7 Upon analyzing the influence of the physiological conditions in the stomach and small intestine on pomegranate bioactive compounds bioavailability using an in vitro availability method,8 it was demonstrated

that pomegranate phenolic compounds are available during digestion in a high amount (29%). Nevertheless, due to pH, anthocyanins are largely transformed into non-red forms, or degraded. Thus, active components of PJ are indeed absorbed and subsequently affect biological processes which are related to atherogenesis Inhibitors,research,lifescience,medical protection. POMEGRANATE CONSUMPTION ATTENUATES ATHEROSCLEROSIS DEVELOPMENT PJ is suggested as the “heart-healthy” fruit juice,9 and it was indeed shown to attenuate cardiovascular diseases.10 Measurements of the arterial stiffness of the common selleck products carotid arteries in 73 patients with at least one cardiovascular risk factor who consumed PJ (Wonderful variety, 240 mL/day for 1 year), Inhibitors,research,lifescience,medical showed trends to increased arterial elasticity in the PJ-treated group versus the placebo-treated group (who received beverage of similar caloric content, flavor, and color). The effect of a daily consumption of PJ for 3 months on myocardial perfusion in 45 patients who had coronary

Inhibitors,research,lifescience,medical heart disease (CHD) was also studied.11 Patients were randomly assigned into one of two groups: a PJ group (240 mL/day) or a placebo group. The experimental and control groups showed similar levels of stress-induced ischemia at baseline. After 3 months, however, the extent of stress-induced ischemia decreased in the pomegranate group,

but increased in the control group. This benefit was observed without changes in cardiac medications, blood sugar, hemoglobin Inhibitors,research,lifescience,medical A1c, body weight, or blood pressure, in either group.11 We next investigated the effects of PJ consumption by patients with carotid artery stenosis (CAS) on carotid lesion size, in association with changes in oxidative stress.12 Ten patients were supplemented with PJ for up to 1 year, and Inhibitors,research,lifescience,medical nine CAS patients who did not consume PJ served as a control group. Blood samples were collected before treatment and after 3, 6, 9, and 12 months of PJ consumption. Patients’ carotid intima-media thickness (CIMT) was compared between the PJ group and the control group. While in the control patients Entinostat group (no PJ) CIMT increased by 10% after 1 year (Figure 1A), PJ consumption resulted in a significant CIMT reduction, by up to 35% (Figure 1B). Analysis of the mean CIMT (of the left and right common carotid arteries) before and during PJ consumption revealed a gradual reduction of 13%, 22%, 26%, and 35%, as observed after 3, 6, 9, and 12 months of PJ consumption, respectively, in comparison to selleck bio baseline values. On examination of the internal carotid arteries, flow velocities were calculated at the stenotic sites and expressed by peak systolic velocity (PSV) and end-diastolic velocity (EDV).