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Mitochondrial Function and Root-Filled Teeth - Detrimental and Unknown Interfaces in Systemic Immune Diseases
Johann Lechner1, Wolfgang Mayer2
1Immunology, Clinic Integrative Dentistry, Munich, Germany.
International Journal of General Medicine
|August 9, 2020
Summary
Root-filled teeth (RFT) can release toxins that reduce cellular energy production. This study found that toxins from RFTs decreased adenosine triphosphate (ATP) activity in patient cells, suggesting a link to mitochondriopathies.
Area of Science:
- Biochemistry
- Immunology
- Dental Medicine
Background:
- Mitochondriopathy is increasingly linked to immune system disorders.
- The potential for root-filled teeth (RFT) to release toxins has been debated, but their impact on mitochondrial adenosine triphosphate (ATP) activity is under-researched.
- Limited methods exist for assessing toxin release from teeth.
Purpose of the Study:
- To investigate toxin release from RFTs.
- To determine the effect of RFT-derived toxins (Tox-sol) on mitochondrial ATP activity in patients.
Main Methods:
- Root-filled teeth (RFTs) were extracted and placed in an aqueous solution for 24 hours to create a toxin solution (Tox-sol).
- Toxin release was assessed using a volatile sulfur compound indicator (VSCI).
- Peripheral blood mononuclear cells (PBMCs) from patients were exposed to diluted Tox-sol (1:100), and changes in mitochondrial ATP activity were measured.
Main Results:
- Exposure to Tox-sol reduced overall ATP activity by approximately 10% in the study population (n=30).
- Three distinct patient responses were observed: significantly reduced ATP activity (n=16), neutral effect (n=10), and increased ATP activity (n=4).
- Non-disease-specific inhibition of ATP activity was noted in patients with rheumatism, neurological disorders, allergies, and tumors.
Conclusions:
- Toxins from RFTs can inhibit mitochondrial ATP activity, potentially contributing to mitochondriopathies.
- A practical VSCI effectively indicated toxic sulfur compounds released from RFTs.
- While disease-specific effects were not identified within the study's limitations, RFT toxins warrant further investigation as a factor in disease development.
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