JP2004238349A - Antiobestic agent or/and prophylactic agent for arteriosclerosis containing terminalia catappa as active ingredient - Google Patents

Antiobestic agent or/and prophylactic agent for arteriosclerosis containing terminalia catappa as active ingredient Download PDF

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Publication number
JP2004238349A
JP2004238349A JP2003030793A JP2003030793A JP2004238349A JP 2004238349 A JP2004238349 A JP 2004238349A JP 2003030793 A JP2003030793 A JP 2003030793A JP 2003030793 A JP2003030793 A JP 2003030793A JP 2004238349 A JP2004238349 A JP 2004238349A
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Japan
Prior art keywords
plant
momotamana
active ingredient
organic solvent
mixture
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
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JP2003030793A
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Japanese (ja)
Inventor
Masaaki Yasue
正明 安江
Mariko Koizumi
真理子 小泉
Morio Inafuku
盛雄 稲福
Sunao Inafuku
直 稲福
Tetsuya Fujino
哲也 藤野
Megumi Yonaha
恵 与那覇
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Asahi Breweries Ltd
Ryukyu Bio Resource Development Co Ltd
Original Assignee
Asahi Breweries Ltd
Ryukyu Bio Resource Development Co Ltd
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Priority to JP2003030793A priority Critical patent/JP2004238349A/en
Publication of JP2004238349A publication Critical patent/JP2004238349A/en
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a medicine or a food or beverage effective for prophylaxis/treatment of obesity/arteriosclerosis by utilizing a bioregulatory function which Terminalia catappa has in order to find an active ingredient from a food or a material based upon the food in prophylaxis/treatment of obesity/arteriosclerosis. <P>SOLUTION: It was confirmed by animal experience that a plant body of Terminalia catappa or its extract has bioactivity which has not been known hitherto. The medicine/food or beverage having antiobestic action or action for preventing/improving arteriosclerosis comprises the plant body of Terminalia catappa or an extract obtained by carrying out extraction treatment of the plant body of Terminalia catappa with water or an organic solvent alone or a mixture thereof as an active ingredient. <P>COPYRIGHT: (C)2004,JPO&NCIPI

Description

【0001】
【発明の属する技術分野】
本発明はモモタマナより得られる抗肥満又は/及び動脈硬化予防物質及びその用途に関する。
【0002】
【従来の技術】
