CA2410453A1

CA2410453A1 - Neuroprotective peptides

Info

Publication number: CA2410453A1
Application number: CA002410453A
Authority: CA
Inventors: Virginia Smith-Swintosky; Michael Renzi; Carlos Plata-Salaman; Linda Jolliffe; Francis Farrell; Dana L. Johnson
Original assignee: Individual
Current assignee: Janssen Pharmaceuticals Inc
Priority date: 2000-05-26
Filing date: 2001-05-23
Publication date: 2001-12-06
Also published as: CN1318084C; EP1296702A4; CN1452492A; MXPA02011727A; IL153079A0; JP2003534384A; AU7490401A; NZ522924A; BR0111182A; HK1058484A1; WO2001091780A1; ZA200210304B; AU2001274904B2; EP1296702A1

Abstract

Methods of treating diseases of the nervous system by administration of compositions having the neurological therapeutic activity of human erythropoietin are disclosed. These compositions include therapeutic agents such as peptides, peptide dimers, polypeptides, and proteins that have the full range of biological activity of human erythropoietin or only certain biological activities of erythropoietin. Improved therapeutic regimens where the erythropoietin is administered at concentrations below those required to stimulate hematopoiesis are also provided.

Description

NEUROPROTECTIVE PEPTIDES
CROSS-REFERENCE TO RELATED APPLICATION
This application claims the benefit of United States Provisional Application Serial No. 60/207654, filed May 26, 2000.
FIELD OF THE INVENTION
The present invention is directed to methods of treating diseases and conditions involving the nervous system by administration of compositions having the therapeutic activity of human erythropoietin. These compositions include therapeutic agents such as peptides, peptide dimers, polypeptides, and proteins that have the full range of biological activity of human erythropoietin or only certain biological activities of erythropoietin. The present invention also provides improved therapeutic regimens wherein the therapeutic agent is administered at concentrations below those required to stimulate hematopoiesis.

Erythropoietin (EPO) is a glycoprotein hormone produced by the kidney in response to tissue hypoxia that stimulates red blood cell production in the bone marrow. The gene for erythropoietin has been cloned and expressed in Chinese hamster ovary (CHO) cells as described in United States Patent No. 4,703,008. Recombinant human erythropoietin (r-HuEPO or Epoetin alfa) has an amino acid sequence identical to that of human urinary erythropoietin, and the two are indistinguishable in chemical, physical and innnunological tests. Recombinant human erythropoietin acts by increasing the number of cells capable of differentiating into mature erythrocytes, triggering their differentiation and augmenting hemoglobin synthesis in developing erythroblasts i(Krantz SB. Blood (1991) 77:
419-434, Beckman BS, Mason-Garcia M. The Faseb Journal (1991) 5: 2958-2964).

Epoetin alfa has been well tolerated in studies conducted to date.
Hypertensive encephalopathy and seizures have occasionally been described in dialysis patients treated with Epoetin alfa, particularly during the early phase of therapy when hematocrit is rising. (Eschbach JW, Egrie JC, Downing MR, Browne JIB, Adamson JW. New Engl J Med (1987) 316:
73-78, Winearls CG, Oliver DO, Pippard MJ, et al. Lancet (1986) 2 (8517): 1175-1177).
Such reports became more rare as experience of use of the compound developed. Occasionally, cancer patients treated with Epoetin alfa have experienced an increase in blood pressure associated with a significant increase in hematocrit. The risk, however, appears substantially lower than in chronic renal failure patients.
No antibody titers against Epoetin alfa could be demonstrated and confirmed in subjects treated with Epoetin alfa for up to 2 years, indicating the absence of immunological sensitivity to Epoetin alfa. Skin rashes and urticaria have been observed rarely and when reported have been mild and transient in nature, but these events suggest allergic hypersensitivity to some components of the Epoetin alfa formulation.
Epoetin alfa is approved for sale in many countries for the treatment of anemia in chronic renal failure (dialysis and predialysis), anemia in zidovudine treated HTV
positive patients (LTS), anemia in cancer patients receiving platinum-based chemotherapy, as a facilitator of autologous blood pre-donation, and as a peri-surgical adjuvant to reduce the likelihood of requiring allogeneic blood transfusions in patients undergoing orthopedic surgery.
EPO influences neuronal stem cells, likely during embryonic development, and possibly during in vitro experiments of differentiation. (Juul et al Pediatr Dev Pathol (1999) 2(2) 148 - 158. Juul et al Pediatr Res (1998) 43(1) 40 - 49.) Further, neonates and infants that suffer CNS injury via hypoxia, meningitis, and intraventricular hemorrhage, show an EPO induced neuroprotective effect (Juul et al Ped Res (1999) 46(5) 543 -547.) EPO helps prevent apoptosis of neural tissue in cases of injury that create hypoxia.
This may be the result of EPO produced locally by astrocytes (Morishita et al Neuroscience (1996) 76(1) 105 - 116). Neuroprotection has been demonstrated in gerbil hippocampal and rat cerebrocortical tissue (Sakanaka et al PNAS (1998) 95(8) 4635 - 4640.
Sadamoto et aI
Biochem Biophys Res Commun (1998) 253(1) 26 - 32).
EPO induces biological effects of PC12 cells, including changes in Ca2+, changes in membrane potential, and promotion of neuronal survival. This has been interpreted that EPO
can stimulate neural function and viability (Koshimura et al J. Neurochem (1999) 72(6) 2565-2572. Tabria et al Iht JDev Neurosci (1995) 13(3/4) 241- 252.).
O'Brien et al propose that a 17 amino acid peptide sequence of EPO can act through the EPO -R (Erythropoietin receptor) to induce biological activity in NS20Y, SK-N-MC, and PC 12 cells, which includes sprouting, differentiation and neuroprotection.
Curiously this peptide does not promote proliferation of hematologic cells, thus it appears inactive in cell lines well understood for their sensitivity to EPO activity. (Campana et al Iht J Mol Med (1998) 1(1) 235 - 241 and United States Patent No.'s 5,700,909, issued on 12/23/1999, 5,571,787, issued on 11/5/1996, 5,714,459, issued on 2/3/1998, and 5,696,080, issued on 12/9/1997, all to O'Brien et al.) EPO may influence neuronal stem cell commitment to drive differentiation of neurons as opposed to astrocytes or oligodendrocytes. This is compared to a similar activity of EPO, where it functions to drive commitment of hematopoietic stem cells to produce red blood cells (RBCs). There is an apparent relationship between CNS hypoxic injury, resulting in the production of EPO from astrocytes that commits neuronal stem cells to differentiate into neurons, while simultaneously acting as a neuroprotective function for existing neurons.
(WIPO publication number W099/21966, published on 5/6/1999, Weiss et al.) SUMMARY OF THE INVENTION
The present invention is directed to methods of treating diseases and conditions involving the nervous system by administration of compositions having the neurological therapeutic activity of human erythropoietin.

In a first embodiment, the present invention is directed to a method for treating a patient having a disorder characterized by neurotoxicity, neurodegeneration or neurological damage, comprising administering to said patient a therapeutically effective amount of a peptide comprising one or more monomeric peptides of 8 to about 40 amino acids in length that bind to EPO receptor, each monomeric peptide comprising a sequence of amino acids X4XSXaXbX6XcXdX7 (SEQ ID NO: 47), wherein XaisGorA;
Xb is P or A;
X~isTorA;
Xd is selected from W, A, and F;
X4 is selected from R, H, Y, L, and W, or X4 is nonexistent;
XS is selected from F, M, and I;
X6 is independently selected from the 20 genetically coded L-amino acids or the stereoisomeric D-amino acids; and X~ is selected from D, V, E, I, and L.
In particular, said sequence is X3X4XSGPX6TWX~X$ (SEQ ID NO: 1), wherein X3 is selected from C, E, A, a-amino-y-bromobutyric acid, and homocysteine (Hoc);
and X8 is selected from C, K, A, a=amino-y-bromobutyric acid, and homocysteine (Hoc).

In a second embodiment, the present invention is directed to peptides which behave as cell-surface receptor agonists and antagonists, as well as dimers and multimers of such peptides which exhibit binding and signal initiation of growth factor-type receptors. In one embodiments the present invention provides peptides which behave as EPO agonists. These peptides may be dimers or multirners of such peptides, preferably 14 to about 20 residues in length, comprising a core amino acid sequence of X3Xa XSGPX6TWX~X$ (SEQ ID NO: 1) wherein each amino acid is indicated by standard one letter abbreviation; X3 can be C, E, A, a-amino-'y-bromobutyric acid, or Hoc, where Hoc is homocysteine; X4 can be R, H, Y, L, or W, or X4 is nonexistent; XS can be M, F, or I;
X6 is independently any one of the 20 genetically coded L-amino acids or the stereoisomeric D-amino acids; X~ can be D, E, I, L, or V; and X$ can be C, K, A, a-amino-y-bromobutyric acid, or Hoc, where Hoc is homocysteine.
Preferably, the monomeric peptide unit of the dimer or multimer comprises a core sequence of amino acids YXZX3X4XSGPX6TWX~X$ (SEQ ID NO: 2), wherein each of XZ
and X6 is independently any one of the 20 genetically coded L-amino acids; X3 is C; and X8 is C.
Preferably, the monomeric peptide unit of the dimer comprises a core sequence of amino acids X,YX2X3X4XSGPX6TWX~X8X9X,oX" (SEQ ID NO: 3), wherein each of X,, XZ, X6, X9, Xlo, and X,1 is independently selected from the 20 genetically coded L-amino acids.
Particularly, X3 can be C, E, A; X4 can be R, H, or Y, or X4 is nonexistent;
XS can be M, F, or I; X~ can be D or V; and X8 can be C, K, or A.
In a more preferred embodiment, both X3 and X8 are C and thus, the monomeric peptide unit of the dimer comprises a core sequence of amino acids XI YXZ CX4 ~TWX~ CX9 X,o Xl, (SEQ ID NO: 4). Particularly, the monomeric peptide unit comprises a core sequence of amino acids X, YXZ CX4 XS GPX6 TWX~ CX9 Xlo Xl, (SEQ ID NO:

