Benefits
Healthy platelet function
In randomized, double-blind trials Fruitflow lowered platelet aggregation measured in blood samples drawn from the people who took it. In the largest, 90 healthy adults, aggregation to a low dose of ADP fell 21.3 percent from baseline three hours after the higher serving, while the control supplement produced no significant change. The European Commission authorised the wording that water-soluble tomato concentrate helps maintain normal platelet aggregation, which contributes to healthy blood flow. This is a laboratory measure of how platelets behave, not a measured reduction in clots or in cardiovascular events.
Blood flow, as worded in the authorised claim
The authorised European wording links maintained platelet aggregation to healthy blood flow, but that link is the regulator's inference from platelet measurements: no Fruitflow trial has measured blood flow or circulation in a person. Do not treat it as a substitute for aspirin or for any prescribed blood thinner. In the one trial that compared them, Fruitflow suppressed platelet function by about a third as much as 75 mg of daily aspirin, and nothing in that trial examined the stomach.
Fast and lasting effect
A single serving lowered platelet aggregation about three hours later in cannulated volunteers, and the change was still present more than 12 hours on. The size depended on how hard the platelets were pushed: 2.9 percent inhibition at a strong ADP stimulus, 20.0 percent at a weak one. In a separate crossover study the effect was still measurable 24 hours after a 150 mg dose.
Mechanism of action
Platelet aggregation inhibition
In laboratory work the tomato compounds blocked platelet aggregation triggered by ADP, collagen, thrombin and arachidonate, an effect linked to glycoprotein IIb/IIIa and to platelet secretion. Unlike aspirin, the action is reversible rather than an irreversible block of cyclooxygenase, so it wears off as the dose clears.
From platelets to blood flow: an inferred step
Lower platelet activation would be expected to reduce the tendency of platelets to stick to vessel walls. Endothelial function and blood flow have not been measured in any human Fruitflow trial, so this step is inferred from the platelet data rather than shown.
Clinical trials
Double-blind randomized crossover trial in 47 healthy adults, comparing Fruitflow with acute and 7-day 75 mg aspirin over a 5-hour timecourse. All study costs, supplements and equipment were provided by Provexis plc, which sells the ingredient, and four of the six authors were Provexis employees at the time. (O'Kennedy et al. 2017, European Journal of Clinical Nutrition)
Healthy adults.
Fruitflow lowered platelet aggregation and thromboxane A2 generation and extended the time to form a clot, against both baseline and control. A single dose of aspirin and a dose of Fruitflow were about equally effective, but aspirin taken daily for seven days was roughly three times as effective, so the paper concludes Fruitflow's suppression of platelet function is about one third that of daily 75 mg aspirin. Plasma clotting times were unchanged, and taking Fruitflow together with aspirin added nothing significant. Responses varied widely between people. Platelet function is a laboratory measure: the trial did not follow anyone for heart attacks, strokes or clots.
Half of this paper is in vitro work on isolated platelets. The human half is a 7-hour time-course in 23 cannulated volunteers given a drink containing tomato extract equivalent to six tomatoes. It is not described as double-blind or placebo-controlled: that design belongs to the companion 90-person crossover published in the same issue of the journal. The work was carried out by Provexis plc, which sells the ingredient. (O'Kennedy et al. 2006, American Journal of Clinical Nutrition)
Healthy adults.
Three hours after the drink, platelet aggregation measured in drawn blood was inhibited by 2.9 percent at a strong ADP stimulus and by 20.0 percent at a weak one, and the change persisted beyond 12 hours. Coagulation measures were unchanged. The in vitro half of the paper linked the effect to glycoprotein IIb/IIIa and to platelet secretory mechanisms.