近年、食生活の高脂肪・高カロリー化により、国民の肥満傾向が徐々に進んでいる。上半身肥満、耐糖能異常、高中性脂肪、高血圧は「死の四重奏」と呼ばれ、これらが重なると加速度的に動脈硬化や心疾患の罹患率が高まり、生命を脅かすとされている。このような生理学的異常の発現には、遣伝因子とともに食生活をはじめとする環境因子が大きく関わっているため、予防・改善するためには時として生活習慣を大きく変える必要があり、持続困難な自己規制を強いられることがある。誰もが受け入れられるような簡便な肥満・動脈硬化予防・改善手段が望まれている。
【0003】
近年、食品又はこれに準ずる天然物から様々な有用物質が見出され、その生理機能を生かした機能性食品がブームになりつつある。機能性食品は、半健常の人が日常的に摂取することで血液脂質、血糖値、血圧等の改善が期待され、簡便な健康増進・疾病予防手段を提供しうる。
モモタマナは学名を「Terminalia catappa」、別名を「コバテイシ(枯葉手樹)」という。沖縄からアジア・アフリカの海岸、小笠原諸島に自生するシクンシ科の樹木であり、種子はアーモンドに似た風味で食用になる。しかしモモタマナの生理機能に着目した研究は少なく、機能性食品又は医薬品の原材料としては殆ど用いられていない。しかしその葉等はポリフェノール類を多く含んでおり、脂肪分の吸収阻害作用を始めとする抗肥満作用、さらには動脈硬化、心疾患等の生活習慣病の予防・治療効果が期待される。
【0004】
【発明が解決しようとする課題】
今後も国民の健康を脅かすであろう肥満・動脈硬化を予防・治療するにあたり、食品又は食品に準ずるものから有効成分を見いだす必要がある。本発明はモモタマナの有する生体調節機能を利用して、肥満・動脈硬化の予防・治療に有効な薬剤、又は飲食品を提供することを目的とする。
【0005】
【課題を解決するための手段】
本発明は上記目的を達成するためになされたもので、モモタマナの植物体もしくはその抽出エキスが、これまで知られていなかったような生理活性を有することを動物実験により確認して本発明を完成するに至った。
【0006】
すなわち本発明は、モモタマナの植物体、もしくは植物体を、水又は有機溶媒単独、又はそれらの混合物で抽出処理して得られるエキスを有効成分し、抗肥満作用もしくは動脈硬化予防・改善作用を持つ医薬品・飲食品を提供する。
【0007】
【発明の実施の形態】
モモタマナの植物体をそのまま使用する場合には、葉、果実、種子、幹もしくは根を生の状態、あるいは乾燥の後、適切な大きさに細砕、もしくは粉末化する。
【0008】
エキスの抽出に際しては、水、アルコール、又はその他の有機溶媒等が用いられる。これらを混合したものを用いても差し支えない。好ましい抽出溶媒は水、あるいは水とアルコール等との混合溶媒である。抽出は、室温抽出、加熱抽出さらには加圧抽出等にて行われる。―般的には室温〜125℃で行われる。植物体からの抽出処理後、遠心分離等により固形分と液体を分離し、さらに必要に応じて濾過等の処理を行った後、減圧濃縮等で濃縮する。さらに、真空乾燥、凍結乾燥等により粉末化することもできる。粉末化に際して、適当な賦形剤を加えても差し支えない。
【0009】
加工された植物体又は抽出エキスは、経口の医薬品として用いることができ、また食品素材と混合して飲食品とすることができる。性状としては固体状又は液体状を呈し、医薬品としては経口剤として錠剤、カプセル剤、顆粒剤、シロップ剤等の剤型をとる。
植物体あるいはエキスを医薬品として人体に投与するときは、1回あたり0.1〜1000mg(乾燥重量)/kg体重の量、好ましくは0.3〜300mg(乾燥重量)/kg体重の量を、1日に1ないし数回経口投与する。
【0010】
飲食品とする場合、これと混合する食品素材は固形物(粉状、薄片状、塊状など)、半固形物(ゼリー状、水飴状など)、もしくは液状物等のいずれであっても良い。飲食品1gあたりの植物体あるいはエキス含有量は、0.3〜300mg(乾燥重量)であることが望ましい。
本発明のモモタマナの植物体あるいは抽出エキスを含有する医薬品及び飲食品は、抗肥満作用、動脈硬化予防改善作用を有するので、成人病・生活習慣病の予防及び治療上有効なものである。
【0011】
【実施例】
以下、本発明を実施例によってさらに具体的に説明するが、本発明はこれに限定されるものではない。
【0012】
実施例1(モモタマナ熱水抽出エキスの調製)
100gのモモタマナ葉を細かく粉砕して1Lの蒸留水に懸濁し、100℃で2時間煮沸した。懸濁液を冷却の後、5000Gで15分間遠心分離して上清を採取し、凍結乾燥して24.8gのエキス粉末を得た。フォリン・チオカルテ法によりモモタマナエキス中のポリフェノール含有量を測定したところ、(−)カテキン換算で44%であった。
【0013】
実施例2(錠剤、カプセル剤)
モモタマナ葉粉末 10.0g
乳糖 75.0g
ステアリン酸マグネシウム 15.0g
合計 100.0g
上記の各重量部を均一に混合し、常法に従って錠剤、カプセル剤とした。
【0014】
実施例3(錠剤、カプセル剤)
実施例1で調製したエキス粉末 10.0g
乳糖 75.0g
ステアリン酸マグネシウム 15.0g
合計 100.0g
上記の各重量部を均一に混合し、常法に従って錠剤、カプセル剤とした。
【0015】
実施例4(散剤、顆粒剤)
モモタマナ葉粉末 20.0g
澱粉 30.0g
乳糖 50.0g
合計 100.0g
上記の各重量部を均一に混合し、常法に従って散剤、顆粒剤とした。
【0016】
実施例5(散剤、顆粒剤)
実施例1で調製したエキス粉末 20.0g
澱粉 30.0g
乳糖 50.0g
合計 100.0g
上記の各重量部を均一に混合し、常法に従って散剤、顆粒剤とした。
【0017】
実施例6(飴)
ショ糖 20.0g
水飴(75%固形分) 70.0g
水 9.5g
着色料 0.45g
香料 0.045g
モモタマナ葉粉末 0.005g
合 計 100.0g
上記の各重量部の各成分を用い、常法に従って飴とした。
