首页> 美国卫生研究院文献>Schizophrenia Bulletin >168. Neuroadaptations to Antipsychotic Drugs: Optimizing use of Current Medication Through a Deeper Understanding of Antipsychotic Drug Action in the Brain and Body
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168. Neuroadaptations to Antipsychotic Drugs: Optimizing use of Current Medication Through a Deeper Understanding of Antipsychotic Drug Action in the Brain and Body

机译:168.对抗精神病药物的神经适应:通过更深入地了解大脑和身体中的抗精神病药物的作用优化当前药物的使用

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摘要

>Overall Abstract: Antipsychotic drugs, all of which block the dopamine D2 receptor to a greater or lesser extent, are the mainstay for the pharmacological treatment of schizophrenia. Engaging in a deeper understanding of how antipsychotics act on the brain and body, at the cellular, molecular and physiological level is vital to comprehend both the beneficial and the potentially harmful actions of these medications and importantly stimulate development of novel therapeutics. To address this timely and clinically relevant issue, we propose 4 talks covering the most up-to-date clinical and preclinical data focusing on (1) antipsychotic treatment efficacy and failure, (2) brain-mediated cardiometabolic side effects, (3) evidence from human postmortem studies that attempt to dissect neuropathological effects of antipsychotic drugs from organic schizophrenia neurobiology, and (4) the emerging interactions of antipsychotic drugs with the immune system. The 4 proposed speakers are:(1) Dr Davide Amato: “Effects of antipsychotic treatment on synaptic dopamine levels and its relevance for antispychotic treatment efficacy and failure: preliminary results from a meta-analysis of microdialysis studies”(2) Dr Margaret Hahn: “Olanzapine impairs central insulin action leading to dysregulation of hepatic glucose production”(3) Dr Clare Beasley: “Post-mortem studies of glial pathology: dissecting drug from disease effects”(4) Dr Anthony Vernon “Do antipsychotics inflame the brain?”The final part of the workshop will then be given over to an open discussion led by the chair, cochair, and moderator with the workshop audience.Professor Gary Remington will chair the session and Professor Lars Jarkog has agreed to act as moderator / discussant.Our aim is to stimulate discussion on these highly clinically relevant topics and consider how we might use current and evolving knowledge and new methodologies in the fields of neuropharmacology and neuroscience, to advance our understanding of the long-term impact of antipsychotic treatment. Ultimately, this may inform the clinical use of these drugs and pave the way for development of novel treatment strategies or optimized antipsychotic drugs.
机译:>总体摘要:抗精神病药都可以或多或少地阻断多巴胺D2受体,是精神分裂症药理治疗的主要手段。深入了解抗精神病药物如何在细胞,分子和生理学水平上作用于大脑和身体,对于理解这些药物的有益作用和潜在有害作用以及重要地刺激新型疗法的发展至关重要。为了解决这个及时且与临床相关的问题,我们提出了4个讲座,涵盖了最新的临床和临床前数据,重点是(1)抗精神病药的治疗效果和衰竭,(2)脑介导的心脏代谢副作用,(3)证据试图从有机精神分裂症神经生物学中剖析抗精神病药的神经病理学作用的人类验尸研究;以及(4)抗精神病药与免疫系统的新兴相互作用。拟议的四位发言人是:(1)Davide Amato博士:“抗精神病药物治疗对突触多巴胺水平的影响及其与抗精神分裂症疗效和失败的相关性:微透析研究的荟萃分析的初步结果”(2)Margaret Hahn博士: “奥氮平削弱中枢胰岛素作用,导致肝葡萄糖生成失调”(3)克莱尔·比斯利(Clare Beasley)博士:“神经胶质病理的验尸研究:将药物从疾病作用中分离出来”(4)安东尼·弗农(Anthony Vernon)博士“抗精神病药会刺激大脑吗?”研讨会的最后部分将由主持人,联合主席和主持人与研讨会的听众进行公开讨论,加里·雷明顿教授将主持会议,拉尔斯·贾科格教授同意担任主持人/讨论者。目的是激发对这些与临床高度相关的主题的讨论,并考虑如何在神经药理学和神经科学领域中使用当前和不断发展的知识和新方法ce,以加深我们对抗精神病药物治疗的长期影响的认识。最终,这可能会为这些药物的临床使用提供信息,并为开发新的治疗策略或优化抗精神病药物铺平道路。

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