JP2010168399A - Pharmaceutical for controlling elevation of blood sugar - Google Patents
Pharmaceutical for controlling elevation of blood sugar Download PDFInfo
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- JP2010168399A JP2010168399A JP2010100544A JP2010100544A JP2010168399A JP 2010168399 A JP2010168399 A JP 2010168399A JP 2010100544 A JP2010100544 A JP 2010100544A JP 2010100544 A JP2010100544 A JP 2010100544A JP 2010168399 A JP2010168399 A JP 2010168399A
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本発明は、血糖の上昇を抑制するための薬剤に関するものである。 The present invention relates to a drug for suppressing an increase in blood sugar.
今日、欧米先進国を中心として糖尿病などの生活習慣病が蔓延しつつあり、我が国も例外ではなく、食環境の欧米化に伴う生活習慣病の急増が顕在化している。その結果、肥満症や高血糖症の人口が急激に増加している。 Today, lifestyle-related diseases such as diabetes are spreading in developed countries in Europe and the United States, and Japan is no exception, and the rapid increase in lifestyle-related diseases associated with the westernization of the food environment has become apparent. As a result, the population of obesity and hyperglycemia is increasing rapidly.
高血糖が持続すると、血管内蛋白との糖化反応等により、動脈硬化、腎障害、網膜症、その他の重篤な糖尿病合併症へとつながる。また、糖尿病によりインスリンに対する感受性が低下した状態では、高インスリン血症により、脂質代謝異常が起こり、高脂血症が誘発される。 If hyperglycemia persists, it leads to arteriosclerosis, nephropathy, retinopathy, and other serious diabetic complications due to glycation reaction with intravascular proteins. Further, in a state where the sensitivity to insulin is decreased due to diabetes, hyperinsulinemia causes abnormal lipid metabolism and hyperlipidemia is induced.
これらの症状を緩和するための薬剤として、抗高脂血症作用および血糖値降下作用を示す数多くの化合物が今日までに報告されている(特許文献1などを参照されたい)。
しかるに、従来の糖尿病の治療効果が高い医療用医薬品の多くは化学的手法により合成されたものであり、その性質上、副作用が強い上に多剤服用による重複毒性の問題などが存在するため、長期間に亘る使用には適していない。 However, many of the conventional ethical drugs with high therapeutic effects for diabetes are synthesized by chemical methods, and because of their nature, there are strong side effects and the problem of multiple toxicity due to multiple doses. Not suitable for long-term use.
本発明は、このような従来の問題点を解消すべく案出されたものであり、その主な目的は、生活習慣病の中核を占める糖尿病の進行を安全に抑制することのできる薬剤を提供することにある。 The present invention has been devised to solve such conventional problems, and its main purpose is to provide a drug that can safely suppress the progression of diabetes, which is the core of lifestyle-related diseases. There is to do.
このような目的を果たすために、本発明においては、血糖の上昇を抑制するための薬剤として、牡蠣の少なくとも肉から熱水抽出などで取り出したエキスの含有物を用いるものとした。 In order to achieve such an object, in the present invention, as an agent for suppressing an increase in blood sugar, an extract containing at least oyster meat extracted by hot water extraction or the like is used.
このような本発明のエキスによれば、血糖の上昇を抑制する作用が得られるので、糖尿病に関連する疾患の進行を副作用を伴わずに抑制する上に大きな効果が得られる。 According to such an extract of the present invention, an effect of suppressing an increase in blood sugar can be obtained, and thus a great effect can be obtained in suppressing the progression of a disease related to diabetes without causing side effects.
以下に本発明について詳細に説明する。 The present invention is described in detail below.
