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Peripheral and Central Pathways of α3 Glycine Receptors as Non-Opioid Molecular Targets to Treat Pain

α3 甘氨酸受体的外周和中枢通路作为非阿片类药物分子靶点治疗疼痛

基本信息

批准号：
10612086
负责人：
YAN XU
金额：
$ 52.94万
依托单位：
UNIVERSITY OF PITTSBURGH AT PITTSBURGH
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-05-01 至 2027-01-31
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10612086
关键词：
Absence of pain sensation Acute Address American Analgesics Behavior Binding Binding Sites Brain Brain region Cannabidiol Cannabinoids Chemosensitization Collaborations Complement Coupling Data Dose Drug Addiction Drug Binding Site Drug Targeting Drug abuse Electrophysiology (science)Equilibrium Formalin Foundations Future Genetic Glycine Receptors Human Hypersensitivity In Situ Hybridization In Vitro Inflammatory Investigation Knock-out Knockout Mice Knowledge Laboratories Lead Legal patent Marijuana Mechanics Mediating Microinjections Midbrain structure Molecular Molecular Target Morphine Motivation Mus Names Neurons Neuropathy Nociception Nucleus Accumbens Operant Conditioning Opioid Opioid Receptor Pain Pain management Pathway interactions Peripheral Persistent pain Pharmaceutical Preparations Play Population Process Protein Family Rattus Regulation Research Personnel Rewards Risk Risk Reduction Rodent Role Self Administration Signal Pathway Signal Transduction Site Specificity Spinal Spinal Cord Spinal cord posterior horn Substantia nigra structure Testing Time Transmembrane Domain Tyrosine 3-Monooxygenase United States National Institutes of Health Ventral Tegmental Area Vertebral column abuse liability antinociception behavior test cellular targeting chronic constriction injury chronic pain chronic pain management conditioned place preference coping cross reactivity design dopaminergic neuron dorsal horn drug candidate drug seeking behavior drug-like compound experience in silico in vivo inflammatory pain knockout animal morphine administration neurotransmission non-opioid analgesic novel therapeutics opioid epidemic pain model pain perception pain processing pain signal painful neuropathy pharmacologic positive allosteric modulator public health relevance receptor reconstitution scaffold screening side effect structural biology tool transmission process

项目摘要

Over 100 million Americans experience some forms of physical pain, a quarter of whom struggle daily to cope with chronic and persistent pain conditions. One of the risks associated with existing analgesic drugs, beyond some manageable side effects, is the potential for drug dependence and abuse. Glycinergic inhibition plays a pivotal role in spinal nociception. Enhancing glycine receptor (GlyR) activities by positive allosteric modulators (PAMs) has been recognized as a promising alternative to opioids for treating chronic pain. By combining structural biology, electrophysiology, and in vivo studies, we discovered a novel drug binding site in the human GlyRs that mediates marijuana’s analgesic action independent of its psychoactive side effects. We further discovered a new molecular scaffold that potentiates GlyRs with little cross reactivity with opioid receptors and other psychotropic receptors. A lead drug candidate from this scaffold was found to be specific positive allosteric modulators for α3-containing GlyRs and have higher potencies than morphine in suppressing neuropathic and inflammatory pain in rodents. Using RNAscope for in situ hybridization, we also discovered abundant colocalization of α3GlyR with a special group of projection neurons in the midbrain. These intriguing findings led us to hypothesize that α3GlyRs in the superficial layer of the spinal dorsal horn and in the midbrain play a dual role as important targets for analgesia and as inhibitory regulators for the reward circuits, respectively. We have collected ample preliminary data to support the following three specific aims: Aim 1: Investigate the role of spinal α3GlyR as an effective molecular target to alleviate mechanical and thermal hypersensitivity in neuropathic and inflammatory pain; Aim 2: Understand α3GlyR’s regulation of the midbrain projection neurons as a key cellular target for antinociception and anti-psychomotor stimulation; and Aim 3: Elucidate the coupling of glycinergic and dopaminergic signaling pathways to harness the dual action of selective positive allosteric modulation of α3GlyRs for both analgesia and reduction of reward-seeking behavior, focusing on drug-seeking and instrumental learning of self-administration tests. These mechanism-guided investigations will complement and further enhance the discovery of new α3GlyR-targeting drugs for safe and effective pain treatment.

超过1亿美国人经历过某种形式的身体疼痛，其中四分之一