Key result
Blockade of Kv7-mediated current with XE-991 significantly reduced rheobase from 482 pA to 366 pA, increased firing rate gain, and eliminated subthreshold voltage oscillations in rat neocortical pyramidal neurons.
Absolute Event Rate: 366% vs 482%
p-value: p=0.001
Kv7 channels play important roles in subthreshold regulation of excitability and generation of theta-frequency subthreshold oscillations in neocortical pyramidal neurons.
Alters rat pyramidal excitability in vitro; leaves open Kv7 modulation of human cortical function or disease.
After block of Kv1- and Kv2-mediated K(+) currents in acutely dissociated neocortical pyramidal neurons from layers II/III of rat somatosensory and motor cortex, the remaining current is slowly activating and persistent. We used whole cell voltage clamp to show that the Kv7 blockers linopirdine and XE-991 blocked a current with similar kinetics to the current remaining after combined block of Kv1 and Kv2 channels. This current was sensitive to low doses of linopirdine and activated more slowly and at more negative potentials than Kv1- or Kv2-mediated current. The Kv7-mediated current decreased in amplitude with time in whole cell recordings, but in most cells the current was stable for several minutes. Current in response to a traditional M-current protocol was blocked by muscarine, linopirdine, and XE-991. Whole cell slice recordings revealed that the Q₁₀ for channel deactivation was ∼2.5. Sharp electrode current-clamp recordings from adult pyramidal cells demonstrated that block of Kv7-mediated current with XE-991 reduced rheobase, shortened the latency to firing to near rheobase current, induced more regular firing at low current intensity, and increased the rate of firing to a given current injection. XE-991 did not affect single action potentials or spike frequency adaptation. Application of XE-991 also eliminated subthreshold voltage oscillations and increased gain for low-frequency inputs (<10 Hz) without affecting gain for higher frequency inputs. These data suggest important roles for Kv7 channels in subthreshold regulation of excitability, generation of theta-frequency subthreshold oscillations, regulation of interspike intervals, and biasing selectivity toward higher frequency inputs.
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Guan et al. (2011) studied this question. Kv7 blockers (linopirdine and XE-991) vs. Control solution was evaluated on Rheobase (Irh) (p=0.001). Blockade of Kv7-mediated current with XE-991 significantly reduced rheobase from 482 pA to 366 pA, increased firing rate gain, and eliminated subthreshold voltage oscillations in rat neocortical pyramidal neurons.
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