JP2013517847A5 - - Google Patents
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- JP2013517847A5 JP2013517847A5 JP2012550219A JP2012550219A JP2013517847A5 JP 2013517847 A5 JP2013517847 A5 JP 2013517847A5 JP 2012550219 A JP2012550219 A JP 2012550219A JP 2012550219 A JP2012550219 A JP 2012550219A JP 2013517847 A5 JP2013517847 A5 JP 2013517847A5
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- cardiac glycoside
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- 239000008194 pharmaceutical composition Substances 0.000 claims 64
- 210000002569 neurons Anatomy 0.000 claims 16
- LPMXVESGRSUGHW-HBYQJFLCSA-N Ouabain Chemical group O[C@@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@H]1O[C@@H]1C[C@@]2(O)CC[C@H]3[C@@]4(O)CC[C@H](C=5COC(=O)C=5)[C@@]4(C)C[C@@H](O)[C@@H]3[C@@]2(CO)[C@H](O)C1 LPMXVESGRSUGHW-HBYQJFLCSA-N 0.000 claims 10
- 239000002368 cardiac glycoside Substances 0.000 claims 10
- 210000003061 neural cell Anatomy 0.000 claims 5
- 229940053128 Nerve Growth Factor Drugs 0.000 claims 4
- 102000015336 Nerve Growth Factor Human genes 0.000 claims 4
- 108010025020 Nerve Growth Factor Proteins 0.000 claims 4
- 230000027455 binding Effects 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 4
- 230000002708 enhancing Effects 0.000 claims 4
- 150000002500 ions Chemical class 0.000 claims 4
- 239000003446 ligand Substances 0.000 claims 4
- 230000001537 neural Effects 0.000 claims 4
- 230000002276 neurotropic Effects 0.000 claims 4
- LTMHDMANZUZIPE-PUGKRICDSA-N Digoxin Chemical group C1[C@H](O)[C@H](O)[C@@H](C)O[C@H]1O[C@@H]1[C@@H](C)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@@H]3C[C@@H]4[C@]([C@@H]5[C@H]([C@]6(CC[C@@H]([C@@]6(C)[C@H](O)C5)C=5COC(=O)C=5)O)CC4)(C)CC3)C[C@@H]2O)C)C[C@@H]1O LTMHDMANZUZIPE-PUGKRICDSA-N 0.000 claims 3
- LTMHDMANZUZIPE-AMTYYWEZSA-N Digoxin Natural products O([C@H]1[C@H](C)O[C@H](O[C@@H]2C[C@@H]3[C@@](C)([C@@H]4[C@H]([C@]5(O)[C@](C)([C@H](O)C4)[C@H](C4=CC(=O)OC4)CC5)CC3)CC2)C[C@@H]1O)[C@H]1O[C@H](C)[C@@H](O[C@H]2O[C@@H](C)[C@H](O)[C@@H](O)C2)[C@@H](O)C1 LTMHDMANZUZIPE-AMTYYWEZSA-N 0.000 claims 3
- 241000124008 Mammalia Species 0.000 claims 3
- 229960005156 digoxin Drugs 0.000 claims 3
- 210000003867 nerve cell Anatomy 0.000 claims 3
- HTIQEAQVCYTUBX-UHFFFAOYSA-N Amlodipine Chemical compound CCOC(=O)C1=C(COCCN)NC(C)=C(C(=O)OC)C1C1=CC=CC=C1Cl HTIQEAQVCYTUBX-UHFFFAOYSA-N 0.000 claims 2
- 206010059512 Apoptosis Diseases 0.000 claims 2
- FFGPTBGBLSHEPO-UHFFFAOYSA-N Carbamazepine Chemical compound C1=CC2=CC=CC=C2N(C(=O)N)C2=CC=CC=C21 FFGPTBGBLSHEPO-UHFFFAOYSA-N 0.000 claims 2
- HSUGRBWQSSZJOP-RTWAWAEBSA-N Diltiazem Chemical compound C1=CC(OC)=CC=C1[C@H]1[C@@H](OC(C)=O)C(=O)N(CCN(C)C)C2=CC=CC=C2S1 HSUGRBWQSSZJOP-RTWAWAEBSA-N 0.000 claims 2
- VZFRNCSOCOPNDB-AJKFJWDBSA-N Domoic Acid Chemical compound OC(=O)[C@@H](C)\C=C\C=C(/C)[C@H]1CN[C@H](C(O)=O)[C@H]1CC(O)=O VZFRNCSOCOPNDB-AJKFJWDBSA-N 0.000 claims 2
