Abstract
There is abundant evidence that taurine functions as an antioxidant in a variety of biological systems. Taurine reacts with HOCl, a potent oxidizing agent generated by activated neutrophils, to form the less toxic product, N-chlorotaurine (20). This reaction retards damage to ocular surfaces exposed to HOCl (13). Taurine protects cultured lymphoblastoid cells against iron-ascorbate or retinol-induced oxidant damage and enhances cell viability (16,17). Taurine supplementation protects the lung from oxidant-induced damage following exposure to ozone (2) or nitrogen dioxide (7). Taurine alone or in combination with niacin reduces pulmonary fibrosis following intratracheal installation of the oxidants, amiodarone (26) or bleomycin (27). Finally, taurine attenuates adriamycin-induced cardiotoxicity in perfused chick hearts by decreasing myocardial lipid peroxidation (9).
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© 1994 Springer Science+Business Media New York
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Trachtman, H., Sturman, J.A. (1994). Taurine and Experimental Kidney Disease. In: Huxtable, R.J., Michalk, D. (eds) Taurine in Health and Disease. Advances in Experimental Medicine and Biology, vol 359. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-1471-2_16
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DOI: https://doi.org/10.1007/978-1-4899-1471-2_16
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