KR920703068A - Treatment of Neurodegenerative Diseases - Google Patents

Treatment of Neurodegenerative Diseases

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Publication number
KR920703068A
KR920703068A KR1019920700591A KR920700591A KR920703068A KR 920703068 A KR920703068 A KR 920703068A KR 1019920700591 A KR1019920700591 A KR 1019920700591A KR 920700591 A KR920700591 A KR 920700591A KR 920703068 A KR920703068 A KR 920703068A
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adenosine
disease
modulator
substance
concentration
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KR1019920700591A
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Korean (ko)
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머랜고스 폴
그루버 해리
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폴 레이킨드
젠시아 파머슈티컬즈, 인코포레이티드
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Publication of KR920703068A publication Critical patent/KR920703068A/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/70Carbohydrates; Sugars; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Epidemiology (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Treatment Of Fiber Materials (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

내용 없음No content

Description

신경변성 질환의 치료방법Treatment of Neurodegenerative Diseases

[도면의 간단한 설명][Brief Description of Drawings]

제1도는 메탐페타민-유도 파킨슨 증후군의 발달에 대한 케타민 및 CHA의 효과를 나타낸 그래프이다.1 is a graph showing the effects of ketamine and CHA on the development of methamphetamine-induced Parkinson's syndrome.

제2도는 메탐페타민-유도 파킨슨 증후군의 발달에 대한 케타민 및 CHA의 효과(카페인의 존재 및 부재하의 효과를 나타낸 그래프이다.FIG. 2 is a graph showing the effects of ketamine and CHA (with and without caffeine) on the development of methamphetamine-induced Parkinson's syndrome.

제3도는 티로신 히드록실라아제 활성의 MPTP-유도 감소에 대한 CHA의 효과를 나타낸 그래프이다.3 is a graph showing the effect of CHA on MPTP-induced reduction of tyrosine hydroxylase activity.

제4도는 티로신 히드록실라아제 활성의 MPTP-유도 감소에 대한 CHA와 MK-801의 효과의 비교를 나타낸 그래프이다.4 is a graph showing the comparison of the effects of CHA and MK-801 on MPTP-induced reduction of tyrosine hydroxylase activity.

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (26)

