あるいは、パルパー
・フィニッシャー等を用いて搾汁する等の方法が挙げら
れる。[0010] Here, a method of obtaining the serum of the tomato juice containing the ACE inhibitor from the tomato fruit is as follows.
Obtain tomato juice from tomato fruit according to the usual method.
As a specific method of obtaining a juice, the washed and sorted raw tomatoes are crushed using a crusher or the like, heated with a tube heater or the like to sterilize and deactivate enzymes, and then extracted using an extractor or the like. For example, a method of squeezing or squeezing using a pulper / finisher or the like can be used.
【0011】次に、上記搾汁液からACE阻害物質を含
有する漿液を得る方法としては、上記搾汁液を遠心分離
器にかけて高分子量沈殿物と漿液に分離する方法が適当
である。遠心条件は、1000〜15000G、好まし
くは10000〜15000Gで、遠心時間は8〜12
分が好ましい。また、更に必要に応じて、このようにし
て得られたトマト漿液を加熱濃縮する、あるいは逆浸透
膜により濃縮することにより、ACE阻害物質含有濃度
が高いトマト漿液濃縮液を得ることができる。ここで、
濃縮倍率については、これを配合する組成物の剤形等を
考慮して適宜選択することが可能である。例えば、トマ
ト搾汁液漿液の濃縮物を、飲食品に用いる場合には、濃
縮の割合は2〜8倍が好ましく、4〜6倍に濃縮するこ
とがより好ましい。濃縮の倍率が小さいと血圧上昇作用
が十分でない場合があり、また濃縮倍率を大きくし過ぎ
ると酸味が強くなり飲食品の食味を損なうことがある。Next, as a method for obtaining a serum containing an ACE inhibitor from the above-mentioned juice, a method of separating the above-mentioned juice into a high-molecular-weight precipitate and a serum by a centrifugal separator is suitable. The centrifugation conditions are 1000-15000G, preferably 10,000-15000G, and the centrifugation time is 8-12.
Minutes are preferred. Further, if necessary, the tomato serum obtained in this way is concentrated by heating or concentrated by a reverse osmosis membrane, so that a tomato serum concentrate having a high ACE inhibitor-containing concentration can be obtained. here,
The concentration ratio can be appropriately selected in consideration of, for example, the dosage form of the composition containing the compound. For example, when a concentrate of tomato juice serum is used for food or drink, the concentration ratio is preferably 2 to 8 times, and more preferably 4 to 6 times. If the concentration ratio is small, the blood pressure increasing effect may not be sufficient, and if the concentration ratio is too large, the acidity becomes strong and the taste of the food or drink may be impaired.
【0012】また、上記トマト漿液から更にACE阻害
物質をより高濃度に含有する分子量4000以下の水溶
性化合物を取り出す方法としては、トマト漿液を排除限
界分子量約4000の透析膜、例えば、スペクトラムポ
ア/3(スペクトラムメディカルインダストリー社製)
等を用いて5〜20倍量の水に対して12〜24時間程
度の透析を行う方法が挙げられる。分子量4000以下
の水溶性化合物は透析外液中に含まれるので、透析外液
を減圧濃縮等の処理後、本発明の食品組成物に配合する
ことができるが、必要に応じて、得られた(濃縮)透析
液をゲル濾過カラムクロマトグラフィー等で脱塩したも
の、更にこれを減圧濃縮したもの等を本発明の食品組成
物に配合することも可能である。As a method for extracting a water-soluble compound having a higher molecular weight of 4000 or less and containing an ACE inhibitor at a higher concentration from the tomato serum, a dialysis membrane having an exclusion limit molecular weight of about 4000, for example, a spectrum pore / 3 (manufactured by Spectrum Medical Industry)
For example, a method of performing dialysis for about 12 to 24 hours against 5 to 20 times the amount of water using the method described above. Since the water-soluble compound having a molecular weight of 4000 or less is contained in the external dialysis solution, the external dialysis solution can be added to the food composition of the present invention after the treatment such as concentration under reduced pressure. (Concentration) A dialysate obtained by desalting by gel filtration column chromatography or the like, and a concentrate obtained by concentrating the dialysate under reduced pressure can be added to the food composition of the present invention.
