Multiple sclerosis (MS) is the most common inflammatory demyelinating disease of the central nervous system (CNS) in young adults. The proinflammatory cytokines such as interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), and nitric oxide (NO) which are known to be produced by inflammatory cells play a key role in the pathogenesis of MS. Some metabolic changes may have an effect on axonal transmission, and white blood cells NO and other inflammatory mediators such as cytokines may be affected from cooling process. In this study, we evaluated the effects of body cooling procedure on proinflammatory cytokines such as TNF-α, IFN-γ, and NO levels. Twenty patients with MS were evaluated. Thirteen of the patients were women, 7 were men (mean age: 33.6 ± 7.5 yrs.). Body temperature was reduced by an average of 1°C approximately in 1 hour with using the "Medivance Arctic Sun Temperature Management System" device. In our study, the decrease in TNF-α, IFN-γ levels after the cooling procedure has no statistical significance, whereas the decrease in the mean level of NO level after the cooling procedure is 4.63 ± 7.4 μmol/L which has statistical significance (P = 0.002). These results suggested that the decrease in NO level improves conduction block in demyelinated axonal segments after cooling procedure in multiple sclerosis.
Keyphrases
- multiple sclerosis
- nitric oxide
- rheumatoid arthritis
- dendritic cells
- induced apoptosis
- mass spectrometry
- young adults
- minimally invasive
- immune response
- oxidative stress
- cell cycle arrest
- ms ms
- spinal cord injury
- end stage renal disease
- white matter
- ejection fraction
- newly diagnosed
- chronic kidney disease
- prognostic factors
- signaling pathway
- climate change
- endoplasmic reticulum stress
- adipose tissue
- hydrogen peroxide
- cell death
- insulin resistance
- nitric oxide synthase
- skeletal muscle
- cell proliferation
- pi k akt