Taylor K E, Cahusac P M
Department of Psychology, University of Stirling, U.K.
Neuropharmacology. 1994 Jan;33(1):103-8. doi: 10.1016/0028-3908(94)90103-1.
The selective glutamate metabotropic receptor agonist (1S,3R)-1-aminocyclopentane-1,3-dicarboxylic acid (1S,3R-ACPD) was applied iontophoretically to cells in the rat primary somatosensory cortex (SI) in vivo. In contrast to other in vivo studies, distinct excitatory and depressant effects were observed. The excitatory responses could not be blocked by ionotropic antagonists, as evidence that they were mediated by a metabotropic receptor. The depressant effects were most pronounced on natural synaptic transmission, suggesting that a presynaptic receptor may be involved, although responses to iontophoretically applied agonists were also affected. Comparison with the presumed presynaptic glutamate receptor agonist L-2-amino-4-phosphonobutyrate (L-AP4) suggest that the depressant effects of 1S,3R-ACPD could be partially mediated by a presynaptic autoreceptor.
将选择性代谢型谷氨酸受体激动剂(1S,3R)-1-氨基环戊烷-1,3-二羧酸(1S,3R-ACPD)通过离子电泳法应用于活体大鼠初级体感皮层(SI)的细胞。与其他体内研究不同,观察到了明显的兴奋和抑制作用。离子型拮抗剂无法阻断兴奋反应,这证明它们是由代谢型受体介导的。抑制作用在自然突触传递中最为明显,这表明可能涉及突触前受体,尽管对离子电泳施加的激动剂的反应也受到了影响。与假定的突触前谷氨酸受体激动剂L-2-氨基-4-膦酰丁酸(L-AP4)的比较表明,1S,3R-ACPD的抑制作用可能部分由突触前自身受体介导。