PMID- 1383740 OWN - NLM STAT- MEDLINE DCOM- 19921123 LR - 20190702 IS - 0027-5107 (Print) IS - 0027-5107 (Linking) VI - 270 IP - 2 DP - 1992 Nov 16 TI - Genotoxicities of nitropyrenes and their modulation by apigenin, tannic acid, ellagic acid and indole-3-carbinol in the Salmonella and CHO systems. PG - 87-95 AB - Four naturally occurring compounds, indole-3-carbinol (I3C), apigenin (Api), ellagic acid (EA) and tannic acid (TA), were tested for their inhibitory effects against 1-nitropyrene- (1-NP) or 1,6-dinitropyrene (1,6-DNP)-induced genotoxicity in Salmonella tester strains and Chinese hamster ovary (CHO) cells. Api and TA strongly inhibited the bacterial mutagenesis induced by nitropyrenes, while I3C and EA had little or no effect. For example, in TA98, 0.2 mumole Api resulted in 48% and 56% inhibition of the mutagenicity induced by 4 nmole 1-NP and 0.035 nmole 1,6-DNP, respectively. With an equal dose, TA caused 46% and 50% reduction of the mutagenicity induced by 1-NP and 1,6-DNP, respectively. As expected, a good correlation was observed between the antimutagenicity of nitropyrenes and their inhibitory effect on nitroreductase activity. This indicated that one of the possible antimutagenic mechanisms of Api or TA was to inactivate the metabolism of nitropyrenes. Two biological end-points, cytotoxicity and sister-chromatid exchange (SCEs), were used to screen the antigenotoxic effects of these compounds in CHO cells. At the sub-cytotoxic dose, I3C, Api and TA all protected against the cytotoxicity induced by 1-NP and 1,6-DNP, but only TA and Api gave a significant reduction of the frequency of SCEs. Moreover, this reduction was found to be highly dose-dependent. FAU - Kuo, M L AU - Kuo ML AD - Institute of Toxicology, College of Medicine, National Taiwan University, Taipei. FAU - Lee, K C AU - Lee KC FAU - Lin, J K AU - Lin JK LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Netherlands TA - Mutat Res JT - Mutation research JID - 0400763 RN - 0 (Antimutagenic Agents) RN - 0 (Antioxidants) RN - 0 (Flavonoids) RN - 0 (Hydrolyzable Tannins) RN - 0 (Indoles) RN - 0 (Oils, Volatile) RN - 0 (Pyrenes) RN - 19YRN3ZS9P (Ellagic Acid) RN - 66Q2ZUF83N (1,6-dinitropyrene) RN - C11E72455F (indole-3-carbinol) RN - EC 1.7.- (Nitroreductases) RN - TD1665I8Q4 (1-nitropyrene) SB - IM MH - Animals MH - *Antimutagenic Agents MH - Antioxidants MH - CHO Cells/drug effects MH - Chamomile MH - Chromosome Aberrations MH - Cricetinae MH - Cricetulus MH - Ellagic Acid/*pharmacology MH - Flavonoids/*pharmacology MH - Hydrolyzable Tannins/*pharmacology MH - Indoles/*pharmacology MH - Mutagenicity Tests MH - Nitroreductases/metabolism MH - Oils, Volatile/*pharmacology MH - Plants, Medicinal MH - Pyrenes/*toxicity MH - Salmonella typhimurium/drug effects MH - Sister Chromatid Exchange EDAT- 1992/11/16 00:00 MHDA- 1992/11/16 00:01 CRDT- 1992/11/16 00:00 PHST- 1992/11/16 00:00 [pubmed] PHST- 1992/11/16 00:01 [medline] PHST- 1992/11/16 00:00 [entrez] AID - 0027-5107(92)90119-M [pii] AID - 10.1016/0027-5107(92)90119-m [doi] PST - ppublish SO - Mutat Res. 1992 Nov 16;270(2):87-95. doi: 10.1016/0027-5107(92)90119-m.