【0013】この様にして得られるトマト搾汁液の漿液
及び/又はその濃縮物は、ACE阻害物質をトマト果実
やトマト搾汁液に比べて高濃度に含有するものであり、
また、トマト搾汁液の漿液に含まれる分子量4000以
下の水溶性化合物は、トマト搾汁液の漿液及び/又はそ
の濃縮物に比べてACE阻害物質を高濃度に含有するも
のである。更に、これらを製造する過程においてトマト
の有する風味を損なうことがないので、得られるトマト
搾汁液の漿液及び/又はその濃縮物、あるいはトマト搾
汁液の漿液に含まれる分子量4000以下の水溶性化合
物は、良好なトマト風味を十分に有するものである。[0013] The serum of the tomato juice and / or its concentrate obtained in this way contains an ACE inhibitor at a higher concentration than tomato fruits and tomato juice.
In addition, the water-soluble compound having a molecular weight of 4000 or less contained in the serum of the tomato juice contains a higher concentration of the ACE inhibitor than the serum of the tomato juice and / or its concentrate. Furthermore, since the flavor of the tomatoes is not impaired in the process of producing them, the resulting serum of the tomato juice and / or its concentrate, or the water-soluble compound having a molecular weight of 4000 or less contained in the serum of the tomato juice is , With a good tomato flavor.
【0014】本発明の食品組成物は、上記トマト搾汁液
の漿液及び/又はその濃縮物、あるいはトマト搾汁液の
漿液に含まれる分子量4000以下の水溶性化合物を含
むものであり、これに含まれるACE阻害物質による血
圧上昇抑制作用を有し、且つ、トマトの良好な風味を十
分に保持するものである。The food composition of the present invention contains a water-soluble compound having a molecular weight of 4000 or less contained in the serum of the tomato juice and / or a concentrate thereof, or the serum of the tomato juice. It has an effect of suppressing an increase in blood pressure by an ACE inhibitor and sufficiently retains a good flavor of tomato.
【0015】本発明の食品組成物に、この様なトマト搾
汁液の漿液及び/又はその濃縮物、あるいはトマト搾汁
液の漿液に含まれる分子量4000以下の水溶性化合物
を配合する場合、種々の食品へ、食品で通常用いられる
任意成分と共に配合することができる。例えば、クラッ
カー、ケーキ、クッキー、ゼリー等の菓子類やジュー
ス、野菜飲料、アルコール飲料等のドリンク類、パン等
の主食、ソース類、ケチャップ等の調味料等が挙げられ
る。When the food composition of the present invention is mixed with a water-soluble compound having a molecular weight of 4000 or less contained in such a serum of tomato juice and / or a concentrate thereof or a serum of tomato juice, , Can be blended with optional components commonly used in foods. Examples include confectionery such as crackers, cakes, cookies, and jellies, drinks such as juices, vegetable drinks, alcoholic drinks, staple foods such as bread, sauces, and seasonings such as ketchup.
【0016】また、本発明の食品組成物は、健康食品、
健康飲料として通常用いられている各種形態、例えば、
散剤、顆粒剤、錠剤、カプセル剤、液剤等も含むもので
あり、これらの製剤化に際しては、賦形剤、結合剤、崩
壊剤、滑沢剤、矯味矯臭剤、増量剤、被覆剤等の通常、
健康食品、健康飲料の製剤化に用いられる任意成分を任
意の量、配合することが可能であり、これらは上記製剤
を一般に製造する方法と同様の製法で製造することがで
きる。Further, the food composition of the present invention comprises a health food,
Various forms usually used as health drinks, for example,
It also includes powders, granules, tablets, capsules, liquids, etc., and in formulating these, excipients, binders, disintegrants, lubricants, flavoring agents, bulking agents, coating agents, etc. Normal,
It is possible to mix optional components used in the formulation of health foods and health drinks in an arbitrary amount, and these can be produced by the same method as that for producing the above-mentioned preparations in general.
【0017】[0017]
【発明の実施の形態】以下に本発明の実施の形態を説明
する。 (1)トマト健康飲料(トマト漿液、トマト漿液の8倍
濃縮液) トマト搾汁液は、トマトジュース製造の常法に従い調製
した。すなわち、洗浄及び選別した生トマトをクラッシ
ャーを用いて破砕し、チューブヒータで約70℃の予熱
を行い殺菌および酵素失活を行った後、エクストラクタ
ーを用いて搾汁した。その後、搾汁液を約120℃で約
50秒間加熱して殺菌し、得られたトマト搾汁液の一部
を後述の血圧上昇抑制試験用として凍結保存した。Embodiments of the present invention will be described below. (1) Tomato health drink (tomato serum, 8-fold concentrated tomato serum) Tomato juice was prepared according to a conventional method for producing tomato juice. That is, the washed and sorted raw tomatoes were crushed using a crusher, preheated to about 70 ° C. with a tube heater to sterilize and deactivate enzymes, and then squeezed using an extractor. Thereafter, the juice was heated at about 120 ° C. for about 50 seconds for sterilization, and a part of the obtained tomato juice was stored frozen for use in a blood pressure increase suppression test described below.
