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      Pathobiology of magnesium deficiency: a cytokine/neurogenic inflammation hypothesis.

      The American journal of physiology
      Animals, Cytokines, blood, physiology, Inflammation, etiology, metabolism, physiopathology, Magnesium Deficiency, Mice, Mice, Inbred BALB C, Models, Biological, Nervous System Physiological Phenomena, Rats, Rats, Sprague-Dawley, Substance P, Time Factors

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          Abstract

          During the progression of Mg deficiency in a rodent model, we have observed dramatic increases in serum levels of inflammatory cytokines [interleukin-1 (IL-1), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-alpha)] after 3 wk on a Mg-deficient diet. Sequential analyses of these cytokine changes in the serum of rats revealed an initial rise at day 12, followed by a major elevation in all three cytokine levels by day 21. Of greater interest was an early peak in the serum level of the neuropeptide substance P after only 5 days on the diet. This "neuronal" tachykinin is thought to be released from neural tissues, and it is known to stimulate production of certain cytokines, including IL-1, IL-6, and TNF-alpha. In addition, there was a concomitant increase in histamine levels, which may have resulted from stimulation and degranulation of mast cells by substance P. Thus we hypothesize that the release of substance P may be the earliest pathophysiological event leading to stimulation of the inflammatory cytokines, which may then stimulate the free radical mechanisms of injury previously confirmed by our work.

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