Targeting deregulated oxidative stress in skin inflammatory diseases: An update on clinical importance

Abdul Q Khan1, Maha Victor Agha1, Khalid Sultan A M Sheikhan1

  • 1Translational Research Institute, Academic Health System, Hamad Medical Corporation, Doha, Qatar.

Insights

This review explores how oxidative stress contributes to inflammatory skin diseases like atopic dermatitis and psoriasis. It highlights natural products as potential treatments targeting reactive oxygen species (ROS) for better patient outcomes.

Area of Science:

  • Dermatology
  • Immunology
  • Biochemistry

Background:

  • The skin acts as a primary defense against environmental exposures.
  • Increased pollution and industrialization correlate with rising rates of skin conditions like dermatitis and psoriasis.
  • Cutaneous inflammatory diseases are complex, necessitating further research for improved patient care.

Purpose of the Study:

  • To review novel insights into reactive oxygen species (ROS) signaling in atopic dermatitis and psoriasis.
  • To explore the role of oxidative stress in the pathogenesis and complications of inflammatory skin diseases.
  • To examine the therapeutic potential of natural products in managing these conditions.

Main Methods:

  • Literature review of pre-clinical and clinical studies.
  • Analysis of signaling mechanisms involving ROS in skin inflammation.
  • Evaluation of natural products for cutaneous disease management.

Main Results:

  • Oxidative stress is increasingly implicated in the pathogenesis and complications of inflammatory skin diseases.
  • ROS-induced signaling pathways are critical in conditions like atopic dermatitis and psoriasis.
  • Natural products show promise for managing symptoms and complications.

Conclusions:

  • Targeting oxidative stress is a promising therapeutic strategy for inflammatory skin diseases.
  • Understanding ROS mechanisms can lead to novel treatment approaches.
  • Natural products offer a viable avenue for managing skin inflammation and its sequelae.