Psoriasis

Psoriasis is a chronic inflammatory immune disease that causes itchy, scaly red patches to develop on the skin. These patches tend to flare up and then go into remission, and although some medications help manage symptoms, many patients continue to experience adverse side effects (1). Psoriasis involves overactivation of TH 17, a type of cell that causes an inflammatory response. This is likely because the cells that suppress TH 17, called T regulatory cells (Tregs), are impaired in people with psoriasis (2, 3). Treatments that can either decrease TH 17 activity or increase Treg function have the potential to reduce the symptoms present in psoriasis (4). Additionally, patients with psoriasis exhibit weakened blood circulation due to decreased availability of nitric oxide (5).

Extivita Therapies for Psoriasis:

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Extivita Therapies for Psoriasis Recovery:

Hyperbaric Oxygen Therapy

Hyperbaric Oxygen Therapy

Hyperbaric Oxygen Therapy

Supplements

Hyperbaric Oxygen Therapy

Nutritional IV Therapy

Pulsed Electromagnetic Field Therapy (PEMF)

Pulsed Electromagnetic Field Therapy

Hyperbaric Oxygen Therapy for Psoriasis:

Hyperbaric Oxygen Therapy - Chapel Hill
Hyperbaric oxygen therapy (HBOT) is known the increase levels of reactive oxygen species (ROS) which modulate signaling pathways that induce cell protection (6). Increased levels of ROS are associated with improved Treg function, suggesting a potential for reducing the inflammatory response in psoriasis (4, 6).

This potential has been realized in animal models where HBOT reduced the symptoms of psoriasis (4). HBOT has also been shown to successfully remove symptoms of severe psoriasis vulgaris in human patients (7). Lastly, HBOT may improve blood circulation in patients with psoriasis by increasing levels of nitric oxide (5, 6).
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Effects of HBOT on Psoriasis:

Grows New Blood Vessels

New Blood Vessel Formation

Hyperbaric oxygen therapy stimulates the formation of new blood vessels, healing injured tissues that were unable to get nutrients and oxygen.

Decreases Inflammation

Decreased Inflammation

Hyperbaric oxygen therapy reduces systemic inflammation by increasing anti-inflammatory gene expression and decreasing proinflammatory genes.
Increases Stem Cell Production

Increased Stem Cell Activity

Hyperbaric oxygen therapy mobilizes stem progenitor cells (SPCs) from the bone marrow, creating the opportunity for tissue regeneration.

IV Therapy for Psoriasis:

People with psoriasis have been shown to have insufficient antioxidant activity. Such a dysfunction plays a key role in the inflammation involved in this disease process (8). Multiple parts of the Myers’ IV, including magnesium, vitamin C, and vitamin B12 have been shown to reduce oxidative stress and inflammation present in psoriasis (9, 10, 11). Additionally, glutathione been shown to reduce symptoms due to its potent antioxidant properties (12,13).

Learn More About Nutritional IV Therapy
Hyperbaric Oxygen Therapy - Chapel Hill
BEMER Pulsed Electromagnetic Field Therapy in Durham, NC

Pulsed Electromagnetic Field Therapy for Psoriasis:

PEMF is a form of pulse electromagnetic frequency (PEMF) therapy. PEMF has many positive benefits, one of them being its anti-inflammatory effects (14, 15). Because psoriasis is an inflammatory disease, PEMF’s proven anti-inflammatory properties have the potential to reduce symptoms. Studies show that presence of systemic microvascular dysfunction in individuals with psoriasis (12). BEMER therapy improves microcirculation and when used with HBOT, can be powerful treatment for psoriasis.

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News & Research for Psoriasis:

Hyperbaric oxygen – its mechanisms and efficacy

Hyperbaric oxygen – its mechanisms and efficacy

Jan 4, 2012 | , , , , , , , ,

Principal mechanisms of HBO2 are based on intracellular generation of reactive species of oxygen and nitrogen. Reactive species are recognized to play a central role in cell signal transduction cascades and the discussion will focus on these pathways. Systematic reviews and randomized clinical trials support clinical use of HBO2 for refractory diabetic wound healing and radiation injuries; treatment of compromised flaps and grafts and ischemia-reperfusion disorders is supported by animal studies and a small number of clinical trials, but further studies are warranted.

