JP4160276B2 - Food and drink with uric acid level lowering agent and uric acid level lowering effect - Google Patents

Food and drink with uric acid level lowering agent and uric acid level lowering effect Download PDF

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JP4160276B2
JP4160276B2 JP2001176842A JP2001176842A JP4160276B2 JP 4160276 B2 JP4160276 B2 JP 4160276B2 JP 2001176842 A JP2001176842 A JP 2001176842A JP 2001176842 A JP2001176842 A JP 2001176842A JP 4160276 B2 JP4160276 B2 JP 4160276B2
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uric acid
tea
acid level
food
level lowering
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JP2002370980A (en
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歩 野澤
明夫 杉本
隆巳 角田
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株式会社 伊藤園
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  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Non-Alcoholic Beverages (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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Description

【0001】
【産業上の利用分野】
本発明は、体内の尿酸値を効果的に低下させることができる尿酸値低下剤、及びそのような薬理効果を備えた飲食物に関する。
【0002】
【従来の技術及び発明が解決しようとする課題】
からだの中では、食べ物から摂取したプリン体を肝臓で分解するなどして毎日ほぼ一定量の尿酸を産生している。この尿酸は、血液等の体液に溶けて循環し、産生量とほぼ同量が主に腎臓から尿中へ濾し取られて排泄されている。ところが、何らかの原因(例えば食生活、飲酒、ストレス、腎臓機能の低下、薬剤による影響、遺伝的要因など)で尿酸産生量と排泄量とのバランスが崩れると、体内の尿酸量が増え過ぎて高尿酸血症になることがある。ちなみに、血液中の尿酸濃度(血清尿酸値)は、一般的に男性3.8〜7.0mg/dL、女性2.4〜5.8mg/dLの範囲が管理基準値とされ、男女ともに尿酸値7.0mg/dLを超えると高尿酸血症発症の可能性が高いとされている。
【0003】
高尿酸血症そのものはなんの症状もないが、これを放っておくと痛風をはじめとする様々な疾病を引き起こすことになる。すなわち、血液中の尿酸の濃度が上昇して飽和濃度を超えると、溶けなくなった尿酸はナトリウムと塩を作って結晶を形成する。尿酸の濃度が高い状態が続くと、この尿酸塩結晶が体内の各部位に沈着して、例えば関節内に尿酸塩が沈着して痛風を引き起したり、腎臓内で結晶化すれば尿路結石や腎障害などを引き起こしたりするのである。また、高尿酸血症は心筋梗塞などの虚血性心疾患の原因となるとも言われている。
【0004】
現在、尿酸値を下げる薬としては、ベンズブロマロンなどの尿酸排泄を促進する薬と、アロプリノールなどの尿酸合成を阻害する薬とがあり、患者の高尿酸血症のタイプに合わせて処方されている。現在処方されているこれらの薬は、尿酸値のコントロール剤として極めて優秀であり、薬の服用によって血清尿酸値を正常に戻すことができる。しかしながら、高尿酸血症そのものは非常に治りにくい病気であるため、薬の服用を中止すると再び高尿酸血症の状態に戻ってしまう。このため、高尿酸血症を根本的に治療するためには長期に渡って根気よく薬を服用し続ける必要がある。
このような点から、高尿酸血症の治療剤としては、長期間安心して無理なく服用できるもの、例えば古くから日常的に摂取されてきた天然物に由来するものが望まれていた。
【0005】
ところが、従来、天然物由来の高尿酸血症の治療剤或いは尿酸値低下剤として開示されていたものは極僅かであった。例えば、特開平6−311868号が、シラカンバ樹液を主成分とする食用液には痛風などに効果がある旨を開示し、特開平6−247868号は、クロレラを有効成分とする尿酸値低下剤を開示している程度であった。
