首页> 美国卫生研究院文献>The Journal of Neuroscience >Pairing the cholinergic agonist carbachol with patterned Schaffer collateral stimulation initiates protein synthesis in hippocampal CA1 pyramidal cell dendrites via a muscarinic NMDA-dependent mechanism
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Pairing the cholinergic agonist carbachol with patterned Schaffer collateral stimulation initiates protein synthesis in hippocampal CA1 pyramidal cell dendrites via a muscarinic NMDA-dependent mechanism

机译:将胆碱能激动剂卡巴胆碱与模式化的Schaffer侧支刺激配对通过毒蕈碱型NMDA依赖性机制启动海马CA1锥体细胞树突中的蛋白质合成。

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摘要

Effects of afferent stimulation on local synthesis of protein in CA1 pyramidal cell dendrites were studied using light microscope autoradiography. Tissue was fixed with paraformaldehyde immediately after 3 min exposure to 3H-leucine in order to trap 3H associated with macromolecules. The rate of 3H-leucine incorporation into dendrites of resting hippocampal slices was 10% the rate of incorporation into cell somata. Ninety percent of the incorporation into the somata was inhibited by cycloheximide (300 microM); none of the incorporation into dendrites was blocked by cycloheximide. Thus, there is no measurable extramitochondrial synthesis of protein in the dendrites of the resting slice. Slices were exposed to 50 microM carbachol and the Schaffer collateral afferents to the CA1 pyramidal cells were stimulated intermittently at 10 Hz over a 20 min period. In this case, 3H incorporation into dendrites was increased almost threefold over resting levels, with no effect on label over the cell somata. There was no associated increase in uptake of free 3H-leucine, and the increase in label was completely blocked by cycloheximide. Thus, associating carbachol and afferent stimulation appears to activate de novo protein synthesis in the dendrites. Neither the carbachol alone nor the Schaffer collateral stimulation alone increased synthesis. The activation of dendrite synthesis was completely blocked by 5 microM atropine, and also by 50 microM D-aminophosphonovalerate. It did not occur when carbachol was paired with steady stimulation of the Schaffer collaterals at 1 Hz for 20 min, rather than with the patterned high- frequency stimulation. Thus, associating a cholinergic agonist with a level of neural activity that occurs in CA3 and CA1 pyramidal cells during exploratory behavior (Muller et al., 1987) initiates local protein synthesis in target dendrites. This effect is dependent on muscarinic cholinergic receptors and NMDA-type glutamate receptors. The possible relationship of this phenomenon to mechanisms of learning is discussed.
机译:使用光学显微镜放射自显影技术研究传入刺激对CA1锥体细胞树突中蛋白质局部合成的影响。暴露于3H-亮氨酸3分钟后立即用低聚甲醛固定组织,以捕获与大分子相关的3H。 3H-亮氨酸掺入静息海马切片的树突中的比率是掺入细胞体细胞中的比率的10%。环己酰亚胺(300 microM)抑制了90%的结合到躯体中。并没有被环己酰亚胺阻止并入树枝状晶体。因此,在静止切片的树突中没有可测量的线粒体蛋白质合成。将切片暴露于50 microM的卡巴胆碱中,并在20分钟的时间内以10 Hz的频率间歇刺激到CA1锥体细胞的Schaffer侧支传入。在这种情况下,树突中的3H掺入量比静止水平增加了近三倍,而对细胞体细胞的标记没有影响。游离3H-亮氨酸的摄取没有相关的增加,并且标记的增加被环己酰亚胺完全阻止了。因此,将卡巴胆碱和传入刺激相关联似乎激活了树突中的从头蛋白质合成。单独的卡巴胆碱或单独的Schaffer侧支刺激均不能增加合成。 5 microM阿托品和50 microM D-氨基膦酸戊酸酯完全阻止了枝晶合成的激活。当卡巴胆碱与Schaffer侧支以1 Hz持续刺激20分钟,而不是与模式化的高频刺激配对时,则不会发生这种情况。因此,在探索行为期间,将胆碱能激动剂与在CA3和CA1锥体细胞中发生的神经活动水平相关联(Muller等人,1987),启动了目标树突中的局部蛋白质合成。此作用取决于毒蕈碱胆碱能受体和NMDA型谷氨酸受体。讨论了这种现象与学习机制的可能关系。

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