Development of a preclinical candidate for the treatment of alcoholism

开发治疗酒精中毒的临床前候选药物

• 批准号: 8322858
• 负责人: Richard M. van Rijn
• 金额: $ 8.84万
• 依托单位: ERNEST GALLO CLINIC AND RESEARCH CENTER
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-20 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8322858
• 关键词: Adverse effects; Affect; Agonist; Alcohol abuse; Alcohol consumption; Alcohol withdrawal syndrome; Alcoholism; Alcohols; Anti-Anxiety Agents; Anxiety; Binding; Biological Assay; Chronic; Development; Disease; Drug Delivery Systems; Drug Interactions; Drug usage; Ethanol; FDA approved; G-Protein-Coupled Receptors; Goals; Hyperalgesia; In Vitro; Individual; Intervention; Lead; Left; Ligands; Methods; Molecular; Mus; Naltrexone; Nature; Opioid; Opioid Receptor; Pharmaceutical Preparations; Pharmacology; Physiological; Play; Population Heterogeneity; Property; Relapse; Research; Rewards; Role; Screening procedure; Societies; Stimulus; Testing; Therapeutic; Time; Withdrawal; alcohol behavior; alcohol exposure; alcoholism therapy; clinically relevant; delta opioid receptor; design; drinking; drinking behavior; drug efficacy; in vitro Assay; in vivo; kappa opioid receptors; mouse model; novel; pre-clinical; preference; radioligand; receptor; response

DESCRIPTION (provided by applicant): Alcoholism and alcohol related illnesses put a large strain on society. While therapeutics are available, none are universally effective among the diverse population of treatment seeking individuals. My research is focused on elucidating the role of two delta opioid receptor subtypes (DOR1 and DOR2) in alcohol abuse disorders. Their ability to affect both ethanol consumption and anxiety make these DOR subtypes promising potential novel drug targets to treat alcoholism. So far I have discovered that the DOR subtypes have unique and sometimes opposing effects on ethanol consumption and anxiety. Moreover, I determined that the DOR1's pharmacology may result from an interaction of the DOR with the MOR forming a DOR-MOR heteromer. My research is designed to determine the mechanism behind the unique pharmacology of the DOR subtypes and exploit it to develop novel drugs that can treat alcohol abuse disorders better and with fewer side effects than the currently available medication. One integral part of my research is resolving how chronic ethanol exposure results in an increase in the number of functional DORs. Additionally, I have designed a unique method to identify drugs that selectively interact with receptor heteromers using a high throughput in vitro assay. I intend to further test compounds identified in this assay using mice models of alcoholism, determining their effects on ethanol intake, anxiety, reward and ethanol withdrawal. My ultimate goal is to validate a DOR-subtype as a new target for intervention in alcohol abuse and determine the properties of the most ideal DOR-subtype selective drug as a preclinical lead.

描述（由申请人提供）：酒精中毒和酒精相关疾病给社会带来了很大的压力。虽然有治疗方法，但没有一种在寻求治疗的不同人群中普遍有效。我的研究重点是阐明两种δ阿片受体亚型（DOR 1和DOR 2）在酒精滥用障碍中的作用。它们影响乙醇消耗和焦虑的能力使这些DOR亚型成为治疗酒精中毒的潜在新药物靶点。到目前为止，我已经发现DOR亚型对乙醇消耗和焦虑有独特的，有时是相反的影响。此外，我确定DOR 1的药理学可能是由于DOR与莫尔相互作用形成DOR-莫尔异聚体。我的研究旨在确定DOR亚型独特药理学背后的机制，并利用它开发新型药物，这些药物可以比目前可用的药物更好地治疗酒精滥用疾病，且副作用更少。我的研究的一个组成部分是解决慢性乙醇暴露如何导致功能性DOR数量增加。此外，我还设计了一种独特的方法来识别药物，选择性地与受体异聚体相互作用，使用高通量的体外试验。我打算使用酒精中毒小鼠模型进一步测试在该测定中鉴定的化合物，确定它们对乙醇摄入、焦虑、奖励和乙醇戒断的影响。我的最终目标是验证DOR亚型作为酒精滥用干预的新靶点，并确定最理想的DOR亚型选择性药物作为临床前先导药物的特性。

项目成果

Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization.

二氧化钛纳米管通过抑制巨噬细胞糖酵解促进M2极化，最终加速内皮化

• DOI: 10.1002/iid3.429
• 发表时间: 2021-09
• 期刊: Immunity, inflammation and disease
• 作者: Yu WP;Ding JL;Liu XL;Zhu GD;Lin F;Xu JJ;Wang Z;Zhou JL
• 通讯作者: Zhou JL

Unique Behavioral and Neurochemical Effects Induced by Repeated Adolescent Consumption of Caffeine-Mixed Alcohol in C57BL/6 Mice.

• DOI: 10.1371/journal.pone.0158189
• 发表时间: 2016
• 期刊: PloS one
• 影响因子: 3.7
• 作者: Robins MT;Lu J;van Rijn RM
• 通讯作者: van Rijn RM