METHODS OF INHIBITING SEIZURE IN A SUBJECT

Bibliographic Details
Title: METHODS OF INHIBITING SEIZURE IN A SUBJECT
Document Number: 20090281522
Publication Date: November 12, 2009
Appl. No: 12/179856
Application Filed: July 25, 2008
Abstract: The present invention relates to methods of inhibiting seizure in a subject. In particular, the invention provides methods of increasing brain leptin levels in a subject.
Inventors: Thio, Kwee Liu Lin (St. Louis, MO, US); Yamada, Kelvin A. (St. Louis, MO, US)
Assignees: Washington University in St. Louis (St. Louis, MO, US)
Claim: 1. A method of inhibiting seizures in a subject, the method comprising intranasally administering a composition comprising leptin to the subject.
Claim: 2. The method of claim 1, wherein the seizures are focal or general seizures.
Claim: 3. The method of claim 1, wherein the subject is human.
Claim: 4. The method of claim 1, wherein the composition comprises a leptin polypeptide having at least about 4 amino acids.
Claim: 5. The method of claim 1, wherein the composition comprises a leptin polypeptide having at least any 4 contiguous amino acids from a primary amino acid sequence at least 75% homologous to an amino acid sequence selected from the group consisting of SEQ ID NOS: 1 and 2.
Claim: 6. A method of inhibiting seizures in a subject, the method comprising administering a compound that activates the leptin receptor in the brain of the subject.
Claim: 7. The method of claim 6, wherein the compound comprises a leptin receptor activator selected from the group consisting of a polypeptide, non-polypeptide, and combinations thereof.
Claim: 8. The method of claim 7, wherein the polypeptide is a leptin polypeptide having at least about 4 amino acids.
Claim: 9. The method of claim 7, wherein the polypeptide is a leptin polypeptide having at least any 4 contiguous amino acids from a primary amino acid sequence at least 75% homologous to an amino acid sequence selected from the group consisting of SEQ ID NOS: 1 and 2.
Claim: 10. The method of claim 7, wherein the non-polypeptide is a small molecule agonist having the ability to bind to the leptin receptor and activate signaling pathways selected from the group consisting of JAK/STAT, P13, and combinations thereof.
Claim: 11. The method of claim 6, wherein the compound activates the leptin receptor such that the brain leptin levels are increased to greater than about 15 pg/mg in the subject.
Claim: 12. The method of claim 6, wherein the compound activates the leptin receptor such that the brain leptin levels are increased to greater than about 20 pg/mg in the subject.
Claim: 13. The method of claim 6, wherein the compound is administered mucosally.
Claim: 14. The method of claim 6, wherein the compound is administered intranasally.
Claim: 15. A method of inhibiting seizures in a subject, the method comprising administering a composition comprising leptin to the subject, such that the brain leptin levels are increased to greater than about 15 pg/mg in the subject.
Claim: 16. The method of claim 15, wherein the brain leptin levels are increased to greater than about 20 pg/mg in the subject.
Claim: 17. The method of claim 15, wherein the composition comprises a leptin polypeptide having at least about 4 amino acids.
Claim: 18. The method of claim 15, wherein the composition comprises a leptin polypeptide having at least any 4 contiguous amino acids from a primary amino acid sequence at least 75% homologous to an amino acid sequence selected from the group consisting of SEQ ID NOS: 1 and 2.
Claim: 19. The method of claim 15, wherein the composition is administered mucosally.
Claim: 20. The method of claim 15, wherein the composition is administered intranasally.
Current U.S. Class: 604/522
Current International Class: 61
Accession Number: edspap.20090281522
Database: USPTO Patent Applications
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Language:English