【0018】
実施例7(飴)
ショ糖 20.0g
水飴(75%固形分) 70.0g
水 9.5g
着色料 0.45g
香料 0.045g
実施例1で調製したエキス粉末 0.005g
合 計 100.0g
上記の各重量部の各成分を用い、常法に従って飴とした。
【0019】
実施例8(ジュース)
濃縮ミカン果汁 15.0g
果糖 5.0g
クエン酸 0.2g
香料 0.1g
色素 0.15g
アスコルビン酸ナトリウム 0.048g
実施例1で調製したエキス粉末 0.002g
水 79.5g
合 計 100.0g
上記の各重量部の各成分を用い、常法に従ってジュースとした。
【0020】
実施例9(クッキー)
薄力粉 32.0g
全卵 16.0g
バター 16.0g
砂糖 25.0g
水 10.8g
ベーキングパウダー 0.198g
モモタマナ葉粉末 0.002g
合 計 100.0g
上記の各重量部の各成分を用い、常法に従ってクッキーとした。
【0021】
実施例10(クッキー)
薄力粉 32.0g
全卵 16.0g
バター 16.0g
砂糖 25.0g
水 10.8g
べーキングパウダー 0.198g
実施例1で調製したエキス粉末 0.002g
合 計 100.0g
上記の各重量部の各成分を用い、常法に従ってクッキーとした。
【0022】
実施例11(モモタマナのリパーゼ阻害作用)
1mg/mLのブタ膵臓リパーゼ、水もしくは1mg/mLモモタマナエキス粉末水溶液、0.1mMオレイン酸メチルウンべリフェロンを1容:1容:2容で混合し、室温で60分間反応させた。5容の0.1N塩酸を加えた後、さらに5容の0.1Mクエン酸3ナトリウムを加え、励起320nm、吸収450nmの蛍光量を測定することで、リパーゼ活性によりオレイン酸メチルウンべリフェロンから遊離した4−メチルウンべリフェロン量を算出した。モモタマナエキス粉末水溶液の添加により、4ーメチルウンべリフェロンの遊離量は36%低下し、モモタマナがリパーゼ阻害活性を有することが確認された。
【0023】
実施例12(モモタマナの脂肪分吸収抑制作用)
6週齢の雄性ddY系マウス(一群9匹)から眼窩採血を行い、10mL/kgのサラダ油を経口投与した後、直ちに10mL/kgの水もしくは0.25g/mLモモタマナエキス粉末水溶液を経口投与した。180分後に再度眼窩採血を行い、血漿を分離して中性脂肪濃度を測定した。モモタマナの投与により、サラダ油負荷180分後の血漿中性脂肪値が顕著に抑制された(表1)。
【0024】

Figure 2004238349
【0025】
実施例13(モモタマナの抗肥満作用)
4週齢の雄性ICR系マウスを9匹ずつ2群に分け、それぞれに精製飼料(AINー93G)、及びモモタマナ葉粉末を1%添加した精製飼料を7週間自由摂取させた。飼育終了後動物の体長(ヒトの身長に相当)・体重測定及び全採血を行い、血漿を分離して中性脂肪値、総コレステロール値、血糖値を測定した。精巣周囲脂肪と肝臓を摘出した後秤量し、肝臓中の中性脂肪、総コレステロール濃度を測定した。
表2に示した通り、エサにモモタマナを添加したところ、体長には変化が見られなかったものの、精巣周囲脂肪の重量が著しく低下し、体重も低下傾向を示した。
【0026】
Figure 2004238349
さらに表3に示した通り、モモタマナを与えた群の中性脂肪値、総コレステロール値、血糖値は、いずれも精製飼料のみを与えた群より低値であった。
【0027】
Figure 2004238349
また表4に示した通り、モモタマナを与えた群の肝臓中の中性脂肪、コレステロール蓄積量は、精製飼料のみを与えた群より著しく低値であった。
【0028】
Figure 2004238349
【0029】
【発明の効果】
本発明によれば、モモタマナを原料として、抗肥満作用及び動脈硬化予防・改善作用を有する物質を得ることができた。更にこれを、医薬品や飲食品の材料として容易に利用することができた。[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to an antiobesity or / and arteriosclerosis preventive substance obtained from Momotamana and its use.
[0002]
[Prior art]
2. Description of the Related Art In recent years, the tendency of obesity in the people has been gradually increasing due to high fat and high calorie diet. Upper body obesity, impaired glucose tolerance, high triglyceride fat, and high blood pressure are called "quartets of death", and when they overlap, the incidence of arteriosclerosis and heart disease accelerates at an accelerated rate, and is thought to be life-threatening. Since the development of such physiological abnormalities is greatly influenced by environmental factors such as dietary factors, as well as transmission factors, it is sometimes necessary to make significant changes in lifestyle to prevent or improve the condition, making it difficult to sustain May be forced to self-regulate. There is a demand for a simple obesity / arteriosclerosis prevention / improvement method that can be accepted by everyone.
