JP2001145471A - Food material derived from purple sweet potato and having blood circulation-improving effect - Google Patents

Food material derived from purple sweet potato and having blood circulation-improving effect

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Publication number
JP2001145471A
JP2001145471A JP32914699A JP32914699A JP2001145471A JP 2001145471 A JP2001145471 A JP 2001145471A JP 32914699 A JP32914699 A JP 32914699A JP 32914699 A JP32914699 A JP 32914699A JP 2001145471 A JP2001145471 A JP 2001145471A
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JP
Japan
Prior art keywords
extract
food
blood circulation
improving
blood flow
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
Application number
JP32914699A
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Japanese (ja)
Other versions
JP3587359B2 (en
Inventor
Akitomo Kume
晃智 粂
Yasuko Sawai
保子 澤井
Hajime Sumio
肇 角尾
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Meiji Dairies Corp
Original Assignee
Meiji Milk Products Co Ltd
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Filing date
Publication date
Application filed by Meiji Milk Products Co Ltd filed Critical Meiji Milk Products Co Ltd
Priority to JP32914699A priority Critical patent/JP3587359B2/en
Publication of JP2001145471A publication Critical patent/JP2001145471A/en
Application granted granted Critical
Publication of JP3587359B2 publication Critical patent/JP3587359B2/en
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Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain a blood circulation improver containing as active ingredient an aqueous solvent extract derived from purple sweet potatoes, and to obtain a food (material) containing an effective amount of the active ingredient. SOLUTION: The blood circulation improver and food (material) are obtained based on having found that purple sweet potatoes have the rat life-lengthening effect for rats under hypoxic conditions, cerebral blood flow (oxygen supply quantity)-increasing effect and blood vessel-relaxing effect as well as antioxidative ability having been known so far.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明が属する技術分野】[Field of the Invention]

【従来の技術】今日、経済状態や食環境の変化に伴っ
て、疾病構造も大きく変化し、低栄養時代に多発してい
た感染症が減少し、脳血管障害、癌、虚血性疾患、糖尿
病、アレルギー疾患などが増加している。その結果、
「医食同源」のコンセプトから、食事成分によるこれら
疾病の予防や改善に関心が高まっており、健康食品ブー
ムが引き起こされることとなった。しかしながら、な
お、健康食品への期待は、食品メーカーはもとより、医
薬品、化粧品などの周辺産業にも広がりをみせている。
その中で、健康食品の購買動向は、「疾病改善型」にシ
フトしており、癌、血流改善、視力改善などがテーマと
なっている。そこで、様々な機能性食品素材が脚光を浴
びている。
2. Description of the Related Art Today, with the changes in economic conditions and dietary environment, the disease structure has changed drastically, infectious diseases frequently occurring in the age of malnutrition have decreased, cerebrovascular disorders, cancer, ischemic diseases, diabetes , Allergic diseases and the like are increasing. as a result,
The concept of “medical and dietary sources” has raised interest in preventing and ameliorating these diseases by dietary components, and has led to a health food boom. However, expectations for health foods are spreading not only to food manufacturers but also to peripheral industries such as pharmaceuticals and cosmetics.
Among them, the purchasing trend of health foods has shifted to “disease improvement type”, and themes are cancer, improvement of blood flow, and improvement of vision. Therefore, various functional food materials have been spotlighted.

【0002】その内の1つにムラサキサツマイモが挙げ
られる。ムラサキサツマイモの新用途開発による高付加
価値に関する研究が、九州農業試験場をはじめとする農
水省の各研究機関で実施されている。その結果、ムラサ
キサツマイモは、肝機能改善作用、抗変異原性、アンギ
オテンシンI変換酵素阻害活性(吉元誠, 山川理, 須田
郁夫, 食品と開発. 健康産業新聞社, 33: 15-17, 199
8)等の生理機能を有することが明らかとなっている。
しかしながら、これまでに、ムラサキサツマイモの抽出
物の血液循環改善作用に関する報告はなされていない。
[0002] One of them is purple potato. Research on high value-added by developing new uses of purple potatoes is being conducted at Kyushu Agricultural Experiment Station and other research institutions of the Ministry of Agriculture and Fisheries. As a result, purple potato has liver function improving effect, anti-mutagenicity, angiotensin I converting enzyme inhibitory activity (Masayoshi Yoshimoto, Osamu Yamakawa, Ikuo Suda, Food and Development. Kenko Sangyo Shimbun, 33: 15-17, 199
It has been revealed that it has physiological functions such as 8).
However, there has been no report on the blood circulation improving effect of the extract of purple potato.

【0003】[0003]

【発明が解決しようとする課題】本発明は、ムラサキサ
ツマイモ由来の水性溶媒抽出物、該抽出物を有効成分と
して含有する血液循環改善剤、血液循環を改善する食品
製造への該抽出物の有効量の使用、及び該抽出物の有効
量を含有する食品を提供することを課題とする。
DISCLOSURE OF THE INVENTION The present invention relates to an aqueous solvent extract derived from purple potato, a blood circulation improving agent containing the extract as an active ingredient, and an effect of the extract for producing a food for improving blood circulation. It is an object to use a quantity and to provide a food containing an effective amount of the extract.

