JP5253746B2 - Composition for prevention and / or treatment of lifestyle-related diseases - Google Patents
Composition for prevention and / or treatment of lifestyle-related diseases Download PDFInfo
- Publication number
- JP5253746B2 JP5253746B2 JP2007061432A JP2007061432A JP5253746B2 JP 5253746 B2 JP5253746 B2 JP 5253746B2 JP 2007061432 A JP2007061432 A JP 2007061432A JP 2007061432 A JP2007061432 A JP 2007061432A JP 5253746 B2 JP5253746 B2 JP 5253746B2
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- JP
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- Prior art keywords
- magnesium
- composition
- pantethine
- group
- serum
- 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.)
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- DJWYOLJPSHDSAL-ROUUACIJSA-N pantethine Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSSCCNC(=O)CCNC(=O)[C@H](O)C(C)(C)CO DJWYOLJPSHDSAL-ROUUACIJSA-N 0.000 claims description 28
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Description
本発明は、生活習慣病の予防および／または治療用の新規な組成物、より詳しくは、高脂血症予防および／または治療用組成物に関する。 The present invention relates to a novel composition for preventing and / or treating lifestyle-related diseases, and more particularly to a composition for preventing and / or treating hyperlipidemia.
パンテチンは、血清総コレステロール低下作用、血清中性脂肪低下作用、血清ＨＤＬコレステロール増加作用等が知られ、パントテン酸欠乏症の予防および治療、消耗性疾患、甲状腺機能亢進症、妊産婦、授乳婦などのパントテン酸の需要が増大し、食事からの摂取が不十分な際の補給、高脂血症、弛緩性便秘、ストレプトマイシンおよびカナマイシンによる副作用の予防および治療、急・慢性湿疹、血液疾患の血小板数および出血傾向の改善のうち、パントテン酸の欠乏または代謝障害が関与すると推定される場合に用いられている（非特許文献１参照）。
酸化マグネシウムや水酸化マグネシウムなどのマグネシウム化合物の多くは、制酸作用、瀉下作用が知られ、制酸薬や瀉下薬として用いられている（非特許文献２および３参照）。
Pantethine is known to lower serum total cholesterol, lower serum triglyceride, increase serum HDL cholesterol, etc., and to prevent and treat pantothenic acid deficiency, debilitating diseases, hyperthyroidism, pregnant women, and lactating women. Supplementation when demand for acid increases and insufficient intake from the diet, prevention and treatment of side effects caused by hyperlipidemia, flaccid constipation, streptomycin and kanamycin, acute / chronic eczema, platelet count and bleeding in blood disorders It is used when it is estimated that pantothenic acid deficiency or metabolic disorder is involved in the improvement of the trend (see Non-Patent Document 1).
Many magnesium compounds such as magnesium oxide and magnesium hydroxide are known to have antacid action and axillary action, and are used as antacids and axides (see Non-Patent Documents 2 and 3).
本発明は、新規な生活習慣病の予防および／または治療用組成物、より具体的には血清脂質代謝改善用組成物を提供するものである。 The present invention provides a novel composition for preventing and / or treating lifestyle-related diseases, more specifically, a composition for improving serum lipid metabolism.
本発明者らは、鋭意研究を行った結果、パンテチン類とマグネシウム化合物を併用すると、優れた血清総コレステロール低下作用、血清中性脂肪低下作用、血清ｎｏｎＨＤＬコレステロール低下作用を示すことを見出し、パンテチン類およびマグネシウム化合物を含有する組成物が、生活習慣病の予防および／または治療用組成物として有用であることを新たに見出し、本発明を完成した。 As a result of intensive studies, the present inventors have found that when pantetins and a magnesium compound are used in combination, they exhibit excellent serum total cholesterol lowering action, serum neutral fat lowering action, and serum nonHDL cholesterol lowering action. The inventors have newly found that a composition containing a magnesium compound is useful as a composition for preventing and / or treating lifestyle-related diseases, and completed the present invention.
すなわち、本発明はパンテチン類およびマグネシウム化合物を含有する組成物に関するものであり、以下の発明に関する。
（１）パンテチン類、およびマグネシウム化合物を含有する組成物。
（２）１日当たりの投与（服用）量として、パンテチン類を１〜２０００ｍｇ、およびマグネシウム化合物を１００〜１５０００ｍｇ含有する組成物。
（３）パンテチン類がパンテチンである上記（１）または（２）記載の組成物。
（４）マグネシウム化合物が、塩化マグネシウム、酸化マグネシウム、水酸化マグネシウム、硫酸マグネシウム、炭酸マグネシウム、ケイ酸マグネシウムおよびメタケイ酸アルミン酸マグネシウムからなる群より選ばれる１または２以上のである上記（１）〜（３）のいずれか１つに記載の組成物。
（５）パンテチン、および酸化マグネシウムまたは水酸化マグネシウムを含有する組成物。
（６）医薬用である上記（１）〜（５）のいずれか１つに記載の組成物。
（７）食品用である上記（１）〜（５）のいずれか１つに記載の組成物。
（８）生活習慣病の予防および／または治療用である上記（１）〜（５）のいずれか１つに記載の組成物。
（９）血清脂質代謝改善用である上記（１）〜（５）のいずれか１つに記載の組成物。
（１０）剤形が経口投与製剤である上記（１）〜（９）のいずれか１つに記載の組成物。
（１１）剤形が錠剤、カプセル剤、散剤、細粒剤、液剤、トローチ剤、ゼリー剤、舐剤またはシロップ剤である上記（１）〜（９）のいずれか１つに記載の組成物。
That is, the present invention relates to a composition containing panthetins and a magnesium compound, and relates to the following inventions.
(1) A composition containing panthetins and a magnesium compound.
(2) A composition containing 1 to 2000 mg of pantethine and 100 to 15000 mg of a magnesium compound as the amount of administration (dose) per day.
(3) The composition according to (1) or (2) above, wherein the pantethine is pantethine.
(4) The above (1) to (1), wherein the magnesium compound is one or more selected from the group consisting of magnesium chloride, magnesium oxide, magnesium hydroxide, magnesium sulfate, magnesium carbonate, magnesium silicate and magnesium aluminate metasilicate. The composition according to any one of 3).
(5) A composition containing pantethine and magnesium oxide or magnesium hydroxide.
(6) The composition according to any one of (1) to (5), wherein the composition is for pharmaceutical use.
(7) The composition according to any one of (1) to (5), which is for food.
(8) The composition according to any one of (1) to (5) above, which is used for prevention and / or treatment of lifestyle-related diseases.
(9) The composition according to any one of (1) to (5), which is used for improving serum lipid metabolism.
(10) The composition according to any one of (1) to (9) above, wherein the dosage form is an orally administered preparation.
(11) The composition according to any one of (1) to (9) above, wherein the dosage form is a tablet, capsule, powder, fine granule, solution, troche, jelly, electuary or syrup .
後記実施例から明らかなように、パンテチン類とマグネシウム化合物を併用すると、優れた血清総コレステロール低下作用、血清中性脂肪低下作用、血清ｎｏｎＨＤＬコレステロール低下作用、すなわち血清脂質代謝改善作用を示した。したがって、パンテチン類およびマグネシウム化合物を含有する組成物は、生活習慣病の予防および／または治療用組成物として有用であり、このものは医薬または食品として利用することができ、有用なものである。 As will be apparent from the examples described later, when pantethines and a magnesium compound were used in combination, an excellent serum total cholesterol lowering effect, serum neutral fat lowering effect, serum nonHDL cholesterol lowering effect, that is, serum lipid metabolism improving effect was exhibited. Therefore, a composition containing panthetins and a magnesium compound is useful as a composition for preventing and / or treating lifestyle-related diseases, and it can be used as a medicine or food and is useful.
本発明にかかるパンテチン類は、公知の化合物であり、その入手方法としては、市販品を用いてもよく、また公知の方法に基づき製造することもできる。パンテチン類としては、パントテニルアルコール、パントテニルエチルエーテル、アセチルパントテニルエチルエーテル、ベンゾイルパントテニルエチルエーテル、ジカルボエトキシパントテン酸エチルエステル、パンテテイン、パンテチン、ホスホパンテテイン、パントテン酸、パントテン酸の塩などを挙げることができる。パントテン酸の塩としては、塩酸塩、硝酸塩、硫酸塩等の鉱酸塩、ナトリウム塩、カリウム塩、カルシウム塩、マグネシウム塩等のアルカリ金属塩、アルカリ土類金属塩等を挙げることができる。本発明において、パンテチン類としては、パンテチン、パントテン酸、パントテン酸の塩が好ましく、パントテン酸の塩としては、パントテン酸カルシウムが好ましい。 The pantethine according to the present invention is a known compound, and as a method for obtaining it, a commercially available product may be used, or it can be produced based on a known method. Panthetins include pantothenyl alcohol, pantothenyl ethyl ether, acetyl pantothenyl ethyl ether, benzoyl pantothenyl ethyl ether, dicarboethoxy pantothenic acid ethyl ester, pantethein, panthetin, phosphopantethein, pantothenic acid, pantothenic acid salt, etc. Can be mentioned. Examples of the salt of pantothenic acid include mineral salts such as hydrochloride, nitrate and sulfate, alkali metal salts such as sodium salt, potassium salt, calcium salt and magnesium salt, and alkaline earth metal salt. In the present invention, pantethins, pantothenic acid, and pantothenic acid salts are preferred as pantetins, and calcium pantothenate is preferred as the pantothenic acid salt.
本発明にかかるマグネシウム化合物は、公知の化合物であり、その入手方法としては、市販品を用いてもよく、また公知の方法に基づき製造することもできる。マグネシウム化合物としては、塩化マグネシウム、酸化マグネシウム、水酸化マグネシウム、硫酸マグネシウム、炭酸マグネシウム、ケイ酸マグネシウムやメタケイ酸アルミン酸マグネシウムなどを挙げることができる。本発明において、マグネシウム化合物としては、酸化マグネシウム、水酸化マグネシウムが好ましい。 The magnesium compound according to the present invention is a known compound, and as a method for obtaining it, a commercially available product may be used, or it can be produced based on a known method. Examples of the magnesium compound include magnesium chloride, magnesium oxide, magnesium hydroxide, magnesium sulfate, magnesium carbonate, magnesium silicate and magnesium aluminate metasilicate. In the present invention, the magnesium compound is preferably magnesium oxide or magnesium hydroxide.
本発明の組成物には、本発明にかかるパンテチン類およびマグネシウム化合物以外に、さらに以下に示す成分を配合してもよい。配合可能な成分としては、プラバスタチンナトリウム、シンバスタチン、アトルバスタチンカルシウム水和物などのＨＭＧ−ＣｏＡ還元酵素阻害剤、ベザフィブラート、クロフィブラート、シンフィブラート、イコサペント酸エチル、ポリエンホスファチジルイコリン、デキストラン硫酸ナトリウム、γ−オリザノール、ニコモール、ニセリトロール、クリノフィブラート、コレスチラミン、エラスターゼＥＳ、メリナミド、プロブコールやＤＰＡ（ドコサペンタエン酸）、ＤＨＡ（ドコサヘキサエン酸）、ＥＰＡ（エイコサペンタエン酸）、γ−リノレン酸、リノール酸、異性化リノール酸などの脂肪酸類、デキストリン、ポリデキストロース、アルギン酸、アルギン酸ナトリウム、キチン、キトサン、セルロース、ヘミセルロース、リグニン、マンナン、カルボキシメチルセルロース、カラギナンなどの食物繊維類、リコペン、アスタキサンチン、α−カロテン、β−カロテン、γ−カロテン、ルテイン、ゼアキサンチン、クリプトキサンチンなどのカロチノイド類、コンドロイチン硫酸、コンドロイチン硫酸ナトリウム、フコイダンなどのムコ多糖、レシチン、ホスファチジルコリン、ホスファチジルイノシトールなどのリン脂質、大豆タンパク質、タウリン、メチオニン、アルギニン、シテインなどのタンパク・アミノ酸、ビール酵母、紅麹などの菌・酵母、ヘスペリジン、ナリンゲニン、ルチン、ケルセチン、プロアントシアニジン、カテキン、ガロタンニン、ダイゼイン、ゲニスチンなどのポリフェノール類、アスコルビン酸、ニコチン酸、ニコチン酸アミド、葉酸、トコトリエノール、トコフェロール、リボフラビン、ピリドキシンなどのビタミン類、Ｌ−カルニチン、ｄｌ−塩化カルニチン、酒石酸水素コリン、イノシトール、コエンザイムＱ１０などのビタミン類似成分、イノシトールヘキサニコチネート、ヘプロニカート、ニコチン酸トコフェロールなどのビタミン誘導体、プラセンタエキスなどの動物由来成分、スピルリナ、ニンニク、月見草油、ブルーベリー、イチョウ葉、ショウキョウ、セイヨウサンザシ、カシュウ、トチュウ、シゴカ、人参、クコシ、ウコン、レイシ、田七人参、プランタゴ オバタなどのハーブ・生薬およびこれらの抽出物等を挙げることができるが、上記のもののみに限定されるべきものではない。これらの成分は、単一成分を配合してもよく、２種以上のものを組み合わせて配合してもよい。 In addition to the pantethines and magnesium compounds according to the present invention, the following components may be further blended in the composition of the present invention. Ingredients that can be added include HMG-CoA reductase inhibitors such as pravastatin sodium, simvastatin, atorvastatin calcium hydrate, bezafibrate, clofibrate, simfibrate, ethyl icosapentate, polyenephosphatidylcholine, dextran sulfate sodium, γ- Oryzanol, nicomol, niceritrol, clinofibrate, cholestyramine, elastase ES, melinamide, probucol, DPA (docosapentaenoic acid), DHA (docosahexaenoic acid), EPA (eicosapentaenoic acid), γ-linolenic acid, linoleic acid, isomerism Fatty acids such as linoleic acid, dextrin, polydextrose, alginic acid, sodium alginate, chitin, chitosan, cellulose, hemicellulose, ligni Dietary fibers such as chloroquine, mannan, carboxymethylcellulose, carrageenan, lycopene, astaxanthin, α-carotene, β-carotene, γ-carotene, lutein, zeaxanthin, cryptoxanthine and other carotenoids, chondroitin sulfate, chondroitin sulfate sodium, fucoidan, etc. Phospholipids such as mucopolysaccharide, lecithin, phosphatidylcholine, phosphatidylinositol, proteins and amino acids such as soy protein, taurine, methionine, arginine, cytein, fungi and yeast such as brewer's yeast, red yeast rice, hesperidin, naringenin, rutin, quercetin, Polyphenols such as proanthocyanidins, catechins, gallotannins, daidzein, genistin, ascorbic acid, nicotinic acid, nicotinamide, folic acid, toco Rienoru, vitamins tocopherol, riboflavin, etc. pyridoxine, L- carnitine, dl-carnitine chloride, choline bitartrate, inositol, vitamin similar components such as coenzyme Q 10, inositol hexanicotinate, Hepuronikato, vitamin derivatives such as tocopherol nicotinate , Animal ingredients such as placenta extract, herbs such as spirulina, garlic, evening primrose oil, blueberry, ginkgo biloba, ginger, hawthorn, kashi, eucommia, staghorn, carrot, kokushi, turmeric, litchi, ginseng, plantago obata -Herbal medicines and extracts thereof can be mentioned, but should not be limited to the above. These components may be blended as a single component or in combination of two or more.
本発明の組成物は、経口的、非経口的に投与することができるが、経口的に投与することが好ましい。経口的に投与する製剤としては、錠剤、カプセル剤、散剤、細粒剤、液剤、トローチ剤、ゼリー剤、舐剤、シロップ剤等を挙げることができる。本発明の組成物は、医薬、飲料や固形物などの食品として用いることができる。 The composition of the present invention can be administered orally or parenterally, but is preferably administered orally. Examples of the preparation to be administered orally include tablets, capsules, powders, fine granules, solutions, troches, jellies, electuaries and syrups. The composition of this invention can be used as foodstuffs, such as a pharmaceutical, a drink, and a solid substance.
製剤化は、公知の製剤技術により行うことができ、製剤中には適当な製剤添加物を加えることができる。製剤添加物は、本発明の効果を損なわない範囲で適宜加えればよい。製剤添加物としては、賦形剤、結合剤、崩壊剤、流動化剤、乳化剤、安定化剤等を挙げることができる。 Formulation can be performed by known formulation techniques, and appropriate formulation additives can be added to the formulation. What is necessary is just to add a formulation additive suitably in the range which does not impair the effect of this invention. Examples of the formulation additive include an excipient, a binder, a disintegrant, a fluidizer, an emulsifier, and a stabilizer.
本発明の組成物における、パンテチン類、およびマグネシウム化合物の配合比は、パンテチン類：マグネシウム化合物が１：０．０１〜１：１００が好ましく、１：０．１〜１：１０がさらに好ましい。 The compounding ratio of panthetins and magnesium compounds in the composition of the present invention is preferably 1: 0.01 to 1: 100, more preferably 1: 0.1 to 1:10 for panthetines: magnesium compounds.
本発明の組成物の投与（配合）量は、性別、年齢、症状、投与方法、投与回数、投与時期等により適宜検討を行い、適当な投与（配合）量を決めればよい。例えば、経口投与の場合、パンテチン類については、１日当たり１〜２０００ｍｇ投与（配合）することが好ましく、５〜１０００ｍｇ投与（配合）することがさらに好ましい。マグネシウム化合物については、１日当たり１００〜１５０００ｍｇ投与（配合）することが好ましく、４００〜２０００ｍｇ投与（配合）することがさらに好ましい。 The administration (formulation) amount of the composition of the present invention may be appropriately determined according to sex, age, symptoms, administration method, number of administrations, administration timing, etc., and an appropriate administration (composition) amount may be determined. For example, in the case of oral administration, pantetins are preferably administered (mixed) at 1 to 2000 mg per day, and more preferably 5 to 1000 mg (mixed). The magnesium compound is preferably administered (mixed) at 100 to 15000 mg per day, and more preferably 400 to 2000 mg (mixed).
本発明の組成物は、本発明にかかる全成分を含む単一の製剤として製し、これを投与（服用）してもよいし、また本発明に係る各成分を分けて別の製剤とし、それら製剤を同時または順次投与（服用）可能としたキット製剤としてもよい。 The composition of the present invention is manufactured as a single preparation containing all the components according to the present invention and may be administered (taken), or each component according to the present invention is divided into separate preparations, These preparations may be kit preparations that can be administered simultaneously or sequentially (taken).
本発明の組成物は、優れた血清脂質代謝改善作用（血清総コレステロール低下作用、血清中性脂肪低下作用、血清ｎｏｎＨＤＬコレステロール低下作用）を示すことから、生活習慣病の予防および／または治療に有用である。本発明の組成物の効能・効果、適応症としては、具体的には、高脂血症、糖尿病、肥満、心筋梗塞、動脈硬化症、脳梗塞、脳卒中、狭心症、高コレステロールに伴う諸症状の改善：頭痛、頭重、肩・首筋のこり、手足のしびれ・冷え、レイノー症候群などを挙げることができる。 The composition of the present invention exhibits an excellent effect of improving serum lipid metabolism (serum total cholesterol lowering action, serum triglyceride lowering action, serum nonHDL cholesterol lowering action), and thus is useful for prevention and / or treatment of lifestyle-related diseases. It is. Specifically, the efficacy, effect and indication of the composition of the present invention include hyperlipidemia, diabetes, obesity, myocardial infarction, arteriosclerosis, cerebral infarction, stroke, angina pectoris, and high cholesterol. Symptom improvement: Headache, head weight, stiff shoulders / neck muscles, numbness / coldness of limbs, Raynaud's syndrome.
以下に、実施例を示して本発明を説明するが、本発明はこれらにのみ限定されるべきものではない。 Hereinafter, the present invention will be described with reference to examples. However, the present invention should not be limited to these examples.
１．血清脂質に対する作用
（１）動物
３週齢の雄性Ｓｌｃ：Ｓｙｒｉａｎハムスター（日本エスエルシー株式会社）をＦ２飼料（日本クレア株式会社）で約１週間予備飼育した後、Ｑｕｉｃｋ Ｆａｔ飼料（日本クレア株式会社）に切り替え、２週間の高脂肪食負荷を行った。なお、正常食群はそのままＦ２飼料を与えた。
1. Action on Serum Lipid (1) Animal After three weeks old male Slc: Syrian hamster (Japan SLC Co., Ltd.) was preliminarily raised with F2 feed (Clea Japan Co., Ltd.) for about 1 week, Quick Fat diet (Clea Japan Co., Ltd.) ) And a high fat diet load for 2 weeks. The normal diet group was fed with F2 feed as it was.
