Neuroendocrine Contribution to Behavior & Cognition in the Female Lifespan

神经内分泌对行为的贡献

• 批准号: 8505465
• 负责人: C. Neill NEILL EPPERSON
• 金额: $ 19.1万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-01 至 2015-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8505465
• 关键词: Acute; Address; Aging; Allopregnanolone; American; Anxiety; Applications Grants; Area; Behavior; Brain; Brain region; Clinical Research; Cognition; Collaborations; Commit; Communities; DSM-V; Data; Data Collection; Development; Development Plans; Diagnosis; Diagnostic; Discipline of obstetrics; Disease; Dose; Drops; Endocrine; Endocrine system; Estrogens; Female; Fluoxetine; Fostering; Functional Magnetic Resonance Imaging; Functional disorder; Funding; Future; Gender; Genetic Polymorphism; Goals; Gonadal Steroid Hormones; Grant; Grant Review Process; Gynecology; Hormonal; Hormonal Change; Hour; Human; Impaired cognition; Individual; International; Investigation; K-Series Research Career Programs; Knowledge; Laboratories; Longevity; Luteal Phase; Magnetic Resonance Spectroscopy; Major Depressive Disorder; Measurement; Measures; Menopause; Menstrual cycle; Mental disorders; Mentors; Mentorship; Metabolism; Methods; Molecular; Mood Disorders; Moods; National Institute of Drug Abuse; National Institute on Aging; Nature; Neurobiology; Neuropharmacology; Neurosciences; Neurosecretory Systems; Neurotransmitters; Occipital lobe; Pathogenesis; Pennsylvania; Perimenopause; Peripheral; Pharmaceutical Preparations; Phase; Plasma; Population; Population Study; Positioning Attribute; Postpartum Depression; Premenstrual syndrome; Progesterone; Protons; Proxy; Psychiatry; Psychophysiology; Recovery; Reproductive Process; Research; Research Design; Research Methodology; Research Personnel; Resources; Scanning; Selective Serotonin Reuptake Inhibitor; Serotonin; Societies; Staging; Surface; Symptoms; System; Technology; Therapeutic; Time; Training; Translating; Translational Research; Tryptophan; Universities; Variant; Woman; Work; Writing; base; behavioral health; career; career development; cingulate cortex; cognitive change; disturbance in affect; effective therapy; experience; gamma-Aminobutyric Acid; interest; member; neurosteroids; patient oriented research; placebo controlled study; pre-clinical; premenstrual dysphoric disorder; professor; programs; proliferative phase Menstrual cycle; reproductive; response; skills; tool; treatment duration

The overarching objective that has guided my research endeavors, collaborations and training opportunities has been to determine the mechanism by which sex hormones and neurosteroids interact with neurotransmitters to modulate behavior, mood, and cognition in women. With my previous two mentored K awards, I was able to develop a unique clinical research program that relied heavily on knowledge gained from molecular and basic neuroscience to inform our investigations of the pathogenesis of premenstrual dysphoric disorder (PMDD), postnatal depression (PPD), and perimenopausal mood and cognitive changes. To this end, I have employed an array of research paradigms and technologies with the goal of translating preclinical findings to the human laboratory. I have relied heavily on the use of proton magnetic resonance spectroscopy (1H-MRS) to explore the relationship between sex hormones, neurosteroids and gamma-aminobutyric acid (GABA) function in women across the menstrual cycle. In the past year, we have moved towards the use of hormonal and pharmacologic challenge paradigms to address changes in GABA concentrations and whether individual factors such as diagnosis, neurosteroid metabolism, and/or genetic polymorphisms, are responsible for observed variations in response. It is this paradigm that I propose to pursue during K24-funding. While 1H-MRS as a tool is excellent for exploring the interaction between progesterone (via allopregnanolone) and GABA, it is not the appropriate technology for questions related to estrogen and serotonin interactions, which may be critical to mood and cognition in aging women. Our previous work using the tryptophan depletion paradigm in menopausal women (Epperson et al., 2007b; Amin et al., 2006b) led me to become increasingly interested in the utility of functional magnetic resonance imaging (fMRI). My lab recently received funding from the National Institute on Aging to study the individual and interactive effects of estrogen and serotonin on cognition and brain activation in menopausal women. This grant will provide important opportunities for me to hone my skills with fMRI and to mentor new trainees. These are just two lines of investigations that I wish to pursue during K24 funding. I have described in this application several other areas of on-going work and how they will not only provide avenues for continued research, but fertile ground for the development of future investigators in patient-oriented research. It is my increasing focus on mentoring junior investigators that motivates me to apply for a K24 instead of submitting a competitive renewal for my K02. As my KO2 is drawing to an end (12/31/09), timely funding of this K24 grant will insure that I can focus on both the research career development plans and project outlined herein, as well as commit substantial effort to fostering the careers of junior researchers. Without K24 funding, I will have to assume additional, non-research related activities in my new Tenured Associate Professor position at the University of Pennsylvania, which is beginning September 1, 2009. My translational research and educational endeavors over the past 9 years have insured that I am uniquely poised to advance our understanding of neuroendocrine contribution to mood and behavior in women. With the full support of both the Departments of Psychiatry and Obstetrics/Gynecology at Penn, I am situated in an intellectually rich and supportive academic community that is certain to further my career development as well as that of individuals I mentor.

