JPS60199818A - Anemia preventing agent - Google Patents

Anemia preventing agent

Info

Publication number
JPS60199818A
JPS60199818A JP59055080A JP5508084A JPS60199818A JP S60199818 A JPS60199818 A JP S60199818A JP 59055080 A JP59055080 A JP 59055080A JP 5508084 A JP5508084 A JP 5508084A JP S60199818 A JPS60199818 A JP S60199818A
Authority
JP
Japan
Prior art keywords
anemia
tryptophan
animal
animal tissue
preventing agent
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
JP59055080A
Other languages
Japanese (ja)
Other versions
JPH0436135B2 (en
Inventor
Kenji Hara
健次 原
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.)
Kao Corp
Original Assignee
Kao Corp
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 Kao Corp filed Critical Kao Corp
Priority to JP59055080A priority Critical patent/JPS60199818A/en
Publication of JPS60199818A publication Critical patent/JPS60199818A/en
Publication of JPH0436135B2 publication Critical patent/JPH0436135B2/ja
Granted legal-status Critical Current

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  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PURPOSE:A safe anemia preventing agent, obtained by incorporating l-tryptophan or a derivative thereof as an active constituent in an animal tissue extract, etc., and capable of very remarkably preventing iron deficiency anemia. CONSTITUTION:An anemia preventing agent, obtained by incorporating l-tryptophan or a derivative thereof, e.g. n-acetyl-l-tryptophan or 5-hydroxytryptophan, in a substance selected from an animal tissue extract, pulverized animal tissue or enzymic decomposition product. A mammal, e.g. cattle or pig, bird, fish or shellfish, etc. may be used as the animal, and the liver or blood is preferably used in the case of particularly a large animal. A pharmaceutical containing the tissue extract, etc. and l-tryptophan at 1:0.1-20 compounding ratio has particularly good anemia preventing effect.

Description

【発明の詳細な説明】 本発明は貧血予防剤に関する。[Detailed description of the invention] The present invention relates to an anemia preventive agent.

近年、鉄欠乏性貧血が増加しており、社会的間m&こな
っている。例えば、学童期以前の幼児、思春期の女子な
ど、身体の発育の著しい人達でバランスのとfしていな
い食事をしている者、更に後者で特に生理の開始時期に
ある者は鉄欠乏に陥ることが多い。また妊産婦では、妊
娠、分娩、産褥を迎じて胎児・\の鉄補給、出産時の出
血、乳汁を介し一乙の刹生先への鉄補給などによシ著し
い鉄欠乏状+rM ’xきたすことがしばしばである。
In recent years, iron-deficiency anemia has been increasing and has become a social problem. For example, people with rapidly growing bodies, such as pre-school children and adolescent girls, who eat an unbalanced diet, and among the latter, especially those who are at the beginning of their menstrual period, may be at risk of iron deficiency. I often fall into it. In addition, during pregnancy, delivery, and the puerperium, pregnant women can develop severe iron deficiency +rM'x due to iron supplementation of the fetus/\, bleeding during childbirth, and iron supplementation of the baby's body through breast milk. This is often the case.

一旦鉄欠乏状態に陥ると、その当初は貧血を改善するた
めに、経口鉄剤の投与に頼らざる會得ない。然し、貧血
の改善をみた後でも、その改善状態を維持してい(には
日常の食事あるいは栄養補助食品による鉄補給が必要で
ちゃ、日常服用するのに適した安全かつ効果的な貧血予
防剤か望まれていた。
Once a person falls into a state of iron deficiency, he or she must initially rely on administration of oral iron preparations to improve the anemia. However, even after the anemia has improved, iron supplementation through daily diet or nutritional supplements is necessary to maintain the improved state. It was desired.

本発明′4は、斯かる実状におい−C鋭意研究した結果
、動物の組織抽出物、粉砕物及び酵素分解物よシなる群
から選ばれた1種若しくは2株以上の混合物とL〜トリ
プトファン若しくはその誘導体全併用することによシ鉄
欠乏注貧血が極めて顕著に予防されること全見出し、本
発明を完成した。
As a result of intensive research into the actual situation, the present invention '4 has developed a mixture of one or more strains selected from the group consisting of animal tissue extracts, pulverized products, and enzymatic decomposition products, and L to tryptophan or The present invention has been completed based on the discovery that iron deficiency anemia can be significantly prevented by the combined use of all of the derivatives.

