Endocannabinoid Metabolism in Cannabis Users: PET Studies with the Novel Probe [1

大麻使用者的内源性大麻素代谢：使用新型探针进行 PET 研究 [1

• 批准号: 8707416
• 负责人: Isabelle Boileau
• 金额: $ 14.61万
• 依托单位: CENTRE FOR ADDICTION AND MENTAL HEALTH
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-08-01 至 2017-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8707416
• 关键词: American; Brain; Brain imaging; Cannabis; Cannabis-Related Disorder; Carbon; Clinic; Clinical; Cues; Data; Development; Disease; Drug Targeting; Endocannabinoids; Enzymes; Euphoria; Gatekeeping; Genetic Polymorphism; Goals; Health; Human; Human Genetics; Illicit Drugs; Image; Individual; Investigation; Investments; Knowledge; Label; Life; Link; Measurement; Measures; Metabolism; Patients; Pharmacologic Substance; Pharmacological Treatment; Pharmacotherapy; Positron-Emission Tomography; Relative (related person); Risk; Rodent Model; Role; Severities; Signal Transduction; Substance Use Disorder; System; Testing; Therapeutic; Time; Translations; Withdrawal; addiction; anandamide; base; cannabinoid receptor; clinical application; disorder prevention; drug development; enzyme activity; evidence base; fatty acid amide hydrolase; genetic association; in vivo; inhibitor/antagonist; interest; neuroimaging; novel; novel strategies; pre-clinical; prevent; public health relevance; radioligand; relating to nervous system; research study; response; social; therapeutic development; tool

DESCRIPTION (provided by applicant): Cannabis is the most prevalent illicit drug consumed by Americans and its abuse is associated with significant consequences to social and personal health, including addiction. In this regard, a third of individuals experimenting with cannabis progress to develop abuse, and of those who try to quit, 70% fail. There are currently no approved pharmacotherapies for cannabis use disorder (CUD). Evidence from preclinical and human genetic studies suggests the involvement of Fatty Acid Amide Hydrolase (FAAH), the enzyme metabolizing the major endocannabinoid anandamide in CUD. In particular, studies of FAAH functional polymorphisms suggest that higher enzyme activity is linked to greater risk for CUD as well as increased severity of withdrawal, cannabis-induced euphoria, and cue- induced neural response. As well, pharmacological studies in rodent models of CUD suggest that FAAH inhibitors alleviate cannabis withdrawal. Together these findings suggest that FAAH inhibitors, which have been avidly developed by pharmaceutical companies and are currently being tested in CUD, might offer a possible therapeutic avenue for the treatment of this disorder. Despite evidence suggesting the involvement of FAAH in CUD and the investment in developing FAAH-targeting drugs, there are no direct data on this enzyme in CUD. We are the only group world-wide to have developed a (PET) radioligand, [11C]-CURB, which allows direct measurement of FAAH. We are uniquely suited to investigate the role of FAAH in CUD as we have the clinical and scientific expertise in the field of CUD (Huestis, Le Foll, George) and imaging (Boileau) and have the only available neuroimaging tool (Wilson, Houle) to investigate this question. There is an urgent need to accelerate the translation, into clinic, of pharmacotherapies already in development for CUD, by providing neuroimaging information which could advance our understanding of endocannabinoid metabolism in CUD. Following upon our development of [11C]-CURB, our major specific aim and hypothesis is to establish by PET imaging whether FAAH activity is elevated in CUD and whether differences are related to addiction severity. Confirmation of this hypothesis, in a 2 year proof-of-concept study, can help identify a drug target to treat (perhaps prevent) CUD and can guide clinical application of treatment approaches (using FAAH inhibitors) already in development. The potential impact of this project is immense, as it provides the first imaging investigation of endocannabinoid metabolism in CUD. The knowledge generated by this project will provide the basis for the further development of evidence-based therapeutic approaches targeting FAAH. The availability of compounds targeting FAAH that are in development by major pharmaceutical companies allows for a quick translation of our human brain findings into the clinic.

大麻是美国人消费的最普遍的非法药物，其滥用与社会和个人健康的重大后果有关，包括成瘾。在这方面，三分之一的人尝试大麻发展为滥用，而那些试图戒烟的人中，70%失败。目前还没有批准的药物治疗大麻使用障碍（CUD）。 来自临床前和人类遗传学研究的证据表明脂肪酸酰胺水解酶（FAAH）参与其中，FAAH是CUD中主要内源性大麻素anandamide的代谢酶。特别是，FAAH功能多态性的研究表明，较高的酶活性与CUD的更大风险以及戒断、大麻诱导的欣快和提示诱导的神经反应的严重程度增加有关。同样，在啮齿动物模型中进行的药理学研究表明FAAH抑制剂可缓解大麻戒断症状。这些研究结果表明，FAAH抑制剂已经被制药公司积极开发，目前正在CUD中进行测试，可能为治疗这种疾病提供一种可能的治疗途径。尽管有证据表明FAAH参与CUD和开发FAAH靶向药物的投资，但没有关于这种酶在CUD中的直接数据。 我们是全球唯一开发出（PET）放射性配体[11 C]-CURB的团队，该配体可直接测量FAAH。我们非常适合研究FAAH在CUD中的作用，因为我们在CUD（Huestis，Le Foll，乔治）和成像（Boileau）领域拥有临床和科学专业知识，并且拥有唯一可用的神经成像工具（Wilson，Houle）来研究该问题。 有一个迫切需要加快翻译，进入临床，药物治疗已经在开发中的CUD，通过提供神经影像学信息，可以提高我们的理解，内源性大麻素代谢的CUD。在我们开发[11 C]-CURB之后，我们的主要具体目标和假设是通过PET成像确定CUD中FAAH活性是否升高以及差异是否与成瘾严重程度相关。 在为期2年的概念验证研究中证实这一假设，可以帮助确定治疗（可能预防）CUD的药物靶标，并可以指导已经开发的治疗方法（使用FAAH抑制剂）的临床应用。该项目的潜在影响是巨大的，因为它提供了第一个在CUD内源性大麻素代谢的成像研究。该项目产生的知识将为进一步开发针对FAAH的循证治疗方法提供基础。主要制药公司正在开发的靶向FAAH的化合物的可用性允许我们将人类大脑的发现快速转化为临床。

项目成果

Fatty acid amide hydrolase binding is inversely correlated with amygdalar functional connectivity: a combined positron emission tomography and magnetic resonance imaging study in healthy individuals.

• DOI: 10.1503/jpn.200010
• 发表时间: 2021-03-17
• 期刊: Journal of psychiatry & neuroscience : JPN
• 作者: Green DGJ;Kim J;Kish SJ;Tyndale RF;Hill MN;Strafella AP;Tong J;McCluskey T;Westwood DJ;Houle S;Lobaugh NJ;Boileau I
• 通讯作者: Boileau I

Circulating Endocannabinoids and N-Acylethanolamines in Individuals with Cannabis Use Disorder-Preliminary Findings.

• DOI: 10.3390/brainsci13101375
• 发表时间: 2023-09-27
• 期刊: Brain sciences
• 影响因子: 3.3

Fatty acid amide hydrolase levels in brain linked with threat-related amygdala activation.

• DOI: 10.1016/j.ynirp.2022.100094
• 发表时间: 2022-06
• 期刊: Neuroimage. Reports
• 作者: Green DG;Westwood DJ;Kim J;Best LM;Kish SJ;Tyndale RF;McCluskey T;Lobaugh NJ;Boileau I
• 通讯作者: Boileau I