...
首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >The diurnal rhythm of adenosine levels in the basal forebrain of young and old rats.
【24h】

The diurnal rhythm of adenosine levels in the basal forebrain of young and old rats.

机译:幼年和老年大鼠基底前脑中腺苷水平的昼夜节律。

获取原文
获取原文并翻译 | 示例

摘要

There are significant decrements in sleep with age. These include fragmentation of sleep, increased wake time, decrease in the length of sleep bouts, decrease in the amplitude of the diurnal rhythm of sleep, decrease in rapid eye movement sleep and a profound decrease in electroencephalogram Delta power (0.3-4 Hz). Old rats also have less sleep in response to 12 h-prolonged wakefulness (W) indicating a reduction in sleep drive with age. The mechanism contributing to the decline in sleep with aging is not known but cannot be attributed to loss of neurons implicated in sleep since the numbers of neurons in the ventral lateral preoptic area, a region implicated in generating sleep, is similar between young (3.5 months) and old (21.5 months) rats. One possibility for the reduced sleep drive with age is that sleep-wake active neurons may be stimulated less as a result of a decline in endogenous sleep factors. Here, we test this hypothesis by focusing on the purine, adenosine (AD), one such sleep factor thatincreases after prolonged W. In experiment 1, microdialysis measurements of AD in the basal forebrain at 1 h intervals reveal that old (21.5 months) rats have more extracellular levels of AD compared with young rats across the 24 h diurnal cycle. In experiment 2, old rats kept awake for 6 h (first half of lights-on period) accumulated more AD compared with young rats. If old rats have more AD then why do they sleep less? To investigate whether changes in sensitivity of the AD receptor contribute to the decline in sleep, experiments 3 and 4 determined that for the same concentration of AD or the AD receptor 1 agonist, cyclohexyladenosine, old rats have less sleep compared with young rats. We conclude that even though old rats have more AD, a reduction in the sensitivity of the AD receptor to the ligand does not transduce the AD signal at the same strength as in young rats and may be a contributing factor to the decline in sleep drive in the elderly.
机译:随着年龄的增长,睡眠会明显减少。这些包括睡眠碎片化,增加的唤醒时间,睡眠周期的减少,睡眠昼夜节律幅度的减少,快速眼动睡眠的减少以及脑电图Delta功率(0.3-4 Hz)的大幅降低。老老鼠对12小时长时间的清醒(W)的反应也较少,这表明随着年龄的增长睡眠驱动力降低。衰老导致睡眠减少的机制尚不清楚,但不能归因于与睡眠有关的神经元的丧失,因为前外侧腹侧视前区(与产生睡眠有关的区域)中的神经元数量在年轻人之间(3.5个月)相似。 )和年长(21.5个月)的老鼠。随着年龄的增长而减少睡眠驱动力的一种可能性是,由于内源性睡眠因子的减少,觉醒的活跃神经元受到的刺激可能更少。在这里,我们通过关注嘌呤,腺苷(AD)(一种在W延长后会增加的睡眠因子)来检验这一假设。在实验1中,以每1 h的间隔对基底前脑中的AD进行微透析测量显示,这只老年大鼠(21.5个月)在整个24小时的昼夜周期中,与年轻大鼠相比,AD的细胞外水平更高。在实验2中,与年轻大鼠相比,保持清醒6小时(开灯时间的前半段)的老大鼠积累了更多的AD。如果年老的老鼠有更多的AD,那么为什么他们睡得更少呢?为了研究AD受体敏感性的变化是否会导致睡眠下降,实验3和4确定,对于相同浓度的AD或AD受体1激动剂环己基腺苷,与年轻大鼠相比,老年大鼠的睡眠较少。我们得出的结论是,即使老年大鼠具有更多的AD,但AD受体对配体的敏感性下降并不会以与年轻大鼠相同的强度转导AD信号,并且可能是导致睡眠驱动力下降的一个因素。老人

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号