Spinal Cord Research Help
AboutCategoriesLatest ResearchContact
Subscribe
Spinal Cord Research Help

Making Spinal Cord Injury (SCI) Research Accessible to Everyone. Simplified summaries of the latest research, designed for patients, caregivers and anybody who's interested.

Quick Links

  • Home
  • About
  • Categories
  • Latest Research
  • Disclaimer

Contact

  • Contact Us
© 2025 Spinal Cord Research Help

All rights reserved.

  1. Home
  2. Research
  3. Physiology
  4. Single-atom catalysts-based catalytic ROS clearance for efficient psoriasis treatment and relapse prevention via restoring ESR1

Single-atom catalysts-based catalytic ROS clearance for efficient psoriasis treatment and relapse prevention via restoring ESR1

Nature Communications, 2023 · DOI: 10.1038/s41467-023-42477-y · Published: October 27, 2023

PhysiologyBiomedicalDermatology

Simple Explanation

Psoriasis, a common skin disease with a high recurrence rate, is linked to elevated levels of reactive oxygen species (ROS). This study introduces biomimetic iron single-atom catalysts (FeN4O2-SACs) capable of scavenging ROS. These catalysts mimic natural antioxidant enzymes, effectively reducing psoriasis-like symptoms and preventing relapse in experiments. The core mechanism involves the upregulation of estrogen receptor 1 (ESR1), a protein found to be reduced in psoriasis patients. This research suggests a new approach to psoriasis treatment, termed psoriasis catalytic therapy (PCT), inspired by multienzyme bionics (MIB), which offers a 'safe, effective, and long-term' therapeutic modality.

Study Duration
Not specified
Participants
Mice
Evidence Level
Not specified

Key Findings

  • 1
    FeN4O2-SACs exhibit multiple enzyme-mimicking activities, analogous to natural antioxidant enzymes, demonstrating broad-spectrum ROS scavenging capability.
  • 2
    In vitro and in vivo experiments demonstrate that FeN4O2-SACs effectively ameliorate psoriasis-like symptoms and prevent relapse, showing augmented efficacy compared to calcipotriol.
  • 3
    The upregulation of estrogen receptor 1 (ESR1) is identified as the core protein upregulated in psoriasis treatment through RNA sequencing and bioinformatic analysis.

Research Summary

This study introduces a 'psoriasis catalytic therapy' strategy using biomimetic materials (FeN4O2-SACs) to continuously scavenge overexpressed ROS, thereby ameliorating psoriatic lesions and preventing recurrence. FeN4O2-SACs effectively inhibit hyperproliferation and inflammatory infiltration in psoriasis by ROS elimination, demonstrating superior efficacy compared to clinical calcipotriol in IMQ-induced psoriasis-like mouse models. Mechanistically, FeN4O2-SACs treatment inhibits ESR1 deficiency via ESR1 upregulation, leading to significant reductions in psoriasis recurrence, highlighting a promising therapeutic pathway.

Practical Implications

Therapeutic Modality

Psoriasis catalytic therapy (PCT) offers a novel therapeutic modality for psoriasis treatment and relapse prevention.

Drug Development

Multienzyme-inspired bionics (MIB) can guide the development of new drugs that mimic the function of multiple natural enzymes.

Clinical Application

FeN4O2-SACs demonstrate potential for clinical application due to their ability to effectively treat psoriasis-like symptoms and prevent relapse without significant side effects.

Study Limitations

  • 1
    The study focuses on mice, and further research is needed to validate these findings in human clinical trials.
  • 2
    The long-term effects and potential toxicity of FeN4O2-SACs require further investigation.
  • 3
    The precise mechanisms of ESR1 upregulation by FeN4O2-SACs need further elucidation.

Your Feedback

Was this summary helpful?

Back to Physiology