【0006】
そこで本発明は、古くから日常的に摂取され、誰でも安心して摂取することができる天然物由来の成分を有効成分とする尿酸値低下剤、及び尿酸値低下効果を備えた飲食物を提供せんとするものである。
【0007】
【課題を解決するための手段】
本発明は、古くから日常的に摂取されている茶に由来する茶ポリフェノールを有効成分として含有する尿酸値低下剤及び尿酸値低下効果を備えた飲食物を提供するものである。
【0008】
本発明の尿酸値低下剤及び飲食物は、摂取することによって高尿酸血症の状態にある尿酸値を効果的に低下させて正常に戻すことができる。しかも、古くから日常的に愛飲され、誰でも安心して摂取できる茶に由来する成分を有効成分とするものであるから、長期間安心して服用することができ、高尿酸血症を根本的に治療するための治療剤として極めて有用である。また、日常的に無理なく摂取できるから高尿酸血症の予防剤としても極めて有用である。更には、痛風をはじめ、高尿酸血症を原因とする様々な疾病の治療剤または予防剤、これらの薬理効果を備えた飲食物としても有用である。
【0009】
【発明の実施の形態】
上記の如く、本発明の尿酸値低下剤は、茶を抽出して得られるポリフェノールすなわち茶ポリフェノールを有効成分として含有する尿酸値低下剤及び尿酸値低下効果を備えた飲食物である。
【0010】
ここで、本発明における茶ポリフェノールとは、茶ポリフェノールは、フラバン-3-オールの基本構造を有する次の茶カテキン類すなわち(-)-エピカテキン、(-)-エピガロカテキン、(-)-エピカテキンガレート、(-)-エピガロカテキンガレート、(±)-カテキン、(-)-ガロカテキン、(-)-カテキンガレート、(-)-ガロカテキンガレート、或いは、遊離型テアフラビン、テアフラビンモノガレートA、テアフラビンモノガレートB、テアフラビンジガレート、これらいずれかの重合体、及びこれらのうちの二種類以上の共重合体からなる群から選ばれたいずれか或いは二種類以上の混合物、中でも茶カテキン類、その中でも特に(-)-エピカテキンガレート及び(-)-エピガロカテキンガレートを50%以上含有してなるもののが本発明の有効成分として好ましい。
なお、上記の茶カテキン類を含む混合物をレトルト殺菌すると、これら茶カテキン類の重合体や共重合体が生じることが知られている。
【0011】
これらの茶ポリフェノールは、ツバキ科に属する茶樹(Camellia sinensis )から得られる葉、茎、木部、根、実のいずれか、或いはこれらの2種類以上の混合物から得られる茶から抽出することができ、その茶としても、茶生葉、紅茶やプアール茶等の発酵茶、ウーロン茶や包種茶等の半発酵茶、緑茶や釜煎り緑茶、ほうじ茶等の不発酵茶のいずれか、又は、これらの2種類以上の混合物であればよく、それぞれの茶から抽出して得られるもの(単独)、又はそれぞれの茶から抽出したもの混合物を用いることができる。抽出方法としては、現在既知の任意の方法によって抽出及び精製を行えばよく、また、市販の茶ポリフェノールを使用することもできる。
【0012】
本発明の有効成分は、茶ポリフェノールのみで構成することも勿論可能であるが、茶ポリフェノールを高濃度で含有する茶抽出物を本発明の有効成分とすることも可能である。また、既に尿酸値低下効果の知られた成分を加えて有効成分とすることもできる。
上記の茶ポリフェノールを高濃度で含有する茶抽出物としては、例えば、上記の茶を水、温水または熱水、好ましくは40℃〜100℃の温熱水中でも90〜100℃の熱水にて抽出して得られた抽出物、更に好ましくはこの抽出物を樹脂吸着や限外濾過・逆浸透濾過等の濾過、或いは酢酸エチル等を使用した分配抽出などの精製手段によって茶カテキン含有量を高める方向に精製して得られる茶抽出物、或いは更にこれらの茶抽出物を濃縮或いは乾燥させた茶抽出エキスを挙げることができる。この際、茶ポリフェノール含有濃度は、25〜97%、好ましくは30〜90%であり、この茶抽出物の具体例としては、緑茶を熱水抽出処理し、この抽出物を乾燥させて茶カテキン濃度を約30%とした緑茶エキス(伊藤園社製商品名:テアフラン30A)や、緑茶を熱水抽出処理し、この抽出物を茶カテキン以外の成分を排除するためにカラム法により処理し乾燥させて、茶ポリフェノール濃度を約85〜95%とした緑茶エキス(伊藤園社製商品名:テアフラン90S)などを例示することができる。
【0013】
本発明の尿酸値低下剤は、医薬品、医薬部外品、健康食品や健康飲料、食品添加剤、飼料、飼料用添加剤など様々な用途に使用することができ、その際の形態としては、凍結乾燥或いは噴霧乾燥等により乾燥させて乾燥粉末として提供することもできるし、液剤、錠剤、散剤、顆粒、糖衣錠、カプセル、懸濁液、乳剤、アンプル剤、注射剤、その他任意の形態に調製して提供することもできる。
医薬品として提供する場合、例えば、有効成分をそのまま精製水又は生理食塩水などに溶解して調製することも可能である。
