TY - JOUR
T1 - Extracellular buffer choice influences acid-base responses and gastrointestinal symptoms
T2 - Buffers and GI responses
AU - Peacock, J.
AU - Sparks, S.A.
AU - Middlebrook, I.
AU - Hilton, N.P.
AU - Tinnion, D.
AU - Leach, N.
AU - Saunders, Bryan
AU - McNaughton, L.R.
PY - 2021/11/2
Y1 - 2021/11/2
N2 - Aim: To compare the pharmokinetic and gastrointestinal (GI) symptom responses between an equal dose of sodium bicarbonate and sodium citrate using delayed-release capsules. Methods: Thirteen active males (age 20.5 ± 2.1 y, height 1.82 ± 0.1 m and body mass 76.5 ± 9.6 kg) consumed either 0.3 g.kg1 BM sodium bicarbonate, sodium citrate or a placebo, using a double-blind, randomised crossover design. Blood bicarbonate [HCO3–]) concentration, pH and GI symptoms were measured pre-ingestion and every 10 min for 180 min post-consumption. Results: [HCO3–] concentration (P < 0.001) and pH (P = 0.040) were significantly higher in the sodium bicarbonate condition compared with sodium citrate condition up to 3 h post-consumption. Peak blood HCO3–concentration was significantly higher with sodium bicarbonate compared with citrate (P < 0.001). Mean GI symptom scores were lower (P = 0.037) for sodium citrate (1.5 ± 1.8 AU) than bicarbonate (2.6 ± 3.1 AU), with considerable inter individual variability. No GI symptoms were reported following consumption of the placebo. Conclusion: Both substances alter [HCO] values significantly, with sodium bicarbonate causing significantly higher pH and [HCO3-] values than the same dose of sodium citrate, but results in slightly more severe GI symptom
AB - Aim: To compare the pharmokinetic and gastrointestinal (GI) symptom responses between an equal dose of sodium bicarbonate and sodium citrate using delayed-release capsules. Methods: Thirteen active males (age 20.5 ± 2.1 y, height 1.82 ± 0.1 m and body mass 76.5 ± 9.6 kg) consumed either 0.3 g.kg1 BM sodium bicarbonate, sodium citrate or a placebo, using a double-blind, randomised crossover design. Blood bicarbonate [HCO3–]) concentration, pH and GI symptoms were measured pre-ingestion and every 10 min for 180 min post-consumption. Results: [HCO3–] concentration (P < 0.001) and pH (P = 0.040) were significantly higher in the sodium bicarbonate condition compared with sodium citrate condition up to 3 h post-consumption. Peak blood HCO3–concentration was significantly higher with sodium bicarbonate compared with citrate (P < 0.001). Mean GI symptom scores were lower (P = 0.037) for sodium citrate (1.5 ± 1.8 AU) than bicarbonate (2.6 ± 3.1 AU), with considerable inter individual variability. No GI symptoms were reported following consumption of the placebo. Conclusion: Both substances alter [HCO] values significantly, with sodium bicarbonate causing significantly higher pH and [HCO3-] values than the same dose of sodium citrate, but results in slightly more severe GI symptom
KW - Alkalosis
KW - Sodium bicarbonate
KW - Sodium citrate
KW - Alkalosis, Sodium bicarbdelayed-release capsules
UR - https://doi.org/10.1080/15438627.2021.1896517
U2 - 10.1080/15438627.2021.1896517
DO - 10.1080/15438627.2021.1896517
M3 - Article (journal)
SN - 1543-8627
VL - 29
SP - 505
EP - 516
JO - Research in Sports Medicine: An International Journal
JF - Research in Sports Medicine: An International Journal
IS - 6
ER -