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Treating Surfaces with a Cold Atmospheric Pressure Plasma using the COST-Jet
Published on: November 2, 2020
Cold Atmospheric Plasma Promotes Anti-Inflammatory and Regenerative Responses in Oral Soft Tissue through
Tien Ngoc Thuy Nguyen1,2, Byung-Hoon Kim1,2
1Convergence research center for treatment of oral soft tissue disease (MRC), Chosun University, Gwangju 61452, Republic of Korea.
Cold atmospheric plasma (CAP) therapy uses reactive oxygen and nitrogen species to reduce oral inflammation and promote tissue healing by regulating cellular redox balance and mitochondrial function.
Area of Science:
- Biomedical Engineering
- Oral Biology
- Plasma Medicine
Background:
- Cold atmospheric plasma (CAP) is explored for oral soft-tissue regeneration and inflammation control.
- Understanding the underlying mechanisms, particularly redox and mitochondrial regulation, is crucial for therapeutic application.
Purpose of the Study:
- To investigate how helium-based CAP influences redox balance and mitochondrial function in lipopolysaccharide (LPS)-challenged human gingival fibroblasts (HGF-1).
- To elucidate the role of reactive oxygen and nitrogen species (RONS) and hydrogen peroxide (H2O2) in mediating CAP's anti-inflammatory and regenerative effects.
Main Methods:
- Human gingival fibroblasts (HGF-1) were stimulated with LPS and treated with helium CAP.
- Optical emission spectroscopy and infrared thermography characterized the plasma.
- Intracellular H2O2 levels, NF-κB activation, inflammatory cytokine secretion (IL-6, IL-1β, TNF-α), collagen I expression, cell migration, proliferation, and mitochondrial function (ROS, membrane potential, biogenesis) were assessed.
- Catalase was used to confirm the role of H2O2.
Main Results:
- CAP generated a nonthermal plasma plume rich in RONS.
- CAP transiently increased H2O2 without cytotoxicity, restoring redox balance and suppressing oxidative stress.
- CAP attenuated LPS-induced NF-κB activation and reduced IL-6, IL-1β, and TNF-α secretion.
- CAP enhanced collagen I expression, cell migration, and proliferation, indicating a shift towards regeneration.
- CAP activated the PGC-1α/NRF-1/TFAM pathway, improving mitochondrial function and promoting biogenesis.
- Catalase treatment abolished CAP's effects, confirming H2O2 as the key mediator.
Conclusions:
- CAP is a non-pharmacological, redox-regulatory tool for oral soft-tissue inflammation and regeneration.
- CAP integrates oxidative and mitochondrial signaling to resolve inflammation and promote healing.
- Hydrogen peroxide is identified as the central mediator of CAP's therapeutic effects in this context.
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