硝基
化学
甲基乙二醛
糖基化
抗氧化剂
血红蛋白
氧化应激
高铁血红蛋白
氧化磷酸化
蛋白质羰基化
生物化学
酶
有机化学
脂质过氧化
受体
作者
O. V. Kosmachevskaya,E. I. Nasybullina,I. S. Pugachenko,Н. Н. Новикова,А. Ф. Топунов
出处
期刊:Antioxidants
[Multidisciplinary Digital Publishing Institute]
日期:2022-10-11
卷期号:11 (10): 2007-2007
被引量:12
标识
DOI:10.3390/antiox11102007
摘要
Donors of nitroxyl and nitroxyl anion (HNO/NO-) are considered to be promising pharmacological treatments with a wide range of applications. Remarkable chemical properties allow nitroxyl to function as a classic antioxidant. We assume that HNO/NO- can level down the non-enzymatic glycation of biomolecules. Since erythrocyte hemoglobin (Hb) is highly susceptible to non-enzymatic glycation, we studied the effect of a nitroxyl donor, Angeli's salt, on Hb modification with methylglyoxal (MG) and organic peroxide-tert-butyl hydroperoxide (t-BOOH). Nitroxyl dose-dependently decreased the amount of protein carbonyls and advanced glycation end products (AGEs) that were formed in the case of Hb incubation with MG. Likewise, nitroxyl effectively protected Hb against oxidative modification with t-BOOH. It slowed down the destruction of heme, formation of carbonyl derivatives and inter-subunit cross-linking. The protective effect of nitroxyl on Hb in this system is primarily associated with nitrosylation of oxidized Hb and reduction of its ferryl form, which lowers the yield of free radical products. We suppose that the dual (antioxidant and antiglycation) effect of nitroxyl makes its application possible as part of an additional treatment strategy for oxidative and carbonyl stress-associated diseases.
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