【0004】[0004]

【課題を解決するための手段】本発明者らは、上記課題
を解決するために種々研究した結果、ムラサキサツマイ
モが、これまで知られていた抗酸化能に加え、低酸素下
におけるラットの延命効果を有することを見いだし、そ
の作用機作の解明を試み、血管弛緩作用により脳血流量
増加を確認した。つまり低酸素下において、脳血流量が
増加し脳に酸素供給量とエネルギー源であるグルコース
供給量を増加させることにより延命効果を示しているこ
とを明らかにし、本発明を完成するに至った。
Means for Solving the Problems The present inventors have conducted various studies in order to solve the above-mentioned problems, and as a result, it has been found that, in addition to the antioxidant ability known so far, the survival of rats under hypoxia was improved. We found that it had an effect, tried to elucidate its mechanism of action, and confirmed that cerebral blood flow increased due to vasorelaxation. In other words, it has been clarified that the cerebral blood flow rate increases under hypoxia, and that the life extension effect is exhibited by increasing the oxygen supply amount and the glucose supply amount to the brain, thereby completing the present invention.

【0005】すなわち、本発明は、(1)ムラサキサツ
マイモ由来の水性溶媒抽出物を有効成分として含有する
血液循環改善剤、(2)上記抽出物を有効成分として含
有する脳代謝機能改善剤、(3)水性溶媒が水、又は含
水アルコールである(1)の抽出物、(4)水、又は含
水アルコールがpH約5以下の弱酸性である(3)の抽
出物、(5)血液循環を改善する機能を有する食品の製
造のための(1)の有効量の抽出物の使用、(6)脳代
謝を改善する機能を有する食品の製造のための(1)の
有効量の抽出物の使用、(7)食品が、健康食品、機能
性食品、又は特定保健用食品である(5)、又は(6)
の抽出物の使用、(8)(1)の抽出物の有効量を含有
する血液循環改善用食品、(9)(1)の抽出物の有効
量を含有する脳代謝改善用食品、及び(10) 健康食
品、機能性食品、又は特定保健用食品である(8)又は
(9)の食品、からなる。
That is, the present invention provides (1) a blood circulation improving agent containing an aqueous solvent extract derived from purple potato as an active ingredient, (2) a brain metabolic function improving agent containing the above extract as an active ingredient, 3) The extract of (1) in which the aqueous solvent is water or hydroalcohol, (4) the extract of (3) in which water or hydroalcohol is weakly acidic with a pH of about 5 or less, and (5) the blood circulation. Use of an effective amount of the extract of (1) for producing a food having an improving function, (6) Use of an effective amount of the extract of (1) for producing a food having a function of improving brain metabolism. Use, (7) the food is a health food, a functional food, or a food for specified health use (5) or (6)
Use of the extract of (8), a food for improving blood circulation containing an effective amount of the extract of (1), (9) a food for improving brain metabolism containing an effective amount of the extract of (1), and ( 10) The food of (8) or (9), which is a health food, a functional food, or a food for specified health use.

【0006】[0006]

【発明の実施の形態】本発明に用いる原料のムラサキサ
ツマイモは、例えば、アヤムラサキ、山川紫、種子島在
来、頴娃紫、知覧紫、ナカムラサキ等を含むが、これら
の中で、アヤムラサキが好ましい。アヤムラサキは、在
来種の山川紫に知覧系を交配して九州109号を選抜
し、九州109号に低糖多収のサツマヒカリを交配して
得られた品種で1995年に農林登録された(吉元誠,山川
理,須田郁夫: 食品と開発.33(8):15-17, 1998)。
BEST MODE FOR CARRYING OUT THE INVENTION The raw purple potato used as a raw material in the present invention includes, for example, Ayamurasaki, Yamakawa purple, Tanegashima native, Ei purple, Chiran purple, Nakamurasaki, etc. Among them, Ayamurasaki is preferred. Ayamurasaki is a breed obtained by crossing the native species Yamakawa purple with Chiran-kei and selecting Kyushu 109, and crossing Kyushu 109 with low-sugar high-yield Satsuma Hikari, which was registered in Agriculture and Forestry in 1995 (Yoshimoto). Makoto, Osamu Yamakawa, Ikuo Suda: Food and Development. 33 (8): 15-17, 1998).

【0007】これらのムラサキサツマイモは、生のま
ま、或いは凍結したものを、抽出効率を上げるために、
少切片に細断或いは粉末とする。本発明のムラサキサツ
マイモの抽出物は、水抽出、水性溶媒抽出、超臨界抽
出、ミセル抽出等を用いて得ることが可能である。水抽
出、或いは水性溶媒抽出法を用いる場合について説明す
る。抽出溶媒は、水又は水性アルコールを用いる。アル
コールとしては、例えば、メタノール、エタノール、プ
ロパノール、等が挙げられるが、これらの中ではエタノ
ールが好ましい。水性アルコールを用いる場合、水とア
ルコールの混合比率は特に限定されないが、アルコール
が30〜70重量%が好ましい。水性溶媒のpHは、中
性でもよいが、好ましくはpH約5以下の弱酸性に設定
する。さらに好ましくは、pH4〜3である。pHの調
整剤は公知であり、例えば、クエン酸、酒石酸、リンゴ
酸等の有機酸、或いは、塩酸、硫酸、リン酸などの無機
酸が挙げられる。溶媒の量は、抽出原料1重量部に対し
て、2〜20重量部、好ましくは、5〜10重量部であ
る。抽出温度は、室温でもよいが、抽出効率を上げるた
めには加温する。その場合は、デンプンが糊化する温度
(64℃)より低い温度に設定する。好ましくは50〜
60℃である。抽出時間は、室温の場合1昼夜、加温し
た場合2〜10時間を目安とする。
[0007] These purple potatoes are used to improve the extraction efficiency of raw or frozen potatoes.
Cut into small pieces or powder. The extract of purple potatoes of the present invention can be obtained using water extraction, aqueous solvent extraction, supercritical extraction, micellar extraction and the like. The case of using water extraction or aqueous solvent extraction will be described. Water or aqueous alcohol is used as the extraction solvent. Examples of the alcohol include methanol, ethanol, and propanol, and among them, ethanol is preferable. When aqueous alcohol is used, the mixing ratio of water and alcohol is not particularly limited, but the alcohol is preferably 30 to 70% by weight. The pH of the aqueous solvent may be neutral, but is preferably set to a weakly acidic pH of about 5 or less. More preferably, the pH is 4 to 3. pH adjusters are known and include, for example, organic acids such as citric acid, tartaric acid and malic acid, and inorganic acids such as hydrochloric acid, sulfuric acid and phosphoric acid. The amount of the solvent is 2 to 20 parts by weight, preferably 5 to 10 parts by weight, based on 1 part by weight of the extraction raw material. The extraction temperature may be room temperature, but it is heated to increase the extraction efficiency. In that case, the temperature is set lower than the temperature (64 ° C.) at which the starch gelatinizes. Preferably 50 to
60 ° C. The extraction time is approximately one day and night at room temperature, and 2 to 10 hours when heated.

