Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA; University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-9014, USA.
Department of Biochemistry and Molecular Biology, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Cell Rep Med. 2024 Sep 17;5(9):101714. doi: 10.1016/j.xcrm.2024.101714. Epub 2024 Sep 5.
Metabolic dysfunction-associated steatotic liver disease (MASLD) prevalence is increasing annually and affects over a third of US adults. MASLD can progress to metabolic dysfunction-associated steatohepatitis (MASH), characterized by severe hepatocyte injury, inflammation, and eventual advanced fibrosis or cirrhosis. MASH is predicted to become the primary cause of liver transplant by 2030. Although the etiology of MASLD/MASH is incompletely understood, dysregulated fatty acid oxidation is implicated in disease pathogenesis. Here, we develop a method for estimating hepatic β-oxidation from the metabolism of [D]octanoate to deuterated water and detection with deuterium magnetic resonance methods. Perfused livers from a mouse model of MASLD reveal dysregulated hepatic β-oxidation, findings that corroborate in vivo imaging. The high-fat-diet-induced MASLD mouse studies indicate that decreased β-oxidative efficiency in the fatty liver could serve as an indicator of MASLD progression. Furthermore, our method provides a clinically translatable imaging approach for determining hepatic β-oxidation efficiency.
代谢功能障碍相关脂肪性肝病(MASLD)的患病率逐年上升,影响了超过三分之一的美国成年人。MASLD 可进展为代谢功能障碍相关脂肪性肝炎(MASH),其特征为严重的肝细胞损伤、炎症,最终发展为晚期纤维化或肝硬化。预计到 2030 年,MASH 将成为肝移植的主要原因。尽管 MASLD/MASH 的病因尚不完全清楚,但脂肪酸氧化失调与疾病发病机制有关。在这里,我们开发了一种从[D]辛烷酸代谢到氘化水并通过氘磁共振方法检测的方法来估计肝β-氧化。MASLD 小鼠模型的灌注肝脏显示出肝β-氧化失调,这一发现与体内成像结果一致。高脂肪饮食诱导的 MASLD 小鼠研究表明,脂肪肝中β氧化效率的降低可以作为 MASLD 进展的指标。此外,我们的方法为确定肝β氧化效率提供了一种可临床转化的成像方法。