Although Golgi cells (GoCs), the main type of inhibitory interneuron in the cerebellar granular layer (GL), are thought to play a central role in cerebellar network function, their excitable properties have remained unexplored. GoCs fire rhythmically in vivo and in slices, but it was unclear whether this activity originated from pacemaker ionic mechanisms. We explored this issue in acute cerebellar slices from 3-week-old rats by combining loose cell-attached (LCA) and whole-cell (WC) recordings. GoCs displayed spontaneous firing at 1-10 Hz (room temperature) and 2-20 Hz (35-37 degrees C), which persisted in the presence of blockers of fast synaptic receptors and mGluR and GABA(B) receptors, thus behaving, in our conditions, as pacemaker neurons. ZD 7288 (20 mu M), a potent hyperpolarization-activated current (I-h) blocker, slowed down pacemaker frequency. The role of subthreshold Na+ currents (I-Na,I-sub) could not be tested directly, but we observed a robust TTX-sensitive, non-inactivating Na+ current in the subthreshold voltage range. When studying repolarizing currents, we found that retigabine (5 mu M), an activator of KCNQ K+ channels generating neuronal M-type K+ (I-M) currents, reduced GoC excitability in the threshold region. The KCNQ channel antagonist XE991 (5 mu M) did not modify firing, suggesting that GoC I-M has low XE991 sensitivity. Spike repolarization was followed by an after-hyperpolarization (AHP) supported by apamin-sensitive Ca2+-dependent K+ currents (I-apa). Block of I-apa decreased pacemaker precision without altering average frequency. We propose that feed-forward depolarization is sustained by I-h and I-Na,I-sub, and that delayed repolarizing feedback involves an I-M-like current whose properties remain to be characterized. The multiple ionic mechanisms shown here to contribute to GoC pacemaking should provide the substrate for fine regulation of firing frequency and precision, thus influencing the cyclic inhibition exerted by GoCs onto the cerebellar GL.
Ionic mechanisms of autorhythmic firing in rat cerebellar Golgi cells
2006
Abstract
Although Golgi cells (GoCs), the main type of inhibitory interneuron in the cerebellar granular layer (GL), are thought to play a central role in cerebellar network function, their excitable properties have remained unexplored. GoCs fire rhythmically in vivo and in slices, but it was unclear whether this activity originated from pacemaker ionic mechanisms. We explored this issue in acute cerebellar slices from 3-week-old rats by combining loose cell-attached (LCA) and whole-cell (WC) recordings. GoCs displayed spontaneous firing at 1-10 Hz (room temperature) and 2-20 Hz (35-37 degrees C), which persisted in the presence of blockers of fast synaptic receptors and mGluR and GABA(B) receptors, thus behaving, in our conditions, as pacemaker neurons. ZD 7288 (20 mu M), a potent hyperpolarization-activated current (I-h) blocker, slowed down pacemaker frequency. The role of subthreshold Na+ currents (I-Na,I-sub) could not be tested directly, but we observed a robust TTX-sensitive, non-inactivating Na+ current in the subthreshold voltage range. When studying repolarizing currents, we found that retigabine (5 mu M), an activator of KCNQ K+ channels generating neuronal M-type K+ (I-M) currents, reduced GoC excitability in the threshold region. The KCNQ channel antagonist XE991 (5 mu M) did not modify firing, suggesting that GoC I-M has low XE991 sensitivity. Spike repolarization was followed by an after-hyperpolarization (AHP) supported by apamin-sensitive Ca2+-dependent K+ currents (I-apa). Block of I-apa decreased pacemaker precision without altering average frequency. We propose that feed-forward depolarization is sustained by I-h and I-Na,I-sub, and that delayed repolarizing feedback involves an I-M-like current whose properties remain to be characterized. The multiple ionic mechanisms shown here to contribute to GoC pacemaking should provide the substrate for fine regulation of firing frequency and precision, thus influencing the cyclic inhibition exerted by GoCs onto the cerebellar GL.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