[0003]
In recent years, various useful substances have been found in foods or natural products equivalent thereto, and functional foods utilizing their physiological functions are becoming a boom. Functional foods are expected to improve blood lipids, blood sugar levels, blood pressure and the like when semi-healthy people take them on a daily basis, and can provide a simple means for promoting health and preventing disease.
Momotamana has a scientific name of "Terminaria catappa " and another name of "Koba Teishi". It is a tree of the family Aridaceae native to the Ogasawara Islands from Okinawa to the coasts of Asia and Africa, and its seeds are edible with a flavor similar to almonds. However, there are few studies focusing on the physiological function of Momotamana, and it is hardly used as a raw material for functional foods or pharmaceuticals. However, the leaves and the like contain a large amount of polyphenols, and are expected to have an anti-obesity effect including a fat absorption inhibitory effect, and a preventive / therapeutic effect for lifestyle-related diseases such as arteriosclerosis and heart disease.
[0004]
[Problems to be solved by the invention]
In the future, in preventing and treating obesity and arteriosclerosis, which will threaten the health of the nation, it is necessary to find active ingredients from foods or food equivalents. An object of the present invention is to provide a drug or a food or drink that is effective in preventing and treating obesity and arteriosclerosis by utilizing the biological regulation function of Momotamana.
[0005]
[Means for Solving the Problems]
The present invention has been made in order to achieve the above object, and completed the present invention by confirming, through animal experiments, that a plant of Momotamana or an extract thereof has a physiological activity that has not been known so far. I came to.
[0006]
That is, the present invention has an anti-obesity effect or an anti-arteriosclerosis-preventing / ameliorating effect, comprising as an active ingredient an extract obtained by extracting a plant of Momota mana, or a plant, with water or an organic solvent alone, or a mixture thereof. Provide medicines and foods and beverages.
