JP2000103741A - Lipase inhibitor - Google Patents
Lipase inhibitorInfo
- Publication number
- JP2000103741A JP2000103741A JP10277896A JP27789698A JP2000103741A JP 2000103741 A JP2000103741 A JP 2000103741A JP 10277896 A JP10277896 A JP 10277896A JP 27789698 A JP27789698 A JP 27789698A JP 2000103741 A JP2000103741 A JP 2000103741A
- Authority
- JP
- Japan
- Prior art keywords
- food
- extracts
- lipase inhibitor
- leaf
- gambir
- 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.)
- Granted
Links
Landscapes
- Medicines Containing Plant Substances (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Non-Alcoholic Beverages (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、安全性が高く、脂肪の
吸収を押さえ、肥満や心疾患、動脈硬化などを防ぐ、食
品に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a food which is highly safe, suppresses fat absorption, and prevents obesity, heart disease, arteriosclerosis, and the like.
【0002】[0002]
【従来の技術】我が国では食生活が欧米化し、年々脂肪
摂取量は増加し、かつ、社会生活の中で運動する量も減
少し、肥満或いは肥満傾向の人が増加し、かつ心疾患、
動脈硬化なども増加している。対応として脂肪摂取量を
減少させ、適度な運動をするようにしていく必要がある
が、なかな容易に実施できない。このため、摂取した脂
肪の吸収を押さえることでも、肥満や心疾患、動脈硬化
などに対応する必要がある。2. Description of the Related Art In Japan, dietary habits have become westernized, the amount of fat intake increases year by year, the amount of exercise in social life decreases, the number of obese or obese people increases, and heart disease,
Atherosclerosis is also increasing. As a response, it is necessary to reduce fat intake and exercise moderately, but it is not easy to carry out. Therefore, it is necessary to cope with obesity, heart disease, arteriosclerosis, and the like by suppressing the absorption of ingested fat.
【0003】阿仙薬はアカネ科のUncaria ga
mbirの葉及び若枝を水で煮て製した乾燥水製エキス
であり、収斂性吐瀉薬として用いたり、口腔清涼剤とし
て広く用いられている。[0003] Asenyaku is Uncaria ga of the family Rubiaceae.
It is a dry water extract made by boiling mbir leaves and shoots with water, and is widely used as an astringent antidiarrheal or as an oral freshener.
【0004】グァバは、バンジロウあるいは番石榴と呼
ばれ、フトモモ科バンジロウ属の植物で、学名をプジジ
ウム グアヤバ エル(Psidium guajaba L.)という。
一般には、その実を生食、ジャム、ジュース等で食す
る。分布は、原産は熱帯アメリカであるが、熱帯、亜熱
帯の各地で広く栽培され、日本では九州南部で栽培さ
れ、琉球諸島では野生化している。また、グアバは、薬
として腸炎、赤痢、消化不良性下痢に用いられており、
葉はお茶の代用とされている。また、本願出願人が出願
した特開平5−246837号公報では、グアバの葉の
溶媒抽出物を化粧料として用いることにより美白、肌荒
れ防止等の利用が図られている。[0004] Guava is called a bunjirou or a gemstone and is a plant belonging to the genus bunjiro in the family Myrtaceae, and its scientific name is Psidium guajaba L.
Generally, the berries are eaten raw, jam, juice, or the like. It is native to tropical America, but is widely cultivated in tropical and subtropical areas, cultivated in southern Kyushu in Japan, and wild in the Ryukyu Islands. Guava is also used as a drug in enteritis, dysentery, and indigestive diarrhea.
Leaves are considered a substitute for tea. Further, in Japanese Patent Application Laid-Open No. 5-246837 filed by the applicant of the present application, the use of a solvent extract of guava leaves as a cosmetic material is used to prevent whitening and rough skin.
【0005】メドウスィートは学名Filipendu
la ulmariaといい、和名はセイヨウナツユキ
ソウという。ヨーロッパ、アジアを原産とするが、北ア
メリカ等に帰化している多年草である。[0005] Medousite has a scientific name of Filipendu
It is called la ulmaria, and its Japanese name is S. It is native to Europe and Asia, but is a natural perennial plant in North America and elsewhere.
【0006】[0006]
【発明が解決しようとする課題】安全で、肥満や心疾
患、動脈硬化に有効なリパーゼ阻害剤を得る。A lipase inhibitor which is safe and effective for obesity, heart disease and arteriosclerosis is obtained.