医薬部外品としては、医薬部外品に通常配合する成分を加えて調製し、これを瓶ドリンク飲料等の飲用形態、或いはタブレット、カプセル、顆粒等の形態として提供することができる。
飲食物としては、例えば、本発明の有効成分に、食品素材(果実やゼリーなども含む)、乳成分、炭酸、賦形剤(造粒剤含む)、希釈剤、或いは更に甘味剤、フレーバー、小麦粉、でんぷん、糖、油脂類等の各種タンパク質、糖質原料やビタミン、ミネラル、その他の生理活性成分、ホルモン、栄養成分などから選ばれた一種或いは二種以上を加えて、スポーツ飲料、果実飲料、茶飲料、野菜ジュース、乳性飲料、アルコール飲料、ゼリー飲料、炭酸飲料などの各種飲料、ゼリー、チューインガム、チョコレート、アイスクリーム、キャンディ、ビスケットなどの菓子類、スナック、パン、ケーキなどの澱粉系加工食品、魚肉練り製品、畜肉製品、豆腐、チーズなどのタンパク質系加工食品、味噌やしょうゆ、ドレッシングなどの調味料、その他、サプリメント、飼料、ペットフードなど様々な形態として提供することができる。
【0014】
本発明における有効成分の含有量は、用途によっても異なるが、医薬品であれば、カテキン乾燥重量換算にして0.001〜1重量%、特に0.01〜0.5重量%配合することが好ましく、飲食品であれば、カテキン乾燥重量換算にして0.001〜1重量%、特に0.01〜0.5重量%配合することが好ましい。
摂取量としては、カテキン乾燥重量換算で一日に10〜5000mg、好ましくは100〜1500mg程度が好ましい。
【0015】
(試験)
一缶190mLあたりテアフラン90S(:商品名、伊藤園社製)230mgを含有し、かつ味の改良のために若干量のサイクロデキストリン、ビタミンC及び香料を添加してなる被験飲料を作成した。上記のテアフラン90Sは、茶ポリフェノール含量92%、茶カテキン含量としては63%(そのうち、EGCg50%、ECg13%)であった。また、被験飲料はレトルト殺菌してあるため茶カテキン類の重合物や異性体を含んだ混合物飲料となっている。
【0016】
血清尿酸値の管理基準値上限である7.0mg/dLを超える血清尿酸値濃度を持つ20歳以上の男性7名(高尿酸血症群)と、血清尿酸値濃度が6.5mg/dL未満の20歳以上の男性9名(正常尿酸値群)とを被験者とし、それぞれの被検者に上記被験試料を8週間にわたり1日3回の食事と共に摂取してもらい、試験開始直前、試験開始から4週、6週及び8週後のそれぞれの時点で血清尿酸値を測定した。図1は、高尿酸血症群の平均血清尿酸値(mg/dL)を経時的に示したグラフであり、図2は、正常尿酸値群の平均血清尿酸値(mg/dL)を経時的に示したグラフである。
【0017】
この結果、血中尿酸値が7.0mg/dLを超える高尿酸血症群では血中の尿酸値が有意に低下した。その一方、血中尿酸値が6.5mg/dL未満の正常尿酸値群では大きな変動は認められなかった。いずれの群も摂取期間中、被験者には何ら副作用は認められず、摂取に際して抵抗感もなかった。
これより、本被験飲料は安全かつ無理なく継続的に摂取することができ、特に血清尿酸値が高値を示す者に対して効果的に尿酸値を低下せしめ得ることが判明した。
【0018】
(実施例1)
以下の処方で尿酸値低下剤としてのタブレットを作成した。
【0019】
茶抽出物(テアフラン90S又はテアフラン30A) … 120mg
ビタミンC … 50mg
乳化オリゴ糖 … 90mg
造粒剤 … 60mg
結晶セルロース … 80mg
還元麦芽糖水飴 … 90mg
スクロース … 100mg
香料 … 適量
【0020】
(実施例2)
以下の処方で尿酸値低下効果を備えた飲食物としてのある飲料を作成した。
【0021】
茶抽出物(テアフラン90S又はテアフラン30A) … 150mg
ビタミンC … 50mg
果糖ぶどう液糖 … 10g
水溶性食物繊維 … 500mg
香料 … 適量
イオン交換水 … 100mLに調整
【図面の簡単な説明】
【図1】高尿酸血症群7名の平均血清尿酸値(mg/dL)を経時的に示したグラフである。
【図2】正常尿酸値群9名の平均血清尿酸値(mg/dL)を経時的に示したグラフである。
[0001]
[Industrial application fields]
The present invention relates to a uric acid level-lowering agent that can effectively reduce the uric acid level in the body, and foods and drinks having such a pharmacological effect.
[0002]
[Prior art and problems to be solved by the invention]
