Vance R E, Teel R W
Department of Physiology and Pharmacology, Loma Linda University, School of Medicine, CA 92350.
Cancer Lett. 1989 Sep 15;47(1-2):37-44. doi: 10.1016/0304-3835(89)90174-2.
Tannic acid, a naturally occurring plant phenol, inhibited rat liver S9 mediated mutagenesis of benzo[a]pyrene in Salmonella typhimurium by 32-77% at concentrations of 5-50 micrograms/mutagenesis plate. Tannic acid (10-40 microM) had no affect on the formation of organosoluble metabolites of benzo[a]pyrene or of its water-soluble conjugates. It did, however, inhibit benzo[a]pyrene (B[a]P) metabolite binding to calf thymus DNA by 40% at a concentration of 40 microM and inhibited benzo[a]pyrene 7,8-dihydrodiol-9,10-epoxide (BPDE): deoxyguanosine adduct formation in calf thymus DNA by 12-54% at concentrations of 10-40 microM. These results suggest that the antimutagenic effect of tannic acid and inhibition of B[a]P metabolite binding to DNA is by a previously described scavenging mechanism and/or by a DNA-affinity binding mechanism that prevents BPDE interaction with DNA as previously described for ellagic acid.
单宁酸是一种天然存在的植物酚类物质,在鼠伤寒沙门氏菌中,它能抑制大鼠肝脏S9介导的苯并[a]芘诱变作用,当浓度为5 - 50微克/诱变平板时,抑制率为32% - 77%。单宁酸(10 - 40微摩尔)对苯并[a]芘的有机可溶性代谢产物或其水溶性共轭物的形成没有影响。然而,在浓度为40微摩尔时,它确实能抑制苯并[a]芘(B[a]P)代谢产物与小牛胸腺DNA的结合,抑制率达40%;在浓度为10 - 40微摩尔时,能抑制苯并[a]芘7,8 - 二氢二醇 - 9,10 - 环氧化物(BPDE)与小牛胸腺DNA形成脱氧鸟苷加合物,抑制率为12% - 54%。这些结果表明,单宁酸的抗诱变作用以及对B[a]P代谢产物与DNA结合的抑制作用,是通过先前描述的清除机制和/或DNA亲和结合机制实现的,该机制如同先前对鞣花酸的描述一样,可阻止BPDE与DNA相互作用。