TY - JOUR
T1 - Gastrointestinal tract, hepatic, hindlimb, and renal recovery of CO2 in vivo
AU - Gresham, J. D.
AU - Okamura, K.
AU - Williams, P. E.
AU - Jabbour, K.
AU - Flakoll, P. J.
PY - 2000
Y1 - 2000
N2 - Whole body oxidative rates of labeled substrates are often measured by collecting expired air and determining the amount of labeled CO2 that is produced. However, the CO2 produced may not be completely recovered under all circumstances, and there is a wide variation in values reported under different experimental conditions (~50-100%). The potential contribution of specific organs to this variation has not been defined. In vivo studies using healthy, postabsorptive, multicatheterized conscious canines were conducted to determine gastrointestinal tract, hepatic, hindlimb, and renal recoveries of NaH14CO3 during a 180-min constant infusion [0.022 ± 0.002 (SE) μCi·kg-1·min-1]. Before the constant infusion period, a bolus infusion of NaH14CO3 (1.76 ± 0.16 μCi/kg) was given, and the rate of decay in blood was measured over a 15-min period to determine pool size. The pool size for the distribution of 14CO2 was ~80% of the total body pool (16.0 ± 1.7 liters). Whole body recovery was 97.2 ± 6.7%. The recoveries across the liver, gut, leg, and kidney were 99.9 ± 1.3, 98.0 ± 1.4, 96.7 ± 2.6, and 99.9 ± 2.1%, respectively. In conclusion, hepatic, gastrointestinal tract, hindlimb, and renal recoveries of CO2 in vivo were near 100%, suggesting that CO2 loss is not greater in gluconeogenic organs and that corrections for incomplete recovery of CO2, when measuring oxidation of substrates across these organs under normal postabsorptive conditions, would be very minor.
AB - Whole body oxidative rates of labeled substrates are often measured by collecting expired air and determining the amount of labeled CO2 that is produced. However, the CO2 produced may not be completely recovered under all circumstances, and there is a wide variation in values reported under different experimental conditions (~50-100%). The potential contribution of specific organs to this variation has not been defined. In vivo studies using healthy, postabsorptive, multicatheterized conscious canines were conducted to determine gastrointestinal tract, hepatic, hindlimb, and renal recoveries of NaH14CO3 during a 180-min constant infusion [0.022 ± 0.002 (SE) μCi·kg-1·min-1]. Before the constant infusion period, a bolus infusion of NaH14CO3 (1.76 ± 0.16 μCi/kg) was given, and the rate of decay in blood was measured over a 15-min period to determine pool size. The pool size for the distribution of 14CO2 was ~80% of the total body pool (16.0 ± 1.7 liters). Whole body recovery was 97.2 ± 6.7%. The recoveries across the liver, gut, leg, and kidney were 99.9 ± 1.3, 98.0 ± 1.4, 96.7 ± 2.6, and 99.9 ± 2.1%, respectively. In conclusion, hepatic, gastrointestinal tract, hindlimb, and renal recoveries of CO2 in vivo were near 100%, suggesting that CO2 loss is not greater in gluconeogenic organs and that corrections for incomplete recovery of CO2, when measuring oxidation of substrates across these organs under normal postabsorptive conditions, would be very minor.
UR - http://www.scopus.com/inward/record.url?scp=0033765764&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0033765764&partnerID=8YFLogxK
U2 - 10.1152/jappl.2000.89.5.2000
DO - 10.1152/jappl.2000.89.5.2000
M3 - Article
C2 - 11053355
AN - SCOPUS:0033765764
SN - 8750-7587
VL - 89
SP - 2000
EP - 2006
JO - Journal of applied physiology
JF - Journal of applied physiology
IS - 5
ER -