US2004265847A1PendingUtilityA1

Method for treating Alzheimer's disease

47
Assignee: MASTERS COLIN LOUISPriority: Nov 12, 1991Filed: Nov 19, 2003Published: Dec 30, 2004
Est. expiryNov 12, 2011(expired)· nominal 20-yr term from priority
A61P 25/28G01N 33/6896Y10S436/811G01N 2800/2821
47
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

The present invention is directed to methods for treating Alzheimer's Disease by modulating divalent cation, trivalent cation and/or heparin interaction with amyloid precursor protein (APP). In particular, the present invention is directed to methods for treating Alzheimer's Disease by administering to a patient with Alzheimer's Disease a therapeutically effective amount of a zinc binding agent for modulating the interaction of zinc and/or heparin with APP and thereby preventing the aberrant processing of APP.

Claims

exact text as granted — not AI-modified
1 - 24 . (Canceled)  
     
     
         25 . A method for treating Alzheimer's disease in a patient comprising subjecting said patient to a therapeutically effective amount of an agent which is capable of crossing the blood brain barrier, wherein said agent modulates the interaction within the central nervous system between a divalent or trivalent cation and/or heparin with amyloid precursor protein (APP) of said patient.  
     
     
         26 . The method according to  claim 25 , wherein the cation is a divalent cation.  
     
     
         27 . The method according to  claim 26 , wherein said divalent cation is zinc.  
     
     
         28 . The method according to  claim 25 , wherein a therapeutically effective amount of a zinc-binding agent is administered to said patient.  
     
     
         29 . The method according to  claim 28 , wherein said zinc-binding agent is selected from sodium citrate, 1,2-diethyl-3-hydroxypyridin-4-one, and 1-hydroxyethyl-3-hydroxy-2-methylpyridin-4-one.  
     
     
         30 . The method according to  claim 28 , wherein said zinc-binding agent is orally administered to said patient.  
     
     
         31 . A method for altering protease-mediated digestion of amyloid precursor protein (APP) in a patient with Alzheimer's disease, comprising the step of administering to said patient to an effective amount of an agent which is capable of crossing the blood brain barrier, wherein said agent modulates the interaction within the central nervous system between a divalent or trivalent cation and/or heparin with amyloid precursor protein (APP) of said patent.  
     
     
         32 . The method according to  claim 31 , wherein the cation is a divalent cation.  
     
     
         33 . The method according to  claim 32 , wherein said divalent cation is zinc.  
     
     
         34 . The method according to  claim 31 , wherein said agent is a zinc-binding agent.  
     
     
         35 . The method according to  claim 34 , wherein said zinc-binding agent is selected from sodium citrate, 1,2-diethyl-3-hydroxypyridin-4-one, and 1-hydroxyethyl-3-hydroxy-2-methylpoyridin-4-one.  
     
     
         36 . The method according to  claim 34 , wherein said zinc-binding agent is orally administered to said patient.  
     
     
         37 . A method of reducing incorrect protease-mediated processing of amyloid precursor protein (APP) in a patient with Alzheimer's disease comprising the step of administering said patient to an effective amount of an agent which is capable of crossing the blood brain barrier, wherein said agent modulates the interaction within the central nervous system between a divalent or trivalent cation and/or heparin with amyloid precursor protein (APP) of said patient.  
     
     
         38 . The method according to  claim 37 , wherein said cation is a divalent cation.  
     
     
         39 . The method according to  claim 38 , wherein said divalent cation is zinc.  
     
     
         40 . The method according to  claim 37 , wherein said agent is zinc-binding agent.  
     
     
         41 . The method according to  claim 40 , wherein said zinc-binding agent is selected from sodium citrate, 1,2-diethyl-3-hydroxypyridin-4-one, and 1-hydroxyethyl-3-hydroxy-2-methylpyridin-4-one.  
     
     
         42 . The method according to  claim 41 , wherein said zinc-binding agent is orally administered to said patient.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.