The effect of plant phenolics on the formation of 7,12-dimethylbenz[ a]anthracene–DNA adducts and TPA-stimulated polymorphonuclear neutrophils chemiluminescence in vitro

• Published in: Toxicology (Amsterdam) 2003-08, Vol.189 (3), p.199-209
• Main Authors: Ignatowicz, Ewa, Balana, Bartosz, Vulimiri, Suryanarayana V., Szaefer, Hanna, Baer-Dubowska, Wanda
• Format: Article
• Language: English
• Subjects: 7,12-Dimethylbenz[ a]anthracene; 9,10-Dimethyl-1,2-benzanthracene - analogs & derivatives; 9,10-Dimethyl-1,2-benzanthracene - metabolism; Animals; Biological and medical sciences; Chemiluminescence; Chlorogenic Acid - pharmacology; DNA - metabolism; DNA adducts; DNA Adducts - biosynthesis; Enzyme Inhibitors - pharmacology; General pharmacology; Human neutrophils; Humans; Hydrolyzable Tannins - pharmacology; Hydroxybenzoates - pharmacology; Luminescent Measurements; Male; Medical sciences; Methylcholanthrene - metabolism; Neutrophils - drug effects; Neutrophils - metabolism; Pharmacognosy. Homeopathy. Health food; Pharmacology. Drug treatments; Phenols - pharmacology; Plant phenolics; Rats; Rats, Wistar; Reactive Oxygen Species - metabolism; Respiratory Burst - drug effects; Resveratrol; Stilbenes - pharmacology; Tetradecanoylphorbol Acetate - pharmacology
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/S0300-483X(03)00148-3

Phenolics, common plant constituents, form up an important part of human diet and are considered potential chemopreventive agents. In the present study, structurally diverse phenolics, such as tannic acid, protocatechuic acid, chlorogenic acid and resveratrol, were investigated for their inhibitory effects on covalent binding of 7,12-dimethylbenz[ a]anthracene (DMBA) to DNA in vitro and the suppression of oxidative burst in 12- O-tetradecanoylphorbol-13-acetate (TPA)-stimulated human polymorphonuclear neutrophils (PMNs). 32P-postlabeling analysis of DNA incubated with DMBA in the presence of 3-methylcholanthrene (3-MC)-induced microsomes produced three major adducts derived from anti-, syn- and anti-dihydrodiol epoxides through reactions with dGuo and dAdo, respectively. Phenolic compounds at the concentration of 150 μM reduced the levels of all DMBA–DNA adducts by 55–98%. The most dramatic effect was observed in case of tannic acid, which completely inhibited the formation of DMBA–dAdo adducts. Chlorogenic acid was the least effective inhibitor of DMBA–DNA adducts formation particularly syn-DMBADE–dAdo (20%). Human neutrophils showed a significant dose-related decrease of TPA-induced chemiluminescence after pretreatment with phenolic compounds. The most effective inhibitors were tannic acid and resveratrol with IC 50=5.19 and 5.76 μM, respectively. These results suggest that the suppression of reactive oxygen species (ROS) and carcinogen–DNA adducts formation may be important for anticarcinogenic activity of the examined phenolics.