IMR Press / FBS / Volume 12 / Issue 1 / DOI: 10.2741/S539
Review
Anti-atherosclerotic and cardiovascular protective benefits of Brazilian nuts
Show Less
1 Instituto de Ciencias Biologicas e da Saude, Campus Universitario do Araguaia, Universidade Federal de Mato Grosso, Av. Valdon Varjao, 6390, Setor Industrial, Barra do Garcas, 78.600-000, MT, Brazil
Send correspondence to: Carlos K B Ferrari, ICBS, Campus do Araguaia, Universidade Federal de Mato Grosso (UFMT), Av. Valdon Varjao, 6390, Setor Industrial, Barra do Garças, 78. 600-000, MT, Brazil, Tel: 55663402-0717, Fax: 55663402-0718, E-mail: drcarlosferrari.ufmt@gmail.com
Front. Biosci. (Schol Ed) 2020, 12(1), 38–56; https://doi.org/10.2741/S539
Published: 1 January 2020
(This article belongs to the Special Issue New trends in atherosclerosis research)
Abstract

Brazil nuts are rich in magnesium, selenium, arginine and other amino acids, dietary fiber, tocopherols (vitamin E), phytosterols, linoleic acid, linolenic acid, sitosterols, monounsaturated and polyunsaturated fatty acids, polyphenols and other amino acids. Due to such a rich mixture of nutrients, Brazil nuts protect LDL from peroxidation, and improve endothelial function, blood pressure, lipid metabolism, and decrease endothelial inflammatory markers, DNA oxidation, and blood lipids (cholesterol, LDL, triglycerides). Here, we review and propose biological mechanisms by which bioactive compounds of Brazil nuts afford protections against atherosclerosis and cardiovascular diseases. Just a few nuts per day provide sufficient cardiovascular benefits, including protection against development and progression of atherosclerosis.

Keywords
Atherosclerosis
beta-sitosterol
Linolenic acid
Magnesium
Tocopherol
Selenium
Arginine
Review
2. INTRODUCTION

Obtained from a South American tree, from Lecythidaceae family, the Brazil nut (Bertholletia excelsa) is an edible oleaginous seed found in the Amazon river basin, including Brazil, Peru, Ecuador, Colombia, and Venezuela (1). Brazil nuts are rich in oil (60-70%), protein (17%), fiber, selenium (Se), magnesium (Mg), potassium (K), phosphorus (P), zinc (Zn), calcium (Ca), copper (Cu), iron (Fe), niacin, thiamine, tocopherol, and vitamin B6 (1). Although Brazil nut is considered the richest food source of Se, the value of this microelement is higher in alkaline and neutral soils and lower in acidic lands (2). In this context, Brazil nuts from the Amazon region soils are very rich in Se, whereas Brazil nuts growing in soils from the neighborhood states, the so-called Legal Amazon, tend to have a lower concentration of this microelement (2,3). The objective of this review is to update the relationship of dietary intake of Brazil nuts and the mechanistic role of their bioactive compounds against atherosclerosis and cardiovascular disease.

3. EPIDEMIOLOGICAL ASPECTS

The two oldest studies regarding nuts, recorded in the MEDLINE, are descriptions of Trapa bispinosa and Anacardium occidentale, respectively published in 1927 and 1930 (4,5). Fraser et al. (6) developed the Adventist Health Study and reported that dietary intake of nuts (5 times per week) was associated with a 48% decrease in the risk of mortality from coronary heart disease (6). Six years later, the Nurses’ Health Study found that regular intake of nuts diminished the risk of coronary heart disease (CHD) and non-fatal myocardial infarction (7). The PREDIMED study, a Spanish cohort study covering 7,216 men and women, concluded that frequent consumption of Brazil nut (>3 servings per week) reduced overall, cardiovascular, and cancer mortality (8). In some populations, intake of Brazil nuts is frequent (9). Some studies suggested an association between dietary intake of nuts and decreased risk of other cardiovascular diseases, stroke, and possibly type 2 diabetes mellitus (10-12).

4. ATHEROPROTECTIVE EFFECT OF CONSTITUENTS OF BRAZIL NUTS

Brazil nuts are considered very nutritious, since they contain considerable amounts of fiber, macronutrients, micronutrients and bioactive compounds, such as phytosterols, phenolics, and flavonoids (1, 13, 14).

4.1. Dietary intake of Brazil nuts and protection against atherosclerosis

It has been suggested that frequent nut consumption is associated with decreased levels of total cholesterol (TC) in blood, improvements on blood pressure, vascular function, oxidative stress, inflammation, and also lowering of visceral adiposity and metabolic syndrome (15-20). Since 2006, Brazil nuts have been considered a rich source of bioactive compounds with antioxidant activity whose intake brings benefits to our health (16). Evaluating twenty foods, some of them regularly eaten by the Brazilian population, it was reported that Brazil nuts had the highest total antioxidant capacity in vitro (21). The values of the TEAC assay found in that study (21) were similar to those found in another study (22). Beyond improvement of body antioxidant status, dietary intake of Brazil nuts also increases Se levels increasing Se-dependent GPX as showed by three Brazilian studies in pre-school children, adults, and elderly subjects (23-25). If Brazil nuts enhance body antioxidant status it also decreases peroxidative reactions such as DNA oxidation and lipid peroxidation (23, 26, 27). A Brazilian study evaluated the effects of Brazil nut supplementation (one nut per day) on blood TC and blood glucose of 130 healthy volunteers (28). Authors found that Brazil nut supplementation significantly decreased both TC and blood glucose levels with no effect on malondialdehyde (MDA), HDL fraction, LDL fraction, C-reactive protein, and triglycerides. Lipid peroxidation and an inflammatory micro-environment on subendothelial space are responsible for atherosclerosis pathogenesis, including transformation of vessel macrophages into foam cells, apoptosis and necrosis of foam cells and progression of both atherosclerosis and thrombosis (26, 29-31). Dietary intake of Brazil nuts and Brazil nuts flour also decreases TC, triglycerides, apolipoprotein-A1 as well as oxidized LDL particles (32-34). Intake of defatted Brazil nuts improved GPX3 and decreased the oxidation of LDL in hyperlipidemic and hypertensive Brazilian patients (34). Farther those atheroprotective mechanisms, eating Brazil nuts has been also associated with decreased inflammatory biomarkers (IL-1, IL-6, INF-γ, TNF-α) in human subjects (35). Cardoso et al. (36) studied the possible role of Brazil nut supplementation on antioxidant and anti-inflammatory response. Authors observed that intake of Brazil nut augmented the expression of nuclear factor E2-related factor (Nrf2), a mechanism which was associated with increased antioxidant response and decreased lipid peroxidation, and decreased inflammatory response as measured by lowered levels of C-reactive protein, and interleukin-6 (IL-6) in hemodialysis patients (36). Evaluating 17 obese female subjects receiving 3 to 5 units of Brazil nuts per day, this small sample randomized controlled trial reported that intake of Brazil nuts decreased TC and LDL cholesterol, triglycerides and oxidized form of LDL, effects that were accompanied by improved red blood cell viscosity, but other microvascular parameters were not significantly affected (37). Mukuddem-Petersen et al. (38), based on results of their systematic review, proposed that regular intake (≥5 times per week) of 50 to 100g of nuts may significantly reduce total cholesterol and LDL cholesterol in normal and hyperlipidemic subjects. Health benefits of eating Brazil nuts are summarized in Table 1.