本発明が提供する血糖上昇を伴う疾患に対する抑制作用を示す薬剤は、牡蠣から抽出したエキスを含有するものである。この牡蠣のエキスは、ベッコウガキ、マガキ、イタボガキなどの牡蠣属(Ostea gigas Thunb.)を、貝殻もろともに、或いは肉のみを取り出し、それを生のまま、或いは乾燥させた後に粉砕したものを原料とし、熱水抽出などの公知の抽出法を利用して取り出したものである。 The medicine which shows the inhibitory action with respect to the disease accompanying the increase in blood glucose provided by this invention contains the extract extracted from the oyster. This oyster extract is made from oyster genus (Ostea gigas Thunb.) Such as beetle oysters, oysters, lobsters, etc., with shells or only meat taken and raw or dried and then ground. And extracted using a known extraction method such as hot water extraction.
この抽出液を濃縮処理することにより、液体製剤を得ることができる。さらにこの濃縮液を噴霧乾燥もしくは凍結乾燥することにより、粉末製剤を得ることができる。 A liquid preparation can be obtained by concentrating the extract. Furthermore, a powder formulation can be obtained by spray-drying or freeze-drying this concentrated solution.
なお、牡蠣からのエキスの抽出方法及び精製方法については公知の方法を適用し得るので、ここではこれ以上の説明は省略する。 In addition, since the well-known method can be applied about the extraction method and extraction method of the extract from an oyster, further description is abbreviate | omitted here.
本発明による薬剤を医薬品として用いる際には、予防や治療に有効な量の牡蠣のエキスが製薬学的に許容できる担体または希釈剤と共に製剤化されると良い。その他にも、結合剤、吸収促進剤、滑沢剤、乳化剤、界面活性剤、酸化防止剤、防腐剤、着色剤、香料、甘味料などを添加しても良い。 When the drug according to the present invention is used as a pharmaceutical, an effective amount of oyster extract for prevention or treatment is preferably formulated together with a pharmaceutically acceptable carrier or diluent. In addition, a binder, an absorption accelerator, a lubricant, an emulsifier, a surfactant, an antioxidant, an antiseptic, a colorant, a fragrance, a sweetener, and the like may be added.
このような医薬製剤において、有効成分である牡蠣エキスの担体成分に対する配合割合は、1.0〜80.0重量%の範囲であり、特に5.0〜50.0重量%の範囲が好ましい。 In such a pharmaceutical preparation, the blending ratio of the oyster extract, which is an active ingredient, to the carrier component is in the range of 1.0 to 80.0% by weight, particularly preferably in the range of 5.0 to 50.0% by weight.
医薬製剤の剤形としては、顆粒剤、細粒剤、錠剤、丸剤、カプセル剤、噴霧剤、溶液剤、懸濁液剤、軟膏剤、ゲル剤、ペースト剤、クリーム剤などを挙げることができ、その投与経路としては、経口、静脈内、筋肉内、皮下、関節腔など、種々の投与経路を挙げることができる。また、有効成分の投与量および投与頻度は、病状、年齢、性別、投与経路などに応じて適宜に変更することができる。 Pharmaceutical dosage forms include granules, fine granules, tablets, pills, capsules, sprays, solutions, suspensions, ointments, gels, pastes, creams, etc. As the administration route, various administration routes such as oral, intravenous, intramuscular, subcutaneous and articular cavity can be mentioned. Further, the dose and frequency of administration of the active ingredient can be appropriately changed according to the disease state, age, sex, administration route and the like.
本発明による牡蠣のエキスは、薬剤に添加しても良い。この薬剤は、生体機能の調節など、生理面での働き(3次機能)を十分に発揮するように製造された食品を指し、例えば、「健康・栄養食品アドバイザリー・スタッフ・テキストブック」(平成15年7月30日、第一出版株式会社発行、第92、93頁)に記載されている通り、一般の食品はもとより、いわゆる健康食品とは一線を画する別のものとして定義されたものである。このような牡蠣エキスを含有する薬剤を適時摂取することにより、糖尿病の発症および進行を安全に抑制することができる。 You may add the oyster extract by this invention to a chemical | medical agent. This drug refers to foods that are produced so as to fully exert physiological functions (tertiary functions) such as regulation of biological functions. For example, “Health and Nutrition Food Advisory Staff Textbook” (Heisei Heisei) As defined in July 30, 2015, published by Daiichi Shuppan Co., Ltd., pages 92, 93), it is defined as something different from so-called health foods as well as general foods. It is. The onset and progression of diabetes can be safely suppressed by taking a drug containing such an oyster extract in a timely manner.
