Several lines of evidence from epidemiological and intervention studies suggest that dietary intake of tomatoes and tomato products is associated with decreased risk of CVD(Reference Street, Comstock and Salkeld1–Reference Gianetti, Pedrinelli and Petrucci4). In a multicentre case–control study in ten European countries, plasma levels of lycopene, which represents more than 80 % of total tomato carotenoids, were found to be protective with regard to acute myocardial infarction(Reference Kohlmeier, Kark and Gomez-Gracia2). In corroboration, low lycopene concentrations are evidently associated with an increased incidence of CVD.
Compelling experimental data support the protective role of tomato ingredients against processes involved in atherogenesis. Antioxidant effects of lycopene play a key role(Reference Levy, Zaltsberg and Ben-Amotz5, Reference Upritchard, Sutherland and Mann6). Lycopene has free radical-scavenging properties and accordingly reduces oxidative stress(Reference Klebanov, Kapitanov and Teselkin7). Dietary supplementation of lycopene has been associated with reduction in lipid peroxidation and LDL oxidation(Reference Levy, Zaltsberg and Ben-Amotz5, Reference Upritchard, Sutherland and Mann6, Reference Agarwal and Rao8, Reference Devaraj, Mathur and Basu9). In addition, a number of other anti-atherogenic mechanisms have been reported. Lycopene inhibited cytokine-induced expression of vascular cell adhesion molecule-1 and intercellular cell adhesion molecule-1, thereby reducing monocyte adhesion to human endothelial cells(Reference Martin, Wu and Meydani10, Reference Hung, Huang and Chen11). Lycopene showed anti-proliferative properties in smooth muscle cells by preventing platelet-derived growth factor-BB-induced migration and proliferation(Reference Lo, Hung and Tseng12). Furthermore, lycopene exerted a hypocholesterolaemic effect by inhibiting cholesterol synthesis(Reference Fuhrman, Elis and Aviram13).
There is some evidence that tomato carotenoids also have beneficial effects on endothelial function, which plays a key role in vascular homoeostasis. Serum lycopene concentrations were inversely related to soluble intercellular adhesion molecule-1, a marker of endothelial function and inflammation(Reference van Herpen-Broekmans, Klöpping-Ketelaars and Bots14, Reference Hozawa, Jacobs and Steffes15). Lycopene supplementation prevented endothelial dysfunction in mice fed an atherogenic diet(Reference Suganuma and Inakuma16). Until now, it remains unclear whether tomato ingredients could have an impact on endothelial function in humans. The aim of the present study was therefore to investigate whether acute or long-term consumption of tomato products ameliorates peripheral endothelial function in human volunteers in a randomised, cross-over dietary intervention study.
Subjects and methods
Study design
Non-smoking healthy postmenopausal women were recruited by press advertisements. A total of thirty-one women were invited for clinical examination. Subjects with cardiovascular risk factors such as high blood cholesterol, diabetes, arterial hypertension and obesity were excluded. All measures of clinical parameters were required to lie within normal ranges for study inclusion: lipid profile, blood pressure, BMI, as well as routine internal and endocrine parameters. Eight subjects were excluded for not meeting the inclusion criteria. Three subjects refused to participate. Twenty subjects received the allocated interventions, one person did not yield evaluable endothelial function measurements. A total of nineteen healthy women completed the study. None of the participants had taken medication for at least 3 months before entering the study. The participants were asked not to consume tomato products at least 2 weeks before and during the study.
