Ma Bennett, Carr Brian A, Krolikowski Paul, Chang Frank N
Department of Drug Metabolism, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
Chem Res Toxicol. 2007 Jan;20(1):72-8. doi: 10.1021/tx060166z.
The cytotoxic effects of blattellaquinone (BTQ), a sex pheromone produced by adult female German cockroaches, have been studied using human lung adenocarcinoma A549 cells. 1,4-Benzoquinone (BQ), a toxic chemical implicated in benzene toxicity, was used as a reference compound. Both BQ and BTQ showed comparable toxicity toward A549 cells, with LD50 values estimated to be 14 and 19 microM, respectively. These two compounds increased the formation of an oxidized fluorescent probe, 2',7'-dichlorofluorescein, but had no effect on the cellular GSSG level. Interestingly, BTQ increased the level of 8-epi-prostaglandin F2alpha and was 4-fold more efficient in depleting cellular GSH content than BQ. Of the five GSH adducts of BTQ isolated, three were identified as mono-GSH conjugates, and the other two were di-conjugates. Mass spectrometric and NMR analyses of the di-conjugates showed that the second GSH molecule displaced the isovaleric acid moiety, potentially via a nucleophilic substitution reaction. The ability of BTQ to conjugate a second GSH molecule without quinone regeneration indicated that it may be a more effective cross-linking agent than BQ. Future experiments may be needed to evaluate the overall safety of BTQ before the commercialization of the compound as a cockroach attractant.
成年雌性德国小蠊产生的性信息素blattellaquinone(BTQ)的细胞毒性作用已通过人肺腺癌A549细胞进行了研究。1,4 - 苯醌(BQ)是一种与苯毒性有关的有毒化学物质,用作参考化合物。BQ和BTQ对A549细胞均显示出相当的毒性,其半数致死剂量(LD50)值估计分别为14和19微摩尔。这两种化合物增加了氧化荧光探针2',7'-二氯荧光素的形成,但对细胞内谷胱甘肽二硫化物(GSSG)水平没有影响。有趣的是,BTQ增加了8-表-前列腺素F2α的水平,并且在消耗细胞内谷胱甘肽(GSH)含量方面比BQ高效4倍。在分离出的BTQ的五种GSH加合物中,三种被鉴定为单GSH共轭物,另外两种为双共轭物。对双共轭物的质谱和核磁共振分析表明,第二个GSH分子可能通过亲核取代反应取代了异戊酸部分。BTQ在不进行醌再生的情况下结合第二个GSH分子的能力表明,它可能是比BQ更有效的交联剂。在将该化合物作为蟑螂引诱剂商业化之前,可能需要进行进一步的实验来评估BTQ的整体安全性。