Presynaptic calcium current modulation by a metabotropic glutamate receptor

被引:327
作者
Takahashi, T [1 ]
Forsythe, ID [1 ]
Tsujimoto, T [1 ]
BarnesDavies, M [1 ]
Onodera, K [1 ]
机构
[1] UNIV LEICESTER,DEPT CELL PHYSIOL & PHARMACOL,ION CHANNEL GRP,LEICESTER LE1 9HN,LEICS,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1126/science.274.5287.594
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metabotropic glutamate receptors (mGluRs) regulate transmitter release at mammalian central synapses. However, because oi 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.
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页码:594 / 597
页数:4
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