【0018】上記で得られたトマト搾汁液に対して12
000G、8分間の遠心分離処理を行い、トマト搾汁液
の漿液を得た。このトマト漿液を本発明のトマト健康飲
料として、その一部を後述の血圧上昇抑制試験用に凍結
保存した。The tomato juice obtained above was added to 12
Centrifugation was performed at 000 G for 8 minutes to obtain a serum of the tomato juice. A part of the tomato serum was used as a healthy tomato beverage of the present invention, and a part thereof was frozen and stored for a blood pressure increase suppression test described below.
【0019】次に、得られたトマト漿液を可溶性固形分
の濃度として8倍に減圧加熱濃縮し、これを本発明の別
のトマト健康飲料として凍結保存した。また、この様に
して得られたトマト漿液又はその8倍濃縮液よりなる本
発明のトマト健康飲料は、トマトの風味を十分に保持し
ていた。Next, the obtained tomato serum was concentrated by heating under reduced pressure to 8 times the concentration of soluble solids, and this was frozen and stored as another tomato health drink of the present invention. Moreover, the tomato health drink of the present invention comprising the tomato serum or the 8-fold concentrated solution obtained in this way sufficiently retained the flavor of tomato.
【0020】(2)トマト健康飲料(トマト漿液の低分
子画分) まず、上記(1)と同様にしてトマト搾汁液の漿液を製
造した。得られたトマト漿液をスペクトラムポア/3
(排除限界分子量約4000、スペクトラムメディカル
インダストリー社製)を用いて9倍量の水に対して一晩
の透析を行い、透析外液をゲル濾過クロマトグラフィー
にかけて脱塩した。この溶液を減圧加熱濃縮し、トマト
漿液に含まれる分子量4000以下の水溶性化合物を本
発明のトマト健康飲料として得た。また、このトマト漿
液の低分子画分よりなる本発明のトマト健康飲料はトマ
トの風味を十分に保持するものであった。(2) Healthy Tomato Drink (Low Molecular Fraction of Tomato Serum) First, a serum of tomato juice was prepared in the same manner as in (1) above. The obtained tomato serum is added to the spectrum pore / 3
(Exclusion limit molecular weight: about 4000, manufactured by Spectrum Medical Industry) was used to dialyze against 9 times the volume of water overnight, and the dialysate was desalted by gel filtration chromatography. This solution was concentrated by heating under reduced pressure to obtain a water-soluble compound having a molecular weight of 4000 or less contained in the tomato serum as the healthy tomato beverage of the present invention. Further, the healthy tomato drink of the present invention comprising the low molecular weight fraction of the tomato serum had a sufficient tomato flavor.
【0021】上記(1)で得られたトマト搾汁液及び本
発明のトマト健康飲料であるトマト漿液、トマト漿液の
8倍濃縮液、更に(2)で得られた本発明のトマト健康
飲料であるトマト漿液に含まれる分子量4000以下の
水溶性化合物を用いて以下の方法で、ACE阻害作用お
よび血圧上昇抑制作用を評価した。The tomato juice obtained in the above (1), the tomato serum which is the tomato health drink of the present invention, an 8-fold concentrated solution of the tomato serum, and the tomato health drink of the present invention obtained in (2). Using a water-soluble compound having a molecular weight of 4,000 or less contained in tomato serum, the ACE inhibitory effect and the blood pressure increase suppressing effect were evaluated by the following methods.
【0022】[0022]
【実施例1】 ACE阻害作用 本発明のトマト由来の食品組成物は、ACEの昇圧作用
を阻害する作用を有し、これにより血圧上昇を抑制する
ものである。ACEは、主に2つの血圧調節系に関与
し、昇圧作用を示す酵素である。一つはアンジオテンシ
ノーゲンからレニンにより生成されるアンジオテンシン
I(昇圧作用なし)のC末端ジペプチド(His−Le
u)を切断し強力な昇圧ペプチドであるアンジオテンシ
ンIIを生成する系であり、もう一つは、内因性の降圧
ペプチドであるブラジキニンを切断し不活性化させる系
であるが、本発明に用いるトマト由来の成分が、アンジ
オテンシンIからアンジオテンシンIIを生成する系を
阻害して昇圧ペプチドであるアンジオテンシンIIの生
成を抑制することで、ACEの昇圧作用を阻害すること
を示す実験結果について説明する。Example 1 ACE Inhibiting Effect The tomato-derived food composition of the present invention has an effect of inhibiting the ACE pressor action, thereby suppressing an increase in blood pressure. ACE is an enzyme mainly involved in two blood pressure regulating systems and exerting a blood pressure effect. One is the C-terminal dipeptide (His-Le) of angiotensin I (no pressor action) produced by renin from angiotensinogen.
u) to cleave a potent pressurizing peptide, angiotensin II, and another to cleave and inactivate the endogenous antihypertensive peptide, bradykinin. Experimental results showing that the derived component inhibits the system that produces angiotensin II from angiotensin I and inhibits the production of angiotensin II, which is a pressor peptide, thereby inhibiting the ACE's pressor action.
