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1.
Br J Nutr ; 116(4): 639-47, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27464461

ABSTRACT

Previous studies have shown that the intake of freeze-dried strawberry powder (FDSP) improves select markers of cardiovascular health in adults with cardiovascular risk factors; however, whether these improvements can be observed in at-risk adolescents is unknown. A randomised, double-blind, cross-over study enrolled twenty-five overweight or obese males, aged 14-18 years, to consume 50 g of a FDSP or a control powder, daily for 1 week. Before and after each test period, measures of microvascular function, plasma nitrate/nitrite, platelet reactivity and blood lipids were collected at baseline and acutely 1 h after FDSP intake. Acute plasma nitrate/nitrite levels increased 1 h after consuming the FDSP during Study Visit 1 before daily FDSP intake (P<0·001) and during Study Visit 2 after 1 week of FDSP intake (P<0·001) compared with control powder intake. As a group, fasting nitrate/nitrite levels did not significantly change after 1 week of control or FDSP intake. However, for those individuals where fasting nitrate levels increased after short-term FDSP intake compared with controls, an increase in reactive hyperaemia index (RHI) was observed (P=0·014), whereas RHI was unchanged in those individuals who did not have a significant increase in nitrate (P=0·396). Taken together, these data support the concept that strawberries can provide vascular health benefits to heavier adolescent males.


Subject(s)
Cardiovascular Diseases/prevention & control , Diet , Fragaria , Overweight/diet therapy , Pediatric Obesity/diet therapy , Adolescent , Beverages , Biomarkers/blood , Cardiovascular Diseases/etiology , Cross-Over Studies , Double-Blind Method , Fasting/blood , Freeze Drying , Humans , Hyperemia , Lipids/blood , Male , Nitrates/blood , Nitrites/blood , Overweight/blood , Overweight/complications , Pediatric Obesity/blood , Pediatric Obesity/complications , Platelet Activation , Postprandial Period , Powders , Risk Factors
2.
J Nutr Biochem ; 26(12): 1458-66, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26396054

ABSTRACT

Improved vascular function after the incorporation of walnuts into controlled or high-fat diets has been reported; however, the mechanism(s) underlying this effect of walnuts is(are) poorly defined. The objective of the current study was to evaluate the acute and short-term effects of walnut intake on changes in microvascular function and the relationship of these effects to plasma epoxides, the cytochrome-P450-derived metabolites of fatty acids. Thirty-eight hypercholesterolemic postmenopausal women were randomized to 4 weeks of 5 g or 40 g of daily walnut intake. All outcomes were measured after an overnight fast and 4 h after walnut intake. Microvascular function, assessed as the reactive hyperemia index (RHI), was the primary outcome measure, with serum lipids and plasma epoxides as secondary measures. Compared to 5 g of daily walnut intake, consuming 40 g/d of walnuts for 4 weeks increased the RHI and Framingham RHI. Total cholesterol and low- and high-density cholesterol did not significantly change after walnut intake. The change in RHI after 4 weeks of walnut intake was associated with the change in the sum of plasma epoxides (r=0.65, P=.002) but not with the change in the sum of plasma hydroxyeicosatetraenoic acids. Of the individual plasma epoxides, arachidonic-acid-derived 14(15)-epoxyeicosatrienoic acid was most strongly associated with the change in microvascular function (r=0.72, P<.001). These data support the concept that the intake of walnut-derived fatty acids can favorably affect plasma epoxide production, resulting in improved microvascular function.


Subject(s)
Epoxy Compounds/blood , Juglans , Microcirculation/physiology , Nuts , Aged , Arachidonic Acid/chemistry , Cholesterol, HDL/metabolism , Cholesterol, LDL/metabolism , Diet , Diet, High-Fat , Fatty Acids/blood , Fatty Acids/metabolism , Female , Humans , Hypercholesterolemia/metabolism , Hyperemia/metabolism , Linoleic Acid/blood , Lipids/blood , Lipoproteins/blood , Middle Aged , Oxylipins/blood , Oxylipins/metabolism
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