Sigma ligands for neuronal regeneration and functional recovery
The invention discloses methods and compositions useful for facilitating neuronal regeneration and functional recovery in neurodegenerative diseases. The methods and compositions utilize ligands for the sigma receptors. These molecules can be delivered alone or in combination with agents which treat or prevent neurodegenerative diseases such as those caused by ischemic stroke, diabetic peripheral neuropathy, cancer therapy induced neuropathy, multiple sclerosis, amyotrophic lateral sclerosis, traumatic brain injury, spinal cord injury, Huntington's disease or Parkinson's disease. In other methods, the sigma receptor ligands are administered after stroke to facilitate functional recovery. The administration of the sigma receptor ligands effects faster functional recovery.
1 . A method of treating a mammalian subject to facilitate neuronal regeneration after onset of a neurodegenerative disease, which comprises administering to the subject an effective amount of a sigma receptor ligand, or salts or solvates thereof
2 . The method as claimed in claim 1 , which further comprises assessing the subject for evidence of neuronal regeneration.
3 . The method as claimed in claim 2 , wherein the evidence of neuronal regeneration is functional recovery in the subject.
4 . The method as claimed in claim 3 , wherein the functional recovery is recovery in a motor skill, cognitive skill, speech, sensory perception or sensory function.
5 . The method as claimed in claim 4 , wherein the functional recovery is recovery in a motor skill.
6 . The method as claimed in claim 4 , wherein the functional recovery is recovery in a cognitive skill.
7 . The method as claimed in claim 2 , wherein the evidence of neuronal regeneration is a structural change in the brain or spinal cord of the subject.
8 . The method as claimed in claims 2 , wherein the sigma ligand is administered repeatedly to the subject until evidence of neuronal regeneration is found.
9 . The method as claimed in claim 8 , wherein the sigma ligand is administered daily.
10 . The method as claimed in claim 1 , wherein the neurodegenerative disease is selected from ischemic stroke, traumatic brain injury and spinal cord injury.
11 . The method as claimed in claim 10 , wherein the treatment is started at least 24 hours after the ischemic stroke, traumatic brain injury or spinal cord injury.
12 . The method as claimed in claim 10 , wherein the treatment is started at least 48 hours after the ischemic stroke, traumatic brain injury or spinal cord injury.
13 . The method as claimed in claim 1 , which further comprises exposing the subject to a stimulating environment.
14 . The method as claimed in claim 1 , wherein the sigma ligand is a selective sigma-1 ligand.
15 . The method as claimed in claim 1 , wherein the sigma ligand is a selective sigma-2 ligand.
16 . The method as claimed in claim 1 , wherein the mammalian subject is a human.
17 . A pharmaceutical composition, which comprises a sigma ligand or salts or solvates thereof for treating a mammalian subject to facilitate neuronal regeneration after onset of a neurodegenerative disease, and a pharmaceutically acceptable excipient.
18 . The pharmaceutical composition as claimed in claim 17 , which further comprises assessing the subject for evidence of neuronal regeneration.
19 . The pharmaceutical composition as claimed in claim 18 , wherein the neuronal regeneration is evidenced by functional recovery.
20 . The pharmaceutical composition as claimed in claim 19 , wherein the functional recovery is recovery in a motor skill, cognitive skill, speech, sensory perception or sensory function.
21 . The pharmaceutical composition as claimed in claim 20 , wherein the functional recovery is recovery in a motor skill.
22 . The pharmaceutical composition as claimed in claim 20 , wherein the functional recovery is recovery in a cognitive skill.
23 . The pharmaceutical composition as claimed in claim 18 , wherein the neuronal regeneration is evidenced by a structural change in the brain or spinal cord of the subject.
24 . The pharmaceutical composition as claimed in claim 17 , wherein the sigma ligand is administered repeatedly to the subject until evidence of neuronal regeneration is found.
25 . The pharmaceutical composition as claimed in claim 24 , wherein the sigma ligand is administered daily.
26 . The pharmaceutical composition as claimed in claim 17 , wherein the sigma ligand is a selective sigma-1-ligand.
27 . The pharmaceutical composition as claimed in claim 17 , wherein the sigma ligand is a selective sigma-2 ligand.
28 . The pharmaceutical composition as claimed in claim 17 , wherein the neurodegenerative disease is selected from ischemic stroke, traumatic brain injury and spinal cord injury.
29 . The pharmaceutical composition as claimed in claim 28 , wherein the treatment is started at least 24 hours after the ischemic stroke, traumatic brain injury or spinal cord injury.
30 . The pharmaceutical composition as claimed in claim 28 , wherein the treatment is started at least 48 hours after the ischemic stroke, traumatic brain injury or spinal cord injury.
31 . The pharmaceutical composition as claimed in claim 17 , which further comprises exposing the subject to a stimulating environment.
32 . The pharmaceutical composition as claimed in claim 17 , wherein the mammalian subject is a human.
33 . A method for facilitating functional recovery after onset of a neurodegenerative disease in a mammalian subject in need thereof, the method comprising:
administering a pharmaceutically effective amount of a ligand for the sigma receptor to the subject.
34 . The method of claim 33 , wherein the ligand is selected from the group consisting of fluvoxamine, 4-IBP, PRE-084, igmesine, OPC-14523, BD-737, and BHDP, or salts, or solvates thereof.
35 . The method of claim 34 , which further comprises exposing the subject to a stimulating environment.
36 . The method of claim 35 , wherein the neurodegenerative disease is selected from the group consisting of ischemic stroke, diabetic peripheral neuropathy, spinal cord injury, traumatic brain injury, multiple sclerosis, amyotrophic lateral sclerosis, Huntington's disease and Parkinson's disease.
37 . The method of claim 36 , wherein the neurodegenerative disease is ischemic stroke.
38 . The method of claim 36 , wherein the ligand is administered during or immediately after a stroke.
39 . The method of claim 36 , wherein the ligand is fluvoxamine, or salts, or solvates thereof.
40 . The method of claim 36 , wherein the ligand is 4-IBP, or salts, or solvates thereof.
41 . The method of claim 36 , wherein the ligand is PRE-084, or salts, or solvates thereof.
42 . The method of claim 36 , wherein the ligand is igmesine.
43 . The method of claim 36 , wherein the ligand is OPC-14523.
44 . The method of claim 36 , wherein the ligand is BD-737.
45 . The method of claim 36 , wherein the ligand is BHDP.
46 . The method of claim 36 , wherein the ligand is administered within 24 hours of the disease onset.
47 . The method of claim 36 , wherein the ligand is administered within 48 hours of the disease onset.
48 . The method of claim 36 , wherein the ligand is administered for at least 2 weeks.
49 . The method of claim 36 , wherein the ligand is administered for 1 month.
50 . The method of claim 36 , wherein the ligand is administered for 3 months.
51 . The method of claim 36 , wherein the ligand is administered for 3 months or longer.
52 . The method of claim 36 , wherein the ligand is administered continuously.
53 . The method of claim 36 , wherein the subject is human.