- -1 Puroshirarijin Substances 0.000 claims 2
- SGTNSNPWRIOYBX-UHFFFAOYSA-N Verapamil Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 claims 2
- 230000036982 action potential Effects 0.000 claims 2
- 239000005409 aflatoxin Substances 0.000 claims 2
- 229960000528 amlodipine Drugs 0.000 claims 2
- 102000004965 antibodies Human genes 0.000 claims 2
- 108090001123 antibodies Proteins 0.000 claims 2
- 230000006907 apoptotic process Effects 0.000 claims 2
- 229960000623 carbamazepine Drugs 0.000 claims 2
- 230000002860 competitive Effects 0.000 claims 2
- 229960004166 diltiazem Drugs 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-L glutamate group Chemical group N[C@@H](CCC(=O)[O-])C(=O)[O-] WHUUTDBJXJRKMK-VKHMYHEASA-L 0.000 claims 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 2
- 229910052744 lithium Inorganic materials 0.000 claims 2
- 239000002207 metabolite Substances 0.000 claims 2
- 230000002336 repolarization Effects 0.000 claims 2
- 230000002588 toxic Effects 0.000 claims 2
- 231100000331 toxic Toxicity 0.000 claims 2
- 229960001722 verapamil Drugs 0.000 claims 2
- 230000002964 excitative Effects 0.000 claims 1
- 230000004936 stimulating Effects 0.000 claims 1
Claims (32)
- 哺乳動物の標的神経細胞を死滅させるための、増強薬と刺激薬とを含む医薬組成物であって、前記増強薬が、刺激薬により誘導される興奮シグナルの毒性作用を増強するのに十分な量で、前記神経細胞に局所的に送達され、前記刺激薬が、前記神経細胞を過度に刺激して前記神経細胞のアポトーシスを促進するのに十分な量で、前記神経細胞に局所的に送達されることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記増強薬が強心配糖体であることを特徴とする医薬組成物。
- 請求項2に記載の医薬組成物において、前記強心配糖体がジゴキシン、プロシラリジン、又はウアビン(ouabin)であることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記刺激薬がグルタメート又はドーモイ酸であることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記刺激薬が強心配糖体であることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記刺激薬が神経成長因子(NGF)受容体に対する抗体であることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記増強薬が、神経特異的受容体に対して親和性を有する向神経性リガンドに連結されることを特徴とする医薬組成物。
- 請求項1に記載の医薬組成物において、前記刺激薬が、神経特異的受容体に対して親和性を有する向神経性リガンドに連結されることを特徴とする医薬組成物。
- 哺乳動物の標的神経細胞を死滅させるための、増強薬とチャネル遮断薬とを含む医薬組成物であって、前記増強薬が、前記チャネル遮断薬の毒性作用を増強するのに十分な量で、前記神経細胞に局所的に送達され、前記チャネル遮断薬が、前記神経細胞の活動電位及び再分極を遮断するのに十分な量で、前記神経細胞に局所的に送達されることを特徴とする医薬組成物。
- 請求項9に記載の医薬組成物において、前記増強薬が強心配糖体であることを特徴とする医薬組成物。
- 請求項10に記載の医薬組成物において、前記強心配糖体がジゴキシン、プロシラリジン、又はウアビン(ouabin)であることを特徴とする医薬組成物。
- 請求項9に記載の医薬組成物において、前記チャネル遮断薬が代謝産物であることを特徴とする医薬組成物。
- 請求項9に記載の医薬組成物において、前記チャネル遮断薬がベラパミル、カルバマゼピン、アムロジピン、又はジルチアゼムであることを特徴とする医薬組成物。
- 請求項9に記載の医薬組成物において、前記チャネル遮断薬が競合イオンであることを特徴とする医薬組成物。
- 請求項14に記載の医薬組成物において、前記競合イオンがリチウムであることを特徴とする医薬組成物。
- 請求項9に記載の医薬組成物において、前記増強薬が、神経特異的受容体に対して親和性を有する向神経性リガンドに連結されることを特徴とする医薬組成物。
- 哺乳動物の標的神経細胞を死滅させるための、刺激薬とチャネル遮断薬とを含む医薬組成物であって、前記刺激薬が、前記神経細胞を過度に刺激して前記神経細胞のアポトーシスを促進するのに十分な量で、前記神経細胞に局所的に送達され、前記チャネル遮断薬が前記神経細胞の活動電位及び再分極を遮断するのに十分な量で、前記神経細胞に局所的に送達されることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記刺激薬がグルタメート又はドーモイ酸であることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記刺激薬が強心配糖体であることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記刺激薬が、神経成長因子(NGF)受容体に対する抗体であることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記チャネル遮断薬が代謝産物であることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記チャネル遮断薬がベラパミル、カルバマゼピン、アムロジピン、又はジルチアゼムであることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記チャネル遮断薬が競合イオンであることを特徴とする医薬組成物。