Table 1 Health benefits of Brazil nuts
Source of micronutrients
Fiber Polyphenols Fatty acids Phytosterols Sphingolipids Amino acids (arginine) Glutathione peroxidase Phosphorus (P) Potassium (K) Calcium (Ca) Copper (Cu) Iron (Fe) Selenium (Se) Magnesium (Mg) Zinc (Zn) Vitamin B1 (thiamine) Vitamin B3 (niacin) Vitamin B6 Vitamin E (tocopherol)
Antioxidant activity
Increased expression of nuclear factor E2-related factor (Nrf2) Decrease in reactive oxygen species (ROS) Decrease in reactive nitrogen species Decrease in lipid peroxidation Decrease in DNA peroxidation Decrease in LDL peroxidation
Anti-inflammatory activity
Decrease in the blood levels of IL-1, IL-6, INF-γ, TNF-α Decrease in vascular inflammation
Antidiabetic activity
Decrease in blood glucose level Decrease in pancreatic load
Anti-atherosclerosis activity
Decrease in formation of macrophage foam cells Decrease in atherogenesis Decrease in total amount of cholesterol, triglycerides, and apolipoprotein-A in the blood Improves blood viscosity
4.2. Dietary fiber and atherosclerosis

Dietary intake of fiber reduced the risk of peripheral artery disease, stroke, and cardiovascular disease (30). Brazil nut is a good source of dietary fiber (DF) (8g/100g) (14, 39) which has been associated with cardiovascular health. In the Los Angeles Atherosclerosis Study, regular intake of DF has been associated with reduced progression of atherosclerosis as measured by arterial intima-media thickness (IMT) (40). A French study showed that DF intake was negatively associated with decreased apolipoprotein B, total cholesterol (TC), blood glucose, and triglycerides (41). The highest tercile of dietary intake of linoleic acid and DF were inversely associated with blood triglyceride levels in Japanese-Brazilian descendants (42). The PREDIMED, a Spanish population study, showed that high intake of DF (>35g per day) significantly reduced the risk of carotid atherosclerosis (43). DF intake has a beneficial role on prevention of atherosclerosis and CHD, since it decreases TC and inflammation, two important factors that modify the development and progression of the disease (29, 44). Recently, it was shown that in children and adolescents, the risk of increased carotid IMT was decreased by 59% by the intake of nuts (45).

4.3. The atheroprotective effect of micronutrients of Brazil nuts
4.3.1. Magnesium (Mg)

Brazil nut is an important food source of Mg, since it contains 365mg to 393mg/100g of this microelement (39). Mg deficiency has been linked to endothelial dysfunction, arterial stiffening, atherosclerosis, mortality due to coronary heart disease mortality and sudden cardiac death (SCD) (46-51). Dietary intake of Mg reduced arterial calcification and stiffening and improves arterial flow-mediated dilation and decreases carotid IMT (50, 52).

4.3.2. Selenium (Se)

The richest source of Se in the planet is represented by Brazil nut (1-3). It is important to note that selenium content varies according to soil conditions. Brito et al. (53) reported Se values since 1. 4µg/g until 91. 69µg/g. Se is an antioxidant, e. g., a free radical scavenger, active site (selenocysteine) of the glutathione peroxidase (GPX) enzyme complex, thyroid hormone deiodinases, thioredoxin-reductases, and 25 types of selenoproteins (54-60). Se deficiency impairs antioxidant defenses by decreasing glutathione peroxidase synthesis as well as selenoproteins, plasma Se, erythrocyte Se status (54, 61), and has been linked to the pathogenesis of a heart disease, firstly described in China at 1964, the Keshan’s disease (62, 63). However, restoration of Se levels efficiently recovered cardiac, mitochondrial and cytosolic GPX values in laboratory animal studies and human studies (61, 64). In a short-term clinical trial, Se supplementation during 8 weeks were sufficient to promote reduction on fasting blood glucose and TC in human volunteers (65). In the SUBRANUT study, Se supplementation increased selenoprotein p, plasma Se, erythrocyte Se, and the levels of GPX isoforms, GPX-1 and GPX-3 (65). The same study, showed that rare single nucleotide polymorphisms were associated with decreased Se biomarkers even after supplementation, and that Se supplementation increased expression of GPX-1 only in subjects with polymorphism at rs1050450, whereas expression of selenoprotein p were lower only in subjects with rs7579 polymorphism.

4.4. Arginine and other amino acids

Brazil nut is a good source of protein and amino acids. It is rich in essential amino acids like leucine, valine, lysine, methionine, and phenylalanine, but it also contains a considerable amount of non-essential amino acids such as glycine, proline, serine, alanine. It contains also the highest arginine amounts among the oilseeds, and has a higher content of aspartic and glutamic acids (66). Some studies from the 90’s suggested that arginine could decrease formation of atherosclerotic plaques (67-69), but other studies showed no anti-atherogenic effect or even a proatherogenic effect of arginine (70-73). The study of Oomen et al. (71) demonstrated no effect of dietary arginine on CHD mortality, whereas Bahls et al. (73) reported deleterious atherosclerotic effects of dietary arginine. Many studies have been suggested that arginine can improve endothelial dysfunction in animals due to improvement of nitric oxide biosynthesis (68, 69, 74, 75), but a recent meta-analysis found no beneficial effects of arginine on endothelial function (76). However, a study reported that dietary intake of arginine, cysteine, glycine, lysine, tyrosine, and glutamic acid was associated with diminished arterial stiffness and blood pressure values (77).