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References
  1. “Psoriasis – Symptoms and Causes.” Mayo Clinic. www.mayoclinic.org, https://www.mayoclinic.org/diseases-conditions/psoriasis/symptoms-causes/syc-20355840. Accessed 27 July 2020.
  2. Quaglino, P., et al. “Th1, Th2, Th17 and Regulatory T Cell Pattern in Psoriatic Patients: Modulation of Cytokines and Gene Targets Induced by Etanercept Treatment and Correlation with Clinical Response.” Dermatology (Basel, Switzerland), vol. 223, no. 1, 2011, pp. 57–67. PubMed, doi:10.1159/000330330.
  3. Sugiyama, Hideaki, et al. “Dysfunctional Blood and Target Tissue CD4+CD25high Regulatory T Cells in Psoriasis: Mechanism Underlying Unrestrained Pathogenic Effector T Cell Proliferation.” Journal of Immunology (Baltimore, Md.: 1950), vol. 174, no. 1, Jan. 2005, pp. 164–73. PubMed, doi:10.4049/jimmunol.174.1.164.
  4. Kim, Hyung-Ran, et al. “Reactive Oxygen Species Prevent Imiquimod-Induced Psoriatic Dermatitis through Enhancing Regulatory T Cell Function.” PLoS ONE, vol. 9, no. 3, Mar. 2014. PubMed Central, doi:10.1371/journal.pone.0091146.
  5. Alba, Billie K., et al. “Endothelial Function Is Impaired in the Cutaneous Microcirculation of Adults with Psoriasis through Reductions in Nitric Oxide-Dependent Vasodilation.” American Journal of Physiology. Heart and Circulatory Physiology, vol. 314, no. 2, 01 2018, pp. H343–49. PubMed, doi:10.1152/ajpheart.00446.2017.
  6. Thom, Stephen R. “Hyperbaric Oxygen – Its Mechanisms and Efficacy.” Plastic and Reconstructive Surgery, vol. 127, no. Suppl 1, Jan. 2011, pp. 131S-141S. PubMed Central, doi:10.1097/PRS.0b013e3181fbe2bf.
  7. Butler, Glenn, et al. “Therapeutic Effect of Hyperbaric Oxygen in Psoriasis Vulgaris: Two Case Reports and a Review of the Literature.” Journal of Medical Case Reports, vol. 3, Aug. 2009, p. 7023. PubMed Central, doi:10.1186/1752-1947-0003-0000007023.
  8. Yildirim, M., et al. “The Role of Oxidants and Antioxidants in Psoriasis.” Journal of the European Academy of Dermatology and Venereology: JEADV, vol. 17, no. 1, Jan. 2003, pp. 34–36. PubMed, doi:10.1046/j.1468-3083.2003.00641.x.
  9. Zheltova, Anastasia A., et al. “Magnesium Deficiency and Oxidative Stress: An Update.” BioMedicine, vol. 6, no. 4, Nov. 2016. PubMed Central, doi:10.7603/s40681-016-0020-6.
  10. Office of Dietary Supplements – Vitamin C. ods.od.nih.gov, https://ods.od.nih.gov/factsheets/VitaminC-HealthProfessional/. Accessed 31 July 2020.
  11. Al-Daghri, Nasser M., et al. “Association of Vitamin B12 with Pro-Inflammatory Cytokines and Biochemical Markers Related to Cardiometabolic Risk in Saudi Subjects.” Nutrients, vol. 8, no. 9, Sept. 2016. PubMed Central, doi:10.3390/nu8090460.
  12. Prussick, Ronald, et al. “Psoriasis Improvement in Patients Using Glutathione-Enhancing, Nondenatured Whey Protein Isolate: A Pilot Study.” The Journal of Clinical and Aesthetic Dermatology, vol. 6, no. 10, Oct. 2013, pp. 23–26.
  13. Gaucher, Caroline, et al. “Glutathione: Antioxidant Properties Dedicated to Nanotechnologies.” Antioxidants, vol. 7, no. 5, Apr. 2018. PubMed Central, doi:10.3390/antiox7050062.
  14. Ross, Christina L., et al. “The Use of Pulsed Electromagnetic Field to Modulate Inflammation and Improve Tissue Regeneration: A Review.” Bioelectricity, vol. 1, no. 4, Mary Ann Liebert, Inc., publishers, Dec. 2019, pp. 247–59. liebertpub.com (Atypon), doi:10.1089/bioe.2019.0026.
  15. Selvam, Ramasamy, et al. “Low Frequency and Low Intensity Pulsed Electromagnetic Field Exerts Its Antiinflammatory Effect through Restoration of Plasma Membrane Calcium ATPase Activity.” Life Sciences, vol. 80, no. 26, June 2007, pp. 2403–10. PubMed, doi:10.1016/j.lfs.2007.03.019.
  16. Alba, Billie K et al. “Endothelial function is impaired in the cutaneous microcirculation of adults with psoriasis through reductions in nitric oxide-dependent vasodilation.” American journal of physiology. Heart and circulatory physiology vol. 314,2 (2018): H343-H349. doi:10.1152/ajpheart.00446.2017