【0008】抽出操作を停止した後、残さを取り除き、
抽出液を回収する。残さの除去は、濾過、遠心分離等の
公知の固液分離手段を適宜組み合わせて用いる。抽出液
はそのままで機能性食品素材の添加物として用いること
ができるが、水性アルコールを抽出溶媒として用いた場
合は、アルコール部分を留去するのが望ましい。該抽出
液は、濃縮又は乾燥し、軟エキス又は乾燥粉末としても
よい。これらの一連の操作は公知(例えば、不和 亮,
上杉利幸, “医薬品の開発11”,仲井由宣編,p287-310,
廣川書店,平成元年; 市尾義昌“続医薬品の開発15”,
原田正敏編,p123-146,廣川書店,平成4年)であり、当業
者であれば、これらの公知技術を適宜修正して、軟エキ
スや乾燥粉末を得ることが可能である。
After stopping the extraction operation, the residue is removed,
Collect the extract. For the removal of the residue, known solid-liquid separation means such as filtration and centrifugation are appropriately used in combination. The extract can be used as it is as an additive to the functional food material, but when aqueous alcohol is used as the extraction solvent, it is desirable to distill off the alcohol portion. The extract may be concentrated or dried to a soft extract or a dry powder. These series of operations are known (for example, Ryo Fuka,
Toshiyuki Uesugi, “Development of Pharmaceuticals 11”, edited by Yoshinobu Nakai, p287-310,
Hirokawa Shoten, 1989; Yoshimasa Ichio “Development of Continued Pharmaceuticals 15”,
Harada Masatoshi, ed., P123-146, Hirokawa Shoten, 1992), and those skilled in the art can appropriately modify these known techniques to obtain soft extracts and dry powders.

【0009】また、さらに、吸着樹脂や膜等を用いて、
上記抽出液中のタンパク質、糖質、脂質等を除去しても
よい。吸着樹脂としては、無極性の多孔質重合樹脂が好
ましく、該樹脂を充填したカラムを用いる。該樹脂とし
ては、スチレン系樹脂、アクリル酸系樹脂が挙げられ、
例えば、HP-20、HP-50、SP-206、SP-8
25(三菱化学(株)製)等や、アンバーライトXAD
-4(有機化学工業(株)製)等を用いることができ
る。通液は、例えば、SV=1〜10の範囲で行う。
Further, using an adsorbing resin or a membrane,
Proteins, carbohydrates, lipids and the like in the extract may be removed. As the adsorption resin, a nonpolar porous polymer resin is preferable, and a column filled with the resin is used. Examples of the resin include a styrene-based resin and an acrylic acid-based resin,
For example, HP-20, HP-50, SP-206, SP-8
25 (manufactured by Mitsubishi Chemical Corporation) and Amberlite XAD
-4 (manufactured by Organic Chemical Industry Co., Ltd.) or the like can be used. The liquid is passed, for example, in the range of SV = 1 to 10.

【0010】このようにして得られた本発明の抽出物
は、抽出液そのまま(残さを含んでいてもよい)、その
濃縮液、エキス、ペースト、或いは乾燥粉末等を含む。
本発明の抽出物は、後述する試験例に示すように、血液
循環の促進、酸素供給量の増加等の生理活性を有する。
結果として脳代謝機能改善作用が期待できる。
[0010] The extract of the present invention thus obtained includes an extract as it is (may contain a residue), a concentrate thereof, an extract, a paste, a dry powder and the like.
The extract of the present invention has physiological activities such as promotion of blood circulation and increase in oxygen supply, as shown in Test Examples described later.
As a result, an effect of improving brain metabolic function can be expected.

【0011】本発明の抽出物(エキスの場合)を血液循
環改善剤として経口投与する場合は、成人に対しては、
エキスの固形分として、1日当たり50〜2000mg
相当を投与する。ここで、エキスの固形分とは、エキス
の溶媒を蒸発させた後の残さをいう。また、該エキスを
単独で、或いは食品衛生上許容される配合物を混合し
て、栄養補助食品、健康食品、機能性食品、或いは特定
保健用食品に加工することもできる。例えば、安定化
剤、保存剤、着色料、香料ビタミン等の配合物を、上記
エキスに適宜添加して混合し、常法により錠剤(タブレ
ット)状、粒状、顆粒状、粉末状、カプセル状、液状、
クリーム状、飲料等の食品に適した形態にて使用するこ
とができる。
When the extract of the present invention (in the case of an extract) is orally administered as a blood circulation improving agent,
50 to 2000 mg per day as solid content of extract
Administer the equivalent. Here, the solid content of the extract refers to the residue after evaporating the solvent of the extract. The extract may be used alone or in combination with a food-hygienically acceptable compound to be processed into a dietary supplement, a health food, a functional food, or a food for specified health use. For example, compounds such as stabilizers, preservatives, coloring agents, and flavoring vitamins are appropriately added to the above extract and mixed, and tablets (tablets), granules, granules, powders, capsules, Liquid,
It can be used in a form suitable for foods such as creams and beverages.