4.5. Fatty acids, phytosterols, and sphingolipids

Bertholletia excelsa nuts are rich food sources of both monounsaturated (omega-9= oleic acid) and polyunsaturated (n-6 or omega-6, the cis-linoleic acid) fatty acids as well as tocopherols (α and γ), and phytosterols such as β-sitosterol and stigmasterol, with considerable amounts of campesterol, another important phytosterol (78, 79). It should be emphasized that phytosterols can reduce both TC and inflammatory biomarkers decreasing the risk of atherosclerosis and thrombosis (80-82). The composition of monounsaturated, polyunsaturated fatty acids and fiber of those nuts are responsible for the protective effect against cardiovascular diseases (83). Monounsaturated and polyunsaturated fatty acids have antioxidant activity and their regular intake protects brain, heart and other tissues, organs and cells against cell degeneration, cell death and aging (84). Furthermore, both mono- and polyunsaturated fats have anti-inflammatory properties and also acts as lipid-layers that can stabilize mitochondrial membranes, improving cell respiratory function which is associated with increased lifespan and decreased risk of cardiometabolic and neurodegenerative diseases (85, 86). It is important to note that Brazil nuts are very rich in β-tocopherol (88. 3%), unsaturated free fatty acids, monounsaturated fatty acids (linoleic acid-39.3%; linolenic acid-36.1%), β-sitosterol (76%) and other phytosterols (87). High dietary intake of linoleic acid was recently associated with decreased levels of blood lipids (total cholesterol and its fractions) in population of more than 340,000 subjects (88). Dietary linolenic acid is inversely associated with waist circumference, blood lipids, inflammatory biomarkers, and positively associated with HDL cholesterol levels (89, 90). Using a structured lipid containing equal proportions of linoleic and linolenic fatty acids, it was reported that this product decreased lipid liver weight, serum TC, LDL cholesterol, and triglycerides, but enhanced serum HDL cholesterol levels (91). One of the oldest studies regarding the cholesterol lowering effects of sitosterol was published in more than 60 years ago. Sitosterol administration to human subjects resulted in lowered levels of TC, phospholipids, and triglycerides (92). In 1956, one of the first studies regarding ß-sitosterol supplementation on blood lipids, an experimental rabbit model of atherosclerosis, reported that ß-sitosterol added to diet decreased liver cholesterol and blood TC (93). In the same year, a human experimental study observed that ß-sitosterol supplementation reduced TC in blood (94). In 1963, it was reported that ß-sitosterol decreased blood and arterial TC levels (95).

During many decades, other experimental animal and human studies corroborated the anti-atherosclerotic role of ß-sitosterol and other phytosterols (96). Brazil nuts are also rich in stigmasterol (1). However, there is a very rare genetic condition in which phytosterols accumulate in body tissues, including in the arterial walls, the sitosterolemia is associated with high levels of cholesterol and increased risk of cardiac events (97). ß-sitosterol administration in a hamster experimental model of atherosclerosis decreased by 20% the plasma cholesterol compared to cholesterol-fed group, and that phytosterol also lowered liver cholesterol (98). ß-sitosterol decreased inflammatory biomarkers such as interleukin-6 and tumor necrosis factor-alfa reducing fatty liver and body adiposity (99). Brazil nuts are a rich source of food sphingolipids (100). Food sphingolipids are suggested to decrease serum LDL and to enhance HDL levels (101). Long-term dietary of sphingomyelin did no atherogenic effect, but significantly decreased atherogenesis in mice (102). Brazil nuts also have significant amounts of squalene (1). The role of squalene in atherosclerosis is still controversial. Some studies found squalene in arterial fatty plaques, whereas other studies found that squalene increase cholesterol levels, others found no effect on blood cholesterol, and other papers also reported a cholesterol lowering effect (103). This lipid has been pointed as having an antioxidant role protecting LDL from oxidation due to down-regulation of CD36 receptor expression, decreasing the risk of atherosclerosis (104). In a mice model, dietary intake of squalene was linked to enhanced levels of HDL cholesterol (105). A review regarding health benefits of squalene showed that this compound seems to be beneficial against atherosclerosis, since it protects lipoproteins against peroxidation, and improves HDL cholesterol levels (106). It should be assumed that more basic and clinical studies regarding to the potential roles of squalene are necessary.

4.6. Tocopherols

Although some studies did not report the occurrence of β-tocopherol in Brazil nuts, in fact both major forms of tocopherol (α, β, γ) are found in those seeds (87, 100). Vitamin E should also be considered a mitochondrial stabilizer agent. It has been observed that vitamin E deficiency was associated with increased lipid peroxidation and partially impaired mitochondrial respiration, since NADH-CoQ10 reductase and cytochrome oxidase activities were diminished in skeletal muscle cells (107). However, the same authors reported increased mitochondrial activities and lipid peroxidation in the liver. Other authors have found mitochondrial failure during liver aging in vitamin E-deficient rats (107). Far beyond its general protective effect on biological membranes (108), tocopherol blocks the oxidative decay of respiratory complex III (109). β-tocopherol is an antioxidant, membrane stabilizer, and nutrient which knowledge has been well established (110). Tocopherols can stabilize mitochondrial and plasma membranes and protect LDL cholesterol from oxidative modification fostered by oxygen, nitrogen, and chlorine reactive species (111, 112). Beyond those activities, tocopherols can also trigger anti-inflammatory effects on liver, connective tissues, brain and other organs (113).

4.7. Polyphenols

Brazil nuts are rich in phenolic compounds (1, 78, 113). John and Shahidi (22) revealed a substantial antioxidant activity of Brazil nuts, measured by trolox equivalent antioxidant capacity test (TEAC assay), DPPH radical scavenging test, Hydroxyl radical scavenging capacity test, oxygen radical absorbance capacity (ORAC), and reducing power test. Authors also describe the following polyphenolics found in Brazil nuts: citric acid, gallocatechin, catechin, vanillic acid, taxifolin, myrecetin-3-o-rhamnoside, elagic acid, and quercetin among others. Catechin can protect endothelial function reducing the expression of vascular adhesion molecules and other molecules associated with inflammatory endothelial activation (114). Elagic acid can contribute to improve HDL cholesterol and to decrease TC and LDL cholesterol (115). Quercetin feeding can modulate serum lipids, raising HDL levels, but decreasing serum triglycerides (116). Furthermore, quercetin can reduce oxidized LDL and blood pressure in human subjects (117). Polyphenols also display antioxidant, anti-inflammatory and anti-apoptotic activities which can rescue cell life, decreasing cell degeneration and death. Their ingestion displays positive impacts on reduction of both morbidity and mortality as well as improvement on life span (30, 45). Polyphenols can scavenge free radicals and reactive oxygen and nitrogen species, as well as they can reduce platelet activity, decreasing the risk of thrombosis. Furthermore, polyphenols display anti-inflammatory properties (118). Both antioxidant and anti-inflammatory activities can reduce atherogenesis, decreasing the development of fatty plaques (29, 30). Polyphenols can specifically reduce oxidation of cholesterol oxidation which is also related to decreased risk of atherosclerosis (Cory et al., 2018, Williamson, 2017). Since atherosclerosis is used to be associated with thrombosis, it is relevant to mention that polyphenols can foster the production of nitric oxide, scavenge free radicals, and inhibit platelet aggregation by multiple pathways (15, 118, 119). It is important to note that when Brazil nut is sold peeled off it is expected that the samples can have some reduction of polyphenol content (118).

Based on the studies above referred, the major anti-atherosclerotic mechanisms associated with eating Brazil nuts are represented in Figure 1.

Figure 1

Biological mechanisms of bioactive compounds from Brazil nuts against atherosclerosis.

5. SUMMARY AND PERSPECTIVES

Eating Brazil nuts can afford protection against atherosclerosis. However, this dietary intake should be accompanied by healthy eating habits which comprise a difficult issue in public health nutrition (9, 120). More research is still important to determine the possible effects of Brazil nut intake in other endothelial regulators and its effects on atherosclerosis and thrombosis risk.

