JPH06271464A - Arachidonic acid-containing composition for prevention or improvement of alimentary disorder - Google Patents

Arachidonic acid-containing composition for prevention or improvement of alimentary disorder

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Publication number
JPH06271464A
JPH06271464A JP5060065A JP6006593A JPH06271464A JP H06271464 A JPH06271464 A JP H06271464A JP 5060065 A JP5060065 A JP 5060065A JP 6006593 A JP6006593 A JP 6006593A JP H06271464 A JPH06271464 A JP H06271464A
Authority
JP
Japan
Prior art keywords
arachidonic acid
containing composition
acid
prevention
oils
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP5060065A
Other languages
Japanese (ja)
Inventor
Yoshio Shimizu
良雄 清水
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.)
Tokiwa Pharmaceutical Co Ltd
Original Assignee
Tokiwa Yakuhin Kogyo KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tokiwa Yakuhin Kogyo KK filed Critical Tokiwa Yakuhin Kogyo KK
Priority to JP5060065A priority Critical patent/JPH06271464A/en
Publication of JPH06271464A publication Critical patent/JPH06271464A/en
Pending legal-status Critical Current

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  • Seasonings (AREA)
  • Medicinal Preparation (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Fodder In General (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

PURPOSE:To provide an arachidonic acid-containing composition for prevention or improvement of alimentary disorders, useful as a food, a medicine, a feed, etc. CONSTITUTION:There is provided an arachidonic acid-containing composition for prevention or improvement of alimentary disorders, containing fats and oils of >=2wt.% arachidonic acid content as the essential component. An economical composition for prevention or improvement of alimentary disorders can be provided by using fats and oils containing high-concentration arachidonic acid.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、比較的多量のアラキド
ン酸を含有する油脂を必須成分として配合した消化器系
粘膜の保護を通して消化器系障害を予防または治療する
食品や医薬、動物用飼料等として有用なアラキドン酸含
有組成物に関する。
FIELD OF THE INVENTION The present invention relates to foods, pharmaceuticals and animal feeds for preventing or treating digestive system disorders through protection of digestive system mucosa containing fats and oils containing a relatively large amount of arachidonic acid as an essential component. The present invention relates to an arachidonic acid-containing composition useful as the above.

【0002】[0002]

【従来の技術】現在、エタノール等の有害物質により、
胃や肝臓の粘膜が損傷を受けて、胃炎や肝障害を起こす
人が増加している。しかも、例えば、肝硬変に消化器系
潰瘍を併発する頻度は高く、5〜15%にも達する。そ
の理由として、これまでは、肝臓におけるガストリン代
謝が低下して血中ガストリン濃度が増大し、胃酸分泌が
亢進されるためであると言われてきた。
2. Description of the Related Art Currently, due to harmful substances such as ethanol,
An increasing number of people have gastric inflammation or liver damage due to damage to the mucous membranes of the stomach and liver. Moreover, for example, the frequency of complications of digestive system ulcer in cirrhosis is high, reaching 5 to 15%. It has been said that the reason for this is that the gastrin metabolism in the liver is lowered, the blood gastrin concentration is increased, and the gastric acid secretion is enhanced.

【0003】しかし、最近では、プロスタグランディン
の生理作用として細胞保護作用や胃酸分泌抑制作用が明
らかになり、プロスタグランディンが防御因子を統括的
に調節することがわかってきた。実際、消化器系潰瘍の
患者はプロスタグランディンの量が極端に低下してお
り、現在のところ、その治療法としては、プロスタグラ
ンディンを患者の胃に直接投与する方法が採用されてい
る。しかし、プロスタグランディンは副作用が強いの
で、それに代わるものが求められている。
However, recently, as a physiological action of prostaglandin, a cytoprotective action and a gastric acid secretion inhibitory action have been clarified, and it has been found that prostaglandin comprehensively regulates defense factors. In fact, patients with gastrointestinal ulcer have extremely low levels of prostaglandin, and at present, the method of treatment is to administer prostaglandin directly to the stomach of the patient. However, since prostaglandins have strong side effects, alternatives are required.

