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首页> 外文期刊>Age. >Old-onset caloric restriction effects on neuropeptide Y- and somatostatin-containing neurons and on cholinergic varicosities in the rat hippocampal formation
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Old-onset caloric restriction effects on neuropeptide Y- and somatostatin-containing neurons and on cholinergic varicosities in the rat hippocampal formation

机译:热量限制对大鼠海马形成中神经肽Y和生长抑素的神经元以及胆碱能静脉曲张的新发热量限制作用

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Abstract Caloric restriction is able to delay age-related neurodegenerative diseases and cognitive impairment. In this study, we analyzed the effects of old-onset caloric restriction that started at 18 months of age, in the number of neuropeptide Y (NPY)- and somatostatin (SS)-contain-ing neurons of the hippocampal formation. Knowing that these neuropeptidergic systems seem to be dependent of the cholinergic system, we also analyzed the number of cholinergic varicosities. Animals with 6 months of age (adult controls) and with 18 months of age were used. The animals aged 18 months were randomly assigned to controls or to caloric-restricted groups. Adult and old control rats were maintained in the ad libitum regimen during / 6 months. Caloric-restricted rats were fed, during 6 months, with 60 % of the amount of food consumed by controls. We found that aging induced a reduction of the total number of NPY- and SS-positive neurons in the hippocampal formation accompanied by a decrease of the cholinergic varicosities. Conversely, the 24-month-old-onset caloric-restricted animals maintained the number of those peptidergic neurons and the density of the cholinergic varicosities similar to the 12-month control rats. These results suggest that the aging-associated reduction of these neuropeptide-expressing neurons is not due to neuronal loss and may be dependent of the cholinergic system. More importantly, caloric restriction has beneficial effects in the NPY- and SS-expressing neurons and in the cholinergic system, even when applied in old age.
机译:摘要热量限制能够延缓与年龄有关的神经退行性疾病和认知障碍。在这项研究中,我们分析了从18个月大时开始的旧发热量限制对海马形成的神经肽Y(NPY)和生长抑素(SS)神经元数量的影响。知道这些神经肽能系统似乎依赖于胆碱能系统,我们还分析了胆碱能静脉曲张的数量。使用6个月龄(成年对照)和18个月龄的动物。将18个月大的动物随机分为对照组或热量限制组。成年和老对照组大鼠在6个月内保持随意治疗。限制热量的大鼠在6个月内接受了对照所消耗食物量的60%。我们发现衰老引起海马结构中NPY和SS阳性神经元总数的减少,同时胆碱能静脉曲张减少。相反,与12个月的对照组相比,发病24个月的受热量限制的动物保持了这些肽能神经元的数量和胆碱能静脉曲张的密度。这些结果表明,这些表达神经肽的神经元与衰老相关的减少不是由于神经元丢失,可能与胆碱能系统有关。更重要的是,热量限制在表达NPY和SS的神经元以及胆碱能系统中也具有有益的作用,即使在老年时也是如此。

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