Study subjects consumed a buttered roll with or without tomato purée (70 g) in the morning after an overnight fast, in accordance with computer-generated randomisation numbers in a cross-over study design. Lycopene content was determined in the commercially available tomato purée used in the study (Smart Price Tomatenmark, Wal-Mart, Germany). Products from one batch were used throughout the study. Endothelial function was assessed at six time points for each patient: at baseline, 24 h and 7 d after consumption of a buttered roll with tomato purée (tomato period); second baseline after 14 d of tomato-free diet; 24 h and 7 d after daily consumption of a buttered roll without tomato purée (control period). At all six time points, blood pressure and heart rate were assessed at rest, and blood was collected for assessment of lycopene levels and measurement of plasma levels for total cholesterol, HDL-cholesterol, LDL-cholesterol and TAG. The study was approved by the Charité University Hospital Ethics Committee, and participants provided their written informed consent. The study was carried out in accordance with The Code of Ethics of the World Medical Association (Declaration of Helsinki).
Determination of lycopene plasma levels
Carotenoids were extracted according to Bieri et al. (Reference Bieri, Brown and Smith17), and with slight modification(Reference Fröhlich, Kaufmann and Bitsch18). Echinenone (CaroteNature, Lupsingen, Switzerland) was used as internal standard. All the experiments were carried out under subdued light to prevent photodegradation and isomerisation. The plasma extracts were analysed on a C30 (250 × 4·6 mm, 5 μm) column (Trentec, Rutesheim, Germany), preceded by a C18 ProntoSil 120-5-C18 H (10 × 4·0 mm, 5 μm) guard column (Bischoff, Leonberg, Germany) at 10 ± 1°C with diode array detection at 470 nm. The mobile phase (1·0 ml/min) consisted of methanol (MeOH) and methyl tert-butyl-diethyl ether (MTBE). The following gradient procedure was used: (1) initial condition with 90 % MeOH and 10 % MTBE; (2) a 40 min linear gradient to 50 % MeOH and 50 % MTBE; (3) 50 % MeOH and 50 % MTBE for 20 min; (4) a 10 min linear gradient to 90 % MeOH and 10 % MTBE; (5) 90 % MeOH and 10 % MTBE for 10 min. Lycopene was quantified using (all-E)-lycopene reference material (CaroteNature, Lupsingen, Switzerland). The concentration of the lycopene stock solution was checked periodically in n-hexane at 472 nm by using its extinction coefficient E (1 %, 1 cm): 3450(Reference Craft, Brown and Smith19). The plasma lycopene levels were given as total lycopene (sum of all detected lycopene isomers).
Measurement of endothelial function of the brachial artery
Endothelial function was measured by high-resolution vascular ultrasound with a 13 MHz linear array transducer (Sonoline An-tares, Siemens, Germany) as recently described(Reference Jochmann, Lorenz and Krosigk20). Briefly, endothelium-dependent flow-mediated dilation (FMD) was assessed by measuring the change in brachial artery diameter for 2 min after reactive hyperaemia for 5 min, according to the established guidelines(Reference Corretti, Anderson and Benjamin21, Reference Pyke and Tschakovsky22). Endothelium-independent nitro-mediated dilation was measured after sublingual application of nitroglycerine spray (0·4 mg) for 6 min. To improve the accuracy and reproducibility of the measurements, an attached device fixed the ultrasound probe at one site of the brachial artery during the entire period of measurement. FMD and nitro-mediated dilation were defined as the maximum percentage change in brachial artery diameter compared with baseline measurement. Analyses of diameter changes were conducted offline (Tom Tec Imaging Systems, Unterschleissheim, Germany) by two different investigators blinded to subject treatment.
Statistical analysis
All the statistical analyses were two-sided with the level of significance accepted at P < 0·05. A linear mixed model with random effects for the control period and without random effects for the lycopene period (all participants had a positive slope over the three time points) was used for comparisons of plasma lycopene contents between the time points (time as fixed effect). Spearman's correlations were used for determinations of intra- and interobserver variability in endothelial function measurements and for associations between FMD and plasma lycopene levels. Statistical analysis was performed using SPSS, release 15.0 (SPSS, Inc., Chicago, IL, USA). The linear mixed models were programmed with R (version 2.6.2).
