Fukunaga Kohji
Department of Pharmacology, Tohoku University Graduate School of Pharmaceutical Sciences, Japan.
Clin Calcium. 2015 Feb;25(2):247-54.
Low-threshold Ca2+ spikes are mediated by T-type Ca2+ channels, which have fast inactivation and slow deactivation kinetics (transient) , and single channel conductance. The activation are triggered by -60 to -65 mV. T-type Ca2+ channels are predominantly expressed in the brain and heart pacemaker cells. Three subtypes of T-type Ca2+ channels Cav3.1 (α1G), Cav3.2 (α1H), Cav3.3 (α1I) encoding by CACNA1G, CACNA1H, CACNA1I genes have been cloned. Although high-threshold voltage-gated Ca2+ channels have auxiliary α2δ, β, γ subunits, T-type Ca2+ channels are composed only by α1 subunit. Although T-type Ca2+ channels are involved in the pace making in heart and a robust low-threshold Ca2+ spike in neurons, the physiological functions in the memory and synaptic plasticity remain unclear. In this paper, I would like to focus on the pathophysiological relevance of T-type Ca2+ channels in the brain functions including cognition.
低阈值Ca2+尖峰由T型Ca2+通道介导,该通道具有快速失活和缓慢失活动力学(瞬态)以及单通道电导。其激活由-60至-65 mV触发。T型Ca2+通道主要在脑和心脏起搏器细胞中表达。由CACNA1G、CACNA1H、CACNA1I基因编码的T型Ca2+通道的三个亚型Cav3.1(α1G)、Cav3.2(α1H)、Cav3.3(α1I)已被克隆。虽然高阈值电压门控Ca2+通道有辅助性α2δ、β、γ亚基,但T型Ca2+通道仅由α1亚基组成。尽管T型Ca2+通道参与心脏起搏以及神经元中强烈的低阈值Ca2+尖峰形成,但其在记忆和突触可塑性方面的生理功能仍不清楚。在本文中,我将重点关注T型Ca2+通道在包括认知在内的脑功能中的病理生理相关性。