【0004】最近、プロスタグランディンの生物学的前
駆体であるアラキドン酸が注目されている。アラキドン
酸は、生体内では、リノール酸から、γ−リノレン酸、
ジホモ-γ-リノレン酸を経て合成されるが、この合成ア
ラキドン酸がプロスタグランジンに変換され、消化器系
障害の予防や治療に効果を発揮すると考えられている。
Recently, arachidonic acid, which is a biological precursor of prostaglandin, has been receiving attention. Arachidonic acid, in vivo, from linoleic acid, γ-linolenic acid,
It is synthesized via dihomo-γ-linolenic acid, and it is believed that this synthetic arachidonic acid is converted into prostaglandins, which is effective in the prevention and treatment of digestive system disorders.

【0005】したがって、消化器系障害の予防や治療の
ために、リノール酸やアラキドン酸を投与することが有
効と考えられ、例えば、特開昭59−62522号に
は、リノール酸やアラキドン酸を界面活性剤と共に水溶
性の組成物として経口投与し、消化器系障害の予防や治
療に用いることが提案されている。この場合、投与され
たリノール酸やアラキドン酸は、胃や十二指腸粘膜中の
リン脂質に取り込まれ、プロスタグランディンに変換さ
れ、胃や十二指腸粘膜を保護する。
Therefore, it is considered effective to administer linoleic acid or arachidonic acid for the prevention or treatment of gastrointestinal disorders. For example, in JP-A-59-62522, linoleic acid or arachidonic acid may be administered. It is proposed to be orally administered as a water-soluble composition together with a surfactant and used for the prevention and treatment of digestive system disorders. In this case, the administered linoleic acid and arachidonic acid are taken up by phospholipids in the stomach and duodenal mucosa and converted into prostaglandin, which protects the stomach and duodenal mucosa.

【0006】しかし、リノール酸を用いる場合はともか
く、アラキドン酸を用いた実用的な消化器系障害の予防
または治療剤は未だ見当らない。すなわち、リノール酸
は通常の油脂食品中に多量に含有されており、その入手
は容易で、食物としての摂取によって所望の効果を期待
できるものの、アラキドン酸は魚や肉、卵等の食品に少
量含有されているにすぎず、消化器系障害の予防や治療
に十分な量を安価に入手することは困難である。また、
特開昭59−62522号では、精製された遊離脂肪酸
形態のアラキドン酸を使用しているが、これは高価であ
るので、実用的ではない。
Regardless of the case of using linoleic acid, however, a practical preventive or therapeutic agent for digestive system disorders using arachidonic acid has not been found yet. That is, linoleic acid is contained in a large amount in ordinary oil and fat foods, and it is easily available, and although a desired effect can be expected by ingestion as food, arachidonic acid is contained in a small amount in foods such as fish, meat and eggs. However, it is difficult to obtain a sufficient amount at a low cost for the prevention and treatment of digestive system disorders. Also,
In JP 59-62522, purified arachidonic acid in free fatty acid form is used, but this is not practical because it is expensive.

【0007】さらに、リノール酸からのアラキドン酸の
生合成はエタノール等の有害物質によって阻害されるの
で、消化器系障害を起こした患者はアラキドン酸の量が
健常例より低下している。そこで、リノール酸ではな
く、アラキドン酸を直接投与することが必要となる。
Furthermore, since the biosynthesis of arachidonic acid from linoleic acid is inhibited by harmful substances such as ethanol, the amount of arachidonic acid in patients with gastrointestinal disorders is lower than that in healthy cases. Therefore, it is necessary to directly administer arachidonic acid instead of linoleic acid.

