Short and long-term impact of neonatal seizures on hippocampal granule cell integ

新生儿癫痫发作对海马颗粒细胞整合的短期和长期影响

基本信息

批准号：
7849034
负责人：
Steve C Danzer
金额：
$ 7.5万
依托单位：
CINCINNATI CHILDRENS HOSP MED CTR
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-06-01 至 2011-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7849034
关键词：
Abnormal Cell Accounting Acute Adult Age Animals Anticonvulsants Apoptosis Biological Models Birth Brain Brain region Bromodeoxyuridine Cell Aging Cell Count Cell Death Cell Differentiation process Cells Cellular Structures Child Cognition Cognitive Cognitive deficits Computer Assisted Confocal Microscopy Control Animal Dendrites Development Embryonic Development Employee Strikes Epilepsy Exhibits Generations Genetic Recombination Green Fluorescent Proteins Hilar Hippocampus (Brain)Human Imagination Immunohistochemistry Impact Seizures Incidence Infant Kainic Acid Label Laboratories Language Development Lead Learning Length Life Location Maps Mediating Memory Morphology Mus Neonatal Neuroglia Neurons Newborn Infant Normal Cell Pattern Phenotype Population Predisposition Presynaptic Terminals Productivity Recurrence Relative (related person)Reporter Resistance Saline Seizures Status Epilepticus Stem cells Structure Tamoxifen Time Vertebral column brain cell caspase-3 cell age density early childhood experience granule cell insight juvenile animal mature animal morphometry mouse model neurogenesis postnatal progenitor protein expression public health relevance self-renewal treatment strategy

项目摘要

DESCRIPTION (provided by applicant): The hippocampus is a structure located deep in the brain that is critical for memory, language development, cognition and even imagination. Surprisingly, this is one of the few regions of the adult brain where new brain cells are generated. These new cells are important for the proper functioning of the hippocampus. Unfortunately, recent studies demonstrate that these new cells are vulnerable to seizures. Seizure activity in the brain can cause these immature cells to form the wrong connections with other brain cells. In adults, these abnormal cells likely lead to cognitive problems and perhaps even the development of epilepsy. Distressingly, in children, the situation may be even worse. First, children exhibit a much lower seizure threshold than adults. Seizures in children, therefore, are common. Second, the developmental period during which children exhibit higher seizure incidence overlaps with the peak period of hippocampal development. Large numbers of hippocampal cells are generated in infants, and these cells undergo extensive development through early childhood. Seizures during this period could lead to the abnormal wiring of large numbers of hippocampal cells. In contrast, the generation of neurons in almost all other brain regions is largely complete by birth. To determine whether new hippocampal cells are uniquely vulnerable to insult, and whether disruption of these cells might account for the severe cognitive deficits experienced by children who have intense or recurrent seizures, we utilize a mouse model system in which newly generated hippocampal cells are labeled with green fluorescent protein (GFP). GFP reveals the complete structure of these cells, and by selectively labeling newly generated cells, the population hypothesized to be must vulnerable can be tracked as the animals develop to assess how they connect with other brain cells. The development of immature cells exposed to neonatal seizures will be compared to cells from normal animals using confocal microscopy. These studies will provide important insights into the long-term consequences of neonatal seizures, will inform clinicians about how aggressively to treat children having seizures with anticonvulsant drugs and will help to establish whether disrupted hippocampal cell integration might account for the negative consequences of neonatal seizures. PUBLIC HEALTH RELEVANCE: Seizures in children are common. The long term consequences of these seizures, however, are still unclear. Here, we will examine the impact of neonatal seizures on the development of a brain region critical for learning, language development, cognition and imagination. These studies will help to determine whether and how neonatal seizures harm young brains, and will guide the development of mitigating strategies and treatments.

描述（由申请人提供）：海马体是位于大脑深处的结构，对于记忆、语言发展、认知甚至想象力至关重要。令人惊讶的是，这是成人大脑中少数产生新脑细胞的区域之一。这些新细胞对于海马体的正常运作非常重要。不幸的是，最近的研究表明这些新细胞很容易癫痫发作。大脑中的癫痫发作活动会导致这些未成熟的细胞与其他脑细胞形成错误的连接。在成年人中，这些异常细胞可能会导致认知问题，甚至可能导致癫痫的发展。令人痛苦的是，对于儿童来说，情况可能更糟。首先，儿童的癫痫发作阈值比成人低得多。因此，儿童癫痫发作很常见。其次，儿童癫痫发作率较高的发育期与海马发育的高峰期重叠。婴儿体内产生大量海马细胞，这些细胞在幼儿期经历广泛的发育。在此期间的癫痫发作可能会导致大量海马细胞的异常连接。相比之下，几乎所有其他大脑区域的神经元的生成基本上在出生时就已完成。为了确定新的海马细胞是否特别容易受到损伤，以及这些细胞的破坏是否可能导致患有剧烈或反复发作的儿童经历的严重认知缺陷，我们利用了小鼠模型系统，其中新生成的海马细胞被标记为绿色荧光蛋白（GFP）。 GFP揭示了这些细胞的完整结构，并且通过选择性地标记新生成的细胞，可以在动物发育过程中追踪被假设为脆弱的细胞群，以评估它们如何与其他脑细胞连接。将使用共聚焦显微镜将暴露于新生儿癫痫发作的未成熟细胞的发育与来自正常动物的细胞进行比较。这些研究将为新生儿癫痫发作的长期后果提供重要的见解，将告知临床医生如何积极地使用抗惊厥药物治疗癫痫发作的儿童，并将有助于确定海马细胞整合破坏是否可能解释新生儿癫痫发作的负面后果。公共卫生相关性：儿童癫痫发作很常见。然而，这些癫痫发作的长期后果仍不清楚。在这里，我们将研究新生儿癫痫发作对学习、语言发展、认知和想象力至关重要的大脑区域发育的影响。这些研究将有助于确定新生儿癫痫发作是否以及如何损害年轻的大脑，并将指导缓解策略和治疗的制定。