US2012252750A1PendingUtilityA1

Formulations for reducing neuronal degeneration

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Assignee: SHEA THOMAS BPriority: Jul 25, 2003Filed: Apr 2, 2012Published: Oct 4, 2012
Est. expiryJul 25, 2023(expired)· nominal 20-yr term from priority
A61P 25/16A23L 33/15A23V 2002/00A61K 31/355A61K 31/00A61P 25/28A61K 31/525A61K 31/22
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Claims

Abstract

Nutriceutical and pharmaceutical formulations for treating neurodegenerative disorders such as Alzheimer's disease are provided. Nutriceutical formulations include two or more of folate, vitamin E, and acetyl-L-carnitine (ALCAR). Pharmaceutical formulations include two or more of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM).

Claims

exact text as granted — not AI-modified
1 . A method for treating a neurodegenerative disorder in a mammal, the method comprising administering to the mammal an amount of a formulation effective to reduce a level of reactive oxygen species (ROS) in an in vitro neural cell culture, wherein the formulation comprises, folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms. 
     
     
         2 . The method of  claim 1 , wherein the formulation comprises folate, vitamin E, ALCAR, NAC, and SAM. 
     
     
         3 . The method of  claim 1 , wherein the mammal suffers from a neurodegenerative disorder selected from the group consisting of Alzheimer's disease, Parkinson's disease, or amyotrophic lateral sclerosis (ALS). 
     
     
         4 . The method of  claim 1 , wherein the mammal is a human. 
     
     
         5 . The method of  claim 1 , wherein a level of reactive oxygen species (ROS) in the mammal is reduced compared to a reference. 
     
     
         6 . A composition comprising, folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms, wherein a unit dose of the composition reduces a level of reactive oxygen species (ROS) in an in vitro neural cell culture. 
     
     
         7 . The composition of  claim 6 , wherein the composition comprises folate, vitamin E, ALCAR, NAC, and SAM. 
     
     
         8 - 25 . (canceled) 
     
     
         26 . The composition of  claim 6 , wherein the unit dose comprises about 200-2000 μg folate. 
     
     
         27 . The composition of  claim 6 , wherein the unit dose comprises about 50-3000 I.U. vitamin E. 
     
     
         28 . The composition of  claim 6 , wherein the unit dose comprises about 200-4000 mg ALCAR. 
     
     
         29 . The composition of  claim 6 , wherein the unit dose comprises about 200-2000 mg NAC. 
     
     
         30 . The composition of  claim 6 , wherein the unit dose comprises about 400-2000 mg SAM. 
     
     
         31 . The composition of  claim 6 , wherein the unit dose comprises about 20-500 mg DZA. 
     
     
         32 . The composition of  claim 7 , wherein the unit dose comprises about 200-2000 μg folate, about 50-3000 I.U. vitamin E, about 200-4000 mg ALCAR, about 200-2000 mg NAC, and about 400-2000 mg SAM. 
     
     
         33 . The composition of  claim 7 , wherein the unit dose comprises about 400-1500 μg folate, about 50 I.U. vitamin E, about 500-3000 mg ALCAR, about 500-1500 mg NAC, and about 400-1500 mg SAM. 
     
     
         34 . The composition of  claim 7 , wherein the unit dose of the composition comprises about 200-2000 μg folate, about 200-4000 mg ALCAR, about 400-2000 mg SAM, and about 200-2000 mg NAC. 
     
     
         35 . The composition of  claim 7 , wherein the unit dose of the composition comprises about 400-1500 μg folate, about 500-3000 mg ALCAR, about 400-1500 mg SAM, and about 500-1500 mg NAC. 
     
     
         36 . A composition comprising folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms, wherein a unit dose of the composition improves memory in a subject. 
     
     
         37 . A method of improving memory in a subject, comprising administering a composition of any one of  claim 6 ,  7 , or  26 - 35  to the subject, such that memory is improved.

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