5), where X4 can be R or H; XS can be F or M; X6 can be I, L, T, M, or V; X~
is D or V;
X9 can be G, K, L, Q, R, S, or T; and Xlo can be A, G, P, R, or Y. More particularly, the monomeric peptide unit of the dimer will comprise a core sequence of amino acids X, YXZ CX4 XS GPX6 TWX~ CX9 Xlo X" (SEQ ID NO: 6), where X, can be D, E, L, N, S, s T, or V; XZ can be A, H, K, L, M, S, or T; X4 is R or H; X9 can be K, R, S, or T; and Xlo is P.
Preferably, the monomeric peptide unit of the dimer will comprise a core sequence of amino acids X, YXZ CX4 XS GPX6 TWX~ CX9 Xlo X,1 (SEQ ID NO: 6), where Xl can be D, E, L, N, S, T, or V; XZ can be A, H, K, L, M, S, or T; X4 is R or H; X9 can be K, R, S, or T;
and Xlo is P.
Particularly preferred monomeric peptide units of the dimers include:
GGLYLCRFGPVTWDCGYKGG (SEQ ID N0:7);

GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID
N0:8);

GGDYHCRMGPLTWVCKPLGG (SEQ ID N0:9);

VGNYMCHFGPITWVCRPGGG (SEQ ID NO:10);

GGVYACRMGPITWVCSPLGG (SEQ ID NO:11);

VGNYMAHMGPITWVCRPGG (SEQ ID N0:12);

GGTYSCHFGPLTWVCKPQ (aka EMP-16) (SEQ ID
N0:13);

GGLYACHMGPMTWVCQPLRG (aka EMP-36) (SEQ ID
N0:14);

TIAQYICYMGPETWECRPSPKA (aka EMP-38) (SEQ ID
NO:15);

YSCHFGPLTWVCK (aka EMP-20 (SEQ ID
N0:16);

YCHFGPLTWVC (aka EMP-23) (SEQ ID
N0:17);

SCHFGPLTWVCK (aka EMP-24) (SEQ ID
N0:18);

GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID
N0:19);

GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID
N0:20);

GGTYSCFGPLTWVCKPQGG (aka EMP-27) (SEQ ID
NO:21);

TYSCHFGPLTWVCKPQGG (aka EMP-17) (SEQ ID
N0:22);

TYSCHFGPLTWVCKPQ (aka EMP-18) (SEQ ID
NO:23);

YSCHFGPLTWVCKP (aka EMP-19) (SEQ ID
N0:24);

YSCHFGPLTWVC (aka EMP-21) (SEQ ID
N0:25);

YSCHFGALTWVCK (aka EMP-22) (SEQ ID
N0:26);

GGCRIGPITWVCGG (aka EMP-25) (SEQ ID
N0:27);

HFGPLTWV (aka EMP-26) (SEQ ID
N0:28);

GGTTSCHFGPLTWVCKPQGG (aka EMP-7) (SEQ ID N0:29);

GGTFSCHFGPLTWVCKPQGG (aka EMP-8) (SEQ ID N0:30);

GGTYSCHFGALTWVCKPQGG (aka EMP-10) (SEQ ID N0:31);

GGTYSCHFGPATWVCKPQGG (aka EMP-11) (SEQ ID N0:32);

GGTYSCHFGPLAWVCKPQGG (aka EMP-12) (SEQ ID N0:33);

GGTYSCHFGPLTAVCKPQGG (aka EMP-13) (SEQ ID N0:34);

GGTYSCHFGPLTFVCKPQGG (aka EMP-14) (SEQ ID N0:35);

GGTYSCHFGPLTWVCKAQGG (aka EMP-15) (SEQ ID N0:36);

GGTXSCHFGPLTWVCKPQGG (aka EMP-28, X = D-Tyr) (SEQ ID
N0:37);

GGTXSCHFGPLTWVCKPQGG (aka EMP-29, X =p-NOZ-Phe) (SEQ ID N0:3 8);

GGTXSCHFGPLTWVCKPQGG (aka EMP-30, X =p-NHZ-Phe) (SEQ ID N0:39);

GGTXSCHFGPLTWVCKPQGG (aka EMP-31, X =p-F-Phe) (SEQ
ID N0:40);

GGTXSCHFGPLTWVCKPQGG (aka EMP-32, X =p-I-Phe) (SEQ
ID N0:41);

GGTXSCHFGPLTWVCKPQGG (aka EMP-33, X = 3,5-dibromo-Tyr) (SEQ ID N0:42);

Ac-GGTYSCHFGPLTWVCKPQGG (aka EMP-34) (SEQ ID N0:43);

GGLYACHMGPMTWVCQPLGG (aka EMP-35) (SEQ ID N0:44);

LGRI~YSCHFGPLTWVCQPAKI~D (aka EMP-37) (SEQ ID NO:45);
and GGTYSEHFGPLTWVKKPQGG (aka EMP-39) (SEQ ID N0:46).
Preferably, monomeric peptide units of the dimers include:
GGTYSCHFGPLTWVCI~PQGG (aka EMP-1) (SEQ ID N0:8);

GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID N0:19);

GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID N0:20);
and YCHFGPLTWVC (aka EMP-23) (SEQ ID N0:17).

In accordance with the present invention the monomeric units of the dimers can be the same or different.
In a preferred embodiment polyethylene glycol (PEG) may be employed as a linker to form the dimeric peptides of the present invention through a covalent bond.
In another embodiment, the present invention is directed to pharmaceutical compositions comprising at least one peptide of the invention and a pharmaceutical carrier to be used in a method of treating or preventing neurotoxicity.
In a further embodiment, the present invention provides a method for therapeutically treating a mammal having a disease or condition resulting from a neurotoxic or neurodegenerative or neuro-damaging event by administration of at least one of the peptides of the present invention.
In a still further embodiment, a method for therapeutically treating a mammal having a neurotoxic, neuro-damaging or neurodegenerative condition which may be modulated by EPO by using at least one of the peptides of the present invention is provided.
BRIEF DESCRIPTION OF THE DRAWING
Figure 1 Panel A and Panel B show that EPO receptor is expressed in rat hippocampal and cortical cultures.
Figure 2 shows that EPO receptor is expressed in neuronal cell lines: PC12 and SK-N-MC cells.
Figure 3 shows EPO induced gene expression in PC12 cells. (Top) Total RNA
isolated from PC-12 cells treated with 1 nm EPO for 24 hr was subject to RT-PCR to quantify the changes in gene expression of specific BCL family members. Pre-treatment with EPO resulted in a 6 fold increase in the expression of the anti-apoptotic gene BCL~, and a greater than 5 fold decrease in the expression of the pro-apoptotic Bak. These results are consistent with the gene chip results suggesting a possible mechanism for EPO's protective effects. (Bottom) Agarose gels showing RT-PCR products representing the regulation of s Bcl,~, and Bak. m - markers, 1 - RT-PCR negative control, lane 2 - No Treatment, lane 3 -50 ng/ml NGF, lane 4 - EPO 1 nm.
Figure 4 shows that rhEPO protects rat cerebral cortical neurons against glutamate toxicity.
. Figure 5 shows that rhEPO protects rat PC12 cells against glutamate-induced cell death. 7 day cultures of PC-12 cells were treated with erythropoietin for 24 hours before being exposed to a toxic concentration of glutamate (200 um). Cultures were allowed to recover for 24 hours and cell survival was determined using a Trypan Blue exclusion assay. 1 to 10 pm Erythropoietin given 24 hours prior to a 15 minute exposure to glutamate significantly increased cell survival (p<.001, student's t-test. The protective activity of EPO
decreased at higher doses.
Figure 6 shows that rhEPO protects rat PC 12 cells against NGF withdrawal-induced cell death. Cultures of PC-12 cells were grown in the presence of NGF for 7 days and then treated with EPO for 24 hours before they were switched to media without NGF.
Cell survival was determined by counting the number of viable cells immediately following the removal of NGF and comparing it to the number of viable cells at 12 hr, 24 hr, 48 hr and 72 hr following growth factor withdrawal. Cell viability was determined based on morphological characteristics including phase brightness, presence of axons and absence of membrane blebbing. Treatment with EPO increased the number of viable cells at each time point following growth factor withdrawal with an optimum concentration of 10 pm.
Figure 7 shows that rhEPO promotes neurite outgrowth in rat cerebral cultures.
Figure 8 shows that rhEPO promotes neurite outgrowth in rat hippocampal cultures.
Figure 9 shows that EMP-1 promotes neurite outgrowth in rat cerebral cortical cultures.
Figure 10 shows that EMP-1 promotes neurite outgrowth in rat hippocampal cultures.
Figure 11 shows that EMP-6 promotes neurite outgrowth in rat cerebral cortical cultures.
Figure 12 shows that EMP-6 promotes neurite outgrowth in rat hippocampal cultures.
Figure 13 shows that EMP-9 promotes neurite outgrowth in rat cerebral cortical cultures.
Figure 14 shows that EMP-9 promotes neurite outgrowth in rat hippocampal cultures.

