JPH1059844A - Improving medicine for perception response function - Google Patents

Improving medicine for perception response function

Info

Publication number
JPH1059844A
JPH1059844A JP21555096A JP21555096A JPH1059844A JP H1059844 A JPH1059844 A JP H1059844A JP 21555096 A JP21555096 A JP 21555096A JP 21555096 A JP21555096 A JP 21555096A JP H1059844 A JPH1059844 A JP H1059844A
Authority
JP
Japan
Prior art keywords
perception
medicine
improving
dementia
function
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
JP21555096A
Other languages
Japanese (ja)
Inventor
Kazuyoshi Yazawa
一良 矢澤
Chikako Ishikawa
千夏子 石川
Kazuo Miyanaga
和夫 宮永
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.)
KANAGAWA KAGAKU KENKYUSHO KK
Sagami Chemical Research Institute
Original Assignee
KANAGAWA KAGAKU KENKYUSHO KK
Sagami Chemical Research Institute
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 KANAGAWA KAGAKU KENKYUSHO KK, Sagami Chemical Research Institute filed Critical KANAGAWA KAGAKU KENKYUSHO KK
Priority to JP21555096A priority Critical patent/JPH1059844A/en
Publication of JPH1059844A publication Critical patent/JPH1059844A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To obtain an improving medicine for perception responsive function applied to not only improvement of perception function lowered by senility, dementia, cerebropathy, etc., but also development of the perception function of healthy subject without side effects by using a specific unsaturated fatty acid as an active ingredient. SOLUTION: This improving medicine for perception responsive function is obtained by using docosahexaenoic acid as an active ingredient. The improving medicine for the perception responsive function is useful as a medicine for improving an auditory stimulation. The medicine is also useful as a medicine concerning dementia, especially a remedy or a preventive for the dementia. Not only a free acid but also its salt, ester, glyceride, phospholipid, choline compound, ascorbic acid compound, amino acid compound, etc., are used as the docosahexaenoic acid. The formulation amount of the docosahexaenoic acid based on the improving medicine for perception responsive function is 10-100wt.%, preferably 50-100wt.%.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は脳の認知応答機能改
善薬に関し、更に詳しくは、ドコサヘキサエン酸を有効
成分として含有することを特徴とする聴覚刺激に対する
認知応答機能改善薬に関するものである。
The present invention relates to a drug for improving the cognitive response function of the brain, and more particularly, to a drug for improving the cognitive response function to auditory stimulation characterized by containing docosahexaenoic acid as an active ingredient.

【0002】[0002]

【従来の技術】近年の人口の高齢化にともない、痴呆症
に対する薬剤の開発は医学的にも社会的にもますます重
要な課題となっており、優れた痴呆症関連薬剤に対する
期待は大きい。
2. Description of the Related Art With the aging of the population in recent years, the development of drugs for dementia has become an increasingly important issue both medically and socially, and there is great expectation for excellent dementia-related drugs.

【0003】ドコサヘキサエン酸は脳や網膜の興奮性膜
に多く含まれている不飽和脂肪酸で、アラキドン酸カス
ケードを阻害する作用を有することが知られている。ま
たこのほかに、幾つかの有用な生理作用を有することが
知られており、学習能力増強剤、記憶力増強剤、痴呆予
防剤、痴呆治療剤、抗痴呆薬または脳機能改善効果を有
する機能性食品等(特開平7-82146号、特開平5-117147
号、特開平2-49723号)の特許出願がなされている。しか
しながら、認知応答機能の改善作用、すなわち、ヒトに
視覚、体性感覚、聴覚などの刺激を与えた場合やヒトが
課題を遂行する場合に大脳から誘発された事象関連電位
の成分で、認知応答機能を反映する生理学的指標として
知られるP300のピークの潜時の減少作用、更には、痴呆
症患者の事象関連電位を増幅させその波形を正常化する
ことは全く知られていない。
[0003] Docosahexaenoic acid is an unsaturated fatty acid contained in a large amount in excitable membranes of the brain and retina and is known to have an action of inhibiting the arachidonic acid cascade. In addition, it is known to have some useful physiological actions, such as a learning ability enhancer, a memory enhancer, a dementia prevention agent, a dementia treatment agent, an anti-dementia agent or a functional having an effect of improving brain function. Food etc. (JP-A-7-82146, JP-A-5-117147
No. 2, JP-A-2-49723). However, the effect of improving cognitive response function, that is, the component of the event-related potential evoked from the cerebrum when a human is given a stimulus such as vision, somatic sensation, or hearing, or when a human performs a task, There is no known effect of reducing the latency of the peak of P300, which is known as a physiological index reflecting function, and further normalizing the waveform by amplifying the event-related potential of dementia patients.

