US2017105980A1PendingUtilityA1

Methods For Treating Nicotinic Acetylcholine Receptor Associated Diseases

Assignee: CHILDREN'S MEDICAL CENTER CORPPriority: Nov 12, 2010Filed: May 20, 2016Published: Apr 20, 2017
Est. expiryNov 12, 2030(~4.3 yrs left)· nominal 20-yr term from priority
Inventors:Takao K. Hensch
A61P 27/02A61P 25/18A61K 31/713G01N 33/74A61K 31/445A61P 25/00C12N 15/113G01N 2800/16G01N 2800/30A61K 31/00A61K 45/06A61K 31/55G01N 2800/7057C12N 2310/14
30
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Claims

Abstract

The present invention provides methods and compositions for treating subjects suffering from a disorder associated with a nicotinic acetylcholine receptor (nAChR), methods for treating a subject having a disorder that would benefit from an increase in neural plasticity, and methods for modulating the plasticity of the primary visual cortex in subjects by modulating the expression, stability, and/or activity of Lynx1.

Claims

exact text as granted — not AI-modified
1 .- 24 . (canceled) 
     
     
         25 . A method for increasing the plasticity of a population of neural cells, the method comprising contacting a population of neural cells with a moiety that decreases the level or an activity of Lynx1, thereby increasing the plasticity of the population of neural cells. 
     
     
         26 . The method of  claim 25 , wherein the moiety is a cholinesterase inhibitor. 
     
     
         27 . The method of  claim 26 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil, galantamine, rivastigmine, and tetrahydroaminoacridine. 
     
     
         28 . The method of  claim 25 , wherein the moiety is a small inhibitory RNA (siRNA). 
     
     
         29 . The method of  claim 25 , wherein the population of neural cells is in vitro. 
     
     
         30 . The method of  claim 25 , wherein the activity of Lynx1 is the ability of Lynx1 to bind to a nicotinic acetylcholine receptor or reduce nicotinic acetylcholine receptor sensitivity to acetylcholine. 
     
     
         31 . The method of  claim 25 , wherein the population of neural cells is part of an auditory cortex or part of a motor cortex of a subject. 
     
     
         32 . A method for modulating the plasticity of a population of neural cells in an auditory cortex in a subject in need thereof, the method comprising:
 administering to the subject an amount of a moiety sufficient to decrease the level or an activity of Lynx1 in a population of neural cells in an auditory cortex, thereby increasing the plasticity of the population of neural cells in the auditory cortex of the subject.   
     
     
         33 . The method of  claim 32 , wherein the moiety is a cholinesterase inhibitor. 
     
     
         34 . The method of  claim 33 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil, galantamine, rivastigmine, and tetrahydroaminoacridine. 
     
     
         35 . The method of  claim 32 , wherein the moiety is a small inhibitory RNA (siRNA). 
     
     
         36 . A method for modulating the plasticity of a population of neural cells in a motor cortex in a subject in need thereof, the method comprising:
 administering to the subject an amount of a moiety sufficient to decrease the level or an activity of Lynx1 in a population of neural cells in a motor cortex, thereby increasing the plasticity of the population of neural cells in the motor cortex of the subject.   
     
     
         37 . The method of  claim 36 , wherein the moiety is a cholinesterase inhibitor. 
     
     
         38 . The method of  claim 37 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil, galantamine, rivastigmine, and tetrahydroaminoacridine. 
     
     
         39 . The method of  claim 36 , wherein the moiety is a small inhibitory RNA (siRNA). 
     
     
         40 . A method for treating a subject suffering from stroke, the method comprising: administering to the subject a therapeutically effective amount of a moiety that decreases the level or an activity of Lynx1 in the subject, thereby treating the subject suffering from stroke. 
     
     
         41 . The method of  claim 40 , wherein the moiety is a cholinesterase inhibitor. 
     
     
         42 . The method of  claim 41 , wherein the cholinesterase inhibitor is selected from the group consisting of donepezil and galantamine. 
     
     
         43 . The method of  claim 40 , wherein the composition is orally administered to the subject.

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