Figure 15 shows that EMP-23 promotes neurite outgrowth in rat cerebral cortical cultures.
Figure 16 shows that EMP-23 promotes neurite outgrowth in rat hippocampal cultures.
Figure 17 shows that EMP-27 promotes neurite outgrowth in rat cerebral cortical cultures.
Figure 1 ~ shows that EMP-27 promotes neurite outgrowth in rat hippocampal cultures.
Figure 19 shows that EPO protects against ischemic injury: study I continuous iv infusion via osmotic mini-pump.
Figure 20 shows plasma determinations for study I.
Figure 21 shows that EPO does not protect against ischemic injury: study II
single iv bolus dose.
Figure 22 shows plasma determinations for study II.
Figure 23 shows that EPO protects against ischemic injury: study III repeat iv bolus dosing.
Figure 24 shows plasma determinations: study III.
DETAILED DESCRIPTION
"Erythropoietin" (EPO) used herein includes those peptides, peptide dimers, polypeptides, and proteins that have the full range of biological activity (for example, hematopoietic and neurological activities) of human erythropoietin or only certain biological activities (for example, hematopoietic or neurological activities only) of erythropoietin, as well as erythropoietin analogs, erythropoietin isoforms, erythropoietin mimetics, erythropoietin fragments, hybrid erythropoietin proteins, fusion proteins, oligomers and multimers of the above, homologues of the above, glycosylation pattern variants of the above, and muteins of the above, regardless of the biological activity of same, and further regardless of the method of synthesis or manufacture thereof including, but not limited to, recombinant, whether produced from cDNA or genomic DNA, synthetic, transgenic, and gene activated methods. Specific examples of erythropoietin include, Epoetin alfa (EPREX~, ERYPO~, PROCRIT°), NEORECORMON, Novel erythropoiesis stimulating protein (NESP
to or ARANESP, a hyperglycosylated analog of recombinant human erythropoietin (Epoetin) described in European patent application EP640619), human erythropoietin analog - human serum albumin fusion proteins such as those described in the international patent application WO 99/66054, erythropoietin mutants such as those described in the international patent application WO 99/38890, erythropoietin omega, which may be produced from an Apa I
restriction fragment of the human erythropoietin gene described in United States Patent No.
5,688,679, altered glycosylated human erythropoietin such as those described in the international patent application WO 99/11781, PEG conjugated erythropoietin analogs such as those described in WO 98/05363 or United States Patent No. 5,643,575.
Specific examples of cell lines modified for expression of endogenous human erythropoietin are described in international patent applications WO 99/05268 and WO 94/12650.
The generally preferred form of EPO is purified, recombinant human EPO (rhEPO), currently formulated and distributed under the trademarks of EPREX~, ERYPO~, or PROCRIT~.
The abbreviation "EMP" as used herein refers to peptide mimetics of EPO, particularly certain peptides described in United States Patent No.'s 5,767,078 and 5,773,569.
Following is a list of amino acid abbreviations used in the present specification for various peptides. The individual amino acid residues are identified according to a single letter and three letter code that is readily known and used by those of ordinary skill in the art.
AMINO ACID ABBREVIATIONS
3-Letter 1-Letter alanine ala A
valine val V
leucine leu L
isoleucine ile I
proline pro P
phenylalanine phe F
tryptophan trp W
methionine met M
glycine gly G

serine ser S

threonine thr T

cysteine cys C

tyrosine tyr Y

asparagine asn N

glutamine gln Q

aspartic acid asp D

glutamic acid glu E

lysine lys K

arginine arg R

histidine his H

In a first embodiment, the present invention is directed to methods of treating neuronal cells with a pharmaceutical composition comprising a therapeutically active peptide that behaves as cell-surface receptor agonists as well as dimers and multimers of such peptides that exhibit binding and signal initiation of growth factor-type receptors. In one embodiment, the present invention provides peptides that behave as EPO
agonists.
Particularly, these peptides may be dimers or multimers that have two 'monomeric' peptide units of 8 to 40 or more amino acids, preferably 14 to about 20 residues in length, comprising a core amino acid sequence of X3 X4 XS GPX6 TWX~ X8 (SEQ ID NO: 1) where each amino acid is indicated by standard one letter abbreviation; X3 can be C, E, A, a-amino-y-bromobutyric acid, or Hoc, where Hoc is homocysteine; X4 can be R, H, Y, L, or W, or X4 is nonexistent; XS can be M, F, or I; X6 is independently any one of the 20 genetically coded L-amino acids or the stereoisomeric D-amino acids; X~ can be D, E, I, L, or V;
and X8 can be C, K, A, a-amino-y-bromobutyric acid, or Hoc, where Hoc is homocysteine, provided that either X3 or X8 is C or Hoc. Preferably, the monomeric peptide unit of the dimer or multimer comprises a core sequence YXZX3X4XSGPX6TWX~XB (SEQ ID NO: 2) where each amino acid is indicated by standard one letter abbreviation; each X,, X2, X6, X9, X,o, and Xl, is independently selected from the 20 genetically coded L-amino acids; X3 can be C, E, A, a-amino-y-bromobutyric acid, or Hoc, where Hoc is homocysteine; X4 can be R, H, Y, L, or W, or X4 is nonexistent; XS can be M, F, or I; X~ can be D, E, I, L, or V; and X8 can be C, K, A, a-amino-y-bromobutyric acid, or Hoc, where Hoc is homocysteine. More preferably, either X3 or X8 is C or Hoc.
Preferably, the monomeric peptide unit of the dimer or multimer comprises a core sequence of amino acids YXZX3X4XSGPX6TWX~XB (SEQ ID NO: 2), wherein each of XZ
and X6 is independently any one of the 20 genetically coded L-amino acids; X3 is C; and X8 is C.
Preferably, the monomeric peptide unit of the dimer comprises a core sequence of amino acids X,YXZX3X4XSGPX6TWX~X$X9XloX" (SEQ ID NO: 3), wherein each of Xl, X2, X6, X9, Xlo, and X11 is independently selected from the 20 genetically coded L-amino acids.
Particularly, X3 can be C, E, A; X4 can be R, H, or Y, or X4 is nonexistent;
XS can be M, F, or I; X~ can be D or V; and X8 can be C, K, or A.
In a more preferred embodiment, both X3 and X$ are C and thus, the monomeric peptide unit of the dimer comprises a core sequence of amino acids Xl YXZ CX4 TWX~ CX9 Xlo X11 (SEQ ID NO: 4). Particularly, the monomeric peptide unit comprises a core sequence of amino acids Xl YXZ CX4 XS GPX6 TWX~ CX9 Xlo X11 (SEQ ID NO:
5), where X4 can be R or H; XS can be F or M; X6 can be I, L, T, M, or V; X~
is D or V;
X9 can be G, K, L, Q, R, S, or T; and Xlo can be A, G, P, R, or Y. More particularly, the monomeric peptide unit of the dimer will comprise a core sequence of amino acids Xl YXZ CX4 XS GPX6 TWX~ CX9 Xlo X11 (SEQ ID NO: 6), where Xl can be D, E, L, N, S, T, or V; XZ can be A, H, K, L, M, S, or T; X4 is R or H; X9 can be K, R, S, or T; and Xlo is P.
Preferably, the monomeric peptide unit of the dimer will comprise a core sequence of amino acids Xl YXZ CX4 XS GPX6 TWX~ CX9 Xlo X11 (SEQ ID NO: 6), where Xl can be D, E, L, N, S, T, or V; XZ can be A, H, K, L, M, S, or T; X4 is R or H; X9 can be K, R, S, or T;
and Xlo is P.

Particularly preferred monomeric peptide units of the dimers include:
GGLYLCRFGPVTWDCGYKGG (SEQ ID N0:7);

GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID
N0:8);

GGDYHCRMGPLTWVCKPLGG (SEQ ID N0:9);

VGNYMCHFGPITWVCRPGGG (SEQ ID NO:10);

GGVYACRMGPITWVCSPLGG (SEQ ID NO:11);

VGNYMAHMGPITWVCRPGG (SEQ ID N0:12);

GGTYSCHFGPLTWVCKPQ (aka EMP-16) (SEQ ID
N0:13);

GGLYACHMGPMTWVCQPLRG (aka EMP-36) (SEQ ID
N0:14);

TIAQYICYMGPETWECRPSPKA (aka EMP-38) (SEQ ID
NO:15);

YSCHFGPLTWVCK (aka EMP-20 (SEQ ID
N0:16);

YCHFGPLTWVC (aka EMP-23) (SEQ ID
N0:17);

SCHFGPLTWVCK (aka EMP-24) (SEQ ID
N0:18);

GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID
N0:19);

GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID
N0:20);

GGTYSCFGPLTWVCKPQGG (aka EMP-27) (SEQ ID
N0:21);

TYSCHFGPLTWVCKPQGG (aka EMP-17) (SEQ ID
N0:22);

TYSCHFGPLTWVCKPQ (aka EMP-18) (SEQ ID
N0:23);

YSCHFGPLTWVCKP (aka EMP-19) (SEQ ID
N0:24);

YSCHFGPLTWVC (aka EMP-21) (SEQ ID
N0:25);

YSCHFGALTWVCK (aka EMP-22) (SEQ ID
N0:26);

GGCRIGPITWVCGG (aka EMP-25) (SEQ ID
N0:27);

HFGPLTWV (aka EMP-26) (SEQ ID
N0:28);

GGTTSCHFGPLTWVCKPQGG (aka EMP-7) (SEQ ID
N0:29);

GGTFSCHFGPL'TWVCKPQGG (aka EMP-8) (SEQ ID
N0:30);

GGTYSCHFGALTWVCKPQGG (aka EMP-10) (SEQ ID
N0:31);

GGTYSCHFGPATWVCKPQGG (aka EMP-11) (SEQ ID
N0:32);

GGTYSCHFGPLAWVCKPQGG (aka EMP-12) (SEQ ID
N0:33);

GGTYSCHFGPLTAVCKPQGG (aka EMP-13) (SEQ ID
N0:34);

GGTYSCHFGPLTFVCKPQGG (aka EMP-14) (SEQ ID
N0:35);

GGTYSCHFGPLTWVCKAQGG (aka EMP-15) (SEQ ID
N0:36);

GGTXSCHFGPLTWVCKPQGG (aka EMP-28, X = D-Tyr) (SEQ
ID N0:37);

GGTXSCHFGPLTWVCI~PQGG (aka EMP-29, X =p-NOZ Phe) (SEQ ID N0:38);

GGTXSCHFGPLTWVCKPQGG (aka EMP-30, X =p-NHi Phe) (SEQ ID N0:39);

GGTXSCHFGPLTWVCKPQGG (aka EMP-31, X =p-F-Phe) (SEQ
ID N0:40);

GGTXSCHFGPLTWVCKPQGG (aka EMP-32, X =p-I-Phe) (SEQ
ID N0:41);

GGTXSCHFGPLTWVCKPQGG (aka EMP-33, X = 3,5-dibromo-Tyr) (SEQ ID N0:42);

Ac-GGTYSCHFGPLTWVCKPQGG (aka EMP-34) (SEQ ID N0:43);

GGLYACHMGPMTWVCQPLGG (aka EMP-35) (SEQ ID N0:44);

LGRKYSCHFGPLTWVCQPAKKD (aka EMP-37) (SEQ ID N0:45);
and GGTYSEHFGPLTWVI~PQGG (aka EMP-39) (SEQ ID N0:46).

Most preferably, monomeric peptide units of the dimers include:

GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID N0:8);

GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID N0:19);

GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID N0:20); and YCHFGPLTWVC (aka EMP-23) (SEQ ID N0:17).

