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Radiation-induced brain injury and cognitive dysfunction in aging rats

辐射引起的老年大鼠脑损伤和认知功能障碍

基本信息

批准号：
8624536
负责人：
Carol Milligan
金额：
$ 21.63万
依托单位：
WAKE FOREST UNIVERSITY HEALTH SCIENCES
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：
2009-05-06 至 2016-02-29
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8624536
关键词：
Acute Address Adult Affect Age-Years Aging Agonist Animal Model Animals Anti-Inflammatory Agents Binding Brain Brain Injuries Brain Neoplasms Cancer Patient Cells Chronic Clinic Clinical Clinical Treatment Cognitive Cognitive deficits Cranial Irradiation Development Dose Elderly Epidemiologic Studies Event Foundations Future Gene Expression Immune Impaired cognition Inflammation Inflammatory Inflammatory Response Injury Investigation Knowledge Long-Term Survivors Measures Mediating Mediator of activation protein Memory Metastatic malignant neoplasm to brain Microglia Modeling Molecular Nature Neoplasm Metastasis Neurobiology Neurons Oxidative Stress Pathway interactions Patients Pattern Phenotype Pioglitazone Population Primary Brain Neoplasms Proliferating Public Health Radiation Radiation-Induced Change Rattus Regimen Relative (related person)Research Risk Rodent Running Severities Testing Tissues Translating age effect aging brain autocrine biological adaptation to stress brain cell brain tissue cell type clinically relevant cognitive function cytokine effective therapy executive function expectation indexing inflammatory marker killings middle age paracrine prevent receptor relating to nervous system research study response therapy development young adult

项目摘要

DESCRIPTION (provided by applicant): Whole brain irradiation (WBI) is an effective treatment for brain tumors and metastases but 50% or more of the long-term survivors treated with WBI suffer cognitive deficits attributed to radiation-induced injury to normal brain tissue. The cellular and molecular mechanisms underlying the deficits are not well understood, but it is clear that radiation kills proliferating cells and also induces acute and chronic oxidative stress and inflammatory responses that alter the function of surviving cells. Although investigations of the mechanisms of radiation-induced brain injury in animal models have begun to reveal key pathways and mediators, translating the knowledge gained from these studies to the clinic is difficult since experimental studies of radiation-induced brain injury in adult rodents have used, almost without exception, very young adults. In contrast, in the clinical population, the majority of adult patients treated with WBI are 50 years of age or older. Since brain aging is accompanied by changes both in proliferating cell populations and in basal levels of inflammation and oxidative stress, the effects of WBI on the older brain are likely to be substantially different from the effects in young adults. This expectation is supported by our preliminary studies and by epidemiological evidence that aging increases the likelihood and the severity of radiation-induced cognitive decline. Treatment of radiation-induced cognitive dysfunction would benefit tremendously from a better understanding of the cellular and molecular responses that follow WBI, but it is critical to test radiation-induced changes in neurobiological measures and cognitive functions following a clinically relevant regimen of WBI and in animals that best model the relevant clinical population. The experiments proposed here will i) provide the first direct test of the effects of aging on radiation-induced deficits in a range of cognitive functions, ii) clarify the key cellular and molecular events that contribute to those functional changes, and iii) test whether treatment with the peroxisomal proliferator-activated receptor (PPAR)? agonist, pioglitazone, an anti-inflammatory agent, prevents radiation-induced cognitive dysfunction in old rats. The information that will be provided by this quantitative analysis of radiation-induced injury in young and old rats is critical to translational efforts to develop therapies to prevent or ameliorate radiation-induced cognitive dysfunction. In the absence of such studies, one runs the significant risk of targeting mechanisms of injury that may be of lesser significance in the primary clinical population.

描述(申请人提供)：全脑照射(WBI)是一种治疗脑肿瘤和转移瘤的有效方法，但接受WBI治疗的长期幸存者中有50%或更多的人患有认知障碍，可归因于辐射对正常脑组织的损伤。这些缺陷背后的细胞和分子机制尚不清楚，但很明显，辐射会杀死增殖细胞，并诱导急性和慢性氧化应激和炎症反应，从而改变存活细胞的功能。尽管在动物模型中对放射性脑损伤机制的研究已经开始揭示关键的途径和媒介，但将这些研究获得的知识转化到临床是困难的，因为成年啮齿动物放射性脑损伤的实验研究几乎无一例外地使用了非常年轻的成年人。相比之下，在临床人群中，接受WBI治疗的大多数成人患者年龄在50岁或以上。由于大脑老化伴随着增殖细胞数量以及炎症和氧化应激基础水平的变化，WBI对老年人大脑的影响可能与年轻人的影响有很大不同。这一预期得到了我们的初步研究和流行病学证据的支持，这些证据表明，衰老会增加辐射导致的认知能力下降的可能性和严重性。更好地了解WBI后的细胞和分子反应将对治疗辐射引起的认知功能障碍大有裨益，但在临床相关的WBI方案和最佳模拟相关临床人群的动物中测试辐射诱导的神经生物学指标和认知功能的变化是至关重要的。这里提出的实验是否将提供第一个直接测试老化对辐射诱导的一系列认知功能缺陷的影响，ii)阐明导致这些功能变化的关键细胞和分子事件，以及iii)测试是否使用过氧化体增殖物激活受体(PPAR)治疗？激动剂吡格列酮是一种抗炎药，可以预防辐射诱导的老年大鼠认知功能障碍。这种对幼年和老年大鼠辐射损伤的定量分析将提供的信息，对于开发预防或改善辐射诱导的认知功能障碍的治疗方法的翻译努力至关重要。在缺乏这样的研究的情况下，人们面临着靶向损伤机制的重大风险，这在初级临床人群中可能不那么重要。