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Mechanisms and Biomarkers (WG 4) page 50<br />

__________________________________________________________________________________________<br />

Further evidence on tomato/lycopene action have been reported by Riso et al. (1999) who<br />

demonstrated a significant reduction in DNA damage (evaluated by the comet assay) of<br />

lymphocytes challenged ex vivo with H2O2 after the consumption of both 60 g tomato puree<br />

(about 16.5 mg lycopene) for 3 weeks, and 25 g tomato puree (about 7 mg lycopene) for 2<br />

weeks (Porrini and Riso, 2000). They also found an inverse relation between DNA damage<br />

and plasma and lymphocyte lycopene concentration (Porrini and Riso, 2000), supporting the<br />

hypothesis of a consistent contribution of lycopene on cell protection from the oxidative<br />

damage but not excluding the contribution of other tomato antioxidants. This inverse<br />

relationship was also demonstrated by the cell culture group in this Network.<br />

Protein oxidation<br />

More research is needed to investigate the possible effect of lycopene and tomato products on<br />

the prevention of protein oxidation as few data are available. Rao and Agarwal (1998b) found<br />

a trend towards lower protein oxidation estimated by measuring the loss of reduced thiol<br />

groups, after 1 week consumption of different tomato based products, as previously reported,<br />

however this decrease was not significant.<br />

Immunomodulation<br />

The first site of extracellular ROS attack on the cell is the poly unsaturated fatty acid-rich cell<br />

membrane which is very susceptible to oxidative stress. Lipid peroxidation alters membrane<br />

fluidity (Baker and Meydani, 1994) disrupts membrane integrity and modulates cell function,<br />

signal transduction and phagocyte response, to compromise all aspects of the immune system.<br />

Watzl et al. (1999) recently demonstrated that 2 weeks of tomato juice consumption<br />

significantly enhanced IL-2 and IL-4 secretion but not lymphocyte proliferation compared<br />

with values obtained after a low carotenoid diet. However the period of depletion itself<br />

suppressed cytokine secretion and cell proliferation, supporting an effect of restoring the<br />

original condition more than a specific or unique effect of tomato consumption.<br />

Plasma antioxidant capacity and other protective effect<br />

The total peroxyl radical trapping potential of plasma (TRAP), as an index of antioxidant<br />

capacity, should provide indication of the modification in reactivity due to increased plasma<br />

antioxidants following an intervention with tomato products. However different authors<br />

suggest that TRAP can not be appropriate for studying the in vivo effect of the consumption<br />

of lipophilic antioxidant rich foods on plasma antioxidant capacity.

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