【0007】[0007]
【課題を解決する手段】鋭意検討した結果、阿仙薬、グ
ァバの葉、メドウスィートの葉の溶媒抽出物を配合する
ことによって問題を解決できることがわかった。これら
の抽出方法は水或いは親水性有機溶媒、或いはこれらの
混液を用いて抽出すればよい。As a result of diligent studies, it has been found that the problem can be solved by blending a solvent extract of Asenyaku, guava leaves, and medosweet leaves. These extraction methods may be performed using water, a hydrophilic organic solvent, or a mixture thereof.
【0008】これらを食品に配合すれば、容易に摂取で
きる。配合できる食品は特に限定はなく、飲料等に配合
してダイエット食品や健康食品に応用できる。また、一
般の食事に利用することもできる。[0008] If these are added to food, they can be easily taken. The food that can be blended is not particularly limited, and can be blended into beverages and the like and applied to diet foods and health foods. It can also be used for ordinary meals.
【0009】[0009]
【実施例】以下に製造例、実施例によって、更に具体的
に説明するが、本発明は、この製造例、実施例によっ
て、限定されるものでないことは云うまでもない。EXAMPLES The present invention will be described more specifically with reference to the following production examples and examples. However, it goes without saying that the present invention is not limited to these production examples and examples.
【0010】〔実施例1〕阿仙薬10gに50%エタノ
ール水溶液300mlを加えて時々撹拌しつつ5日間放置
した。これを濾過後、エバポレートした後、凍結乾燥し
た。[Example 1] 10 g of Asen medicine was added with 300 ml of a 50% aqueous ethanol solution and left for 5 days with occasional stirring. After filtration, evaporation and freeze-drying.
【0011】〔実施例2〕グァバの葉(乾燥品)10g
に50%エタノール水溶液300mlを加えて時々撹拌し
つつ5日間放置した。これを濾過後、エバポレートした
後、凍結乾燥した。[Example 2] 10 g of guava leaves (dried product)
Was added to the mixture, and the mixture was left for 5 days with occasional stirring. After filtration, evaporation and freeze-drying.
【0012】〔実施例3〕メドウスィートの葉(乾燥
品)10gに50%エタノール水溶液300mlを加えて
時々撹拌しつつ5日間放置した。これを濾過後、エバポ
レートした後、凍結乾燥した。[Example 3] To 10 g of leaves of meduus sweet (dried product), 300 ml of a 50% aqueous ethanol solution was added, and the mixture was left for 5 days with occasional stirring. After filtration, evaporation and freeze-drying.
【0013】 〔処方例1〕錠剤 (1) 実施例1の抽出物 200g (2) 乳糖 500g (3) コーンスターチ 290g (4) ステアリン酸Mg 20g (1)、(2)及び170gのコーンスターチを混和
し、70gのコーンスターチから作ったペーストととも
に顆粒化、この顆粒に50gのコーンスターチと(4)
とを加え、混合物を圧隙錠剤機で圧縮して錠剤を100
0錠打錠製造した。[Prescription Example 1] Tablet (1) 200 g of extract of Example 1 (2) Lactose 500 g (3) Corn starch 290 g (4) Mg stearate 20 g (1), (2) and 170 g of corn starch are mixed. , Granulate with a paste made from 70 g of corn starch, add 50 g of corn starch to the granules and (4)
And the mixture is compressed on a press tablet machine to reduce the tablets to 100
0 tablets were manufactured.
【0014】〔処方例2〕飲料 実施例2の抽出物 1g キシリトール 10g ビタミンB1塩酸塩 0.5mg ビタミンB2 0.2mg ビタミンC 500mg ナイアシン 1.0mg パントテン酸Ca 0.2mg 上記の原料を計量混合し、精製水で100mlにした。Formulation Example 2 Beverage Extract of Example 2 1 g Xylitol 10 g Vitamin B 1 hydrochloride 0.5 mg Vitamin B 2 0.2 mg Vitamin C 500 mg Niacin 1.0 mg Ca pantothenate 0.2 mg Weigh the above ingredients Mix and make up to 100 ml with purified water.
【0015】〔処方例3〕処方例1の実施例1の抽出物
を実施例3に変えて作成したもの[Formulation Example 3] The extract prepared in Example 1 of Formulation Example 1 was changed to Example 3.