신경조직 중에 및 신경조직 부근에 아데노신의 세포의 농도를 증가시키는 것으로 이루어지는, 이환동물의 증가된 흥분성 아미노산의 방출에 기인하여, 신경 변성 질환에 유발되거나 또는 신경 변성 질환을 유발시키는 흥분성 중독에 의해 유발된 신경조직 손상을 예방하기 위한 방법.Caused by neurodegenerative disease or by excitatory intoxication which causes or is degenerative due to increased release of excitatory amino acids in affected animals, which consists in increasing the concentration of adenosine cells in and near neural tissue. Method for preventing damaged nerve tissue. 제1항에 있어서, 신경조직 중에 및 신경조직 부근에 아데노신의 세포외 농도를 증가시키는 물질을 치료학상 효과적인 양으로 동물에게 투여함으로써 아데노신 농도를 증가시킴을 특징으로 하는 방법.The method of claim 1, wherein the adenosine concentration is increased by administering to the animal a therapeutically effective amount of a substance that increases the extracellular concentration of adenosine in and near the nerve tissue. 제2항에 있어서, 상기 물질이 아데노신 조절제, 아데노신 길항물질 또는 아데노신 운반 억제제를 포함함을 특징으로 하는 방법.The method of claim 2, wherein the substance comprises an adenosine modulator, an adenosine antagonist or an adenosine transport inhibitor. 제3항에 있어서, 상기 물질이 아데노신 길항물질을 포함함을 특징으로 하는 방법.4. The method of claim 3 wherein said substance comprises an adenosine antagonist. 제3항에 있어서, 상기 물질이 아데노신 조절제를 포함함을 특징으로 하는 방법.4. The method of claim 3, wherein said substance comprises adenosine modulators. 제2항에 있어서, 상기 신경조직이 뇌 또는 척수임을 특징으로 하는 방법.The method of claim 2, wherein said neural tissue is brain or spinal cord. 제6항에 있어서, 상기 흥분성 중독이 뇌손상에 의해 유발되거나 뇌손상을 유발시킴을 특징으로 하는 방법.7. The method of claim 6, wherein the excitatory poisoning is caused by or causes brain injury. 제2항에 있어서, 상기 신경변성 질환이 파킨슨 병, 알쯔하이머 병, 근위축성 측삭 경화증 또는 헌팅톤병임을 특징으로 하는 방법.The method of claim 2, wherein the neurodegenerative disease is Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis or Huntington's disease. 제8항에 있어서, 상기 물질이 아데노신 조절제, 아데노신 길항물질 또는 아데노신 운반 억제제를 포함함을 특징으로 하는 방법.The method of claim 8, wherein said substance comprises an adenosine modulator, an adenosine antagonist or an adenosine transport inhibitor. 신경조직 중에 아데노신의 세포외 농도를 증가시키는 것을 포함하는, 환자의 신경변성 질환과 관련된 신경조직 손상을 감소시키기 위한 방법.A method for reducing neuronal damage associated with neurodegenerative disease in a patient, comprising increasing extracellular concentrations of adenosine in neural tissue. 제10항에 있어서, 아데노신 농도 증가제를 치료학상 효과적인 양으로 환자에게 투여함으로써 아데노신 농도를 증가시킴을 특징으로 하는 방법.The method of claim 10, wherein the adenosine concentration is increased by administering an adenosine concentration increasing agent to the patient in a therapeutically effective amount. 제11항에 있어서, 아데노신 증가제가 아데노신 조절제, 아데노신 길항물질, 또는 아데노신 운반 억제제를 포함함을 특징으로 하는 방법.12. The method of claim 11, wherein the adenosine enhancer comprises an adenosine modulator, an adenosine antagonist, or an adenosine transport inhibitor. 제12항에 있어서, 아데노신 농도 증가제가 아데노신 조절제를 포함함을 특징으로 하는 방법.The method of claim 12, wherein the adenosine concentration increasing agent comprises an adenosine modulator. 제13항에 있어서, 아데노신 조절제가 푸린 누클레오시드 또는 유사체 또는 이들의 프로드러그를 포함함을 특징으로 하는 방법.The method of claim 13, wherein the adenosine modulator comprises purine nucleosides or analogs or prodrugs thereof. 제14항에 있어서, 아데노신 조절제가 AICA 리보시드 또는 AICA 리보시드 프로드러그 또는 유사체를 포함함을 특징으로 하는 방법.The method of claim 14, wherein the adenosine modulator comprises an AICA riboside or AICA riboside prodrug or analog. 제12항에 있어서, 아데노신 농도 증가제가 아데노신 길항물질을 포함함을 특징으로 하는 방법.The method of claim 12 wherein the adenosine concentration increasing agent comprises an adenosine antagonist. 제12항에 있어서, 신경 변성 질환이 파킨슨 병, 알쯔하이머 병, 근위축성 측삭 경화증 또는 헌팅톤병임을 특징으로 하는 방법.The method of claim 12, wherein the neurodegenerative disease is Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis or Huntington's disease. 아데노신의 세포외 농도를 증가시키는 물질을 치료학상 효과적인 양으로 예방 투여하는 것을 포함하는, 신경변성 질환과 관련된 신경조직 손상을 억제하기 위한 방법.A method for inhibiting neuronal damage associated with a neurodegenerative disease, comprising prophylactically administering a therapeutically effective amount of a substance that increases the extracellular concentration of adenosine. 제18항에 있어서, 신경 변성 질환이 파킨슨 병을 포함함을 특징으로 하는 방법.19. The method of claim 18, wherein the neurodegenerative disease comprises Parkinson's disease. 제18항에 있어서, 상기 물질이 아데노신 조절제, 아데노신 길항물질 또는 아데노신 운반 억제제를 포함함을 특징으로 하는 방법.19. The method of claim 18, wherein said substance comprises an adenosine modulator, an adenosine antagonist or an adenosine transport inhibitor. 제20항에 있어서, 상기 물질이 아데노신 길항물질을 포함함을 특징으로 하는 방법.21. The method of claim 20, wherein said substance comprises an adenosine antagonist. 제20항에 있어서, 상기 물질이 아데노신 조절제를 포함함을 특징으로 하는 방법.21. The method of claim 20, wherein said substance comprises an adenosine modulator. 제20항에 있어서, 상기 신경 변성 질환이 파킨슨 병, 알쯔하이머 병, 근위축성 측삭 경화증 또는 헌팅톤 병 임을 특징으로 하는 방법.The method of claim 20, wherein the neurodegenerative disease is Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis or Huntington's disease. 아데노신의 세포외 농도를 증가시키는 물질을 치료학상 효과적인 양으로 이환 동물에게 투여하는 것을 포함하는, 이환 동물의 신경 변성 질환과 관련된 진행성 뇌의 치매를 감소시키기 위한 방법.A method for reducing progressive brain dementia associated with neurodegenerative disease in a diseased animal, comprising administering to the affected animal a therapeutically effective amount of a substance that increases the extracellular concentration of adenosine. 제24항에 있어서, 상기 물질이 아데노신 조절제, 아데노신 길항물질 또는 아데노신 운반 억제제임을 특징으로 하는 방법.The method of claim 24, wherein the substance is an adenosine modulator, adenosine antagonist or adenosine transport inhibitor. 제25항에 있어서, 상기 신경 변성 질환이 파킨슨 병, 알쯔하이머 병, 근위축성 측삭 경화증 또는 헌팅톤 병임을 특징으로 하는 방법.The method of claim 25, wherein the neurodegenerative disease is Parkinson's disease, Alzheimer's disease, amyotrophic lateral sclerosis or Huntington's disease. ※ 참고사항:최초출원 내용에 의하여 공개되는 것임.※ Note: The information is disclosed by the first application.
KR1019920700591A 1989-09-15 1990-09-12 Treatment of Neurodegenerative Diseases KR920703068A (en)

