The current epidemic of opiate addiction has led to nearly 50 thousand deaths a year in the U.S. Much like the earlier cocaine/crack epidemic, it has proved devastating to individuals, families and communities. The most successful treatment of long-term opiate use disorder (OUD) is still one of maintenance using methadone. This is far from a cure, leaving people functional but still addicted to a narcotic. While the use of powerful opiate blocking drugs, such as naloxone and naltrexone, has demonstrated great value in rescuing victims of opiate overdose, they have proved disappointing in the long term treatment of OUD. The use of these drugs often produces devastating withdrawal symptoms forcing patients to turn to opiates for relief. A better approach to long term OUD treatment is clearly needed. The difficulty in treating OUD stems from the fact that opiate use damages the natural motivational and reward mechanisms in the brain. Curing addiction requires restoring this mechanism. Unfortunately, both opiates and the drugs used to treat OUD, compromise the opiate receptor protein, a key component of the reward mechanism. What is needed is a drug that acts as a switch, blocking the effects of opiates while allowing the reward mechanism to continue to work normally. This requires a new type of drug that operates on the protein control (allosteric) site. The proposal employs high performance computer modeling technology along with biological assays to search for such a drug. If successful it will identify lead compounds that result in drugs that treat and possibly cure opiate addiction.
Public Health Relevance Statement: Project Narrative The project will develop new therapeutic agents for treating opiate use disorder that are non-narcotic and avoid devastating withdrawal symptoms. Our pharmacological approach targets the negative allosteric binding site in order to selectively inhibit exogenous opiates while allowing endogenous agonists to function properly, thereby allowing the brain to restore its natural motivational and reward mechanisms. Successful completion of this project will directly benefit the 2 million sufferers of long term opiate use disorder in the U.S. by providing a novel treatment protocol.
Project Terms: Achievement; addiction; Agonist; Agreement; Allosteric Site; Area; base; Binding; Binding Sites; Biological Assay; Biotechnology; Brain; Capital; Cells; Cessation of life; Communities; Computer Models; Coupled; Crack Cocaine; Cyclic AMP; Databases; Development; Docking; drug candidate; drug discovery; Drug usage; Effectiveness; Epidemic; Family; Fluorescence; Goals; high end computer; illicit opioid; Individual; inhibitor/antagonist; Investigational New Drug Application; Laboratory Study; Lead; lead candidate; Legal patent; Location; Maintenance; Methadone; molecular dynamics; Motivation; mu opioid receptors; Naloxone; Naltrexone; Narcotics; novel; novel therapeutics; Opiate Addiction; Opioid; Opioid agonist; opioid overdose; Opioid Receptor; opioid use; opioid use disorder; Outcome; Patients; Pharmaceutical Preparations; Pharmacology; Phase; prescription opioid; Proteins; receptor; receptor internalization; Receptor Signaling; Rewards; Sales; salvinorin A; Signal Transduction; Site-Directed Mutagenesis; small molecule; small molecule therapeutics; stem; Technology; Therapeutic; Therapeutic Agents; Toxic effect; Treatment Protocols; United States National Institutes of Health; Validation; Withdrawal Symptom; Work
