Ϫ ]), oxygen uptake (V O2) kinetics, and exercise tolerance in normoxia (N) and hypoxia (H). In a doubleblind, crossover study, 12 healthy subjects completed cycle exercise tests, twice in N (20.9% O2) and twice in H (13.1% O2). Subjects ingested either 140 ml/day of NO 3 Ϫ -rich beetroot juice (8.4 mmol NO3; BR) or NO 3 Ϫ -depleted beetroot juice (PL) for 3 days prior to moderate-intensity and severe-intensity exercise tests in H and N. Preexercise plasma [NO 2 Ϫ ] was significantly elevated in H-BR and N-BR compared with H-PL (P Ͻ 0.01) and N-PL (P Ͻ 0.01). The rate of decline in plasma [NO 2 Ϫ ] was greater during severe-intensity exercise in H-BR [Ϫ30 Ϯ 22 nM/min, 95% confidence interval (CI); Ϫ44, Ϫ16] compared with H-PL (Ϫ7 Ϯ 10 nM/min, 95% CI; Ϫ13, Ϫ1; P Ͻ 0.01) and in N-BR (Ϫ26 Ϯ 19 nM/min, 95% CI; Ϫ38, Ϫ14) compared with N-PL (Ϫ1 Ϯ 6 nM/min, 95% CI; Ϫ5, 2; P Ͻ 0.01). During moderate-intensity exercise, steady-state pulmonary V O2 was lower in H-BR (1.91 Ϯ 0.28 l/min, 95% CI; 1.77, 2.13) compared with H-PL (2.05 Ϯ 0.25 l/min, 95% CI; 1.93, 2.26; P ϭ 0.02), and V O2 kinetics was faster in H-BR (: 24 Ϯ 13 s, 95% CI; 15, 32) compared with H-PL (31 Ϯ 11 s, 95% CI; 23, 38; P ϭ 0.04). NO 3 Ϫ supplementation had no significant effect on V O2 kinetics during severe-intensity exercise in hypoxia, or during moderate-intensity or severe-intensity exercise in normoxia. Tolerance to severe-intensity exercise was improved by NO 3 Ϫ in hypoxia (H-PL: 197 Ϯ 28; 95% CI; 173, 220 vs. H-BR: 214 Ϯ 43 s, 95% CI; 177, 249; P ϭ 0.04) but not normoxia. The metabolism of NO 2 Ϫ during exercise is altered by NO 3 Ϫ supplementation, exercise, and to a lesser extent, hypoxia. In hypoxia, NO 3 Ϫ supplementation enhances V O 2 kinetics during moderate-intensity exercise and improves severe-intensity exercise tolerance. These findings may have important implications for individuals exercising at altitude. hypoxia; beetroot juice; nitric oxide; efficiency; performance NITRIC OXIDE (NO) IS A UBIQUITOUS, water-soluble, free radical gas that plays a crucial role in many biological processes. Effective NO production is important in normal physiological functioning, from the regulation of blood flow, muscle contractility, and mitochondrial respiration to host defense, neurotransmission, and glucose and calcium homeostasis (11,17,60). NO production via the oxidation of L-arginine, in a process catalyzed by nitric oxide synthase (NOS), may be blunted in conditions of reduced O 2 availability (52). It is now widely accepted that NO can also be generated via an alternative pathway, whereby inorganic nitrate (NO 3 Ϫ ) is reduced to nitrite (NO 2 Ϫ ) and further to NO. This NOS-and O 2 -independent NO 3 Ϫ -NO 2 Ϫ -NO pathway represents a complementary system for NO synthesis spanning a broad range of redox states (49). In addition to being produced endogenously, the body's NO 3 Ϫ stores can be increased via the diet, with green leafy vegetables and beetroot being particularly rich in NO 3 Ϫ . Upon ingestion, inorganic NO 3 Ϫ is absorbed from the ...