Abstract
Reactive oxygen species (ROS) are a causal factor in aging, atherosclerosis,carcinogenesis, and infarction (Sheweita and Khoshhal, Curr Drug Metab 8:519–525, 2007). In bone metabolism, ROS play a dual role, with different actions under physiological and pathological conditions (Sontakke and Tare, Clin Chim Acta 318:145–148, 2002). Reactive oxygen species include hydroxyl radicals, superoxide anion radicals, hydrogen peroxide, and nitric oxide; ROS lead to oxidation of enzymes and protein oxidation and degradation. The effects of ROS are eliminated by antioxidant enzymes such as superoxide dismutase (SOD), glutathione peroxidase, and catalase. Oxidative stress occurs when the effects of ROS are greater than the antioxidant mechanisms in biological systems, and cellular damage occurs. The full effect of oxidative stress on bone remodeling is unknown, but there is evidence that both pro-oxidants and antioxidants play a role in skeletal integrity in health and disease.
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Schenck, P.A. (2011). Oxidative Stress and Calcium Metabolism. In: Mandelker, L., Vajdovich, P. (eds) Studies on Veterinary Medicine. Oxidative Stress in Applied Basic Research and Clinical Practice. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-071-3_3
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DOI: https://doi.org/10.1007/978-1-61779-071-3_3
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