ANTIOXIDANT/PROOXIDANT EFFECTS OF BIOACTIVE POLYPHENOLICS

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ISSN: 1579-4377 ANTIOXIDANT/PROOXIDANT EFFECTS OF BIOACTIVE POLYPHENOLICS S. Touriño, D. Lizárraga, A. Carreras, C. Matito, V. Ugartondo, M. Mitjans, J.J. Centelles, M. P. Vinardell, L. Juliá, M. Cascante, and J. L. Torres*, Institute for Chemical and Environmental Research (IIQAB-CSIC), Jordi Girona 18-26, 08034 Barcelona, Spain; Department of Biochemistry and Molecular Biology, Associated Unit to CSIC, Universitat de Barcelona, Av. Diagonal 645, 08028 Barcelona, Spain. Departament de Fisiologia, Associated Unit to CSIC, Facultat de Farmàcia, Universitat de Barcelona, Av. Joan XXIII s/n, 08028-Barcelona, Spain. ABSTRACT Pine, grape and witch hazel byproducts are rich sources of polyphenols. From extracts (OW) soluble in both ethyl acetate and water we have generated a collection of fractions differing in percentage of pyrogallol groups. The mixtures were highly active as free radical scavengers against DPPH. The phenolics protected red blood cells from free radical induced hemolysis and were mildly cytotoxic to HaCat keratinocytes. They also inhibited the proliferation of tumoral SK-Mel 28 melanoma cells. Our results show that there is a relationship between percentage of pyrogallol groups, scavenging efficiency, cell antioxidant effect, cytotoxicy and antiproliferation. Interestingly, the most effective antioxidants were also the most cytotoxic and effective antiproliferative agents. This could be due to a dual antioxidant/prooxidant effect of polyphenols. KEYWORDS polyphenols, tannins, proanthocyanidins, catechins, antioxidants, hemolysis, cell proliferation, cytotoxicity.

INTRODUCTION Polyphenols are broadly considered beneficial for human health because they are capable of scavenging free radicals and reactive oxygen species (ROS) (Rice-Evans et al., 1996). Interestingly, polyphenols may be scavengers and ROS forming agents at the same time (Alanko et al., 1999). Strongly reducing species such as pyrogallol (three adjacent phenol groups) containing ( )-epigallocatechin (EGC) and ( )-epigallocatechingallate (EGCG) are able to form the superoxide radical from molecular oxygen (Kondo et al., 1999). Moreover, the orto-quinones formed by the loss of two electrons from pyrogallol and catechol (two adjacent phenol groups) moieties may participate in enzymatic redox cycling with the formation of superoxide and other ROS (Boots et al., 2007). These redox reactions may have a determinant influence over cell functions such as the cell cycle and apoptosis and the pyrogallol group appears to play a crucial role (Lizárraga et al., 2007). To establish structure/activity relationships of oligomeric condensed and hydrolysable tannins (Figure 1) we have generated over the years a complete collection of fractions differing in size and pyrogallol content (Torres et al., 2002; Touriño et al., 2008; Touriño et al., 2005). Polyphenols from grape (Vitis vinifera) pomace and pine (Pinus pinaster) bark were essentially procyanidins (Figure 1) with low gallate (Figure 1, R 2 = galloyl) content or no galloylation at all, respectively. Witch hazel (Hamamelis virginiana) bark fractions contained a high proportion of gallates included in both prodelphinidins and hydrolysable tannins. We summarize and compare here our results on free radical scavenging, cytotoxicity and antiproliferative activity against skin related cell lines. 3349

RESULTS AND DISCUSSION The collection of polyphenolic fractions was obtained by a combination of chromatographic techniques as shown in Scheme 1. Table 1 summarizes the results on the structural characterization of the fractions and their activity as scavengers, cell protecting agents against oxidative stress and antiproliferative agents on skin related cell lines. Table 1. Percentage of pyrogallol groups and activity of fractions from pine bark (P fractions), grape pomace (G fractions) and Witch hazel (H fractions) Fractions %G a DPPH b ED 50 a Percentage of pyrogallol grups of proanthocyanidins (PA, pine and grape) or PA + Hydrolyzable tannins (Witch hazel, including hamamelitannin, methyl gallate, pentagalloylgallate and gallic acid). PA percentage galloylation was estimated by thiolysis with cysteamine. Liquid chromatography-mass spectrometry (LC MS/MS) was used for the identification of the other gallates and gallic acid. b DPPH (1,1-diphenyl-2-picrylhydrazyl free radical) assay ED 50 micrograms of fraction able to scavenge 50% of DPPH divided by micromoles DPPH, mean of three experiments. c Antioxidant protective activity on erythrocytes in the presence of the free radical promoter AAPH (2,2 -Azobis (amidinopropane) dihydrochloride), concentration (micrograms/ml ± SE) inhibiting 50% of the hemolysis induced by AAPH. d Cytotoxicity on HaCat keratinocytes after 72 h of treatment, concentration (micrograms/ml ± SE) reducing cell viability by 50%. e Antiproliferative activity on SK-Me-28 melanoma cells concentration (micrograms/ml ± SE) inhibiting cell proliferation by 50%. Nt, not tested. AAPH c HaCaT d SK-Mel-28 e OWP 0 80.0 40.4 ± 1.4 248.2 ± 24.5 122 ± 4 IVP 0 59.5 34.2 ± 2.7 132.5 ± 12.9 137 ± 5 VP 0 153.8 nt nt 213 ± 4 VIP 0 47.8 nt nt 146 ± 4 VIIIP 0 84.0 37.7 ± 2.8 150.3 ± 1.3 134 ± 3 OWG 15 52.6 36.5 ± 1.3 121.2 ± 14.7 70 ± 4 IVG 25 37.0 28.6 ± 3.3 103.2 ± 1.3 nt VG <1 52.6 nt nt nt VIG 16 41.6 nt nt nt VIIIG 34 37.0 46.9 ± 3.3 77.8 ± 3.3 213 ± 7 OWH 54.1 42.4 21.5 ± 1.6 41 ± 2 26 ± 2 IVH 70.0 28.6 22.6 ± 1.7 38 ± 3 29 ± 2 VH 24.3 58.8 nt nt 32 ± 2 VIH 81.3 29.5 nt nt 28 ± 2 VIIIH 96.2 26.4 24.5 ± 0.8 68 ± 10 39 ± 2 control Ec 0 49.3 35.38 ± 2.6 245.7 ± 62 nt In general agreement with the literature (Alanko et al., 1999; Tan et al., 2000), our comparative results show that there is a relationship between percentage of pyrogallol groups, scavenging efficiency, cell antioxidant effect, cytotoxicy and antiproliferation. Interestingly, the more effective the antioxidants were, the more cytotoxic and antiproliferative they also were. This could be due to a dual antioxidant/prooxidant effect of polyphenols or better, to their capacity to either scavenge or generate radicals depending on the environment. The generation of the superoxide radical and other ROS by phenolics might be behind their mild effect on cell growth and apoptotic/necrotic death. The common 3350