【0023】1)イン・ビトロでの試験 用いた試薬は、0.15Mホウ酸緩衝液、酵素溶液とし
てACE(シグマ社製)を0.1unit/mLの濃度
で含有するホウ酸緩衝液、基質溶液として(−)−ヒッ
プリル−L−ヒスチジル−L−ロイシン・n水和物(和
光純薬(株)製)を4.02mg/mLの濃度で含有す
るホウ酸緩衝液(350mMのNaCl含有)であっ
た。また、試験に用いたACE阻害サンプルは、上記
(1)で得られたトマト漿液及び(2)で得られたトマ
ト漿液に含まれる分子量4000以下の水溶性化合物で
あった。1) In vitro test The reagents used were 0.15 M borate buffer, a borate buffer containing ACE (manufactured by Sigma) as an enzyme solution at a concentration of 0.1 unit / mL, and a substrate. Borate buffer (containing 350 mM NaCl) containing (-)-hippuryl-L-histidyl-L-leucine n-hydrate (manufactured by Wako Pure Chemical Industries, Ltd.) at a concentration of 4.02 mg / mL as a solution. Met. The ACE inhibition sample used in the test was a water-soluble compound having a molecular weight of 4000 or less contained in the tomato serum obtained in (1) and the tomato serum obtained in (2).
【0024】まず、ACE阻害サンプル80μL、酵素
溶液20μL、基質溶液100μLを氷冷下で試験管内
で混ぜ、37℃にて50分間の酵素反応を行った。これ
に、1N塩酸(氷冷)250μLを加えて反応停止を行
い、次いで、酢酸エチル1.5mLを加えて撹拌後、遠
心分離(3000rpm、5分)し、酢酸エチル層を1
mL試験管に分取した。これを加熱し、酢酸エチルを蒸
発・乾固後、1.25mLの水に溶解し、228nmの
吸光度を測定した。First, 80 μL of the ACE inhibition sample, 20 μL of the enzyme solution, and 100 μL of the substrate solution were mixed in a test tube under ice cooling, and the enzyme reaction was carried out at 37 ° C. for 50 minutes. The reaction was stopped by adding 250 μL of 1N hydrochloric acid (ice-cooled) thereto, followed by adding 1.5 mL of ethyl acetate and stirring, followed by centrifugation (3000 rpm, 5 minutes) to separate the ethyl acetate layer for 1 hour.
Dispensed into mL test tubes. This was heated, and ethyl acetate was evaporated and dried, then dissolved in 1.25 mL of water, and the absorbance at 228 nm was measured.
【0025】酵素活性の評価は、ACE阻害サンプルの
代わりにホウ酸緩衝液を添加した場合の酵素活性に対す
る阻害率を算出することで行った。すなわち、ACE阻
害サンプルを加えた時の吸光度をS、AEC阻害サンプ
ルの代わりにホウ酸緩衝液を添加した場合の値をC、酵
素溶液の代わりにホウ酸緩衝液で反応させたときの値を
Bとすると、ACE阻害サンプルの阻害率は以下の式で
導かれる。The evaluation of the enzyme activity was carried out by calculating the rate of inhibition of the enzyme activity when a borate buffer was added instead of the ACE-inhibited sample. That is, the absorbance when the ACE inhibition sample was added was S, the value when the borate buffer was added instead of the AEC inhibition sample was C, and the value when the reaction was performed with the borate buffer instead of the enzyme solution was C. If B, the inhibition rate of the ACE-inhibited sample is derived by the following equation.
【0026】[0026]
【数1】 阻害率(%)=((C−S)/(C−B))*100 この式により求められた上記(1)で得られたトマト漿
液及び(2)で得られたトマト漿液に含まれる分子量4
000以下の水溶性化合物(共にアッセイ系での最終濃
度)のイン・ビトロでのACE阻害活性を表1に示す。## EQU1 ## Inhibition rate (%) = ((CS) / (CB)) * 100 The tomato serum obtained in the above (1) and the tomato obtained in the above (2), which are obtained by this equation. Molecular weight 4 contained in serum
Table 1 shows the in vitro ACE inhibitory activity of 000 or less water-soluble compounds (both final concentrations in the assay system).
