scholarly journals The use of oxygen consumption as an indicator of energy assimilation in full sib groups of rainbow trout

1980 ◽  
Vol 12 (4) ◽  
pp. 422
Author(s):  
JB Kinghorn
1993 ◽  
Vol 71 (11) ◽  
pp. 2167-2173 ◽  
Author(s):  
John R. Bailey ◽  
William R. Driedzic

Rainbow trout (Oncorhynchus mykiss) were acclimated to 5 and 20 °C. Oxygen consumption of isolated perfused hearts was measured at 5 or 15 °C with either glucose or palmitate as the exogenous fuel source. With glucose as the fuel there was no significant difference in oxygen consumption of hearts from either acclimation group at either temperature. With palmitate as the fuel source, hearts from fish acclimated to and tested at 5 °C had significantly higher oxygen consumption than hearts from fish acclimated to 20 °C and tested at either 5 or 15 °C. Hearts from fish both acclimated to and tested at 5 °C had a higher oxygen consumption with palmitate than when glucose was supplied. This reflects the preference for fatty acid fuels found in cold acclimated muscle tissue, and consequently the amount of oxygen required to utilize fats. Under all experimental conditions, 14CO2 production from either (6-14C)glucose or (1-14C)palmitate could account for less than 0.5% of oxygen consumption. Tissue chemical analysis showed that most of the label from (6-14C)glucose appeared in acid-soluble (glycolytic intermediates, citric acid cycle intermediates, amino acids, etc.) and lipid fractions while most of the label from (1-14C)palmitate appeared in lipid- or acid-soluble or acid precipitate (protein material) fractions. This indicates considerable dilution of exogenous fuels in endogenous pools, which could account for the discrepancy in measured O2 consumption and 14CO2 production. Glucose catabolism was little affected by either acute or chronic changes in temperature other than an increase in glucose incorporation into the glycogen pool. Hearts from fish both acclimated to and tested at 5 °C showed an increased handling of exogenous fatty acids as reflected by elevated rates of catabolism and incorporation into intracellular lipids.


1994 ◽  
Vol 29 (4) ◽  
pp. 245-251 ◽  
Author(s):  
Atsushi Yamamoto ◽  
Takaji Iida

1992 ◽  
Vol 167 (1) ◽  
pp. 155-169 ◽  
Author(s):  
M. Scarabello ◽  
G. J. Heigenhauser ◽  
C. M. Wood

Juvenile rainbow trout (approximately 6 g) were exercised to exhaustion in two 5 min bouts given 6 h apart. Resting levels of whole-body lactate and glycogen were restored prior to the second bout. The rate of O2 consumption increased about threefold 5 min after each bout of exercise, while recovery time decreased from 4 h after the first bout to 2–3 h after the second. The excess post-exercise oxygen consumption, i.e. ‘oxygen debt’, was significantly reduced by 40% after the second exercise bout, despite almost identical rates of lactate clearance and glycogen resynthesis. The rates of CO2 and ammonia excretion increased sixfold and threefold, and recovery times decreased from 4–6 h to 3 h and from 3 h to 1.5 h, respectively. After the first bout, whole-body lactate levels peaked at 5 min post-exercise at about 8.5 times pre-exercise levels. After the second bout, lactate levels peaked at 0 min post-exercise and fell more rapidly during recovery. Whole-body glycogen levels decreased by 70% and 80% and ATP levels decreased by 75% and 65% after the first and second bouts, respectively, while glucose levels increased about 1.5-fold immediately after both bouts. Creatine phosphate levels decreased by 70% and 80% after the first and second bouts, respectively. After 6 h of recovery, creatine phosphate levels were higher after the second bout than after the first. These findings suggest that exhaustive exercise may cause a ‘non-specific’ increase in metabolic rate not directly related to the processing of metabolites, which is reduced upon a subsequent exercise bout. This is in contrast with the classical ‘oxygen debt hypothesis’, which states that the oxygen debt and lactate clearance are linked. Furthermore, it appears that two sequential exercise bouts are sufficient to induce a ‘training effect’, i.e. improved rates of metabolic recovery.


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