Naie Katja, Gundimi Sabine, Siegmund Herbert, Heinemann Uwe, Manahan-Vaughan Denise
Synaptic Plasticity Research Group, Johannes Mueller Institute for Physiology, Charité, Berlin, Germany.
Eur J Pharmacol. 2006 Mar 27;535(1-3):104-13. doi: 10.1016/j.ejphar.2006.01.030. Epub 2006 Mar 20.
In vivo, activation of group III metabotropic glutamate (mGlu) receptors leads to a reduction of basal synaptic transmission in the hippocampus, and depending on the experimental conditions in vitro, leads to neuroprotection or neurotoxicity. Here, the cellular response to cerebral application of L(+)-2-amino-4-phosphonobutanoic acid (AP4) was investigated in the CA1 region and dentate gyrus of freely moving rats. Drugs were applied via the lateral ventricle, and electrophysiological measurements were obtained via chronically implanted electrodes. AP4 produced a slowly developing depression of evoked responses in both hippocampal regions which lasted for over 4 h. Effects could be reversed by application of high frequency tetanus. Histological evaluation, 4 h or 7 d, following a single, acute AP4 injection into the lateral cerebral ventricle showed that AP4-mediated synaptic depression either amplified (CA1) or attenuated (dentate gyrus) excitotoxic neuronal death, strongly depending on the sub-region investigated. Effects were long-lasting, being still evident 7 days after AP4 application. In both hippocampal areas, the effects obtained were subtle, however, with the CA1 region being more potently affected. Interestingly, effects in the dentate gyrus comprised a slight enhancement of live cell number coupled with deterioration in cell area, suggesting that cell proliferation triggered by group III mGlu receptor activation may have masked neurotoxic effects mediated by activation of this receptor. These results show that although AP4 induces a slow-onset synaptic depression in both sub-regions, cell viability is differentially influenced by activation of group III mGlu receptors in the CA1 region and dentate gyrus.
在体内,III组代谢型谷氨酸(mGlu)受体的激活会导致海马体基础突触传递的减少,并且根据体外实验条件的不同,会导致神经保护或神经毒性。在此,研究了自由活动大鼠的CA1区和齿状回对脑内应用L(+)-2-氨基-4-膦酰丁酸(AP4)的细胞反应。药物通过侧脑室给药,并通过长期植入的电极进行电生理测量。AP4在两个海马区均产生了缓慢发展的诱发反应抑制,持续超过4小时。高频强直刺激可逆转这种效应。单次急性向侧脑室注射AP4后4小时或7天的组织学评估表明,AP4介导的突触抑制要么放大(CA1区)要么减弱(齿状回)兴奋性毒性神经元死亡,这在很大程度上取决于所研究的亚区域。效应具有持久性,在应用AP4 7天后仍很明显。在两个海马区获得的效应都很细微,然而,CA1区受影响更明显。有趣的是,齿状回的效应包括活细胞数量略有增加以及细胞面积恶化,这表明III组mGlu受体激活引发的细胞增殖可能掩盖了该受体激活介导的神经毒性作用。这些结果表明,尽管AP4在两个亚区域均诱导了缓慢起效的突触抑制,但CA1区和齿状回中III组mGlu受体的激活对细胞活力的影响存在差异。