METHODS OF TREATING ANXIETY DISORDERS
Disclosed are methods of treating an anxiety disorder, e.g., obsessive compulsive disorder, in an individual, comprising identifying an individual in need thereof and treating that individual to antagonize opioid receptor activity and to restore normal monoaminergic tone within the synapse.
1 . A method of treating an anxiety disorder comprising identifying a patient suffering from or at risk of suffering from an anxiety disorder, and administering to the patient a first compound and a second compound, wherein said first compound is an opioid antagonist or opioid receptor partial agonist and said second compound modulates monoaminergic synaptic activity.
2 . The method of claim 1 , wherein the monoaminergic synaptic activity is at least one monoaminergic synaptic activity selected from serotonin synaptic activity, norepinephrine synaptic activity, and dopamine synaptic activity.
3 . The method of claim 1 , wherein the anxiety disorder is obsessive compulsive disorder.
4 . The method of claim 1 , wherein the first compound is a MOP receptor antagonist.
5 . The method of claim 1 , wherein the first compound is selected from alvimopan, norbinaltorphimine, nalmefene, naloxone, naltrexone, methylnaltrexone, and nalorphine, and pharmaceutically acceptable salts, enantiomers, metabolites or prodrugs thereof.
6 . The method of claim 1 , wherein the first compound is naltrexone, 6-beta-naltrexol, or a pharmaceutically acceptable salt or prodrug thereof.
7 . The method of claim 6 , wherein the first compound indirectly modulates a dopamine pathway.
8 . The method of claim 1 , wherein said second compound is a selective serotonin reuptake inhibitor (SSRI), reuptake promoter, or a specific 5-HT receptor agonist.
9 . The method of claim 8 , wherein said SSRI is selected from fluoxetine, fluvoxamine, sertraline, paroxetine, citalopram, escitalopram, sibutramine, duloxetine, and venlafaxine, and pharmaceutically acceptable salts or prodrugs thereof.
10 . The method of claim 8 , wherein said SSRI is fluoxetine or a pharmaceutically acceptable salt or prodrug thereof.
11 . The method of claim 1 , wherein said first compound and said second compound are administered nearly simultaneously.
12 . The method of claim 1 , wherein the second compound is bupropion or a metabolite thereof.
13 . The method of claim 1 , wherein said first compound is naltrexone and said second compound is fluoxetine.
14 . The method of claim 1 , wherein said first compound is naltrexone and said second compound is bupropion.
15 . A method of treating a movement disorder comprising identifying a patient suffering from or at risk of suffering from a movement disorder, and administering to the patient a first compound and a second compound, wherein said first compound is an opioid antagonist or opioid receptor partial agonist and said second compound modulates monoaminergic synaptic activity.
16 . The method of claim 15 , wherein the monoaminergic synaptic activity is at least one monoaminergic synaptic activity selected from serotonin synaptic activity, norepinephrine synaptic activity, and dopamine synaptic activity.
17 . The method of claim 15 , wherein the movement disorder is Tourette syndrome.
18 . The method of claim 15 , wherein the movement disorder is tics.
19 . The method of claim 15 , wherein the first compound is a MOP receptor antagonist.
20 . The method of claim 15 , wherein said second compound is a selective serotonin reuptake inhibitor (SSRI) or a specific 5-HT receptor agonist.
21 . The method of claim 15 , wherein said first compound is naltrexone and said second compound is fluoxetine.
22 . The method of claim 15 , wherein said first compound is naltrexone and said second compound is bupropion.