6. ACKNOWLEDGEMENTS

Author wish to acknowledge the work of the editors and reviewers that significantly improved this manuscript.

Abbreviations
Abbreviation Expansion

CHD: coronary heart disease, DF: dietary fiber, K: potassium, Mg: magnesium, TC: total cholesterol, Se: selenium, TEAC assay = trolox equivalent antioxidant capacity

References
[1]
YangJBrazil nuts and associated health benefits: A reviewLWT Food Sci Technol20094215731580DOI: 10.1016/j.lwt.2009.05.019 2. E. C. Silva Jr, L. H. O. Wadt, K. E. Silva, R. M. B. Lima, K. D. Batista, M. C. Guedes, G. S. Carvalho, T. S. Carvalho, A. R. Reis and G. Lopes: Natural variation of selenium in Brazil nuts and soils from the Amazon region. Chemosphere 188, 650-658 (2017). DOI: 10.1016/j.chemosphere.2017.08.158 PMid:28923728
[2]
MaiharaV. AGonzagaI. BSilvaV. LFávaroD. I. TVasconcelosM. B. ACozzolinoS. M. FDaily dietary selenium intake of selected Brazilian population groupsJ Radioanal Nucl Chem2004259465468DOI: 10.1023/B:JRNC.0000020919.58559.dd
[3]
Chatterjee M. K The food value of the nut of Anacardium occidentale (HijliBadam) Ind Med Gaz 1930 65 12 15
[4]
Brahmachari B. B Chatterjee N. K The food value of Trapa bispinosa Ind Med Gaz 1927 62 365 370
[5]
FraserG. ESabatéJBeesonLStrahanT. MA possible protective effect of nut consumption on risk of coronary heart disease. The Adventist Health StudyArch Int Med199215214161424DOI: 10.1001/archinte.152.7.1416 DOI: 10.1001/archinte.1992.00400190054010
[6]
HuF. BStampferM. JMansonJ. ERimmE. BColditzG. ARosnerB. ASpeizerF. EHennekensC. HWillettW. CFrequent nut consumption and risk of coronary heart disease in women: prospective cohort studyBMJ199831713411345DOI: 10.1136/bmj.317.7169.1341 PMid:9812929 PMCid:PMC28714
[7]
MM. Guasch-FerréBullóMMartínez-GonzálezM. ARosECorellaDEstruchRMM. FitóArósFWärnbergJFiolMLapetraJVinyolesELamuela-RaventósR. MSerra-MajemLPintóXRuiz-GutiérrezVBasoraJSalas-SalvadóJFrequency of nut consumption and mortality risk in the PREDIMED nutrition intervention trialBMC Med201311164DOI: 10.1186/1741-7015-11-164 PMid:23866098 PMCid:PMC3738153
[8]
Wadi J. M. L Ferrari C. K. B Knowledge and intake of functional foods by primary health care professionals from a Legal Amazon region, Brazil Rev Bras Obes Nutr Emagrec 2017 11 313 321
[9]
SabatéJAngYNuts and health outcomes: new epidemiologic evidenceAm J Clin Nutr200989S1643S1648DOI: 10.3945/ajcn.2009.26736Q PMid:19321572
[10]
ShaoCTangHZhaoWHeJNut intake and stroke risk: A dose-response meta-analysis of prospective cohort studiesSci Rep2016630394DOI: 10.3945/ajcn.2009.26736Q PMid:19321572
[11]
ChenG. CZhangRMartínez-GonzálezM. AZhangZ. -LBonaccioM. LDamR. M. vanQinL. -QNut consumption in relation to all-cause and cause-specific mortality: a meta-analysis of 18 prospective studiesFood Funct2017838933905DOI: 10.1039/C7FO00915A PMid:28875220
[12]
Fernandes I. M Chagas E. A Filho A. A. de Mello Maldonado S. A. S Santos R. C. dos Costa H. N. R. da Ribeiro P. R. E Madrid M. E. H Avilla O. V Melo A. C. G. R. de Duarte E. D. R. S Composição mineralógica e nutricional da castanha do Brasil Bertholletia excelsa HB cultivada em São João da Baliza (Roraima). Gramado, RS, Anais do 57o Congresso Brasileiro de Química. 2017
[13]
MichalakMKieltyka-DadasiewiczANut oils and their dietetic and cosmetic significance: a reviewJ Oleo Sci201868111120DOI: 10.5650/jos.ess18216 PMid:30651417
[14]
LudoviciVBarthelmesJNageleM. PFlammerA. JPolyphenolsSudano Ianti-platelet nutraceutical?Cur Pharm Des201824146157DOI: 10.2174/1381612823666171109104600 PMid:29119922
[15]
BlomhoffRCarlsenM. HAndersenL. FjrD. R. Jacobs Health benefits of nuts: potential role of antioxidantsBrit J Nutr2006965260DOI: 10.1017/BJN20061864 PMid:17125534
[16]
RosEHealth benefits of nut consumptionNutrients20102652682DOI: 10.3390/nu2070652 PMid:22254047 PMCid:PMC3257681
[17]
AlissaE. MFernsG. AFunctional foods and nutraceuticals in the primary prevention of cardiovascular diseasesJ Nutr MetabolArticle ID 569486, 16 pages2012DOI: 10.1155/2012/569486 PMid:22570771 PMCid:PMC3335253
[18]
O’NeilC. EIIIV. L. FulgoniNicklasT. ATree nut consumption is associated with better adiposity measures and cardiovascular and metabolic syndrome health risk factors in U. S. Adults: NHANES 2005-2010Nutr J20151464DOI: 10.1186/s12937-015-0052-x PMid:26123047 PMCid:PMC4484644
[19]
Cardona-AlvaradoM. IOrtegaF. JRamírez-ChávezETejeroM. EMolina-TorresJFernández-RealJ. MPerez-LuqueE. LAlmonds and walnuts consumption modifies PUFAS profiles and improves metabolic inflammation beyond the impact on anthropometric measureThe Open Nutr J2018128998DOI: 10.2174/1874288201812010089
[20]
FerrariC. K. BPercárioSSilvaJ. C. C. BTorresE. A. F. SAn apple plus a Brazil nut a day keeps the doctors away: Antioxidant Capacity of Foods and their Health BenefitsCur Pharm Des201622189195DOI: 10.2174/1381612822666151117122715 PMid:26572874
[21]
JohnJ. AShahidiFPhenolic compounds and antioxidant activity of Brazil nut (Bertholettia excelsa)J Funct Foods20102196209DOI: 10.1016/j.jff.2010.04.008
[22]
MartensI. B. GCardosoB. RHareD. JNiedzwieckiM. MLajoloF. MMartensACozzolinoS. M. FSelenium status in preschool children receiving a Brazil nut-enriched dietNutrition20153113391343DOI: 10.1016/j.nut.2015.05.005 PMid:26429652
[23]