次に本発明による牡蠣エキスを含有した薬剤の血糖上昇抑制効果の検証結果について説明する。 Next, the verification result of the blood glucose rise inhibitory effect of the chemical | medical agent containing the oyster extract by this invention is demonstrated.
7週齢、雌性の自然発症高血糖(KKAy)マウスに対し、予備飼育期間(一週間)中は固形飼料を与えつつ血糖測定および状態観察を行い、空腹時の血糖の平均値がほぼ一定となるように10匹ずつ2群に群分けした。そして各群の一方(Control群)に対して溶剤の懸濁液を、他方(被験物質投与群)に対して被験物質としての牡蠣エキスの懸濁液を、それぞれ1日1回28日間連続的に強制経口投与し、投与期間中の血糖値の変動を、投与開始時、7日目、14日目、21日目に、測定日の午前10時に眼窩静脈叢から採血して空腹時血糖値を測定した。 7 weeks old, female spontaneously hyperglycemic (KKAy) mice were subjected to blood glucose measurement and state observation while feeding solid chow during the preliminary breeding period (one week), and the average value of fasting blood glucose was almost constant. In this way, 10 animals were divided into 2 groups. Then, a suspension of solvent for one group (Control group) of each group and a suspension of oyster extract as a test substance for the other (test substance administration group) were each once continuously for 28 days. The blood glucose level during the administration period was collected from the orbital venous plexus at 10 am on the measurement day on the 7th, 14th and 21st days, and the fasting blood glucose level was measured. Was measured.
なお、被験物質の体重比投与量は、200mg/kg相当量とした。試験結果は平均値±標準偏差で表し、有意差検定はstudent's-tを用いた。 In addition, the body weight ratio dose of the test substance was 200 mg / kg equivalent. Test results are expressed as mean ± standard deviation, and student's-t was used for the significance test.
その結果、図1に示す通り、溶剤の懸濁液のみを与えた、つまり被験物質を与えなかった陽性対照群の空腹時血糖値は、試験開始時が140.01mg/dlであったのに対し、21日後には、230.10mg/dlと糖尿病血糖値を呈し、しかも更に上昇傾向にあった。 As a result, as shown in FIG. 1, the fasting blood glucose level of the positive control group that received only the suspension of the solvent, that is, the test substance was 140.01 mg / dl at the start of the test. On the other hand, after 21 days, diabetic blood glucose level of 230.10 mg / dl was exhibited, and it was further increased.
これに対し、被験物質を投与した群の空腹時血糖値は、投与後21日目に210.30mg/dlと陽性対照群に対して有為な(約−20mg/dl)血糖上昇抑制効果を示し、その後も顕著に血糖上昇が抑制された。
In contrast, the fasting blood glucose level of the group administered with the test substance was 210.30 mg / dl on
以上により、牡蠣の主に肉から抽出したエキスを含有した懸濁液には、自然発症高血糖(KKAy)マウスに対する血糖上昇抑制効果のあることが実証された。 As described above, it was demonstrated that a suspension containing an extract of oysters mainly extracted from meat has an effect of suppressing an increase in blood glucose in spontaneously hyperglycemic (KKAy) mice.
本発明による薬剤は、インスリン依存性糖尿病、およびインスリン非依存性糖尿病からなる群から選択される血糖上昇を伴う疾患などの予防、改善、或いは治療に用いることができる。 The drug according to the present invention can be used for prevention, amelioration, or treatment of a disease accompanied by an increase in blood glucose selected from the group consisting of insulin-dependent diabetes and non-insulin-dependent diabetes.
