CN1891215B - 对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 - Google Patents
对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 Download PDFInfo
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- CN1891215B CN1891215B CN200610099685.5A CN200610099685A CN1891215B CN 1891215 B CN1891215 B CN 1891215B CN 200610099685 A CN200610099685 A CN 200610099685A CN 1891215 B CN1891215 B CN 1891215B
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- arachidonic
- docosahexenoic
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Abstract
Description
Claims (8)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2005191624A JP5697293B2 (ja) | 2005-06-30 | 2005-06-30 | 器質的脳障害に起因する高次脳機能の低下に対する改善作用を有する組成物 |
JP2005-191624 | 2005-06-30 | ||
JP2005191624 | 2005-06-30 |
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CN201410745897.0A Division CN104666290A (zh) | 2005-06-30 | 2006-06-29 | 对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 |
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CN1891215A CN1891215A (zh) | 2007-01-10 |
CN1891215B true CN1891215B (zh) | 2015-08-19 |
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CN201410745897.0A Pending CN104666290A (zh) | 2005-06-30 | 2006-06-29 | 对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 |
CN200610099685.5A Expired - Fee Related CN1891215B (zh) | 2005-06-30 | 2006-06-29 | 对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 |
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CN201410745897.0A Pending CN104666290A (zh) | 2005-06-30 | 2006-06-29 | 对器质性脑损伤引起的高级脑功能下降具有改善作用的组合物 |
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US (2) | US20090048215A1 (zh) |
EP (1) | EP1896136A2 (zh) |
JP (1) | JP5697293B2 (zh) |
KR (1) | KR101344053B1 (zh) |
CN (2) | CN104666290A (zh) |
AU (1) | AU2006266751B2 (zh) |
CA (1) | CA2613343C (zh) |
RU (1) | RU2008103363A (zh) |
WO (1) | WO2007004685A2 (zh) |
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JP2003048831A (ja) | 2001-08-02 | 2003-02-21 | Suntory Ltd | 脳機能の低下に起因する症状あるいは疾患の予防又は改善作用を有する組成物 |
JP4993852B2 (ja) | 2004-09-17 | 2012-08-08 | サントリーホールディングス株式会社 | ストレスに起因する行動異常を伴う症状あるいは疾患の予防又は改善作用を有する組成物 |
JP5967855B2 (ja) | 2005-06-30 | 2016-08-10 | サントリーホールディングス株式会社 | 日中活動量の低下および/又はうつ症状の改善作用を有する組成物 |
WO2008081989A1 (ja) * | 2006-12-28 | 2008-07-10 | Suntory Holdings Limited | 神経再生剤 |
EP2689782B1 (en) | 2007-06-26 | 2020-05-13 | N.V. Nutricia | Improving memory in subjects with mini-mental state examination of 24-26 |
WO2009002148A1 (en) | 2007-06-27 | 2008-12-31 | N.V. Nutricia | Food composition for prodromal dementia patients |
WO2009002145A1 (en) | 2007-06-26 | 2008-12-31 | N.V. Nutricia | Lipid composition for improving function of brain functioning |
WO2009002146A1 (en) | 2007-06-26 | 2008-12-31 | N.V. Nutricia | Supporting activities of daily living |
JP2009019025A (ja) * | 2007-07-13 | 2009-01-29 | Suntory Ltd | 非ヒト動物の老化又は痴呆に伴う疾患又は症状の改善剤 |
US8343753B2 (en) | 2007-11-01 | 2013-01-01 | Wake Forest University School Of Medicine | Compositions, methods, and kits for polyunsaturated fatty acids from microalgae |
PL2609812T3 (pl) | 2007-12-20 | 2019-02-28 | N.V. Nutricia | Ciekły produkt zawierający nukleotydy/nukleozydy |
US20110082205A1 (en) * | 2009-10-01 | 2011-04-07 | Panker Cynthia A | Docosahexaenoic Acid Gel Caps |
WO2011047095A1 (en) | 2009-10-13 | 2011-04-21 | Martek Biosciences Corporation | Reducing the risk of pathological effects of traumatic brain injury |
JP6178761B2 (ja) * | 2013-07-10 | 2017-08-09 | ライオン株式会社 | 内服剤 |
US9610302B2 (en) | 2013-12-05 | 2017-04-04 | Buriva, LLC. | Composition containing phospholipid-DHA and B vitamins |
US9233114B2 (en) | 2013-12-05 | 2016-01-12 | Buriva, LLC | Dietary supplement containing phospholipid-DHA derived from eggs |
US9216199B2 (en) | 2013-12-05 | 2015-12-22 | Buriva, LLC | Nutritional supplement containing phospholipid-DHA derived from eggs |
US9549937B2 (en) | 2013-12-05 | 2017-01-24 | Burvia, LLC. | Composition containing phospholipid-DHA and folate |
US10456368B2 (en) | 2016-09-26 | 2019-10-29 | Garrett E. Wdowin | Compositions for mitigating brain trauma and methods thereof |
