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Cysteamine is a stable aminothiol with radioprotective activities.1 It reduces ionizing radiation-induced death and chromosomal damage in mice in a dose-dependent manner.1,2 Cysteamine binds rapidly and temporarily to plasma proteins upon administration and this activity is directly correlated to its radioprotective effects.2 In vitro, 0.1 mM cysteamine depletes 90% of free cystine from cystinotic fibroblasts.3 Formulations containing cysteamine have been used to treat nephropathic cystinosis and reduce glomerular deterioration in humans.4
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1. The protective effect of cysteamine on young mice exposed to roentgen rays. Acta. Radiol. 42(6), 485-493 (1954).
2. The effect of cysteamine, cystamine and hypoxia on mortality and bone marrow chromosome aberrations in mice after total body roentgen irradiation. Acta. Radiol. 44(3), 243-248 (1955).
3. Cystinosis. Intracellular cystine depletion by aminothiols in vitro and in vivo. J. Clin. Invest. 58(1), 180-189 (1976).
4. Predicted reciprocal serum creatinine at age 10 years as a measure of renal function in children with nephropathic cystinosis treated with oral cysteamine. Pediatr. Nephrol. 4(2), 129-135 (1990).