【0027】[0027]
【表1】 [Table 1]
【0028】この結果から、上記(1)で得られたトマ
ト漿液及び(2)で得られたトマト漿液に含まれる分子
量4000以下の水溶性化合物はともにイン・ビトロで
のACE阻害活性に優れることがわかった。また、両サ
ンプルの50%阻害濃度より、トマト漿液に比べトマト
漿液に含まれる分子量4000以下の水溶性化合物の方
がACE阻害活性が100倍以上強いことがわかった。From these results, it is clear that both the tomato serum obtained in the above (1) and the water-soluble compound having a molecular weight of 4000 or less contained in the tomato serum obtained in the above (2) are excellent in ACE inhibitory activity in vitro. I understood. In addition, the 50% inhibitory concentration of both samples showed that the ACE inhibitory activity of the water-soluble compound having a molecular weight of 4000 or less contained in tomato serum was 100 times or more stronger than that of tomato serum.
【0029】2)イン・ビボでの試験 上述のようにACEは、非活性状態のアンジオテンシン
I(以下、「ANGI」と略す)を、血圧上昇作用を持
つANGIIに変換する酵素である。従って、ANGI
を静脈投与すると、血中のACEによってANGIIに
変換され、血圧が上昇する。ところが予めACE阻害剤
を投与しておくと、ANGIを投与しても血圧が上がら
なくなる。この現象をラット(ウィスター系、体重30
0g、雄(清水実験材料))を用いて観察した。ACE
阻害物質としては、上記(2)で得られたトマト漿液に
含まれる分子量4000以下の水溶性化合物を用いた。2) In Vivo Test As described above, ACE is an enzyme that converts inactive angiotensin I (hereinafter abbreviated as "ANGI") to ANGII which has a blood pressure increasing effect. Therefore, ANGI
Is intravenously converted to ANGII by ACE in the blood and increases blood pressure. However, if an ACE inhibitor is administered in advance, blood pressure will not increase even if ANGI is administered. This phenomenon was observed in rats (Wistar strain, body weight 30).
0 g, male (Shimizu experimental material)). ACE
As the inhibitor, a water-soluble compound having a molecular weight of 4000 or less contained in the tomato serum obtained in the above (2) was used.
【0030】具体的な実験方法を説明すると、まず、ラ
ットに生理食塩水200μLを投与し、この時に血圧が
変化しないことを確認した後、ラットにANGI(10
0〜150ng/kg)を投与した。この時の血圧上昇
値がコントロールとなるが、10〜20mmHg上昇が
望ましく、この値をプレコントロールとした。次にAC
E阻害物質を150μL投与し、更にANGI(100
〜150ng/kg)を投与する。この時の血圧上昇値
をトライアルとして、最初にANGIを投与したときの
血圧上昇と比較した。ACE阻害物質が作用していれ
ば、このトライアルはプレコントロールに比べ小さい値
となる。その後、更にANGI(100〜150ng/
kg)を投与し、この時の血圧上昇値をポストコントロ
ールとした。この時、ACE阻害物質が代謝されてしま
っていれば、この時の血圧上昇値ポストコントロールは
最初にANGIを投与したときの血圧上昇値とほぼ同じ
であると考えられる。A specific experimental method will be described. First, 200 μL of physiological saline is administered to rats, and it is confirmed that the blood pressure does not change at this time.
0-150 ng / kg). The blood pressure increase value at this time serves as a control, but a 10-20 mmHg increase is desirable, and this value was used as a pre-control. Then AC
E inhibitor was administered at 150 μL, and ANGI (100
150150 ng / kg). The blood pressure increase value at this time was used as a trial and compared with the blood pressure increase when ANGI was first administered. If the ACE inhibitor is acting, this trial will be smaller than the pre-control. Thereafter, ANGI (100-150 ng /
kg), and the blood pressure increase value at this time was used as post control. At this time, if the ACE inhibitor has been metabolized, it is considered that the blood pressure elevation value at this time is almost the same as the blood pressure elevation value when ANGI was first administered.
【0031】ここで上記実験において、ラットの血圧
は、麻酔下(ウレタン麻酔、1.0〜1.5g/kg)
で左頚動脈にカテーテルを挿入し、血管内の脈圧を、圧
トランスデューサー(DT−12、(ビゴ・スペクトラ
ムド社製))を介して連続的に測定された。また、AN
GIやACE阻害物質の投与方法は、大腿静脈に挿入し
たカテーテルから投与し、投与速度は100μL/mi
nとし、1回の投与量は200μL以下にとどめた。In the above experiment, the blood pressure of the rat was measured under anesthesia (urethane anesthesia, 1.0 to 1.5 g / kg).