指导我的研究工作，合作和培训机会的总体目标是确定性激素和神经类固醇与神经递质相互作用以调节女性行为，情绪和认知的机制。通过我之前的两次指导K奖，我能够开发出一个独特的临床研究计划，该计划在很大程度上依赖于从分子和基础神经科学中获得的知识，以告知我们对经前焦虑症（PMDD），产后抑郁症（PPD）和围月经期情绪和认知变化的发病机制的调查。为此，我采用了一系列研究范式和技术，目的是将临床前发现转化为人类实验室。我在很大程度上依赖于质子磁共振波谱（1H-MRS）的使用，以探讨性激素，神经类固醇和γ-氨基丁酸（GABA）功能在整个月经周期的妇女之间的关系。在过去的一年中，我们已经转向使用激素和药理学挑战范式，以解决GABA浓度的变化，以及是否个别因素，如诊断，神经类固醇代谢和/或遗传多态性，是负责观察到的反应变化。我建议在K24资助期间追求的正是这种范式。 虽然1H-MRS作为一种工具是探索孕酮（通过别孕烯醇酮）和GABA之间的相互作用，它不是与雌激素和5-羟色胺相互作用，这可能是关键的情绪和认知在老年妇女的问题的适当技术。我们先前在绝经期妇女中使用色氨酸耗竭范例的工作（Epperson等人，2007 b; Amin等人，2006 b）使我对功能性磁共振成像（fMRI）的实用性越来越感兴趣。我的实验室最近得到了国家老龄化研究所的资助，研究雌激素和血清素对更年期妇女认知和大脑激活的个体和交互作用。这笔赠款将为我提供重要的机会，磨练我的技能与功能磁共振成像和指导新学员。 这只是我希望在K24资助期间进行的两条调查路线。我在本申请中描述了其他几个正在进行的工作领域，以及它们如何不仅为继续研究提供途径，而且为未来研究人员在以患者为导向的研究中的发展提供肥沃的土壤。这是我越来越注重指导初级调查员，促使我申请K24，而不是提交一个有竞争力的更新我的K 02。由于我的KO 2即将结束（2009年12月31日），及时资助K24赠款将确保我能够专注于本文概述的研究职业发展计划和项目，并致力于培养初级研究人员的职业生涯。如果没有K24的资助，我将不得不承担额外的，非研究相关的活动在我的新的终身副教授在宾夕法尼亚大学的位置，这是2009年9月1日开始。在过去的9年里，我的翻译研究和教育努力确保了我能够独特地提高我们对女性情绪和行为的神经内分泌贡献的理解。在宾夕法尼亚大学精神病学和产科/妇科部门的全力支持下，我位于一个智力丰富和支持性的学术社区，这肯定会促进我的职业发展以及我所指导的个人。