すなわち本発明は、動物の組織抽出物、粉砕物及び酵素
分解物よシなる群から選ばれた物質(以下、「動物の組
織抽出物等」と称する)、並びにt−トリプトファン若
しくはその誘導体を有効成分とする貧血予防剤勿提供す
めものである。
That is, the present invention effectively utilizes a substance selected from the group consisting of animal tissue extracts, pulverized products, and enzymatically decomposed products (hereinafter referred to as "animal tissue extracts, etc."), as well as t-tryptophan or its derivatives. It is recommended as an anemia preventive agent as a component.

本発明で使用する動物としては、ウシ、ブタ、ウマ、ヒ
ツジ、イヌ、ウサギ、ヤギ等の哺乳動物;ニワトリ、ア
ヒル、シチメンチョウ、ホロホロチヨウ等の鳥類:カキ
、アミ、オキアミ、ヤツメウナギ、小魚等の魚貝類;ス
ツポン、カメ等の爬虫類等を挙げることができる。動物
の組織としては、これら動物の全体及びその臓器、例え
ば肝臓、血液等のいずれをも使用できるが、特に大型動
物の場合に肝臓又は血液全使用するのが好適である3゜
動物の組織抽出物は、組絨全例えば温湯若しくは熱湯で
長時間煮出して抽出する方法、35〜45Cでプロテア
ーゼあるいはプロテアーゼとリパーゼを作用させること
によシ酵素分解しつつ抽出する方法等によシ製造される
。動物の粉砕物としては、動物そのものの粉砕物のほか
、液体窒素で凍結した後に粉砕したもの、凍結乾燥物を
粉砕したもの等を挙げることができる。動物の酵素分解
物とは、動物及びその粉砕物をプロテアーゼあるいはプ
ロテアーゼとリパーゼで分解したものであるnプロテア
ーゼとしては、例えば動物由来のベズシン、膵ソロデア
ーゼ、微生物由来のアスベルギルx (Aspcrgi
llus )属、バチルス(Bacillus )属及
びストレプトマイセス(Streptomyces )
属グロテアーゼ、植物由来のパパイン、プロメチイン4
1ffl用することができる。
Examples of animals used in the present invention include mammals such as cows, pigs, horses, sheep, dogs, rabbits, and goats; birds such as chickens, ducks, turkeys, and guinea fowl; oysters, mysids, krill, lampreys, small fish, etc. Examples include fish and shellfish; reptiles such as stinging turtles and turtles. As the animal tissue, any of the whole animal and its organs such as liver and blood can be used, but in the case of large animals, it is particularly preferable to use the whole liver or blood. The product can be produced by extracting the entire bulk, for example, by boiling it in hot or boiling water for a long time, or by extracting it while enzymatically decomposing it by allowing protease or protease and lipase to act at 35 to 45C. Examples of the pulverized animal product include, in addition to the pulverized animal itself, those pulverized after freezing with liquid nitrogen, and pulverized freeze-dried products. An enzymatically decomposed product of an animal is a product obtained by decomposing an animal or its pulverized product with protease or protease and lipase.N proteases include, for example, animal-derived bezucin, pancreatic soloidease, and microorganism-derived asbergyl x (Aspcrgi).
llus), Bacillus and Streptomyces
genus grotease, papain of plant origin, promethiine 4
It can be used for 1ffl.

本発明に用いるt−トリプトファンの誘導体としては、
例えば1】−アセチル−を−トリプトファン、5−ヒド
ロキシトリプトファン等が挙げられる。
The t-tryptophan derivatives used in the present invention include:
Examples include 1]-acetyl-tryptophan, 5-hydroxytryptophan, and the like.

本発明の貧血予防剤の有効成分として使用される動物の
組織抽出物等及びt −) IJブトファン若しくはそ
の誘導体は、食品素材あるいは食品添加物として使用さ
れている極めて安全性の高いものであシ、マウスに対す
る急性毒性試験による50チ致死量は、雄の腹腔内投与
でいずれも50y/紛以上である。
Animal tissue extracts, etc. and t-) IJ butophane or its derivatives used as active ingredients of the anemia preventive agent of the present invention are extremely safe and are used as food materials or food additives. The lethal dose of 50 y/mt in acute toxicity tests for mice was 50 y/mt or more when administered intraperitoneally to males.

