Transplacental Arsenic Induced Hepatic Dysfunction and Vascular Disease

描述（由申请人提供）：心血管疾病是美国人死亡的主要原因。长期摄入砷会导致动脉粥样硬化，并与心肌梗死和中风的死亡率增加有关。早期生活中的砷暴露可能在成年后动脉粥样硬化的发展中起重要作用，正如在母亲饮用高砷水的地区，婴儿死于晚期动脉粥样硬化引起的心肌梗死的报告所表明的那样。经胎盘砷暴露可破坏肝脏DNA甲基化模式，从而改变肝脏基因表达。基础肝病是动脉粥样硬化的独立危险因素。因此，砷暴露诱导的肝脏疾病可能易患动脉粥样硬化，在美国饮用水中广泛暴露于砷可能导致动脉粥样硬化和心血管疾病死亡。我们的工作假设是，砷暴露破坏了肝脏基因表达的表观遗传控制，使肝脏易于发生炎症，这是一种致动脉粥样硬化的触发因素，导致易感动物加速动脉粥样硬化。初步数据表明，动脉粥样硬化倾向的载脂蛋白E基因敲除（ApoE -/-）小鼠经胎盘暴露于饮用水中的砷发展明显的血管疾病的10周龄没有高脂饮食和肝脏基因表达表明促炎状态。这项探索性资助申请的目的是：1）通过测定孕妇和胎儿血砷水平的砷暴露反应，测定动脉粥样硬化病变形成的暴露/时间依赖性，（病变形成的速率和程度），评估砷暴露-血管反应性变化的反应和动脉病变性质的特征（病变细胞，纤维化和炎症）在砷暴露小鼠; 2）通过表征肝脏病理学来探索经胎盘砷诱导的肝脏变化，确定肝功能障碍的循环生物标志物，并检验肝脏变化和血管病变之间存在时间相关性的假设。变化将在出生时以及10、16和24周龄时检查组织，以确定子宫内砷暴露诱导的疾病过程和分子变化的稳定性。拟议研究的目的是确定是否有一个阈值水平的砷暴露所需的加速动脉粥样硬化使用ApoE模型。该模型与人类动脉粥样硬化的相关性在于，产前暴露于砷的人在以后的生活中可能更容易受到饮食影响。这些研究将为砷诱导动脉粥样硬化的机制以及胎儿砷暴露在疾病进展中的作用提供重要信息。该模型也将为今后砷致动脉粥样硬化机制的研究提供丰富的资源，包括确定砷效应的关键发展阶段，以及砷暴露诱导的DNA甲基化、染色质结构、基因表达和遗传印记变化的分子研究。公共卫生相关性：在美国，饮用水中的砷暴露是一个主要问题。早期砷暴露对成人疾病进展的影响尚不清楚，但可能非常重要。本研究利用小鼠胚胎砷暴露诱发血管疾病的模型，研究胚胎砷暴露对肝脏发育的影响，这些影响可能在成年早期引起血管疾病。

DESCRIPTION (provided by applicant): Cardiovascular disease is the major cause of death in the U.S. Chronic arsenic ingestion causes atherosclerosis and is associated with increased mortality from myocardial infarction and stroke. Early life arsenic exposure may play a significant role in development of atherosclerosis in adult life, as suggested by reports of infant deaths from myocardial infarction caused by advanced arteriosclerosis in regions where mothers consumed water with high levels of arsenic. Transplacental arsenic exposure can disrupt liver DNA methylation patterns and thus alter liver gene expression. Underlying liver disease is an independent risk factor for atherosclerosis. Hence, arsenic exposure induced liver disease may predispose to atherogenesis, and widespread exposure to arsenic in drinking water in the U.S. likely contributes to atherogenesis and death from cardiovascular disease. Our working hypothesis is that arsenic exposure disrupts epigenetic control of hepatic gene expression predisposing the liver to inflammation that is an atherogenic trigger resulting in accelerated atherosclerosis in susceptible animals. Preliminary data indicate that atherosclerosis-prone apolipoprotein E knockout (ApoE -/-) mice transplacentally exposed to arsenic in drinking water develop overt vascular disease by 10 weeks of age without high lipid diet and that liver gene expression suggests a pro-inflammatory state. The aims of this exploratory grant application are 1) to refine and to optimize this newly developed model of transplacental arsenic induced atherogenesis by determining arsenic exposure response of arsenic blood levels in pregnant females and fetuses, determining exposure/time dependence of atherosclerotic lesion formation (rate and extent of lesion formation), assessing arsenic exposure-response of changes in vascular reactivity and characterizing the nature of arterial lesions (lesion cellularity, fibrosis and inflammation) in arsenic exposed mice; 2) explore transplacental arsenic-induced hepatic changes by characterizing liver pathology, determining circulating biomarkers of liver dysfunction and test the hypothesis that there is a temporal correlation between hepatic changes and vascular changes. Tissues will be examined at birth and at 10, 16 and 24 weeks of age to determine the course of disease and stability of molecular changes induced by in utero arsenic exposure. The goal of the proposed studies is to determine whether there is a threshold level of arsenic exposure necessary to accelerate atherogenesis using the ApoE model. The relevance of this model to human atherosclerosis is that people prenatally exposed to arsenic are likely more susceptible to dietary influences later in life. These studies will provide important information on the mechanisms of arsenic induced atherosclerosis and the role that fetal arsenic exposure plays in disease progression. This model also will be a rich resource for future research on the mechanism of arsenic induced atherosclerosis including determination of the critical stages of development for the arsenic effect, and molecular studies of arsenic exposure induced changes in DNA methylation, chromatin structure, gene expression and genetic imprinting. PUBLIC HEALTH RELEVANCE: Exposure to arsenic drinking water is a major concern in the United States. The effect of early life arsenic exposure on adult disease progression is unknown but potentially very important. This project uses a mouse model of fetal arsenic exposure induced vascular disease to investigate effects of fetal arsenic exposure on liver development that likely cause vascular disease by young adulthood.