【0016】リパーゼ抑制試験方法 試験品(実施例の0.5%水溶液)1.0ml、基質溶液
1.0ml、酵素溶液1.0mlを試験管に計り取り40℃
の恒温水槽に15分間放置した。15分後、冷水5.0
ml加え、温度を室温に戻し425nmによる吸光度を測定
した。試験品の替わりに精製水を用いて対照としリパー
ゼ抑制の抑制率を計算した。Lipase Inhibition Test Method 1.0 ml of a test product (0.5% aqueous solution of the example), 1.0 ml of a substrate solution, and 1.0 ml of an enzyme solution are weighed in a test tube and subjected to 40 ° C.
For 15 minutes. After 15 minutes, cold water 5.0
The temperature was returned to room temperature, and the absorbance at 425 nm was measured. Purified water was used in place of the test sample, and the inhibition rate of lipase inhibition was calculated as a control.
【0017】上記の実験で使用した試薬の作成方法は 1.基質溶液 pNP-Valerate溶液を0.5mlを基質用緩衝液で50mlに
定容 2.pNP-Valerate溶液(Pentanoic acid 4-nitrophenyl
ester) Pentanoic acid 4-nitrophenyl ester0.132gをメ
タノールで10mlに定容した。 3.基質用緩衝液(0.05M-TrisBuffer) トリス(ヒドロキシメチル)アミノメタンを3.03
g、オレフィンスルホン酸を0.20gを精製水で500
mlに定容後、塩酸でpH7.7に調製 4.酵素溶液 リパーゼ(SIGMA;Type2)10mgを希釈用緩衝液で20ml
に定容した。 5.希釈用緩衝液(0.05M-TrisBuffer) トリス(ヒドロキシメチル)アミノメタンを12.12
g、オレフィンスルホン酸を0.80g、塩化カルシウム
一水和物を0.32gを精製水で2000mlに定容し
た。The method of preparing the reagents used in the above experiment was as follows. 1. Substrate solution 0.5 ml of pNP-Valerate solution is made up to 50 ml with substrate buffer. pNP-Valerate solution (Pentanoic acid 4-nitrophenyl
ester) Pentanoic acid 4-nitrophenyl ester (0.132 g) was made up to 10 ml with methanol. 3. Substrate buffer (0.05M-TrisBuffer) Tris (hydroxymethyl) aminomethane was added to 3.03.
g, 0.20 g of olefinsulfonic acid in purified water 500
After adjusting the volume to ml, adjust to pH 7.7 with hydrochloric acid. Enzyme solution Lipase (SIGMA; Type 2) 10 mg in dilution buffer 20 ml
Fixed volume. 5. Dilution buffer (0.05M-TrisBuffer) Tris (hydroxymethyl) aminomethane was added to 12.12.
g, olefin sulfonic acid 0.80 g, and calcium chloride monohydrate 0.32 g were made up to 2000 ml with purified water.
【0018】結果を表−1に示す。The results are shown in Table 1.
【表1】 [Table 1]
【0019】使用テスト 成人8名に毎日3回、1回あたり処方例1或いは処方例
3を1錠、処方例2を100g3ヶ月間食べて貰い、ア
ンケートした。なお、比較例は実施例より製造例の抽出
物を水にかえたものである。(比較例1,2) これを
2群16名で実施した。判定基準は以下のようでアンケ
ートの結果をまとめたのが以下の表である。 処方例の方が非常によい 3 処方例の方がかなりよい 2 処方例の方がややよい 1 差がない 0 比較例の方がややよい −1 比較例の方がかなりよい −2 比較例の方が非常によい −3Usage Test Eight adults were asked to eat one tablet of Formulation Example 1 or Formulation Example 3 at a time, and 100 g of Formulation Example 2 for three months at a time. In the comparative example, the extract of the production example was replaced with water from the example. (Comparative Examples 1 and 2) This was performed by 16 people in two groups. The following table summarizes the results of the questionnaire with the following criteria. Formulation example is very good 3 Formulation example is considerably better 2 Formulation example is slightly better 1 No difference 0 Comparative example is slightly better -1 Comparative example is much better -2 Comparative example Is much better -3
【0020】実験の方法は表−2のように行った。The experiment was performed as shown in Table 2.
【表2】 [Table 2]
【0021】結果ひ表−3のようになった。The results are shown in Table 3 below.
【表3】 [Table 3]
【0022】[0022]
【効果】阿仙薬、グァバの葉、メドウスィートの葉の溶
媒抽出物を配合したリパーゼ阻害剤は安全性が高く炭水
化物の吸収を押さえ、肥満や心疾患、動脈硬化などを防
ぐ。[Effect] A lipase inhibitor containing a solvent extract of asenyaku, guava leaf, and medosweet leaf is highly safe, suppresses carbohydrate absorption, and prevents obesity, heart disease, and arteriosclerosis.
