2019
DOI: 10.1080/09637486.2019.1580683
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Acute dietary nitrate does not reduce resting metabolic rate or oxidative stress marker 8-isoprostane in healthy males and females

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Cited by 4 publications
(3 citation statements)
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“…An increased dietary nitrate intake induced upregulation of catalase, superoxide dismutase, glutathione peroxidase, mitofusin 2 and PGC1α in PBMCs in patients with metabolic syndrome [ 99 ]. Nevertheless, no significant effects of dietary nitrate supplementation were found on markers of oxidative stress (i.e., malondialdehyde, mitochondrial superoxide, 8-isoprostane) in other studies [ 100 102 ], which clearly emphasizes the need for further basic and translational research in this area.…”
Section: Introductionmentioning
confidence: 79%
“…An increased dietary nitrate intake induced upregulation of catalase, superoxide dismutase, glutathione peroxidase, mitofusin 2 and PGC1α in PBMCs in patients with metabolic syndrome [ 99 ]. Nevertheless, no significant effects of dietary nitrate supplementation were found on markers of oxidative stress (i.e., malondialdehyde, mitochondrial superoxide, 8-isoprostane) in other studies [ 100 102 ], which clearly emphasizes the need for further basic and translational research in this area.…”
Section: Introductionmentioning
confidence: 79%
“…The macroscopic effect of these mechanisms was tested in a 3-day dietary nitrate supplementation trial showing a reduction of REE by 4.2% (−82 kcal/day) measured by indirect calorimetry in healthy subjects [ 52 ]. However, these initial findings have not been replicated in subsequent studies of different duration (i.e., 2 h or 7 days) as no significant changes were found for REE after nitrate supplementation [ 53 , 54 ]. All these studies were conducted in energy balance whereas our study purposively investigated whether dietary nitrate may amplify the expected (i.e., due to the decrease in metabolically active tissue) reduction in REE post-weight loss induced by CR.…”
Section: Discussionmentioning
confidence: 97%
“…Alternatively, rather than increasing NO production per se the rich concentration of polyphenols and other antioxidants in BRJ (37) could act in concert with any NO that is produced, either by prolonging NO bioavailability and/or by protecting cellular machinery from other reactive nitrogen and/or oxygen species. However, numerous studies to date have failed to reveal any influence of either acute or repeated BRJ intake on markers of oxidative stress in various populations (38)(39)(40)(41)(42)(43). For example, we recently determined the effects of daily ingestion of either NO 3 − -containing or NO 3 − -free BRJ for 2 wk on plasma 8-hydroxydeoxyguanosine (8-OHdG), protein carbonyls (PCs), and 4-hydroxynonenal (4-HNE), markers of oxidative damage to DNA/RNA, proteins/amino acids, and lipids, respectively, in 65-79 y old men and women (43).…”
Section: Discussionmentioning
confidence: 99%