Fernando H, Huang C R, Milliman A, Shu L, LeBreton P R
Department of Chemistry, University of Illinois at Chicago 60607-7061, USA.
Chem Res Toxicol. 1996 Dec;9(8):1391-402. doi: 10.1021/tx960134j.
Reactions of the benzo[a]pyrene (BP) and benz[a]anthracene (BA) metabolites, (+/-)-trans-7 8-dihydroxy-anti-9, 10-epoxy-7, 8, 9, 10-tetrahydro-BP (BPDE), (+/-)-trans-3, 4-dihydroxy-anti- 1,2-epoxy-1,2,3,4-tetrahydro-BA (BADE), (+/-)-BP-4,5-oxide (BPO), and (+/-)-BA-5, 6-oxide (BAO), were examined under pseudo-first-order conditions at varying Na+ (2.0-100 Mm) and native calf thymus DNA (ctDNA) concentrations. In 0.2 mM ctDNA and 2.0 mM Na+, at a pH of 7.3 most BPDE, BADE, BPO, and BAO (87-95%) undergo DNA catalyzed hydrolysis or rearrangement. For BPDE and BPO, overall, pseudo-first-order rate constants, k, in 2.0 mM Na+ and 0.2 mM ctDNA are 21-72 times larger than values obtained without DNA. For BADE and BAO, the rate constants are less strongly influenced by DNA; k values in 0.2 mM ctDNA are only 9-12 times larger than values obtained without DNA. Kinetic data for BPDE, BPO, BADE, and BAO and DNA intercalation association constants (KA) for BP and BA diols which are model compounds indicate that KA values for BPDE and BPO in 2.0 mM Na+ are 6.6-59 times larger than those of BADE and BAO. The greater DNA enhancement of rate constants for BPDE and BPO, versus BADE and BAO, correlates with the larger KA values of the BP metabolites. DNA adducts, which account for less than 10% of the yields, also form. For BPDE in 0.20 mM ctDNA, k decreases 5.1 times as the Na+ concentration increases from 2.0 to 100 mM. Nevertheless, the DNA adduct level remains constant over the range of Na+ concentrations examined. These results provide evidence that, for BPDE in 0.20 mM DNA and 2.0 mM Na+, ctDNA adduct formation follows a mechanism which is similar to that for DNA catalyzed hydrolysis. The pseudo-first-order rate constant for adduct formation, kAd, given approximately by kAd approximately equal to (kcat,AdKA[DNA])/(1 + KA[DNA]), where kcat,Ad is a catalytic rate constant. for BADE, BPO, and BAO, the influence of varying DNA and Na+ concentrations on k values is similar to that for BPDE, and provides evidence that the formation of adducts follows the same rate law.
在不同的钠离子浓度(2.0 - 100 mM)和天然小牛胸腺DNA(ctDNA)浓度下,在准一级反应条件下研究了苯并[a]芘(BP)和苯并[a]蒽(BA)代谢物,即(±)-反式-7,8-二羟基-反式-9,10-环氧-7,8,9,10-四氢-BP(BPDE)、(±)-反式-3,4-二羟基-反式-1,2-环氧-1,2,3,4-四氢-BA(BADE)、(±)-BP-4,5-氧化物(BPO)和(±)-BA-5,6-氧化物(BAO)的反应。在0.2 mM ctDNA和2.0 mM钠离子条件下,pH为7.3时,大多数BPDE、BADE、BPO和BAO(87 - 95%)会发生DNA催化的水解或重排。总体而言,对于BPDE和BPO,在2.0 mM钠离子和0.2 mM ctDNA中的准一级反应速率常数k比无DNA时得到的值大21 - 72倍。对于BADE和BAO,速率常数受DNA的影响较小;在0.2 mM ctDNA中的k值仅比无DNA时得到的值大9 - 12倍。BPDE、BPO、BADE和BAO的动力学数据以及作为模型化合物的BP和BA二醇的DNA插入缔合常数(KA)表明,在2.0 mM钠离子中,BPDE和BPO的KA值比BADE和BAO的KA值大6.6 - 59倍。与BADE和BAO相比,BPDE和BPO的速率常数受DNA增强的程度更大,这与BP代谢物较大的KA值相关。也会形成占产率不到10%的DNA加合物。对于0.20 mM ctDNA中的BPDE,随着钠离子浓度从2.0 mM增加到100 mM,k降低5.1倍。然而,在所研究的钠离子浓度范围内,DNA加合物水平保持恒定。这些结果提供了证据,即在0.20 mM DNA和2.0 mM钠离子条件下,ctDNA加合物的形成遵循一种与DNA催化水解相似的机制。加合物形成的准一级反应速率常数kAd大致由kAd≈(kcat,AdKA[DNA])/(1 + KA[DNA])给出,其中kcat,Ad是催化速率常数。对于BADE、BPO和BAO,不同的DNA和钠离子浓度对k值的影响与BPDE相似,并提供了加合物形成遵循相同速率定律的证据。