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Mechanism and Optimization of CBD-mediated analgesic effects

CBD介导的镇痛作用机制及优化

基本信息

批准号：
10662464
负责人：
ZHIGANG HE
金额：
$ 67.09万
依托单位：
BOSTON CHILDREN'S HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2019
资助国家：
美国
起止时间：
2019-09-15 至 2024-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10662464
关键词：
Absence of pain sensation Adult Analgesics Attenuated Binding Brain Stem Calcium Cannabidiol Cannabinoids Cannabinol Cannabis Cerebral cortex Chlorides Data Disinhibition Dorsal Dose Family GABA Receptor Glycine Glycine Receptors Hyperactivity Image Imaging technology Immediate-Early Genes Impairment In Vitro Intrathecal Injections Killer Cells Knock-out Light Lumbar spinal cord structure Maps Mediating Medical Methods Minor Modeling Molecular Monitor Mus Neural Inhibition Neurons Pain Pain management Peripheral Peripheral nerve injury Population Publications Receptor Cell Reporter Genes Route Signal Transduction Somatosensory Cortex Spinal Spinal Cord Stimulus Testing Tetrahydrocannabinol Vertebral column Viral Vector blood-brain barrier crossing cannabichromene cannabigerol cell type cellular targeting chloride-cotransporter potassium chronic pain management design effective therapy in vivo inflammatory pain inhibitor innovation insight marijuana use mechanical allodynia nerve injury neuromechanism novel novel strategies pain model pain processing painful neuropathy pharmacologic response side effect small hairpin RNA spared nerve transmission process

项目摘要

Abstract Substantial evidence indicates that cannabis is effective for the treatment of chronic pain in adults, but medical use of cannabis is restricted by its main psychoactive component tetrahydrocannabinol (THC). Minor cannabinoids, such as cannabidiol (CBD), do not have psychotropic activity. However, their analgesic effects are not as potent as THC and the neural mechanisms by which minor cannabinoids-mediated analgesia may be optimized remain largely unknown. Accordingly, the overall objective of this project is to identify neural mechanisms involved in minor cannabinoids signaling in order to optimize their analgesic effects. In light of compelling evidence that CBD acts on a1 and a3-glycine receptors (GlyRs), which are only a part of molecular players in neuropathic pain, we will investigate the effects and mechanisms of the combination of CBD or other minor cannabinoids with manipulations based on KCC2, a neuron-specific chloride extruder expressed in most neurons. Our test hypothesis is that CBD's mechanistic effects may be modulated by KCC2 dose-dependently and increasing KCC2 activity in spinal cord and/or cortex may enhance CBD analgesia. Specifically, we will determine whether modulating KCC2 activity will alter CBD analgesia in a dose-dependent manner, and define circuit mechanisms by which KCC2 modulates CBD analgesia. In addition to CBD, we will also examine whether KCC2 activity will regulate the analgesic effects of a family of CBD-related minor cannabinoids. Identifying the novel circuit targets and mechanisms of minor cannabinoids-mediated analgesia will not only help optimize non- psychoactive cannabinoid-based therapies but also provide routes to develop effective new treatments with minimal side-effects.

摘要