Effects of Nitric Oxide on Synaptic Transmission in the Neonatal Hippocampus

一氧化氮对新生儿海马突触传递的影响

• 批准号: 7896243
• 负责人: Santina Agnes Zanelli
• 金额: $ 17.1万
• 依托单位: UNIVERSITY OF VIRGINIA
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7896243
• 关键词: 7-nitroindazole; Action Potentials; Acute; Adverse effects; Affect; Age; Aminobutyric Acids; Area; Brain; Brain Hypoxia-Ischemia; Brain Injuries; Calcium; Cells; Characteristics; Confocal Microscopy; Data; Development; Disease; Electrophysiology (science); Endoplasmic Reticulum; Exposure to; Frequencies; Functional disorder; Generations; Glutamates; Hippocampus (Brain); Hypoxia; Image; In Vitro; Ischemic-Hypoxic Encephalopathy; Kinetics; Knock-out; Knockout Mice; Lead; Link; Long-Term Effects; Mediating; Medicine; Membrane; Membrane Potentials; Mentorship; Monitor; Morbidity - disease rate; Mus; Neonatal; Neurodevelopmental Impairment; Neurons; Newborn Infant; Nitric Oxide; Nitric Oxide Synthase Type I; Outcome; Pathway interactions; Perinatal; Positioning Attribute; Predisposition; Production; Property; Reperfusion Therapy; Research; Resistance; Rest; Rodent; Role; Ryanodine; Seizures; Slice; Stroke; Synapses; Synaptic Transmission; Techniques; Testing; Thapsigargin; Time; Toxic effect; Universities; Virginia; Wild Type Mouse; animal data; hippocampal pyramidal neuron; in vivo; inhibitor/antagonist; mortality; neonatal hypoxic-ischemic brain injury; neonate; neuronal excitability; neurotoxic; neurotransmission; neurotransmitter release; new therapeutic target; novel; patch clamp; pediatric department; postnatal; postsynaptic; presynaptic; prevent; public health relevance; research study; skills; theories; two-photon; voltage clamp

DESCRIPTION (provided by applicant): Hypoxic-ischemic brain injury is a major problem in perinatal medicine. It is the most common cause of seizures in the newborn and can lead to significant neurodevelopmental impairments. Current therapies available to neonates with seizures have limited efficacy and animal data suggest they may have significant toxicities. The mechanisms by which hypoxia leads to increased seizure susceptibility are incompletely understood. In preliminary experiments, we found that pharmacologic inhibition of neuronal nitric oxide synthase (nNOS) prevents hypoxia-reoxygenation seizures in immature rodents. Further, we also found that both hypoxia-reoxygenation and exogenous nitric oxide (NO) exposure resulted in increased neuronal excitability in CA1 neurons from P7 mice. In addition to changes in membrane properties, NO exposure resulted in enhanced glutamatergic and GABAergic synaptic transmission in cultured hippocampal neurons. Finally, our preliminary data also shows that NO increases intraterminal calcium concentration in cultured hippocampal neurons. In the proposed experiments, we will test the hypothesis that nNOS-mediated NO production during hypoxia-reoxygenation leads to neuronal hyperexcitability and synaptic transmission dysfunction in the neonatal hippocampus. Using wild-type and nNOS knockout mice , we will complete the following 3 aims: (1) To investigate the effects of hypoxia-reoxygenation and NO on CA1 neuronal excitability using current-clamp electrophysiology; (2) To investigate the effects of hypoxia-reoxygenation and NO on glutamatergic and GABAergic synaptic transmission in CA1 pyramidal neurons using voltage-clamp electrophysiology; and (3) To determine the effects of NO on synaptic calcium dynamics using using calcium imaging and confocal microscopy techniques. Experiments will be conducted at the University of Virginia with the support of the Department of Pediatrics and under the mentorship of Dr Kapur, an expert in the field of electrophysiology. With Dr Kapur's guidance the candidate will acquire new skills, including patch-clamp electrophysiology and in vitro synaptic calcium imaging, that will place the candidate in an ideal position to study the acute and long term effects of hypoxia-induced seizures in the immature brain. PUBLIC HEALTH RELEVANCE: The identification of the mechanisms of hypoxic hyperexcitability such as those mediated by NO may lead to novel pathways for the development of new therapies for neonatal seizures. This is an important area of research because of the limited efficacy, possible acute toxicities and long-term adverse effects of the treatments currently available to newborn with seizures.

描述（由申请人提供）：缺氧缺血性脑损伤是围产期医学的一个主要问题。它是新生儿癫痫发作的最常见原因，可导致显著的神经发育障碍。目前可用于癫痫发作新生儿的治疗方法疗效有限，动物数据表明它们可能具有显著的毒性。缺氧导致癫痫发作易感性增加的机制尚不完全清楚。在初步实验中，我们发现神经元一氧化氮合酶（nNOS）的药理学抑制可以预防未成熟啮齿动物的缺氧-复氧癫痫发作。此外，我们还发现，缺氧-复氧和外源性一氧化氮（NO）暴露导致增加的神经元兴奋性CA 1神经元从P7小鼠。除了膜特性的变化，NO暴露导致培养的海马神经元中谷氨酸能和GABA能突触传递增强。最后，我们的初步数据还表明，NO增加培养的海马神经元内钙离子浓度。在拟议的实验中，我们将测试的假设，nNOS介导的NO生产过程中缺氧-复氧导致神经元过度兴奋和突触传递功能障碍的新生儿海马。本研究以野生型和nNOS基因敲除小鼠为研究对象，主要完成以下三个方面的工作：（1）采用电流钳技术研究缺氧-复氧和NO对海马CA 1区神经元兴奋性的影响;（2）采用电压钳技术研究缺氧-复氧和NO对海马CA 1区锥体神经元多巴胺能和GABA能突触传递的影响;（3）应用钙离子成像和共聚焦显微镜技术研究NO对突触钙动力学的影响。实验将在弗吉尼亚大学儿科系的支持下进行，并在电生理学领域专家Kapur博士的指导下进行。在Kapur博士的指导下，候选人将获得新的技能，包括膜片钳电生理学和体外突触钙成像，这将使候选人处于理想的位置，以研究缺氧诱导癫痫发作对未成熟大脑的急性和长期影响。 公共卫生关系：缺氧过度兴奋的机制，如NO介导的识别可能会导致新的途径，为新生儿癫痫发作的新疗法的发展。这是一个重要的研究领域，因为目前对新生儿癫痫发作的治疗效果有限，可能存在急性毒性和长期不良反应。