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硫醇对N-亚硝基噻唑烷合成过程中一种诱变污染物的抑制作用。

Inhibitory effects of thiols on a mutagenic contaminant from the synthesis of N-nitrosothiazolidine.

作者信息

Miller A J, Fiddler W

出版信息

Mutat Res. 1987 Sep;180(1):75-9. doi: 10.1016/0027-5107(87)90068-6.

Abstract

The effect of S9 and various thiols were studied for potential modifying effects on a mutagenic trace artifact ('NTHZ') formed during the synthesis of N-nitrosothiazolidine (NTHZ) from cysteamine, formaldehyde and nitrite. Induced and uninduced S9 prepared from Syrian hamster livers reduced mutagenic activity in Salmonella TA100. Incorporation of boiled S9 into the preincubation medium produced similar effects, indicating a non-enzymatic mechanism for the detoxification reaction. Thiols alone also lowered revertant yields, and inhibitory efficacy was, in general, related to the pKa of the compound. At equimolar concentrations mutagenic activity was reduced in the following order (pKa values in parentheses): Thioglycolate (10.7) greater than mercaptoethanol (9.6) greater than reduced glutathione (8.8) greater than cysteine (8.35) greater than cystine (8.2). N-Acetylcysteine (9.52) and cysteamine (8.35), however, did not fit this pattern. The results of this study suggest that normal hepatic mechanisms may minimize 'NTHZ' genotoxicity thereby reducing potential health risks associated with its exposure.

摘要

研究了S9和各种硫醇对在由半胱胺、甲醛和亚硝酸盐合成N-亚硝基噻唑烷(NTHZ)过程中形成的诱变微量假象物(“NTHZ”)的潜在修饰作用。从叙利亚仓鼠肝脏制备的诱导型和未诱导型S9降低了鼠伤寒沙门氏菌TA100中的诱变活性。将煮沸的S9加入预孵育培养基中产生了类似的效果,表明解毒反应存在非酶机制。单独的硫醇也降低了回复突变率,并且抑制效果通常与化合物的pKa有关。在等摩尔浓度下,诱变活性按以下顺序降低(括号内为pKa值):巯基乙酸(10.7)大于巯基乙醇(9.6)大于还原型谷胱甘肽(8.8)大于半胱氨酸(8.35)大于胱氨酸(8.2)。然而,N-乙酰半胱氨酸(9.52)和半胱胺(8.35)不符合这种模式。本研究结果表明,正常的肝脏机制可能会使“NTHZ”的遗传毒性降至最低,从而降低与其接触相关的潜在健康风险。

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