Eid T, Jorritsma-Byham B, Schwarcz R, Witter M P
Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, USA.
Exp Brain Res. 1996 May;109(2):209-18. doi: 10.1007/BF00231782.
Neurons in layer III of the medial entorhinal area (MEA) in the rat are extremely vulnerable to local injections of amino-oxyacetic acid and to experimentally induced limbic seizures. A comparable specific pathology has been noted in surgical specimens from patients with temporal lobe epilepsy. Efforts to understand this preferential neuronal vulnerability led us to study the neural input to this layer in the rat. Iontophoretic injection of the retrograde tracer fast blue, aimed at layer III of the MEA, resulted in retrogradely labeled neurons in the presubiculum in all the injected hemispheres. The nucleus reuniens thalami, the anteromedial thalamic nucleus, the ventral portion of the claustrum (endopiriform nucleus), the dorsomedial parts of the anteroventral thalamic nucleus, and the septum-diagonal band complex were labeled less frequently. In only one experiment, retrogradely labeled neurons were observed in the ventrolateral hypothalamus and in the brainstem nucleus raphe dorsalis. Since projections from claustrum to the entorhinal cortex has not been studied in the rat with modern sensitive anterograde tracing techniques, iontophoretic injections of the anterograde tracer Phaseolus vulgaris-leucoagglutinin were placed into the ventral portion of the claustrum. Anterogradely labeled fibers in the entorhinal area proved not to be confined to the MEA, since a prominent projection distributed to the lateral entorhinal area as well. In both areas, the densest terminal labeling was present in layers IV-VI, whereas layer III appeared to be only sparsely labeled. The present data indicate that of all potential afferents only those from the presubiculum distribute preferentially to layer III of the MEA. This, in turn, suggests a potentially important role of the presubiculum in the seizure-related degeneration of neurons in layer III of the MEA.
大鼠内侧内嗅区(MEA)III层中的神经元极易受到局部注射氨基氧乙酸以及实验性诱发的边缘叶癫痫发作的影响。在颞叶癫痫患者的手术标本中也发现了类似的特定病理情况。为了理解这种神经元的优先易损性,我们对大鼠该层的神经输入进行了研究。将逆行示踪剂快蓝离子导入注射至MEA的III层,结果在所有注射半球的前下托中均出现了逆行标记的神经元。丘脑连合核、丘脑前内侧核、屏状核(内梨状核)腹侧部分、丘脑前腹侧核背内侧部分以及隔区 - 斜角带复合体被标记的频率较低。仅在一项实验中,在腹外侧下丘脑和脑干中缝背核观察到了逆行标记的神经元。由于尚未采用现代敏感的顺行追踪技术对大鼠中屏状核到内嗅皮质的投射进行研究,因此将顺行示踪剂菜豆凝集素离子导入注射至屏状核腹侧部分。结果表明,内嗅区中顺行标记的纤维并不局限于MEA,因为有一个明显的投射也分布到了外侧内嗅区。在这两个区域中,IV - VI层的终末标记最为密集,而III层似乎仅有稀疏标记。目前的数据表明,在所有潜在的传入纤维中,只有来自前下托的纤维优先分布到MEA的III层。这反过来表明,前下托在MEA III层神经元与癫痫相关的变性过程中可能发挥重要作用。