CominettiCBortoliM. C. dePurgattoEOngT. PMorenoF. SJrA. B. GarridoCozzolinoS. M. FAssociations between glutathione peroxidase-1 Pro-198Leu polymorphism, selenium status and DNA damage levels in obese women after consumption of Brazil nutsNutrition201127891896DOI: 10.1016/j.nut.2010.09.003 PMid:21208780
[24]
Cardoso-BRApolinárioDBandeiraV. SBusseA. LMagaldiR. MJacob-filhoWCozzolinoS. MEffects of Brazil nut consumption on selenium status and cognitive performance in older adults with mild cognitive impairment: a randomized controlled pilot trialEur J Nutr201655107116DOI: 10.1007/s00394-014-0829-2 PMid:25567069
[25]
LuJChenBChenTGuoSXueXChenQZhaoMXiaLZhuZZhengLYinHComprehensive metabolomics identified lipid peroxidation as a prominent feature in human plasma of patients with coronary heart diseasesRedox Biol201712899907DOI: 10.1016/j.redox.2017.04.032 PMid:28472752 PMCid:PMC5415551
[26]
Stockler-PintoM. BMafraDMoraesCLoboJBoaventuraG. TFarageN. ESilvaW. SCozzolinoS. FMalmOBrazil nut (Bertholletia excelsa, H. B. K.) improves oxidative stress and inflammation biomarkers in hemodialysis patientsBiol Trace Elem Res2014158105112DOI: 10.1007/s12011-014-9904-z PMid:24504745
[27]
ColpoEVilanovaC. D. AReetzL. G. BDuarteM. M. M. FFariasI. L. GMullerE. IMullerA. L. HFloresE. M. MWagnerRRochaJ. B. T. daA single consumption of high amounts of the Brazil nuts improves lipid profile of healthy volunteersJ Nutr Metab20132013653185DOI: 10.1155/2013/653185 PMid:23840948 PMCid:PMC3693158
[28]
SanthakumarA. BBattinoMJMJ. M. Alvarez-SuarezDietary polyphenols: structures, bioavailability and protective effects against atherosclerosisFood Chem Toxicol20181134965DOI: 10.1016/j.fct.2018.01.022 PMid:29360556
[29]
MossJ. W. EWilliamsJ. ORamjiD. PNutraceuticals as therapeutic agents for atherosclerosisBBA Mol Bas Dis2018186415621572DOI: 10.1016/j.bbadis.2018.02.006 PMid:29454074 PMCid:PMC5906642
[30]
Ferrari C. K. B Free radicals, lipid peroxidation and antioxidants in apoptosis: implications for cancer, cardiovascular and neurological diseases Biologia (Bratislava) 2000 55 581 590
[31]
CarvalhoR. FHugheninG. V. BLuizR. RMoreiraA. S. BOliveiraG. M. MRosaGIntake of partially defatted Brazil nut flour reduces serum cholesterol in hypercholesterolemic patients- a randomized controlled trialNutr J20151459DOI: 10.1016/j.bbadis.2018.02.006 PMid:29454074 PMCid:PMC5906642
[32]
FernandesD. CAlvesA. MCastroG. S. FJordãoA. ANavesM. M. VEffects of Baru almond and Brazil nut against hyperlipidemia and oxidative stress in vivoJ Food Res201543846DOI: 10.1016/j.bbadis.2018.02.006 PMid:29454074 PMCid:PMC5906642
[33]
HugheninG. VOliveiraG. MMoreiraA. SSaint’PierreT. DGonçalvesR. APinheiro-MulderA. RTeodoroA. JLuizR. RRosaGImprovement of antioxidant status after Brazil nut intake in hypertensive and dyslipidemic subjectsNutr J20151454DOI: 10.1186/s12937-015-0043-y PMid:26022214 PMCid:PMC4477321
[34]
ColpoEVilanovaC. D. D. AReetzL. G. BDuarteM. M. M. FFariasI. L. GMeinerzD. FMarianoD. O. CVendrusculoR. GBoligonA. ACorteC. L. DWagnerRAthaydeM. LRochaJ. B. T daBrazil nut consumption by healthy volunteers improves inflammatory parametersNutrition201430459465DOI: 10.1016/j.nut.2013.10.005 PMid:24607303
[35]
Cardoso-BRApolinárioDBandeiraV. SBusseA. LMagaldiR. MJacob-filhoWCozzolinoS. MEffects of Brazil nut consumption on selenium status and cognitive performance in older adults with mild cognitive impairment: a randomized controlled pilot trialEur J Nutr201655107116DOI: 10.1016/j.nut.2013.10.005 PMid:24607303
[36]
MaranhãoP. AKraemer-AguiarL. GCLC. L. de OliveiraKuschnirM. C. CVieiraY. RSouzaM. G. CKouryJ. CBouskelaEBrazil nuts intake improves lipid profile, oxidative stress and microvascular function in obese adolescents: a randomized controlled trialNutr Metab2011832DOI: 10.1186/1743-7075-8-32 PMid:21619692 PMCid:PMC3123174
[37]
Mukuddem-PetersenJOosthuizenWJerlingJ. CA systematic review of the effects of nuts on blood lipid profiles in humansJ Nutr200513520822089DOI: 10.1093/jn/135.9.2082 PMid:16140880
[38]
BRASIL. Tabela Brasileira de Composição de Alimentos (TACO). Campinas, 4ª Ed., NEPA/UNICAMP 2011 64
[39]
WuHDwyerK. MFanZShircoreAFanJDwyerJ. HDietary fiber and progression of atherosclerosis: the Los Angeles Atherosclerosis StudyAm J Clin Nutr20037810851091DOI: 10.1093/ajcn/78.6.1085 PMid:14668268
[40]
LaironDArnaultNBertraisSPlanellsRCleroEHercbergSBoutron-RualtM. -CDietary fiber intake and risk factors for cardiovascular disease in French adultsAm J Clin Nutr20058211851194DOI: 10.1093/ajcn/82.6.1185 PMid:16332650
[41]
BevilacquaM. RGimenoS. G. AMatsumuraL. KFerreiraS. R. GGROUPJAPANESE BRAZILIANS DIABETES STUDY Hiperlipidemias e fatores dietéticos: estudo transversal entre nipo-brasileirosArq Bras Endocrinol Metab200751547558DOI: 10.1590/S000427302007000400008
[42]
Buil-CosialesPIrimiaPRosERiverolMGilabertRMartinez-VilaENúñezIDiez-EspinoJMartínez-GonzálezM. ASerrano-MartínezMDietary fibre intake is inversely associated with carotid intima-media thickness: a cross-sectional assessment in the PREDIMED StudyEur J Clin Nutr20096312131229DOI: 10.1038/ejcn.2009.45 PMid:19550433
[43]
BernaudF. S. RRodriguesT. CDietary fiber – adequate intake and effects on metabolism healthArq Bras Endocrinol Metab201357397405DOI: 10.1590/S0004-27302013000600001
[44]
AghayanMAsghariGYuzbashianEDehghanPHaghighianH. KMirmiranPJavadiMAssociation of nuts and unhealthy snacks with subclinical atherosclerosis among children and adolescents with overweight and obesityNutr Metabol20191623DOI: 10.1186/s12986-019-0350-y PMid:31007705 PMCid:PMC6454780
