The effect of a dietary nitrate supplementation in the form of a single shot of beetroot juice on static and dynamic apnoea performance

Introduction: The purpose of the present study was to assess the effects of acute nitrate (NO3-)-rich beetroot juice supplementation on peripheral oxygen saturation (SpO2), heart rate (HR), and pulmonary gas exchange during submaximal static and dynamic apnoea. Methods: Nine (six male, three female) trained apneists (age: 39.6 ± 8.2 years, stature: 170.4 ± 11.5cm, body mass: 72.0 ± 11.5 kg) performed three submaximal static apnoeas at 60%, 70% and 80% of the participant’s current reported personal best time, followed by three submaximal (~ 75% or personal best distance) dynamic apnoeas following the consumption of either a 140 ml concentrated NO3--rich beetroot juice (BRJ; 7.7 mmol NO3-) or a NO3--depleted placebo (PLA; 0.1 mmol NO3-) in double-blind randomised manner. HR and SpO2 were measured via fingertip pulse oximetry at the nadir, and online gas analysis was used to assess pulmonary oxygen uptake (V̇O2) during recovery following breath-holds. Results: There were no differences (P <0.05) between conditions for HR (PLA = 59 ± 11 bpm and BRJ = 61 ± 12 bpm), SpO2 (PLA = 83 ± 14% and BRJ = 84 ± 9%) or V̇O2 (PLA = 1.00 ± 0.22 L.min-1 and BRJ = 0.97 ± 0.27 L.min-1). Conclusion: The consumption of 7.7mmol of beetroot juice supplementation prior to a series of submaximal static and dynamic apnoeas did not induce a significant change in SpO2, HR and V̇O2, when compared to placebo. Therefore there is no apparent physiological response that may benefit free-divers as a result of the supplementation

Phospho-Rasputin Stabilization by Sec16 Is Required for Stress Granule Formation upon Amino Acid Starvation

Most cellular stresses induce protein translation inhibition and stress granule formation. Here, using Drosophila S2 cells, we investigate the role of G3BP/Rasputin in this process. In contrast to arsenite treatment, where dephosphorylated Ser142 Rasputin is recruited to stress granules, we find that, upon amino acid starvation, only the phosphorylated Ser142 form is recruited. Furthermore, we identify Sec16, a component of the endoplasmic reticulum exit site, as a Rasputin interactor and stabilizer. Sec16 depletion results in Rasputin degradation and inhibition of stress granule formation. However, in the absence of Sec16, pharmacological stabilization of Rasputin is not enough to rescue the assembly of stress granules. This is because Sec16 specifically interacts with phosphorylated Ser142 Rasputin, the form required for stress granule formation upon amino acid starvation. Taken together, these results demonstrate that stress granule formation is fine-tuned by specific signaling cues that are unique to each stress. These results also expand the role of Sec16 as a stress response protein