JP2012520883A - アルツハイマー病及び骨粗鬆症の治療並びに老化の軽減 - Google Patents
アルツハイマー病及び骨粗鬆症の治療並びに老化の軽減 Download PDFInfo
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Abstract
Description
本明細書に開示されている特徴はすべて、任意の組合せで組み合わせることができる。本明細書に開示されている各特徴は、同一の、等価の、又は類似の目的を果たす代替の特徴により置き換えることができる。したがって、明示的に別段の指定のない限り、開示されている各特徴は、一般的な一連の等価の又は類似の特徴の一例に過ぎない。
Claims (42)
- 疾患を治療するための方法であって、
それを必要としている対象へ、
酸化的リン酸化阻害剤、イオノフォア、及びアデノシン5’−一リン酸活性化タンパク質キナーゼ(AMPK)活性化剤からなる群から選択される第一の薬剤、
抗炎症活性を持つ第二の薬剤、及び
セロトニン活性を持つか維持する第三の薬剤
を含有する有効量の組成物を投与することを含み、
前記疾患が、アルツハイマー病、骨粗鬆症、睡眠時無呼吸、勃起機能不全、マッカードル病、又は炭水化物代謝障害である上記方法。 - 第一の薬剤が、メトホルミン、フェンホルミン、ブホルミン、エフェドリン、チロキシン、サリチルアニリド、又はサリチル酸である、請求項1に記載の方法。
- 第一の薬剤が、塩酸メトホルミンである、請求項2に記載の方法。
- 第二の薬剤が、非ステロイド性抗炎症性化合物である、請求項1に記載の方法。
- 第二の薬剤が、アスピリン、ジクロフェナク、イブプロフェン、インドメタシン、アセトアミノフェン、ニメスリド、又はCOX−2阻害剤である、請求項1に記載の方法。
- 第二の薬剤が、アスピリンである、請求項5に記載の方法。
- 第三の薬剤が、セロトニン又はセロトニン再取り込み阻害剤である、請求項1に記載の方法。
- 第三の薬剤が、硫酸セロトニン、セロトニンクレアチニン硫酸複合体、又は塩酸セロトニンである、請求項7に記載の方法。
- 前記組成物が、第一の薬剤5〜5,000mg、第二の薬剤1〜5,000mg、及び第三の薬剤0.1〜1000mg、又は同一の比の量で含有する、請求項1に記載の方法。
- 前記組成物が、第一の薬剤5〜1,500mg、第二の薬剤1〜1,000mg、及び第三の薬剤0.1〜100mg、又は同一の比の量で含有する、請求項9に記載の方法。
- 前記組成物が、第一の薬剤5〜1,000mg、第二の薬剤1〜500mg、及び第三の薬剤0.1〜50mg、又は同一の比の量で含有する、請求項10に記載の方法。
- 前記組成物が、塩酸メトホルミン、アスピリン、及びセロトニンクレアチニン硫酸複合体を含有する、請求項1に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜5,000mg、アスピリン1〜5,000mg、及びセロトニンクレアチニン硫酸複合体0.1〜1,000mg、又は同一の比の量で含有する、請求項12に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜1,500mg、アスピリン1〜1,000mg、及びセロトニンクレアチニン硫酸複合体0.1〜100mg、又は同一の比の量で含有する、請求項13に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜1,000mg、アスピリン1〜500mg、及びセロトニンクレアチニン硫酸複合体0.1〜50mg、又は同一の比の量で含有する、請求項14に記載の方法。
- 前記組成物が、薬学的に許容できる担体をさらに含む、請求項1に記載の方法。
- 前記組成物が、活性成分として第一、第二、及び第三の薬剤のみを含有する、請求項1に記載の方法。
- 第一の薬剤が、AMPK活性化剤である、請求項1に記載の方法。
- 前記組成物が、活性成分として第一、第二、及び第三の薬剤のみを含有する、請求項18に記載の方法。
- AMPK活性化剤が、メトホルミン、フェンホルミン、ブホルミン、5’−アミノイミダゾール−4−カルボキシアミド−リボヌクレオシド、チエノピリドン、レスベラトロール、ノートカトン、チアゾール及びアディポネクチンからなる群から選択される、請求項18に記載の方法。
- 第一の薬剤が、酸化的リン酸化阻害剤又はイオノフォアである、請求項1に記載の方法。
- 老化又は疲労を軽減するための方法であって、
それを必要としている対象へ、
酸化的リン酸化阻害剤、イオノフォア、及びAMPK活性化剤からなる群から選択される第一の薬剤、
抗炎症活性を持つ第二の薬剤、及び
セロトニン活性を持つか維持する第三の薬剤
を含有する有効量の組成物を投与することを含む上記方法。 - 第一の薬剤が、メトホルミン、フェンホルミン、ブホルミン、エフェドリン、チロキシン、サリチルアニリド、又はサリチル酸である、請求項22に記載の方法。
- 第一の薬剤が、塩酸メトホルミンである、請求項23に記載の方法。
- 第二の薬剤が、非ステロイド性抗炎症性化合物である、請求項22に記載の方法。
- 第二の薬剤が、アスピリン、ジクロフェナク、イブプロフェン、インドメタシン、アセトアミノフェン、ニメスリド、又はCOX−2阻害剤である、請求項22に記載の方法。
- 第二の薬剤が、アスピリンである、請求項26に記載の方法。
- 第三の薬剤が、セロトニン又はセロトニン再取り込み阻害剤である、請求項22に記載の方法。