In the body, purine bodies taken from food are broken down by the liver, producing a certain amount of uric acid every day. This uric acid is dissolved and circulated in body fluids such as blood, and almost the same amount as the production amount is mainly filtered from the kidneys into the urine and excreted. However, if the balance between uric acid production and excretion is lost due to some cause (for example, eating habits, alcohol consumption, stress, decreased kidney function, effects of drugs, genetic factors, etc.), the amount of uric acid in the body increases too much. May cause uricemia. By the way, the uric acid concentration in blood (serum uric acid level) is generally controlled within the range of 3.8 to 7.0 mg / dL for men and 2.4 to 5.8 mg / dL for women. If the value exceeds 7.0 mg / dL, the possibility of developing hyperuricemia is considered high.
[0003]
Hyperuricemia itself has no symptoms, but leaving it alone can cause various diseases including gout. That is, when the concentration of uric acid in the blood rises and exceeds the saturation concentration, uric acid that has become insoluble forms a salt with sodium to form crystals. If the concentration of uric acid continues to be high, these urate crystals will be deposited in various parts of the body.For example, if urate is deposited in the joints to cause gout, or crystallizes in the kidney, the urinary tract It can cause stones and kidney damage. Hyperuricemia is also said to cause ischemic heart diseases such as myocardial infarction.
[0004]
Currently, drugs that lower uric acid levels include drugs that promote excretion of uric acid, such as benzbromarone, and drugs that inhibit uric acid synthesis, such as allopurinol, and are prescribed according to the type of hyperuricemia in patients. Yes. These drugs currently prescribed are extremely excellent as a control agent for uric acid level, and the serum uric acid level can be returned to normal by taking the drug. However, since hyperuricemia itself is a very difficult disease to cure, if you stop taking the medicine, it will return to the state of hyperuricemia again. For this reason, in order to fundamentally treat hyperuricemia, it is necessary to continue taking the medicine patiently for a long time.
