Chrachri Abdesslam, Williamson Roddy
Department of Biological Sciences, University of Plymouth, Portland Square, Drake Circus, Plymouth PL4 8AA, UK.
Brain Res. 2004 Sep 10;1020(1-2):178-87. doi: 10.1016/j.brainres.2004.06.027.
Spontaneous excitatory postsynaptic currents (sEPSCs) were recorded from two different classes of neurons in the optic lobes of the cuttlefish brain and their synaptic activities analyzed and compared. The cell types were as follows: efferent centrifugal neurons, with cell bodies in the inner granule layer and axons projecting to the retina, and interneurons local to the medulla. For both neuronal groups, the sEPSCs reversal potentials were around 0 mV and there were no significant differences in their mean amplitude and rise times. However, the sEPSCs from the centrifugal neurons had a significantly higher frequency and faster decay time constant than those recorded from the medulla. Tetrodotoxin (TTX) reduced the mean frequency of the sEPSCs from both the medulla and centrifugal neurons by 69.66 +/- 4.05% and 57.80 +/- 3.87%, respectively, implying that more than half of these excitatory synaptic inputs were due to action potential-mediated release of neurotransmitter. Pharmacological examination revealed that the centrifugal neurons were driven by spontaneous synaptic inputs mediated by glutamatergic and cholinergic receptors, because co-application of the glutamate antagonist kynurenic acid (KYNA) and the nicotinic antagonist mecamylamine hydrochloride (MCM) resulted in complete blockade of these excitatory inputs. For the medulla neurons, the synaptic inputs were driven by glutamate and other transmitters yet to be identified. Evoked EPSCs (eEPSCs) were recorded from both types of neurons by stimulating the appropriate optic nerve bundles; in centrifugal neurons, the eEPSCs were blocked by co-application of KYNA and MCM, whereas in the medulla neurons, KYNA alone either totally or partially blocked the eEPSCs.
在乌贼脑视叶中,从两类不同的神经元记录了自发性兴奋性突触后电流(sEPSCs),并对它们的突触活动进行了分析和比较。细胞类型如下:传出离心神经元,其细胞体位于内颗粒层,轴突投射到视网膜,以及髓质局部的中间神经元。对于这两类神经元,sEPSCs的反转电位均约为0 mV,其平均幅度和上升时间没有显著差异。然而,离心神经元的sEPSCs频率显著更高,衰减时间常数更快,比从髓质记录到的sEPSCs更快。河豚毒素(TTX)分别将髓质和离心神经元的sEPSCs平均频率降低了69.66±4.05%和57.80±3.87%,这意味着这些兴奋性突触输入中超过一半是由动作电位介导的神经递质释放引起的。药理学检查表明,离心神经元由谷氨酸能和胆碱能受体介导的自发性突触输入驱动,因为谷氨酸拮抗剂犬尿喹啉酸(KYNA)和烟碱拮抗剂盐酸美加明(MCM)共同应用导致这些兴奋性输入完全被阻断。对于髓质神经元,突触输入由谷氨酸和其他尚未确定的递质驱动。通过刺激适当的视神经束,从这两类神经元记录诱发的兴奋性突触后电流(eEPSCs);在离心神经元中,eEPSCs被KYNA和MCM共同应用阻断,而在髓质神经元中,单独使用KYNA可完全或部分阻断eEPSCs。