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      Brazil nuts intake improves lipid profile, oxidative stress and microvascular function in obese adolescents: a randomized controlled trial

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          Abstract

          Background

          Obesity is a chronic disease associated to an inflammatory process resulting in oxidative stress that leads to morpho-functional microvascular damage that could be improved by some dietary interventions. In this study, the intake of Brazil nuts ( Bertholletia excelsa), composed of bioactive substances like selenium, α- e γ- tocopherol, folate and polyunsaturated fatty acids, have been investigated on antioxidant capacity, lipid and metabolic profiles and nutritive skin microcirculation in obese adolescents.

          Methods

          Obese female adolescents (n = 17), 15.4 ± 2.0 years and BMI of 35.6 ± 3.3 kg/m 2, were randomized 1:1 in two groups with the diet supplemented either with Brazil nuts [BNG, n = 08, 15-25 g/day (equivalent to 3 to 5 units/day)] or placebo [PG (lactose), n = 09, one capsule/day] and followed for 16 weeks. Anthropometry, metabolic-lipid profiles, oxidative stress and morphological (capillary diameters) and functional [functional capillary density, red blood cell velocity (RBCV) at baseline and peak (RBCV max) and time (TRBCV max) to reach it during post-occlusive reactive hyperemia, after 1 min arterial occlusion] microvascular variables were assessed by nailfold videocapillaroscopy at baseline (T0) and after intervention (T1).

          Results

          T0 characteristics were similar between groups. At T1, BNG (intra-group variation) had increased selenium levels ( p = 0.02), RBCV ( p = 0.03) and RBCV max ( p = 0.03) and reduced total (TC) ( p = 0.02) and LDL-cholesterol ( p = 0.02). Compared to PG, Brazil nuts intake reduced TC ( p = 0.003), triglycerides ( p = 0.05) and LDL-ox ( p = 0.02) and increased RBCV ( p = 0.03).

          Conclusion

          Brazil nuts intake improved the lipid profile and microvascular function in obese adolescents, possibly due to its high level of unsaturated fatty acids and bioactive substances.

          Trial Registration

          Clinical Trials.gov NCT00937599

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          Most cited references27

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          Oxidative stress and metabolic syndrome.

          Metabolic syndrome is a collection of cardiometabolic risk factors that includes obesity, insulin resistance, hypertension and dyslipidemia. Although there has been significant debate regarding the criteria and concept of the syndrome, this clustering of risk factors is unequivocally linked to an increased risk of developing type 2 diabetes and cardiovascular disease. Metabolic syndrome is often characterized by oxidative stress, a condition in which an imbalance results between the production and inactivation of reactive oxygen species. Reactive oxygen species can best be described as double-edged swords; while they play an essential role in multiple physiological systems, under conditions of oxidative stress, they contribute to cellular dysfunction. Oxidative stress is thought to play a major role in the pathogenesis of a variety of human diseases, including atherosclerosis, diabetes, hypertension, aging, Alzheimer's disease, kidney disease and cancer. The purpose of this review is to discuss the role of oxidative stress in metabolic syndrome and its major clinical manifestations (namely coronary artery disease, hypertension and diabetes). It will also highlight the effects of lifestyle modification in ameliorating oxidative stress in metabolic syndrome. Discussion will be limited to human data.
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            A walnut diet improves endothelial function in hypercholesterolemic subjects: a randomized crossover trial.

            Epidemiological studies suggest that nut intake decreases coronary artery disease (CAD) risk. Nuts have a cholesterol-lowering effect that partly explains this benefit. Endothelial dysfunction is associated with CAD and its risk factors and is reversed by antioxidants and marine n-3 fatty acids. Walnuts are a rich source of both antioxidants and alpha-linolenic acid, a plant n-3 fatty acid. To test the hypothesis that walnut intake will reverse endothelial dysfunction, we randomized in a crossover design 21 hypercholesterolemic men and women to a cholesterol-lowering Mediterranean diet and a diet of similar energy and fat content in which walnuts replaced approximately 32% of the energy from monounsaturated fat. Participants followed each diet for 4 weeks. After each intervention, we obtained fasting blood and performed ultrasound measurements of brachial artery vasomotor function. Eighteen subjects completing the protocol had suitable ultrasound studies. Compared with the Mediterranean diet, the walnut diet improved endothelium-dependent vasodilation and reduced levels of vascular cell adhesion molecule-1 (P<0.05 for both). Endothelium-independent vasodilation and levels of intercellular adhesion molecule-1, C-reactive protein, homocysteine, and oxidation biomarkers were similar after each diet. The walnut diet significantly reduced total cholesterol (-4.4+/-7.4%) and LDL cholesterol (-6.4+/-10.0%) (P<0.05 for both). Cholesterol reductions correlated with increases of both dietary alpha-linolenic acid and LDL gamma-tocopherol content, and changes of endothelium-dependent vasodilation correlated with those of cholesterol-to-HDL ratios (P<0.05 for all). Substituting walnuts for monounsaturated fat in a Mediterranean diet improves endothelium-dependent vasodilation in hypercholesterolemic subjects. This finding might explain the cardioprotective effect of nut intake beyond cholesterol lowering.
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              Impaired microvascular function in obesity: implications for obesity-associated microangiopathy, hypertension, and insulin resistance.

