Kelly A, Maguire C, Lynch M A
Department of Physiology, Trinity College, Dublin, Ireland.
Neuroscience. 2000;95(2):359-65. doi: 10.1016/s0306-4522(99)00460-1.
Previous findings have indicated that nerve growth factor may play a role in the expression of long-term potentiation in perforant path-granule cell synapses and that nerve growth factor treatment restores the ability of aged rats to sustain long-term potentiation. In this study, we have attempted to analyse the changes which occur in nerve growth factor release and tyrosine receptor kinase phosphorylation following tetanization in tissue prepared from dentate gyrus of young rats, as well as aged rats which did or did not sustain long-term potentiation. We report that KCl-stimulated nerve growth factor release was significantly increased in slices of the dentate gyrus or whole hippocampus, but not in synaptosomes prepared from the dentate gyrus. KCl-induced nerve growth factor release was also significantly enhanced in slices prepared from tetanized, compared with untetanized, tissue obtained from young rats and aged rats which sustained long-term potentiation; this response was absent in tissue prepared from aged rats which failed to sustain long-term potentiation, perhaps due to the enhanced basal nerve growth factor release observed in this tissue. Tetanization increased tyrosine receptor kinase phosphorylation in the dentate gyrus of young rats and aged rats which sustained long-term potentiation. In parallel with the changes in nerve growth factor release, tyrosine receptor kinase phosphorylation was markedly increased in untetanized tissue, which may contribute to the lack of effect in tetanized tissue prepared from aged rats which failed to sustain long-term potentiation. We observed that nerve growth factor concentration and tyrosine receptor kinase expression were decreased in aged, compared with young, rats. The data suggest that deficits in nerve growth factor release and subsequent signalling may contribute to age-related deficits in long-term potentiation.
先前的研究结果表明,神经生长因子可能在穿通通路-颗粒细胞突触的长时程增强表达中发挥作用,并且神经生长因子治疗可恢复老年大鼠维持长时程增强的能力。在本研究中,我们试图分析在年轻大鼠以及经历或未经历长时程增强的老年大鼠齿状回制备的组织中,强直刺激后神经生长因子释放和酪氨酸受体激酶磷酸化所发生的变化。我们报告称,KCl刺激的神经生长因子释放在齿状回切片或整个海马中显著增加,但在从齿状回制备的突触体中未增加。与未强直刺激的组织相比,在经历强直刺激的年轻大鼠和经历长时程增强的老年大鼠所获得的组织制备的切片中,KCl诱导的神经生长因子释放也显著增强;在未经历长时程增强的老年大鼠所制备的组织中未出现这种反应,这可能是由于在该组织中观察到基础神经生长因子释放增加所致。强直刺激增加了经历长时程增强的年轻大鼠和老年大鼠齿状回中的酪氨酸受体激酶磷酸化。与神经生长因子释放的变化并行,未强直刺激的组织中酪氨酸受体激酶磷酸化显著增加,这可能导致在未经历长时程增强的老年大鼠强直刺激组织中缺乏效应。我们观察到,与年轻大鼠相比,老年大鼠的神经生长因子浓度和酪氨酸受体激酶表达降低。数据表明,神经生长因子释放及后续信号传导的缺陷可能导致与年龄相关的长时程增强缺陷。