[0007]
BEST MODE FOR CARRYING OUT THE INVENTION
In the case of using the plant body of Momotamana as it is, leaves, fruits, seeds, stems or roots are raw or dried, and then ground or powdered to an appropriate size.
[0008]
In extracting the extract, water, alcohol, or another organic solvent is used. A mixture of these may be used. A preferred extraction solvent is water or a mixed solvent of water and alcohol. The extraction is performed by room temperature extraction, heat extraction, and pressure extraction. -Generally at room temperature to 125 ° C. After the extraction treatment from the plant body, the solid content and the liquid are separated by centrifugation or the like, and further, if necessary, subjected to treatment such as filtration, and then concentrated under reduced pressure. Further, it can be powdered by vacuum drying, freeze drying or the like. Upon powdering, an appropriate excipient may be added.
[0009]
The processed plant or the extracted extract can be used as an oral pharmaceutical, or can be mixed with food materials to produce a food or drink. It takes a solid or liquid form as a property, and a pharmaceutical takes an oral dosage form such as a tablet, capsule, granule, syrup and the like.
When a plant or an extract is administered to the human body as a pharmaceutical, the dose of the plant or extract should be 0.1 to 1000 mg (dry weight) / kg body weight per dose, preferably 0.3 to 300 mg (dry weight) / kg body weight. Administer orally once or several times a day.
[0010]
In the case of food or drink, the food material mixed therewith may be any of a solid (powder, flake, lump, etc.), a semi-solid (jelly, syrup, etc.) or a liquid. The content of the plant or extract per 1 g of food or drink is desirably 0.3 to 300 mg (dry weight).
Pharmaceuticals and foods and drinks containing the plant or extract of Momotamana of the present invention have an anti-obesity effect and an effect of preventing and improving arteriosclerosis, and thus are effective in preventing and treating adult diseases and lifestyle-related diseases.
[0011]
【Example】
Hereinafter, the present invention will be described more specifically with reference to Examples, but the present invention is not limited thereto.
[0012]
Example 1 (Preparation of Momotamana hot water extract)
100 g of Momotamana leaves were finely ground, suspended in 1 L of distilled water, and boiled at 100 ° C. for 2 hours. After cooling the suspension, the suspension was centrifuged at 5000 G for 15 minutes, and the supernatant was collected and freeze-dried to obtain 24.8 g of extract powder. The polyphenol content in the peach tamana extract measured by the Folin-Ciocarte method was 44% in terms of (-) catechin.
[0013]
Example 2 (tablets, capsules)
Momotamana leaf powder 10.0g
Lactose 75.0g
Magnesium stearate 15.0g
100.0g in total
The above parts by weight were uniformly mixed to obtain tablets and capsules according to a conventional method.
[0014]
Example 3 (tablets, capsules)
10.0 g of the extract powder prepared in Example 1
Lactose 75.0g
Magnesium stearate 15.0g
100.0g in total
The above parts by weight were uniformly mixed to obtain tablets and capsules according to a conventional method.
[0015]
Example 4 (powder, granule)
Momotamana leaf powder 20.0g
Starch 30.0g
Lactose 50.0g
100.0g in total
The above parts by weight were uniformly mixed to give powders and granules according to a conventional method.
[0016]
Example 5 (powder, granule)
20.0 g of extract powder prepared in Example 1
Starch 30.0g
Lactose 50.0g
100.0g in total
The above parts by weight were uniformly mixed to give powders and granules according to a conventional method.
[0017]
Example 6 (candy)
Sucrose 20.0g
70.0g syrup (75% solids)
9.5 g of water
0.45 g coloring
Spice 0.045g
Momotamana leaf powder 0.005g
Total 100.0g
A candy was prepared according to a conventional method using the above components in each part by weight.
[0018]
Example 7 (candy)
Sucrose 20.0g
70.0g syrup (75% solids)
9.5 g of water
0.45 g coloring
Spice 0.045g
0.005 g of extract powder prepared in Example 1
Total 100.0g
A candy was prepared according to a conventional method using the above components in each part by weight.