- 請求項23に記載の医薬組成物において、前記競合イオンがリチウムであることを特徴とする医薬組成物。
- 請求項17に記載の医薬組成物において、前記刺激薬が、神経特異的受容体に対して親和性を有する向神経性リガンドに連結されることを特徴とする医薬組成物。
- 哺乳動物の標的神経細胞を死滅させるための、強心配糖体を含む医薬組成物であって、前記強心配糖体が、前記神経細胞を死滅させるのに十分な量で、前記神経細胞に局所的に送達されることを特徴とする医薬組成物。
- 請求項26に記載の医薬組成物において、前記強心配糖体がジゴキシンであることを特徴とする医薬組成物。
- 請求項27に記載の医薬組成物において、前記量が0.0001〜10mMであることを特徴とする医薬組成物。
- 請求項26に記載の医薬組成物において、前記強心配糖体がプロシラリジンであることを特徴とする医薬組成物。
- 請求項29に記載の医薬組成物において、前記量が0.0001〜10mMであることを特徴とする医薬組成物。
- 哺乳動物の標的神経細胞を死滅させるための、アフラトキシンを含む医薬組成物であって、前記アフラトキシンが、前記神経細胞を死滅させるのに十分な量で、前記神経細胞に局所的に送達されることを特徴とする医薬組成物。
- 請求項31に記載の医薬組成物において、前記量が0.00001〜0.003mMであることを特徴とする医薬組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US33683810P | 2010-01-26 | 2010-01-26 | |
US61/336,838 | 2010-01-26 | ||
PCT/US2011/022653 WO2011094367A1 (en) | 2010-01-26 | 2011-01-26 | Methods, devices, and agents for denervation |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016115237A Division JP2016199559A (ja) | 2010-01-26 | 2016-06-09 | 除神経のための方法、装置、及び薬剤 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2013517847A JP2013517847A (ja) | 2013-05-20 |
JP2013517847A5 true JP2013517847A5 (ja) | 2014-03-13 |
JP5952195B2 JP5952195B2 (ja) | 2016-07-13 |
Family
ID=43735722
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012550219A Expired - Fee Related JP5952195B2 (ja) | 2010-01-26 | 2011-01-26 | 除神経のための方法、装置、及び薬剤 |
JP2016115237A Pending JP2016199559A (ja) | 2010-01-26 | 2016-06-09 | 除神経のための方法、装置、及び薬剤 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016115237A Pending JP2016199559A (ja) | 2010-01-26 | 2016-06-09 | 除神経のための方法、装置、及び薬剤 |
Country Status (6)
Country | Link |
---|---|
US (3) | US20110184337A1 (ja) |
EP (2) | EP3246035A1 (ja) |
JP (2) | JP5952195B2 (ja) |
CN (2) | CN105640501A (ja) |
CA (1) | CA2787062C (ja) |
WO (1) | WO2011094367A1 (ja) |
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- 2011-01-26 US US13/014,702 patent/US20110184337A1/en not_active Abandoned
- 2011-01-26 WO PCT/US2011/022653 patent/WO2011094367A1/en active Application Filing
- 2011-01-26 CA CA2787062A patent/CA2787062C/en not_active Expired - Fee Related
- 2011-01-26 CN CN201180006941.0A patent/CN102892454B/zh not_active Expired - Fee Related
- 2011-01-26 JP JP2012550219A patent/JP5952195B2/ja not_active Expired - Fee Related
- 2011-01-26 US US13/014,700 patent/US8975233B2/en not_active Expired - Fee Related
- 2011-01-26 EP EP11703963A patent/EP2528649A1/en not_active Withdrawn
- 2011-04-28 US US13/096,446 patent/US9056184B2/en not_active Expired - Fee Related
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2016
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