本発明に用いる動物の組織抽出物等とt−)リグトファ
ン若しくはその誘導体の配合比に、貧血状態、投与方法
等によって適宜選択できるが、一般には動物の組織抽出
物等1に対して、A−)リグトファン若しくはその誘導
体’t−0,01〜100の割合で、特に0.1〜20
の割合で混合して製剤するのが好ましく、このとき本発
明の貧血予防剤の効果が最も良好に発揮される。
The blending ratio of the animal tissue extract, etc. used in the present invention and t-)ligtophan or its derivative can be appropriately selected depending on the anemia condition, administration method, etc., but in general, the ratio of A- ) Ligtophan or its derivative 't-0.01 to 100, especially 0.1 to 20
It is preferable to mix and formulate the anemia prophylactic agent of the present invention in a ratio of .

本発明の貧血予防剤は、常法によシ、動物の組織抽出物
等とt−)リプトファン若しくはその誘導体及び製剤化
に必要な添加剤とを混合し、錠剤、丸剤、顆粒剤、カプ
セル剤等の経口製剤、注射剤等の非経口剤に製剤化する
ことができる。
The anemia preventive agent of the present invention can be prepared by mixing an animal tissue extract, etc. with t-)liptophan or a derivative thereof and additives necessary for formulation, and preparing tablets, pills, granules, etc. according to a conventional method. It can be formulated into oral preparations such as capsules and parenteral preparations such as injections.

本発明の貧血予防剤の投与量は、貧血の程度及び投与方
法によっても異なるが、例えば成人で1日あたシ有助成
分証で0.5〜10Fが望ましい。
The dosage of the anemia preventive agent of the present invention varies depending on the degree of anemia and the administration method, but is preferably 0.5 to 10 F per day for adults, for example.

実施例I SD系ラット(雄性、6週令、体重3502前後、1群
7匹)ヲ、スツポン粉末、t−)リプトファン、あるい
にスツポン粉末と!−トリグトファンを配合した粉末飼
料(第1表)で10日間飼育したのち、同飼料で飼育を
続けながら、毎日1回頚静脈よル体重の約1/200 
(約1.75m)の血液を20日間採血して実験的貧血
状態を生せしめつつ、随時赤血球数、ヘマトクリット値
、ヘモグロビン値の測定を行なった。その結果を第1図
〜第3図に示す。
Example I SD rats (male, 6 weeks old, weight around 3502, 7 rats per group) wo, stupon powder, t-) liptophan, or stupon powder! - After being fed a powdered feed containing trigtophan (Table 1) for 10 days, while continuing to be fed the same feed, the jugular vein was fed once a day, approximately 1/200 of the body weight.
(approximately 1.75 m) of blood was collected for 20 days to create an experimental anemia state, and the red blood cell count, hematocrit value, and hemoglobin value were measured from time to time. The results are shown in FIGS. 1 to 3.

M1図〜第3図から明らかなように、スツポン粉末とt
−1リプトフアンとを併用すると、これt単独で用いた
場合に比べ貧血の予防効果が高められた。
As is clear from Fig. M1 to Fig.
When used in combination with t-1 liptophan, the anemia preventive effect was enhanced compared to when used alone.

実施例2゜ 〔組成〕 スツポン凍結粉砕物 66.7% を一トリプトファン 16.6 コーンスターチ 4.9 結晶セルロース &3 カルボキシメチルセルロースカルシウム 3.5ヘマト
クリツト値が30〜35%の貧血状態の26〜35才の
女性10名に上記組成の錠剤(o、5? )?!−1日
4錠1ケ月間服用させたところ、1ケ月後のへマドクリ
ット値が全員35〜40%となり、貧血状態を大巾に改
善することができた。
Example 2 [Composition] 66.7% frozen and crushed stupon 1 tryptophan 16.6 corn starch 4.9 crystalline cellulose & 3 carboxymethyl cellulose calcium 3.5 Anemic 26-35 year olds with hematocrit values of 30-35% Tablets with the above composition (o, 5?) were given to 10 women? ! - When the patients were given 4 tablets a day for 1 month, their hematocrit values were 35-40% after 1 month, and their anemia status was significantly improved.

