JP2001039887A - Prophylactic/therapeutic preparation for dementia and prophylactic/therapeutic method for dementia using the same - Google Patents
Prophylactic/therapeutic preparation for dementia and prophylactic/therapeutic method for dementia using the sameInfo
- Publication number
- JP2001039887A JP2001039887A JP11215312A JP21531299A JP2001039887A JP 2001039887 A JP2001039887 A JP 2001039887A JP 11215312 A JP11215312 A JP 11215312A JP 21531299 A JP21531299 A JP 21531299A JP 2001039887 A JP2001039887 A JP 2001039887A
- Authority
- JP
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- Prior art keywords
- dementia
- extract
- preparation
- astragalus
- therapeutic
- Prior art date
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、これまで予防およ
び治療が困難とされた痴呆症の予防・治療に関し、痴呆
の十分な予防及び治療を可能とする画期的予防・治療製
剤および該製剤を用いた痴呆の予防あるいは治療方法に
関する。TECHNICAL FIELD The present invention relates to the prevention and treatment of dementia, which has been difficult to prevent and treat so far, and an epoch-making prophylactic / therapeutic preparation capable of sufficiently preventing and treating dementia and the preparation. And a method for preventing or treating dementia using the same.
【0002】[0002]
【従来の技術】痴呆は、一般的には加齢に伴って発生す
るが、このほかにも薬剤による後遺的障害としても引き
起こされる。 薬剤による痴呆の代表としては、パーキ
ンソン病の治療薬として使用されているドーパの長期投
与によるものがある。 すなわちパーキンソン病は、錐
体外路系変性疾患であり、多くの場合、中年以後に発症
する。臨床的には無動、筋固縮、静止時振戦、姿勢反射
異常、自律神経症状などを主な特徴とし、とくに治療薬
として知られるL−ドーパは、長期にわたる使用により
痴呆が発生する。2. Description of the Related Art Dementia generally occurs with aging, but is also caused as a sequelae by drugs. A representative example of drug-induced dementia is long-term administration of dopa, which is used as a therapeutic drug for Parkinson's disease. That is, Parkinson's disease is an extrapyramidal degenerative disease that often develops after middle age. Clinically, it is characterized by immobility, muscle rigidity, tremor at rest, abnormal posture reflex, and autonomic nervous symptoms. L-dopa, which is known as a therapeutic agent, causes dementia due to long-term use.
【0003】[0003]
【発明が解決しようとする課題】これまでに痴呆症に対
する有効な治療・改善薬剤がないことから、その十分な
予防・治療に使用できる画期的製剤の開発が望まれ、特
にパーキンソン病治療薬として広く使用されているドー
パによって誘発される後遺的痴呆障害発生の予防あるい
は治療に使用できる製剤の開発が望まれていた。Since there has been no effective therapeutic or ameliorating agent for dementia so far, it has been desired to develop an epoch-making preparation which can be used for its sufficient prevention and treatment. It has been desired to develop a preparation that can be used for preventing or treating the occurrence of sequelae of dementia induced by dopa, which is widely used.
【0004】[0004]
【課題を解決するための手段】そこで本発明者らは、漢
方の生薬系を中心に鋭意研究を重ねた結果、生薬として
の黄耆および晋耆からの抽出エキスが痴呆症の予防・治
療に有効であること、またとくに黄耆および晋耆エキス
がドーパ誘発性痴呆の予防・治療に有効であることを初
めて明らかとし、発明を完成するに至った。Means for Solving the Problems The inventors of the present invention have conducted intensive studies mainly on Chinese herbal medicines. As a result, the extracts from Astragalus and Astragalus as herbal medicines are useful for the prevention and treatment of dementia. The present invention was first clarified to be effective, and in particular, it was found that Astragali and Shinki extract are effective for prevention and treatment of dopa-induced dementia, and completed the invention.
