The static discharge rate of Renshaw cells (studied in deafferented, intercollicularly decerebrate cats) has a nonlinear dependence on the frequency of trains of stimulus impulses to alpha-motor axons in the ventral root. This dependence is well described by a rectangular hyperbola that approaches saturation with increasing stimulus frequency. The tendency to saturate is independent of the number of motor axons exciting a Renshaw cell. On average, the stimulus frequency at which the discharge rate reaches half its saturation value lies between 10 and 15 Hz. The effect of Renshaw cell activity -- measured as the antidromic inhibition of individual alpha-motoneurons -- reflects the forms of the static frequency characteristics. An electric circuit analog of the Renshaw cell membrane is presented which serves to explain the qualitative features of the static input-output relations; the nonlinearity is the result of synapses with linear properties acting together at the cell membrane.
In decerebrate cats, the dynamic responses of Renshaw cells to step changes in input were determined separately both for changes in the number of alpha-axons excited and for changes in the frequency at which they were stimulated. Together, these two input variables to the Renshaw cells describe the level of activity in the motor output from the spinal cord. In either case, the dynamic responses of the interneurons depend only on their static activity before and after an input step occurs, but are otherwise indistinguishable. This favors the interpretation that the two input variables are equivalent under dynamic conditions, i.e., Renshaw cells respond to total motor output.
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