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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Brain-derived neurotrophic factor increases inhibitory synapses, revealed in solitary neurons cultured from rat visual cortex.
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Brain-derived neurotrophic factor increases inhibitory synapses, revealed in solitary neurons cultured from rat visual cortex.

机译:脑源性神经营养因子增加抑制性突触,在从大鼠视皮层培养的孤立神经元中发现。

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To elucidate chronic actions of brain-derived neurotrophic factor (BDNF) on GABAergic synapses, we examined effects of a long-term application of BDNF for 10-15 days on autapses (synapses) of solitary GABAergic neurons cultured from rat visual cortex. Solitary neuron preparations were used to exclude a possible contamination of BDNF actions on excitatory neurons in dissociated neuron culture or slice preparations. Neurons were confirmed to be GABAergic pharmacologically with bicuculline, a selective antagonist for GABAA receptors and immunocytochemically with antibody against glutamic acid decarboxylase 65, a GABA synthesizing enzyme. To evaluate GABAergic synaptic function, evoked and/or miniature inhibitory postsynaptic currents (IPSCs) were recorded in the whole-cell voltage-clamp mode. The treatment with BDNF at a concentration of 100 ng/ml enhanced the amplitude of evoked IPSCs and the frequency of miniature IPSCs. In contrast, BDNF did not have a detectable effect on the amplitude of miniature IPSCs and the paired pulse ratio of IPSCs evoked by two, successive activations. To evaluate morphological changes, neurons were immunocytochemically stained with antibodies against microtubule-associated protein 2, to visualize somatodendritic region and synapsin I, to visualize presynaptic sites. The quantitative analysis indicated that BDNF increased the area of soma, the numbers of primary dendrites and dendritic branching points, the total length of dendrites and the number of synaptic sites. Such an action of BDNF was seen in both subgroups of GABAergic neurons, parvalbumin-positive and -negative neurons. To visualize functionally active presynaptic sites, neurons were stained with a styryl dye, FM1-43. BDNF increased the number of stained sites that was correlated with the frequency of miniature IPSCs. These results suggest that the chronic treatment with BDNF promotes dendritic and synaptic development of GABAergic neurons in visual cortex.
机译:为了阐明脑源性神经营养因子(BDNF)对GABA能突触的慢性作用,我们研究了长期应用BDNF 10-15天对从大鼠视皮层培养的孤立GABA能神经元的突触(突触)的影响。在分离的神经元培养物或切片制剂中,单独的神经元制剂用于排除BDNF作用于兴奋性神经元的可能污染。在药理学上,神经元与双瓜氨酸(一种GABAA受体的选择性拮抗剂)在药理学上被证实,并且在抗谷氨酸脱羧酶65(一种GABA合成酶)的抗体上免疫细胞化学。为了评估GABA能的突触功能,以全细胞电压钳模式记录诱发和/或微型抑制性突触后电流(IPSC)。浓度为100 ng / ml的BDNF处理可增强诱发的IPSC的幅度和微型IPSC的频率。相比之下,BDNF对微型IPSC的幅度和两次连续激活所引起的IPSC的成对脉冲比没有可检测的影响。为了评估形态学变化,用针对微管相关蛋白2的抗体对神经元进行免疫细胞化学染色,以观察躯体树突区域和突触蛋白I,以观察突触前位点。定量分析表明,BDNF增加了体细胞的面积,初级树突的数量和树突分支点,树突的总长度以及突触位点的数量。 BDNF的这种作用在GABA能神经元,小白蛋白阳性和阴性神经元两个亚组中均可见。为了可视化功能活跃的突触前位点,神经元用苯乙烯基染料FM1-43染色。 BDNF增加了染色位点的数量,其与微型IPSC的频率相关。这些结果表明,BDNF的慢性治疗促进了视觉皮层中GABA能神经元的树突和突触发育。

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