EPO is administered by any suitable means as appropriate for the particular patient being treated, as would be apparent to one skilled in the art. The phrase "therapeutically effective" as used herein will vary from patient-to-patient, and depending on the particular range of biological activities possessed by the EPO molecule being administered.
Typically, for EPO
having hematopoietic activity, a therapeutically effective amount will be from about 1 to 500 LU./kg body weight and more preferably from 50 to 300 LU./kg body weight especially when erythropoietin is administered via subcutaneously. For EPO molecules not possessing hematopoietic activity the therapeutically effective dose may be more or less that an EPO
molecule having hematopoietic activity. The preferred methods of administration are intravenous (iv) and subcutaneous (sc), with subcutaneous being generally preferred.
Hematopoietically active EPO is administered within the range of about 50 -1000 U/kg per dose, one to five times per week. In another embodiment, the EPO composition is administrated is directly to the nervous system. This administration route includes, but is not limited to, the intracerebral, intraventricular, intracerebroventricular, intrathecal, intracisternal, intraspinal and/or peri-spinal routes of administration, which can employ intracranial and intravertebral needles, and catheters with or without pump devices. Infusion doses can range, for example, from about 1.0 to 50,000 U/kg/min of EPO composition over a period ranging from several minutes to several days. Hematopoietically active EPO administration is delayed or withheld if the patient, male or female, exhibits a hemoglobin level in excess of about 15 g/dL.
The present invention provides in one embodiment a method to treat acute and chronic neurodegenerative disorders comprising administration of EPO or analogs thereof.
Acute neurodegenerative disorders include, but are not limited to, various types of acute neurodegenerative disorders associated with neuronal cell death or compromise including cerebrovascular insufficiency, focal or diffuse brain trauma, diffuse brain damage, and spinal cord injury. Examples of acute neurodegenerative disorders are: cerebral ischemia or infarction including embolic occlusion and thrombotic occlusion, reperfusion following acute ischemia, perinatal hypoxic-ischemic injury, cardiac arrest, as well as intracranial hemorrhage of any type (such as epidural, subdural, subarachnoid and intracerebral), and intracranial and intravertebral lesions (such as contusion, penetration, shear, compression and laceration), and whiplash shaken infant syndrome. Chronic neurodegenerative disorders that can be treated with one or more methods of the present invention include, but are not limited to, Alzheimer's disease, Pick's disease, diffuse Lewy body disease, progressive supranuclear palsy (Steel-Richardson syndrome), multisystem degeneration (Shy-Drager syndrome), chronic epileptic conditions associated with neurodegeneration, motor neuron diseases including amyotrophic lateral sclerosis, degenerative ataxias, cortical basal degeneration, ALS-Parkinson's-Dementia complex of Guam, subacute sclerosing panencephalitis, Huntington's disease, Parkinson's disease, synucleinopathies (including multiple system atrophy), primary progressive aphasia, striatonigral degeneration, Machado-Joseph disease /
spinocerebellar ataxia type 3 and olivopontocerebellar degenerations, Gilles De La Tourette's disease, bulbar and pseudobulbar palsy, spinal and spinobulbar muscular atrophy (Kennedy's disease), primary lateral sclerosis, familial spastic paraplegia, Werdnig-Hoffmann disease, Kugelberg-Welander disease, Tay-Sach's disease, Sandhoff disease, familial spastic disease, Wohlfart-Kugelberg-Welander disease, spastic paraparesis, progressive multifocal leukoencephalopathy, familial dysautonomia (Riley-Day syndrome), and prion diseases (including, but not limited to Creutzfeldt-Jakob, Gerstmann-Straussler-Scheinlcer disease, Kuru and fatal familial insomnia).
Because of the combination of neuroprotection and neurite outgrowth induced by rhEPO, other clinical conditions can be treated with one or more methods of the present invention include treating and / or preventing the neurological (including, but not limited to, cognitive) and psychiatric (including, but not limited to, psychopathology, depression, or anxiety), manifestations associated with peripheral diseases including, but not limited to, EPO deficiency (e.g., renal disease), blood loss of any kind (including, but not limited to, hemodialysis, peritoneal dialysis, diagnostic sampling, occult gastrointestinal bleeding), renal failure and end-stage renal disease, renal transplantation, and other conditions associated with anemia and neurological and neuropsychiatric manifestations, including, but not limited to, hematological and non-hematological malignancies / cancer, symptoms or complications in patients receiving chemotherapy (including, but not limited to, cisplatin) and other drugs (including, but not limited to, zidovudine), other hematological disorders (including, but not limited to, sickle cell anemia and thalassemia), inflammatory and infectious disorders (including, but not limited to, human immunodeficiency viral infections), chronic systemic autoimmune diseases (including, but not limited to, systemic lupus erythematosus), Henoch Schonlein Purpura, and hemolytic uremic syndrome. Also included in the present invention are the treatment and / or prevention of neurological and neuropsychiatric manifestations resulting from chemical, toxic, infectious and radiation injury of the nervous system and as a result of prematurity, as well as the treatment and / or prevention of neurological and neuropsychiatric consequences of encephalopathies including, but not limited to, those of anoxic-ischemia, hepatic, glycemic, uremic, electrolyte and endocrine origin.
Also, because of the combination of neuroprotection and neurite outgrowth induced by rhEPO, this molecule can also be applicable for the treatment and / or prevention of plexopathies (including plexus palsies), multifocal neuropathies, sensory neuropathies, motor neuropathies, sensory-motor neuropathies, infections neuropathies, autonomic neuropathies, sensory-autonomic neuropathies, demyelinating neuropathies (including, but not limited to, Guillain-Barre syndrome and chronic inflammatory demyelinating polyradiculoneuropathy), other inflammatory and immune neuropathies, neuropathies induced by drugs, neuropathies induced by pharmacological treatments, neuropathies induced by toxins, traumatic neuropathies (including, but not limited to, compression, crush, laceration and segmentation neuropathies), metabolic neuropathies, endocrine and paraneoplastic neuropathies, and other neuropathies such as Charcot-Marie-Tooth disease (type la, 1b, 2, 4a,1=X
linked), Friedreich's ataxia, metachromatic leukodystrophy, Refsum's disease, adrenomyeloneuropathy, Ataxia-telangiectasia, Dejerine-Sottas neuropathy (types A and B), Lambert-Eaton syndrome, and disorders of the cranial nerves.
The following examples illustrate the present invention without, however, limiting the same thereto.

rhEPO is expressed in nrimarv rat neuronal cultures and in neuronal cell lines Primary Neurohal Cell Culture Dissociated hippocampal and cortical cell cultures were established from embryonic day 18 rat fetuses as previously described (Mattson et al., 1994). Briefly, fetuses were removed via cesarean section from pregnant moms (Sprague-Dawley) anesthetized with halothane according to the AVMA Panel on Euthanasia. Pups were decapitated and the brains were removed and placed in HEPES-buffered Hank's Balanced Salt solution (HBSS;
Gibco). The hippocampi and cortices were dissected out and pooled according to tissue-type.
Tissue was trypsinized for 15 min (lmg/ml trypsin-HBSS; Worthington), rinsed with fresh HBSS, incubated in trypsin inhibitor (lmg/ml; Sigma) for 5 min, rinsed again with fresh HBSS and then triturated in lml fresh HBSS with a fire-polished glass pipette.
Dissociated cells were seeded at. 30,000 cells/well onto poly-D-lysine coated 96-well plates (Collaborative BioScience). Each well contained 1001 of Eagle's Minimal Essential Media (MEM; Gibco) supplemented with 26mM NaHC03 (Sigma), 56mM glucose (Sigma), lSmM
KCl (Sigma), 1mM sodium pyruvate (Sigma), l.lmM L-glutamine (Sigma), 10% (v/v) heat-inactivated fetal bovine serum (Hyclone), and 0.001% gentamicin sulfate (Sigma) (pH 7.4).
Cells were allowed to attach for 24h in a humidified 37°C 5% COZ
incubator before experimental treatment. The culture media was aspirated and exchanged with fresh media every three days.

Imrnunocytochemistry Parallel hippocampal and cortical cultures were treated as described above and were processed for immunocytochemistry (ICC) as described previously (Smith Swintosky et al., 1997). Briefly, cells were plated onto four-chamber poly-D-lysine coated glass slides (LabTek, Napersville, IL). On the seventh day in culture, the culture media was removed and the cells were washed once with Dulbecco's phosphate buffered saline (DPBS; Sigma) and then fixed with 10% phosphate-buffered formalin for l5min at room temperature. After fixation, the cultures were rinsed with DPBS and placed in blocking serum for lOmin (normal horse serum; 1:50 dilution in DPBS; Vector Labs, Burlingame, CA). Cultures were rinsed again and then incubated for 30min in an anti-mouse monoclonal antibody specific to the EPO receptor (EBP-7); 1:75 dilution in antibody diluent (Zymed, South San Francisco, CA). Cultures were rinsed several times with DPBS, then exposed to biotinylated secondary antibody for 30min (Vector Labs).
Cultures were rinsed a final time and then incubated for 30min in avidin-biotinylated horseradish peroxidase complex (mouse IgG ABC kit, Vector Labs). The presence of the primary antibody was detected using 3'3-diaminobenzidine tetrahydrochloride (DAB, Biomeda, Foster City, CA) - two exposures for Smin each. Cells were then counterstained with hematoxylin, dehydrated, cleared, coverslipped and photographed under an Olympus BX-2 light microscope.
Results Robust staining for EPO receptor was observed in both neurons and glia within hippocampal and cortical cultures (Figure la and Figure 1b). EPO receptor expression levels appear to increase with time in culture.
Discussion These results show that EPO plays a role in early development of the nervous system, particularly the hippocampus and cerebral cortex.
Irnmunohistochemistry of neuronal cell lines The neuronal cell lines PC-12, derived from a pheochromocytoma of the rat adrenal gland (Greene and Tischler, 1976), and SK-N-MC, obtained from a neuroepithelioma of a brain of human origin (Spengler et al., 1973), were used: PC-12 cells can be reversibly induced to the neuronal phenotype in the presence of nerve growth factor (NGF). PC-12 cells were grown on poly-D-Lysine coated tissue culture dishes in DMEM containing 10% horse serum and 5% FBS and in the presence of 0.1 pg/ml NGF for 7 days to induce the neuronal phenotype. SK-N-MC cells were cultured in minimal essential media supplemented with 1.0 mM Sodium pyruvate, 1.5 g/L sodium bicarbonate, 2mM glutamine and 10% FBS for 4 days.
PC-12 and SK-N-MC cells were cultured in a 96 well plate from Greiner, conducive for microscopy. On the day of the experiment cells were fixed in 10% Formalin containing 10%
sucrose and incubated in blocking buffer (40 mM Tris HCL, Ph 8.0, 27mh NaCI, and 0.2%Tween 20). Receptors for erythropoietin were detected by incubating the cells with a rabbit polyclonal, anti-erythropoietin receptor antibody (C-20 from Santa Cruz) and a FITC
conjugated secondary antibody. Labeled cells were visualized using a fluorescent microscope (ATTO).
Results A polyclonal antibody against the erythropoietin receptor labeled both SK-N-MC
and PC-12 cells as seen in Figure 2 (right panels). All SK-N-MC cells visible at low magnification appeared to be labeled with the antibody. The majority of PC-12 cells that were detectable were labeled with the anti-erythropoietin receptor antibody. A
few intact PC-12 cells that retained a characteristic neuronal phenotype in this preparation showed staining throughout the axonal process as well as in the cell body. Secondary antibody alone did not label either cell type (Figure 2, left panels).
Therefore, these results demonstrate that these cell lines, SK-N-MC cells from a human neuroepithelioma and PC-12 cells from a rat pheochromocytoma, express the erythropoietin receptor. These cell lines are therefore responsive to erythropoietin and can provide a good system to study the effects of erythropoietin on neurons. .

