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THE EFFECTS OF ANOXIA UPON ENERGY SOURCES AND SELECTED METABOLIC INTERMEDIATES IN THE BRAINS OF FISH, FROG AND TURTLE 1
Author(s) -
McDougal D. B.,
Holowach J.,
Howe M. C.,
Jones E. M.,
Thomas C. A.
Publication year - 1968
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1968.tb08956.x
Subject(s) - glycogen , turtle (robot) , creatine , glycolysis , biology , hexokinase , medicine , endocrinology , fish <actinopterygii> , rana , carassius auratus , phosphocreatine , phosphate , phosphofructokinase , metabolic rate , energy metabolism , metabolism , biochemistry , ecology , fishery
— The levels of the main cerebral energy reserves, ATP, P‐creatine, glycogen and glucose, and of several glycolytic intermediates and lactate, were measured in the brains of fish ( Carassius auratus ), turtle ( Pseudemys scripta elegans ) and frog ( Rana pipiens ). The levels of glycogen in these brains were 2‐9 times higher than those reported for mammals. In frog, cerebral glycogen levels were 35 per cent higher during the winter than in spring. The P‐creatine: ATP ratios were 3 instead of the more usual (mammalian) value of 1. The levels of other intermediates were similar to those found in mammalian brain. When anoxia was produced by decapitation, changes in the various substances measured were similar to those in mammalian brain, but were much slower. The initial rate at which high‐energy phosphate was used could be calculated from these changes. Values of 1.1 m‐equiv./kg/min for fish and frog and of 0.46 m‐equiv./kg/min for turtle were found, which are 1/20 and 1/50, respectively, of the rate in mouse brain. The rate of disappearance of high‐energy phosphate reserves followed first‐order kinetics for 4 hr in turtle and for at least an hour in the other species. Changes in metabolites as the experiment progressed were interpreted to indicate a progressively falling intracellular pH, prolonged inhibition of phosphofructokinase, and a long period of hexokinase inhibition.