[0019]
Example 8 (juice)
Concentrated orange juice 15.0g
Fructose 5.0g
Citric acid 0.2g
Spice 0.1g
0.15 g of pigment
Sodium ascorbate 0.048g
0.002 g of extract powder prepared in Example 1
79.5 g of water
Total 100.0g
A juice was prepared using the above-mentioned respective parts by weight and in accordance with a conventional method.
[0020]
Example 9 (cookie)
Soft flour 32.0g
16.0 g of whole egg
16.0 g of butter
Sugar 25.0g
10.8g of water
Baking powder 0.198g
Momotamana leaf powder 0.002g
Total 100.0g
A cookie was prepared according to a conventional method using the above components in each part by weight.
[0021]
Example 10 (cookie)
Soft flour 32.0g
16.0 g of whole egg
16.0 g of butter
Sugar 25.0g
10.8g of water
Baking powder 0.198g
0.002 g of extract powder prepared in Example 1
Total 100.0g
A cookie was prepared according to a conventional method using the above components in each part by weight.
[0022]
Example 11 (lipase inhibitory action of Momotamana)
1 mg / mL porcine pancreatic lipase, water or a 1 mg / mL aqueous solution of momotamana extract, and 0.1 mM methylumbelliferone oleate were mixed at a volume ratio of 1: 1: 1: 2 and reacted at room temperature for 60 minutes. After adding 5 volumes of 0.1N hydrochloric acid, 5 volumes of 0.1M trisodium citrate are further added, and the amount of fluorescence at an excitation of 320 nm and an absorption of 450 nm is measured, thereby releasing from methylumbelliferone oleate by lipase activity. The amount of 4-methylumbelliferone thus obtained was calculated. The addition of the aqueous solution of momotamana extract reduced the release amount of 4-methylumbelliferone by 36%, confirming that momotamana had a lipase inhibitory activity.
[0023]
Example 12 (Fat absorption inhibition effect of momotamana)
Orbital blood was collected from 6-week-old male ddY mice (9 mice per group), and 10 mL / kg of salad oil was orally administered, followed immediately by 10 mL / kg of water or 0.25 g / mL aqueous solution of momotamana extract powder. . After 180 minutes, orbital blood was collected again, the plasma was separated, and the neutral fat concentration was measured. The administration of Momotamana significantly suppressed the plasma triglyceride level 180 minutes after the salad oil load (Table 1).
[0024]
Figure 2004238349
[0025]
Example 13 (Anti-obesity action of Momotamana)
Four-week-old male ICR mice were divided into two groups of nine each, and each group was allowed to freely ingest a purified feed (AIN-93G) and a purified feed to which 1% of momotamana leaf powder was added, for 7 weeks. After breeding, the animals were measured for body length (corresponding to human height) and body weight, and whole blood was collected. Plasma was separated and neutral fat, total cholesterol, and blood glucose were measured. The peritesticular fat and the liver were excised and weighed to measure the levels of neutral fat and total cholesterol in the liver.
As shown in Table 2, when momotamana was added to the food, there was no change in body length, but the weight of the peri-testicular fat was significantly reduced, and the body weight also tended to decrease.
[0026]
Figure 2004238349
Furthermore, as shown in Table 3, the triglyceride, total cholesterol, and blood glucose levels of the group receiving momotamana were lower than those of the group receiving only the purified feed.
[0027]
Figure 2004238349
In addition, as shown in Table 4, the amount of triglyceride and cholesterol accumulated in the liver of the group to which momotamana was fed was significantly lower than the group to which only the purified feed was fed.
[0028]
Figure 2004238349
[0029]
【The invention's effect】
ADVANTAGE OF THE INVENTION According to this invention, the substance which has an anti-obesity effect and an arteriosclerosis prevention / amelioration effect was able to be obtained from Momotamana as a raw material. Furthermore, it could be easily used as a material for medicines and foods and drinks.