EPO induced gene exbression in PC12 cells Cell Culture PC-12 cells (from a rat Pheochromocytoma) were cultured on poly-D-Lysine coated tissue culture plastic in DMEM containing 10 % FBS and 5% Horse serum. To induce the neuronal phenotype in PC-12 cells, serum was removed and the cells were treated with NGF
(50 ng/ml). Cells were grown for 7 days in the presence of the NGF then used for experiments.
EPO Treatment and RNA isolation PC-12 cells were cultured as described in Example 1 in a 10 cm poly-D-lysine coated tissue culture dish. Cells were incubated in the presence of lU/ml of EPO for 24 hr. Total RNA was then isolated using a Qiagen RNAeasy mini prep kit and used for RT-PCR.
Quantitative RT PCR
Real time reverse transcription and PCR were performed in a single reaction using a light cycler and an RNA amplification kit from Roche Molecular Biochemicals.
RNA was quantitated and added in equal amounts to reaction mix that includes the dsDNA
specific dye SYBR green I. Specific PCR reaction products are quantitated by detecting the amount of fluorescence in the reaction at each PCR cycle. Final analysis was performed using the data analysis software included with the light cycler instrument.
Summary Pre-treatment of PC-12 cells with EPO (lU/ml) for 24 hr resulted in significant changes in the gene expression of the bcl-2 family members bcl~ and bak as seen in Figure 3. Cells treated with EPO showed a 6-fold increase in the expression of the anti-apoptotic gene, bcl~,, and a 5-fold decrease in the expression of the pro-apoptotic gene, bak. EPO has been shown previously to increase the survival of red blood cell progenitor cells by increasing bcl~, expression (Silva et al., 1996). These results show that EPO
uses a similar mechanism to protect neurons from undergoing apoptosis in response to injury.
The regulation of bak shows that EPO can effect the expression of additional genes to elicit this effect.

rhEPO neuroprotection and neurite outgrowth effects on rat hippocampal and cortical cells and PC 12 cells Primary Neuronal Cell Culture Dissociated hippocampal and cortical cell cultures were established from embryonic day 18 rat fetuses as previously described (Mattson et al., 1994). Briefly, fetuses were removed via cesarean section from pregnant moms (Sprague-Dawley) anesthetized with halothane according to the AVMA Panel on Euthanasia. Pups were decapitated and the brains were removed and placed in HEPES-buffered Hank's Balanced Salt solution (HBSS;
Gibco). The hippocampi and cortices were dissected out and pooled according to tissue-type.
Tissue was trypsinized for 15 min (lmg/ml trypsin-HBSS; Worthington), rinsed with fresh HBSS, incubated in trypsin inhibitor (lmg/ml; Sigma) for 5 min, rinsed again with fresh HBSS and then triturated in lml fresh HBSS with a fire-polished glass pipette.
Dissociated cells were seeded at 30,000 cells/well onto poly-D-lysine coated 96-well plates (Collaborative BioScience). Each well contained 1001 of Eagle's Minimal Essential Media (MEM; Gibco) supplemented with 26mM NaHC03 (Sigma), 56mM glucose (Sigma), lSmM
KCl (Sigma), 1mM sodium pyruvate (Sigma), l.lmM L-glutamine (Sigma), 10% (v/v) heat inactivated fetal bovine serum (Hyclone), and 0.001 % gentamicin sulfate (Sigma) (pH 7.4).
Cells were allowed to attach for 24h in a humidified 37°C 5% COZ
incubator before experimental treatment. The culture media was aspirated and exchanged with fresh media every three days.
Glutarnate Toxicity Assay Cortical cells were seeded at 200,000 cells/dish onto polyethylenimine-coated 35mm culture dishes. Each dish contained 1.5m1 MEM supplemented as described above.
On the seventh day in culture, four fields per pre-marked dish were visualized with a Nikon Diaphot inverted microscope (10x magniEcation) and photographed prior to experimental treatment.
Immediately following, the cultures were treated with vehicle or recombinant human erythropoietin (rhEPO; lot #41C514; SO~,M stock in 0.2M citrate, 0.585g.L NaCl diluted to appropriate concentrations in Dulbecco's phosphate buffered saline (DPBS;
Sigma) + 0.1%
bovine serum albumin (BSA; Sigma)). Twenty-four hours later the cultures were treated with 100~,M glutamate (Sigma). Twenty-four hours post-glutamate, the four fields from each dish were photographed again. Cell survival was measured by counting viable cells in each field pre- and post-experimental treatment. Neurons were considered viable if they had neurites that were uniform in diameter and smooth in appearance, and somata that were smooth and round to oval in shape. Data were expressed as percent of control (vehicle;
mean ~ SD).
PC12 Cell Culture PC-12 cells (from a rat Pheochromocytoma) were cultured on poly-D-Lysine coated tissue culture plastic in DMEM containing 10 % FBS and 5% Horse serum. To induce the neuronal phenotype in PC-12 cells, serum was removed and the cells were treated with NGF
(50 ng/ml). Cells were grown for 7 days in the presence of the NGF then used for experiments.
Glutamate Toxicity PC-12 cells were cultured as described above. 24 hr prior to insult, cells were treated with rhEPO at concentrations ranging from 1 pm to 1 nm. On the day of the experiment, cells were exposed to 200 ~,M glutamate for 30 min. Cells were then washed 2 times with fresh media to remove the glutamate and cultured in fresh media containing NGF but no EPO.
After 24 hr cells were assayed for viability using a trypan blue exclusion assay. Briefly, media was removed and the cells were incubated in 0.4% Trypan Blue for 5 min.
Cells were then washed gently with PBS, then fixed with 10% formalin. Cell viability was determined by counting the total number of cells vs. the number of trypan blue positive (dead) cells.
NGF withdrawal PC-12 cells were cultured as described above in a 96 well poly-d-lysine coated multi-well plate and treated with rhEPO (1 pm to 10 nm) for 24 hr prior to NGF
withdrawal. On the day of the experiment the cells were washed with buffer 3 times to remove NGF and then cultured in fresh media without NGF. Immediately following NGF washout cells were counted (t=0) to determine the number of living cells.
Cell viability was based on morphological characteristics including phase brightness, presence of axons, and absence of blebbing. Cell counts were performed at 12 hr, 24 hr, 48 hr and 72 hr and the number of viable cells were scored.
Neurite Outgrowth Assay Twenty-four hours after plating, cultures were treated with vehicle (PBS+0.1%
BSA), 100ng of various growth factors (brain derived neurotrophic factor (BDNF;
Promega), glial derived neurotrophic factor (GDNF; Promega), nerve growth factor (NGF;
Boehringer Mannheim), basic fibroblast growth factor (bFGF; Boehringer Mannheim), insulin-like growth factor -1 (IGF-l; Boehringer Mannheim), neurotrophin-3 (NT3;
Calbiochem), neurotrophin-4 (NT4; Calbiochem), ciliary neurotrophic factor (CNTF;
Calbiochem), epidermal growth factor (EGF; Calbiochem), vascular endothelial growth factor (VEGF;
Calbiochem)), or rhEPO (prepared same as above; l OfM - l OnM)). Each treatment condition was run in quadruplicate or octuplicate. On the third day in culture, the media was aspirated off and replaced with fresh media and test compound. At one week in culture, the cells were fixed with 10% phosphate-buffered formalin for l5min, then rinsed with DPBS
(Sigma) and placed in blocking serum for 30 min (horse serum; 1:50 dilution in DPBS;
Vector Labs).
Cultures were rinsed again with DPBS and then incubated in primary antibody for 2 hr (microtubule-associated protein-2 (MAP-2) is a selective marker for dendritic processes;
anti-mouse monoclonal (Chemicon); 1:1000 dilution of MAP-2 in antibody diluent (Zymed)). Negative control wells were incubated in antibody diluent alone.
Background signal was determined by blank wells (cell-free) incubated with or without antibody.
Cultures were rinsed again with DPBS and then placed in fluorescein for 1 hr (FITC; anti-mouse IgG; rat adsorbed; 1:50 dilution in DPBS; Vector Labs). Cultures were rinsed a final time with DPBS and then the plates were read on a Cytofluor 4000 fluorescence plate reader.
Neurite outgrowth was expressed as percent change from control (vehicle; mean fluorescence ~ SD).