Applications Claiming Priority (3)

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US40791389A 1989-09-15 1989-09-15
US07/407,913 1989-09-15
PCT/US1990/005180 WO1991004032A1 (en) 1989-09-15 1990-09-12 Methods of treating neurodegenerative conditions

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KR920703068A true KR920703068A (en) 1992-12-17

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JP (1) JPH05506842A (en)
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AU (1) AU643235B2 (en)
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WO (1) WO1991004032A1 (en)

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ATE206755T1 (en) * 1991-08-09 2001-10-15 Massachusetts Inst Technology USES OF A PROTEIN KINASE OF CLAY AND NEUROFILAMENT PK40
DK62592D0 (en) * 1992-05-14 1992-05-14 Novo Nordisk As
EP0582164B1 (en) * 1992-07-31 1998-12-23 Bristol-Myers Squibb Company Adenosine re-uptake inhibiting derivatives of diphenyl oxazoles, thiazoles and imidazoles
US5589467A (en) * 1993-09-17 1996-12-31 Novo Nordisk A/S 2,5',N6-trisubstituted adenosine derivatives
US5780450A (en) * 1995-11-21 1998-07-14 Alcon Laboratories, Inc. Use of adenosine uptake inhibitors for treating retinal or optic nerve head damage
DE19707655A1 (en) * 1997-02-26 1998-08-27 Hoechst Ag Combination preparation for use in dementia
US6440455B1 (en) * 1997-09-02 2002-08-27 Children's Medical Center Corporation Methods for modulating the axonal outgrowth of central nervous system neurons

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US4575498A (en) * 1983-07-21 1986-03-11 Duke University Method for restoring depleted purine nucleotide pools
US4912092A (en) * 1986-03-27 1990-03-27 The Regents Of The University Of California Methods for increasing extracellular adenosine and for stabilizing mast cells

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NO920983D0 (en) 1992-03-13
AU6401590A (en) 1991-04-18
EP0491792A1 (en) 1992-07-01
JPH05506842A (en) 1993-10-07
WO1991004032A1 (en) 1991-04-04
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NO920983L (en) 1992-03-13
AU643235B2 (en) 1993-11-11

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