Doré S, Kar S, Rowe W, Quirion R
Douglas Hospital Research Centre, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Neuroscience. 1997 Oct;80(4):1033-40. doi: 10.1016/s0306-4522(97)00154-1.
The insulin-like growth factors (IGF-I and IGF-II) and insulin are localized within distinct brain regions and their respective functions are mediated by specific membrane receptors. High densities of binding sites for these growth factors are discretely and differentially distributed throughout the brain, with prominent levels localized to the hippocampal formation. IGFs and insulin, in addition to their growth promoting actions, are considered to play important roles in the development and maintenance of normal cell functions throughout life. We compared the anatomical distribution and levels of IGF and insulin receptors in young (five month) and aged (25 month) memory-impaired and memory-unimpaired male Long Evans rats as determined in the Morris water maze task in order to determine if alterations in IGF and insulin activity may be related to the emergence of cognitive deficits in the aged memory-impaired rat. In the hippocampus, [125I]IGF-I receptors are concentrated primarily in the dentate gyrus (DG) and the CA3 sub-field while high amounts of [125I]IGF-II binding sites are localized to the pyramidal cell layer, and the granular cell layer of the DG. [125I]insulin binding sites are mostly found in the molecular layer of the DG and the CA1 sub-field. No significant differences were found in [125I]IGF-I. [125I]IGF-II or [125I]insulin binding levels in any regions or laminae of the hippocampus of young vs aged rats. and deficits in cognitive performance did not relate to altered levels of these receptors in aged memory-impaired vs aged memory-unimpaired rats. Other regions. including various cortical areas, were also examined and failed to reveal any significant differences between the three groups studied. It thus appears that IGF-I, IGF-II and insulin receptor sites are not markedly altered during the normal ageing process in the Long Evans rat, in spite of significant learning deficits in a sub-group (memory-impaired) of aged animals. Hence. recently reported changes in IGF-I receptor messenger RNA levels in aged memory-impaired rats are apparently not reflected at the level of the translated protein.
胰岛素样生长因子(IGF-I和IGF-II)及胰岛素定位于不同的脑区,它们各自的功能由特定的膜受体介导。这些生长因子的高密度结合位点在全脑呈离散性和差异性分布,其中海马结构中的水平尤为突出。IGF和胰岛素除了具有促进生长的作用外,还被认为在整个生命过程中正常细胞功能的发育和维持中发挥重要作用。我们比较了年轻(5个月)和老年(25个月)的记忆受损和记忆未受损雄性Long Evans大鼠中IGF和胰岛素受体的解剖分布及水平,这些大鼠在莫里斯水迷宫任务中的表现用于确定IGF和胰岛素活性的改变是否可能与老年记忆受损大鼠认知缺陷的出现有关。在海马中,[125I]IGF-I受体主要集中在齿状回(DG)和CA3亚区,而大量的[125I]IGF-II结合位点定位于锥体细胞层和DG的颗粒细胞层。[125I]胰岛素结合位点大多见于DG的分子层和CA1亚区。在年轻大鼠与老年大鼠海马的任何区域或层中,[125I]IGF-I、[125I]IGF-II或[125I]胰岛素的结合水平均未发现显著差异。而且,老年记忆受损大鼠与老年记忆未受损大鼠相比,认知能力的缺陷与这些受体水平的改变无关。还检查了包括不同皮质区域在内的其他区域,未发现所研究的三组之间有任何显著差异。因此,尽管老年动物亚组(记忆受损)存在明显的学习缺陷,但在Long Evans大鼠的正常衰老过程中,IGF-I、IGF-II和胰岛素受体位点并未明显改变。因此,最近报道的老年记忆受损大鼠中IGF-I受体信使RNA水平的变化显然未在翻译后的蛋白质水平得到体现。