Results Neuroprotection study with primary neuronal cultures: Pretreatment of cultures with rhEPO for 24h prior to glutamate administration resulted in a significant increase in neuronal survival (Figure 4). Cell survival was maximally increased approximately 200%
over parallel cultures treated with glutamate alone. The neuroprotective effect of rhEPO was concentration-dependent, with the greatest effects observed at pM
concentrations in which cell survival was greater than or equal to vehicle (no glutamate) treated cultures.
Neuronrotection study with PC 12 cells: Pre-treatment with EPO resulted in a significant decrease in cell death induced by both glutamate toxicity and growth factor withdrawal in PC-12 cells (Figures 5 and 6). The peak concentration for the neuroprotective effect in both experiments was 10 pm. The dose response curve for the neuroprotective effect of EPO was bi-phasic with the ability of EPO to protect cells against cytotoxicity decreasing at concentrations above 10 pm, with no significant effect at 1 nm. These results suggest that EPO is able to prevent an apoptotic response in neurons exposed to a variety of cytotoxic insults Neurite outgrowth study with primary neuronal cultures: Cultures treated with rhEPO
resulted in a significant increase in neurite outgrowth as measured by MAP2-FITC
immunofluorescence. The neurite outgrowth promoting effect was concentration dependent with maximal activity observed at pM levels (Figures 7 and 8). The results indicate that rhEPO treatment induced a larger outgrowth response in the hippocampal cultures (12-44%
over control) than in the cortical cultures (15-29% over control). A
comparison between rhEPO and known growth factors indicates that they exhibit regional differences in their neurite outgrowth promoting abilities. rhEPO's ability to increase neurite outgrowth in cortical cultures is greater than or equal to that of known growth factors.
This observation is compelling and important since few factors have such effects on cortical cells. On the other hand, many growth factors exert strong outgrowth responses in the hippocampus (38-86%
over control). Compared to such growth factors, rhEPO showed moderate yet robust outgrowth promoting activity; however, its activity was superior to several growth factors including BDNF, NGF and VEGF.
2s Discussion The neuroprotection studies confirmed previous evidence that rhEPO is protective at pM concentrations against glutamate toxicity and serum withdrawal in vitro.
Surprisingly we discovered that rhEPO promotes neurite outgrowth in primary mammalian neural cells. The effect was robust for hippocampal and cortical cells. The effect was potent with efficacy observed at sub-picomolar concentrations, far more potent than any previous EPO related observation. Moreover, in cerebral cortical neurons, which respond to few growth factors, rhEPO was superior in inducing neurite outgrowth relative to the majority of known growth factors.
From a therapeutic perspective, the observation that rhEPO promotes neuroprotection and neurite outgrowth in cerebral cortical neurons is very important. During neurodegeneration, neural cells can be in different stages of the process.
Some may be stressed, others experience significant neurite retraction and loss of synaptic input, and eventually all affected cells will succumb to death. A therapeutic agent that can intervene in this process at multiple levels can be of great benefit to the recovery of the neural cells and eventually neural function. The present data support that rhEPO accomplishes this task by protecting the cells, by enhancing their survival, by promoting re-establishment ~of synaptic contacts and connections, and by stabilizing the neuronal and neural circuitry.
It should also be specified that the data are particularly important, considering that very few growth factors are effective in cerebral cortical neurons, and also that very few growth factors display the dual activity as neuroprotectants and promoters of neurite outgrowth in cortical neurons. It is particularly relevant that this dual activity of rhEPO was observed at sub-picomolar / picomolar concentrations.

EPO MIMETIC PEPTIDES STIMULATE NEURITE OUTGROWTH

Cell Culture Dissociated hippocampal and cortical cell cultures were established from embryonic day 1 ~ rat fetuses as previously described (Mattson et al., 1994). Briefly, fetuses were removed via cesarean section from pregnant moms (Sprague-Dawley) anesthetized with halothane according to the AVMA Panel on Euthanasia. Pups were decapitated and the brains were removed and placed in HEPES-buffered Hank's Balanced Salt solution (HBSS;
Gibco). The hippocampi and cortices were dissected out and pooled according to tissue-type.
Tissue was trypsinized for 15 min (lmg/ml trypsin-HBSS; Worthington), rinsed with fresh HBSS, incubated in trypsin inhibitor (lmg/ml; Sigma) for 5 min, rinsed again with fresh HBSS and then triturated in lml fresh HBSS with a fire-polished glass pipette.
Dissociated cells were seeded at 30,000 cells/well onto poly-D-lysine coated 96-well plates (Collaborative BioScience). Each well contained 1001 of Eagle's Minimal Essential Media ,(MEM; Gibco) supplemented with 26mM NaHC03 (Sigma), 56mM glucose (Sigma), lSmM
KCl (Sigma), 1mM sodium pyruvate (Sigma), l.lmM L-glutamine (Sigma), 10% (v/v) heat-inactivated fetal bovine serum (Hyclone), and 0.001% gentamicin sulfate (Sigma) (pH 7.4).
Cells were allowed to attach for 24h in a humidified 37°C 5% COZ
incubator before experimental treatment. The culture media was aspirated and exchanged with fresh media every 3 days.
Neu~ite Outgrowth Assay Twenty-four hours after plating, cultures were treated with vehicle (PBS+0.1%
BSA), 100ng of various growth factors (brain derived neurotrophic factor (BDNF;
Promega), glial-derived neurotrophic factor (GDNF; Promega), nerve growth factor (NGF;
Boehringer Mannheim), basic fibroblast growth factor (bFGF; Boehringer Mannheim), insulin-like growth factor -1 (IGF-l; Boehringer Mannheim), neurotrophin-3 (NT3;
Calbiochem), neurotrophin-4 (NT4; Calbiochem), ciliary neurotrophic factor (CNTF;
Calbiochem), epidermal growth factor (EGF; Calbiochem), vascular endothelial growth factor (VEGF;
Calbiochem)), or Epo mimetic peptides (EMP1, EMP6, EMP9, EMP23 and EMP27;
diluted in DPBS+0.1% BSA; lOfM - lOnM; Table 1). Each treatment condition was run in quadruplicate. On the third day in culture, the media was aspirated off and replaced with fresh media and test compound. At one week in culture, the cells were fixed with 10%

phosphate-buffered formalin for l5min, then rinsed with DPBS (Sigma) and placed in blocking serum for 30 min (horse serum; 1:50 dilution in DPBS; Vector Labs).
Cultures were rinsed again with DPBS and then incubated in primary antibody for 2 hr (microtubule-associated protein-2 (MAP-2) is a selective marker for dendritic processes;
anti-mouse monoclonal (Chemicon); 1:1000 dilution of MAP-2 in antibody diluent (Zymed)).
Negative control wells were incubated in antibody diluent alone. Background signal was determined by blank wells (cell-free) incubated with or without antibody. Cultures were rinsed again with DPBS and then placed in fluorescein for 1 hr (FITC; anti-mouse IgG; rat adsorbed; 1:50 dilution in DPBS; Vector Labs). Cultures were rinsed a final time with DPBS
and then the plates were read on a Cytofluor 4000 fluorescence plate reader. Neurite outgrowth was expressed as percent change from control (vehicle; mean fluorescence ~ SEM).
Table 1:
Erythropoeitin Mimetic Peptides (EMP) SEQ.ID.NO Sequence Sequence name 21 , EMP-27 GGTYSC-FGPLTWVCKPQGG

Results 15 Neurite out,~rowth studX: Cultures treated with EMP's resulted in a significant increase in neurite outgrowth as measured by MAP2-FITC immunofluorescence. The neurite outgrowth promoting effect was concentration dependent with maximal activity observed at pM levels (Figures 9-18). The results indicate that EMP's displayed different activity profiles. At the concentrations tested, EMP-1 and 6 displayed typical bell-shaped dose-20 response profiles in hippocampal cultures with peak activity observed between 30-300pM
(83-117% increase over vehicle). EMP-9 and 27 exhibited a flat response profile in hippocampal cultures with peak activity observed at similar concentrations as EMP-1 and 6, but the amplitude of the response was greatly attenuated (29-32% increase over vehicle).
EMP-23 had a modest response to EPO in hippocampal cultures with peak activity observed between 30pM-1nM that led to a 43-46% increase over vehicle response. In the cortical cultures, EMP-1, 9 and 27 exhibited response profiles similar to most known growth factors -a flat response overall with maximal activity occurring between 30-300pM
reaching 32-40%
above the vehicle response. EMP-6 and 23 displayed typical bell-shaped dose-response profiles with peak activity observed between 30-300pM resulting in a 68-87%
increase in outgrowth over vehicle response levels. Overall, EMP-6 promoted robust neurite outgrowth activity in both hippocampal and cortical cultures; whereas, EMP-1 showed selective effects in hippocampal cultures over cortical cultures and EMP-23 effects were greater in cortical cultures than hippocampal cells. EMP-9 and 27 neurite outgrowth responses were less impressive overall.
A comparison between the EMP's and known growth factors indicated that they exhibit regional differences in their neurite outgrowth promoting abilities.
The EMP's ability to increase neurite outgrowth in cortical cultures was greater than or equal to that of known growth factors (Figure 9-18). This observation is compelling and important since few factors have such effects on cortical cells. On the other hand, many growth factors exert strong outgrowth responses in the hippocampus (38-86% over control). Compared to such growth factors, the EMP's showed moderate yet robust outgrowth promoting activity;
however, they displayed superior activity over BDNF, NGF and VEGF.
Discussion EMP's promote neurite outgrowth in mammalian cells. The effect was robust for hippocampal and cortical cells. The neurite outgrowth promoting effect was superior to that of various growth factors. The effect was potent with efficacy observed at picomolar concentrations.
It should also be specified that the data are particularly important, considering that very few growth factors or mimetics are effective in cerebral cortical neurons in promoting neurite outgrowth. It is particularly relevant that this activity of the EMPs was observed at sub-picomolar / picomolar concentrations.

EPO protects against ischemic inj~urv Subjects Male spontaneous hypertensive rats (Charles River) weighing between 250-300g were weighed and then anesthetized with ketamine (100mg/ml)/xylazine (20mg/ml) cocktail (1.2m1/kg; i.p.). The level of anesthetic was assessed by corneal reflex (air puff to eye) and leg jerk in response to tail or foot pinch. Once the rat was anesthetized, it was placed on a small animal surgical board and restrained during the surgical procedure. The rat's body temperature was monitored continuously with a rectal probe and maintained at 37°C with a homeostatic heating pad.
Experimental model of cerebral ischemia Rats were rendered ischemic by tandem occlusion of the left common carotid artery and the left middle cerebral artery for 2h followed by 22h of reperfusion using a modification of the technique described by Brint and co-workers (J. Cereb Blood Flow Metab 8:474-485, 1988). Specifically, the left CCA was isolated through an incision in the ventral surface of the neck. For isolation of the ipsilateral MCA, a second incision was made between the lateral canthus of the left eye and the corresponding external auditory canal to bare the underlying skull. The MCA was exposed through a Smm burrhole drilled 2-3mm rostral to the fusion of the zygomatic arch and the squamosal bone under direct visualization with a Zeiss operating microscope. The dura was opened with a sterile 26g needle and a platinum alloy wire (O.lmm diameter) was inserted beneath the MCA just superior to the inferior cortical vein. The MCA was temporarily occluded by elevation and compression of the vessel across the alloy wire, as described by Aronowski and colleagues (Stroke, 25:2235-2240, 1994). Concurrently, the CCA was occluded with an aneurysm clip. The duration of occlusion of the CCA and the MCA was 2h. At the end of this period, the wire and the clip were carefully removed to allow reperfusion of the vessels and the incision area was sutured shut. The rat was placed in an isolation cage to recover before returning to his home cage. .