【0005】すなわち、請求項1の発明は、生薬として
の黄耆あるいは晋耆エキス(各エキスに含有される活性
を有する化合物類を含む)のうち、少なくとも1種を含
む痴呆予防・治療用製剤に関する。 また請求項2の発
明は、痴呆がドーパ誘発性痴呆である請求項1記載の痴
呆予防・治療製剤に関する。 さらに請求項3の発明
は、痴呆予防・治療用製剤が健康食品である請求項1記
載の痴呆予防・治療製剤に関する。[0005] That is, the invention of claim 1 is a preparation for the prevention and treatment of dementia, comprising at least one of astragalus or radix as a crude drug (including compounds having an activity contained in each extract). About. The invention of claim 2 relates to the preventive / therapeutic preparation for dementia according to claim 1, wherein the dementia is dopa-induced dementia. Furthermore, the invention of claim 3 relates to the preparation for prevention / treatment of dementia according to claim 1, wherein the preparation for prevention / treatment of dementia is a health food.
【0006】さらに請求項4の発明は、痴呆予防治療用
製剤が医薬品である請求項1記載の痴呆予防・治療製剤
に関する。 さらに請求項5の発明は、生薬としての黄
耆あるいは晋耆エキス(各エキスに含有される活性を有
する化合物類を含む)のうち、少なくとも1種を含む痴
呆予防・治療用製剤を用いた痴呆の予防あるいは治療方
法に関する。Further, the invention of claim 4 relates to the preparation for preventing and treating dementia according to claim 1, wherein the preparation for preventing and treating dementia is a pharmaceutical. Further, the invention of claim 5 provides a dementia using a preparation for the prevention and treatment of dementia, which comprises at least one of astragalus or radix as a crude drug extract (including compounds having an activity contained in each extract). The present invention relates to a method for preventing or treating the disease.
【0007】[0007]
【発明の実施の形態】以下において本発明の具体的な内
容を説明すると、本発明は痴呆症の予防・治療に、生薬
としての黄耆あるいは晋耆エキス及びそれらエキスに含
有される活性を有する化合物を用いることを特徴とする
ものである。 さらにここでいう黄耆あるいは晋耆は、
いずれも漢方の分野における生薬としてのものを意味
し、黄耆あるいは晋耆は、抽出エキスの形態で利用され
る。BEST MODE FOR CARRYING OUT THE INVENTION The specific contents of the present invention will be described below. The present invention has an Astragalus or Shinki extract as a crude drug and an activity contained in these extracts for the prevention and treatment of dementia. It is characterized by using a compound. In addition, Kioki or Shinoki here,
Each of them means a herbal medicine in the field of Chinese medicine, and Asagi or Shinoki is used in the form of an extract.
【0008】またここでいう黄耆あるいは晋耆の抽出エ
キスには、それらのエキスに含有される活性を有する化
合物類をも含むものとする。 さらに痴呆の予防あるい
は治療に使用される上記した薬剤のなかには、脳機能を
改善する作用を有するものもある。 生薬としての黄耆
あるいは晋耆からのエキス抽出は、適当な抽出溶媒を用
いて行なえるが、湯煎やエタノール抽出方法、クロマト
グラフィー法等を用いることができる。[0008] The extract of Astragalus or Astragalus referred to herein also includes active compounds contained in these extracts. Furthermore, some of the above-mentioned drugs used for the prevention or treatment of dementia have an effect of improving brain function. Extraction from Astragalus or Astragalus as a crude drug can be carried out using an appropriate extraction solvent, but hot water roasting, ethanol extraction, chromatography and the like can be used.
【0009】この場合、抽出液の塩濃度やpHを変化さ
せることにより、より効率的にエキスの抽出をおこなう
ことができる。 またこの場合黄耆エキスあるいは晋耆
エキスを用いて抗痴呆作用を検出できる適当な評価系に
て活性のスクリーニングを行い、本活性を指標として黄
耆エキスあるいは晋耆エキスをクロマトグラフィー等で
分画することにより活性化合物を分離精製することがで
きる。In this case, the extract can be more efficiently extracted by changing the salt concentration or pH of the extract. In this case, screening for activity is carried out with an appropriate evaluation system that can detect the anti-dementia effect using Astragalus extract or Astragalus extract, and this activity is used as an index to fractionate Astragalus extract or Astragalus extract by chromatography etc. By doing so, the active compound can be separated and purified.