Claims (1)
牡蠣の肉を貝殻と共に、生のまま、あるいは乾燥した後に粉砕したものを原料として用いて抽出して得たエキスを含有することを特徴とする血糖上昇を抑制するための薬剤。
A drug for suppressing an increase in blood sugar,
A drug for suppressing an increase in blood glucose, characterized by containing an extract obtained by extracting raw materials of oyster meat together with shells, raw or dried and ground.
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JP2010100544A JP2010168399A (en) | 2010-04-26 | 2010-04-26 | Pharmaceutical for controlling elevation of blood sugar |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013192515A (en) * | 2012-03-21 | 2013-09-30 | Lion Corp | Oyster extract |
WO2016009594A1 (en) * | 2014-07-15 | 2016-01-21 | 株式会社渡辺オイスター研究所 | Hepatoprotective agent, glucose metabolism-improving agent, and anti-obesity agent |
JP2018118910A (en) * | 2017-01-23 | 2018-08-02 | 株式会社渡辺オイスター研究所 | Oyster extract having sleep improvement action based sleep efficiency deterioration suppressing action, sleep difficulty improvement action, and sleep related matters for quality of life (hereinafter referred to as qol), and having action for suppressing increase in awakening mid-sleep by maintaining total arousal frequency |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS552654A (en) * | 1978-06-22 | 1980-01-10 | Kaihoo Kk | Insulin secretion accelerator |
JP2001352946A (en) * | 2000-06-09 | 2001-12-25 | Fusae Nishihara | Oyster extracted essence comprising low-molecular fraction at high concentration and method for producing the same |
JP2004067557A (en) * | 2002-08-05 | 2004-03-04 | Sonoko:Kk | Medicine or functional food for controlling itch |
JP2005015414A (en) * | 2003-06-27 | 2005-01-20 | Sonoko:Kk | Medicine or functional food for suppressing/relieving symptom of allergic disease |
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2010
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS552654A (en) * | 1978-06-22 | 1980-01-10 | Kaihoo Kk | Insulin secretion accelerator |
JP2001352946A (en) * | 2000-06-09 | 2001-12-25 | Fusae Nishihara | Oyster extracted essence comprising low-molecular fraction at high concentration and method for producing the same |
JP2004067557A (en) * | 2002-08-05 | 2004-03-04 | Sonoko:Kk | Medicine or functional food for controlling itch |
JP2005015414A (en) * | 2003-06-27 | 2005-01-20 | Sonoko:Kk | Medicine or functional food for suppressing/relieving symptom of allergic disease |
Non-Patent Citations (1)
Title |
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JPN6008048444; 太田隆男: 'カキ(Crassostrea gigas)中の血小板凝集抑制物質' 愛知医科大学医学会雑誌 Vol.18, No.6, 1990, p.589-604 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013192515A (en) * | 2012-03-21 | 2013-09-30 | Lion Corp | Oyster extract |
WO2016009594A1 (en) * | 2014-07-15 | 2016-01-21 | 株式会社渡辺オイスター研究所 | Hepatoprotective agent, glucose metabolism-improving agent, and anti-obesity agent |
JPWO2016009594A1 (en) * | 2014-07-15 | 2017-07-27 | 株式会社渡辺オイスター研究所 | Liver protective agent, glucose metabolism improving agent and anti-obesity agent |
JP2018118910A (en) * | 2017-01-23 | 2018-08-02 | 株式会社渡辺オイスター研究所 | Oyster extract having sleep improvement action based sleep efficiency deterioration suppressing action, sleep difficulty improvement action, and sleep related matters for quality of life (hereinafter referred to as qol), and having action for suppressing increase in awakening mid-sleep by maintaining total arousal frequency |
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