Study Design Studv I: EPO and vehicle delivered via osmotic mini-pump Twenty-hours prior to the onset of ischemia, an osmotic mini-pump (Model 1003D;
Alza) filled with vehicle or EPO was placed between the scapula of the rat. A
catheter attached to the pump was inserted and tethered within the right jugular vein for continuous infusion of drug at a rate of 1 ~1/hr. Rats were divided into five groups:
(1) sham-operated vehicle-treated, (2) ischemic vehicle treated, (3) ischemic 1.32U/day EPO treated, (4) ischemic 132U/day EPO treated and (5) ischemic 1321U/day EPO treated. On Day Two, rats were rendered ischemic as described above. Twenty-two hours later, the rats were evaluated for behavioral performance, a blood sample was collected for terminal plasma levels of EPO and then the rat was euthanized, brain removed, sectioned and stained for histological analysis.
Studv II: EPO and vehicle delivered as a single intravenous bolus in'eci tion On Day One, the rats were rendered ischemic as described above. Rats were divided into four groups: (1) ischemic vehicle treated, (2) ischemic 1000U/kg EPO
treated, (3) ischemic 2500U/kg EPO treated and (4) SOOOU/lcg EPO treated. Fifteen minutes post-occlusion, the rats received vehicle or EPO as an intravenous bolus injection.
Twenty-two hours later, the rats were evaluated for behavioral performance, a blood sample was collected for terminal plasma levels of EPO and then the rat was euthanized, brain removed, sectioned and stained for histological analysis.
Studv III: EPO and vehicle delivered as repeat intravenous bolus in'ections On Day One, the rats were rendered ischemic as described above. Rats were divided into two groups: (1) ischemic vehicle treated and (2) ischemic 2500U/kg EPO
treated.
Drug was administered as an intravenous bolus at lSmin, 2h, 4h and 6h post occlusion for a total dose of 10,000U/kg. Twenty-two hours later, the rats were evaluated for behavioral performance, a blood sample was collected for terminal plasma levels of EPO and then the rat was euthanized, brain removed, sectioned and stained for histological analysis.

Outcome measures Plasma Determinations: Blood samples were collected from each rat via the orbital sinus at the time of sacrifice. Plasma was separated out, frozen and analyzed by EPO ELISA
for determination of plasma concentration (U/ml).
Infarct Volume: Brains were removed, blocked into lmm slabs and stained with 2,3,5-triphenyl tetrazolium chloride dye (TTC; Sigma) for 15 min at room temperature.
Stained sections were stored in 10% buffered formalin at 4oC. Sections were visualized by a Nikon SMZ-U microdissecting scope. Images of each brain section were captured with a CCD camera and processed using Image Pro Phase III software in order to calculate infarct volume.
Results tud I: EPO given at 132 or 1321U/day as a continuous infusion via osmotic mini-pump significantly reduced infarct volume (Figure 19). Plasma concentrations correlated with the protective effect (Figure 20).
Studv II: EPO given as a single iv bolus 15 min post-occlusion did not protect against ischemic damage in this model at 1000, 2500 or 5000U/kg (Figure 21). Plasma concentrations were low in each group (Figure 22).
Stud,~EPO given as a repeat iv bolus of 2500U/kg at l5min, 2h, 4h and 6h post-occlusion led to a significant decrease in infarct volume (Figure 23). Plasma concentrations are presently being determined (Figure 24).
Discussion Data support that continuous or repeat dosing with low to moderate concentrations of EPO can significantly reduce infarct volume in spontaneous hypertensive rats rendered ischemic via the transient tandem occlusion of the CCA and MCA. The results also support that there is a critical relationship between the amount and timing of EPO
administration for the protective effect to occur. Low doses of EPO given over an extended period of time can be more beneficial than high doses given the same way or as a single bolus infusion. This is in agreement with the in vitro data indicating that EPO maximal protective effect is observed at low doses (pM) and actually looses efficacy at higher doses (~.M).

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Claims

WHAT IS CLAIMED IS:

1. A method for treating a patient having a condition mediated by neurotoxicity, neurodegeneration or neurological damage, comprising administering to said patient a therapeutically effective amount of a peptide comprising one or more monomeric peptides of 8 to about 40 amino acids in length that bind to EPO receptor, each monomeric peptide comprising a sequence of amino acids X4X5XaXbX6XcXdX7 (SEQ
ID NO: 47), wherein Xa is G or A;
Xb is P or A;
Xc is T or A;
Xa is selected from W, A, and F;
X4 is selected from R, H, Y, L, and W, or X4 is nonexistent;
X5 is selected from F, M, and I;
X6 is independently selected from the 20 genetically coded L-amino acids or the stereoisomeric D-amino acids; and X7 is selected from D, V, E, I, arid L.

2. The method of claim 1, wherein said sequence is X4 X5GPX6TWX7 (SEQ ID NO:
48.

3. The method of claim 2, wherein said sequence is X3X4X5GPX6TWX7X8 (SEQ ID
NO:
1), wherein X3 is selected from C, E, A, .alpha.-amino-y-bromobutyric acid, and homocysteine (Hoc); and, X8 is selected from C, K, A, .alpha.-amino-y-bromobutyric acid, and homocysteine (Hoc).

4. The method of claim 3 with the proviso that either X3 or X8 is C or homocysteine (Hoc).

5. The method of claim 4 wherein X3 or X8 is C.

6. The method of claim 3 wherein X3 is selected from C, E, and A;

X4 is selected from R, H, and Y, or X4 is nonexistent;

X6 is selected from V, L, I, M, E, and A; and X7 is D or V; and X8 is selected from C, K and A.

7. The method of claim 3 wherein said peptide is a dimer of each of said monomeric peptides comprising a sequence of amino acids YX2X3X4X5GPX6TWX7X8 (SEQ ID
NO: 2), wherein X2 and X6 are each independently selected from the 20 genetically coded L-amino acids;

X3 is C; and X8 is C.

8. The method of claim 7 wherein X2 is selected from L S H M A and I, or X2 is nonexistent; and X6 is selected from V, L, I, M, E, and A.

9. The method of claim 7 wherein each of said monomeric peptides comprises a sequence of amino acids X1YX2X3X4X5GPX6TWX7X8X9X10X11 (SEQ ID NO: 3), wherein each of X1, X2, X6, X9, X10, and X11 is independently selected from the 20 genetically coded L-amino acids.

10. The peptide dimer of claim 9 wherein X3 is selected from C, E, and A;
X4 is selected from R, H, and Y, or X4 is nonexistent;
X7 is D or V;
X8 is C or K.
X9 is K, G, L, Q, R, S, or T; and X10 is A,G,P,R,or Y.

11. The method of Claim 10 wherein X1 is D, E, L, N, S, T or V;
X2 is selected from L, S, H, M, A, and I, or X2 is nonexistent;
X9 is selected from K, Q, R, S, and G; and X10 is selected from P, Y, and A.

12. The method of claim 3 wherein said peptide is a dimer of each of said monomeric peptides comprising a sequence of amino acids X'X2X3X4X5GPX6TWX7X8 (SEQ ID
NO: 49), wherein X' is selected from D-Tyr, p-NO2-Phe, p-NH2-Phe, p-F-Phe, p-I-Phe, and 3,5-dibromo-Tyr.

13. The method of claim 12 wherein said sequence is X'CHFGPLTWVC.

14. The method of claim 1 wherein each of said monomeric peptides comprise a sequence independently selected from GGLYLCRFGPVTWDCGYKGG (SEQ ID NO:7);
GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID NO:8);
GGDYHCRMGPLTWVCKPLGG (SEQ ID NO:9);
VGNYMCHFGPITWVCRPGGG (SEQ ID NO:10);
GGVYACRMGPITWVCSPLGG (SEQ ID NO:11);
VGNYMAHMGPITWVCRPGG (SEQ ID NO:12);
GGTYSCHFGPLTWVCKPQ (aka EMP-16) (SEQ ID NO:13);
GGLYACHMGPMTWVCQPLRG (aka EMP-36) (SEQ ID NO:14);
TIAQYICYMGPETWECRPSPKA (aka EMP-38) (SEQ ID NO:15);
YSCHFGPLTWVCK (aka EMP-20 (SEQ ID NO:16);
YCHFGPLTWVC (aka EMP-23) (SEQ ID NO:17);
SCHFGPLTWVCK (aka EMP-24) (SEQ ID NO:18);
GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID NO:19);
GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID NO:20);
GGTYSCFGPLTWVCKPQGG (aka EMP-27) (SEQ ID NO:21);
TYSCHFGPLTWVCKPQGG (aka EMP-17) (SEQ ID NO:22);
TYSCHFGPLTWVCKPQ (aka EMP-18) (SEQ ID NO:23);
YSCHFGPLTWVCKP (aka EMP-19) (SEQ ID NO:24);
YSCHFGPLTWVC (aka EMP-21) (SEQ ID NO:25);

YSCHFGALTWVCK (aka EMP-22) (SEQ ID NO:26);
GGCRIGPITWVCGG (aka EMP-25) (SEQ ID NO:27);
HFGPLTWV (aka EMP-26) (SEQ ID NO:28);
GGTTSCHFGPLTWVCKPQGG (aka EMP-7) (SEQ ID NO:29);
GGTFSCHFGPLTWVCKPQGG (aka EMP-8) (SEQ ID NO:30);
GGTYSCHFGALTWVCKPQGG (aka EMP-10) (SEQ ID NO:31);
GGTYSCHFGPATWVCKPQGG (aka EMP-11) (SEQ ID NO:32);
GGTYSCHFGPLAWVCIPQGG (aka EMP-12) (SEQ ID NO:33);
GGTYSCHFGPLTAVCKPQGG (aka EMP-13) (SEQ ID NO:34);
GGTYSCHFGPLTFVCKPQGG (aka EMP-14) (SEQ ID NO:35);
GGTYSCHFGPLTWVCKAQGG (aka EMP-15) (SEQ ID NO:36);
GGTXSCHFGPLTWVCKPQGG (aka EMP-28, X = D-Tyr) (SEQ
ID NO:37);
GGTXSCHFGPLTWVCKPQGG (aka EMP-29, X =p-NOZ Phe) (SEQ ID NO:38);
GGTXSCHFGPLTWVCKPQGG (aka EMP-30, X =p-NHZ-Phe) (SEQ ID NO:39);
GGTXSCHFGPLTWVCKPQGG (aka EMP-31, X =p-F-Phe) (SEQ
ID NO:40);
GGTXSCHFGPLTWVCKPQGG (aka EMP-32, X =p-I-Phe) (SEQ
ID NO:41);
GGTXSCHFGPLTWVCIPQGG (aka EMP-33, X = 3,5-dibromo-Tyr) (SEQ ID NO:42);
Ac-GGTYSCHFGPLTWVCKPQGG (aka EMP-34) (SEQ ID NO:43);
GGLYACHMGPMTWVCQPLGG (aka EMP-35) (SEQ ID NO:44);
LGRKYSCHFGPLTWVCQPAKIGD (aka EMP-37) (SEQ ID NO:45);
and GGTYSEHFGPLTWVKKPQGG (aka EMP-39) (SEQ ID NO:46).

