PUBLICATION

Influence of hypoxia and of hypoxemia on the development of cardiac activity in zebrafish larvae

Authors
Jacob, E., Drexel, T., Schwerte, T., and Pelster, B.
ID
ZDB-PUB-020920-2
Date
2002
Source
American journal of physiology. Regulatory, integrative and comparative physiology   283(4): R911-917 (Journal)
Registered Authors
Pelster, Bernd, Schwerte, Thorsten
Keywords
anaerobic metabolism; cardiac output; convective oxygen transport
MeSH Terms
  • Anaerobiosis/physiology
  • Animals
  • Cardiac Output
  • Diffusion
  • Environment
  • Heart/physiopathology*
  • Heart Rate
  • Hypoxia/physiopathology*
  • Larva/physiology
  • Oxygen/analysis
  • Oxygen/blood
  • Oxygen/metabolism
  • Partial Pressure
  • Reference Values
  • Skin/metabolism
  • Temperature
  • Time Factors
  • Water/chemistry
  • Zebrafish/growth & development*
  • Zebrafish/physiology*
PubMed
12228061 Full text @ Am. J. Physiol. Regul. Integr. Comp. Physiol.
Abstract
Cardiac activity and anaerobic metabolism were analyzed in zebrafish larvae raised under normoxia (PO(2) = 20 kPa) and under chronic hypoxia (PO(2) = 10 kPa) at three different temperatures (25, 28, and 31 degrees C). Heart rate increased with development and with temperature. Under normoxia, cardiac output increased significantly at high temperature (31 degrees C), but not at 28 or at 25 degrees C. Under chronic hypoxia, however, heart rate as well as cardiac output increased at all temperatures in larvae at about hatching time or shortly thereafter. Cardiac activity of larvae raised for 2 wk after fertilization with a reduced hemoglobin oxygen-carrying capacity in their blood (hypoxemia; due to the presence of CO or of phenylhydrazine in the incubation water) was not different from control animals. Whole body lactate content of these animals did not increase. Thus there was no indication of a stimulated anaerobic energy metabolism. The increase in cardiac activity observed during hypoxia suggests that at about hatching time receptors are present that sense hypoxic conditions, and this information can be used to induce a stimulation of convective oxygen transport to compensate for a reduction in bulk oxygen diffusion in the face of a reduced oxygen gradient between environmental water and tissues. Under normoxia, however, the PO(2) gradient between environmental water and tissues and diffusional oxygen transport assure sufficient oxygen supply even if hemoglobin oxygen transport in the blood is severely impaired. Thus, under normoxic conditions and with a normal metabolic rate of the tissues, convective oxygen transport is not required until ~2 wk after fertilization.
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