Use of GLP-1 analogues for the treatment of disorders associated with dysfunctional synaptic transmission
The present invention relates to a peptide analogue of glucagon-like peptide-1 (7-36), which is useful to prophylactically prevent, improve, or reverse the diminished cognitive function associated with these types of disorders, by increasing (or sustaining) the LTP of synaptic transmission. Moreover, sustaining LTP may find utility in the prophylaxis of neurological disease by delaying the onset of impaired cognitive processes, and could serve as a treatment, not only for the diminished cognitive function caused by neurodegeneration, but also for the dysfunctional cognitive processes associated with trauma or age.
1. A method of improving memory in a subject comprising administering to the subject a pharmaceutically acceptable amount of a peptide analogue of glucagon-like peptide-1 (7-36) selected from the group consisting of a peptide analogue 10 to 31 amino acids in length and comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO: 1; a peptide analogue 10 to 31 amino acids in length comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO: 1 and further comprising N-terminal glycation; a peptide consisting of the sequence identified in SEQ ID NO: 1; a peptide consisting of SEQ ID NO:1 with N-terminal glycation; a peptide analogue 10 to 31 amino acids in length and comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-His and D-His, X 2 is selected from L-Val and D-Val, and X 3 is selected from L-Glu and D-Glu; a peptide analogue consisting of the sequence identified in SEQ ID NO: 4; a peptide analogue 10 to 31 amino acids in length and comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-Asp and D-Asp, X 2 is selected from L-Ala and D-Ala, and X 3 is selected from L-Glu and D-Glu; a peptide analogue consisting of the sequence identified in SEQ ID NO: 3; a peptide analogue 10 to 31 amino acids in length and comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-His and D-His, X 2 is selected from L-Ala and D-Ala, and X 3 is selected from L-Pro and D-Pro; a peptide analogue consisting of the sequence identified in SEQ ID NO: 5; a peptide analogue 10 to 31 amino acids in length and comprising at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2, wherein X 2 is Ala or Val and wherein the peptide analogue further comprises addition of L-Glu, D-Glu, or addition of a C-16 palmitoyl fatty acid at Lys(20), or an amino acid substitution by L-Arg or D-Arg at Lys(28) of SEQ ID NO:2; and a peptide analogue Arg(34)Lys(26)-(N-epsilon-(gamma-Glu) (N-alpha-hexadecanoyl))GLP-1(7-37).
2. The method according to claim 1 , wherein the amino acid sequence of the peptide analogue consists of the sequence identified in SEQ ID NO: 1.
3. The method according to claim 1 , wherein the peptide analogue further comprises N-terminal glycation.
4. The method according to claim 2 , wherein the peptide analogue further comprises N-terminal glycation.
5. The method according to claim 1 wherein the peptide analogue is 10 to 31 amino acids in length and the amino acid sequence of the peptide analogue comprises at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-His and D-His, X 2 is selected from L-Val and D-Val, and X 3 is selected from L-Glu and D-Glu.
6. The method according to claim 1 , wherein the amino acid sequence of the peptide analogue consists of the sequence identified in SEQ ID NO: 4.
7. The method according to claim 1 wherein the peptide analogue is 10 to 31 amino acids in length and the amino acid sequence of the peptide analogue comprises at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-Asp and D-Asp, X 2 is selected from L-Ala and D-Ala, and X 3 is selected from L-Glu and D-Glu.
8. The method according to claim 1 , wherein the amino acid sequence of the peptide analogue consists of the sequence identified in SEQ ID NO: 3.
9. The method according to claim 1 wherein the peptide analogue is 10 to 31 amino acids in length and the amino acid sequence of the peptide analogue comprises at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2 wherein X 1 is selected from L-His and D-His, X 2 is selected from L-Ala and D-Ala, and X 3 is selected from L-Pro and D-Pro.
10. The method according to claim 1 , wherein the amino acid sequence of the peptide analogue consists of the sequence identified in SEQ ID NO: 5.
11. The method according to claim 1 wherein the peptide analogue is 10 to 31 amino acids in length and the amino acid sequence of the peptide analogue comprises at least the first 10 amino acids from the N-terminal end of the sequence identified in SEQ ID NO:2, wherein X 2 is Ala or Val; and wherein the peptide analogue further comprises addition of L-Glu, D-Glu, or addition of a C-16 palmitoyl fatty acid at Lys(20), or an amino acid substitution by L-Arg or D-Arg at Lys(28) of SEQ ID NO:2.
12. The method according to claim 1 , wherein the peptide analogue is Arg(34)Lys(26)-(N-epsilon-(gamma-Glu) (N-alpha-hexadecanoyl))GLP-1(7-37).