2. Mechanisms of Action

oxidative stress

Definition

Oxidative stress occurs when there is an imbalance between the production of reactive oxygen species (ROS) and the cellular antioxidant defense mechanisms. ROS, including superoxide radicals, hydrogen peroxide, and hydroxyl radicals, are generated during normal cellular metabolism, particularly in mitochondria. When ROS accumulate beyond the cell's neutralizing capacity, they damage proteins, lipids, and DNA through oxidation reactions. This cellular state is implicated in aging, neurodegenerative diseases, cancer, cardiovascular disorders, and inflammatory conditions. Cells respond through activation of antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase) and transcription factors like NRF2, which regulate protective gene expression. Understanding oxidative stress pathways is crucial for developing therapeutic interventions targeting redox homeostasis.

Visualize oxidative stress in Nodes Bio

Researchers can map oxidative stress networks by visualizing interactions between ROS-generating enzymes, antioxidant defense proteins, and downstream signaling cascades. Network analysis reveals how oxidative damage propagates through cellular pathways, identifies key regulatory nodes like NRF2 and KEAP1, and shows crosstalk between mitochondrial dysfunction and inflammatory responses. This enables identification of therapeutic targets and biomarkers in oxidative stress-related diseases.

Visualization Ideas:

  • ROS-generating enzyme networks connected to antioxidant defense pathways
  • Mitochondrial dysfunction cascades showing oxidative damage propagation to cellular compartments
  • Drug-target networks mapping compounds that modulate oxidative stress responses
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Example Use Case

A pharmaceutical team investigating Alzheimer's disease uses network visualization to map how amyloid-beta accumulation triggers oxidative stress in neurons. They construct a multi-layer network connecting mitochondrial dysfunction, ROS production, lipid peroxidation markers, and neuroinflammatory cytokines. By analyzing network topology, they identify that inhibiting NADPH oxidase reduces oxidative damage propagation through multiple downstream pathways, revealing it as a promising drug target. The visualization also uncovers unexpected connections between oxidative stress markers and tau phosphorylation pathways.

Related Terms

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