[45]
MaierJ. ALow magnesium and atherosclerosis: an evidence-based linkMol Aspect Med200324137146DOI: 10.1016/S0098-2997(02)00095-X
[46]
MaierJ. A. MMalpuech-BrugèreCZimowskaWRayssiguierYMazurALow magnesium promotes endothelial cell dysfunction: implications for atherosclerosis, inflammation and thrombosisBBA Mol Bas Dis200416891321DOI: 10.1016/j.bbadis.2004.01.002 PMid:15158909
[47]
AlturaB. MLiWZhengAZhengTShahN. CShahG. JYangZ. WPerez-AlbelaJ. LAlturaB. TSudden cardiac death in infants, children and young adults: possible roles of dietary magnesium intake and generation of platelet-activating factor in coronary arteriesJ Heart Health2016215DOI: 10.16966/2379-769X.121
[48]
KieboomB. C. TNiemeijerM. NLeeningM. J. GBergM. E. van denFrancoO. HDeckersJ. WHofmanAZietseRStrickerB. HHoornE. J Serum magnesium and the risk of death from coronary heart disease and sudden cardiac deathJ Am Heart Assoc20165e002707DOI: 10.1161/JAHA.115.002707 PMid:26802105 PMCid:PMC4859391
[49]
BraakeA. D. terShanahanC. MBaaijJ. H. F. de Magnesium counteracts vascular calcification. Passive interference or active modulation?Ather Thromb Vasc Biol20173714311445DOI: 10.1161/ATVBAHA.117.309182 PMid:28663256
[50]
KostovKHalachevaLRole of magnesium deficiency in promoting atherosclerosis, endothelial dysfunction, and arterial stiffening as risk factors for hypertensionInt J Mol Sci2018191724DOI: 10.1161/ATVBAHA.117.309182 PMid:28663256
[51]
MofradM. DDjafarianKMozaffariHShab-BidarSEffect of magnesium supplementation on endothelial function: a systematic review and meta-analysis of randomized controlled trialsAtherosclerosis201827398105DOI: 10.1016/j.atherosclerosis.2018.04.020 PMid:29709832
[52]
Brito R. C. M Junior J. B. Pereira KGF K. G. F Dantas Determinação de selênio em castanha-do-brasil e seus produtos. Natal, RN, Brazil, Anais, 37ª Reunião Anual da Sociedade Brasileira de Química, resumo T2390-1.
[53]
FerrariC. K. BMedicinal chemistry of Brazil nuts: An overviewJ Mod Med Chem20186712DOI: 10.12970/2308-8044.2018.06.02
[54]
BehneDKyriakopoulosAMammalian selenium-containing proteinsAnnu Rev Nutr200121453473DOI: 10.1146/annurev.nutr.21.1.453 PMid:11375445
[55]
ZhaoXYaoHFanRZhangZXuSSelenium deficiency influences nitric oxide and selenoproteins in pancreas of chickensBiol Trace Elem Res2014161341349DOI: 10.1007/s12011-014-0139-9 PMid:25319006
[56]
HuangJ. QRenF. ZJiangY. YLeiXCharacterization of Selenoprotein M and its response to Selenium deficiency in chicken brainBiol Trace Elem Res2016170449458DOI: 10.1007/s12011-015-0486-1 PMid:26315306
[57]
BurkR. FHillK. EGlutathione PeroxidasesComprehensive Toxicology, Second Edition, edited by Charlene A. McQueen, Elsevier, Oxford, volume20104229242DOI: 10.1016/B978-0-08-046884-6.00413-9
[58]
YangJHamidSLiuQCaiJXuSZhangZGene expression of selenoproteins can be regulated by thioredoxin (Txn) silence in chicken cardiomyocytesJ Inorg Biochem2017177118126DOI: 10.1016/j.jinorgbio.2017.08.027 PMid:28957736
[59]
ConradMAngeliJ. P. FGlutathione peroxidasesComprehensive Toxicology. Oxford, Elsevier 201810260276DOI: 10.1016/B978-0-12-801238-3.95621-6
[60]
JrG. F. CombsBiomarkers of selenium statusNutrients2015722092236DOI: 10.3390/nu7042209 PMid:25835046 PMCid:PMC4425141
[61]
Lu Y. J Wang K. L Pathologic changes of the conduction system of the heart in 43 cases of Keshan disease Chin Med J 1964 83 430 440
[62]
LevanderO. AThe selenium-coxsackievirus connection: chronicle of a collaborationJ Nutr2000130485488DOI: 10.1093/jn/130.2.485S PMid:10721935
[63]
TanguySToufektsianM. -CBesseSDucrosVLeirisJ. deBoucherFDietary selenium intake affects cardiac susceptibility to ischemia/reperfusion in male senescent ratsAge Ageing200332273278DOI: 10.1093/ageing/32.3.273 PMid:12720612
[64]
DonadioJ. L. SRogeroM. MGuerra-ShinoharaE. MDesmarchelierCBorelPCozzolinoS. M. FSEPP1 polymorphisms modulate serum glucose and lipid response to Brazil nut supplementationEur J Nutr20185718731882DOI: 10.1007/s00394-017-1470-7 PMid:28501922
[65]
FreitasJ. BNavesM. M. VComposição química de nozes e sementes comestíveis e sua relação com a nutrição e a saúdeRev Nutr201023269279DOI: 10.1590/S1415-52732010000200010
[66]
AjiWRavalliSSzabolcsMJiangX. -CSciaccaR. RMichlerR. ECannonP. JL-arginine prevents xanthoma development and inhibits atherosclerosis in LDL receptor knockout miceCirculation199795430437DOI: 10.1161/01. CIR.95.2.430 PMid:9008461
[67]
BögerR. HBode-BögerS. MBrandesR. PPhivthong-ngamLBöhmeMNafeRMüggeAFrölichJ. CDietary L-arginine reduces the progression of atherosclerosis in cholesterol-fed animalsCirculation19979612821290DOI: 10.1161/01. CIR.96.4.1282 PMid:9286960
[68]
CookeJ. PArginineP. S. Tsaoa new therapy for atherosclerosis?Circulation199795311312DOI: 10.1161/01. CIR.95.2.311 PMid:9008440
[69]
JeremyR. WMcCarronHSullivanDEffects of dietary L-arginine on atherosclerosis and endothelium-dependent vasodilatation in the hypercholesterolemic rabbit. Response according to treatment duration, anatomic site, and sexCirculation199694498506DOI: 10.1161/01. CIR.94.3.498 PMid:8759095
[70]
OomenC. MErkM. J. vanFeskensE. JKokF. JKromhoutDArginine intake and risk of coronary heart disease mortality in elderly menArterioscler Thromb Vasc Biol20002021342139DOI: 10.1161/01. ATV.20.9.2134 PMid:10978260
[71]
