Grassi S, Francescangeli E, Goracci G, Pettorossi V E
Institute of Human Physiology, University of Perugia, Italy.
Neuroscience. 1999;94(2):549-59. doi: 10.1016/s0306-4522(99)00284-5.
In rat brainstem slices, we investigated the interaction between platelet-activating factor and group I metabotropic glutamate receptors in mediating long-term potentiation within the medial vestibular nuclei. We analysed the N1 field potential wave evoked in the ventral portion of the medial vestibular nuclei by primary vestibular afferent stimulation. The group I metabotropic glutamate receptor antagonist, (R,S)-1-aminoindan-1,5-dicarboxylic acid, prevented long-term potentiation induced by a platelet-activating factor analogue [1-O-hexadecyl-2-O-(methylcarbamyl)-sn-glycero-3-phosphocholine], as well as the full development of potentiation, induced by high-frequency stimulation under the blocking agent for synaptosomal platelet-activating factor receptors (ginkolide B), at drug washout. However, potentiation directly induced by the group I glutamate metabotropic receptor agonist, (R,S)-3,5-dihydroxyphenylglycine, was reduced by ginkolide B. These findings suggest that platelet-activating factor, whether exogenous or released following potentiation induction, exerts its effect through presynaptic group I metabotropic glutamate receptors, mediating the increase of glutamate release. In addition, we found that this mechanism, which led to full potentiation through presynaptic group I metabotropic glutamate receptor activation, was inactivated soon after application of potentiation-inducing stimulus. In fact, the long-lasting block of the platelet-activating factor and metabotropic glutamate receptors prevented the full potentiation development and the induced potentiation progressively declined to null. Moreover, ginkolide B, given when high-frequency-dependent potentiation was established, only reduced it within 5 min after potentiation induction. We conclude that to fully develop vestibular long-term potentiation requires presynaptic events. Platelet-activating factor, released after the activation of postsynaptic mechanisms which induce potentiation, is necessary for coupling postsynaptic and presynaptic phenomena, through the activation of group I metabotropic glutamate receptors, and its action lasts only for a short period. If this coupling does not occur, a full and long-lasting potentiation cannot develop.
在大鼠脑干切片中,我们研究了血小板活化因子与I组代谢型谷氨酸受体之间的相互作用,该相互作用介导了内侧前庭核内的长时程增强。我们分析了初级前庭传入刺激在内侧前庭核腹侧部分诱发的N1场电位波。I组代谢型谷氨酸受体拮抗剂(R,S)-1-氨基茚满-1,5-二羧酸可阻止血小板活化因子类似物[1-O-十六烷基-2-O-(甲基氨基甲酰基)-sn-甘油-3-磷酸胆碱]诱导的长时程增强,以及在突触体血小板活化因子受体阻断剂(银杏内酯B)存在下,高频刺激在药物洗脱时诱导的增强的完全发展。然而,I组谷氨酸代谢型受体激动剂(R,S)-3,5-二羟基苯甘氨酸直接诱导的增强被银杏内酯B减弱。这些发现表明,血小板活化因子,无论是外源性的还是在增强诱导后释放的,都通过突触前I组代谢型谷氨酸受体发挥作用,介导谷氨酸释放的增加。此外,我们发现,这种通过突触前I组代谢型谷氨酸受体激活导致完全增强的机制,在施加增强诱导刺激后很快就失活了。事实上,血小板活化因子和代谢型谷氨酸受体的长期阻断阻止了完全增强的发展,诱导的增强逐渐下降至零。此外,在高频依赖性增强建立后给予银杏内酯B,仅在增强诱导后5分钟内将其减弱。我们得出结论,要使前庭长时程增强完全发展需要突触前事件。在诱导增强的突触后机制激活后释放的血小板活化因子,对于通过激活I组代谢型谷氨酸受体来耦合突触后和突触前现象是必要的,并且其作用仅持续短时间。如果这种耦合不发生,就无法发展出完全且持久的增强。