Ahmad Sleiman, Kathleen B. Miller, Danicia Flores, Jaqueline Kuan, Kaitlyn Altwasser, Benjamin J. Smith, Tatiana Kozbenko, Robyn Hocking, Scott J. Wood, Janice Huff, Christelle Adam-Guillermin, Nobuyuki Hamada, Carole Yauk, Ruth Wilkins, Vinita Chauhan
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An AOP was constructed utilizing mechanistic information to build empirical support for the key event relationships (KERs) between the MIE of deposition of energy to the AO of learning and memory impairment through multiple key events (KEs). The evidence for the AOP was acquired through a documented scoping review of the literature. In this AOP, the MIE is connected to the AO via six KEs: increased oxidative stress, increased deoxyribonucleic acid (DNA) strand breaks, altered stress response signaling, tissue resident cell activation, increased pro-inflammatory mediators, and abnormal neural remodeling that encompasses atypical structural and functional alterations of neural cells and surrounding environment. Deposition of energy directly leads to oxidative stress, increased DNA strand breaks, an increase of pro-inflammatory mediators and tissue resident cell activation. 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引用次数: 0
摘要
了解辐射诱发的非癌症对中枢神经系统(CNS)的影响对于医疗(如放射治疗)和职业(如核工作人员和宇航员)辐照的风险评估至关重要。在此,我们采用了不良后果途径(AOP)方法来整合认知能力下降领域的相关研究,以确定研究缺口、制定对策并最终用于风险评估。AOP 是一种分析结构,从分子启动事件 (MIE) 开始,以简化的形式描述不良结果 (AO) 的关键事件。我们利用机理信息构建了一个 AOP,通过多个关键事件(KEs),为能量沉积 MIE 与学习和记忆障碍 AO 之间的关键事件关系(KERs)提供经验支持。AOP 的证据是通过对文献进行有据可查的范围审查获得的。在此 AOP 中,MIE 通过六个关键事件与 AO 相连:氧化应激增加、脱氧核糖核酸(DNA)链断裂增加、应激反应信号改变、组织驻留细胞激活、促炎症介质增加以及神经重塑异常(包括神经细胞和周围环境的非典型结构和功能改变)。能量沉积直接导致氧化应激、DNA 链断裂增加、促炎症介质增加和组织常驻细胞活化。这些 KEs 本身相互关联,可导致神经重塑异常,影响学习和记忆过程。已确定的知识差距包括提高对多个 KER 的 AOP 的定量理解,以及通过实验工作对提出的调节因素进行更多测试。从广义上设想,这些工作的成果可以扩展到其他认知障碍,并补充国际辐射管理机构在审查辐射防护系统方面正在开展的工作。
AOP report: Development of an adverse outcome pathway for deposition of energy leading to learning and memory impairment
Understanding radiation-induced non-cancer effects on the central nervous system (CNS) is essential for the risk assessment of medical (e.g., radiotherapy) and occupational (e.g., nuclear workers and astronauts) exposures. Herein, the adverse outcome pathway (AOP) approach was used to consolidate relevant studies in the area of cognitive decline for identification of research gaps, countermeasure development, and for eventual use in risk assessments. AOPs are an analytical construct describing critical events to an adverse outcome (AO) in a simplified form beginning with a molecular initiating event (MIE). An AOP was constructed utilizing mechanistic information to build empirical support for the key event relationships (KERs) between the MIE of deposition of energy to the AO of learning and memory impairment through multiple key events (KEs). The evidence for the AOP was acquired through a documented scoping review of the literature. In this AOP, the MIE is connected to the AO via six KEs: increased oxidative stress, increased deoxyribonucleic acid (DNA) strand breaks, altered stress response signaling, tissue resident cell activation, increased pro-inflammatory mediators, and abnormal neural remodeling that encompasses atypical structural and functional alterations of neural cells and surrounding environment. Deposition of energy directly leads to oxidative stress, increased DNA strand breaks, an increase of pro-inflammatory mediators and tissue resident cell activation. These KEs, which are themselves interconnected, can lead to abnormal neural remodeling impacting learning and memory processes. Identified knowledge gaps include improving quantitative understanding of the AOP across several KERs and additional testing of proposed modulating factors through experimental work. Broadly, it is envisioned that the outcome of these efforts could be extended to other cognitive disorders and complement ongoing work by international radiation governing bodies in their review of the system of radiological protection.