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吸入的甲醛与Fischer 344大鼠鼻黏膜中DNA的共价结合:通过高效液相色谱法分析甲醛和DNA以及进行初步的药代动力学解释。

Covalent binding of inhaled formaldehyde to DNA in the nasal mucosa of Fischer 344 rats: analysis of formaldehyde and DNA by high-performance liquid chromatography and provisional pharmacokinetic interpretation.

作者信息

Casanova M, Deyo D F, Heck H D

机构信息

Department of Biochemical Toxicology and Pathobiology, Chemical Industry Institute of Toxicology, Research Triangle Park, North Carolina 27709.

出版信息

Fundam Appl Toxicol. 1989 Apr;12(3):397-417. doi: 10.1016/0272-0590(89)90015-8.

Abstract

Inhalation of 3HCHO and H14CHO (6 ppm, 6 hr) resulted in the formation of DNA-protein crosslinks in the rat nasal respiratory mucosa. The DNA was extracted and was fractionated into aqueous (AQ) and interfacial (IF) portions. AQ DNA and IF DNA were enzymatically hydrolyzed to deoxyribonucleosides in Tris buffer and analyzed by HPLC with liquid scintillation counting (LSC). HCHO was bound exclusively to the IF DNA, indicating that the HCHO was bound as DNA-protein crosslinks. Hydrolysis of the DNA quantitatively released the HCHO; no evidence was obtained for the formation of hydroxymethyl adducts. An adduct detected previously following incubation of mammalian cells with HCHO, N6-hydroxymethyldeoxyadenosine (hm6dA) [Beland, F.A., Fullerton, N.F., and Heflich, R.H. (1984) J. Chromatogr. 308, 121-131], was shown to be produced by reaction of HCHO with deoxyadenosine (dA) in bis-Tris buffer under conditions similar to those used for hydrolysis of the DNA. This reaction does not occur in Tris buffer. Evidence was obtained that most or all of the hm6dA observed can be explained by this reaction. Based on these results, an improved method to determine the amount of H14CHO bound to DNA was developed: the DNA is hydrolyzed in Tris buffer and analyzed by HPLC, and the released H14CHO is derivatized with dimedone and quantitated by LSC. Rats were exposed to a wide range of H14CHO concentrations (0.3, 0.7, 2, 6, or 10 ppm; 6 hr). DNA-protein crosslinking occurred at all concentrations. The formation of crosslinks was interpreted in terms of a nonlinear pharmacokinetic model incorporating oxidation of inhaled HCHO as a defense mechanism. The slope of the fitted concentration-response curve at 10 ppm is 7.3-fold greater than at 0.3 ppm, and the detoxication pathway is half-saturated at an airborne concentration of 2.6 ppm.

摘要

吸入³HCHO和H¹⁴CHO(6 ppm,6小时)导致大鼠鼻呼吸黏膜中形成DNA-蛋白质交联物。提取DNA并将其分离为水相(AQ)和界面相(IF)部分。将AQ DNA和IF DNA在Tris缓冲液中酶解为脱氧核苷,并用带液体闪烁计数(LSC)的高效液相色谱(HPLC)进行分析。HCHO仅与IF DNA结合,表明HCHO以DNA-蛋白质交联物的形式结合。DNA的水解定量释放出HCHO;未获得形成羟甲基加合物的证据。先前在用HCHO孵育哺乳动物细胞后检测到的一种加合物,N⁶-羟甲基脱氧腺苷(hm⁶dA)[贝兰德,F.A.,富勒顿,N.F.,和赫夫利希,R.H.(1984年)《色谱杂志》308,121 - 131],被证明是在与DNA水解所用条件相似的双Tris缓冲液中,HCHO与脱氧腺苷(dA)反应产生的。此反应在Tris缓冲液中不发生。有证据表明观察到的大部分或全部hm⁶dA都可以用此反应来解释。基于这些结果,开发了一种改进的方法来测定与DNA结合的H¹⁴CHO的量:将DNA在Tris缓冲液中水解并用HPLC分析,释放出的H¹⁴CHO用二甲基酮肟衍生化并用LSC定量。将大鼠暴露于广泛的H¹⁴CHO浓度范围(0.3、0.7、2、6或10 ppm;6小时)。在所有浓度下均发生DNA-蛋白质交联。交联物的形成根据一个包含吸入HCHO氧化作为防御机制的非线性药代动力学模型来解释。在10 ppm时拟合的浓度-反应曲线的斜率比在0.3 ppm时大7.3倍,解毒途径在空气浓度为2.6 ppm时达到半饱和。

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