US20230398088A1 (en) * | 2020-10-30 | 2023-12-14 | The Trustees Of The University Of Pennsylvania | Lipid Prophylactic Brain Injury Treatment |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004028529A1 (en) * | 2002-09-24 | 2004-04-08 | Suntory Limited | Composition with effects of decline prevention, improvement or enhancement of normal responses of cognitive abilities of a healthy person |
EP1419768A1 (en) * | 2001-08-02 | 2004-05-19 | Suntory Limited | Compositions having effects of preventing or ameliorating conditions or diseases caused by brain hypofunction |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4668704A (en) * | 1982-08-09 | 1987-05-26 | Regents Of The University Of California | Method for protecting and healing gastro-duodenal mucosa and the liver of mammals |
US4526902A (en) * | 1983-10-24 | 1985-07-02 | Century Laboratories, Inc. | Combined fatty acid composition for treatment or prophylaxis of thrombo-embolic conditions |
US5198468A (en) * | 1987-06-24 | 1993-03-30 | Efamol Holdings Plc | Essential fatty acid composition |
AU683027B2 (en) * | 1993-01-27 | 1997-10-30 | Scotia Holdings Plc | Triglycerides |
US5583019A (en) * | 1995-01-24 | 1996-12-10 | Omegatech Inc. | Method for production of arachidonic acid |
US6080787A (en) * | 1997-02-21 | 2000-06-27 | Abbott Laboratories | Methods for reducing the incidence of necrotizing enterocolitis |
FR2762993B1 (fr) * | 1997-05-06 | 1999-08-13 | Inst Rech Biolog Sa | Nouvelle utilisation de phospholipides d'origine animale en therapeutique et/ou dietetique |
US5902807A (en) * | 1997-05-12 | 1999-05-11 | Antti Haapalinna | Method for the treatment of mental illness in mammals and a composition therefor |
EP0893064B1 (fr) * | 1997-07-22 | 2003-01-15 | Societe Des Produits Nestle S.A. | Composition lipidique pour formule infantile et procédé de préparation |
US6225444B1 (en) * | 1998-02-10 | 2001-05-01 | Protarga, Inc. | Neuroprotective peptides and uses thereof |
JP2000239168A (ja) * | 1999-02-19 | 2000-09-05 | Bizen Kasei Kk | 脳卒中予防剤およびこれを配合してなる組成物 |
US7208180B2 (en) * | 2000-05-08 | 2007-04-24 | N.V. Nutricia | Method and preparation for the preventing and/or treating vascular disorders and secondary disorders associated therewith |
US20040219208A1 (en) * | 2001-08-03 | 2004-11-04 | Ryu Kawamura | Sustained-release medicines |
US6689810B2 (en) * | 2001-08-21 | 2004-02-10 | Cellular Sciences, Inc. | Method for treating pulmonary disease states in mammals by altering indigenous in vivo levels of nitric oxide |
EP1501493B1 (en) * | 2002-05-03 | 2009-10-07 | Pronova BioPharma Norge AS | Use of epa and dha in secondary prevention of strokes |
CA2522712A1 (en) * | 2003-04-18 | 2004-10-28 | Kyowa Hakko Kogyo Co., Ltd. | Nerve regenerating drug |
IL158552A0 (en) * | 2003-10-22 | 2004-05-12 | Enzymotec Ltd | Lipids containing omega-3 fatty acids |
JP4522075B2 (ja) * | 2003-10-29 | 2010-08-11 | サントリーホールディングス株式会社 | 血管の老化に起因する症状あるいは疾患の予防又は改善作用を有する組成物 |
WO2005072306A2 (en) * | 2004-01-19 | 2005-08-11 | Martek Biosciences Corporation | Reelin deficiency or dysfunction and methods related thereto |
JP2006083136A (ja) * | 2004-09-17 | 2006-03-30 | Suntory Ltd | ストレスに起因する脳機能の低下およびそれに伴う症状あるいは疾患の予防又は改善作用を有する組成物 |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1419768A1 (en) * | 2001-08-02 | 2004-05-19 | Suntory Limited | Compositions having effects of preventing or ameliorating conditions or diseases caused by brain hypofunction |
WO2004028529A1 (en) * | 2002-09-24 | 2004-04-08 | Suntory Limited | Composition with effects of decline prevention, improvement or enhancement of normal responses of cognitive abilities of a healthy person |
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US20150133555A1 (en) | 2015-05-14 |
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EP1896136A2 (en) | 2008-03-12 |
WO2007004685A3 (en) | 2007-06-14 |
CA2613343C (en) | 2015-06-02 |
CN1891215A (zh) | 2007-01-10 |
CN104666290A (zh) | 2015-06-03 |
AU2006266751A1 (en) | 2007-01-11 |
KR101344053B1 (ko) | 2013-12-24 |
JP2007008863A (ja) | 2007-01-18 |
WO2007004685A2 (en) | 2007-01-11 |
RU2008103363A (ru) | 2009-08-10 |
JP5697293B2 (ja) | 2015-04-08 |
US20090048215A1 (en) | 2009-02-19 |
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