Little is known about the physiology of neurons in Caenorhabditis eleg
ans. Using new techniques for in situ patch-clamp recording in C. eleg
ans, we analyzed the electrical properties of an identified sensory ne
uron (ASER) across four developmental stages and 42 unidentified neuro
ns at one stage. We find that ASER is nearly isopotential and fails to
generate classical Na+ action potentials. Rather, ASER displays a hig
h sensitivity to input currents coupled to a depolarization-dependent
reduction in sensitivity that may endow ASER with a wide dynamic range
. Voltage clamp revealed depolarization-activated K+ and Ca2+ currents
that contribute to high sensitivity near the zero-current potential.
The depolarization-dependent reduction in sensitivity can be attribute
d to activation of K+ current at voltages where it dominates the net m
embrane current. The voltage dependence of membrane current was simila
r in all neurons examined, suggesting that C. elegans neurons share a
common mechanism of sensitivity and dynamic range.