              Obesity is associated with an increased risk of developing microangiopathy, hypertension, and insulin resistance. We hypothesized that obesity is a primary cause of microvascular dysfunction, which may contribute to the development of these obesity-related disorders. We examined microvascular function in 16 lean (body mass index 30 kg/m2) healthy women (mean age, 38.9+/-6.7 years) in the basal state and during physiological systemic hyperinsulinemia. We determined skin capillary recruitment after arterial occlusion with capillaroscopy and skin endothelium-(in)dependent vasodilation by iontophoresis of acetylcholine and sodium nitroprusside. Obese women, compared with lean women, had higher systolic blood pressure (P<0.05), impaired insulin sensitivity (P<0.01), impaired capillary recruitment in the basal state (P<0.05) and during hyperinsulinemia (P<0.05), and impaired acetylcholine-mediated vasodilation in the basal state (P<0.05) and during hyperinsulinemia (P<0.01). Sodium nitroprusside-mediated vasodilation was similar in lean and obese women. Capillary recruitment and acetylcholine-mediated vasodilation were positively correlated with insulin sensitivity (r=0.58, P<0.01 and r=0.55, P<0.01, respectively) and negatively with blood pressure (r=-0.64, P<0.001 and r=-0.42, P<0.05, respectively) in both lean and obese women. Obesity is characterized by impaired microvascular function in the basal state and during hyperinsulinemia and, in both lean and obese women, microvascular dysfunction is associated with increased blood pressure and decreased insulin sensitivity. These findings are consistent with a contribution of impaired microvascular function to the development of obesity-related microangiopathy, hypertension, and insulin resistance.
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                Author and article information

                Journal
                Nutr Metab (Lond)
                Nutrition & Metabolism
                BioMed Central
                1743-7075
                2011
                28 May 2011
                : 8
                : 32
                Affiliations
                [1 ]Clinical and Experimental Research Laboratory in Vascular Biology - BioVasc; Rua São Francisco Xavier, 524, Rio de Janeiro, CEP:20550-013 - Brazil
                [2 ]Endocrinology, Department of Internal Medicine; Clinical and Experimental Research Laboratory in Vascular Biology - BioVasc; Rua São Francisco Xavier, 524, Rio de Janeiro, CEP:20550-013 - Brazil
                [3 ]Nutrition Applied Department; Nutrition Institute - Rua São Francisco Xavier, 524, Rio de Janeiro, CEP: 20550-013 - Brazil
                [4 ]Study Center for Adolescent Health - NESA Av 28 de setembro,. 87, CEP: 20551-030, Rio de Janeiro - Brazil
                [5 ]Physiological Sciences Department; Clinical and Experimental Research Laboratory in Vascular Biology - BioVasc; Rua São Francisco Xavier, 524 , Rio de Janeiro CEP:20550-013 - Brazil
                [6 ]Study Center for Nutrition and Oxidative Stress; Nutrition Institute; Rua São Francisco Xavier, 524, Rio de Janeiro, CEP: 20550-013 - Brazil
                [7 ]Physiological Sciences and Clinical Medicine Departments; Clinical and Experimental Research Laboratory in Vascular Biology - BioVasc; Rua São Francisco Xavier, 524 Rio de Janeiro, CEP:20550-013 -Brazil
                Article
                1743-7075-8-32
                10.1186/1743-7075-8-32
                3123174
                21619692
                5547c9d6-55cb-4be9-a738-29e3d2a26c3e
                Copyright ©2011 Maranhão et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 February 2011
                : 28 May 2011
                Categories
                Research

                Nutrition & Dietetics
                microcirculation,obesity,brazil nuts,lipid profile,oxidative stress,adolescents
                Nutrition & Dietetics
                microcirculation, obesity, brazil nuts, lipid profile, oxidative stress, adolescents

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