Sustained Defense Against Oxidative Stress: Chronic Dosing of Hydrogas and Sodium Metasilicate Shows Lasting Anti-Inflammatory Benefits

Can repeated natural supplementation help combat the harmful cycle of oxidative stress and inflammation? New research in a preclinical model suggests it can.

A study led by Prof. Dr. Daniel F. Martins at the Experimental Neuroscience Laboratory (LANEX–UNISUL) investigated the chronic antioxidative effects of two promising agents — Hydrogas and Sodium Metasilicate (SM) — and found encouraging results for long-term inflammation control.

Background: Inflammation, Oxidative Stress, and the Need for Long-Term Solutions

Chronic inflammation underlies a vast array of modern diseases — from autoimmune and cardiovascular conditions to neurodegenerative disorders. One of the main drivers of this persistent inflammation is oxidative stress, a biochemical imbalance where free radicals overwhelm the body’s natural antioxidant defenses.

While short-term interventions may provide temporary relief, lasting control of oxidative stress requires consistent support. This study sought to determine whether repeated, low-dose administration of Hydrogas and Sodium Metasilicate could reduce oxidative damage and bolster endogenous antioxidant systems over time.

Study Design and Methodology

The researchers used a mouse model of persistent inflammation, triggered by injection of Complete Freund’s Adjuvant (CFA) into the paw — a widely accepted model for simulating chronic inflammatory states.

✅ Study Overview:

  • Subjects: 48 mice divided into 6 groups (n = 8 per group)
  • Groups:
    • Control (tap water)
    • Hydrogas
    • Sodium Metasilicate at 0.3 mg/kg
    • Sodium Metasilicate at 1.1 mg/kg
    • Sodium Metasilicate at 3 mg/kg
    • Sodium Metasilicate at 10 mg/kg
  • Dosing Regimen: Twice daily via oral gavage for five consecutive days
  • Evaluated Tissues: Paw skin, spinal cord, and plasma
  • Measured Outcomes:
    • Oxidative damage: Lipid peroxidation (MDA equivalents) and protein oxidation (carbonyls)
    • Antioxidant defenses: Catalase and Superoxide Dismutase (SOD) enzyme activity
  • Analysis: ELISA for biomarkers; statistical testing via One-Way ANOVA and Tukey’s multiple comparisons

 

Key Results: Antioxidant Effects Across Tissues

🔹 Hydrogas

  • Reduced lipid peroxidation in all tissues (paw, spinal cord, plasma)
  • Reduced protein oxidation in paw and spinal cord, but not plasma
  • Increased catalase activity in plasma only
  • No significant change in SOD levels

 

Interpretation: Hydrogas seems to offer systemic protection, particularly effective against lipid oxidation, with modest influence on localized antioxidant enzyme activation.

 

🔹 Sodium Metasilicate

Oxidative Damage (Lipid and Protein Peroxidation):

  • All doses (0.3–10 mg/kg) reduced lipid peroxidation in paw and spinal cord
  • Only 3 mg/kg showed significant reduction in plasma
  • All doses decreased protein carbonyls in paw
  • Only 10 mg/kg significantly reduced protein oxidation in spinal cord
  • No significant effect on plasma protein oxidation

 

Antioxidant Defense (Enzyme Activity):

  • Catalase:
    • No effect in paw tissue
    • Increased in spinal cord at 0.3 mg/kg
    • Increased in plasma at 0.3 and 1.1 mg/kg
  • SOD:
    • Increased in paw at 1.1 and 3 mg/kg
    • Increased in spinal cord at 3 mg/kg
    • No effect in plasma

 

Interpretation: Sodium Metasilicate provides dose-dependent, tissue-specific antioxidant benefits, with the 1.1 and 3 mg/kg doses delivering the most robust activation of antioxidant defenses in inflamed tissues.

 

Conclusion: Chronic Supplementation Shows Promise

This study demonstrates that repeated administration of Hydrogas or Sodium Metasilicate for just five days can:

  • Reduce oxidative damage in both local and systemic tissues
  • Activate endogenous antioxidant enzymes (particularly catalase and SOD)
  • Offer tissue-specific and dose-sensitive benefits

 

While Hydrogas appears to work primarily on systemic markers of oxidative stress, Sodium Metasilicate, especially at intermediate doses, shows a more nuanced and localized antioxidative response, making it a compelling candidate for targeted interventions.

Implications for Future Research

  • Personalized dosing: Finding the right concentration is key, as higher doses do not always yield better results.
  • Mechanistic studies: The differences in tissue response suggest unique biological pathways for each compound.
  • Longer-term studies: Future research should evaluate chronic use over weeks or months to explore full therapeutic potential.
  • Combination strategies: Could Hydrogas and SM be even more effective when combined? Synergistic effects merit investigation.

 

Final Thoughts

As the demand grows for natural and non-toxic therapies to manage chronic inflammation, this study adds valuable insight into the potential of Hydrogas and Sodium Metasilicate. With proper formulation and dose control, they may emerge as effective tools for long-term management of oxidative stress, reducing the burden of inflammation-related diseases.