oxidative rate
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2013 ◽  
Vol 781-784 ◽  
pp. 908-912
Author(s):  
Ping Hui Zhang ◽  
Rong Sheng Xu ◽  
Zhen Dong Zhao ◽  
Liang Wu Bi ◽  
Yan Ju Lu ◽  
...  

Chinese gum rosin were digested by microwave-assisted sample digestion, and then the metal and semimetal elements in it were detected by inductive coupled plasma optical emission spectrometer (ICP-OES). Most metal and semimetal elements mass fractions in gum rosin are less than 5.0mg/kg, among which mass fractions of Al, Ca, Fe, Mg, Na are relatively higher. Some metal and semimetal elements in gum rosin may influence auto-oxidative rate to bring about color changing.


2007 ◽  
Vol 293 (5) ◽  
pp. R2046-R2051 ◽  
Author(s):  
Luke J. Haseler ◽  
Alexander Lin ◽  
Jan Hoff ◽  
Russell S. Richardson

In contrast to their exercise-trained counterparts, the maximal oxidative rate of skeletal muscle in sedentary humans appears not to benefit from supplemental O2 availability but is impacted by severe hypoxia, suggesting a metabolic limitation either at or below ambient O2 levels. However, the critical level of O2 availability at which maximal metabolic rate is reduced in sedentary humans is unknown. Using 31P magnetic resonance spectroscopy and arterial oximetry, phosphocreatine (PCr) recovery kinetics and arterial oxygenation were assessed in six sedentary subjects performing 5-min bouts of plantar flexion exercise followed by 6 min of recovery. Each trial was repeated while breathing one of four different fractions of inspired O2 (FIO2) (0.10, 0.12, 0.15, and 0.21). The PCr recovery rate constant (a marker of oxidative capacity) was unaffected by reductions in FIO2, remaining at a value of 1.5 ± 0.2 min−1 until arterial O2 saturation (SaO2) fell to less than ∼92%, the average value reached breathing an FIO2 of 0.15. Below this SaO2, the PCr rate constant fell significantly by 13 and 31% to 1.3 ± 0.2 and 1.0 ± 0.2 min−1 ( P < 0.05) as SaO2 was reduced to 82 ± 3 and 77 ± 2%, respectively. In conclusion, this study has revealed that O2 availability does not impact maximal oxidative rate in sedentary humans until the O2 level falls well below that of ambient air, indicating a metabolic limitation in normoxia.


2004 ◽  
Vol 97 (3) ◽  
pp. 1077-1081 ◽  
Author(s):  
Luke J. Haseler ◽  
Alexander P. Lin ◽  
Russell S. Richardson

Previously, it was demonstrated in exercise-trained humans that phosphocreatine (PCr) recovery is significantly altered by fraction of inspired O2 (FiO2), suggesting that in this population under normoxic conditions, O2 availability limits maximal oxidative rate. Haseler LJ, Hogan ML, and Richardson RS. J Appl Physiol 86: 2013–2018, 1999. To further elucidate these population-specific limitations to metabolic rate, we used 31P-magnetic resonance spectroscopy to study the exercising human gastrocnemius muscle under conditions of varied FiO2 in sedentary subjects. To test the hypothesis that PCr recovery from submaximal exercise in sedentary subjects is not limited by O2 availability, but rather by their mitochondrial capacity, six sedentary subjects performed three bouts of 6-min steady-state submaximal plantar flexion exercise followed by 5 min of recovery while breathing three different FiO2 (0.10, 0.21, and 1.00). PCr recovery time constants were significantly longer in hypoxia (47.0 ± 3.2 s), but there was no difference between hyperoxia (31.8 ± 1.9 s) and normoxia (30.0 ± 2.1 s) (mean ± SE). End-exercise pH was not significantly different across treatments. These results suggest that the maximal muscle oxidative rate of these sedentary subjects, unlike their exercise-trained counterparts, is limited by mitochondrial capacity and not O2 availability in normoxia. Additionally, the significant elongation of PCr recovery in these subjects in hypoxia illustrates the reliance on O2 supply at the other end of the O2 availability spectrum in both sedentary and active populations.


1999 ◽  
Vol 31 (Supplement) ◽  
pp. S246 ◽  
Author(s):  
T. Hamaoka ◽  
T. Katsumura ◽  
T. Sako ◽  
H. Higuchi ◽  
M. Murakami ◽  
...  

1998 ◽  
Vol 30 (Supplement) ◽  
pp. 232
Author(s):  
T. Hamaoka ◽  
T. Katsumura ◽  
T. Shimomitsu ◽  
N. Murase ◽  
S. Nishio ◽  
...  

1990 ◽  
Vol 259 (3) ◽  
pp. E342 ◽  
Author(s):  
H Hourani ◽  
P Williams ◽  
J A Morris ◽  
M E May ◽  
N N Abumrad

The effects of insulin-induced hypoglycemia (IIH) on leucine kinetics (mumol.kg-1.min-1) and interorgan flow of amino acids (AA) were examined in 2 groups of 18-h fasted conscious dogs. Insulin was infused at 5 mU.kg-1.min-1 for 3 h. IIH (40 +/- 5 mg/dl) resulted in a drop in plasma leucine (114 +/- 10 to 64 +/- 9 microM) and leucine rate of appearance (Ra) (3.1 +/- 0.1 to 2.4 +/- 0.2) within 1 h but gradually increased (P less than 0.05) to 145 +/- 30 microM and 3.8 +/- 0.5 by 3 h. Leucine oxidative rate of disposal (Rd) increased from 0.44 +/- 0.08 to 1.02 +/- 0.35 (P less than 0.01), and nonoxidative Rd dropped initially but was near basal levels by 3 h. When euglycemia was maintained, there was sustained drop in plasma leucine from 122 +/- 12 to 42 +/- 6 mumol/l, leucine Ra from 3.1 +/- 0.4 to 1.8 +/- 0.2, oxidative Rd from 0.36 +/- 0.03 to 0.22 +/- 0.04, and nonoxidative Rd from 2.75 +/- 0.4 to 1.6 +/- 0.2 (all P less than 0.01). IIH was associated with a significant net release of leucine (and other AA) across the gut (0.04 +/- 0.05 to 1.86 +/- 0.30 mumol.kg-1.min-1; P less than 0.05). In the group with euglycemia there was no significant change in the gut balance of leucine. We conclude that IIH is associated with a proteolytic response and that the gut is the major contributor to this response.


1987 ◽  
Vol 253 (5) ◽  
pp. R746-R755 ◽  
Author(s):  
N. Baker ◽  
M. Gan-Elepano ◽  
B. A. Guthrie ◽  
J. F. Mead

We have reexamined the concept of the irreversible disposal rate (IDR) or fractional catabolic rate (FCR) in relation to the oxidation of a major metabolic fuel, plasma free fatty acids (FFA), in mice. We measured the disappearance of intravenously injected [1-14C]palmitate complexed to mouse serum albumin from the circulation of normal mice fed ad libitum and fasted approximately 4 h before tracer injection. We also measured the appearance of expired 14CO2 in the breath. Using multicompartmental analyses (SAAM) we found that, in contrast to earlier studies in this and other mammals where the estimated IDR has always been two to three times greater than the oxidative rate, the IDR (FCR) corresponded closely to the fractional rate of plasma FFA oxidation to CO2. This rate could be estimated accurately in a study of 10- to 15-min duration. In an extended study (5-h duration) we obtained kinetic evidence of a major transport pathway that involves delayed recycling of FFA through at least several unidentified relatively slowly turning compartments.


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