In view of the above, a therapeutic agent for hyperuricemia has been desired that can be taken safely and comfortably for a long period of time, for example, a product derived from a natural product that has been ingested daily since ancient times.
[0005]
However, very few have been disclosed as therapeutic agents for hyperuricemia derived from natural products or agents for lowering uric acid levels. For example, JP-A-6-31868 discloses that an edible liquid mainly composed of birch sap has an effect on gout and the like, and JP-A-6-247868 discloses a uric acid level reducing agent containing chlorella as an active ingredient. Was disclosed.
[0006]
Therefore, the present invention does not provide a uric acid level-lowering agent comprising a natural product-derived ingredient that has been ingested on a daily basis for a long time and can be safely consumed by anyone, and a food or drink with a uric acid level-lowering effect. It is what.
[0007]
[Means for Solving the Problems]
This invention provides the food and drink provided with the uric acid value lowering agent which contains the tea polyphenol derived from the tea which is ingested routinely for a long time as an active ingredient, and the uric acid value lowering effect.
[0008]
By ingesting the uric acid level-lowering agent and food and drink of the present invention, the uric acid level in the state of hyperuricemia can be effectively reduced and returned to normal. Moreover, since it is an ingredient that is derived from tea that has been enjoyed and enjoyed everyday by anyone and can be safely consumed by anyone, it can be taken with confidence for a long period of time and radically treats hyperuricemia Therefore, it is extremely useful as a therapeutic agent. In addition, since it can be taken daily without difficulty, it is extremely useful as a preventive agent for hyperuricemia. Furthermore, it is also useful as a therapeutic or preventive agent for various diseases caused by gout and hyperuricemia, and foods and drinks having these pharmacological effects.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
As described above, the uric acid level-lowering agent of the present invention is a uric acid level-lowering agent containing polyphenol obtained by extracting tea, that is, tea polyphenol as an active ingredient, and a food and drink having a uric acid level-lowering effect.
[0010]
Here, the tea polyphenol in the present invention is the following tea catechins having the basic structure of flavan-3-ol, namely (-)-epicatechin, (-)-epigallocatechin, (-)- Epicatechin gallate, (-)-epigallocatechin gallate, (±) -catechin, (-)-gallocatechin, (-)-catechin gallate, (-)-gallocatechin gallate, or free theaflavin, theaflavin monogallate A , Theaflavin monogallate B, theaflavin digallate, any polymer thereof, and any one or a mixture of two or more selected from the group consisting of two or more of these copolymers, especially tea catechins, Of these, those containing 50% or more of (−)-epicatechin gallate and (−)-epigallocatechin gallate are particularly preferred as the active ingredient of the present invention.
In addition, when the mixture containing said tea catechins is retort-sterilized, it is known that the polymer and copolymer of these tea catechins will arise.
[0011]
These tea polyphenols can be extracted from tea obtained from leaves, stems, xylem, roots and fruits obtained from Camellia sinensis belonging to the camellia family, or a mixture of two or more of these. As the tea, either fresh tea leaves, fermented teas such as black tea and puer tea, semi-fermented teas such as oolong tea and bun tea, green tea, kettle roasted green tea, non-fermented tea such as hoji tea, or these 2 It may be a mixture of more than one kind, and a mixture obtained by extracting from each tea (single) or a mixture extracted from each tea can be used. As an extraction method, extraction and purification may be performed by any currently known method, and a commercially available tea polyphenol can also be used.
[0012]
Of course, the active ingredient of the present invention can be composed only of tea polyphenol, but a tea extract containing tea polyphenol at a high concentration can also be used as the active ingredient of the present invention. In addition, an ingredient already known to have a uric acid value lowering effect can be added to make it an active ingredient.
