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Biophysical Journal 54: 655-667 (1988)
© 1988 the Biophysical Society
ABSTRACT
Until recently, polarographic methods for measuring the time course of transient changes in the rate of oxygen consumption (
QO2) have been applied only to tissue preparations containing thousands of cells. Here, we describe
QO2 measurements on the lateral ocellus of the barnacle (Balanus eburneus) which contains only three photoreceptor cells. The decrement of partial pressure of oxygen (
PO2) elicited by an 80 ms flash of light was measured near the cells with a microelectrode and the
QO2 was calculated from the
PO2 using a model of diffusion with spherical symmetry. As shown by mathematical simulation, the exact shape of the preparation is not crucial for our measurements of the time course of the
QO2. For a given
QO2, the model describes correctly the attenuation of the
PO2 measured at increased distances from the preparation. To know more about the mechanisms controlling the
QO2, we compared it with the electrical response of the photoreceptor cells: both responses have a similar spectral dependence, but only the
QO2 was abolished by a 10-min exposure to 50 µM dinitrophenol or to 3 mM amytal. We conclude that the
QO2 reflects an increase in mitochondrial respiration and that it is initiated by the phototransformation of rhodopsin, as was already found in the honeybee drone retina (Dimitracos and Tsacopoulos, 1985; Jones and Tsacopoulos, 1987).
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