And a catheter was inserted into the left carotid artery, and the pulse pressure in the blood vessel was continuously measured via a pressure transducer (DT-12, manufactured by Vigo Spectrum). Also, AN
The administration method of the GI or ACE inhibitor is to administer from a catheter inserted into the femoral vein, and the administration rate is 100 μL / mi.
n, and the single dose was kept at 200 μL or less.
【0032】この実験を5回行い、プレコントロール、
トライアル、ポストコントロールとして得られた血圧上
昇値の平均値をそれぞれ求めた。これらの値からプレコ
ントロールの平均値を100としたときの他の血圧上昇
平均値の相対値を計算した。結果を表2に示す。This experiment was performed five times, and the pre-control
The average value of the blood pressure elevation values obtained as a trial and post control was determined. From these values, the relative value of the other blood pressure increase average value when the average value of the pre-control was set to 100 was calculated. Table 2 shows the results.
【0033】[0033]
【表2】 [Table 2]
【0034】この結果から明らかなように、トライアル
の血圧上昇値がプレコントロール、ポストコントロール
の血圧上昇値に比べ約60%程度と低く、従って上記
(2)で得られたトマト漿液に含まれる分子量4000
以下の水溶性化合物はイン・ビボでのACE阻害活性に
も優れることがわかった。As is clear from these results, the blood pressure increase value of the trial is about 60% lower than the blood pressure increase values of the pre-control and the post-control, and therefore, the molecular weight contained in the tomato serum obtained in the above (2) 4000
The following water-soluble compounds were also found to be excellent in ACE inhibitory activity in vivo.
【0035】[0035]
【実施例2】 血圧上昇抑制作用 上記(1)で得られたトマト搾汁液及び8倍濃縮トマト
漿液を等量の水で希釈した4倍濃縮トマト漿液(本発明
のトマト健康飲料)を自然発症性高血圧ラットに投与し
てその効果を評価した。尚、評価に用いた自然発症性高
血圧ラットは、高血圧症のモデル動物として一般的であ
り、5〜6週齢で発症して血圧が上昇し始め、その後1
2〜14週齢で平衡状態に達することが知られている。Example 2 Blood Pressure Elevation Suppressing Action Naturally developed 4-fold concentrated tomato serum (the tomato health drink of the present invention) obtained by diluting the tomato juice and 8-fold concentrated tomato serum obtained in (1) above with an equal amount of water. It was administered to rats with essential hypertension to evaluate its effect. The spontaneously hypertensive rats used for the evaluation are generally used as model animals for hypertension, develop onset at 5 to 6 weeks of age, and begin to increase in blood pressure.
It is known to reach equilibrium at 2-14 weeks of age.
【0036】4週齢の自然発症性高血圧ラット(SH
R)21匹を購入(星野試験動物飼育所)し、2週間の
予備飼育を行った後、最高血圧(収縮期血圧、以下「S
BP]と略す)を測定し、この平均値が群間でほぼ等し
くなるように7匹ずつ3群に分けた(体重の平均もでき
るだけ揃えた)。Four-week-old spontaneously hypertensive rats (SH
R) After purchasing 21 animals (Hoshino test animal breeding station) and carrying out preliminary breeding for 2 weeks, systolic blood pressure (systolic blood pressure, hereinafter referred to as "S
BP]), and the animals were divided into three groups of seven each such that the average value was almost the same between the groups (the average of the body weights was also made as uniform as possible).
【0037】予備飼育中は飲料として水を自由に摂取さ
せておいたが、群分け後、3つの群のうちの2群には、
上記(1)で得られたトマト搾汁液及び8倍濃縮トマト
漿液を等量の水で希釈した4倍濃縮トマト漿液をそれぞ
れ飲料として与え、残りの1群はコントロール群として
水を飲料として与えた。これら飲料は全て自由に摂取さ
せ、摂取量は給水瓶の重さで測定した。また、飼料は、
オリエンタル酵母(株)のMF固形飼料を予備飼育から
試験終了まで通じて自由摂取させた。予備飼育期間中は
1ケージ4匹で、群分け後は、1ケージ2匹で飼育し
た。飼育室の温度は25℃に保ち、昼夜は12時間サイ
クル(6:00〜18:00の間点灯)とした。試験
は、予備飼育終了後から6週間行った。尚、上記のよう
な自由摂取でSHRが摂取したトマト搾汁液あるいはト
マト搾汁液漿液の4倍濃縮液の量は、一匹当たり一日約
30gであった。During preliminary breeding, water was freely taken as a drink, but after grouping, two of the three groups contained:
The tomato juice obtained in the above (1) and the 4-fold concentrated tomato serum obtained by diluting the 8-fold concentrated tomato serum with an equal amount of water were provided as drinks, and the remaining group was provided with water as a control group as water. . All of these drinks were allowed to be taken freely, and the amount of intake was measured by the weight of a water bottle. Also, the feed is
The MF solid feed of Oriental Yeast Co., Ltd. was allowed to freely ingest from pre-breeding to the end of the test. During the pre-breeding period, the animals were bred in four cages per cage, and after grouping, they were bred in two cages per cage. The temperature of the breeding room was kept at 25 ° C., and the day and night were cycled for 12 hours (lighted on from 6:00 to 18:00). The test was performed for 6 weeks after the completion of the preliminary breeding. The amount of the tomato juice or the four-fold concentrated solution of the tomato juice serum that the SHR ingested as described above was about 30 g per animal per day.