【0012】さらにまた、食品素材、例えば、ローヤル
ゼリー、クロレラ、スピルリナ、人参、核酸、霊芝、ア
ガリクス・プラゼイ・ムリル、マイタケ、菌糸体(冬虫
夏草培養物等)、キチン・キトサン、レシチン、アロ
エ、イチョウ葉、ウコン、ブルーベリー、ノコギリヤ
シ、大豆イソフラボン、紅麹、等との併用で、これらの
素材の有する本来の生理作用に、さらにプラスした本発
明の抽出物の相乗又は相加効果が期待できる。本発明の
抽出物の原料であるムラサキサツマイモは、すでに食品
として長く使用された実績があり、原料としての安全性
の面でも全く問題はない。その抽出物も毒性試験の結
果、安全な機能性食材として使用できる。
Furthermore, food materials, such as royal jelly, chlorella, spirulina, ginseng, nucleic acid, reishi, agaricus prasei muril, maitake, mycelium (corticides, etc.), chitin chitosan, lecithin, aloe, ginkgo When used in combination with leaves, turmeric, blueberries, saw palmetto, soy isoflavones, red yeast rice, etc., a synergistic or additive effect of the extract of the present invention which is further added to the original physiological action of these materials can be expected. The purple potato, which is a raw material of the extract of the present invention, has already been used as a food for a long time, and there is no problem in terms of safety as a raw material. The extract can also be used as a safe functional food as a result of the toxicity test.

【0013】[0013]

【実施例】以下、試験例を挙げて本発明を具体的に説明
するが、本発明はこれらの具体例に限定されるものでは
ない。以下の試験例に用いたエキスは、アヤムラサキか
ら抽出したエキス(日農化学工業株式会社製、lot.9041
4)である。
EXAMPLES Hereinafter, the present invention will be described specifically with reference to test examples, but the present invention is not limited to these specific examples. The extract used in the following test examples was an extract extracted from Ayamurasaki (Nichino Chemical Co., Ltd., lot.9041).
4).

【0014】[試験例1] 反復経口投与毒性試験 Crj:CD(SD)IGSラット(雄4週齢)に対して、アヤムラ
サキエキス(以下「エキス」という)を、毎日1回、最
高800mg/kgで、連続3週間強制経口投与した。
その結果、一般症状、体重、摂餌量、摂水量、臓器重
量、血球、血液生化学的検査、及び臓器病理所見におい
て、毒性学的な異常は認められなかった。
Test Example 1 Toxicity test for repeated oral administration Ayamurasaki extract (hereinafter referred to as “extract”) was administered to Crj: CD (SD) IGS rats (male 4 weeks old) once daily at a maximum of 800 mg / kg. And gavage administration for 3 consecutive weeks.
As a result, no toxicological abnormalities were observed in general symptoms, body weight, food consumption, water consumption, organ weight, blood cells, blood biochemical tests, and organ pathological findings.

【0015】[試験例2] 低酸素条件下での延命効果 脳は代謝活性の極めて旺盛な組織で、生体の酸素消費量
の20%を消費するといわれている。脳出血、脳梗塞等
による虚血状態が誘起され、脳が低酸素状態に陥ると、
その代謝機能は急激に低下し、生命現象の維持が困難と
なる。すなわち、脳への酸素供給は、生命維持、さらに
は、思考など「人が人たる」に重要である能力維持にと
って不可欠である。イチョウ葉エキスの脳代謝機能亢進
の評価として、低酸素条件下での生存時間の延長効果を
検討した報告(L.Karcher et.al.,Naunyn-Schmiedeber
g's Arch Pharmacol. 327: 31-35, 1984)がある。この
報告にしたがって、以下の投与経路によりエキスの脳に
対する代謝機能改善効果を評価した。
Test Example 2 Life Prolonging Effect Under Hypoxic Conditions The brain is a tissue with a very high metabolic activity, and is said to consume 20% of the oxygen consumption of a living body. Cerebral hemorrhage, ischemic state due to cerebral infarction, etc. is induced, and the brain falls into a hypoxic state,
Its metabolic function declines rapidly, making it difficult to maintain vital phenomena. In other words, the supply of oxygen to the brain is indispensable for sustaining life and maintaining abilities such as thinking, which are important for "human beings". In order to evaluate the enhancement of cerebral metabolic function of ginkgo biloba leaf extract, a report examining the effect of prolonging survival time under hypoxic conditions (L. Karcher et.al., Naunyn-Schmiedeber
g's Arch Pharmacol. 327: 31-35, 1984). According to this report, the effect of improving the metabolic function of the extract on the brain was evaluated by the following administration routes.