JJ. LoscalzoAdverse effects of supplements L-arginine in atherosclerosis: consequences of methylation stress in a complex catabolism?Arterioscler Thromb Vasc Biol20032335DOI: 10.1161/01. ATV.0000040860.71626.9D PMid:12524215
[72]
BahlsMFriedrichNAtzlerDFelixS. BNauckM. ABögerR. HVölzkeHSchwedhelmEDörrML-Arginine and SDMA serum concentrations are associated with subclinical atherosclerosis in the Study of Health in Pomerania (SHIP)PLoS ONE201510e0131293DOI: 10.1371/journal.pone.0131293 PMid:26098562 PMCid:PMC4476678
[73]
FerrariC. K. BFrançaE. LHonorio-FrançaA. CNitric oxide, health and diseaseJ Appl Biomed20097163173DOI: 10.32725/jab.2009.019
[74]
JavanmardS. HNematbakhshMSaneiM. HEarly prevention by L-arginine attenuates coronary atherosclerosis in a model of hypercholesterolemic animals; no positive results for treatmentNutr Metab2009613DOI: 10.32725/jab.2009.019
[75]
Rodrigues-KrauseJKrauseMRochaI. M. G. daUmpierreDFayhA. P. TAssociation of L-arginine supplementation with markers of endothelial function in patients with cardiovascular or metabolic disorders: A systematic review and meta-analysisNutrients20191115DOI: 10.3390/nu11010015 PMid:30577559 PMCid:PMC6357192
[76]
JenningsAMacGregorAWelchAChowienczykPSpectorTCassidyAAmino acid intakes are inversely associated with arterial stiffness and central blood pressure in womenJ Nutr201514521302138DOI: 10.3390/nu11010015 PMid:30577559 PMCid:PMC6357192
[77]
Costa T Jorge N Beneficial bioactive compounds present in nuts and walnuts Unopar Cient Cienc Biol Saude 2011 13 195 203
[78]
AlvesA. MFernandesD. CBorgesJ. FSousaA. G. de ONavesM. M. VOilseeds native to the Cerrado have fatty acid profile beneficial for cardiovascular healthRev Nutr201629859866DOI: 10.1590/1678-98652016000600010
[79]
RochaV. ZRasR. TGagliardiA. CMangiliL. CTrautweinE. ASantosR. DEffects of phytosterols on markers of inflammation: A systematic review and meta-analysisAtherosclerosis20162487683DOI: 10.1016/j.atherosclerosis.2016.01.035 PMid:26987068
[80]
MoghadasianM. HAlsaifMLeKGangadaranSMasisiKTT. BetaShenG. XCombination effects of wild rice and phytosterols on prevention of atherosclerosis in LDL receptor knockout miceHealth Adv201633128135DOI: 10.1016/j.jnutbio.2016.03.015 PMid:27155919
[81]
YiJKnudsenT. ANielsenA. -LDuelundLChristensenMHervellaPNeedhamDMouritsenO. GInhibition of cholesterol transport in an intestine cell model by pine-derived phytosterolsChem Phys Lipid20162006273DOI: 10.1016/j.chemphyslip.2016.06.008 PMid:27372052
[82]
FraserG. ENut consumption, lipids, and risk of coronary eventClin Cardiol1999221115DOI: 10.1002/clc.4960221504 PMid:10410300 PMCid:PMC6655570
[83]
ValenzuelaRSanhuezaJValenzuelaADocosohexaenoic acid (DHA), an important fatty acid in aging and the protection of neurodegenerative diseasesJ Nutr Ther201216372DOI: 10.6000/1929-5634.2012.01.01.6
[84]
SilvaW. J. M. daFerrariC. K. BMitochondrial metabolism, free radicals and agingRev Bras Geriatr Gerontol201114441451DOI: 10.1590/S1809-98232011000300005
[85]
Ferrari C. K. B Functional foods, nutraceuticals and herbs: an approach of cell and molecular anti-ageing mechanisms Agro Food Ind High-Tech 2013 24 10 13
[86]
ChunhiengTHafidiAPiochDBrochierJMontetDDetailed study of Brazil nut (Bertholletia excelsa) oil micro-compounds: phospholipids, tocopherols and sterolsJ Braz Chem Soc20081913741380DOI: 10.1590/S1809-98232011000300005
[87]
ZhaoJ. VSchoolingMEffect of linoleic acid on ischemic heart disease and its risk factors: a Mendelian randomization studyBMC Med20191761DOI: 10.1186/s12916-019-1293-x PMid:30866921 PMCid:PMC6417131
[88]
DumontJGoumidiLGrenier-BoleyBCottelDMarécauxNMontayeMWagnerAArveilerDSimonCFerrièresJRuidavetsJ. -BAmouyelPDallongevilleJMeirhaegheADietary linoleic acid interacts with FADS1 genetic variability to modulate HDL-cholesterol and obesity-related traitsClin Nutr20183716831689DOI: 10.1016/j.clnu.2017.07.012 PMid:28774683
[89]
LenighanY. MMcNultyB. ARocheH. MDietary fat composition: replacement of saturated fatty acids with PUFA as a public health strategy, with emphasis on a-linolenic acidProc Nutr Soc201978234245DOI: 10.1016/j.clnu.2017.07.012 PMid:28774683
[90]
ShagholianMGoliS. A. HShirvaniAAgha-GhazviniM. RAsgarySLiver and serum lipids in Wistar rats fed a novel structured lipid containing conjugated linoleic acid and conjugated linolenic acidGrasas Aceites201970e307DOI: 10.3989/gya.0582181
[91]
BestM. MDuncanC. HLoonE. J. VanWathenJ. DThe effects of sitosterol on serum lipidsAm J Med1955196170DOI: 10.1016/0002-9343(55)90274-6
[92]
BeherW. TAnthonyW. LBakerG. DEffects of beta-sitosterol on regression of cholesterol atherosclerosis in rabbitsCirc Res19564485487DOI: 10.1161/01. RES.4.4.485 PMid:13330195
[93]
FarquharJ. WSmithR. EDempseyM. EThe effect of beta sitosterol on the serum lipids of young men with arteriosclerotic heart diseaseCirculation1956147782DOI: 10.1161/01. CIR.14.1.77 PMid:13356460
[94]
GersonTShorlandF. BDunckleyG. GEffect of ß-sitosterol on cholesterol and lipid metabolism in the ratNature1963200579DOI: 10.1038/200579a0 PMid:14082232
[95]
KassisA. NVanstoneC. AAbuMweisS. SJonesP. JEfficacy of plant sterols is not influenced by dietary cholesterol intake in hypercholesterolemic individualsMetabolism200857339346DOI: 10.1016/j.metabol.2007.10.008 PMid:18249205
[96]
Nghiem-RaoT. HPatelS. BInvestigating sitosterolemia to understand lipid physiologyClin Lipidol20138649658DOI: 10.2217/clp.13.60 PMid:29928317 PMCid:PMC6005666