【0038】上記のように飼育しながらSHRの血圧を
1週間に1度非観血法により測定した。非観血法とは、
ラットの尾動脈の血流を光センサーにて検知して血圧を
測定する方法である。すなわち、尾動脈をカフで徐々に
加圧してゆき、血流が検知できなくなる圧力を測定す
る。この時の圧力をSBPとする。具体的には、50℃
に加熱したホットプレート上約5mmにセットされたス
テンレス製の飼育ケージに15分間SHRを入れ加熱し
(この加熱により、放熱器官でもある尻尾の血管に血液
が十分流れるようになる。)、加熱後、直ちに軍手でS
HRを拘束し、血圧測定装置(KN−210ラット尾動
脈圧、脈拍測定装置;夏目製作所(株))で血圧(SB
P)を測定した。測定は1匹につき5〜6回連続して行
い、1回目(場合によっては1回目と2回目)を除いた
平均をそのSHRのSBPとした。ここで、最初の測定
値を棄却するのは、1回目の測定値がそれ以降の血圧に
比べ極めて高い値を示すことが多いからである。While bred as described above, the blood pressure of SHR was measured once a week by a non-invasive method. What is the non-invasive method?
This is a method of measuring blood pressure by detecting blood flow in the tail artery of a rat with an optical sensor. That is, the tail artery is gradually pressurized with a cuff, and the pressure at which blood flow cannot be detected is measured. The pressure at this time is defined as SBP. Specifically, 50 ° C
The SHR is placed in a stainless steel breeding cage set at about 5 mm on a hot plate heated for 15 minutes and heated (this heating allows blood to flow sufficiently to the blood vessels of the tail, which is also a heat radiating organ), and after heating , Immediately in gloves S
The HR was restrained and the blood pressure (SB) was measured using a blood pressure measurement device (KN-210 rat tail artery pressure, pulse measurement device; Natsume Seisakusho Co., Ltd.).
P) was measured. The measurement was continuously performed 5 to 6 times per animal, and the average excluding the first time (in some cases, the first and second times) was taken as the SBP of the SHR. Here, the reason why the first measurement value is rejected is that the first measurement value often shows an extremely high value as compared with the subsequent blood pressure.
【0039】各群7匹のSBPの平均値と標準偏差とを
求め、また、コントロール群とトマト搾汁液投与群、ト
マト搾汁液漿液の4倍濃縮液投与群との間に有意差が認
められるか否か、スチューデンツ−T法で検定した。結
果を表3及び図1に示す。The average value and standard deviation of the SBP of 7 animals per group were determined, and a significant difference was observed between the control group, the group to which the tomato juice was administered, and the group to which the 4 times concentrated tomato juice was administered. It was tested by the Student's-T method. The results are shown in Table 3 and FIG.
【0040】尚、図1中の*は、そのデータがコントロ
ール群と比較して危険率5%以下で有意であることを示
す印である。The symbol * in FIG. 1 indicates that the data is significant at a risk rate of 5% or less as compared with the control group.