【0016】1) 腹腔内投与 SDIGS系ラット(雄8週齢)を体重に基づいて群分けし
た(1群8匹)。エキスは注射用蒸留水に溶解後、エキ
スとして、10.5mg/kg、52.5mg/kg、
105mg/kg、及び210mg/kgを腹腔内に投
与した。対照群には注射用蒸留水を腹腔内投与した。試
験群及び対照群の投与容量は10ml/kgとした。腹腔内投
与後30分経過した時点で、2匹ずつ順次減圧デシケータ
ーに入れ減圧した(180mmHg)。生存時間の判定
は、180mmHg到達時点から呼吸停止時点までの時
間とした。なお、呼吸停止は外観から観察して判断し
た。統計処理は、Dunnettの多重比較により、対照群と
試験群との同時比較を行った。結果を第1図に示す。図
1から、エキスは、用量依存的に延命効果作用を有する
ことが明らかである。生体は、生命維持に対する緊急時
ににおいて、一番に脳機能を維持する方向に反応するこ
とが知られている。本発明のエキスは、酸素欠乏下で、
脳機能の維持に極めて優れた作用を有することが本試験
で明らかにされた。
1) Intraperitoneal administration SDIGS rats (male, 8 weeks old) were divided into groups based on body weight (8 rats per group). The extract was dissolved in distilled water for injection, and then extracted as 10.5 mg / kg, 52.5 mg / kg,
105 mg / kg and 210 mg / kg were administered intraperitoneally. The control group received intraperitoneal distilled water for injection. The administration volume of the test group and the control group was 10 ml / kg. At 30 minutes after the intraperitoneal administration, two mice were sequentially placed in a vacuum desiccator to reduce the pressure (180 mmHg). The determination of the survival time was defined as the time from the point at which 180 mmHg was reached to the point at which respiration was stopped. The respiratory arrest was determined by observing the appearance. For statistical processing, a control group and a test group were simultaneously compared by Dunnett's multiple comparison. The results are shown in FIG. From FIG. 1, it is apparent that the extract has a life-prolonging effect effect in a dose-dependent manner. It is known that a living body responds to maintaining the brain function most in an emergency for maintaining life. The extract of the present invention, under oxygen deficiency,
The present study revealed that the compound has an extremely excellent effect on maintaining brain function.

【0017】2) 経口投与 エキスの腹腔内投与により、本発明のエキスは脳への酸
素供給を効率化する作用があることが明らかにされた
が、果たして経口摂取でも同様の効果を示すかが、該エ
キスを機能性食品素材として開発する場合には重要であ
る。そこで以下の実験を行った。SDIGS系ラット(雄7
週齢)を体重に基づいて群分けした(1群5匹)。試験
前日に一晩絶食した。エキスは注射用蒸留水に溶解後、
210mg/10ml/kgを経口投与した。対照群に
は注射用蒸留水を経口投与した。試験群及び対照群の投
与容量は10ml/kgとした。経口投与後50分経過し
た時点で、2匹ずつ順次減圧デシケーターに入れ減圧し
た(180mmHg)。生存時間の判定は試験例1と同
様であった。結果を第2図に示す。図2から、エキスの
経口投与は、腹腔内投与と同様に、低酸素下で延命効果
を有することが明らかである。このエキスの有効成分は
現在明らかでないが、少なくとも有効性を示す成分は、
消化管からの吸収が十分に行われていることを示してい
る。すなわち、本発明のエキスは機能性食品素材として
有用である。なお、対照群での生存時間が腹腔内での試
験に比べ短いのは、絶食の影響とラットの週齢によると
考えられる。
2) Oral administration The intraperitoneal administration of the extract has revealed that the extract of the present invention has the effect of increasing the oxygen supply to the brain. This is important when developing the extract as a functional food material. Therefore, the following experiment was performed. SDIGS rats (male 7
Weeks) were grouped based on body weight (5 animals per group). Fasted overnight the day before the test. After the extract is dissolved in distilled water for injection,
210 mg / 10 ml / kg was orally administered. The control group was orally administered distilled water for injection. The administration volume of the test group and the control group was 10 ml / kg. When 50 minutes had passed after oral administration, two animals were placed in a vacuum desiccator sequentially and the pressure was reduced (180 mmHg). The determination of the survival time was the same as in Test Example 1. The results are shown in FIG. From FIG. 2, it is clear that oral administration of the extract has a prolonged life under hypoxia similarly to intraperitoneal administration. The active ingredients of this extract are currently not clear, but at least the ingredients that show efficacy are
This indicates that absorption from the digestive tract is sufficient. That is, the extract of the present invention is useful as a functional food material. The shorter survival time in the control group compared to the intraperitoneal test is considered to be due to the effect of fasting and the age of the rats.

