IP Library Patent Application 12499682
Patent Application
App. No. 12/499,682

Method for Reducing Levels of Disease Associated Proteins

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Patent No.
US None
App. No.
12/499,682
Abstract

The subject invention concerns the reduction of protein aggregation in the neurons of a mammal through the use of a ketogenic treatment such as a ketogenic diet, a physical training regimen and/or administration of agents to increase fatty acid oxidation. Such ketogenic treatment can be useful in the reduction of certain aggregates including amyloid β peptide, polyglutamine containing huntintin protein, polyglutamine containing androgen receptor, polyglutamine containing atrophin-1, polyglutamine containing ataxins, α-synclein, prion protein, tau and superoxide dismutase 1 (SOD1).

Claims (24)

1 . A method of reducing protein aggregation in the brain of a mammal, said method comprising administering a ketogenic treatment so to produce ketosis or a ketogenic state in the mammal for a predetermined period, whereby the protein aggregation is reduced.

2 . The method of claim 1 , wherein the ketosis or ketogenic state comprises maintenance of a serum ketone body level elevated above normal fasting value.

3 . The method of claim 2 , wherein serum ketone level is above 0.2 mM, 0.3 mM, 0.4 mM or higher for one hour or more.

4 . The method of claim 1 , wherein the ketogenic treatment is dietary and comprises:

a) reducing dietary carbohydrates whereby serum insulin level and protein synthesis is reduced, while protein degradation is increased; and

b) increasing dietary lipids whereby cellular lipid metabolism is increased.

5 . The method of claim 4 , wherein the carbohydrate levels are restricted to an amount less than 20%, 10% or 2% of total calories and serum ketone levels are elevated above normal fasting baseline levels.

6 . The method of claim 1 , wherein the ketogenic treatment is induced by an agent that increases fatty acid oxidation.

7 . The method of claim 6 , wherein the agent that increases fatty acid oxidation is selected from the group consisting of L-carnitine and derivatives thereof, caffeine, ephedra alkaloids, non-steroidal anti-inflammatory agents (NSAIDs), statin drugs, and fibrates.

8 . The method of claim 1 , wherein the ketogenic treatment is induced by a physical training regimen.

9 . The method of claim 8 , wherein the physical training regimen comprises activity above 50% of either VO2max or maximal heart rate for a period of greater than 20 minutes.

10 . The method of claim 1 , wherein the ketogenic treatment is induced by a combination of at least two treatments selected from the group consisting of dietary treatment, fatty acid oxidation agent treatment, and physical training regimen.

11 . The method of claim 10 , wherein the dietary treatment is combined with the physical training regimen.

12 . The method of claim 1 , wherein the protein aggregates are selected from the group consisting of amyloid β peptide, polyglutamine containing huntintin protein, polyglutamine containing androgen receptor, polyglutamine containing atrophin-1, polyglutamine containing ataxins, α-synclein, prion protein, tau and superoxide dismutase 1 (SOD1).

13 . The method of claim 1 , further comprising administering a second compound which inhibits aggregate formation or is neuroprotective.

14 . The method of claim 13 , wherein the second compound is selected from the group consisting of Congo red, cystamine, cysteamine, minocycline, ethyl eicosapentaenoate, and riluzole.

15 . The method of claim 1 , wherein the ketogenic treatment is between 1 day and 1 year.

16 . An assay for measuring the effectiveness of ketogenic treatment for the reduction or prevention of protein aggregation in cells, comprising

a) treating said cells in vivo or in vitro with a ketogenic treatment; and

b) determining whether such treatment prevents or reduces protein aggregation in the cells.

17 . The method of claim 16 , wherein the reduction in protein aggregation is at least 25% by weight.

18 . The assay of claim 16 , wherein the in vivo treatment involves ketogenic treatment of a non-human mammal that exhibits neuronal aggregation of a protein associated with a protein aggregation disease under non-ketogenic conditions.

19 . The assay of claim 16 , wherein the non-human mammal is a transgenic mouse that exhibits neuronal protein aggregation under non-ketogenic conditions.

20 . The assay of claim 16 , wherein the in vitro treatment comprises ketogenic treatment of cultured cells which exhibit protein aggregation under non-ketogenic conditions.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Feb 10, 2025
From: NESTLÉ HEALTH SCIENCE US HOLDINGS, INC.
To: CERECIN INC.
Reel/Frame 070168/0946 →
PATENT SECURITY AGREEMENT Recorded Jul 24, 2012
From: ACCERA, INC.
To: NESTLE HEALTH SCIENCE US HOLDINGS, INC., AS COLLATERAL AGENT
Reel/Frame 028624/0001 →
MERGER Recorded Dec 30, 2010
From: NEUERA PHARMACEUTICALS, INC.
To: ACCERA, INC.
Reel/Frame 025558/0250 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2009
From: HENDERSON, SAMUEL T.
To: ACCERA, INC.
Reel/Frame 023475/0726 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2009
From: ACCERA, INC.
To: ACCERA SUBSIDIARY, INC.
Reel/Frame 023475/0759 →
CHANGE OF NAME Recorded Nov 5, 2009
From: ACCERA SUBSIDIARY, INC.
To: NEUERA PHARMACEUTICALS, INC.
Reel/Frame 023475/0859 →