【0041】[0041]
【表3】 [Table 3]
【0042】この結果から、上記実施の形態(1)で得
られたトマト搾汁液を投与されたSHR群、(1)で得
られた8倍濃縮トマト漿液を等量の水で希釈した4倍濃
縮トマト漿液(本発明のトマト健康飲料)を投与された
SHR群は共に、これらの投与を受けなかったコントロ
ール群に比べ総体的に見て血圧上昇が抑制されていると
判断できるが、トマト搾汁液のSHRに対する血圧上昇
抑制作用は十分とは言えないのに比べ、本発明のトマト
健康飲料となる4倍濃縮トマト漿液を投与されたSHR
群は血圧上昇がよく抑制されており、本発明のトマト健
康飲料が血圧上昇抑制作用を十分に有することがわか
る。From these results, the SHR group to which the tomato juice obtained in the above-mentioned embodiment (1) was administered, the 4-fold concentration of the 8-fold concentrated tomato serum obtained in (1) diluted with an equal amount of water In both SHR groups to which the concentrated tomato serum (the tomato health drink of the present invention) was administered, it can be judged that the increase in blood pressure is generally suppressed compared to the control group which did not receive these administrations. The effect of the sap on the increase in blood pressure against SHR is not sufficient, whereas the SHR administered with 4-fold concentrated tomato serum, which is the tomato healthy beverage of the present invention,
In the group, the increase in blood pressure was well suppressed, indicating that the healthy tomato beverage of the present invention has a sufficient blood pressure increase suppressing effect.
【0043】[0043]
【発明の効果】本発明のトマト由来の食品組成物は、ト
マトの良好な風味を保持しながら、且つ、ACEの昇圧
作用を抑制して血圧上昇を抑制する作用に優れることか
ら、本態性高血圧症等を改善するための機能性食品とし
て有望である。EFFECTS OF THE INVENTION The tomato-derived food composition of the present invention is excellent in the action of maintaining high flavor of tomatoes and suppressing ACE's vasopressor action to suppress an increase in blood pressure. It is promising as a functional food for improving diseases and the like.
【図1】 実施例のトマト搾汁液投与SHR群、トマト
搾汁液漿液の4倍濃縮液投与SHR群及びコントロール
SHR群の収縮期血圧(SBP)の経時変化を示す図。BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing the change over time in the systolic blood pressure (SBP) of the SHR group to which the tomato juice was administered, the SHR group to which a 4-fold concentrated solution of the tomato juice was administered, and the control SHR group.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) A23L 1/05 - 1/09 A23L 1/30 JICSTファイル(JOIS)──────────────────────────────────────────────────続 き Continued on the front page (58) Fields surveyed (Int. Cl. 6 , DB name) A23L 1/05-1/09 A23L 1/30 JICST file (JOIS)
Claims (2)
物を有効成分として含有する血圧上昇抑制作用を有する
食品組成物。1. A food composition having an effect of suppressing blood pressure elevation, comprising a serum of tomato juice and / or a concentrate thereof as an active ingredient.
000以下の水溶性化合物を有効成分として含有する血
圧上昇抑制作用を有する食品組成物。2. Molecular weight 4 contained in serum of tomato juice
A food composition having an effect of suppressing blood pressure elevation, comprising a water-soluble compound of 000 or less as an active ingredient.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7198925A JP2905725B2 (en) | 1995-07-01 | 1995-07-01 | Food composition derived from tomato |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7198925A JP2905725B2 (en) | 1995-07-01 | 1995-07-01 | Food composition derived from tomato |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH099892A JPH099892A (en) | 1997-01-14 |
| JP2905725B2 true JP2905725B2 (en) | 1999-06-14 |
Family
ID=16399251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7198925A Expired - Lifetime JP2905725B2 (en) | 1995-07-01 | 1995-07-01 | Food composition derived from tomato |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2905725B2 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005198645A (en) * | 2003-05-22 | 2005-07-28 | Lion Corp | Tomato fermentation broth, antihypertensive agent, method for producing the same, and food and beverage composition |
| JP2006193435A (en) * | 2005-01-11 | 2006-07-27 | Kagome Co Ltd | Fatigue-improving agent |
| JP2007204386A (en) * | 2006-01-31 | 2007-08-16 | Kagome Co Ltd | Asthma attack preventive |
| JP5121257B2 (en) * | 2007-03-01 | 2013-01-16 | キッコーマン株式会社 | Antihypertensive composition |
| JP2009027987A (en) * | 2007-07-27 | 2009-02-12 | Kikkoman Corp | Composition comprising tomato fruit containing γ-aminobutyric acid in high concentration and method for producing the same |
| US20150132371A1 (en) * | 2012-04-23 | 2015-05-14 | University Of Oslo | Use of tomato extract as antihypertensive agent and process for making water soluble sugar free tomato extract |
| GB201223365D0 (en) | 2012-12-24 | 2013-02-06 | Provexis Natural Products Ltd | Compositions |
| US10905733B2 (en) | 2016-11-02 | 2021-02-02 | Provexis Natural Products Limited | Water soluble tomato extract protects against adverse effects of air pollution |
-
1995
- 1995-07-01 JP JP7198925A patent/JP2905725B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH099892A (en) | 1997-01-14 |
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