Claims (8)

モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、体脂肪蓄積予防効果あるいは体脂肪減少効果を有する医薬品。A pharmaceutical having an effect of preventing body fat accumulation or reducing body fat, comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant of Momotamana. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、体脂肪蓄積予防効果あるいは体脂肪減少効果を有する飲食品。A food or drink having an effect of preventing body fat accumulation or reducing body fat, comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant body of Momota mana. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、脂肪分の消化吸収阻害作用あるいは血液中の中性脂肪低下作用を有する医薬品。Pharmaceuticals that have an inhibitory effect on digestion and absorption of fat or a function of lowering triglyceride in blood as an active ingredient, using an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant or a plant of Momotamana . モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、脂肪分の消化吸収阻害作用あるいは血液中の中性脂肪低下作用を有する飲食品。An extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant or a plant of Momotamana as an active ingredient, and having a digestive absorption inhibitory effect of fat or a neutral fat lowering effect in blood. Goods. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、抗コレステロール作用を有する医薬品。A pharmaceutical having an anticholesterol effect, comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant body of Momotamana. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とし、抗コレステロール作用を有する飲食品。A food or drink having an anticholesterol effect, comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant of Momotamana. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とする抗肥満剤。An antiobesity agent comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant of Momotamana or a plant. モモタマナの植物体もしくは植物体から水又は有機溶媒単独、又はそれらの混合物で抽出処理して得たエキスを有効成分とする動脈硬化予防剤。An arteriosclerosis preventive agent comprising, as an active ingredient, an extract obtained by extracting water or an organic solvent alone or a mixture thereof from a plant of Momotamana or a plant.
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005053864A (en) * 2003-08-06 2005-03-03 Ryukyu Bio Resource Kaihatsu:Kk Prophylactic and therapeutic agent for diabetes mellitus disease
JP2005060334A (en) * 2003-08-19 2005-03-10 Okinawa Pref Gov Anti-obesity agent having lipase inhibiting activity and antioxidation activity
EP1628489A1 (en) 2004-08-18 2006-02-22 Sony Corporation Video signal processing apparatus and method
JP2006188486A (en) * 2004-12-07 2006-07-20 Toyo Shinyaku:Kk Body fat accumulation-inhibiting or reducing agent
JP5888574B1 (en) * 2015-07-02 2016-03-22 株式会社東洋新薬 Blood flow improver

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001270833A (en) * 2000-01-18 2001-10-02 Nagaoka Koryo Kk Antiobesity agent
JP2002155083A (en) * 2000-11-22 2002-05-28 Yamanouchi Pharmaceut Co Ltd Hydrazide derivative

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001270833A (en) * 2000-01-18 2001-10-02 Nagaoka Koryo Kk Antiobesity agent
JP2002155083A (en) * 2000-11-22 2002-05-28 Yamanouchi Pharmaceut Co Ltd Hydrazide derivative

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005053864A (en) * 2003-08-06 2005-03-03 Ryukyu Bio Resource Kaihatsu:Kk Prophylactic and therapeutic agent for diabetes mellitus disease
JP2005060334A (en) * 2003-08-19 2005-03-10 Okinawa Pref Gov Anti-obesity agent having lipase inhibiting activity and antioxidation activity
JP4644787B2 (en) * 2003-08-19 2011-03-02 沖縄県 Anti-obesity agent having lipase inhibitory activity and antioxidant properties
EP1628489A1 (en) 2004-08-18 2006-02-22 Sony Corporation Video signal processing apparatus and method
JP2006188486A (en) * 2004-12-07 2006-07-20 Toyo Shinyaku:Kk Body fat accumulation-inhibiting or reducing agent
JP5888574B1 (en) * 2015-07-02 2016-03-22 株式会社東洋新薬 Blood flow improver
JP2017014165A (en) * 2015-07-02 2017-01-19 株式会社東洋新薬 Blood flow improvement agent

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