【0018】[試験例3] 脳血流量増加作用 低酸素下での延命効果を考えた場合、その要因の一つと
して、脳組織への酸素及びエネルギー源であるグルコー
スの供給の促進が考えられる。そこで、脳血流量に対す
る効果を評価した。 SDIGS系ラット(雄6〜
7週齢)を用いた。対照群は3匹、試験群は11匹用い
た。試験前日に一晩絶食した。ウレタン麻酔(1.4g/kg
i.p.)したラットにポリエチレンチューブ(内径0.7
6mm、外径1.22mm)を口から胃底部に到達する
まで挿入した。頭皮を切開し冷却生理食塩水で冷やしな
がら、ミニドリル(日本理化学器械株式会社「NRK ミニ
ター M-11-BS型」)で頭頂骨を剥離し、3〜4mm四方
の小窓を開けた。露出した硬膜上に血流量測定装置(プ
ライムテック株式会社「LASERFLO BPM2」)をセットし
た。血流量が安定するまで20分〜40分間観察した。
血流量が安定した時点で、エキスをポリエチレンチュー
ブを通して経口投与した。エキスは注射用蒸留水に溶解
後、210mg/kg投与した。対照群には注射用蒸留
水を用いた。投与容量は両群とも5ml/kgとした。
エキス投与時間を0分とし、60分間継続して血流量
(100g組織あたり1分間に流れる血液量)を計測し
た。結果を第3図に示す。図3では、代表例を示した。
対照群では血流量に経時的変化は認められないが(図3
(1))、エキス経口投与群では、投与後30分頃から血流
が漸次増加し続ける例(図3(2))、30分付近および5
0〜60分付近に血流量の増加が認められる例(図3
(3))、50〜60分付近に血流量の増加が認められる例
(図3(4))など、幾つかのパターンが認められた。この
血流量の増加する時間は、エキスの体内動態と密接に関
与していると考えられる。これに関しては現在検証中で
あるが、いずれにしても、これらの結果は、エキスの経
口投与により、脳血流量が増加し、結果、酸素供給量を
高め脳代謝機能を改善する効果を有することを示すもの
である。
[Test Example 3] Increase in cerebral blood flow When considering the effect of prolonging life under hypoxia, one of the factors may be to promote the supply of oxygen and glucose as an energy source to brain tissue. . Thus, the effect on cerebral blood flow was evaluated. SDIGS rats (male 6 ~
7 weeks old) was used. Three control groups and 11 test groups were used. Fasted overnight the day before the test. Urethane anesthesia (1.4g / kg
ip) rats into polyethylene tubing (0.7 mm id)
6 mm, outer diameter 1.22 mm) was inserted from the mouth until it reached the fundus. While the scalp was incised and cooled with cooling physiological saline, the parietal bone was peeled off with a mini drill (Nippon Riken Kikai Co., Ltd. “NRK Minitar M-11-BS type”), and a small window of 3 to 4 mm square was opened. A blood flow measuring device ("LASERFLO BPM2") was set on the exposed dura. Observation was performed for 20 to 40 minutes until the blood flow was stabilized.
When blood flow stabilized, the extract was orally administered through a polyethylene tube. The extract was dissolved in distilled water for injection and administered at 210 mg / kg. For the control group, distilled water for injection was used. The administration volume was 5 ml / kg for both groups.
With the extract administration time set to 0 minute, the blood flow rate (the amount of blood flowing per minute per 100 g tissue) was measured for 60 minutes. The results are shown in FIG. FIG. 3 shows a representative example.
In the control group, there was no change in blood flow over time (FIG. 3
(1)) In the group to which the extract was orally administered, the blood flow gradually increased from around 30 minutes after administration (FIG. 3 (2)), around 30 minutes and 5 minutes.
Example in which blood flow increases around 0 to 60 minutes (FIG. 3)
(3)), several patterns were observed, such as an example in which the blood flow increased around 50 to 60 minutes (FIG. 3 (4)). It is considered that the time during which the blood flow increases is closely related to the pharmacokinetics of the extract. In any case, these results indicate that oral administration of the extract has the effect of increasing cerebral blood flow and consequently increasing oxygen supply and improving cerebral metabolic function. It is shown.

【0019】[試験例4] 耳介血流量増加作用 SDIGS系ラット(雄7週齢)3匹を用いて、末梢の血流
改善効果を調べた。ウレタン麻酔(1.4g/kgi.
p)したラットの耳介に血流量測定装置(プライムテッ
ク株式会社「LASERFLO BPM2」)をセットした。20分
〜40分間観察して、血流量が安定しているのを確認し
た上で、エキスを腹腔内投与した。エキスは注射用蒸留
水に溶解後、20mg/kgを投与した。対照群には注
射用蒸留水を用いた。試験群及び対照群の投与容量は1
0ml/kgとした。60分間継続して血流量(100
g組織あたり1分間に流れる血液量)を計測した。代表
的な結果を第4図に示す。
[Test Example 4] Increase of auricular blood flow The effect of improving peripheral blood flow was examined using three SDIGS rats (male, 7 weeks old). Urethane anesthesia (1.4 g / kg i.
p) A blood flow measuring device ("LASERFLO BPM2") was set on the pinna of the rat. After observing for 20 to 40 minutes to confirm that the blood flow rate was stable, the extract was administered intraperitoneally. After the extract was dissolved in distilled water for injection, 20 mg / kg was administered. For the control group, distilled water for injection was used. The administration volume of the test group and the control group is 1
It was 0 ml / kg. Blood flow (100
The amount of blood flowing per minute per g tissue) was measured. Representative results are shown in FIG.

【0020】エキス投与15分から25分にかけ耳介で
の血流量は最大となった。経口投与(脳血流量試験)に
比べ血流量の増加が早い時間で起こるのは、腹腔内投与
によるものであり、消化管からの吸収を必要としないた
めと考えられる。エキスの腹腔内投与により、末梢組織
においても血流改善作用を有することを示すものであ
り、本発明のエキスが、冷え性、肩こり等の末梢血流不
良に有効であることが期待される。
From 15 minutes to 25 minutes after the administration of the extract, the blood flow at the pinna became maximum. It is considered that the reason why the blood flow increases earlier than in the oral administration (cerebral blood flow test) is due to the intraperitoneal administration and does not require absorption from the digestive tract. This indicates that the intraperitoneal administration of the extract has an effect of improving blood flow even in peripheral tissues, and it is expected that the extract of the present invention is effective for poor peripheral blood flow such as coldness and stiff shoulders.

