A-type K+ current dominates somatic excitability of delayed firing neurons in rat substantia gelatinosa.

ABSTRACT

Substantia gelatinosa neurons display three main types of intrinsic firing behavior tonic, adapting, and delayed onset. Here, voltage-gated currents expressed by delayed firing neurons were studied in nucleated patches obtained in spinal cord slices of 3-5 weeks-old rats. Inward Na+ current was negligible under these conditions and was usually occluded by superposition of much larger outward currents. Two kinds of outward currents were found, an A-type (K(A) ) and delayed rectifier (K(DR) ) potassium currents. K(A) activated rapidly (<1.5 ms at >-20 mV) and operated at subthreshold membrane potentials; voltages of steady-state half-maximal activation and inactivation were -38.7 and -87.2 mV, respectively. Inactivation was biexponential with a dominant fast component (~90%, time constant ∼8 ms). K(DR) activated more slowly (<8 ms at >-20 mV), half-maximal activation was -23.6 mV, and decayed mono-exponentially with a time constant 70-110 ms. Maximal amplitudes of K(A) were almost 10-times larger than those of K(DR) , their respective densities were 8.5 and 0.97 µS µm⁻². Tetraethylammonium, 5 mM, blocked K(DR) but not K(A) , whereas both currents were depressed by 5 mM 4-aminopyridine. In current-clamp recordings, 4-action potential but not tetraethylammonium abolished firing delay suggesting the causative role of K(A) . Thus, the predominance of fast K(A) over other somatic currents is a distinctive feature of delayed firing neurons among all other types of substantia gelatinosa neurons and likely explains the appearance of their typical firing delay.