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M Guppy

Publications and source records attributed to M Guppy.

40 records · Page 3Linked to original sources

Metabolic sources of heat and power in tuna muscles. II. Enzyme and metabolite profiles.

Tuna appear able to maintain their muscles at 5-10 degrees C above ambient by balancing heat produced in situ and conserved by a counter-current heat exchanger with heat lost to the sea. Metabolite profiles under three different activity states (rest, burst swimming, and steady state swimming during feeding frenzies at sea) were used to identify which metabolic processes in white and red muscles could account for observed excess temperatures. During burst swimming, transient changes in metabolite levels indicate that the metabolism of both red and white muscle contributes to powering burst swimming; red muscle work is sustained mainly by oxidative metabolism while white muscle work depends upon an intense anaerobic glycolysis. The rate of metabolism in red muscle is easily high enough to account for the measured (10 degrees C) increase in temperature at this time. However, in white muscle, anaerobic glycolysis can account for only about a 2 degrees C maximum rise in temperature. The highest sustained swimming speeds and the highest muscle temperatures in skipjack are found during feeding frenzies at sea. As in burst swimming, during steady-state swimming red muscle temperatures can be accounted for by oxidative metabolism. In the case of white muscle, the lactate measurements indicate that anaerobic glycolysis could only lead to a 0.3 degree C temperature rise. However, if the fraction of utilized glycogen that is not fermented (about 60%) is assumed to be fully oxidized, enough heat is generated to raise white muscle temperatures by over 10 degrees C. The observed excess temperature at this time is about 8-10 degrees C, showing that anarerobic carbohydrate metabolism in white muscle is probably the major heat source during feeding frenzies. These interpretations are fully consistent with enzyme profiles of red and white muscles in tuna. They do not, however, explain why tuna have warm muscles. The latter problem is briefly discussed.

Aerobiosis↗

Role of dehydrogenase competition in metabloic regulation. The case of lactate and alpha-glycerophosphate dehydrogenases.

Many tissues expressing capacities for both anaerobic and aerobic glycolysis contain significant amounts of both lactate dehydrogenase and alpha-glycerophosphate dehydrogenase. Since the first serves in oxidation-reduction balance during anaerobic metabolism, while the second serves in the alpha-glycerophosphate cycle during aerobic metabolism, a provision seemed to be made (through competition for coenzyme) to encourage relatively exclusive function of either one or the other dehydrogenase. Competition for coenzyme was found to depend upon the isoenzyme form of each dehydrogenase (which determines the sensitivity of each reaction to modulators) and the concentration of two key metabolites, alpha-glycerophosphate and creatine phosphate, which differentially influence alpha-glycerophosphate dehydrogenases and lactate dehydrogenases. The sensitivities of various dehydrogenase isoenzymes to these modulators correlated well with their expected roles in the tissue of origin.

Animals↗

Controlling the highest lactate dehydrogenase activity known in nature.

In the shipjack, Euthynnus pelamis, white muscle appears to possess a powerful anaerobic capacity as well as a significant carbohydrate based aerobic potential. Lactate dehydrogenase occurs at higher activities than found thus far anywhere else in nature and clearly functions in anaerobic glycolysis. Alpha-glycerophosphate dehydrogenase also occurs in unusually high activities and appears to play a role in aerobic glycolysis. Regulation of these two reactions is accomplished by temperature, pH, and creatine phosphate levels. High temperature, low pH, and low creatine phosphate levels all appear to favor lactate dehydrogenase over alpha-glycerophosphate dehydrogenase; low temperature, high pH, and high creatine-phosphate levels, all expected during the quiescent state in this species, and when metabolism in aerobic, all favor alpha-glycerophosphate dehydrogenase activity.

Adenosine Triphosphate↗