| Abstract: | Neuronal plasticity and its development were investigated at pyramidal neurons in the cortical slices of rats. The threshold and probability of firing spikes were measured by using whole‐cell recording to assess neuronal excitability. Postsynaptic high frequency activity (HFA) at the pyramidal neurons, evoked by 20 trains (250‐ms interval) of five depolarization‐pulses (1 ms) at 100 Hz, persistently lowered the threshold and increased the probability of firing spikes. After long‐term enhancement of neuronal excitability by HFA was stable, another HFA induced further enhancement. Infusing 1 mM 1,2‐bis(2‐aminophenoxy)‐ethane‐N, N,N′,N′‐tetraacetic acid or 100 μM CaMKII(281–301) into the recording neurons prevented HFA‐induced long‐term enhancement of neuronal excitability. The infusion of 40 μM calcineurin autoinhibitory peptide enhanced neuronal excitability, which occluded HFA effect. HFA‐induced long‐term enhancement of intrinsic excitability expressed at most pyramidal neurons after postnatal day (PND) 14, but not at those before PND 9. Our results show a new type of neuronal plasticity induced by physiological activity at cortical neurons, which requires calcium‐dependent protein phosphorylation and develops during postnatal period. An upregulation of intrinsic excitability at cortical neurons facilitates their activity and broadens signal codes; consequently, their computational ability is upgraded. © 2004 Wiley Periodicals, Inc. J Neurobiol, 2004 |