───────────────────────────────────────────────────── 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) A23L 1/30 A23L 1/30 B 2/52 2/38 C 2/38 2/00 F ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A23L 1/30 A23L 1/30 B 2/52 2/38 C 2/38 2/00 F
Claims (1)
の溶媒抽出物を配合したリパーゼ阻害剤1. A lipase inhibitor containing a solvent extract of asenyaku, guava leaf, and medosuit leaf.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27789698A JP4233645B2 (en) | 1998-09-30 | 1998-09-30 | Lipase inhibitor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27789698A JP4233645B2 (en) | 1998-09-30 | 1998-09-30 | Lipase inhibitor |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000103741A true JP2000103741A (en) | 2000-04-11 |
JP4233645B2 JP4233645B2 (en) | 2009-03-04 |
Family
ID=17589806
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27789698A Expired - Lifetime JP4233645B2 (en) | 1998-09-30 | 1998-09-30 | Lipase inhibitor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4233645B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001131070A (en) * | 1999-04-06 | 2001-05-15 | Taisho Pharmaceut Co Ltd | Riboflavin-formulated liquid composition |
JP2001299242A (en) * | 2000-04-28 | 2001-10-30 | Kanebo Ltd | Food containing gelling agent and method for producing the same |
JP2003026585A (en) * | 2001-07-10 | 2003-01-29 | Maruzen Pharmaceut Co Ltd | Lipase inhibitor |
JP2003342185A (en) * | 2002-05-25 | 2003-12-03 | Bhn Kk | Inhibitor of lipase activity |
JP2010105922A (en) * | 2008-10-28 | 2010-05-13 | Uha Mikakuto Co Ltd | Lox-1 antagonist agent |
JP2012025773A (en) * | 2011-10-14 | 2012-02-09 | Maruzen Pharmaceut Co Ltd | Lipase inhibitor |
WO2012169897A1 (en) * | 2011-05-04 | 2012-12-13 | Renate Kirchner Pro Helse | Weight reducing material |
US8741359B2 (en) | 2001-05-03 | 2014-06-03 | Basf Beauty Care Solutions France S.A.S. | Method for testing a substance which is potentially active in the field of lipolysis and its mainly cosmetic use |
KR20150114835A (en) * | 2014-04-02 | 2015-10-13 | (재)남해마늘연구소 | Sweet jelly comprising natural plant component |
-
1998
- 1998-09-30 JP JP27789698A patent/JP4233645B2/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001131070A (en) * | 1999-04-06 | 2001-05-15 | Taisho Pharmaceut Co Ltd | Riboflavin-formulated liquid composition |
JP4678079B2 (en) * | 1999-04-06 | 2011-04-27 | 大正製薬株式会社 | Riboflavin formulation solution composition |
JP2001299242A (en) * | 2000-04-28 | 2001-10-30 | Kanebo Ltd | Food containing gelling agent and method for producing the same |
US8741359B2 (en) | 2001-05-03 | 2014-06-03 | Basf Beauty Care Solutions France S.A.S. | Method for testing a substance which is potentially active in the field of lipolysis and its mainly cosmetic use |
JP2003026585A (en) * | 2001-07-10 | 2003-01-29 | Maruzen Pharmaceut Co Ltd | Lipase inhibitor |
JP2003342185A (en) * | 2002-05-25 | 2003-12-03 | Bhn Kk | Inhibitor of lipase activity |
JP2010105922A (en) * | 2008-10-28 | 2010-05-13 | Uha Mikakuto Co Ltd | Lox-1 antagonist agent |
WO2012169897A1 (en) * | 2011-05-04 | 2012-12-13 | Renate Kirchner Pro Helse | Weight reducing material |
JP2012025773A (en) * | 2011-10-14 | 2012-02-09 | Maruzen Pharmaceut Co Ltd | Lipase inhibitor |
KR20150114835A (en) * | 2014-04-02 | 2015-10-13 | (재)남해마늘연구소 | Sweet jelly comprising natural plant component |
KR101672758B1 (en) * | 2014-04-02 | 2016-11-04 | (재)남해마늘연구소 | Sweet jelly comprising natural plant component |
Also Published As
Publication number | Publication date |
---|---|
JP4233645B2 (en) | 2009-03-04 |
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