Esvap Elif, Ulgen Kutlu O
Department of Chemical Engineering, Bogazici University, Istanbul 34342, Turkey.
Biomedicines. 2023 Feb 16;11(2):583. doi: 10.3390/biomedicines11020583.
Autism spectrum disorders (ASD) are a heterogeneous group of neurodevelopmental disorders generally characterized by repetitive behaviors and difficulties in communication and social behavior. Despite its heterogeneous nature, several metabolic dysregulations are prevalent in individuals with ASD. This work aims to understand ASD brain metabolism by constructing an ASD-specific prefrontal cortex genome-scale metabolic model (GEM) using transcriptomics data to decipher novel neuroinflammatory biomarkers. The healthy and ASD-specific models are compared via uniform sampling to identify ASD-exclusive metabolic features. Noticeably, the results of our simulations and those found in the literature are comparable, supporting the accuracy of our reconstructed ASD model. We identified that several oxidative stress, mitochondrial dysfunction, and inflammatory markers are elevated in ASD. While oxidative phosphorylation fluxes were similar for healthy and ASD-specific models, and the fluxes through the pathway were nearly undisturbed, the tricarboxylic acid (TCA) fluxes indicated disruptions in the pathway. Similarly, the secretions of mitochondrial dysfunction markers such as pyruvate are found to be higher, as well as the activities of oxidative stress marker enzymes like alanine and aspartate aminotransferases (ALT and AST) and glutathione-disulfide reductase (GSR). We also detected abnormalities in the sphingolipid metabolism, which has been implicated in many inflammatory and immune processes, but its relationship with ASD has not been thoroughly explored in the existing literature. We suggest that important sphingolipid metabolites, such as sphingosine-1-phosphate (S1P), ceramide, and glucosylceramide, may be promising biomarkers for the diagnosis of ASD and provide an opportunity for the adoption of early intervention for young children.
自闭症谱系障碍(ASD)是一组异质性的神经发育障碍,其一般特征为重复行为以及沟通和社交行为方面的困难。尽管具有异质性,但几种代谢失调在ASD个体中普遍存在。这项工作旨在通过利用转录组学数据构建一个特定于ASD的前额叶皮质基因组规模代谢模型(GEM)来理解ASD大脑代谢,以破译新的神经炎症生物标志物。通过均匀采样比较健康模型和特定于ASD的模型,以识别ASD特有的代谢特征。值得注意的是,我们的模拟结果与文献中的结果具有可比性,支持了我们重建的ASD模型的准确性。我们发现,在ASD中,几种氧化应激、线粒体功能障碍和炎症标志物水平升高。虽然健康模型和特定于ASD的模型的氧化磷酸化通量相似,并且该途径的通量几乎未受干扰,但三羧酸(TCA)通量表明该途径存在破坏。同样,发现线粒体功能障碍标志物如丙酮酸的分泌更高,以及氧化应激标志物酶如丙氨酸和天冬氨酸转氨酶(ALT和AST)以及谷胱甘肽二硫化物还原酶(GSR)的活性也更高。我们还检测到鞘脂代谢存在异常,鞘脂代谢与许多炎症和免疫过程有关,但在现有文献中其与ASD的关系尚未得到充分探索。我们认为,重要的鞘脂代谢物,如1 -磷酸鞘氨醇(S1P)、神经酰胺和葡萄糖神经酰胺,可能是诊断ASD的有前景的生物标志物,并为幼儿采用早期干预提供了机会。