Related Documentation:
Several groups have reported the presence of a low-threshold, inactivating Ca2+ channel in the Purkinje cell [2, 3, 4] comparable to the T channel in other neurons [1]. The whole-cell voltage-clamp study of freshly isolated rat Purkinje cells by [4] (their Figs. 1–3) provided all the data necessary to model activation of T calcium (CaT) current (Fig. 2 B). [3] (their Fig. 4C) have shown a higher threshold of activation for CaT current in Purkinje cells, but [2] reported the same threshold as [4]. The equations for CaT current inactivation were based on a combination of steady-state inactivation data from [3] (their Fig. 5A) and time constant data from [4] (their Fig. 2B), which were almost identical to the data from [3] (their Fig. 5C).
[1] AP Fox, MC Nowycky, and RW Tsien. Kinetic and pharmacological properties distinguishing three types of calcium current in chick sensory neurones. Journal of Physiology (Lond.), 394:149–172, 1987.
[2] DL Gruol and CR Deal. Expression of calcium conductances in purkinje neurons in culture. Society for Neuroscience Abstracts, 16:677, 1990.
[3] T Hirano and S Hagiwara. Kinetics and distribution of voltage-gated Ca, Na, and K channels on the somata of rat cerebellar Purkinje cells. Pfluegers Archiv, 413:463–469, 1989.
[4] M Kaneda, M Wakamori, M Ito, and N Akaike. Low-threshold calcium current in isolated Purkinje cell bodies of rat cerebellum. Journal of Neurophysiology, 63:1046–1052, 1990.