【0008】[0008]

【発明が解決しようとする課題】このような事情に鑑
み、本発明者らはアラキドン酸を用いた実用的な消化器
系障害の予防または治療剤を得るべく鋭意研究を行った
結果、例えば、特開昭63−44891号や特開平2−
86789号等に開示されるような微生物学的方法によ
り得られる高濃度のアラキドン酸を含有する油脂がその
目的に好適であり、そのような油脂を配合した組成物で
も、エタノール等の有害物質により障害を起こした消化
器系においてプロスタグランジンの量を増加させ、消化
器系障害の予防および治療に有用であることを見い出
し、本発明を完成するに至った。
In view of such circumstances, the present inventors have conducted diligent research to obtain a practical preventive or therapeutic agent for digestive system disorders using arachidonic acid. JP-A-63-44891 and JP-A-2-
Oils and fats containing a high concentration of arachidonic acid obtained by the microbiological method as disclosed in No. 86789 and the like are suitable for that purpose, and even a composition containing such oils and fats, due to harmful substances such as ethanol. The amount of prostaglandins in the damaged digestive system was increased, and it was found to be useful for the prevention and treatment of digestive system disorders, and the present invention has been completed.

【0009】[0009]

【課題を解決するための手段】すなわち、本発明は、ア
ラキドン酸含有量が2重量%以上の油脂を必須成分とし
てなることを特徴とする消化器系障害の予防または治療
用組成物を提供するものである。ここで、消化器系と
は、エタノール等の有害物質を経口的に摂取した場合に
炎症や潰瘍等の障害が発生する可能性のある体内器官を
意味し、具体的には、食道、胃、十二指腸、小腸等が挙
げられる。
Means for Solving the Problems That is, the present invention provides a composition for preventing or treating a gastrointestinal disorder, which comprises an oil and fat having an arachidonic acid content of 2% by weight or more as an essential component. It is a thing. Here, the digestive system means a body organ in which disorders such as inflammation and ulcer may occur when orally ingesting harmful substances such as ethanol, and specifically, the esophagus, the stomach, Duodenum, small intestine and the like can be mentioned.

【0010】天然に存在する油脂の中に、アラキドン酸
含有量が2重量%に達するものは見当たらないので、本
発明では、アラキドン酸生産能を有する微生物から得ら
れる油脂であって、アラキドン酸含有量が2重量%以
上、好ましくは10〜99重量%、さらに好ましくは2
0〜99重量%の油脂を必須成分として配合する。アラ
キドン酸の量が少なすぎると、その配合効果が期待でき
ないので、かかる油脂は本発明の組成物中のアラキドン
酸含有量が、組成物全体に対して2重量%以上、好まし
くは10重量%以上となるように配合する。
Since no arachidonic acid content of 2% by weight is found among naturally occurring fats and oils, in the present invention, the arachidonic acid-containing fats and oils obtained from a microorganism having an arachidonic acid-producing ability can be used. The amount is 2% by weight or more, preferably 10 to 99% by weight, more preferably 2
0 to 99% by weight of fats and oils is added as an essential component. If the amount of arachidonic acid is too small, the compounding effect cannot be expected, so that the content of arachidonic acid in the composition of the present invention is 2% by weight or more, preferably 10% by weight or more based on the entire composition. Blend so that

【0011】このような比較的高濃度のアラキドン酸を
含有する油脂は、例えば、特開昭63−44891号に
開示の方法に従い、モルティエレラ(Mortierella)属
に属するアラキドン酸生産菌を、炭素源としてグルコー
ス、窒素源として酵母エキスを用い、好ましくは大豆油
の存在下で培養し、アラキドン酸含有画分を抽出、濃縮
することにより、得ることができる。また、特開平2−
86789号に開示の方法に従い、エントモフトラ(En
tomophthora)属糸状菌を、有機多塩基酸を添加した培
地中で培養することにより、アラキドン酸を菌体内に高
濃度で蓄積させ、これを採取することにより、迅速かつ
安価に大量生産することもできる。
Such an oil or fat containing a relatively high concentration of arachidonic acid can be obtained by using an arachidonic acid-producing bacterium belonging to the genus Mortierella as a carbon source according to the method disclosed in JP-A-63-44891. Glucose and yeast extract as a nitrogen source are used, preferably, the culture is carried out in the presence of soybean oil, and the arachidonic acid-containing fraction is extracted and concentrated. In addition, JP-A-2-
In accordance with the method disclosed in No. 86789, Entomotra (En
It is also possible to mass-produce arachidonic acid at a high concentration in the cells by culturing filamentous fungi of the genus Tomophthora) in a medium to which organic polybasic acid is added, and to collect them rapidly and at low cost. it can.

【0012】本発明の組成物は、かかる比較的高濃度の
アラキドン酸を含有する油脂単独またはそれらの混合物
のみで構成してもよく、あるいは、このようなアラキド
ン酸含有油脂に加えて、ドコサヘキサエン酸(以下、D
HAという)や、エイコサペンタエン酸(以下、EPA
という)、γ−リノレン酸、α−リノレン酸、リノール
酸、これらの酸を含有する油脂、例えば、大豆油、ゴマ
油、精製魚油等、また、d−α−トコフェロール等のビ
タミン、カキ肉エキス等のアミノ酸、食酢、食塩、甘味
料、香辛料等の調味料等を適宜含有させてもよい。
The composition of the present invention may be constituted by oils and fats containing such a relatively high concentration of arachidonic acid alone or a mixture thereof, or in addition to such oils and fats containing arachidonic acid, docosahexaenoic acid. (Hereafter, D
HA and eicosapentaenoic acid (hereinafter EPA)
, Γ-linolenic acid, α-linolenic acid, linoleic acid, fats and oils containing these acids, for example, soybean oil, sesame oil, refined fish oil, etc., vitamins such as d-α-tocopherol, oyster meat extract, etc. The amino acid, vinegar, salt, sweetener, seasoning such as spice and the like may be appropriately contained.

【0013】特に、アラキドン酸と共に、DHAを含有
させることにより、アラキドン酸の体内での働きが促進
され、その消化器系障害の予防、治療効果がさらに向上
することが判明した。一般に、DHAは、アラキドン酸
に対する重量比で、0.5〜7倍の割合で添加すると所
望の促進効果が得られる。
In particular, it has been found that by incorporating DHA together with arachidonic acid, the action of arachidonic acid in the body is promoted, and the preventive and therapeutic effects on the digestive system disorders are further improved. Generally, DHA has a desired promoting effect when added in a weight ratio of 0.5 to 7 times with respect to arachidonic acid.

【0014】また、アラキドン酸と共に、カキ肉エキス
を含有させることにより、脂肪酸とアミノ酸の両方を摂
取することができ、より一層の消化器系障害の予防、治
療効果が期待できる。一般に、カキ肉エキスは、アラキ
ドン酸に対する重量比で、2〜150倍、好ましくは1
5〜50倍の割合で添加すると所望の効果が得られる。
By adding oyster meat extract together with arachidonic acid, both fatty acids and amino acids can be ingested, and further preventive and therapeutic effects on digestive system disorders can be expected. Generally, the oyster meat extract has a weight ratio of 2 to 150 times, preferably 1 to arachidonic acid.
The desired effect can be obtained by adding it at a ratio of 5 to 50 times.

【0015】本発明の組成物は、常法により、油剤、エ
マルジョン、ソフトカプセル剤、ハードカプセル剤、錠
剤、顆粒剤、固形剤、チュアブル剤、ドレッシング類、
菓子類等の医薬や食品等の形態にすることができ、消化
器系障害の予防や治療の必要な人に対して経口的に摂取
させることができる。また、必要であれば、可溶化等の
公知の技術に従って、非経口投与用の形態としてもよ
く、例えば、注射剤とすることもできる。
The composition of the present invention is prepared by an ordinary method such as oil, emulsion, soft capsule, hard capsule, tablet, granule, solid, chewable agent, dressing,
It can be in the form of medicine such as confectionery, food, etc., and can be orally ingested by a person in need of prevention or treatment of digestive system disorders. Further, if necessary, it may be in a form for parenteral administration according to a known technique such as solubilization, and for example, an injection may be prepared.

【0016】また、人に限らず、ラット、ネズミ、モル
モット、サル、ヒヒ等の哺乳動物の消化器系障害の予防
や治療にも用いることができ、例えば、常法に従い、飼
料用の固体または液体の添加剤とすることもできる。
Not only humans but also rats, rats, guinea pigs, monkeys, baboons, and other mammals can be used for the prevention and treatment of digestive system disorders. It can also be a liquid additive.

【0017】本発明の組成物は、通常、アラキドン酸の
1日の経口的摂取量が成人の場合、50〜2000mg
/日、好ましくは200〜500mg/日となるように
与える。また、人以外の哺乳動物については、アラキド
ン酸の1日の経口的摂取量が1〜50mg/kg、好ま
しくは5〜10mg/kgとなるように与える。
The composition of the present invention is usually 50 to 2000 mg when the daily oral intake of arachidonic acid is adult.
/ Day, preferably 200 to 500 mg / day. For mammals other than humans, the daily oral intake of arachidonic acid is 1 to 50 mg / kg, preferably 5 to 10 mg / kg.

【0018】[0018]

【実施例】以下に実施例および実験例を挙げて本発明を
さらに詳しく説明するが、本発明はこれらに限定される
ものではない。なお、実施例中の「%」は「重量%」を
意味する。
The present invention will be described in more detail with reference to Examples and Experimental Examples, but the present invention is not limited thereto. In addition, "%" in an Example means "weight%."

【0019】実施例1 以下の処方により、常法に従って、ソフトカプセル剤を
製造した。 成 分 配合量 アラキドン酸含有油脂 50.0% (アラキドン酸を22%以上含有) エイコサペンタエン酸(EPA)含有精製魚油 20.0% (EPAを28%以上、DHAを12%以上含有) ドコサヘキサエン酸(DHA)含有精製魚油 29.8% (EPAを8%以上、DHAを30%以上含有) ビタミンE抽出液 0.2%
Example 1 A soft capsule was prepared according to a conventional method according to the following formulation. Ingredients Content Arachidonic acid-containing fats and oils 50.0% (Containing 22% or more arachidonic acid) Eicosapentaenoic acid (EPA) -containing refined fish oil 20.0% (Containing 28% or more EPA and 12% or more DHA) Docosahexaenoic acid Purified fish oil containing (DHA) 29.8% (containing 8% or more EPA and 30% or more DHA) Vitamin E extract 0.2%

【0020】実施例2 以下の処方により、常法に従って、ドレッシングを製造
した。
Example 2 A dressing was produced according to a conventional method according to the following formulation.

【0021】実施例3 まず、以下の処方により、常法に従って、アラキドン酸
粉末を調製した。
Example 3 First, arachidonic acid powder was prepared according to a conventional method according to the following formulation.

【0022】アラキドン酸含有油脂を溶媒のエタノール
に溶解し、残りの原料を混合したものに、この溶液を添
加し、混合分散させて吸着させた後、加温乾燥して溶媒
を除去し、アラキドン酸粉末とした。こうして得られた
アラキドン酸粉末を用い、以下の処方により、常法に従
って、ハードカプセル剤を製造した。
Arachidonic acid-containing fats and oils were dissolved in ethanol as a solvent, and the remaining raw materials were mixed, and this solution was added, mixed and dispersed for adsorption, and then heated and dried to remove the solvent and arachidone. Acid powder was used. Using the arachidonic acid powder thus obtained, a hard capsule was manufactured according to a conventional method according to the following formulation.

【0023】実施例4 実施例3で調製したアラキドン酸粉末を用い、以下の処
方により、常法に従って、錠剤を製造した。
Example 4 Using the arachidonic acid powder prepared in Example 3, tablets were manufactured according to a conventional method according to the following formulation.

【0024】実験例 動物実験1 (実験方法)SD系の雄ラット(体重約200g)24
尾を6尾ずつ4群に分け、エタノールおよびアラキドン
酸投与の有無により区別し、以下の実験を行った。各群
の動物に、以下の成分からなる飼料を20g/日の量で
経口的に14日間投与した。エタノール投与群には、空
腹時にエタノールを毎回チューブで3g/kg/日の量
で投入した。なお、エタノールの投与期間はアラキドン
酸投与の2週間前からとし、アラキドン酸投与中もエタ
ノールを投入した。
Experimental Example Animal Experiment 1 (Experimental Method) SD male rats (body weight: about 200 g) 24
The tails were divided into 4 groups of 6 tails, which were distinguished by the presence or absence of administration of ethanol and arachidonic acid, and the following experiments were conducted. Animals of each group were orally administered with a feed comprising the following ingredients in an amount of 20 g / day for 14 days. To the ethanol-administered group, ethanol was added by a tube at an amount of 3 g / kg / day each time on an empty stomach. The administration period of ethanol was 2 weeks before the administration of arachidonic acid, and ethanol was added during the administration of arachidonic acid.

【0025】アラキドン酸非投与群には、飼料にラード
10%を添加したものを、アラキドン酸投与群には、ラ
ード7%およびアラキドン酸3%を添加したものを食餌
療法で与えた。2週間後、動物を屠殺して胃を取り出
し、胃の粘膜をガラス片で掻き取り、以下のようにアラ
キドン酸投与の効果を定量的に判定した。なお、ラード
は飽和脂肪酸を多く含み、アラキドン酸を含まない。
The arachidonic acid non-administered group was fed diet with lard 10% added, and the arachidonic acid administration group was fed lard 7% and arachidonic acid 3%. Two weeks later, the animals were sacrificed, the stomach was taken out, the mucous membrane of the stomach was scraped with a glass piece, and the effect of arachidonic acid administration was quantitatively determined as follows. Lard contains a large amount of saturated fatty acids and does not contain arachidonic acid.

【0026】胃粘膜中の総リン脂質濃度(μg/mgタ
ンパク湿量)と、アラキドン酸を多く含むと言われてい
る胃粘膜イノシトール分画中のアラキドン酸濃度(重量
比)の測定 (結果)
Measurement of total phospholipid concentration in gastric mucosa (μg / mg protein wet amount) and arachidonic acid concentration (weight ratio) in gastric mucosal inositol fraction, which is said to contain a large amount of arachidonic acid (result)

【表1】 [Table 1]

【0027】表1に示すように、エタノールを与えてラ
ードだけを加えた場合と、エタノールを与えずにラード
だけを加えた場合とでは、エタノールを与えた方が総リ
ン脂質濃度およびアラキドン酸濃度が低下している。し
かし、アラキドン酸を加えることにより、エタノールを
与えても、胃粘膜中の総リン脂質濃度およびアラキドン
酸濃度はエタノールを与えない場合と同程度であり、正
常値の範囲内である。このことから、アラキドン酸に
は、エタノール等の有害物質による胃粘膜中の総リン脂
質濃度およびアラキドン酸濃度の低下を防止し、ひいて
は胃粘膜を保護する作用のあることがわかる。
As shown in Table 1, when ethanol was added and lard alone was added, and when lard alone was added without ethanol added, ethanol was added to the total phospholipid concentration and arachidonic acid concentration. Is falling. However, even if ethanol is given by adding arachidonic acid, the total phospholipid concentration and the arachidonic acid concentration in the gastric mucosa are about the same as when ethanol is not given, which is within the normal range. From this, it can be seen that arachidonic acid has an action of preventing a decrease in the total phospholipid concentration and arachidonic acid concentration in the gastric mucosa due to harmful substances such as ethanol, and thus protecting the gastric mucosa.