Results
A total of nineteen postmenopausal healthy women (mean age 58·9 (sd 6·3) years) finished the study protocol. Baseline characteristics of the study group are depicted in Table 1. Lycopene content of the tomato purée was determined before the start of the study: 70 g of the purée contained 46·2 mg of lycopene. Thus, the volunteers consumed 46·2 mg of lycopene/d. Plasma levels of lycopene at baseline and after consumption of 70 g tomato purée/d are shown in Fig. 1. A slight decrease in lycopene plasma levels was observed after 7 d in the control group. However, compared with controls, consumption of tomato purée resulted in an increase of lycopene plasma levels by 38 % after 24 h and by 145 % after 7 d.
Owing to the cross-over design of the study, endothelial function was assessed at each time point with tomato purée consumption (tomato period) and without tomato purée (control period) for all the subjects. The intra- and interobserver variabilities were 0·99 and 0·98 for baseline diameter of the arteria brachialis and 0·99 and 0·99 for maximum dilation (FMD), respectively. FMD levels at baselines (control and tomato periods) revealed a broad inter-individual variation, ranging from 2·9 to 14·8 %. Mean baseline FMD was 7·8 (sem 3·3)% before the tomato period and 7·7 (sem 3·2)% before the control period. Compared with baseline, there were no significant differences in FMD after acute (24 h) or chronic (7 d) tomato purée consumption (8·2 (sem 2·8)% after 24 h and 8·3 (sem 2·7)% after 7 d of intervention with tomato purée). In addition, we found no significant differences in FMD between the tomato and control periods at any time point investigated (after 24 h: 8·6 (sem 3·5)% for control and 8·2 (sem 2·8)% for the tomato period; after 7 d: 8·2 (sem 2·7)% for control and 8·3 (sem 2·7)% for the tomato period). Finally, there was no significant correlation between lycopene plasma levels and FMD (Fig. 2). Likewise, endothelium-independent nitro-mediated dilation was not modulated by tomato consumption (data not shown).
Discussion
In a randomised, cross-over dietary intervention study, healthy non-smoking postmenopausal women consumed lycopene from tomato purée for 1 week. Although lycopene was absorbed and resulted in a significant increase in lycopene plasma levels compared with baseline and the control period (no tomato purée), endothelial-dependent vasodilation was not influenced by this intervention.
Experimental evidence suggests that lycopene may ameliorate the endothelial function in animal models. Suganuma & Inakuma(Reference Suganuma and Inakuma16) reported that dietary ingestion of tomato protected hypercholesterolaemic mice from endothelial dysfunction. The uptake of tomato inhibited the increase of lipid peroxides in mouse plasma in their study, suggesting that lycopene may act primarily as an antioxidant in plasma. It is well established that enhanced production or attenuated degradation of reactive oxygen species leads to oxidative stress, a process that affects endothelial function. Reactive oxygen species can interact with and inactivate NO, which is produced by the normal vascular endothelium and is a principal determinant of normal endothelial vascular function. Reduced NO bioavailability results in endothelial dysfunction and increased risk of CVD(Reference Cai and Harrison23). FMD assessment for endothelial function is regarded as a predictor for future cardiovascular events(Reference Halcox, Donald and Ellins24). Purified lycopene supplementation decreased biomarkers of oxidative stress in human subjects(Reference Devaraj, Mathur and Basu9). Very recently, an inverse relationship between lycopene plasma concentration and arterial stiffness as well as oxLDL has been shown in healthy women(Reference Kim, Yoe and Kim25). However, the increase in lycopene plasma levels did not affect plasma lipophilic antioxidant capacity in the present study (data not shown).
Several reasons for the missing effects of tomato purée on endothelial function in the present study may be discussed. First, it is conceivable that the present study group was ‘too healthy’ and basal endothelial function too good to enable detection of significant effects. Since antioxidant mechanisms are very much in the foreground of lycopene properties, situations in which increased oxidative stress and subsequent endothelial dysfunction are present – such as observed in chronic smokers – might have shown different results. In addition, the inclusion of women only could have biased the outcome.
