Tannenbaum S R, Wishnok J S, Leaf C D
Massachusetts Institute of Technology, Cambridge 02139.
Am J Clin Nutr. 1991 Jan;53(1 Suppl):247S-250S. doi: 10.1093/ajcn/53.1.247S.
Nitrosation occurs under a wide variety of conditions by reaction of most types of amines with any of a large number of nitrosating species. Nitrite can be formed in vivo via bacterial reduction of nitrate and by activated macrophages and endothelial cells. The mechanism of nitrite formation by mammalian cells is via enzymatic oxidation of arginine to NO followed by oxidation to N2O3 and N2O4. Nitrosatable amines are found in many foods and some, eg, dimethylamine, are synthesized in the body. Precursors of N-nitroso compounds are thus almost constantly present together under favorable reaction conditions in vivo and there is, consequently, considerable interest concerning possible human health risks arising from endogenous formation of this class of compounds. Among many nitrosation inhibitors, most attention has focused on ascorbic acid, which reacts with many nitrosating agents and which is virtually nontoxic. This presentation discusses the chemistry of ascorbic acid inhibition of nitrosation reactions.
在多种条件下,大多数类型的胺与大量亚硝化剂中的任何一种发生反应都会产生亚硝化作用。亚硝酸盐可通过细菌将硝酸盐还原以及活化的巨噬细胞和内皮细胞在体内形成。哺乳动物细胞形成亚硝酸盐的机制是通过精氨酸酶促氧化为一氧化氮,随后氧化为三氧化二氮和四氧化二氮。许多食物中都含有可亚硝化的胺,有些(如二甲胺)是在体内合成的。因此,在体内有利的反应条件下,N-亚硝基化合物的前体几乎总是同时存在,因此,人们对这类化合物内源性形成可能对人类健康造成的风险相当关注。在众多亚硝化抑制剂中,大多数关注都集中在抗坏血酸上,它能与许多亚硝化剂反应,且几乎无毒。本报告讨论了抗坏血酸抑制亚硝化反应的化学原理。