Stripling J S, Patneau D K
Department of Psychology, University of Arkansas, Fayetteville 72701, USA.
Brain Res. 1999 Sep 11;841(1-2):27-42. doi: 10.1016/s0006-8993(99)01765-5.
Previous research has demonstrated that repeated high-frequency stimulation of the granule cell layer of the olfactory bulb (OB) produces an enduring potentiation of late components (PLC) in potentials evoked in the OB and piriform cortex (PC), while leaving the monosynaptic EPSP produced by OB mitral cells in PC pyramidal cells unaltered. Two experiments were conducted using male Long-Evans rats with chronically implanted electrodes to assess the relative contribution to this potentiation of the two main fiber systems that interconnect the OB and PC: the lateral olfactory tract (LOT), which contains mitral cell axons that synapse on PC pyramidal cells, and the PC association fiber system, which consists of the axons of PC pyramidal cells that synapse on several cell populations within the PC and on granule cells in the OB. The results indicate that stimulation of PC association fibers is both necessary and sufficient to duplicate the pattern of potentiation seen following OB stimulation in previous experiments. LOT stimulation had no consistent effect, and coactivation of the LOT and PC association fibers was no more effective than activation of PC association fibers alone. Possible mechanisms underlying this effect are discussed, including (1) long-term potentiation (LTP) at synapses made by the axons of PC pyramidal cells on neurons in the OB and PC; and (2) repetitive firing in PC pyramidal cells due to regenerative excitation in a population of deep cells in the PC and endopiriform nucleus.
先前的研究表明,反复高频刺激嗅球(OB)颗粒细胞层会使OB和梨状皮质(PC)诱发电位中的晚期成分(PLC)产生持久增强,而PC锥体细胞中OB二尖瓣细胞产生的单突触兴奋性突触后电位(EPSP)则保持不变。使用长期植入电极的雄性Long-Evans大鼠进行了两项实验,以评估连接OB和PC的两个主要纤维系统对这种增强作用的相对贡献:外侧嗅束(LOT),其包含与PC锥体细胞形成突触的二尖瓣细胞轴突;以及PC联合纤维系统,其由PC锥体细胞的轴突组成,这些轴突与PC内的几个细胞群以及OB中的颗粒细胞形成突触。结果表明,刺激PC联合纤维对于复制先前实验中OB刺激后所见的增强模式既必要又充分。LOT刺激没有一致的效果,并且LOT和PC联合纤维的共同激活并不比单独激活PC联合纤维更有效。讨论了这种效应潜在的可能机制,包括:(1)PC锥体细胞轴突与OB和PC中神经元形成的突触处的长时程增强(LTP);以及(2)由于PC和内梨状核中一群深层细胞的再生性兴奋导致PC锥体细胞的重复放电。