実施例3 〔組成〕 ワシ・ヘモグロビン凍結乾燥物 50.0%t−トリグ
トファン 5.θ 中鎖脂肪酸トリグリセライド 44.5天然トコフエロ
ール o5 上記各成分金よく混合し、ソフトゼラチンカプセルに3
00〜宛充横し、1日3粒宛服用する。
Example 3 [Composition] Lyophilized eagle hemoglobin 50.0% t-trigtophan 5. θ Medium-chain fatty acid triglyceride 44.5 Natural tocopherol o5 Mix each of the above ingredients well and place in a soft gelatin capsule.
Take 3 tablets per day.

実施例4 貧血予防、改善飲:P+: 〔組成〕 ■リンゴ酢 10.0重量部 ■クエン” 4.0 ■ビタミンBl O,05 ■ ’ n2o、os ■ ’ B3 0.2 ■ “ B6 0.05 ■アスコルビン酸 0.3 ■カフエイン 0.5 ■グラニユー糖 120.0 [相]蜂蜜 30.0 ■エタノール 10.0’ ■スツポン凍結粉砕物 10.0 @n−アセチル−6−)リブトファ7 2.0■ドリン
ク・フレーバー 4,5 q9ミネラルウオーター バランス 計1000 〔製法〕 ■〜Q?Il″充分攪拌溶解後p過し、ボトルに詰めで
殺菌後製品とする。
Example 4 Anemia prevention and improvement drink: P+: [Composition] ■Apple cider vinegar 10.0 parts by weight■Quen'' 4.0 ■Vitamin Bl O,05 ■'n2o,os ■'B3 0.2 ■“B6 0. 05 ■ Ascorbic acid 0.3 ■ Caffeine 0.5 ■ Granulated sugar 120.0 [Phase] Honey 30.0 ■ Ethanol 10.0' ■ Frozen crushed stupon 10.0 @n-acetyl-6-) ribtofa 7 2 .0■Drink/flavor 4,5 q9 mineral water Balance meter 1000 [Production method] ■~Q? After thoroughly stirring and dissolving, the mixture is filtered and bottled to produce a sterilized product.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図〜第3図は、いずれもラット全実験的貧血状態と
した場合の血液成分の経口変化を示す図面で、第1図な
赤血球数、第2図はへマドクリット値、第3図はヘモグ
ロビン値の経日変化を示す。 −Q : コ ン ト ロ −ル群 −−−〇−−−;1−トリプトファン群−−−−−ロー
−:スッポン粉末群 −一△□: スツポン粉末+を一トリプトファン群以上 (X103Cr+11s7IIIm:i) f、 1 
図採血開始後の日数 第 2 図 (%) 0 10 20 第 3 図 (?/dll)
Figures 1 to 3 are diagrams showing oral changes in blood components when rats are subjected to total experimental anemia. Figure 1 is the red blood cell count, Figure 2 is the hematocrit value, and Figure 3 is the It shows the change in hemoglobin value over time. -Q: Control group ---- ) f, 1
Figure Number of days after blood collection started Figure 2 (%) 0 10 20 Figure 3 (?/dll)

Claims (1)

【特許請求の範囲】[Claims] 1、 動物の組織抽出物、粉砕物及び酵素分解物よシな
る群から選ばれた物質並びにt−)リプトファン若しく
なその誘導体を有効成りとする貧血予防剤。
1. An anemia preventive agent which effectively contains a substance selected from the group consisting of animal tissue extracts, pulverized products, and enzymatically decomposed products, and t-)liptophan or its derivatives.
JP59055080A 1984-03-22 1984-03-22 Anemia preventing agent Granted JPS60199818A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59055080A JPS60199818A (en) 1984-03-22 1984-03-22 Anemia preventing agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59055080A JPS60199818A (en) 1984-03-22 1984-03-22 Anemia preventing agent

Publications (2)

Publication Number Publication Date
JPS60199818A true JPS60199818A (en) 1985-10-09
JPH0436135B2 JPH0436135B2 (en) 1992-06-15

Family

ID=12988723

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59055080A Granted JPS60199818A (en) 1984-03-22 1984-03-22 Anemia preventing agent

Country Status (1)

Country Link
JP (1) JPS60199818A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109481470A (en) * 2019-01-08 2019-03-19 广东海洋大学 A kind of preparation method of fish blood source iron supplementary

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109481470A (en) * 2019-01-08 2019-03-19 广东海洋大学 A kind of preparation method of fish blood source iron supplementary

Also Published As

Publication number Publication date
JPH0436135B2 (en) 1992-06-15

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