【0010】本発明の痴呆の予防・治療製剤としては、
医薬品あるいは健康食品の用途があげられ、また投与経
路としては、ドリンク剤、錠剤、カプセル剤、顆粒剤、
散剤、シロップ剤などによる経口投与、坐剤などによる
非経口投与、注射剤による静脈投与や皮下投与、軟膏剤
による経皮投与があげられる。 また一般的に使用され
る賦形剤、結合剤、崩壊剤、湿潤剤を用いて錠剤等の成
形を行なうこともできる。 さらにこれらに対し、適当
なコーティングを施すこともできる。The preventive / therapeutic preparations for dementia of the present invention include:
It is used for pharmaceuticals or health foods, and administration routes include drinks, tablets, capsules, granules,
Examples include oral administration with powders and syrups, parenteral administration with suppositories and the like, intravenous and subcutaneous administration with injections, and transdermal administration with ointments. Tablets and the like can also be formed using commonly used excipients, binders, disintegrants and wetting agents. Further, an appropriate coating can be applied to these.
【0011】また前記したシロップ剤等の液体製剤で
は、一般的に使用されるレシチン等の乳化剤やメチルセ
ルロース等の懸濁化剤、保存剤を用いて調製することが
できる。 さらに製剤の投与量は、投与形態、患者の症
状や年齢、性別、体重、使用される化合物によって異な
るが、経口投与の場合、成人で1日あたり0.1μg〜
50gを1〜3回に分けて投与できる。より好ましく
は、0.1mg〜5gを1〜3回に分けて投与すること
ができる。 またこれらの抽出エキスの投与量について
は、そのいずれのものにあっても投与の継続期間がある
程度長ければ微量であっても効果がみられる。The above liquid preparations such as syrups can be prepared using commonly used emulsifiers such as lecithin, suspending agents such as methylcellulose, and preservatives. Further, the dosage of the preparation varies depending on the form of administration, the condition and age of the patient, the sex, the body weight, and the compound to be used.
50 g can be administered in 1 to 3 divided doses. More preferably, 0.1 mg to 5 g can be administered in 1 to 3 divided doses. Regarding the dosage of these extracts, even if the amount of the extract is very small as long as the administration period is relatively long, the effect can be seen.
【0012】〔実施例1〕黄耆および晋耆エキスの抗痴
呆作用の評価 黄耆および晋耆エキスの調製 黄耆100gあるいは晋耆100gをフラスコに入れ、
これに蒸留水を加えた。 これを加熱し、60分間沸騰
させた後、室温にて2時間放置した。 放置後、濾過と
遠心分離により上清を分離し、これを凍結乾燥させて黄
耆エキス21g、晋耆エキス20gを調製し、抗痴呆作
用の評価に使用した。[Example 1] Evaluation of anti-dementia action of Astragalus and Astragalus extracts Preparation of Astragalus and Astragalus extract 100 g of Astragalus or Astragalus 100 g in a flask,
Distilled water was added to this. This was heated and boiled for 60 minutes, and then left at room temperature for 2 hours. After standing, the supernatant was separated by filtration and centrifugation, and the supernatant was freeze-dried to prepare 21 g of Astragalus extract and 20 g of Astragalus extract, which were used for evaluation of the anti-dementia effect.
【0013】 ドーパ誘発性痴呆マウスの調製 C57BL/6マウス(雄、8週齢)にL−ドーパ(シ
グマ社製)の単回経口投与(100〜1000mg/k
g)をおこなった。 次に、黄耆エキス(1g/kg/
day)あるいは晋耆エキス(1g/kg/day)を
L−ドーパの投与24時間後から14日間自由摂取させ
たマウスをステップスルー型受動的回避実験装置による
評価に使用した。Preparation of Dopa-induced Dementia Mice A single oral administration (100-1000 mg / k) of L-dopa (Sigma) to C57BL / 6 mice (male, 8 weeks old)
g) was performed. Next, astragalus extract (1 g / kg /
day) or Shinoki extract (1 g / kg / day) was freely taken for 14 days from 24 hours after the administration of L-dopa, and used for evaluation by a step-through passive avoidance experiment apparatus.