【0021】[試験例5] 血管弛緩作用 血流量増加作用の要因を調べるために以下の試験を行っ
た。SDIGS系ラット(雄8〜9週齢)を用いた。ラット
の後頭部を強打後、放血致死させ、大動脈の弓部から横
隔膜までを摘出した。Krebs-Henseleit液中で、血管に
付着した脂肪や結合組織を取り除き、螺旋状に切開した
後等分割して、2本の血管標本を作成した。この標本に
0.5gの負荷をかけ、95%O2+5%CO2を通気し
た、Krebs-Henseleit液を満たしたマグヌス管(10m
l、37℃)中で1時間平衡化した。α作動薬であるフ
ェニレフリン(最終濃度1×10-7M)にて収縮を惹起
後、エキスを最終濃度が0.1mg/ml、0.3mg
/ml、1.1mg/ml、及び3.2mg/mlにな
るように累積的に添加した。弛緩の変化をトランスデュ
ーサを用いて測定した。結果を図5に示す。
[Test Example 5] Vasodilatory action The following test was conducted to examine the factors of the blood flow increasing action. SDIGS rats (male 8-9 weeks old) were used. After banging the occipital region of the rat, the animal was sacrificed by exsanguination, and the aorta was excised from the arch to the diaphragm. In a Krebs-Henseleit solution, fats and connective tissues attached to blood vessels were removed, cut in a spiral shape, and equally divided to prepare two blood vessel specimens. A 0.5 g load was applied to the specimen, and a Magnus tube filled with Krebs-Henseleit solution (10 m in length) aerated with 95% O 2 + 5% CO 2 was used.
1, 37 ° C.) for 1 hour. After inducing contraction by phenylephrine (final concentration 1 × 10 −7 M) which is an α agonist, the extract was added to a final concentration of 0.1 mg / ml and 0.3 mg.
/ Ml, 1.1 mg / ml, and 3.2 mg / ml. The change in relaxation was measured using a transducer. FIG. 5 shows the results.

【0022】図5から、本発明のエキスは、α作動薬に
よる血管の収縮を抑制することが明らかである。すなわ
ち、本発明のエキスは、血管弛緩作用を有し、この作用
が血流量増加の要因の一つとして考えられる。なお、こ
の血管弛緩作用は内皮細胞依存性である結果が得られて
いる。上記一連の試験結果は、本発明のムラサキサツマ
イモ由来の水性溶媒抽出物が血管の機能改善、酸素供給
量の増加等の生理活性に基づく脳機能改善作用を有する
ことを示すものである。
From FIG. 5, it is clear that the extract of the present invention suppresses the contraction of blood vessels due to the α agonist. That is, the extract of the present invention has a vasorelaxant action, and this action is considered as one of the factors for increasing blood flow. In addition, it has been obtained that the vasorelaxation effect is dependent on endothelial cells. The above series of test results show that the aqueous solvent extract derived from the purple potato of the present invention has a cerebral function improving action based on physiological activities such as improvement of blood vessel function and increase in oxygen supply.

【0023】[0023]

【発明の効果】本発明のムラサキサツマイモ由来の水性
溶媒抽出物は、優れた血液循環改善作用を有する。した
がって、該抽出物、或いは該抽出物を含有する食品を日
常の食生活の中で摂取することにより、血液循環が改善
され、末梢血循環不全に関連する各種の疾患、例えば、
冷え性、手足のしびれ、糖尿病、更年期障害、リウマ
チ、神経痛、静脈瘤、脳機能代謝不全等の予防及び改善
に有用である。
Industrial Applicability The aqueous solvent extract derived from purple potato of the present invention has an excellent blood circulation improving effect. Therefore, by ingesting the extract, or a food containing the extract in a daily diet, blood circulation is improved, various diseases related to peripheral blood circulation failure, for example,
It is useful for prevention and improvement of coldness, numbness of limbs, diabetes, menopause, rheumatism, neuralgia, varicose veins, cerebral dysfunction, and the like.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 ラットに対するアヤムラサキエキスの腹腔内
投与後の、低酸素下での、ラットの延命効果を示す図で
ある。SDIGS系ラット(雄8週齢)に対し、アヤムラサ
キエキス、10.5mg/kg、 52.5mg/kg、 105mg/kg、及び21
0mg/kgを腹腔内に投与後、減圧デシケーターに入れ、18
0mmHg到達時点から呼吸停止時点までの時間を計測し
た。バーは平均値±標準偏差を示す。p<0.05
(*)。
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a graph showing the survival effect of rats under hypoxia after intraperitoneal administration of Ayamurasaki extract to rats. Ayamurasaki extract, 10.5 mg / kg, 52.5 mg / kg, 105 mg / kg, and 21 mg / kg for SDIGS rats (male, 8 weeks old)
After intraperitoneal administration of 0 mg / kg, put in a vacuum desiccator,
The time from the point of reaching 0 mmHg to the point of stopping breathing was measured. Bars indicate mean ± standard deviation. p <0.05
(*).

【図2】 同じくラットに対するアヤムラサキエキスの
経口投与後の、低酸素下での、ラットの延命効果を示す
図である。SDIGS系ラット(雄7週齢)は試験前日に一
晩絶食した。アヤムラサキエキス、210mg/kgを経口投与
後、減圧デシケーターに入れ、180mmHg到達時点から呼
吸停止時点までの時間を計測した。バーは平均値±標準
偏差を示す。p<0.01(**)。
FIG. 2 is a graph showing the survival effect of rats under hypoxia after oral administration of Ayamurasaki extract to rats. SDIGS rats (male, 7 weeks old) were fasted overnight the day before the test. After oral administration of Ayamurasaki extract, 210 mg / kg, it was placed in a vacuum desiccator, and the time from the point of reaching 180 mmHg to the point of respiratory arrest was measured. Bars indicate mean ± standard deviation. p <0.01 (**).