【0028】動物実験2 (実験方法)SD系の雄ラット(体重約200g)24
尾を6尾ずつ4群に分け、1つのアラキドン酸非投与群
と、3つのアラキドン酸投与群(投与量5、20、10
0mg/kg)とについて、以下の実験を行った。アラ
キドン酸投与群にアラキドン酸を投与して30分後、す
べての群にエタノールを10mg/kgの量で経口的に
投与した。1時間後、動物を屠殺して胃を取り出し、1
0%ホルマリン液で簡易固定し、潰瘍の長さを測定し
た。
Animal experiment 2 (Experimental method) SD male rat (body weight: about 200 g) 24
The tails were divided into 4 groups of 6 tails each, one arachidonic acid non-administration group and three arachidonic acid administration groups (dose 5, 20, 10
0 mg / kg), the following experiment was conducted. Thirty minutes after the administration of arachidonic acid to the arachidonic acid administration group, ethanol was orally administered to all groups in an amount of 10 mg / kg. After 1 hour, the animals were slaughtered and their stomachs removed and 1
It was simply fixed with 0% formalin solution, and the length of the ulcer was measured.

【0029】(結果)(Result)

【表2】 [Table 2]

【0030】表2に示すように、アラキドン酸を投与し
ない場合に比べて、アラキドン酸を投与した場合の方が
潰瘍の長さは減少している。しかも、アラキドン酸の投
与量が増大するにつれて、潰瘍の長さは著しく減少して
いる。このことから、アラキドン酸には胃粘膜を保護
し、潰瘍の発生を抑制する作用のあることがわかる。
As shown in Table 2, the length of the ulcer is shorter when arachidonic acid is administered than when arachidonic acid is not administered. Moreover, as the dose of arachidonic acid increases, the length of the ulcer decreases significantly. From this, it is understood that arachidonic acid has an action of protecting the gastric mucosa and suppressing the development of ulcer.

【0031】[0031]

【発明の効果】本発明によれば、遊離脂肪酸形態のアラ
キドン酸ではなく、安価に大量生産価可能なアラキドン
酸含有油脂を用いているので、消化器系障害の予防また
は治療用として実用的なアラキドン酸含有組成物が提供
される。さらに、アラキドン酸含有油脂に加えて、DH
A含有油脂やカキ肉エキスを添加すれば、アラキドン酸
の体内での働きが促進され、消化器系障害の予防および
治療効果が向上する。
According to the present invention, since arachidonic acid-containing oils and fats that can be mass-produced inexpensively are used instead of arachidonic acid in the form of free fatty acid, it is practically useful for preventing or treating gastrointestinal disorders. Arachidonic acid-containing compositions are provided. In addition to arachidonic acid-containing fats and oils, DH
Addition of A-containing fats and oils and oyster meat extract promotes the action of arachidonic acid in the body, and improves the preventive and therapeutic effects on digestive system disorders.

フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 9/20 B 7329−4C 9/48 C 7329−4C F 7329−4C 31/20 ACL 9283−4C //(A61K 31/23 35:56) 7431−4C (A61K 31/20 35:56) 7431−4C Continuation of the front page (51) Int.Cl. 5 Identification number Reference number within the agency FI Technical display area A61K 9/20 B 7329-4C 9/48 C 7329-4C F 7329-4C 31/20 ACL 9283-4C // (A61K 31/23 35:56) 7431-4C (A61K 31/20 35:56) 7431-4C

Claims (9)

