Adverse Outcome Pathway on antagonist binding to PPARα leading to body-weight loss

K. Gust, Mitchell S. Wilbanks, Zachary A. Collier, L. Burgoon, E. Perkins
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引用次数: 2

Abstract

The present AOP describes antagonistic chemical binding to the peroxisome proliferator-activated receptor α (PPARα), resulting in preferential binding a co-repressor to the overall PPARα signalling complex causing a chain of events that includes: antagonism of PPARα nuclear signalling, decreased transcriptional expression of PPARα-regulated genes that support energy metabolism, inhibited metabolic energy production (decreased fatty acid beta oxidation and ketogenesis), and increase in catabolism of muscle protein, culminating with starvation-like weight loss. The AOP is likely to be synergised during fasting, starvation or malnutrition events. The adverse outcome of this AOP is body-weight loss, which within the context of dynamic energy budget theory, decreases energy allocations to organismal maturation and reproduction and has been demonstrated to negatively affect ecological fitness.
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拮抗剂与PPARα结合导致体重减轻的不良结局途径
目前的AOP描述了与过氧化物酶体增殖体激活受体α (PPARα)的拮抗化学结合,导致对整个PPARα信号复合物的协同抑制因子的优先结合,导致一系列事件,包括:PPARα核信号的拮抗,支持能量代谢的PPARα调节基因的转录表达减少,抑制代谢能量产生(减少脂肪酸β氧化和生酮),增加肌肉蛋白的分解代谢,最终导致饥饿样的体重减轻。AOP很可能在禁食、饥饿或营养不良的情况下协同工作。这种AOP的不利结果是体重下降,在动态能量预算理论的背景下,它减少了对生物体成熟和繁殖的能量分配,并已被证明对生态适应性产生负面影响。
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