NovoTHOR® is a systemic Photobiomodulation Therapy used by Olympic athletes, professional NFL, MMA, and NBA players to aid their recovery and keep them at peak performance.
Our mission at the AIM Clinic is to bring the best therapies being used by top athletes, such as NovoTHOR®, and make it available to our local community to help reduce chronic disease and pain and enable true healing.
Photobiomodulation therapy (PBM Therapy) is the application of monochromatic light to improve the speed and quality of tissue repair through modulation of inflammation by enhancing mitochondrial function. The NovoTHOR® delivers 2.7kW of power to the body using the wavelengths 660 nm (Red) & 850 nm (Near-Infrared). The goal is to boost energy, increase immunity, decrease inflammation, and activate stem cells for healing. Treatments are 5-20 minutes based on tolerance because it can trigger a Herxheimer and/or Detox reactions for some patients.
Potentially Beneficial For:
Potentially Beneficial For:
Most of the effects of PBM Therapy can be explained by light absorption in the mitochondria which are the energy producers of most of the cells in our body. After the mitochondria absorb these specific wavelengths of light, Nitric Oxide (circulation) is released, ATP (energy) increases, and ROS (oxidative stress) is modulated. This ultimately can lead to Less Pain, Less Inflammation, Less Edema, and Tissue Repair.
These cascading benefits can be found in the below graph:
The benefit on the mitochondria can even be seen visually. With the specic wavelengths of light used in PBM, regular mitochondria ("a" in below picture) can be transformed into “Giant Mitochondria” ("b" in below picture). The sources of mitochondria in our bodies include stem cells, immune cells, muscle cells, nerve cells, and brain cells. This likely explains the diverse benefits seen with NovoTHOR® therapy!
NovoTHOR® is a Class I Medical Devices. NovoTHOR® is built according to current Good Manufacturing Practices (cGMP) and is in compliance with applicable standards as required by FDA.
Dr. Andrew Chevalier and Susie Clare, NP-C are trained by Dr. Frank Shallenberger for Ozone Therapy and Prolozone®.
Please call us today at 603-583-4603 fill out the form below and we will be in contact with you to schedule an appointment.
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1. Karu, T.I., Mitochondrial signaling in mammalian cells activated by red and near-IR radiation. Photochem Photobiol, 2008. 84(5): p. 1091-9.
2. Eells, J.T., et al., Mitochondrial signal transduction in accelerated wound and retinal healing by near-infrared light therapy. Mitochondrion, 2004. 4(5-6): p. 559-67.
3. Karu, T., Mitochondrial mechanisms of photobiomodulation in context of new data about multiple roles of ATP. Photomedicine and Laser Surgery, 2010. 28 (2): p. 159-60.
4. Palacios-Callender, M., et al., Endogenous NO regulates superoxide production at low oxygen concentrations by modifying the redox state of cytochrome c oxidase. Proceedings of the National Academy of Sciences of the United States of America, 2004. 101 (20): p. 7630-5.
5. Cleeter, M.W., et al., Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide. Implications for neurodegenerative diseases. FEBS letters, 1994. 345(1): p. 50-4.
6. Antunes, F., A. Boveris, and E. Cadenas, On the mechanism and biology of cytochrome oxidase inhibition by nitric oxide. Proc. Natl. Acad. Sci. USA, 2004. 101: p. 16774-9.
7. Galkin, A., A. Higgs, and S. Moncada, Nitric oxide and hypoxia. Essays in biochemistry, 2007. 43: p. 29-42.
8. Lane, N., Cell biology: power games. Nature, 2006. 443(7114): p. 901-3.
9. Bolanos, J.P., et al., Nitric oxide-mediated inhibition of the mitochondrial respiratory chain in cultured astrocytes. Journal of neurochemistry, 1994. 63(3): p. 910-6.
10. Chen, S., Natural products triggering biological targets--a review of the anti-inflammatory phytochemicals targeting the arachidonic acid pathway in allergy asthma and rheumatoid arthritis. Current drug targets, 2011. 12(3): p. 288-301.