As the tea extract containing the above-mentioned tea polyphenol at a high concentration, for example, the above tea is extracted with water, hot water or hot water, preferably 90 to 100 ° C. in hot water of 40 ° C. to 100 ° C. In order to increase the tea catechin content by purification means such as resin adsorption, ultrafiltration / reverse osmosis filtration, or partition extraction using ethyl acetate, etc. The tea extract obtained by refining can be used, or the tea extract obtained by concentrating or drying these tea extracts. In this case, the concentration of tea polyphenol is 25 to 97%, preferably 30 to 90%. As a specific example of this tea extract, green tea is subjected to hot water extraction treatment, and the extract is dried to make tea catechin. Green tea extract (trade name: Teaflan 30A, manufactured by ITO EN) with a concentration of about 30% or green tea is extracted with hot water, and this extract is processed by the column method and dried to exclude components other than tea catechins. An example is a green tea extract (trade name: Tea Franc 90S manufactured by ITO EN) with a tea polyphenol concentration of about 85 to 95%.
[0013]
The uric acid level-lowering agent of the present invention can be used for various uses such as pharmaceuticals, quasi drugs, health foods and health drinks, food additives, feeds, feed additives, etc. It can be dried by freeze-drying or spray-drying, etc., and can be provided as a dry powder, or it can be prepared as a liquid, tablet, powder, granule, dragee, capsule, suspension, emulsion, ampoule, injection, or any other form Can also be provided.
When provided as a pharmaceutical product, for example, the active ingredient can be prepared by dissolving it in purified water or physiological saline as it is.
As a quasi-drug, it can be prepared by adding components that are usually blended into a quasi-drug, and this can be provided as a drinking form such as a bottled drink or a form such as a tablet, capsule or granule.
Examples of the food and drink include the active ingredients of the present invention, food ingredients (including fruits and jelly), milk ingredients, carbonic acid, excipients (including granulating agents), diluents, or further sweeteners, flavors, Sports drinks and fruit drinks by adding one or more selected from various proteins such as wheat flour, starch, sugar, fats and oils, carbohydrate raw materials, vitamins, minerals, other physiologically active ingredients, hormones, nutritional ingredients, etc. , Tea beverages, vegetable juices, milk beverages, alcoholic beverages, jelly beverages, carbonated beverages and other beverages, jelly, chewing gum, chocolate, ice cream, candy, biscuits and other sweets, snacks, bread, cakes and other starches Processed foods, fish paste products, livestock meat products, protein-based processed foods such as tofu and cheese, miso, soy sauce, dressings and other seasonings Other supplements, feed, can be provided as a variety of forms, such as pet food.
[0014]
The content of the active ingredient in the present invention varies depending on the use, but in the case of a pharmaceutical, it is preferably 0.001 to 1% by weight, particularly 0.01 to 0.5% by weight in terms of catechin dry weight. If it is a food or drink, it is preferably added in an amount of 0.001 to 1% by weight, particularly 0.01 to 0.5% by weight in terms of dry weight of catechin.
The amount of intake is 10 to 5000 mg per day in terms of dry weight of catechin, preferably about 100 to 1500 mg.
[0015]
(test)
A test beverage containing 230 mg of theafuran 90S (trade name, manufactured by ITO EN) per 190 mL of can, and adding a small amount of cyclodextrin, vitamin C and flavor to improve the taste was prepared. Theafuran 90S had a tea polyphenol content of 92% and a tea catechin content of 63% (of which EGCg was 50% and ECg was 13%). Moreover, since the test beverage is sterilized by retort, it is a mixed beverage containing a polymer or isomer of tea catechins.
