Peroxynitrite donor impairs excitability of hippocampal CA1 neurons by inhibiting voltage-gated potassium currents

Abstract Nitric oxide (NO) reacts rapidly with superoxide anion and produces peroxynitrite (ONOO − ), which is a highly reactive free radical that has been shown to mediate much of the toxicity of NO. ONOO − has also been implicated as playing a role in the pathology of various brain disorders. The aim of this study was to investigate the actions of ONOO − on voltage-activated potassium currents and its effect on membrane excitability in hippocampal CA1 neurons. SIN-1(3-morpholino-sydnonimine), which leads to the simultaneous generation of superoxide anion and NO, and then forms the highly reactive species ONOO − , induced a dose-dependent inhibition in amplitudes of transient potassium currents ( I A ) and delayed rectifier potassium currents ( I K ). SIN-1 (500 μM) produced a hyperpolarizing shift in the activation–voltage curve of both I A and I K and delayed the recovery of I A from inactivity, but did not have a marked effect on the inactivation parameters of I A . However, co-treatment with SIN-1 and Mn(III)tetrakis(4-benzoic acid)porphyrin chloride (MnTBAP, 100 μM), an ONOO − scavenger, had no effects on I A and I K currents. SIN-1 (500 μM) led to increase in action potential duration and decrease in action potential firing rate. The results suggest that changes of I A and I K currents induced by ONOO − in hippocampal neurons have influence on excitability of hippocampal CA1 neurons, which are related to its neurotoxicity.