Dynamics of Ca 2+ and Na + in the dendrites of mouse cerebellar Purkinje cells evoked by parallel fibre stimulation

• Published in: The European journal of neuroscience Vol. 18; no. 10; pp. 2677 - 2689
• Main Authors: Kuruma, Akinori, Inoue, Takafumi, Mikoshiba, Katsuhiko
• Format: Journal Article
• Language: English
• Published: 01-11-2003
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/j.1460-9568.2003.02977.x

Ca
2+
and Na
+
play important roles in neurons, such as in synaptic plasticity. Their concentrations in neurons change dynamically in response to synaptic inputs, but their kinetics have not been compared directly. Here, we show the mechanisms and dynamics of Ca
2+
and Na
+
transients by simultaneous monitoring in Purkinje cell dendrites in mouse cerebellar slices. High frequency parallel fibre stimulation (50 Hz, 3–50‐times) depolarized Purkinje cells, and Ca
2+
transients were observed at the anatomically expected sites. The magnitude of the Ca
2+
transients increased linearly with increasing numbers of parallel fibre inputs. With 50 stimuli, Ca
2+
transients lasted for seconds, and the peak [Ca
2+
] reached ∼100 µ
m
, which was much higher than that reported previously, although it was still confined to a part of the dendrite. In contrast, Na
+
transients were sustained for tens of seconds and diffused away from the stimulated site. Pharmacological interventions revealed that Na
+
influx through α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA) receptors and Ca
2+
influx through P‐type Ca channels were essential players, that AMPA receptors did not operate as a Ca
2+
influx pathway and that Ca
2+
release from intracellular stores through inositol trisphosphate receptors or ryanodine receptors did not contribute greatly to the large Ca
2+
transients.