structural feature mainly responsible for the activities of phenolic fractions appears to be the pyrogallol group both on ring B of gallocatechins/prodelphinidins and on galloyl moieties (gallates). Natural plant polyphenols are considered antioxidants and perceived popularly as beneficial agents for the prevention of many diseases. The concept antioxidant is usually linked to free radical scavenging since it has been accepted that the main underlying cause of cell damage is the production of ROS by the mitochondrial metabolism or by external agents (e.g. radiation) and that ROS are essentially harmful and should be eliminated. But ROS may not be always harmful. First, ROS, as well as reactive nitrogen species (RNS) are key agents in the regulation of cell functions by acting as secondary messengers in intracellular signaling cascades (Alanko et al., 1999; Valko et al., 2007). Second, moderate generation of ROS maybe selectively toxic to cancer cells and may even end up producing an antioxidant effect by fostering the endogenous defense systems. Polyphenols are capable of both scavenging and generating radicals and may exert their beneficial effects by a combination of both mechanisms. ACKNOWLEDGEMENT Financial support of the Spanish Ministry of Education and Science (research grant AGL2006-12210-C03-02/ALI) is acknowledged. REFERENCES 1. Alanko, J., Riutta, A., Holm, P., Mucha, I., Vapaatalo, H. and Metsa-Ketela, T. 1999. Modulation of arachidonic acid metabolism by phenols: relation to their structure and antioxidant/prooxidant properties. Free Radical Biol. Med. 26: 193-201. 2. Boots, A. W., Li, H., Schins, R. P. F., Duffin, R., Heemskerk, J. W. M., Bast, A. and Haenen, G. 2007. The quercetin paradox. Toxicol. Appl. Pharmacol. 222: 89-96. 3. Kondo, K., Kurihara, M., Miyata, N., Suzuki, T. and Toyoda, M. 1999. Scavenging mechanisms of (-)-epigallocatechin gallate and (-)-epicatechin gallate on peroxyl radicals and formation of superoxide during the inhibitory action. Free Radical Biol. Med. 27: 855-863. 4. Lizárraga, D., Lozano, C., Briede, J. J., van Delft, J. H., Touriño, S., Centelles, J. J., Torres, J. L. and Cascante, M. 2007. The importance of polymerization and galloylation for the antiproliferative properties of procyanidin-rich natural extracts. FEBS J. 274: 4802-4811. 5. Rice-Evans, C. A., Miller, N. J. and Paganga, G. 1996. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radical Biol. Med. 20: 933-956. 6. Tan, X. H., Hu, D. R., Li, S. R., Han, Y., Zhang, Y. L. and Zhou, D. Y. 2000. Differences of four catechins in cell cycle arrest and induction of apoptosis in LoVo cells. Cancer Lett. 158: 1-6. 3351

7. Torres, J. L., Varela, B., García, M. T., Carilla, J., Matito, C., Centelles, J. J., Cascante, C., Sort, X. and Bobet, R. 2002. Valorization of grape (Vitis vinifera) byproducts. Antioxidant and biological properties of polyphenolic fractions differing in procyanidin composition and flavonol content. J. Agric. Food Chem. 50: 7548-7555. 8. Touriño, S., Lizárraga, D., Carreras, A., Lorenzo, S., Ugartondo, V., Mitjans, M., Vinardell, M. P., Juliá, L., Cascante, M. and Torres, J. L. 2008. Highly Galloylated Tannin Fractions from Witch Hazel (Hamamelis virginiana) Bark: Electron Transfer Capacity, In Vitro Antioxidant Activity and Effects on Skin Related Cells. Chem. Res. Toxicol.: in press, doi: 10.1021/tx700362u. 9. Touriño, S., Selga, A., Jiménez, A., Juliá, L., Lozano, C., Lizárraga, D., Cascante, M. and Torres, J. L. 2005. Procyanidin fractions from pine (Pinus pinaster) bark: Radical scavenging power in solution, antioxidant activity in emulsion and antiproliferative effect in melanoma cells. J. Agric. Food Chem. 53: 4728-4735. 10. Valko, M., Leibfritz, D., Moncol, J., Cronin, M. T. D., Mazur, M. and Telser, J. 2007. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol. 39: 44-84. 3352