【特許請求の範囲】[Claims] 【請求項1】 アラキドン酸含有量が2重量%以上の油
脂を必須成分としてなることを特徴とする消化器系障害
の予防または治療用アラキドン酸含有組成物。
1. An arachidonic acid-containing composition for preventing or treating digestive system disorders, which comprises an oil and fat having an arachidonic acid content of 2% by weight or more as an essential component.
【請求項2】 油脂のアラキドン酸含有量が10重量%
以上である請求項1記載のアラキドン酸含有組成物。
2. The arachidonic acid content of fats and oils is 10% by weight.
The above is the arachidonic acid-containing composition according to claim 1.
【請求項3】 油脂のアラキドン酸含有量が20重量%
以上である請求項2記載のアラキドン酸含有組成物。
3. The arachidonic acid content of fats and oils is 20% by weight.
The above is the arachidonic acid-containing composition according to claim 2.
【請求項4】 胃粘膜の保護または損傷治療用である請
求項1記載のアラキドン酸含有組成物。
4. The arachidonic acid-containing composition according to claim 1, which is used for protecting gastric mucosa or treating damage.
【請求項5】 ソフトカプセル剤の形態である請求項1
記載のアラキドン酸含有組成物。
5. The method of claim 1 in the form of a soft capsule.
The arachidonic acid-containing composition described.
【請求項6】 さらにドコサヘキサエン酸含有油脂を添
加した請求項1記載のアラキドン酸含有組成物。
6. The arachidonic acid-containing composition according to claim 1, further comprising a fat / oil containing docosahexaenoic acid.
【請求項7】 ドコサヘキサエン酸含有量が、アラキド
ン酸含有量に対して、0.5〜7倍である請求項6記載
のアラキドン酸含有組成物。
7. The arachidonic acid-containing composition according to claim 6, wherein the docosahexaenoic acid content is 0.5 to 7 times the arachidonic acid content.
【請求項8】 カキ肉エキスと混合したハードカプセル
剤の形態である請求項1記載のアラキドン酸含有組成
物。
8. The arachidonic acid-containing composition according to claim 1, which is in the form of a hard capsule mixed with an oyster meat extract.
【請求項9】 カキ肉エキスと混合した錠剤の形態であ
る請求項1記載のアラキドン酸含有組成物。
9. The arachidonic acid-containing composition according to claim 1, which is in the form of a tablet mixed with an oyster meat extract.
JP5060065A 1993-03-19 1993-03-19 Arachidonic acid-containing composition for prevention or improvement of alimentary disorder Pending JPH06271464A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5060065A JPH06271464A (en) 1993-03-19 1993-03-19 Arachidonic acid-containing composition for prevention or improvement of alimentary disorder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5060065A JPH06271464A (en) 1993-03-19 1993-03-19 Arachidonic acid-containing composition for prevention or improvement of alimentary disorder

Publications (1)

Publication Number Publication Date
JPH06271464A true JPH06271464A (en) 1994-09-27

Family

ID=13131316

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH06271464A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002002105A1 (en) * 2000-06-29 2002-01-10 Laxdale Limited Therapeutic combinations of fatty acids
EP1190629A1 (en) * 2000-09-18 2002-03-27 EnergyBalance AG Omega-3 fatty acids in combination with a concentrated vitamin E source
JP2009518332A (en) * 2005-12-06 2009-05-07 エルテーエス ローマン テラピー−ジステーメ アーゲー Unsaturated fatty acids as thrombin inhibitors
US7601523B2 (en) 1995-01-24 2009-10-13 Martek Biosciences Corporation Method for production of arachidonic acid
JP2011098966A (en) * 1998-10-15 2011-05-19 Dsm Ip Assets Bv Pufa supplements
JP2011225458A (en) * 2010-04-15 2011-11-10 Kao Corp Gip rise inhibitor

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7601523B2 (en) 1995-01-24 2009-10-13 Martek Biosciences Corporation Method for production of arachidonic acid
US7666657B2 (en) 1995-01-24 2010-02-23 Martek Biosciences, Inc. Method for production of arachidonic acid
US7736885B2 (en) 1995-01-24 2010-06-15 Martek Biosciences, Inc. Method for production of arachidonic acid
JP2011098966A (en) * 1998-10-15 2011-05-19 Dsm Ip Assets Bv Pufa supplements
WO2002002105A1 (en) * 2000-06-29 2002-01-10 Laxdale Limited Therapeutic combinations of fatty acids
EP1190629A1 (en) * 2000-09-18 2002-03-27 EnergyBalance AG Omega-3 fatty acids in combination with a concentrated vitamin E source
JP2009518332A (en) * 2005-12-06 2009-05-07 エルテーエス ローマン テラピー−ジステーメ アーゲー Unsaturated fatty acids as thrombin inhibitors
JP2011225458A (en) * 2010-04-15 2011-11-10 Kao Corp Gip rise inhibitor

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