V. Vanginneken et al., FISH MUSCLE ENERGY-METABOLISM MEASURED DURING HYPOXIA AND RECOVERY - AN IN-VIVO P-31-NMR STUDY, American journal of physiology. Regulatory, integrative and comparative physiology, 37(5), 1995, pp. 1178-1187
Three fish species were exposed to graded hypoxia levels and allowed t
o recover. Levels of high-energy phosphate compounds in epaxial white
muscle were monitored by in vivo P-31 nuclear magnetic resonance (NMR)
spectroscopy. Furthermore, O-2 consumption of the animals was measure
d. With increasing hypoxia load, metabolic parameters started to chang
e in the following order: phosphocreatine (PCr)-to-P-i ratio (decrease
), O-2 consumption (decrease), [PCr] (decrease), intracellular pH (pH(
i); decrease), P-i (increase), free ADP concentration ([ADP](free); in
crease), [ATP] (decrease). PCr levels fell with the P-O2. After each i
ncrement, the [PCr] reached a stable plateau value while, in some case
s, a recovery was observed. This recovery could be explained because t
he balance between anaerobic and aerobic metabolism is continuously fl
uctuating during hypoxia as a consequence of changes in the activity o
f the fish. Consequently the [ADP](free) are fluctuating, resulting in
an activation of the creatine kinase reaction and the anaerobic glyco
lysis. In all three species, anaerobic glycolysis was activated, but i
n contrast to anoxia exposure, metabolic suppression was absent. The c
hanges of [ADP](free) and [H+] (which influences the position of the c
reatine kinase equilibrium) are species dependent. Species differences
observed in the other parameters were small. It is concluded that the
pattern of the activation of anaerobic metabolism under deep hypoxia
is different from that under anoxia.