Another limitation of the present study represents the duration of the intervention time. It may have been too short, and chronic effects after long-term consumption may play a role in the vasculoprotective effects of tomato products. In a human intervention study, patients with type 2 diabetes were supplemented with tomato juice for 4 weeks. The intervention resulted in a nearly threefold increase in plasma lycopene levels. The authors found an increase in the lag time of Cu-induced oxidation of isolated LDL ex vivo. However, cardiovascular parameters in vivo (plasma lipid levels, blood pressure, levels of C-reactive protein and circulating pro-inflammatory cell adhesion molecules) did not change significantly after intervention in this study(Reference Upritchard, Sutherland and Mann26). Although a fair number of epidemiological indications for beneficial effects of tomato products on the cardiovascular system are available, sound data on intervention studies are sparse. The rationale for the rather short intervention time in the present study was based on other studies with plant-derived interventions. Consumption of red and white wine resulted in significant improvement in endothelial function (FMD) after 3 h in subjects with coronary artery disease(Reference Whelan, Sutherland and McCormick27). Likewise, green and black tea improved FMD in healthy postmenopausal women – the same kind of subjects as employed in the present study – already after 2 h(Reference Jochmann, Lorenz and Krosigk20). In healthy males, ingestion of a flavanol-rich cocoa drink increased FMD 1–4 h after consumption(Reference Schroeter, Heiss and Balzer28). Even more pronounced, an acute (after 2 h) as well as a long-term, sustained increase in FMD was observed after daily consumption of a high-flavanol cocoa drink for a period of 7 d in healthy male smokers(Reference Heiss, Finis and Kleinbongard29). These data indicate the efficacy of food-derived interventions to improve the endothelial function, both after shorter intervention times and in healthy subjects.
Clearly, there is a difference in the time and mode of action between the above-mentioned foods and tomato products in terms of endothelial function measured as FMD. The potential reasons for this discrepancy can only be speculated upon. It may be attributed to the fact that hydrophilic water-soluble polyphenols may influence the cellular processes directly and in a rather short time via activation of cellular surface receptors. Lipophilic carotenoids are mainly transported within lipoproteins in the blood(Reference Goulinet and Chapman30). It can be argued that their hydrophobic nature prevents the direct access to cell receptors and hence immediate cellular responses. Plasma kinetics also differ between polyphenols and lipophilic carotenoids. While plant-derived polyphenols are adsorbed rapidly in the blood within a few hours, carotenoids require a longer time of adsorption. Thus, much longer intervention times might be required to observe the physiological effects with tomato products. However, since we found slightly elevated plasma lycopene levels already after 24 h, and a significant increase after 7 d of intervention, we feel confident that the intervention time in the present study was long enough to detect potential changes in endothelial function.
In conclusion, the present study shows that there is no vascular effect demonstrable by the measurement of FMD after intervention with tomato purée for 7 d in healthy postmenopausal women. Further investigation is warranted to determine whether beneficial effects may be observed in subjects exhibiting various cardiovascular risk factors known to result in endothelial dysfunction.
Acknowledgements
The authors thank Christian Gafert, Marco Russo, Aline Höfer and Vanessa Witzel for their excellent technical assistance. V. S. contributed to study conception, supervision of the study, data interpretation and writing of the manuscript. C. K. participated in the conduction of the human study and data collection. S. H. carried out the measurement of endothelial function and was involved in data generation and data analysis. N. J. participated in the experimental design, data interpretation and preparation of the manuscript. C. J. took part in data analysis and validation. V. B., K. F. and L. M. measured plasma lycopene levels and antioxidant capacities. In addition, they took part in writing of the manuscript. C. G. did the statistical analysis. M. L. was involved in experimental design, data interpretation, data validation and the writing of the manuscript. The authors have no conflicts of interest regarding the paper. The present work was supported by the European Community Sixth Framework Programme (IP 016213).