- 第三の薬剤が、硫酸セロトニン、セロトニンクレアチニン硫酸複合体、又は塩酸セロトニンである、請求項28に記載の方法。
- 前記組成物が、第一の薬剤5〜5,000mg、第二の薬剤1〜5,000mg、及び第三の薬剤0.1〜1000mg、又は同一の比の量で含有する、請求項22に記載の方法。
- 前記組成物が、第一の薬剤5〜1,500mg、第二の薬剤1〜1,000mg、及び第三の薬剤0.1〜100mg、又は同一の比の量で含有する、請求項30に記載の方法。
- 前記組成物が、第一の薬剤5〜1,000mg、第二の薬剤1〜500mg、及び第三の薬剤0.1〜50mg、又は同一の比の量で含有する、請求項31に記載の方法。
- 前記組成物が、塩酸メトホルミン、アスピリン、及びセロトニンクレアチニン硫酸複合体を含有する、請求項22に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜5,000mg、アスピリン1〜5,000mg、及びセロトニンクレアチニン硫酸複合体0.1〜1,000mg、又は同一の比の量で含有する、請求項33に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜1,500mg、アスピリン1〜1,000mg、及びセロトニンクレアチニン硫酸複合体0.1〜100mg、又は同一の比の量で含有する、請求項34に記載の方法。
- 前記組成物が、塩酸メトホルミン5〜1,000mg、アスピリン1〜500mg、及びセロトニンクレアチニン硫酸複合体0.1〜50mg、又は同一の比の量で含有する、請求項35に記載の方法。
- 前記組成物が、薬学的に許容できる担体をさらに含む、請求項22に記載の方法。
- 前記組成物が、活性成分として第一、第二、及び第三の薬剤のみを含有する、請求項22に記載の方法。
- 第一の薬剤が、AMPK活性化剤である、請求項22に記載の方法。
- 前記組成物が、活性成分として第一、第二、及び第三の薬剤のみを含有する、請求項39に記載の方法。
- AMPK活性化剤が、メトホルミン、フェンホルミン、ブホルミン、5’−アミノイミダゾール−4−カルボキシアミド−リボヌクレオシド、チエノピリドン、レスベラトロール、ノートカトン、チアゾール、及びアディポネクチンからなる群から選択される、請求項39に記載の方法。
- 第一の薬剤が、酸化的リン酸化阻害剤又はイオノフォアである、請求項22に記載の方法。
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EP (1) | EP2408434A4 (ja) |
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JP2017523982A (ja) * | 2015-07-06 | 2017-08-24 | ソウル ナショナル ユニバーシティ アールアンドディービー ファウンデーション | Gpcr19作用剤を有効成分として含有する、アルツハイマー病または認知症を予防、治療、または遅延させるための薬学的組成物 |
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JP2013519738A (ja) * | 2010-02-12 | 2013-05-30 | オーシャンズ キング ライティング サイエンスアンドテクノロジー カンパニー リミテッド | ホウ珪酸塩発光材料及びその製造方法 |
JP2017523982A (ja) * | 2015-07-06 | 2017-08-24 | ソウル ナショナル ユニバーシティ アールアンドディービー ファウンデーション | Gpcr19作用剤を有効成分として含有する、アルツハイマー病または認知症を予防、治療、または遅延させるための薬学的組成物 |
KR20200077779A (ko) * | 2018-12-21 | 2020-07-01 | 연세대학교 산학협력단 | 퇴행성 뇌질환 발병 위험성 예측용 조성물 및 이를 이용한 퇴행성 뇌질환의 발병 위험성 예측 방법 |
KR102145438B1 (ko) | 2018-12-21 | 2020-08-18 | 연세대학교 산학협력단 | 퇴행성 뇌질환 발병 위험성 예측용 조성물 및 이를 이용한 퇴행성 뇌질환의 발병 위험성 예측 방법 |
WO2021029434A1 (ja) * | 2019-08-15 | 2021-02-18 | 賢 石井 | 首下がり症候群および胸腰椎脊柱変形の治療薬 |
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US8377947B2 (en) | 2013-02-19 |
US20100234295A1 (en) | 2010-09-16 |
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AU2010225923A1 (en) | 2011-11-10 |
WO2010107702A1 (en) | 2010-09-23 |
CN102395359A (zh) | 2012-03-28 |
EP2408434A1 (en) | 2012-01-25 |
EP2408434A4 (en) | 2013-11-27 |
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