Gary Nicholas C, Misganaw Burook, Hammamieh Rasha, Gautam Aarti
Medical Readiness Systems Biology, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
The Geneva Foundation, Tacoma, WA, United States.
Front Genet. 2024 Jul 25;15:1394630. doi: 10.3389/fgene.2024.1394630. eCollection 2024.
Acute Stress Disorder (ASD) is a psychiatric condition that can develop shortly after trauma exposure. Although molecular studies of ASD are only beginning, groups of metabolites have been found to be significantly altered with acute stress phenotypes in various pre-clinical and clinical studies. ASD implicated metabolites include amino acids (β-hydroxybutyrate, glutamate, 5-aminovalerate, kynurenine and aspartate), ketone bodies (β-hydroxybutyrate), lipids (cortisol, palmitoylethanomide, and N-palmitoyl taurine) and carbohydrates (glucose and mannose). Network and pathway analysis with the most prominent metabolites shows that Extracellular signal-regulated kinases and c-AMP response element binding (CREB) protein can be crucial players. After highlighting main recent findings on the role of metabolites in ASD, we will discuss potential future directions and challenges that need to be tackled. Overall, we aim to showcase that metabolomics present a promising opportunity to advance our understanding of ASD pathophysiology as well as the development of novel biomarkers and therapeutic targets.
急性应激障碍(ASD)是一种在创伤暴露后不久可能出现的精神疾病。尽管对ASD的分子研究才刚刚起步,但在各种临床前和临床研究中,已发现几组代谢物会随着急性应激表型而发生显著变化。与ASD相关的代谢物包括氨基酸(β-羟基丁酸、谷氨酸、5-氨基戊酸、犬尿氨酸和天冬氨酸)、酮体(β-羟基丁酸)、脂质(皮质醇、棕榈酰乙醇胺和N-棕榈酰牛磺酸)和碳水化合物(葡萄糖和甘露糖)。对最突出代谢物的网络和通路分析表明,细胞外信号调节激酶和c-AMP反应元件结合(CREB)蛋白可能是关键因素。在强调了代谢物在ASD中作用的近期主要发现之后,我们将讨论未来潜在的方向以及需要应对的挑战。总体而言,我们旨在表明代谢组学为推进我们对ASD病理生理学的理解以及新型生物标志物和治疗靶点的开发提供了一个很有前景的机会。