Manahan-Vaughan D
Leibniz Institute for Neurobiology, Department of Neurophysiology, Magdeburg, Germany.
Neuropharmacology. 1998 Dec;37(12):1459-64. doi: 10.1016/s0028-3908(98)00150-6.
Activation of group 1 metabotropic glutamate receptors (mGluRs) has been shown to facilitate the induction of tetanically evoked long-term potentiation in vivo, whereas group 2 mGluR antagonists inhibit long-term depression (LTD) in the CA1 region. LTD has not been successfully demonstrated to date in the dentate gyrus of freely moving rats. In this study, it was found that 1-Hz low-frequency stimulation (LFS) when applied via a stimulating electrode chronically implanted in the perforant path, evoked short-term depression (STD) of field excitatory post-synaptic potentials and population spikes measured from the dentate gyrus granule cell layer. Application of the group 2 mGluR agonists (S)-4-carboxyphenylglycine (4C3HPG) or (2S,2'R,3'R)-2-(2',3'-dicarboxycyclopropyl)glycine (DCG-IV) prior to LFS facilitated the expression of LTD. Application of the group 2 mGluR antagonist (2S)-alpha-ethylglutamic acid (EGLU) prior to agonist application prevented the facilitating effect of the agonists on LFS-induced depression. EGLU did not influence the expression of LFS-induced STD. Neither 4C3HPG, DCG-IV nor EGLU had an effect on basal synaptic transmission at the concentrations used. The present study demonstrates that priming of group 2 mGluRs leads to induction of persistent LTD in the dentate gyrus in vivo, consistent with a role for group 2 mGluRs in metaplasticity.
已表明,激活第1组代谢型谷氨酸受体(mGluRs)可促进体内强直刺激诱发的长时程增强的诱导,而第2组mGluR拮抗剂可抑制CA1区的长时程抑制(LTD)。迄今为止,在自由活动大鼠的齿状回中尚未成功证明LTD。在本研究中,发现当通过长期植入穿通路径的刺激电极施加1赫兹低频刺激(LFS)时,可诱发齿状回颗粒细胞层记录到的场兴奋性突触后电位和群体峰电位的短时程抑制(STD)。在LFS之前应用第2组mGluR激动剂(S)-4-羧基苯基甘氨酸(4C3HPG)或(2S,2'R,3'R)-2-(2',3'-二羧基环丙基)甘氨酸(DCG-IV)可促进LTD的表达。在应用激动剂之前应用第2组mGluR拮抗剂(2S)-α-乙基谷氨酸(EGLU)可阻止激动剂对LFS诱导的抑制的促进作用。EGLU不影响LFS诱导的STD的表达。在所使用的浓度下,4C3HPG、DCG-IV和EGLU对基础突触传递均无影响。本研究表明,第2组mGluRs的预激活可导致体内齿状回中持续性LTD的诱导,这与第2组mGluRs在突触可塑性中的作用一致。