15. The method of claim 14 wherein each of said monomeric peptides is independently selected from:
GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID NO:8);
GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID NO:19);
GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID NO:20); and YCHFGPLTWVC (aka EMP-23) (SEQ ID NO:17).

16. The method of claim 1 wherein said peptide is a dimer formed by a polyethylene glycol linker through a covalent bond.

17. The method of claim 16 wherein each monomeric peptides of said dimer are covalently bound N-terminus to N-terminus.

18. The method of claim 16 wherein each monomeric peptides of said dimer are covalently bound N-terminus to C-terminus.

19. The method of claim 1 wherein said monomeric peptides are dimerized on activated benodiazepins, oxazalones, azalactones, aminimides or diketopiperazine.

20. The method of claim 19 wherein said monomeric peptides are covalently bound N-terminus to N-terminus.

21. The method of claim 19 wherein said monomeric peptides are covalently bound N-terminus to C-terminus.

22. The peptide of claim 2, which comprises least one peptide dimer.

23. A method of activating a cell surface receptor to induce neuroprotective biological activity comprising contacting a dimer of peptides of claim 2 with said receptor thereby inducing said neuroprotective biological activity.

24. The method of claim 23 wherein said cell surface receptor is contacted with said dimer in vitro or in vivo.

25. The method of claim 23 wherein said cell surface receptor is EPO receptor.

26. The method of claim 23 wherein said peptide dimer is a cell surface receptor agonist selected form a group consisting of a GH agonist, PDGF agonist, EGF agonist, G-CSF agonist, TPO (thrombopoietin) agonist, VEGF agonist, FGF agonist, insulin agonist, IL-3 agonist, IL-5 agonist, IL-6 agonist and IL-2 agonist.

27. The method of claim 23 wherein said agonist comprises a sequence of amino acids YX2X3X4X5GPX6TWX7X8 (SEQ ID NO: 2) wherein each of X2 and X6 is independently selected from the 20 genetically coded L-amino acids; X3 is C;
X4 is R, H,L or W;X5 is M,F or I; X7 is D,E,I,L or V; and X8 is C.

28. The method of claim 23 wherein said agonist comprises a sequence of amino acids X1YX2X3X4X5GPX6TWX7X8X9X10X11 (SEQ ID NO: 3) wherein each of Xl, X2, X6, X9, X10, and X11 is independently selected from any one of the 20 genetically coded L-amino acids; X3 is C; X4 is R, H, L or W; X5 is M, F or I; X7 is D, E, I, L or V; and X8 is C.

29. The method of claim 23 wherein said agonist comprises a sequence of amino acids X1YX2X3X4X5GPX6TWX7X8X9X10X11 (SEQ ID NO: 3) wherein each of X1, X2, and X11, is independently selected from any one of the 20 genetically coded L-amino acids;X3 is C; X4 is R or H; X5 is For M; X6 is I,L,T,M or V; X7is D or V;X9 is G, K, L, Q, R, S, or T; and X10 is A, G, P, R, or Y.

30. The method of claim 23 wherein said agonist comprises a sequence of amino acids X1YX2X3X4X5GPX6TWX7X8X9X10X11 (SEQ ID NO: 3) wherein X1 is D, E, L, N, S, T
or V; X2 is A, H, K, L, M, S, or T; X3 is C; X4 is R or H; X5 is M, F or I; X6 and X11 are independently any one of the 20 genetically coded L-amino acids; X7 is D, E, I, L
or V; X8 is C; X9 is K, R, S, or T; and X10 is P.

31. The method of claim 23 wherein said agonist is selected from a group consisting of:

GGLYLCRFGPVTWDCGYKGG (SEQ ID NO:7);
GGTYSCHFGPLTWVCKPQGG (aka EMP-1) (SEQ ID NO:8);
GGDYHCRMGPLTWVCKPLGG (SEQ ID NO:9);
VGNYMCHFGPITWVCRPGGG (SEQ ID NO:10);
GGVYACRMGPITWVCSPLGG (SEQ ID NO:11);
VGNYMAHMGPITWVCRPGG (SEQ ID NO:12);
GGTYSCHFGPLTWVCKPQ (aka EMP-16) (SEQ ID NO:13);
GGLYACHMGPMTWVCQPLRG (aka EMP-36) (SEQ ID NO:14);
TIAQYICYMGPETWECRPSPKA (aka EMP-38) (SEQ ID NO:15);
YSCHFGPLTWVCK (aka EMP-20 (SEQ ID NO:16);
YCHFGPLTWVC (aka EMP-23) (SEQ ID NO:17);
SCHFGPLTWVCK (aka EMP-24) (SEQ ID NO:18);
GGTASCHFGPLTWVCKPQGG (aka EMP-6) (SEQ ID NO:19);
GGTYSCHFAPLTWVCKPQGG (aka EMP-9) (SEQ ID NO:20);
GGTYSCFGPLTWVCKPQGG (aka EMP-27) (SEQ ID NO:21);
TYSCHFGPLTWVCKPQGG (aka EMP-17) (SEQ ID NO:22);
TYSCHFGPLTWVCKPQ (aka EMP-18) (SEQ ID NO:23);
YSCHFGPLTWVCKP (aka EMP-19) (SEQ ID NO:24);
YSCHFGPLTWVC (aka EMP-21) (SEQ ID NO:25);
YSCHFGALTWVCK (aka EMP-22) (SEQ ID NO:26);
GGCRIGPITWVCGG (aka EMP-25) (SEQ ID NO:27);
HFGPLTWV (aka EMP-26) (SEQ ID NO:28);
GGTTSCHFGPLTWVCKPQGG (aka EMP-7) (SEQ ID NO:29);
GGTFSCHFGPLTWVCKPQGG (aka EMP-8) (SEQ ID NO:30);
GGTYSCHFGALTWVCKPQGG (aka EMP-10) (SEQ ID NO:31);
GGTYSCHFGPATWVCKPQGG (aka EMP-11) (SEQ ID NO:32);
GGTYSCHFGPLAWVCKPQGG (aka EMP-12) (SEQ ID NO:33);
GGTYSCHFGPLTAVCKPQGG (aka EMP-13) (SEQ ID NO:34);
GGTYSCHFGPLTFVCKPQGG (aka EMP-14) (SEQ ID NO:35);
GGTYSCHFGPLTWVCKAQGG (aka EMP-15) (SEQ ID NO:36);

GGTXSCHFGPLTWVCKPQGG (aka EMP-28, X = D-Tyr) (SEQ ID NO:37);
GGTXSCHFGPLTWVCKPQGG (aka EMP-29, X =p-NO2 Phe) (SEQ ID NO:38);
GGTXSCHFGPLTWVCKPQGG (aka EMP-30, X =p-NH2-Phe) (SEQ ID NO:39);
GGTXSCHFGPLTWVCIkPQGG (aka EMP-31, X =p-F-Phe) (SEQ ID NO:40);
GGTXSCHFGPLTWVCKPQGG (aka EMP-32, X =p-I-Phe) (SEQ ID NO:41);
GGTXSCHFGPLTWVCKPQGG (aka EMP-33, X = 3,5-dibromo-Tyr) (SEQ ID NO:42);
Ac-GGTYSCHFGPLTWVCKPQGG (aka EMP-34) (SEQ ID NO:43);
GGLYACHMGPMTWVCQPLGG (aka EMP-35) (SEQ ID NO:44);
LGRkYSCHFGPLTWVCQPAKKD (aka EMP-37) (SEQ ID NO:45); and GGTYSEHFGPLTWVKKPQGG (aka EMP-39) (SEQ ID NO:46).

32. The method of claim 23 wherein said peptide dimers are formed with a polyethylene glycol linker through a covalent bond.

33. A method of preparing a cell surface receptor agonist comprising dimerizing a cell surface antagonist.

34. The method of claim 33 wherein said cell surface antagonist receptor is a GH
antagonist, PDGF antagonist, EGF antagonist, G-CSF antagonist, EGF antagonist, GM-CSF antagonist, TPO antagonist, VEGF antagonist, FGF antagonist, insulin antagonist, IL-3 antagonist, IL-5 antagonist, IL-6 antagonist, or an IL-2 antagonist.

35. The method of claim 33 wherein said cell surface receptor antagonist is an EPO-R
antagonist.

36. The method of claim 35 wherein said antagonist comprises a sequence of amino acids (X?X2)nX3X4X5GPX6TWX7X8 (SEQ ID NO: 19) wherein X6 is selected from the 20 genetically coded L-amino acids; X3 is C; X4 is R, H, L or W; X5, is M, F or I; X7, is D, E, I, L or V; X8 is C; X2 is selected from the 20 genetically coded L-amino acids, n is 0 or 1 and X? is any of the 20 genetically coded L-amino acids except Y
(tyrosine).

37. The method of Claim 33 where said antagonist is SCHFGPLTWVCK
(SEQ ID NO: 18).