【0014】 ステップスルー型受動的回避実験装置
による評価 白色光で照射した明室(20×10×12cm)と床に
電気ショックを付加することが出来る金属グリッドを取
り付けた暗室(30×30×30cm)からなり、明室
と暗室の間は可動式のギロチンドアで仕切られたステッ
プスルー型受動的回避実験装置を使用して抗痴呆効果の
評価を行った。Evaluation by a step-through passive avoidance experiment device A bright room (20 × 10 × 12 cm) irradiated with white light and a dark room (30 × 30 × 30 cm) fitted with a metal grid capable of applying an electric shock to the floor ), And the anti-dementia effect was evaluated using a step-through type passive avoidance experiment device partitioned by a movable guillotine door between the light room and the dark room.
【0015】前記で調製したマウスを、明室と暗室を
自由に出入りできる状態で約1分間装置内に入れて装置
に慣れさせた。 次に、ギロチンドアを閉め、マウスを
明室に入れて30秒後に再びギロチンドアを開け、マウ
スが四肢を完全に暗室に移動したところでギロチンドア
を閉め、3mA、5秒間の電気ショックを付加した。
24時間後にギロチンドアを開けた状態のステップスル
ー型受動的回避実験装置の明室にマウスを入れ、暗室へ
移動するか否かを観察した。The mouse prepared as described above was put into the apparatus for about 1 minute in a state where the mouse could freely enter and exit the bright room and the dark room, and was used to the apparatus. Next, the guillotine door was closed, the mouse was put in the light room, and after 30 seconds, the guillotine door was opened again. When the mouse had completely moved the extremities to the dark room, the guillotine door was closed, and an electric shock of 3 mA for 5 seconds was applied. .
Twenty-four hours later, the mouse was placed in a bright room of the step-through type passive avoidance experiment device with the guillotine door opened, and it was observed whether or not the mouse moved to a dark room.
【0016】黄耆エキスあるいは晋耆エキス投与群は、
全てのマウスが暗室への移動をしなかったのに対して、
コントロール群のマウスは、全て暗室へ移動したことよ
り、黄耆エキスおよび晋耆エキス投与マウスには学習障
害の改善が認められ、したがって黄耆および晋耆は、痴
呆症の予防・治療にきわめて有効であることが明らかと
なった。[0016] The group administered with the Astragalus extract or the Astragalus extract is
While all mice did not move to the darkroom,
Since all mice in the control group moved to the dark room, mice with administration of Astragalus extract and Aspergillus extract showed improvement in learning disability. Therefore, Astragalus and Astragalus were extremely effective in preventing and treating dementia. It became clear that it was.
【0017】なお上記の実施例においては、痴呆症の予
防・治療薬の評価の一例としてドーパ誘発性痴呆の場合
について説明しているが、薬剤の評価は、本評価系に限
定されない。 また痴呆の評価方法としても、上記実施
例によるほかに、学習能力を評価するステップスルー試
験がある。In the above embodiment, the case of dopa-induced dementia is described as an example of the evaluation of a preventive / therapeutic agent for dementia, but the evaluation of the drug is not limited to this evaluation system. As a method for evaluating dementia, there is a step-through test for evaluating learning ability, in addition to the above-described embodiment.
【0018】[0018]
【発明の効果】以上詳述した通り、本発明は生薬として
の黄耆あるいは晋耆エキス(各エキスに含有される活性
を有する化合物類を含む)のうち、少なくとも1種を含
むものであるから、痴呆予防・治療用製剤として痴呆症
の予防・治療に、また痴呆症の予防・治療方法として画
期的効果をもたらす。 また本発明は、これらの生薬の
単独投与だけでなく、これまでにも知られ、あるいは将
来的に生成される各種の痴呆症改善薬剤との併用使用が
可能である。As described in detail above, the present invention contains at least one of astragalus or radix as a crude drug (including compounds having an activity contained in each extract). It has an epoch-making effect as a prophylactic / therapeutic preparation for the prevention and treatment of dementia and a method for the prevention and treatment of dementia. In addition, the present invention can be used in combination with not only single administration of these crude drugs but also various dementia ameliorating agents known or produced in the future.
