Identifying the mechanisms of action for CBD on chronic arthritis pain
Identifying the mechanisms of action for CBD on chronic arthritis pain
批准号:
9895227
负责人:
YU-SHIN DING
金额:
$25.43万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-15 至 2021-08-31
关键词:
AcuteAdultAffectAgonistAmericanAnalgesicsAnimal ModelAnimalsAnti-Anxiety AgentsAnticonvulsantsAntipsychotic AgentsAutoradiographyBehavior assessmentBehavioralBuspironeCNR1 geneCannabisCapsaicinChronicChronic DiseaseChronic inflammatory painClinical ResearchClinical TrialsDegenerative polyarthritisDevelopmentDoseDropoutDrug TargetingEvaluationExhibitsFAAH inhibitorFutureGoalsInflammatoryInterventionIntractable PainLinkMechanicsMedicalMissionOpioidOpioid AnalgesicsPainPain DisorderPain MeasurementPain managementPatientsPeripheralPharmaceutical PreparationsPharmacologyPositron-Emission TomographyProgressive DiseasePropertyProtocols documentationPublic HealthReflex actionReportingResearchResearch DesignRouteSiteSymptomsTRPV1 geneTestingTetrahydrocannabinolTherapeuticTherapeutic EffectTimeUnited StatesUp-RegulationWeight-Bearing stateWithdrawaladverse event riskarthritic painbasebehavioral studycapsazepinechronic paincostdisabilityevidence baseexperiencehypnoticimaging studyin vivomarijuana usemouse modelneurochemistryneuroimagingnon-opioid analgesicnovelopioid epidemicopioid misuseosteoarthritis painpainful neuropathypreclinical studypreventresponseside effecttreatment strategyuptake
中文摘要
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英文摘要
PROJECT SUMMARY
Chronic pain is a devastating public health issue that affects >20% of all adults in the United States and costs
~$600 billion annually, more than any other medical condition. Nearly 27 million US adults have osteoarthritis,
a chronic and progressive disease for which pain is the primary symptom, making it a common cause of
chronic pain, and a leading cause of disability in the US. The management of pain has often relied on opioid-
based, pharmacologic interventions, which not only lack long-term efficacy but also carry risks for adverse
events and contribute to the national epidemic of opioid misuse. The identification and development of novel
pain management strategies for the treatment of chronic pain, therefore, is a high priority and an unmet need.
Although both THC (the major constituent of cannabis) and CBD exhibit antinociceptive effects—particularly
for chronic inflammatory pain, arthritic pain, and neuropathic pain—CBD holds particular promise as it lacks
psychoactive and addictive properties. Preclinical studies showed that CBD has a wide range of reported
pharmacological effects such as anticonvulsant, analgesic, anxiolytic, anti-inflammatory, hypnotic,
antipsychotic and neuroprotective actions; however, the exact mechanisms of action for these effects have not
been examined in chronic OA pain. The proposed study will be the first PET imaging study to determine the
key targets of CBD that are related to its mechanisms of action on pain treatment in OA. The goal of this study
is to bolster the evidence base and understand the underlying mechanisms of action of CBD by identifying the
neurochemical and behavioral alterations induced by chronic pain in OA and their modulation by CBD, alone or
in combination with other drugs. In this proposal, we will first identify the neurochemical alterations induced by
chronic pain in an OA mouse model, as compared to controls, via state-of-the-art neuroimaging studies. We
will then evaluate the CBD modulation on the neurochemical and behavioral alterations in OA animals, via
neuroimaging studies and behavioral assessment, with an extensive pharmacological, mechanistic-driven
approach to identify/confirm the mechanisms of action of CBD in OA. By doing so, CBD modulation for
neurochemical changes (mechanisms of action) can be directly linked with its analgesic properties, as reflected
in behavioral changes. This strategy will ultimately provide a strong evidence base to identify/confirm the
underlying mechanisms of action of CBD as a potential therapeutic for chronic pain in OA. These
comprehensive sets of neuroimaging and behavioral studies designed to identify the most valid mechanistic
marker attributed to the therapeutic effects of CBD (or a set of mechanistic markers that form a “signature” for
OA) will guide us to fine-tune further mechanistic studies for future clinical trials in patients with OA.
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The Norepinephrine Transporter: A Novel Target for Imaging Brown Adipose Tissue
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依托单位:
PET IMAGING OF NICOTINIC RECEPTORS
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财政年份:2004
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依托单位:
PET Imaging of Nicotinic Receptors
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依托单位:
PET STUDIES OF CATECHOL-OMICRON-METHYLTRANSFERASE
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依托单位:
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依托单位:
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依托单位:
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依托单位:
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依托单位:
海外基金