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隔离饲养的大鼠前额叶皮质中的吊灯状小体减少。

Chandelier cartridges in the prefrontal cortex are reduced in isolation reared rats.

作者信息

Bloomfield Claire, French Sarah J, Jones Declan N C, Reavill Charlie, Southam Eric, Cilia Jackie, Totterdell Susan

机构信息

Department of Pharmacology, University of Oxford, Oxford OX1 3QT, UK.

出版信息

Synapse. 2008 Aug;62(8):628-31. doi: 10.1002/syn.20521.

Abstract

Chandelier neurons are a subset of parvalbumin containing cortical interneurons characterised by their preferential targeting of the axon initial segments of pyramidal neurons. They have been the focus of recent interest after evidence that the arrays of boutons are reduced in the prefrontal cortex of schizophrenic patients, post mortem. Since one chandelier neuron may innervate the axon initial segments of several hundred pyramidal neurons, it is hypothesized that their special connectivity might facilitate synchronisation of cortical outputs and play a key role in working memory. Disruption in their function is therefore thought to play a potentially important role in cortically associated symptoms of schizophrenia. Using the isolation rearing animal model of schizophrenia, we examined immunolabelling for GABA-transporter 1, a marker of chandelier cartridges. We show that the numbers of arrays of chandelier axons are reduced by 36% in the ventral prelimbic cortex of isolation-reared rats, compared with their socially-housed litter mates. This mimics findings in the PFC of schizophrenic patients where GAT-1-positive cartridges are reduced by 40% and is the first study to demonstrate changes in chandelier cartridges in an animal model of schizophrenia.

摘要

吊灯神经元是含有小白蛋白的皮质中间神经元的一个子集,其特征在于它们优先靶向锥体细胞的轴突起始段。在死后证据表明精神分裂症患者前额叶皮质中终扣阵列减少之后,它们成为了近期研究的焦点。由于一个吊灯神经元可能支配数百个锥体细胞的轴突起始段,因此推测它们特殊的连接方式可能有助于皮质输出的同步,并在工作记忆中起关键作用。因此,其功能的破坏被认为在精神分裂症的皮质相关症状中可能起重要作用。利用精神分裂症的隔离饲养动物模型,我们检测了作为吊灯神经元终扣标记物的γ-氨基丁酸转运体1的免疫标记。我们发现,与群居的同窝大鼠相比,隔离饲养大鼠腹侧前扣带回皮质中吊灯轴突终扣阵列的数量减少了36%。这与精神分裂症患者前额叶皮质中γ-氨基丁酸转运体1阳性终扣减少40%的发现相似,并且这是第一项在精神分裂症动物模型中证明吊灯神经元终扣发生变化的研究。

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