【0004】[0004]

【発明が解決しようとする課題】本発明は特定の刺激に
対する応答を速やかに改善する、副作用のない認知応答
機能改善薬を提供する。
DISCLOSURE OF THE INVENTION The present invention provides a cognitive response function-improving drug which rapidly improves response to a specific stimulus without side effects.

【0005】[0005]

【課題を解決するための手段】本発明者らは、上記の課
題を解決すべく鋭意検討を重ねた結果、ドコサヘキサエ
ン酸の投与が事象関連電位(ERP: Event related potent
ial)の成分であるP300のピーク潜時を速め、さらには、
痴呆症患者の事象関連電位を増幅させその波形を改善し
正常化するという新たな知見に基づき、本発明を完成し
た。すなわち、本発明はドコサヘキサエン酸を有効成分
として含有する認知応答機能改善薬に関するものであ
る。
Means for Solving the Problems The present inventors have conducted intensive studies in order to solve the above-mentioned problems, and as a result, it has been found that administration of docosahexaenoic acid causes an event-related potential (ERP).
ial), which accelerates the peak latency of P300.
The present invention has been completed based on the new finding that the event-related potential of a dementia patient is amplified to improve and normalize its waveform. That is, the present invention relates to a cognitive response function improving drug containing docosahexaenoic acid as an active ingredient.

【0006】[0006]

【発明の実施の形態】本発明の認知応答機能改善薬は、
加齢、痴呆、脳障害等によって低下した認知機能の改善
のみならず、健常者における認知機能の向上などに適用
される。本発明におけるドコサヘキサエン酸とは、遊離
酸をはじめ、その塩、エステル、グリセリド、リン脂
質、コリン化合物、アスコルビン酸化合物、アミノ酸化
合物等を意味するものである。このドコサヘキサエン酸
を含む油としては、好ましくは総脂肪酸中のドコサヘキ
サエン酸(遊離酸として)の占める割合が10%以上のもの
をいう。
BEST MODE FOR CARRYING OUT THE INVENTION The drug for improving cognitive response function of the present invention comprises:
The present invention is applied not only to improvement of cognitive function reduced due to aging, dementia, brain disorder, etc., but also to improvement of cognitive function in healthy subjects. The docosahexaenoic acid in the present invention means free acids, salts, esters, glycerides, phospholipids, choline compounds, ascorbic acid compounds, amino acid compounds and the like. The oil containing docosahexaenoic acid preferably refers to an oil in which docosahexaenoic acid (as a free acid) accounts for 10% or more of the total fatty acids.

【0007】本発明の認知応答機能改善薬は治療のため
に経口的あるいは非経口的に投与することができる。経
口投与剤としては散剤、顆粒剤、カプセル剤、錠剤など
の固形製剤あるいはシロップ剤、エリキシル剤などの液
状製剤とすることができる。また、非経口投与剤として
注射剤とすることができる。これらの製剤は活性成分に
薬理学的、製剤学的に認容される製造助剤を加えること
により、公知の製造法、例えば日本薬局方第10版製剤
総則記載の方法ないし適当な改良を加えた方法によって
製造することができる。更に公知の技術により持続性製
剤とすることも可能である。当該製造助剤を用いる場合
は、本発明の認知応答機能改善薬中のドコサヘキサエン
酸(遊離酸として)の配合量は通常は10〜100重量%、
好ましくは50〜100重量%である。
The cognitive response function improving agent of the present invention can be administered orally or parenterally for treatment. Oral preparations can be solid preparations such as powders, granules, capsules and tablets, or liquid preparations such as syrups and elixirs. In addition, injections can be prepared as parenteral administration agents. These preparations are prepared by adding pharmacologically and pharmaceutically acceptable production auxiliaries to the active ingredients to give known production methods, for example, the method described in the Japanese Pharmacopoeia, 10th Edition, General Preparations, or appropriate improvements. It can be manufactured by a method. Furthermore, it is also possible to prepare a sustained-release preparation by a known technique. When using the production aid, the amount of docosahexaenoic acid (as a free acid) in the cognitive response function improving agent of the present invention is usually 10 to 100% by weight,
Preferably it is 50 to 100% by weight.

