Materials and method for suppressing inflammatory and neuropathic pain

Abstract

N-type voltage-gated calcium channels (CaV2.2) are critical mediators of neurotransmitter release and are thought to be involved with transmission of nociception. The use of conventional CaV2.2 blockers in pain therapeutics is limited by side effects. Reported herein is a means to suppress both inflammatory and neuropathic pain without directly blocking CaV2.2, but rather by inhibiting the binding of the axonal collapsin response mediator protein 2 (CRMP-2), a protein known to enhance CaV2.2 function. A 15 amino acid peptide of CRMP-2 fused to the protein transduction domain of the HIV tat protein (TAT CBD3) reduced meningeal blood flow induced by activation of the trigeminovascular system, prevented inflammation-induced tactile hypernociception induced by intraplantar formalin and nocifensive behavior following corneal capsaicin application, and reversed neuropathic hypernociception produced by the antiretroviral drug 2′,3′-dideoxycytidine. Preventing CRMP-2-mediated enhancement of CaV2.2 function suppressed inflammatory and neuropathic nociception, providing a method for treating pain and inflammation.

We claim: 
     
         1 . A compound that uncouples CRMP-2 and CaV2.2, comprising:
 a compound of the formula X-Z,   wherein X is a polypeptide having at least 80 percent identify to at least one polypeptide selected from the groups consisting of: SEQ ID NO.: 12 and SEQ ID NO.: 13 and   Z is at least one polypeptide having at least 80 percent identity to at least one polypeptide selected from the group consisting: of SEQ. ID NO.: 1, SEQ. ID NO.: 3, SEQ. ID NO.:4, SEQ. ID NO.: 5, SEQ. ID NO.: 6, SEQ. ID NO.: 7, SEQ. ID NO.: 8, SEQ. ID NO.: 9, and SEQ. ID NO.: 10, wherein X and Z are fused to one another.   
     
     
         2 . The compound according to  claim 1 , wherein the X and Z are fused to one another via a peptide bond. 
     
     
         3 . The compound according to  claim 1 , wherein X is polypeptide that has at least 90 percent identity to at least one polypeptide selected from the group consisting of SEQ ID NO.: 11 and SEQ ID NO.: 12. 
     
     
         4 . The compound according to  claim 1 , wherein Z is a polypeptide that has at least 90 percent identity to at least one polypeptide selected from the group consisting of SEQ. ID NO.: 1, SEQ. ID NO.: 3, SEQ. ID NO.: 4, SEQ. ID NO.: 5, SEQ. ID NO.: 6, SEQ. ID NO.: 7, SEQ. ID NO.: 8, SEQ. ID NO.: 9, and SEQ. ID NO.: 10. 
     
     
         5 . The compound according to  claim 1 , wherein X is at least one polypeptide that has at least 95 percent identity to at least one polypeptide selected from the group consisting of SEQ ID NO.: 11 and SEQ ID NO.: 12. 
     
     
         6 . The compound according to  claim 1 , wherein
 X is a polypeptide having at least 90 percent homology to at least one polypeptide selected from the groups consisting of: SEQ ID NO.: 12 and SEQ ID NO.: 13 and   Z is a polypeptide having at least 90 percent homology to at least one polypeptide selected from the group consisting: of SEQ. ID NO.: 1, SEQ. ID NO.: 3, SEQ. ID NO. 4: SEQ. ID NO.: 5, SEQ. ID NO.: 6, SEQ. ID NO.: 7, SEQ. ID NO.: 8, SEQ. ID NO.: 9, and SEQ. ID NO.: 10, wherein X and Z are fused to one another.   
     
     
         7 . The compound according to  claim 1 , wherein
 X is a polypeptide having at least 95 percent homology to at least one polypeptide selected from the groups consisting of: SEQ ID NO.: 12 and SEQ ID NO.: 13 and   Z is a polypeptide having at least 95 percent homology to at least one polypeptide selected from the group consisting: of SEQ. ID NO.: 1, SEQ. ID NO.: 3, SEQ. ID NO. 4, SEQ. ID NO.: 5, SEQ. ID NO.: 6, SEQ. ID NO.: 7, SEQ. ID NO.: 8, SEQ. ID NO.: 9, and SEQ. ID NO.: 10, wherein X and Z are fused to one another.   
     
     
         8 . The compound according to  claim 1 , wherein X is at least one polypeptide selected from the group consisting of SEQ ID NO.: 12 and SEQ ID NO.: 13. 
     
     
         9 . The compound according to  claim 1 , wherein Z is a polypeptide selected from the group consisting: of SEQ. ID NO.: 1, SEQ. ID NO.: 3, SEQ. ID NO. 4, SEQ. ID NO.: 5, SEQ. ID NO.: 6, SEQ. ID NO.: 7, SEQ. ID NO.: 8, SEQ. ID NO.: 9, and SEQ. ID NO.: 10. 
     
     
         10 . The compound according to  claim 1 , wherein the compound is SEQ ID NO. 11. 
     
     
         11 . A method of treating a patient, comprising the steps:
 providing at least one compound according to  claim 1  or a pharmaceutically acceptable salt thereof.   
     
     
         12 . The method according to  claim 11 , wherein said compound is formulated for administering to a patient. 
     
     
         13 . The method according to  claim 11 , wherein the method further includes the step of:
 administering at least one therapeutically effective dose of said compound to a patient.   
     
     
         14 . The method according to  claim 13 , wherein the dose is between about 1 mg to about 100 mg of said compound per about 1 kilogram of the patient's body weight. 
     
     
         15 . The method according to  claim 13 , wherein the dose is between about 1 mg to about 20 mg of said compound per about 1 kilogram of the patient's body weight. 
     
     
         16 . The method according to  claim 13 , wherein the patient is a mammal. 
     
     
         17 . The method according to  claim 13 , wherein the patient is a human being. 
     
     
         18 . A kit for treating a patient, comprising;
 at least one therapeutically effective dose of the compound according to  claim 1  or a pharmaceutically acceptable salt thereof.   
     
     
         19 . The kit according to  claim 18 , wherein said compound in the kit is formulated for injection. 
     
     
         20 . The kit according to  claim 18 , wherein said compound in the kit is formulate with at least one additional material that helps to preserve the activity of said compound.