【図3】 ラットに対するアヤムラサキエキスの経口投
与後の脳の血流量増加作用を示す図である。SDIGS系ラ
ット(雄6〜7週齢)は試験前日に一晩絶食した。ポリ
エチレンチューブ経由でアヤムラサキエキス経口投与
(エキス投与時間を0分とする)し、脳の硬膜上の血流
量(100g組織あたり1分間に流れる血液量)を60分
間継続して計測した。
FIG. 3 is a graph showing the effect of increasing the blood flow in the brain after oral administration of Ayamurasaki extract to rats. SDIGS rats (males 6-7 weeks old) fasted overnight the day before the test. Ayamurasaki extract was orally administered through a polyethylene tube (the extract administration time was set to 0 minute), and the blood flow on the dura of the brain (the amount of blood flowing per minute per 100 g of tissue) was continuously measured for 60 minutes.

【図4】 ラットに対するアヤムラサキエキスの腹腔内
投与後の耳介血流量増加作用を示す図である。SDIGS系
ラット(雄7週齢)の耳介に血流量測定装置(プライム
テック株式会社「LASERFLO BPM2」)をセットし、アヤ
ムラサキエキスを腹腔内投与した。60分間継続して血流
量(100g組織あたり1分間に流れる血液量)を計測し
た。
FIG. 4 is a graph showing the effect of increasing auricular blood flow after intraperitoneal administration of Ayamurasaki extract to rats. A blood flow measuring device (LASERFLO BPM2) was set on the pinna of an SDIGS rat (male, 7 weeks old), and Ayamurasaki extract was intraperitoneally administered. The blood flow rate (the amount of blood flowing per minute per 100 g tissue) was measured for 60 minutes.

【図5】 血管弛緩作用を示す図である。SDIGS系ラッ
ト(雄8〜9週齢)の大動脈の血管標本に対し、α作動
薬であるフェニレフリン(最終濃度1×10-7M)にて収縮
を惹起後、アヤムラサキエキスを累積的に添加したマグ
ヌス管中での大動脈標本の弛緩の変化を、トランスデュ
ーサを用いて測定した。
FIG. 5 is a view showing a blood vessel relaxing action. After inducing a contraction with phenylephrine (final concentration: 1 × 10 −7 M) to an aortic vascular specimen of an SDIGS rat (male 8 to 9 weeks old), Ayamurasaki extract was cumulatively added. The change in relaxation of the aortic specimen in the Magnus tube was measured using a transducer.

───────────────────────────────────────────────────── 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) A61P 25/28 A61P 25/28 Fターム(参考) 4B016 LC07 LG06 LP02 4B018 MD53 ME14 MF01 4C088 AB12 AC12 BA09 BA10 CA04 CA23 NA14 ZA15 ZA36 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) A61P 25/28 A61P 25/28 F-term (Reference) 4B016 LC07 LG06 LP02 4B018 MD53 ME14 MF01 4C088 AB12 AC12 BA09 BA10 CA04 CA23 NA14 ZA15 ZA36

Claims (10)

【特許請求の範囲】[Claims] 【請求項1】 ムラサキサツマイモ由来の水性溶媒抽出
物を有効成分として含有する血液循環改善剤。
1. A blood circulation improving agent comprising an aqueous solvent extract derived from purple potato as an active ingredient.
【請求項2】 上記抽出物を有効成分として含有する脳
代謝機能改善剤。
2. A cerebral metabolic function improving agent comprising the above extract as an active ingredient.
【請求項3】 水性溶媒が水、又は含水アルコールであ
る請求項1記載の抽出物。
3. The extract according to claim 1, wherein the aqueous solvent is water or a hydroalcoholic.
【請求項4】 水、又は含水アルコールがpH約5以下
の弱酸性である請求項3記載の抽出物。
4. The extract according to claim 3, wherein the water or the hydrous alcohol is weakly acidic with a pH of about 5 or less.
【請求項5】 血液循環を改善する機能を有する食品の
製造のための請求項1記載の有効量の抽出物の使用。
5. Use of an effective amount of the extract according to claim 1 for the production of a food product having the function of improving blood circulation.
【請求項6】 脳代謝を改善する機能を有する食品の製
造のための請求項1記載の有効量の抽出物の使用。
6. Use of an effective amount of the extract according to claim 1, for the manufacture of a food having a function of improving brain metabolism.
【請求項7】 食品が、健康食品、機能性食品、又は特
定保健用食品である請求項5、又は6に記載の抽出物の
使用。
7. The use of the extract according to claim 5, wherein the food is a health food, a functional food, or a food for specified health use.
【請求項8】 請求項1記載の抽出物の有効量を含有す
る血液循環改善用食品。
8. A food for improving blood circulation, comprising an effective amount of the extract according to claim 1.
【請求項9】 請求項1記載の抽出物の有効量を含有す
る脳代謝改善用食品。
A food for improving cerebral metabolism, comprising an effective amount of the extract according to claim 1.
【請求項10】 健康食品、機能性食品、又は特定保健
用食品である請求項8又は9に記載の食品。
10. The food according to claim 8, which is a health food, a functional food, or a food for specified health use.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004277411A (en) * 2003-02-19 2004-10-07 Toyo Shinyaku:Kk Dried powder of sweet potato starch lees and composition containing the same
CN103330201A (en) * 2013-06-24 2013-10-02 哈尔滨医科大学 Health-care food capable of delaying female climacteric syndrome and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004277411A (en) * 2003-02-19 2004-10-07 Toyo Shinyaku:Kk Dried powder of sweet potato starch lees and composition containing the same
CN103330201A (en) * 2013-06-24 2013-10-02 哈尔滨医科大学 Health-care food capable of delaying female climacteric syndrome and preparation method thereof

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