【0008】本発明において、事象関連電位(ERP: Even
t related potential)の測定は、日本脳波筋電図学会誘
発電位検査法委員会の定めた誘発電位測定指針に従い、
弁別反応時間課題を用いて行った。すなわち、1000Hz(1
0〜20%)と2000Hz(80〜90%)のランダム刺激を持続時間10
0msec、刺激間隔2sec、刺激強度は最低可聴域プラス50
dbの音をヘッドホンにより両耳に呈示し、1000Hzの目標
音が聞こえた時に手元のボタンを押すことにより行っ
た。誘導は前頭部(Frontal)、中央部(Central)、側頭部
(Parietal)、後頭部(Occipital)の各左右、計8箇所よ
り行い、両耳朶を連結し基準電極とした。
In the present invention, an event-related potential (ERP: Even
t related potential) is measured according to the evoked potential measurement guidelines set by the EEG EMG test committee,
The discrimination reaction time task was used. That is, 1000 Hz (1
0-20%) and 2000Hz (80-90%) random stimulus for 10 minutes
0msec, stimulus interval 2sec, stimulus intensity is minimum audible range plus 50
The sound of the db was presented to both ears through headphones, and when the target sound of 1000 Hz was heard, the sound was performed by pressing a button at hand. Leads to frontal (Frontal), central (Central), temporal
(Parietal) and occipital (Occipital) were performed from a total of eight places, and both earlobes were connected to form a reference electrode.

【0009】事象関連電位の各波の同定は、刺激開始か
ら80〜250msecの間の極大陰性電位を自動的あるいは制
御的な刺激分類過程を反映する内因性成分とされるN200
の潜時とし、250〜600msecの間の極大陽性電位を選択的
注意や認知機能を反映して変動する内因性成分とされる
P300の潜時とした。
The identification of each wave of the event-related potential is based on the fact that the maximum negative potential between 80 and 250 msec from the start of the stimulus is regarded as an intrinsic component that reflects the automatic or controlled stimulus classification process.
The latent positive potential between 250 and 600 msec is considered to be an intrinsic component that fluctuates reflecting selective attention and cognitive function
Latency of P300.

【0010】以下、実施例、参考例により本発明を更に
詳細に説明するが、本発明は何らこれらに限定されるも
のではない。
Hereinafter, the present invention will be described in more detail with reference to Examples and Reference Examples, but the present invention is not limited thereto.

【0011】[0011]

【実施例】【Example】

実施例1 健常者21人(表1)に対して、前記の方法により事象関連
電位(ERP)の測定を行った後、DHAトリグリセリド(DHAと
して150mg/粒)を含有するカプセル20粒を内服させ、2
時間後に再度ERPの測定を行った。加算回数は40回で、
平均加算は、標的刺激と標準刺激のそれぞれについて別
々に記録し、N200とP300の潜時を求めた。その結果を表
2に示す。P300のコントロールとして、DHAの投与に対
する反応性のよかったグループを抽出し(n=3)、上記DHA
の投与から1ケ月経過後、無投薬で1回目の測定とその
2時間後に2回目のERPの測定を行った。結果を表3に
示す。
Example 1 Twenty-one healthy subjects (Table 1) were measured for event-related potential (ERP) by the above-mentioned method, and then 20 capsules containing DHA triglyceride (150 mg / particle as DHA) were taken. , 2
After an hour, ERP measurement was performed again. The number of additions is 40,
The average addition was recorded separately for each of the target and standard stimuli, and the latency of N200 and P300 was determined. Table 2 shows the results. As a control for P300, a group that was highly responsive to DHA administration was extracted (n = 3), and the DHA
One month after the administration of No.1, the first measurement was performed without medication, and the second measurement of ERP was performed two hours later. Table 3 shows the results.

【0012】[0012]

【表1】 [Table 1]

【0013】[0013]

【表2】 [Table 2]

【0014】[0014]

【0015】[0015]

【表3】 [Table 3]

【0016】表2より、N200は不変であったが、P300は
何れの部位においても潜時が短くなっていることが観察
された。一方、表3より無投薬では1回目とその2時間
後の測定における潜時の変化は認められなかった。従っ
て、健常者におけるDHAの投与はP300の潜時を速め、短
縮することから認知応答機能の改善効果が認められた。
From Table 2, it was observed that N200 was unchanged, but P300 had a shorter latency at any site. On the other hand, from Table 3, no change in latency was observed between the first measurement and the measurement 2 hours after no-medication. Therefore, administration of DHA in healthy subjects accelerated and shortened the latency of P300, indicating an improvement in cognitive response function.

