Abstract
When slices of the main electric organ of Electrophorus are stimulated electrically, the sequence of temperature changes is briefly positive (Q$_{1}$), then negative (Q$_{2}$) and finally positive (Q$_{3}$). The initial temperature rise Q$_{1}$ is only seen when there are several damaged electroplates in the immediate neighbourhood of the thermistor probe, and is regarded as an artifact. The cooling phase Q$_{2}$ is completed within about 70 ms of the electrical discharge, and its average size on open circuit for a single impulse at 22 degrees C is 60 $\mu $cal/g. The final warming phase Q$_{3}$ is about twice as large, measured from the peak of Q$_{2}$, and its average half-time is 37 s. At lower ambient temperatures the size of Q$_{2}$ is greater (Q$_{10}$ about 1$\cdot $6), and Q$_{3}$ reaches completion rather more slowly. The main object of the experiments was to test the prediction made in 1906 by Bernstein & Tschermak that the electric organ should undergo a cooling equal to the warming of the external resistive load minus the heat of ionic mixing. Simultaneous measurements of the size of Q$_{2}$ and of the external electrical work showed that Q$_{2}$ can be considered as consisting of two components, one of which is the load-dependent 'Bernstein' cooling, while the other is the cooling observed on open circuit which is effectively independent of the current drawn. Not more than a fifth of the open-circuit cooling is likely to arise from the presence of a leakage path round the outer edges of the slice of tissue. After considering several alternatives, it is suggested that the bulk of the open-circuit cooling can possibly be attributed to a coupling between the efflux of K$^{+}$ ions through the innervated faces of the electroplates during the plateau of the discharge and a chemical reaction, perhaps involving a synthesis of ATP by reversal of the sodium pump.

This publication has 10 references indexed in Scilit: