TY - JOUR
T1 - Oxygen delivery and cardiac output during exercise following oral phosphate-glucose
AU - Mannix, E. T.
AU - Stager, J. M.
AU - Harris, A.
AU - Farber, M. O.
PY - 1990/6
Y1 - 1990/6
N2 - Phosphate has been proposed as an ergogenic aid since it may enhance O2 delivery and cardiac work efficiency by increasing plasma phosphate (P Pi), red blood cell phosphate (RBC Pi), 2,3-diphosphoglycerate (DPG), RBC adenosine triphosphate (ATP), and P50. In 10 normal, fasting males we measured cardiac output (Q) by CO2 rebreathing, heart rate (HR), O2 deficit (O2DEF), and O2 con-sumption (VO2) during cycle ergometer exercise (60% of peak VO2). Stroke volume (SV) and arteriovenous O2 difference (A-VO2) were calculated. Following a baseline blood sample (BASE) for P Pi, RBC Pi, DPG, RBC ATP, and P50 (3 h before exercise), a single oral dose of dicalcium phosphate (129 mmol) and glucose (500 ml/10% sol, PHOS), or placebo (PLA), was administered in a random, crossover, double-blind fashion. Blood sampling was repeated immediately before and after exercise (PRE-EX and POST-EX). PHOS induced increases in P Pi (3.87 to 4.35 mg · dl−1, P < 0.05), RBC Pi (3.86 to 4.63 mg · dl−1, P = 0.08), DPG (11.8 to 13.1 μmol · g−1 Hb, P < 0.05), RBC ATP (4.2 to 4.4 μmol · g−1 Hb, P < 0.05), and P50 (26.8 to 27.9 mm Hg, P < 0.05) from BASE to PRE-EX. All variables remained elevated through the exercise period, as evidenced by higher levels than BASE at POST-EX (P < 0.05). However, P50 was not different across conditions at PRE-EX (PHOS P50 = 27.9, PLA P50 = 28.3 mm Hg) or POST-EX (PHOS P50 = 28.0, PLA P50 = 28.1 mm Hg). No differences in Q, SV, HR, O2DEF, VO2, or A-VO2 were noted across conditions. Thus, the acute alterations of the hemato-logical parameters resulting from PHOS do not affect O2 delivery or cardiac output during submaximal exercise.
AB - Phosphate has been proposed as an ergogenic aid since it may enhance O2 delivery and cardiac work efficiency by increasing plasma phosphate (P Pi), red blood cell phosphate (RBC Pi), 2,3-diphosphoglycerate (DPG), RBC adenosine triphosphate (ATP), and P50. In 10 normal, fasting males we measured cardiac output (Q) by CO2 rebreathing, heart rate (HR), O2 deficit (O2DEF), and O2 con-sumption (VO2) during cycle ergometer exercise (60% of peak VO2). Stroke volume (SV) and arteriovenous O2 difference (A-VO2) were calculated. Following a baseline blood sample (BASE) for P Pi, RBC Pi, DPG, RBC ATP, and P50 (3 h before exercise), a single oral dose of dicalcium phosphate (129 mmol) and glucose (500 ml/10% sol, PHOS), or placebo (PLA), was administered in a random, crossover, double-blind fashion. Blood sampling was repeated immediately before and after exercise (PRE-EX and POST-EX). PHOS induced increases in P Pi (3.87 to 4.35 mg · dl−1, P < 0.05), RBC Pi (3.86 to 4.63 mg · dl−1, P = 0.08), DPG (11.8 to 13.1 μmol · g−1 Hb, P < 0.05), RBC ATP (4.2 to 4.4 μmol · g−1 Hb, P < 0.05), and P50 (26.8 to 27.9 mm Hg, P < 0.05) from BASE to PRE-EX. All variables remained elevated through the exercise period, as evidenced by higher levels than BASE at POST-EX (P < 0.05). However, P50 was not different across conditions at PRE-EX (PHOS P50 = 27.9, PLA P50 = 28.3 mm Hg) or POST-EX (PHOS P50 = 28.0, PLA P50 = 28.1 mm Hg). No differences in Q, SV, HR, O2DEF, VO2, or A-VO2 were noted across conditions. Thus, the acute alterations of the hemato-logical parameters resulting from PHOS do not affect O2 delivery or cardiac output during submaximal exercise.
KW - 3-dpg
KW - Cardiac work efficiency
KW - Ergogenic aid
KW - Hemoglobin
KW - Oxygen affinity, 2
KW - Oxygen deficit
UR - http://www.scopus.com/inward/record.url?scp=0025373075&partnerID=8YFLogxK
U2 - 10.1249/00005768-199006000-00011
DO - 10.1249/00005768-199006000-00011
M3 - Article
C2 - 2381302
AN - SCOPUS:0025373075
SN - 0195-9131
VL - 22
SP - 341
EP - 347
JO - Medicine and Science in Sports and Exercise
JF - Medicine and Science in Sports and Exercise
IS - 3
ER -