【0017】実施例2 痴呆症患者に対して、実施例1と同様の方法によりERP
の測定を行い、N200とP300の潜時を求めた。その結果を
表4及び図1、2に示す。
Example 2 ERP was performed on a dementia patient in the same manner as in Example 1.
Was measured to determine the latency of N200 and P300. The results are shown in Table 4 and FIGS.

【0018】[0018]

【表4】 [Table 4]

【0019】表4及び図1、2より明らかなように、DH
Aカプセルの投与はP300の潜時を速め、かつ、ERPの波形
を正常化させた。従って、痴呆症患者においても認知応
答改善効果が認められた。
As is clear from Table 4 and FIGS.
The administration of the A capsule accelerated the latency of P300 and normalized the waveform of ERP. Therefore, a cognitive response improvement effect was also observed in dementia patients.

【0020】参考例1 対象者として、P300のコントロールと重ならないように
実施例1のDHA投与に対する反応性のよかった健常者を
抽出し(n=4)、DHA投与に対する測定から1ケ月後、DHA
トリグリセリドをEPA-エチルエステルのカプセル(エパ
デール:純度90%,300mg)に代えた他は実施例1と同様の
方法によりERPの測定を行い、N200とP300の潜時を求め
た。その結果を表5に示す。
Reference Example 1 As subjects, healthy subjects having good responsiveness to DHA administration in Example 1 were extracted so as not to overlap with the control of P300 (n = 4). One month after the measurement for DHA administration, DHA was performed.
The ERP was measured in the same manner as in Example 1 except that the triglyceride was replaced with EPA-ethyl ester capsules (epadel: purity 90%, 300 mg), and the latency of N200 and P300 was determined. Table 5 shows the results.

【0021】[0021]

【表5】 [Table 5]

【0022】表5より、EPA投与によるP300の潜時の変
化は認められなかた。
From Table 5, no change in the latency of P300 due to EPA administration was observed.

【0023】[0023]

【発明の効果】本発明のドコサヘキサエン酸を有効成分
として含有する認知応答機能改善薬は、健常者や痴呆症
患者の事象関連電位(ERP: Event related potential)P3
00のピーク潜時を速め、認知応答機能を改善する。この
改善効果は加齢、痴呆、脳障害等によって低下した認知
機能の改善のみならず、健常者における認知機能の向上
をも意味するものであり、痴呆の予防、治療薬として有
用である。
EFFECT OF THE INVENTION The cognitive response function-improving agent containing docosahexaenoic acid of the present invention as an active ingredient is useful for the event-related potential (ERP) P3 of healthy subjects and dementia patients.
Increases the peak latency of 00 and improves cognitive response. This improvement effect means not only improvement of cognitive function reduced by aging, dementia, brain disorder, etc., but also improvement of cognitive function in healthy subjects, and is useful as a preventive or therapeutic drug for dementia.

【0024】[0024]

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

【図1】図1は、痴呆症患者に対してのDHAトリグリセ
リド投与前の事象関連電位を示す。
FIG. 1 shows event-related potentials before administration of DHA triglyceride to dementia patients.

【図2】図2は、痴呆症患者に対してのDHAトリグリセ
リド投与後の事象関連電位を示す。
FIG. 2 shows event-related potentials after administration of DHA triglyceride to dementia patients.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ドコサヘキサエン酸を有効成分として含
有することを特徴とする認知応答機能改善薬。
1. A cognitive response function improving drug comprising docosahexaenoic acid as an active ingredient.
【請求項2】 認知が聴覚刺激に対するものである請求
項1に記載の認知応答機能改善薬。
2. The cognitive response function improving drug according to claim 1, wherein the cognition is for an auditory stimulus.
JP21555096A 1996-08-15 1996-08-15 Improving medicine for perception response function Pending JPH1059844A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21555096A JPH1059844A (en) 1996-08-15 1996-08-15 Improving medicine for perception response function

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21555096A JPH1059844A (en) 1996-08-15 1996-08-15 Improving medicine for perception response function

Publications (1)

Publication Number Publication Date
JPH1059844A true JPH1059844A (en) 1998-03-03

Family

ID=16674294

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21555096A Pending JPH1059844A (en) 1996-08-15 1996-08-15 Improving medicine for perception response function

Country Status (1)

Country Link
JP (1) JPH1059844A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015005443A1 (en) * 2013-07-10 2015-01-15 ライオン株式会社 Oral composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015005443A1 (en) * 2013-07-10 2015-01-15 ライオン株式会社 Oral composition
US9480672B2 (en) 2013-07-10 2016-11-01 Lion Corporation Internal composition
JPWO2015005443A1 (en) * 2013-07-10 2017-03-02 ライオン株式会社 Oral composition

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