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OBJECTIVES: Dietary inorganic nitrate from foods such as red beetroot juice (RBJ) can contribute to nitric oxide (NO) bioavailability through the enterosalivary nitrate-nitrite-NO pathway. A critical step in this pathway is the reduction of nitrate to nitrite by oral bacteria. We investigated the effects of inorganic nitrate supplementation, as RBJ or placebo + potassium nitrate (PBO+NIT), on the oral microbiota, and its relationship with saliva and plasma NO metabolites and vascular endothelial function. METHODS: In a randomized, double-blind, placebo-controlled trial, we measured the abundance of oral nitrate-reducing bacteria in saliva samples from 15 middle-aged/older adults with overweight and obesity using 16 rRNA sequencing. We also assessed the relationship of oral nitrate-reducing bacteria with the physiological responses to acute (4 hours) and chronic (4 weeks) RBJ, PBO+NIT, nitrate-free RBJ, and placebo supplementation via measurement of saliva and plasma nitrate/nitrite (NOx), plasma nitrite levels, and reactive hyperemia index (RHI). RESULTS: A significant decrease in the alpha diversity metric, Pileou's Evenness, was detected after chronic consumption of PBO+NIT (0.69 ± 0.05 at week 0 vs. 0.65 ± 0.05 at week 4; P

OBJECTIVES: High-fat meal (HFM) consumption has been shown to impair postprandial endothelial function. Red beetroot juice (RBJ) contains polyphenols, betalains, carotenoids, ascorbic acid, and inorganic nitrate, and has been shown to improve endothelial function. This study investigated the acute and chronic effects of RBJ and its bioactive components on postprandial endothelial function. We hypothesized that a HFM would impair postprandial endothelial function, and that RBJ would attenuate this, in part, through increased circulating nitrate/nitrite (NOx) levels. METHODS: A 4-period randomized, double-blind, placebo-controlled crossover clinical trial was conducted. Fifteen overweight and obese middle-aged/older men and postmenopausal women underwent baseline (T0) assessment of endothelial function (via reactive hyperemia index, RHI) and collection of blood and saliva. Participants consumed one of the following 70 mL treatments (acute exposure): 1) RBJ, 2) nitrate-free RBJ (NF-RBJ), 3) placebo + nitrate (PBO + NIT), and 4) placebo (PBO), followed by a HFM. RHI was measured at 4 hours (T4) post-HFM, and blood and saliva were collected at 1 hour (T1), 2 hours (T2), and T4. Participants then consumed treatments daily for 4 weeks (chronic exposure), and all assessments were repeated before/after the HFM but without consuming treatments. RESULTS: No significant time or treatment effects were observed for RHI. Following acute and chronic exposure to RBJ and PBO + NIT, plasma NOx levels were higher at T0 (chronic only), T1, T2, and T4 compared to PBO and NF-RBJ (P