Hasler J A, Siwela A H, Nyathi C B, Chetsanga C J
Res Commun Chem Pathol Pharmacol. 1986 Mar;51(3):421-4.
This study examined activation of aflatoxin B1 (AFB1) in livers of Schistosoma mansoni-infected and noninfected mice by measuring covalent binding of [3H]AFB1 to cellular macromolecules in vivo and in vitro. During a one week time period after AFB1 treatment of animals, maximal binding of [3H]AFB1 to DNA, RNA and protein in liver occurred during the 1-6 hour period after treatment, with less binding throughout of AFB1 to macromolecules of infected mice. Experiments performed in vitro to determine the capacity of liver microsomes to mediate the binding of AFB1 to calf thymus DNA showed that microsomes from infected mice mediated the binding of less [3H]AFB1 to DNA than those from noninfected animals.
本研究通过测量[3H]黄曲霉毒素B1(AFB1)在体内和体外与细胞大分子的共价结合,检测曼氏血吸虫感染和未感染小鼠肝脏中AFB1的激活情况。在给动物注射AFB1后的一周时间内,[3H]AFB1与肝脏中DNA、RNA和蛋白质的最大结合发生在注射后的1 - 6小时内,且AFB1与感染小鼠大分子的结合在整个过程中较少。体外实验测定肝脏微粒体介导AFB1与小牛胸腺DNA结合的能力,结果显示感染小鼠的微粒体介导的[3H]AFB1与DNA的结合比未感染动物的微粒体少。