Development of a Multiscale Mechanistic Simulation of Acetaminophen Induced Liver

对乙酰氨基酚诱导肝脏的多尺度机制模拟的开发

• 批准号: 8743591
• 负责人: KENNETH W DUNN
• 金额: $ 53.45万
• 依托单位: TRUSTEES OF INDIANA UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-25 至 2018-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8743591
• 关键词: Acetaminophen; Acute; Affect; Analgesics; Animals; Apoptotic; Bile fluid; Biological; Biological Assay; Blood Vessels; Blood flow; Carrier Proteins; Cell Death; Cell surface; Centrilobular hepatic necrosis; Cessation of life; Clinical; Computer Simulation; Data; Development; Discontinuous Capillary; Disease; Dose; Drug Exposure; Drug Kinetics; Endothelium; Environmental Risk Factor; Enzymes; Experimental Models; Exposure to; Fever; Genetic; Genetic Polymorphism; Health; Hepatocyte; Hepatotoxicity; Histology; Home environment; Human; Image; Immune; Indiana; Individual; Injury; Injury to Liver; Institutes; Kinetics; Kupffer Cells; Label; Lead; Life; Link; Liver; Liver Failure; Lobule; Maps; Measurement; Measures; Medicine; Metabolic Pathway; Metabolism; Methods; Microscopic; Microscopy; Mission; Modality; Modeling; Modification; Morphology; Mouse Strains; Mus; National Institute of Diabetes and Digestive and Kidney Diseases; Obstruction; Organ; Organ failure; Outcome; Patients; Pharmaceutical Preparations; Pharmacologic Substance; Population Genetics; Positioning Attribute; Predisposition; Process; Publishing; Reactive Oxygen Species; Reporting; Resources; Risk; S-Phase Fraction; Serologic tests; Serum Markers; Signal Pathway; Simulate; Site; Spatial Distribution; Systems Biology; Techniques; Testing; Therapeutic Agents; Thick; Three-Dimensional Imaging; Time; Tissues; Toxic Environmental Substances; Toxic effect; Toxicology; Toxin; Universities; Variant; Western World; Xenobiotics; acetaminophen overdose; acute liver injury; base; bile canaliculus structure; body system; cell motility; cell type; human data; improved; in vivo; intravital imaging; intravital microscopy; liver function; liver injury; medical schools; model development; neutrophil; novel; open source; predictive modeling; public health relevance; research study; simulation; simulation software; spatiotemporal; tool

DESCRIPTION (provided by applicant): Pharmacological and toxicological processes occur across a wide range of spatial and temporal scales and include multiple organ systems. A Systems Biology in silico toxicological model must include submodels that cover the multiple scales and the multiple tissues relevant to human medicine and toxicology. We will develop a liver centered mechanism based multiscale in silico simulation framework for xenobiotic toxicity and metabolism that incorporates four key biological scales: Population genetic and exposure variation scale Physiologically Based Pharmacokinetic (PBPK) whole body scale Tissue level and multicellular scale Subcellular signaling and metabolic pathways scales The multiscale in silico simulation will be centered on the liver, a critical organ in many toxicological, pharmacological, normal and disease processes. For our initial simulations of toxic challenge to the liver we will build a mechanism based in silico simulation of Acetaminophen (APAP) toxicity. APAP is a widely used over-the-counter pain reliever and fever reducer. An acute overdose of APAP is a leading cause of liver failure in the western world. APAP overdose leads to centrilobular liver necrosis that can progress to liver failure and in some cases patient death. Our multiscale in silico simulation will link existing open source modeling tools for the various spatiotemporal scales into an aggregate in silico model. This approach allows us to leverage existing tools, modeling modalities and models at the individual biological scales. Furthermore, this approach facilitates swapping models at individual scales without extensive modification of the sub-models at the other scales and allows us to leverage existing model development tools and resources. The complete multiscale in silico model will provide a mechanism based framework that incorporates effects at the various scales and will also provide a framework to predict changes in clinically used serum markers of liver function and failure. Our in silico simulation will be calibrated using microscopic imaging in the liver of a living mouse, mouse liver immune-histology, along with standard histology and serology in animal studies of APAP toxicity. The proposed in silico model is a first step in toxicity prediction 1. 2. 3. 4. simulatio that ultimately will lead to improved techniques for prediction toxicity of therapeutic agents and environmental toxins while simultaneously reducing the need for animal toxicity studies.

描述（由申请方提供）：药理学和毒理学过程发生在广泛的空间和时间尺度上，包括多个器官系统。系统生物学计算机毒理学模型必须包括涵盖与人类医学和毒理学相关的多个尺度和多个组织的子模型。我们将开发一个以肝脏为中心的机制为基础的多尺度计算机模拟框架，用于生物外源性毒性和代谢，其中包括四个关键的生物尺度：群体遗传和暴露变化量表基于生理学的药代动力学（PBPK）全身量表组织水平和多细胞量表亚细胞信号传导和代谢途径量表多尺度计算机模拟将以肝脏为中心，在许多毒理学、药理学、正常和疾病过程中的关键器官。对于我们对肝脏毒性挑战的初步模拟，我们将建立一个基于对乙酰氨基酚（APAP）毒性计算机模拟的机制。APAP是一种广泛使用的非处方止痛药和退烧药。急性过量的APAP是西方世界肝衰竭的主要原因。APAP过量导致小叶中心肝坏死，可进展为肝功能衰竭，在某些情况下导致患者死亡。我们的多尺度计算机模拟将把现有的各种时空尺度的开源建模工具链接到一个聚合的计算机模型中。这种方法使我们能够利用现有的工具，建模方式和模型在个人的生物尺度。此外，这种方法便于在单个尺度上交换模型，而无需在其他尺度上大量修改子模型，并允许我们利用现有的模型开发工具和资源。完整的多尺度计算机模拟模型将提供一个基于机制的框架，该框架整合了各种尺度的效应，还将提供一个框架来预测临床使用的肝功能和肝功能衰竭血清标志物的变化。我们的计算机模拟将使用活体小鼠肝脏的显微成像进行校准，小鼠肝脏 免疫组织学，沿着标准组织学和APAP毒性动物研究中的血清学。提出的计算机模型是毒性预测的第一步1。2. 3. 4.模拟，最终将导致改进的技术，用于预测治疗剂和环境毒素的毒性，同时减少对动物毒性研究的需要。