Garattini E, Coccia P, Romano M, Jiritano L, Noseda A, Salmona M
Cancer Res. 1984 Nov;44(11):5150-5.
The role of prostaglandin endoperoxide synthetase in the in vivo activation of benzo(a)pyrene to reactive metabolites capable of interacting irreversibly with cellular macromolecules was studied in guinea pig liver, lung, kidney, spleen, small intestine, colon, and brain. DNA and protein covalent binding experiments were made after systemic administration of acetylsalicylic acid (200 mg/kg) followed by radiolabeled benzo(a)pyrene (4 microgram/kg). Results are compared with a control situation in which the prostaglandin endoperoxide synthetase inhibitor (acetylsalicylic acid) was not administered. No decrease in the level of DNA or protein benzo(a)pyrene-derived covalent binding was observed in any of the tissues studied.
在豚鼠的肝脏、肺、肾脏、脾脏、小肠、结肠和大脑中,研究了前列腺素内过氧化物合成酶在体内将苯并(a)芘激活为能够与细胞大分子发生不可逆相互作用的活性代谢物过程中的作用。在全身给予乙酰水杨酸(200毫克/千克)后,接着给予放射性标记的苯并(a)芘(4微克/千克),然后进行DNA和蛋白质共价结合实验。将结果与未给予前列腺素内过氧化物合成酶抑制剂(乙酰水杨酸)的对照情况进行比较。在所研究的任何组织中,均未观察到DNA或蛋白质中苯并(a)芘衍生的共价结合水平降低。