[97]
LL. LeiZhuHZhangCWangXMaK. YWangLZhaoYChenZ. -YDietary b-sitosterol is more potent in reducing plasma cholesterol than sesamin in hypercholesterolemia hamstersEur J Lipid Sci Technol20171191600349DOI: 10.1002/ejlt.201600349
[98]
KuranoMHasegawaKKunimiMHaraMYatomiYTeramotoTTsukamotoKSitosterol prevents obesity-related chronic inflammationBBA Mol Cel Biol Lip20181863191198DOI: 10.1016/j.bbalip.2017.12.004 PMid:29221711
[99]
AlasalvarCBollingB. WReview of nut phytochemicals, fat-soluble bioactives, antioxidant components and health effectsBrit J Nutr2015113568578DOI: 10.1017/S0007114514003729 PMid:26148924
[100]
VesperHSchmelzE. -MNikolova-KarashianM. NDillehayD. LLynchD. VjrA. H. Merrill Sphingolipids in food and the emerging importance of sphingolipids to nutritionJ Nutr199912912391250DOI: 10.1093/jn/129.7.1239 PMid:10395583
[101]
ChungR. W. SWangZBursilC. AWuB. JBarterP. JRyeK. -AEffect of long-term dietary sphingomyelin supplementation on atherosclerosis in micePLoS ONE201712e0189523DOI: 10.1371/journal.pone.0189523 PMid:29240800 PMCid:PMC5730175
[102]
Lou-BonafonteJ. MArnalCNavarroM. AOsadaJEfficacy of bioactive compounds from extra virgin olive oil to modulate atherosclerosis developmentMol Nutr Food Res20125610431057DOI: 10.1002/mnfr.201100668 PMid:22760979
[103]
Granados-PrincipalSQuilesJ. LRamirez-TortosaC. LOchoa-HerreraJPerez-LopezPPulido-MoranMRamirez-TortosaM. CSqualene ameliorates atherosclerotic lesions through the reduction of CD36 scavenger receptor expression in macrophagesMol Nutr Food Res201256733740DOI: 10.1002/mnfr.201100703 PMid:22648620
[104]
Gabás-RiveraCBarranqueroCMartínez-BeamonteRNavarroM. ASurraJ. COsadaJDietary Squalene increases high density lipoprotein-colesterol and paraoxonase 1 and decreases oxidative stress in MicePLoS ONE20149e104224DOI: 10.1371/journal.pone.0104224 PMid:25117703 PMCid:PMC4130590
[105]
Lou-BonafonteJ. MMartínez-BeamonteRSanclementeTSurraJ. CHerrera-MarcosL. VSanchez-MarcoJArnalCOsadaJCurrent insights into the biological action of squaleneMol Nutr Food Res2018621800136DOI: 10.1002/mnfr.201800136 PMid:29883523
[106]
ArmeniTPrincipatoGQuilesJ. LPieriCBompadreSBattinoMMitochondrial dysfunction during aging: vitamin E deficiency or caloric restriction-two different ways of modulating stressJ Bionerg Biomembr200335181191DOI: 10.1023/A:1023754305218
[107]
BrownK. MMorriceP. CDuthieG. GErythrocyte membrane fatty acid composition of smokers and non-smokers: effects of vitamin E supplementationEur J Clin Nutr199852145150DOI: 10.1038/sj.ejcn.1600536 PMid:9505161
[108]
RafiqueRShapiraA. HCoperJ. MMitochondrial respiratory chain dysfunction in ageing; influence of vitamin E deficiencyFree Radic Res200438157165DOI: 10.1080/10715760310001643311 PMid:15104209
[109]
CanMetCon. Canadian Metabolomics Conference. Showing metabocard for beta-tocopherol (HMDB0006335). Alberta, CA, available at: http://www.hmdb.ca/metabolites/HMDB0006335 [03/29/2019]
[110]
FerrariC. K. BTorresE. A. F. SBiochemical pharmacology of functional foods and prevention of chronic diseases of agingBiomed Pharmacother200357251260DOI: 10.1016/S0753-3322(03)00032-5
[111]
FerrariC. K. BFunctional foods, herbs and nutraceuticals: towards biochemical mechanisms of healthy agingBiogerontology20045275289DOI: 10.1016/S0753-3322(03)00032-5
[112]
YangJLiuR. HHalimLAntioxidant and antiproliferative activities of common edible nut seedsLWT Food Sci Technol20094218DOI: 10.1016/j.lwt.2008.07.007
[113]
CarnevaleRLoffredoLNocellaCBartimocciaSBucciTFalcoE. DePeruzziMChimentiIBiondi-ZoccaiGPignatelliPVioliFFratiGEpicatechin and catechin modulate endothelial activation induced by platelets of patients with peripheral artery diseaseOxid Med Cell Longev2014691015DOI: 10.1016/j.lwt.2008.07.007
[114]
HosseiniBSaedisomeoliaAWoodL. GYaseriMTavasoliSEffects of pomegranate extract supplementation on inflammation in overweight and obese individuals: A randomized controlled clinical trialCompl Ther Clin Pract2016224450DOI: 10.1016/j.ctcp.2015.12.003 PMid:26850805
[115]
PfeufferMAuingerABleyUKraus-StojanowicILaueCWinklerPRüferC. EFrankJBösch-SaadatmandiCRimbachGSchrezenmeirJEffect of quercetin on traits of the metabolic syndrome, endothelial function and inflammation in men with different APOE isoformsNutr Metab Cardiovasc Dis201323403409DOI: 10.1016/j.numecd.2011.08.010 PMid:22118955
[116]
EgertSBosy-WestphalASeiberlJKürbitzCSettlerUPlachta-DanielzikSWagnerA. EFrankJSchrezenmeirJRimbachGWolfframSMüllerM. JQuercetin reduces systolic blood pressure and plasma oxidised low-density lipoprotein concentrations in overweight subjects with a high-cardiovascular disease risk phenotype: a double-blinded, placebo-controlled cross-over studyBr J Nutr200910210651074DOI: 10.1016/j.numecd.2011.08.010 PMid:22118955
[117]
CoryHPassarelliSSzetoJTamezMMatteiJThe role of polyphenols in human health and food systems: a mini-reviewFront Nutr2018587DOI: 10.3389/fnut.2018.00087 PMid:30298133 PMCid:PMC6160559
[118]
WilliamsonGThe role of polyphenols in modern nutritionNutr Bull201742226235DOI: 10.3389/fnut.2018.00087 PMid:30298133 PMCid:PMC6160559
[119]
FerrariC. K. BImplementation of public health policies for healthy lifestyles promotion: what Brazil should tell us?Health Prom Perspect20188243248DOI: 10.15171/hpp.2018.33 PMid:30087849 PMCid:PMC6064754
Share
Back to top