Takahashi T, Forsythe I D, Tsujimoto T, Barnes-Davies M, Onodera K
Department of Neurophysiology, Institute for Brain Research, Faculty of Medicine, University of Tokyo, Tokyo 113, Japan.
Science. 1996 Oct 25;274(5287):594-7. doi: 10.1126/science.274.5287.594.
Metabotropic glutamate receptors (mGluRs) regulate transmitter release at mammalian central synapses. However, because of the difficulty of recording from mammalian presynaptic terminals, the mechanism underlying mGluR-mediated presynaptic inhibition is not known. Here, simultaneous recordings from a giant presynaptic terminal, the calyx of Held, and its postsynaptic target in the medial nucleus of the trapezoid body were obtained in rat brainstem slices. Agonists of mGluRs suppressed a high voltage-activated P/Q-type calcium conductance in the presynaptic terminal, thereby inhibiting transmitter release at this glutamatergic synapse. Because several forms of presynaptic modulation and plasticity are mediated by mGluRs, this identification of a target ion channel is a first step toward elucidation of their molecular mechanism.
代谢型谷氨酸受体(mGluRs)调节哺乳动物中枢突触处的递质释放。然而,由于从哺乳动物突触前终末进行记录存在困难,mGluR介导的突触前抑制的潜在机制尚不清楚。在此,在大鼠脑干切片中,对一个巨大的突触前终末——Held壶腹及其在梯形体内侧核的突触后靶点进行了同步记录。mGluRs的激动剂抑制了突触前终末中高电压激活的P/Q型钙电导,从而抑制了这个谷氨酸能突触处的递质释放。由于几种形式的突触前调节和可塑性是由mGluRs介导的,因此确定靶离子通道是阐明其分子机制的第一步。