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Addressing Hypertension via Nutrition (Stalking a Silent Killer)

by Heather Granato
09/15/2008
Continued from page 8

One of the most consumed beverages in the world, tea, also offers benefits to blood pressure. A recent review out of the University of Missouri-Columbia noted consumption of tea, and its abundant polyphenol epigallocatechin-3-gallate (EGCG), may improve endothelial function and hypertension.47 In fact, animal research has shown green tea extract has the ability to prevent induced hypertension in rats, which was attributed to prevention of oxidative damage, supporting vascular health.48

Polyphenols found in pine bark extract have been investigated for their impact on vascular health. One placebo-controlled, double blind study out of China examined the impact of 100 mg/d of pine bark extract (as Pycnogenol®, from Horphag, supplied by Natural Health Science) on patients with hypertension.49 The intervention improved endothelial function, decreasing endothelin-1 concentrations and increasing NO levels in plasma, although there were no significant changes in heart rate. A 12-week pilot study from New Zealand examined the impact of pine bark extract (as Enzogenol®, from ENZO Nutraceuticals, supplied by B&D Nutritional Ingredients) plus vitamin C on blood pressure and other cardiac parameters.50 Intervention at a dose of 480 mg/d pine bark extract and 240 mg/d vitamin C was associated with a significant reduction in systolic blood pressure.

The majority of research to date on Ginkgo biloba has focused on its possible benefit to cognitive function; however, studies are investigating its possible effect on blood pressure, though results have been mixed. Japanese researchers reported ginkgo extract could decrease salt-related elevation of blood pressure and support vasodilation in rats;51 another Japanese rat trial found a standardized ginkgo extract (as EGb 761) could suppress age-related increases in blood pressure.52 However, additional work from Japan found ginkgo extract worked to reduce blood pressure in younger animals, but impaired peripheral circulation and increased liver weight in aged hypertensive rats, suggesting a need for further investigation on its effects.53

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