Suppressive effects of retinoids, carotenoids and antioxidant vitamins on heterocyclic amine-induced umu C gene expression in Salmonella typhimurium (TA 1535/pSK 1002)

Mutat Res. 1996 Jun 12;368(2):133-40. doi: 10.1016/0165-1218(95)00109-3.

Abstract

Effects of retinoids, carotenoids and antioxidant vitamins were studied by mutagen-induced umu C gene expression system in Salmonella typhimurium (TA 1535/pSK 1002). Retinol (vitamin A), retinol acetate and retinoic acid showed remarkable inhibitory activities, whereas retinol palmitate exhibited significant but weak activity for umu C gene expression in tester bacteria induced by 3-amino-3,4-dimethyl-5H-pyrido[4.3-b]indol (Trp-P-1) in the presence of hepatic metabolizing enzymes (S9 mixture). Carotenoids having provitamin A activity (beta-carotene and canthaxanthin) exhibited moderate suppressive effects on the same experimental system. The ranks of suppressive activities were retinol > retinol acetate > retinoic acid > canthaxanthin > beta-carotene > retinol palmitate and their doses for inhibition by 50% (ID50) were estimated to be 1.2 x 10(-7), 3.0 x 10(-7), 5.4 x 10(-7), 1.5 x 10(-6), 4.0 x 10(-5) and 6.0 x 10(-5) M, respectively. However, they did not cause significant inhibition on umu C gene expression induced by direct-acting mutagen (adriamycin or mitomycin C) in the absence of S9 mixture. Inhibition of umu gene expression appears to be due to inhibition of P450-mediated metabolic activation of the heterocyclic amine Trp-P-1. Ascorbic acid (vitamin C) showed weak but significant suppressive activity at high-dose concentrations (3 x 10(-6) - 10(-4)M). However, alpha-tocopherol did not exhibit significant suppression at all dose concentrations. The significance of the experimental results is discussed from the viewpoint of the chemoprevention against genotoxicity associated with carcinogenesis.

MeSH terms

  • Animals
  • Antimutagenic Agents / pharmacology
  • Antioxidants / pharmacology
  • Bacterial Proteins / drug effects*
  • Bacterial Proteins / genetics
  • Carbolines / toxicity
  • Carotenoids / pharmacology*
  • DNA-Directed DNA Polymerase
  • Dose-Response Relationship, Drug
  • Escherichia coli Proteins*
  • Gene Expression / drug effects*
  • Heterocyclic Compounds / toxicity
  • Liver / drug effects
  • Liver / enzymology
  • Mutagens / toxicity
  • Rats
  • Rats, Sprague-Dawley
  • Retinoids / pharmacology*
  • Salmonella typhimurium / drug effects*
  • Salmonella typhimurium / genetics
  • Vitamins / pharmacology*

Substances

  • Antimutagenic Agents
  • Antioxidants
  • Bacterial Proteins
  • Carbolines
  • Escherichia coli Proteins
  • Heterocyclic Compounds
  • Mutagens
  • Retinoids
  • Vitamins
  • Carotenoids
  • UmuC protein, E coli
  • DNA-Directed DNA Polymerase
  • 3-amino-1,4-dimethyl-5H-pyrido(4,3-b)indole