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Toxicology

By G. Winkelmann

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Andican Á ¨ zdog˘an Á G. Burc¸ak A. Seven Á S. H. Ku¨c¸u¨k Á M. O Department of Biochemistry, Cerrahpas¸ a Medical _ Faculty, Istanbul University, Istanbul, Turkey S. com Increased oxidative stress promotes protein glycation (Selvaraj et al. 2002). As free Cu ions are highly redox active and thus might contribute to oxidative tissue damage, in vivo availability of catalytic Cu is usually restricted to a great extent (Cooper et al. 2005). However, glycation due to chronic hyperglycemia has been reported to damage the Cu-binding properties of 123 44 ceruloplasmin and albumin, the main Cu-binding proteins in plasma (Linder 1991; Islam et al.

1007/s10534-009-9264-x Zinc activates neutrophils’ oxidative burst Marisa Freitas Æ Grac¸a Porto Æ Jose´ L. F. C. Lima Æ Eduarda Fernandes Received: 3 May 2009 / Accepted: 25 August 2009 / Published online: 17 September 2009 Ó Springer Science+Business Media, LLC. 2009 Abstract Zinc has been shown to disturb the innate host defense response by interfering in the activation of neutrophils and subsequent oxidative burst, although the exact role of this metal, either as an activator or inhibitor, remains a matter of controversy among research groups.

65 vs. 001, respectively). These findings reflected the establishment of diabetes mellitus in STZ administered rats. 9 vs. 01). 3 vs. 1 vs. 8 vs. 05, respectively). 1 vs. 01). Pearson correlation analysis results are shown in Table 2. 05). 05) (Figs. 1, 2). 05) (Figs. 05). 05 level 123 Biometals (2010) 23:43–49 47 AGE-peptides and oxidative stress related parameters in diabetic and nondiabetic states. 2 ml) intraperitoneally on every alternate day for 30 days) was reported in STZ-diabetic mice (Sitasawad et al.

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