首页|Reactive Oxygen Species and Oxidative Stress in the Pathogenesis of MAFLD
Reactive Oxygen Species and Oxidative Stress in the Pathogenesis of MAFLD
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NETL
NSTL
万方数据
维普
The pathogenesis of metabolic-associated fatty liver dis-ease (MAFLD) is complex and thought to be dependent on multiple parallel hits on a background of genetic suscep-tibility. The evidence suggests that MAFLD progression is a dynamic two-way process relating to repetitive bouts of metabolic stress and inflammation interspersed with endog-enous anti-inflammatory reparative responses. In MAFLD, excessive hepatic lipid accumulation causes the produc-tion of lipotoxins that induce mitochondrial dysfunction, endoplasmic reticular stress, and over production of reac-tive oxygen species (ROS). Models of MAFLD show marked disruption of mitochondrial function and reduced oxidative capacitance with impact on cellular processes including mi-tophagy, oxidative phosphorylation, and mitochondrial bio-genesis. In excess, ROS modify insulin and innate immune signaling and alter the expression and activity of essential enzymes involved in lipid homeostasis. ROS can also cause direct damage to intracellular structures causing hepatocyte injury and death. In select cases, the use of anti-oxidants and ROS scavengers have been shown to diminish the pro-apoptopic effects of fatty acids. Given this link, endogenous anti-oxidant pathways have been a target of interest, with Nrf2 activation showing a reduction in oxidative stress and inflammation in models of MAFLD. Thyroid hormone recep-tor β (THRβ) agonists and nuclear peroxisome proliferation-activated receptor (PPAR) family have also gained interest in reducing hepatic lipotoxicity and restoring hepatic func-tion in models of MAFLD. Unfortunately, the true interplay between the clinical and molecular components of MAFLD progression remain only partly understood. Most recently, multiomics-based strategies are being adopted for hypoth-esis-free analysis of the molecular changes in MAFLD. Tran-scriptome profiling maps the unique genotype-phenotype associations in MAFLD and with various single-cell tran- scriptome-based projects underway, there is hope of novel physiological insights to MAFLD progression and uncover therapeutic targets.
NETL
NSTL
万方数据
维普