（２）投与検体の調製法
（イ）媒体
０．５％メチルセルロース（ＭＣ）溶液（和光純薬工業株式会社）を使用した。
（ロ）パンテチン１２０ｍｇ/ｍＬ液
８０％パンテチン液を１５０ｍｇ/ｍＬになるように上記媒体で溶解した。
（ハ）酸化マグネシウム１００ｍｇ/ｍＬ溶液
必要量の酸化マグネシウムを秤量し、上記媒体で、１００ｍｇ/ｍＬ溶液になるように溶解した。
（ニ）パンテチン１２０ｍｇ/ｍＬ＋酸化マグネシウム１００ｍｇ/ｍＬ溶液
まず、２倍量のパンテチン２４０ｍｇ/ｍＬ溶液を作製した。次に必要量の酸化マグネシウムにパンテチン２４０ｍｇ/ｍＬ溶液と０．５％ＭＣ溶液を等量ずつ加え酸化マグネシウムの濃度が１００ｍｇ/ｍＬになるようにした。
（ホ）パンテチン１２０ｍｇ/ｍＬ＋水酸化マグネシウム１００ｍｇ/ｍＬ溶液
まず、２倍量のパンテチン２４０ｍｇ/ｍＬ溶液を作製した。次に必要量の水酸化マグネシウムにパンテチン２４０ｍｇ/ｍＬ溶液と０．５％ＭＣ溶液を等量ずつ加え水酸化マグネシウムの濃度が１００ｍｇ/ｍＬになるようにした。
(2) Preparation method of administration specimen (a) Medium A 0.5% methylcellulose (MC) solution (Wako Pure Chemical Industries, Ltd.) was used.
(B) Pantethine 120 mg / mL solution An 80% pantethine solution was dissolved in the above medium to a concentration of 150 mg / mL.
(C) Magnesium oxide 100 mg / mL solution A required amount of magnesium oxide was weighed and dissolved in the above medium so as to be a 100 mg / mL solution.
(D) Pantethine 120 mg / mL + magnesium oxide 100 mg / mL solution First, a double amount of pantethine 240 mg / mL solution was prepared. Next, an equivalent amount of a pantethine 240 mg / mL solution and a 0.5% MC solution were added to the required amount of magnesium oxide so that the concentration of magnesium oxide was 100 mg / mL.
(E) Pantethine 120 mg / mL + magnesium hydroxide 100 mg / mL solution First, a double amount of pantethine 240 mg / mL solution was prepared. Next, pantethine 240 mg / mL solution and 0.5% MC solution were added in equal amounts to the required amount of magnesium hydroxide so that the magnesium hydroxide concentration was 100 mg / mL.
（３）試験法
２週間の高脂肪食負荷の後、１群８匹に分け１日１回連続９日間、上記検体を５ｍＬ/ｋｇハムスターに経口投与し、各薬剤の投与量が表１になるようにした。なお、正常食群、コントロール群は媒体を投与した。
(3) Test method After the high-fat diet load for 2 weeks, the above specimens were orally administered to 5 mL / kg hamster once a day for 9 consecutive days, divided into 8 animals per group. It was made to become. In the normal diet group and the control group, the vehicle was administered.
採血は投与開始前日、投与６日目及び投与９日目の計３回行い、遠心分離（３０００ｒｐｍ、１５分間、４℃）により得られた血清について酵素法を用いて総コレステロール濃度（ｍｇ/ｄＬ）および中性脂肪濃度（ｍｇ/ｄＬ）を測定した。ｎｏｎＨＤＬコレステロール濃度（ｍｇ/ｄＬ）は、沈殿法により得られたＨＤＬ画分中のコレステロール濃度を酵素法で求め、総コレステロール濃度からＨＤＬコレステロール濃度を差し引いて求めた。 Blood was collected a total of three times on the day before the start of administration, the sixth day of administration, and the ninth day of administration, and the serum obtained by centrifugation (3000 rpm, 15 minutes, 4 ° C.) was used to measure the total cholesterol concentration (mg / dL) ) And triglyceride concentration (mg / dL). The nonHDL cholesterol concentration (mg / dL) was determined by determining the cholesterol concentration in the HDL fraction obtained by the precipitation method by an enzymatic method and subtracting the HDL cholesterol concentration from the total cholesterol concentration.
