Development of Dopamine D3 Ligands as Medications for Psychostimulant Addiction
Development of Dopamine D3 Ligands as Medications for Psychostimulant Addiction
批准号:
7784925
负责人:
SUBRAMANIAM ANANTHAN
金额:
$47.82万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2012-08-31
关键词:
Active SitesAdenylate CyclaseAdrenergic ReceptorAffinityAgonistAnimal ModelBindingBinding SitesBiochemistryBiological AssayBiological AvailabilityBlood - brain barrier anatomyBrainCellsCharacteristicsCocaineComplexComputer SimulationContractsCuesDevelopmentDockingDopamineDopamine D1 ReceptorDopamine D2 ReceptorDopamine ReceptorDrug AddictionDrug DesignDrug KineticsDrug ReceptorsDrug usageEnvironmentEvaluationForskolinGoalsHealthHealth SciencesHealthcare SystemsHomology ModelingHumanIn VitroIndividualInstitutesInterdisciplinary StudyKnowledgeLaboratoriesLeadLigand BindingLigandsMethamphetamineModelingModificationNational Institute of Drug AbuseNeuraxisPenetrationPersonal SatisfactionPharmaceutical ChemistryPharmaceutical PreparationsPharmacologyPlasmaPropertyProteinsProtocols documentationPsychostimulant dependencePublic HealthRattusRelapseResearchResearch PersonnelRhodopsinScienceSocietiesSolubilityStructureTechniquesTexasTherapeutic AgentsToxicologyUniversitiesValidationaddictionbasecandidate selectioncomparativecomputational chemistrydesigndisorder later incidence preventiondopamine D3 receptordrug abuse preventiondrug developmentdrug of abuseexperienceimprovedin vivoinsightiterative designlipophilicitynovelpreventpsychostimulantpublic health relevanceradioligandreceptorscaffoldtherapeutic targettool
中文摘要
描述(由申请人提供):我们拟议研究的长期目标是开发治疗药物成瘾的药物。最近的研究提供了令人信服的证据,表明具有拮抗剂或部分激动剂特性的对多巴胺受体D3亚型具有高度选择性的化合物有可能被开发成治疗可卡因、甲基苯丙胺和相关精神兴奋剂成瘾的药物。本文提出一项多学科研究,涉及基于结构的合理药物设计、合成和评估,以识别和开发具有成为临床有用治疗药物潜力的化合物。形成我们研究重点的一个主要考虑是开发新的配体和新的支架,这些配体和支架具有D3受体比其他多巴胺受体亚型的结合和功能选择性,并且具有良好的物理化学和药代动力学特性,可以分布到中枢神经系统。我们最近在设计和合成多巴胺D3受体新配体方面的努力为我们提供了有前途的先导化合物,这些先导化合物可能通过基于结构的药物设计工作进行优化。通过追求以下具体目标,可以实现先导物发现、先导物优化以及进一步开发候选物的识别和选择的预期目标:(1)通过配体对接到经过验证和改进的多巴胺D3受体同源模型的活性位点,预测蛋白质-配体相互作用,通过对先导模板进行特定的合理修饰,设计和合成新的配体。(2)建立D2受体模型,进行配体对接比较研究,深入了解D3和D2受体之间选择性的结构基础,设计具有更高选择性的新配体。(3)通过放射性配体结合试验评估合成的配体在体外对人D3、D2、D4和D1受体的结合亲和力,并通过腺苷酸环化酶试验确定配体的功能活性和选择性。(4)评估有前途的配体,确定其穿过血脑屏障和实现中枢神经系统渗透的能力,以选择化合物进行进一步的研究。在药物设计、合成药物化学、计算化学、生物化学和药理学方面具有丰富经验的研究人员组成的团队,除了加强我们对配体-受体相互作用的基本理解外,还将发现和开发新的药物工具和药物,用于治疗药物成瘾和预防药物复发。
英文摘要
DESCRIPTION (provided by applicant): Our long-term goal of the proposed research is to develop medications for the treatment of drug addiction. Recent research has provided convincing evidence that compounds that are highly selective for the D3 subtype of dopamine receptors with antagonist or partial agonist properties have the potential of being developed into medications for the treatment of addiction to cocaine, methamphetamine, and related psychostimulants. Proposed herein is a multidisciplinary research involving structure-based rational drug design, synthesis, and evaluations to identify and develop compounds with the potential for becoming clinically useful treatment agents. A major consideration that forms the focus of our research is the development of new ligands and novel scaffolds endowed with binding and functional selectivity for the D3 receptor over other dopamine receptor subtypes and with favorable physicochemical and pharmacokinetic properties for distribution into the central nervous system. Our recent efforts on the design and synthesis of novel ligands of the dopamine D3 receptor has provided us with promising lead compounds that could potentially be optimized through structure-based drug design efforts. The envisioned goals of lead discovery, lead optimization, and identification and selection of candidates for further development are to be achieved through the pursuit of the following specific aims: (1) Design and synthesize new ligands through specific rational modifications to the lead templates on the basis of protein-ligand interactions predicted through ligand docking into the active site of a validated and refined homology model of the dopamine D3 receptor. (2) Develop a D2 receptor model and perform comparative ligand docking studies to gain insight into the structural basis of selectivity between the D3 and D2 receptors and to design new ligands with improved selectivity. (3) Evaluate the binding affinity of the synthesized ligands in vitro against human D3, D2, D4 and D1 receptors using cells expressing each subtype of receptor through radioligand binding assays and determine the functional activity and selectivity of the ligands using adenylyl cyclase assay, and (4) Evaluate promising ligands to determine their ability to cross the blood brain barrier and achieve CNS penetration for selecting compounds for further studies. The proposed effort involving a team of researchers with experience in drug design, synthetic medicinal chemistry, computational chemistry and biochemistry and pharmacology should, in addition to enhancing our basic understanding of ligand-receptor interactions, lead to the discovery and development of new pharmacological tools and medications for the treatment of drug addiction and for prevention of relapse to drug use.
PUBLIC HEALTH RELEVANCE: Addiction to stimulant drugs such as cocaine and methamphetamine has a huge impact on the health and well-being of a large number of individuals and imposes a significant burden on the health care system. Results from recent research indicate that compounds that selectively interact with the D3 subtype of dopamine receptor could potentially be useful for treatment of addiction and for prevention of relapse to drug taking. The discovery and development of medications for the treatment of addiction to cocaine, methamphetamine, and related psychostimulants through the proposed research effort will therefore have a significant beneficial impact on the society and public health.
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