【0019】また本発明の化合物の望ましい投与形態
は、経口投与によるものであるが、このほかにも各種の
投与形態での投与が可能であり、また化合物の吸収や生
体内での安定性等を考慮することにより投与形態は適宜
選択できる。The desirable dosage form of the compound of the present invention is oral administration. In addition, the compound can be administered in various dosage forms, and the compound can be absorbed and its stability in a living body. The administration form can be appropriately selected by considering the above.
Claims (5)
エキスに含有される活性を有する化合物類を含む)のう
ち、少なくとも1種を含む痴呆予防・治療用製剤。1. A preparation for the prevention and treatment of dementia, comprising at least one of astragalus or radix as a crude drug extract (including compounds having an activity contained in each extract).
載の痴呆予防・治療製剤。2. The preventive / therapeutic preparation for dementia according to claim 1, wherein the dementia is dopa-induced dementia.
求項1記載の痴呆予防・治療製剤。3. The preparation for preventing or treating dementia according to claim 1, wherein the preparation for preventing or treating dementia is a health food.
1記載の痴呆予防・治療製剤。4. The preparation for preventing or treating dementia according to claim 1, wherein the preparation for preventing or treating dementia is a pharmaceutical.
エキスに含有される活性を有する化合物類を含む)のう
ち、少なくとも1種を含む痴呆予防・治療用製剤を用い
た痴呆の予防あるいは治療方法。5. A method for preventing or treating dementia using a preparation for the prevention and treatment of dementia comprising at least one of the astragalus or radix extracts as active crude drugs (including compounds having an activity contained in each extract). Method of treatment.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP11215312A JP2001039887A (en) | 1999-07-29 | 1999-07-29 | Prophylactic/therapeutic preparation for dementia and prophylactic/therapeutic method for dementia using the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11215312A JP2001039887A (en) | 1999-07-29 | 1999-07-29 | Prophylactic/therapeutic preparation for dementia and prophylactic/therapeutic method for dementia using the same |
Publications (1)
Publication Number | Publication Date |
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JP2001039887A true JP2001039887A (en) | 2001-02-13 |
Family
ID=16670243
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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JP11215312A Pending JP2001039887A (en) | 1999-07-29 | 1999-07-29 | Prophylactic/therapeutic preparation for dementia and prophylactic/therapeutic method for dementia using the same |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006068155A1 (en) * | 2004-12-22 | 2006-06-29 | National University Corporation University Of Toyama | Agent for reconstructing neural network comprising chinese medicine formulation and method of reconstructing neural network |
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JPH06172196A (en) * | 1992-12-04 | 1994-06-21 | Pola Chem Ind Inc | Blood viscosity depressant and composition containing the same |
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1999
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JPS61263905A (en) * | 1985-05-17 | 1986-11-21 | Pola Chem Ind Inc | Cosmetic |
JPH0539305A (en) * | 1990-02-09 | 1993-02-19 | Indena Spa | Immuno suppressive polysaccharide extracted from astragalus membranaceous and pharma- ceutical composition containing same |
JPH06125738A (en) * | 1992-10-16 | 1994-05-10 | Eiko Sangyo Kk | Beverage or food comprising lactose fermentation product containing organic germanium compound |
JPH06172196A (en) * | 1992-12-04 | 1994-06-21 | Pola Chem Ind Inc | Blood viscosity depressant and composition containing the same |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2006068155A1 (en) * | 2004-12-22 | 2006-06-29 | National University Corporation University Of Toyama | Agent for reconstructing neural network comprising chinese medicine formulation and method of reconstructing neural network |
JPWO2006068155A1 (en) * | 2004-12-22 | 2008-06-12 | 国立大学法人富山大学 | Neural network restructuring agent and method for reconstructing neural network by Kampo prescription |
JP5044782B2 (en) * | 2004-12-22 | 2012-10-10 | 国立大学法人富山大学 | Neural network restructuring agent and method for reconstructing neural network by Kampo prescription |
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