結果を表２〜４に示した。なお、有意差検定は、各時点についてコントロール群と薬物投与群の比較（コントロール群 ｖｓ. パンテチン投与群、酸化マグネシウム投与群、パンテチン＋酸化マグネシウム併用群、パンテチン＋水酸化マグネシウム併用群）およびパンテチン＋酸化マグネシウム併用群と各単独群の比較（ｖｓ.パンテチン投与群、酸化マグネシウム投与群）およびパンテチン＋水酸化マグネシウム投与群とパンテチン投与群の比較およびパンテチンと併用するマグネシウム化合物の違いによる比較（パンテチン＋酸化マグネシウム併用群 ｖｓ. パンテチン＋水酸化マグネシウム併用群）の２群間比較を実施した。すなわち、等分散性をＦ検定で有意水準５％で行い、有意であればＡｓｐｉｎ−Ｗｅｌｃｈのｔ検定を、有意でなければＳｔｕｄｅｎｔのｔ検定を行った。 The results are shown in Tables 2-4. In addition, the significant difference test was performed by comparing the control group and the drug administration group at each time point (control group vs. pantethine administration group, magnesium oxide administration group, pantethine + magnesium oxide combination group, pantetin + magnesium hydroxide combination group) and pantetin + Comparison between magnesium oxide combination group and each single group (vs. pantethine administration group, magnesium oxide administration group), comparison between pantethine + magnesium hydroxide administration group and pantethine administration group, and comparison by difference in magnesium compound used together with pantethine (pantethine + Comparison between two groups of the magnesium oxide combination group vs. pantethine + magnesium hydroxide combination group) was performed. That is, the equidispersity was F-tested at a significance level of 5%. If significant, Aspin-Welch t-test was performed, and if not significant, Student t-test was performed.
＊＊ ｐ＜０．０１、＊＊＊ ｐ＜０．００１ コントロール群に対して有意差あり
＃ ｐ＜０．０５、＃＃ ｐ＜０．０１、＃＃＃ ｐ＜０．００１ パンテチン投与群に対して有意差あり
＄ ｐ＜０．０５、＄＄ ｐ＜０．０１ 酸化マグネシウム投与群に対して有意差あり
結果から明らかなように、高脂肪食摂取（コントロール群）により総コレステロール、中性脂肪およびｎｏｎＨＤＬコレステロール濃度が上昇した。パンテチンおよび酸化マグネシウムまたは水酸化マグネシウムを併用した群（パンテチン＋酸化マグネシウム併用群、パンテチン＋水酸化マグネシウム併用群）は、コントロール群と比べ総コレステロール、中性脂肪及びｎｏｎＨＤＬコレステロール濃度低下作用を示し、パンテチン投与群よりも低下作用が顕著だった。パンテチンおよび酸化マグネシウムを併用した群については、酸化マグネシウム投与群に対しても低下作用が顕著であった。パンテチンと併用するマグネシウム化合物の違いによる効果の差は見られなかった。
したがって、パンテチン類およびマグネシウム化合物を併用すると、優れた血清脂質代謝改善作用を示すことがわかった。
** p <0.01, *** p <0.001 Significantly different from control group
# P <0.05, ## p < 0.01, a significant difference with respect to ### p <0.001 pantethine administration group
$ P <0.05, $$ p <0.01 Significantly different from the magnesium oxide administration group As can be seen from the results, total cholesterol, triglyceride and nonHDL cholesterol levels by high fat diet intake (control group) Rose. The group in which pantethine and magnesium oxide or magnesium hydroxide were used in combination (pantethine + magnesium oxide combination group, pantethine + magnesium hydroxide combination group) showed an effect of lowering total cholesterol, neutral fat and non-HDL cholesterol concentrations compared to the control group. The lowering effect was more remarkable than that of the administration group. In the group in which pantethine and magnesium oxide were used in combination, the lowering effect was significant compared to the magnesium oxide administration group. There was no difference in effect due to the difference in the magnesium compound used in combination with panthetin.
Therefore, it was found that when pantethines and a magnesium compound were used in combination, an excellent effect of improving serum lipid metabolism was exhibited.
本発明のパンテチン類とマグネシウム化合物を含有する組成物は、優れた血清総コレステロール低下作用、血清中性脂肪低下作用、血清ｎｏｎＨＤＬコレステロール低下作用、すなわち血清脂質代謝改善作用を示した。したがって、パンテチン類およびマグネシウム化合物を含有する組成物は、脂質代謝が関わる生活習慣病の予防および／または治療用組成物として有用であり、このものは医薬または食品として利用することができる。 The composition containing panthetins and a magnesium compound of the present invention showed excellent serum total cholesterol lowering effect, serum neutral fat lowering effect, serum nonHDL cholesterol lowering effect, that is, serum lipid metabolism improving action. Therefore, a composition containing panthetins and a magnesium compound is useful as a composition for preventing and / or treating lifestyle-related diseases involving lipid metabolism, and can be used as a medicine or food.
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