[0016]
Seven males 20 years or older (hyperuricemia group) with serum uric acid level concentrations exceeding 7.0 mg / dL, which is the upper limit of serum uric acid levels, and serum uric acid levels are less than 6.5 mg / dL Nine males aged 20 years or older (normal uric acid level group) were subjects, and each subject took the test sample with meals three times a day for 8 weeks. Serum uric acid levels were measured at each time point after 4 weeks, 6 weeks and 8 weeks. FIG. 1 is a graph showing the average serum uric acid level (mg / dL) in the hyperuricemia group over time, and FIG. 2 shows the average serum uric acid level (mg / dL) in the normal uric acid level group over time. It is the graph shown in.
[0017]
As a result, the blood uric acid level significantly decreased in the hyperuricemia group in which the blood uric acid level exceeded 7.0 mg / dL. On the other hand, no significant change was observed in the normal uric acid level group with a blood uric acid level of less than 6.5 mg / dL. In any group, no side effects were observed in the subjects during the intake period, and there was no resistance during intake.
From this, it became clear that this test drink can be ingested safely and without difficulty, and can effectively lower the uric acid level particularly for those who have high serum uric acid levels.
[0018]
(Example 1)
The tablet as a uric acid level lowering agent was created with the following prescription.
[0019]
Tea extract (teafuran 90S or teafuran 30A) ... 120mg
Vitamin C ... 50mg
Emulsified oligosaccharide ... 90mg
Granulating agent 60mg
Crystalline cellulose ... 80mg
Reduced maltose starch syrup ... 90mg
Sucrose ... 100mg
Perfume ... appropriate amount [0020]
(Example 2)
A beverage as a food and drink having the effect of lowering the uric acid value with the following formulation was prepared.
[0021]
Tea extract (teafuran 90S or teafuran 30A) ... 150mg
Vitamin C ... 50mg
Fructose grape sugar: 10g
Water-soluble dietary fiber: 500mg
Fragrance ... Appropriate amount of ion-exchanged water ... Adjust to 100 mL [Brief description of the drawings]
FIG. 1 is a graph showing the mean serum uric acid level (mg / dL) of 7 patients with hyperuricemia over time.
FIG. 2 is a graph showing the mean serum uric acid level (mg / dL) of 9 normal uric acid level groups over time.

Claims (3)

血漿尿酸値が高値を示す者に対しては尿酸値を低下させ、血漿尿酸値が正常値を示す者に対しては尿酸値が略変動しない、茶カテキン類を有効成分として含有する尿酸値低下剤。Reduces uric acid levels for those with high plasma uric acid levels and decreases uric acid levels with tea catechins as active ingredients for those with normal plasma uric acid levels. Agent. 前記茶カテキン類は、フラバン-3-オールの基本構造を有する次の茶カテキン類すなわち(-)-エピカテキン、(-)-エピガロカテキン、(-)-エピカテキンガレート、(-)-エピガロカテキンガレート、(±)-カテキン、(-)-ガロカテキン、(-)-カテキンガレート、(-)-ガロカテキンガレート、これらいずれかの重合体、及びこれらのうちの二種類以上の共重合体からなる群から選ばれたいずれか或いは二種類以上の混合物である請求項1に記載の尿酸値低下剤。The tea catechins include the following tea catechins having the basic structure of flavan-3-ol: (−)-epicatechin, (−)-epigallocatechin, (−)-epicatechin gallate, (−)-epi Gallocatechin gallate, (±) -catechin, (-)-gallocatechin, (-)-catechin gallate, (-)-gallocatechin gallate, any of these polymers, and two or more types of these copolymers The uric acid level-lowering agent according to claim 1, which is any one selected from the group consisting of or a mixture of two or more. 前記茶カテキン類としてEGCgとECgの両方を含有し、これらが総カテキン量の50%以上である茶抽出物を0.001〜1重量%配合してなる、請求項1又は2に記載の尿酸値低下剤。The uric acid according to claim 1 or 2, comprising 0.001 to 1% by weight of a tea extract containing both EGCg and ECg as the tea catechins, which are 50% or more of the total catechin amount. Value reducing agent.
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