Godino M C, Torres M, Sánchez-Prieto J
Departamento de Bioquímica, Facultad de Veterinaria, Universidad Complutense, 28040-Madrid, Spain.
FEBS Lett. 2005 Jan 31;579(3):768-72. doi: 10.1016/j.febslet.2004.12.065.
Since cannabinoid receptors inhibit excitatory synaptic transmission by reducing glutamate release, we have examined whether this might occur through the direct inhibition of presynaptic Ca2+ channels. In cerebrocortical nerve terminals, activation of cannabinoid receptors with WIN55,212-2 reduces the KCl-evoked release of glutamate. However, this inhibition is attenuated when N- and P/Q-type Ca2+ channels are blocked. Through Ca2+ imaging in single nerve terminals, we found that WIN55,212-2 reduced the influx of Ca2+ both in nerve terminals that contain N-type Ca2+ channels and those that contain P/Q-type Ca2+ channels. Thus, cannabinoid receptors modulate the two major Ca2+ channels coupled to glutamate release in the cerebral cortex.
由于大麻素受体通过减少谷氨酸释放来抑制兴奋性突触传递,我们研究了这是否可能通过直接抑制突触前Ca2+通道而发生。在大脑皮质神经末梢,用WIN55,212-2激活大麻素受体可减少KCl诱发的谷氨酸释放。然而,当N型和P/Q型Ca2+通道被阻断时,这种抑制作用会减弱。通过对单个神经末梢进行Ca2+成像,我们发现WIN55,212-2在含有N型Ca2+通道的神经末梢和含有P/Q型Ca2+通道的神经末梢中均减少了Ca2+内流。因此,大麻素受体调节大脑皮质中与谷氨酸释放相关的两种主要Ca2+通道。